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Background:
Systematic Review

Failure to Rescue After Surgery for Pancreatic Cancer: A Systematic Review and Narrative Synthesis of Risk Factors and Safety Strategies

1
Department of Quality and Patient Safety, Tokyo Medical University, Tokyo 160-0023, Japan
2
Section of Medical Safety Management, Tokyo Medical University Hospital, Tokyo 160-0023, Japan
3
School of Project Design, Miyagi University, Taiwa 981-3298, Japan
4
Jefferson College of Population Health, Philadelphia, PA 19107, USA
5
Sheps Health Services Research Center, University of North Carolina, Chapel Hill, NC 27599, USA
6
Department of Surgery, Imperial College, London SW7 2BX, UK
7
Department of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, Tokyo 160-0023, Japan
*
Authors to whom correspondence should be addressed.
Cancers 2025, 17(19), 3259; https://doi.org/10.3390/cancers17193259
Submission received: 11 August 2025 / Revised: 4 October 2025 / Accepted: 6 October 2025 / Published: 8 October 2025
(This article belongs to the Special Issue Novel Diagnosis and Treatment Approaches in Pancreatic Cancer)

Abstract

Simple Summary

Failure to rescue (FTR)—death after major postoperative complications—is a persistent, variable problem in pancreatic cancer surgery. The review using PRISMA 2020 checklist and flow diagram screened 83 studies (1992–2025) and included 52 studies (2010–2025) across registry, multicenter, single-center, and audit designs. Due to heterogeneity in designs and FTR definitions (in-hospital, 30/90-day, severity- and complication-specific cases), a narrative synthesis was used; no formal risk-of-bias assessment or meta-analysis was performed. FTR varied by definition: pooled rates were 13.2% for 90-day CD ≥ III (G1); 10.3% for in-hospital/30-day CD ≥ III (G3); and 7.4% for 30-day “serious/major” morbidity (G8), with G1 > G3 (+3.0 pp; RR 1.29) and G3 > G8 (+2.9 pp; RR 1.39; all p < 0.001). Five domains were consistently linked to lower FTR and improved outcomes: (i) centralization to high-volume centers; (ii) evolution of surgical techniques; (iii) optimized perioperative management (early imaging, structured escalation); (iv) patient-specific risk stratification and prehabilitation; and (v) non-technical skills (NTS) including decision-making, situational awareness, communication, teamwork, and leadership. NTS measurement was infrequent, and no study assessed stress or fatigue management. Future work should standardize pancreas-specific FTR definitions, incorporate process-level rescue metrics, and embed NTS assessments with simulation and implementation science to change and strengthen team behaviors and reduce preventable patient mortality.

Abstract

Background: Failure to rescue (FTR), defined as death after major postoperative complications, is a critical quality indicator in pancreatic cancer surgery. Despite advances in surgical techniques and perioperative care, FTR rates remain high and vary across institutions. Methods: This systematic review uses a narrative synthesis followed by PRISMA 2020. A PubMed search (1992–2025) identified 83 studies; after screening, 52 studies (2010–2025) were included. Eligible designs were registry-based, multicenter, single-center, or prospective audits. Given substantial heterogeneity in study designs, FTR definitions, and outcome measures, a narrative synthesis was performed; no formal risk-of-bias assessment or meta-analysis was conducted. Results: Definitions of FTR varied (in-hospital, 30-day, 90-day, severity-based, and complication-specific cases). Reported rates differed by definition: average reported rates were 13.2% for 90-day CD ≥ III (G1); 10.3% for in-hospital/30-day CD ≥ III (G3); and 7.4% for 30-day “serious/major” morbidity (G8). Absolute differences were +3.0 and +2.9 percentage points (exploratory, descriptive comparisons). Five domains were consistently associated with lower FTR: (i) centralization to high-volume centers; (ii) safe adoption/refinement of surgical techniques; (iii) optimized perioperative management including early imaging and structured escalation pathways; (iv) patient-level risk stratification and prehabilitation; and (v) non-technical skills (NTSs) such as decision-making, situational awareness, communication, teamwork, and leadership. Among NTS domains, stress and fatigue management were not addressed in any included study. Limitations: Evidence is predominantly observational with substantial heterogeneity in study designs and FTR definitions; the search was limited to PubMed; and no formal risk-of-bias, publication-bias assessment, or meta-analysis was performed. Consequently, estimates and associations are descriptive/associative with limited certainty and generalizability. Conclusions: NTSs were rarely used or measured across the included studies, with validated instruments; quantitative assessment was uncommon, and no study evaluated stress or fatigue management. Reducing the FTR after pancreatic surgery will require standardized, pancreas-specific definitions of FTR, process-level rescue metrics, and deliberate strengthening of NTS. We recommend a pancreas-specific operational definition with an explicit numerator/denominator: numerator = all-cause mortality within 90 days of surgery; denominator = patients who experience major complications (Clavien–Dindo grade III–V, often labeled “CD ≥ 3”). Addressing the gaps in stress and fatigue management and embedding behavioral metrics into quality improvement programs are critical next steps to reduce preventable mortality after complex pancreatic cancer procedures.

1. Introduction

Pancreatic resection remains one of the most complex and high-risk surgical procedures, with postoperative morbidity and mortality rates regularly reported as high as 30–70% and 2–15%, respectively [1,2,3,4,5,6]. The pancreatoduodenectomy (PD)—most commonly performed for pancreatic cancer but also for other periampullary diseases—is the most technically demanding, frequently complicated by intra-abdominal fluid collections, postoperative pancreatic fistula (POPF), and postpancreatectomy hemorrhage (PPH) [7,8,9,10,11,12]. While perioperative mortality, particularly in pancreatic cancer surgery, has declined over the past few decades due to advances in surgical techniques, patient selection, and perioperative care [13,14], morbidity remains stubbornly high, and complications such as POPF and PPH continue to pose life-threatening risks and long-term morbidity. Postoperative chemotherapy, crucial for improving long-term survival in pancreatic cancer, can be delayed by poorly managed complications; ineffective early management can undermine optimal outcomes. PPH, often triggered by enzymatic erosion of major vessels, is one of the most fatal events after PD and has been identified as a major cause of interhospital transfers and preventable mortality [15,16,17,18].
Because the rescue pathways in pancreatic surgery are uniquely shaped by POPF and PPH, we restricted our scope to pancreatic procedures to ensure clinical comparability across studies. Increasing attention has been paid to the concept of failure to rescue (FTR)—defined as death following a major postoperative complication—which captures individual, team, and institutional variations in their ability to recognize, intervene, and manage surgical complications before they become fatal [19,20,21,22]. A growing body of research in North America and Europe has examined hospital- and patient-level determinants of FTR [8,23,24,25,26], and a number of promising strategies—such as early postoperative imaging [27,28,29], preoperative frailty screening [30,31], robotic surgery [32,33,34], and timely interprofessional interventions—have been proposed to mitigate FTR in high-risk pancreatic surgery. However, the evidence regarding their effectiveness remains mixed, highlighting important organizational, implementation and cultural challenges.
The PRISMA 2020 checklist was used to guide a systematic review with narrative synthesis examining how FTR is defined and reported after pancreatic surgery and identifying modifiable clinical, organizational, and team-based strategies to reduce FTR. Our research questions were: for adults undergoing pancreatic surgery, (1) what definitions and rates of FTR have been reported, and (2) which modifiable clinical, organizational, patient-level, and team (non-technical) strategies are associated with lower FTR?

2. Methods

We conducted a systematic review with a narrative synthesis of existing literature on FTR in pancreatic surgery care, using the PRISMA 2020 guidelines [35]. The review comprised five phases: (1) Identifying the research question, (2) identifying relevant studies, (3) study selection, (4) collating data, and (5) synthesizing results narratively.
Registration statement: The review protocol was not registered in a database such as PROSPERO.
Checklist: A completed PRISMA 2020 checklist is provided in the Supplementary Materials.
PRISMA statement: Reporting follows the PRISMA 2020 guidelines.

2.1. Search Strategy

We conducted a systematic literature search in PubMed to identify studies on FTR after pancreatic surgery. Given the distinctive pathophysiology and rescue pathways in pancreatic surgery—particularly the central role of clinically relevant POPF and delayed post-pancreatectomy hemorrhage—we restricted the scope to pancreatic procedures to enhance comparability, ensure clinically coherent rescue determinants, and avoid cross-procedure ecological bias.
The following search query was used:
(“failure to rescue” [All Fields] OR “FTR” [All Fields] OR “failure-to-rescue” [All Fields])
AND (“pancreatic surgery” [All Fields] OR “pancreatectomy” [All Fields] OR “pancreatoduodenectomy” [All Fields] OR “whipple procedure” [All Fields] OR “distal pancreatectomy” [All Fields] OR “total pancreatectomy” [All Fields]) AND (“1 January 1992” [Date-Publication]: “9 May 2025” [Date-Publication])

2.2. Selection Criteria

Studies were included in the review (1) if they specifically focused on failure to rescue (FTR) in the context of pancreatic surgery, (2) discussed clinical, institutional, or system-level strategies for reducing FTR and (3) reported relevant outcome measures such as morbidity, mortality, or rescue rates. Eligible study designs included randomized controlled trials, observational studies, and multicenter analyses. Reviews were retrieved at the search stage but excluded during eligibility assessment and were used only as background references. To minimize cross-procedure heterogeneity, the scope was restricted a priori to pancreatic procedures.
Studies were excluded if they (1) were not related to pancreatic surgery (e.g., such as those focusing solely on gastric or colorectal surgery), (2) lacked clinical data (e.g., commentaries or expert opinions), (3) were review articles, or (4) were case reports with insufficient information for meaningful analysis. Studies involving a mixed surgical population were included only when pancreatic surgery patients were clearly represented or analyzable. Studies covering hepato-biliary-pancreatic (HBP) procedures as a combined category were included if pancreatic surgery constituted a substantial and integral component of the analysis. All titles, abstracts, and full texts were independently reviewed by two authors (MU and YN) to determine eligibility. Any disagreements were resolved through discussion until a consensus was reached.

2.3. Data Extraction and Synthesis

2.3.1. Data Extraction

We developed a standardized extraction form (available upon request) to capture the study characteristics, patient populations, surgical procedures, definitions of FTR, intervention details (where applicable), and FTR outcome measures. Two reviewers (MU and YN) independently extracted data, and discrepancies were resolved by discussion and consensus.

2.3.2. Definition Framework and Grouping

The cohorts were grouped along three prespecified dimensions to isolate the impact of definitional choices on reported FTR: (i) observation window (in-hospital, 30-day, or 90-day cases); (ii) severity threshold for the qualifying postoperative complication (e.g., Clavien–Dindo ≥ III/IIIa; NSQIP “serious/major”; administrative/registry “any/major”); and (iii) data source (clinical cohort/registry vs. administrative/claims). These dimensions were used to classify each cohort prior to analysis.

2.3.3. Data Synthesis

For each definition grouping, we aggregated deaths and denominators across non-overlapping cohorts and calculated simple pooled proportions with Wilson 95% confidence intervals. To illustrate the magnitude of definition-driven differences, we report unweighted, exploratory contrasts. These calculations are descriptive and hypothesis-generating only and do not constitute a formal meta-analysis; no study-level weighting, heterogeneity modeling, or risk-of-bias assessment was performed. We did not conduct a formal risk-of-bias appraisal nor a formal meta-analysis, owing to substantial heterogeneity across study designs, patient populations, FTR definitions, and outcome measures.

3. Results

3.1. Characteristics of the Included Studies

A total of 52 studies were included through a multi-step selection process based on relevance to failure to rescue (FTR) after pancreatic surgery. The selection process is summarized in Figure 1, which follows the PRISMA 2020 format and includes the reason for exclusion.
We included 52 original studies published between 2010 and 2025. By design, these comprised retrospective analyses of national registries (RN, n = 24), retrospective single-center studies (RS, n = 13), retrospective multicenter studies (RM, n = 8), retrospective international multicenter studies (RI, n = 3), prospective national registry studies (PN, n = 2), prospective multicenter domestic studies (PM, n = 1), and prospective international multicenter studies (PI, n = 1). The number of institutions ranged from 1 (single center) to approximately 4000 (nationwide registry), and sample sizes ranged from 43 to 94,661 patients across the included studies. Review articles were excluded at the eligibility assessment and used only as background references. Study-specific details (authors, year, design, duration, number of institutions, and number of patients) are provided in Table 1.
Pancreatoduodenectomy (PD) was the most frequently reported procedure; distal pancreatectomy (DP) and total pancreatectomy (TP) were also commonly represented. All included cohorts comprised patients undergoing pancreatic surgery. Operative approach (pancreatic cohorts): reported in 22/52 studies; among the 20 with quantifiable shares (patient-weighted n = 121,632), final approach pooled to Open ≈91% and MIS ≈9% (LP ≈4%, Rb ≈0.5%); conversions counted under Open.
Although our search period spanned from 1992 onwards, no eligible studies specifically focusing on FTR in pancreatic surgery were identified prior to 2010. A single potentially relevant study by Ghaferi et al., published in 2009, was excluded due to the inclusion of multiple surgical procedures (AAA, esophageal surgery, CABG) beyond pancreatic surgery [80] and thus did not meet our inclusion criteria. Consequently, all included studies were published from 2010 onward.

3.2. Summary of FTR Descriptions

Of 52 eligible studies, 37 reported some form of failure-to-rescue (FTR). Three studies explicitly reported FTR by procedure and were split accordingly in Table 2 [67,74,77]. For the remaining 15 studies, FTR could not be explicitly determined because the definition and/or rate of FTR was not clearly reported; therefore, we include Table S1, which specifies the missing data for each study.

3.2.1. FTR Definition

The concept of FTR was originally proposed by Silber et al. in 1992, referring to the proportion of patients who died after experiencing major postoperative complications [19]. The principal dimensions were the observation time window, the severity threshold, the definition of complications, and the choice of denominator. FTR definitions clustered around H-CD3 (in-hospital, Clavien–Dindo [CD] ≥ III) and 90-CD3 (90-day cases, CD ≥ III), with additional use of 90-CD3a, 90-Acc3, and administrative/NSQIP variants. Across the entire dataset (40 entries, corresponding to 37 studies), the frequency of definitions by group was: G1 (90-day × CD ≥ III/IIIa/Acc3) in 6 studies, G2 in none, G3 (in-hospital/30-day × CD ≥ III/IIIa) in 9, G4 (90-day × Any, administrative) in 1, G5 (30-day/in-hospital × Any, non-CD) in 2, G6 (in-hospital × Any, administrative/NSQIP) in 9, G7 (90-day × specific complications such as CR-PPH/POPF) in 1, and G8 (alternative or non-comparable definitions) in 12.

3.2.2. Time Windows, Severity Thresholds, and Denominators

All counts refer to 40 study entries. The distribution of observation windows was as follows: in-hospital only in 18 of 40 studies (45.0%), 90-day in 11 studies (27.5%), 30-day in 6 studies (15.0%), mixed in-hospital/30-day in 3 studies (7.5%), in-hospital plus 90-day in 1 study (2.5%), and composite windows in 1 study (2.5%). The severity thresholds applied were as follows: Clavien–Dindo-based definitions (CD ≥ III/IIIa or CD IV) in 20 of 40 studies (50.0%), Accordion ≥3 in 2 studies (5.0%), NSQIP serious/major criteria in 3 studies (7.5%), administrative or claims-defined “major” complications in 6 studies (15.0%), “any event” definitions in 8 studies (20.0%), and ISGPS-specific complications only in 1 study (2.5%). The denominators used were as follows: major complications defined by Clavien–Dindo or Accordion criteria in 20 of 40 studies (50.0%; CD-based in 18 and Accordion-based in 2), major complications identified through claims, ICD, or MSQC coding in 6 studies (15.0%), NSQIP serious/major morbidity in 3 studies (7.5%), any complication in 8 studies (20.0%), and narrow single-study denominators—mixed CD ≥ III or POPF, CD IV only, or ISGPS-specific complications only—in 1 study each (2.5%).

3.2.3. Reported FTR Outcomes

Because no formal meta-analysis or risk-of-bias assessment was undertaken, the pooled values and between-group contrasts below are illustrative only. They should be interpreted as descriptive signals of how definitional choices affect apparent FTR, not as comparative effect estimates. All 95% confidence intervals are binomial (Wilson) around the simple pooled counts (Σn/ΣN) and do not incorporate between-study heterogeneity or study-level weighting.
Among studies using a 90-day window with CD ≥ III complications (G1), the pooled FTR was 13.2% (591/4461; 95% CI 12.3–14.3), with a study-level median 14.7% [10.9–19.5] (range 2.0–21.9%). Restricting capture to in-hospital (±30-day) outcomes at a similar CD threshold (G3) produced a pooled FTR of 10.3% (433/4213; 95% CI 9.4–11.2), with a median of 8.9% [7.1–13.4] (5.1–14.3%). Definitions centered on 30-day “serious/major” morbidity (G8) yielded the lowest pooled rate, 7.4% (1580/21,397; 95% CI 7.0–7.7), with a median of 9.6% [6.5–15.4] (5.3–33.3%). Descriptively, G1 exceeded G3 by 3.0 percentage points (RR 1.29) and G8 by 5.9 points (RR 1.79), while G3 exceeded G8 by 2.9 points (RR 1.39). These contrasts are descriptive only; no hypothesis testing was performed.
Groups that relied on administrative or registry “any/major” coding (G6) produced a pooled FTR of 11.5% (9353/81,332; 95% CI 11.3–11.7). The corresponding study-level median 7.8% [6.2–9.5] (2.9–12.6%) sat appreciably lower than the pooled rate, reflecting the disproportionate influence of very large cohorts on Σn/ΣN. Descriptively, G6 lay between G1 and G8: G1 vs. G6 differed by 1.7 points (RR 1.15), and G6 vs. G8 differed by 4.1 points (RR 1.56). No hypothesis testing was performed.
For complication-specific denominators (G7), exemplified by CR-PPH B/C and CR-POPF B/C, the pooled FTR for CR-PPH was 13.8% (9/65; 95% CI 7.5–24.3), and the combined study-level median across CR-PPH and CR-POPF was 7.6% [4.4–10.7]. Because the denominator is restricted to patients with a particular ISGPS event, these values are not directly comparable with the all-complication denominators used in G1, G3, and G8; they are best interpreted as event-specific fatality among patients who already crossed a high-risk threshold. Where only medians were available, 90-day “any” definitions (G4) clustered in the mid-teens (16.4% [14.9–17.9]; n = 2), in line with a broader denominator and extended follow-up. By contrast, 30-day/in-hospital “any” definitions (G5) centered lower (5.0% [4.1–7.0]; n = 4), echoing the attenuation observed whenever capture is truncated at discharge or 30 days.
We evaluated 15 studies that reported complications and/or mortality but could not be standardized to our FTR definition (90-day mortality among patients with CD ≥ III complications) (Table S1). Frequencies of not reported (NR) codes were: R6 (Counts missing): 8/15 (53.3%), R1 (Severity classification not reported): 7/15 (46.7%), R2 (Time window unspecified): 7/15 (46.7%), R4 (Denominator unclear): 5/15 (33.3%), R3 (No post-discharge death capture): 4/15 (26.7%), R8 (Other): 3/15 (20.0%), R5 (FTR concept not used): 2/15 (13.3%), and R7 (Mixed surgical case-mix): 1/15 (6.7%). Compound deficits were the rule, not the exception. The median number of NR reasons per study was 2 (mean 2.47); 13/15 (86.7%) studies had ≥2 codes.

3.3. Strategies for Reducing FTR in Pancreatic Surgery

We identified five major categories of strategies for reducing failure to rescue (FTR) in pancreatic surgery: (i) organizational or institutional interventions, (ii) evolution and safe implementation of surgical techniques, (iii) perioperative management, (iv) patient-related factors, and (v) non-technical skills (NTS). These categories were derived from the 52 included studies and are summarized in Table 3.

3.3.1. Organizational Strategies

Centralization of pancreatic surgery to high-volume centers is widely recognized as a key strategy to reduce Failure to Rescue (FTR), particularly for high-risk procedures such as pancreaticoduodenectomy and total pancreatectomy. Across national and multi-center datasets, patients treated at high-volume hospitals consistently had lower failure-to-rescue (FTR) rates than those at low-volume hospitals, with absolute gaps of roughly 6–7 percentage points—for example, 12.0% vs. 6.4% [37], 11.1% vs. 5.4% [40], and 21.8% vs. 14.9% [38]—reinforcing a centralization signal beyond differences in complication rates alone. This is largely attributed to the presence of experienced multidisciplinary teams—including anesthesiologists, surgical staff, ICU specialists, interventional radiologists, emergency physicians, as well as a high-performing blood bank—that can promptly manage severe complications such as postoperative hemorrhage, pancreatic fistula, and septic shock [18,23,60,65,66,72,81]. These institutions are also characterized by the routine use of standardized clinical protocols for postoperative monitoring, reoperation criteria, antibiotic therapy, and ICU admission, ensuring timely and consistent responses across the care continuum [41,58,59,68]. Furthermore, continuous quality improvement is embedded in institutional culture through regular morbidity and mortality conferences, benchmarking initiatives, and structured case reviews, which collectively enhance team performance and clinical decision-making [38,63,67,70]. While the degree of centralization varies across countries depending on healthcare systems and geographic factors, the overall benefits of this model in improving FTR outcomes are consistently supported in both national and international studies [8,37,62,76,78].

3.3.2. Evolution of Surgical Techniques

Advancements in surgical techniques, particularly the introduction and expansion of minimally invasive and robotic approaches, have significantly reshaped the landscape of pancreatic surgery [82]. These innovations offer several clinical advantages, including enhanced visualization, improved instrument dexterity, and more precise dissection, which are especially beneficial in complex procedures such as pancreaticoduodenectomy. Evidence suggests that these techniques can reduce intraoperative blood loss and postoperative complication rates, thereby potentially lowering the risks of Failure to Rescue (FTR) [54,77,83]. Consistent with these mechanistic expectations, comparative outcome studies report lower FTR after minimally invasive approaches than open surgery in selected populations—for example, a 90-day Medicare analysis found 13.4% with MIS versus 19.4% with open [42]. Procedure-specific contrasts also show systematically higher FTR after pancreatoduodenectomy (PD) than distal pancreatectomy (DP) across settings and definitions: 21.9% vs. 10.0% at 90 days [74]; 10.7% vs. 8.1% in standard NSQIP and 6.8% vs. 5.6% in pancreas-targeted NSQIP [65]; with longitudinal series preserving the PD > DP gradient despite overall improvements (PD 13.4→10.8→7.4% vs. DP 8.8→7.1→5.9% [63]. Additional cohorts echo this pattern—PD 20.5% versus total pancreatectomy 15.8% [77] and PD 7.5% versus DP 3.1% under CD ≥ IIIa denominators [67]. However, the adoption of advanced surgical techniques is accompanied by substantial technical complexity and steep learning curves with much variation by users. Early implementation of these technologies—especially in low-volume centers—has been associated with increased perioperative mortality, underscoring the need for deliberate institutional preparation, structured training, and careful case selection. To mitigate these risks, the introduction of minimally invasive pancreatic surgery should ideally occur within high-volume centers that possess the infrastructure to support safe implementation [25,64,69]. Several studies have emphasized the importance of structured training programs and stepwise adoption protocols in facilitating safe integration of novel techniques [63,69]. In this context, comprehensive institutional strategies—including readiness assessment to adopt the new technology, regular adverse event and near miss reporting, regular mortality and morbidity conferences [84] and root cause analyses, formal training curricula, mentorship by experienced surgeons, simulation training, and progressive case accumulation—have been shown to reduce technical errors and enhance patient safety [53,69,85]. Importantly, these frameworks enable community and non-academic hospitals to safely adopt complex procedures while maintaining acceptable outcomes [69].
In addition, specific technical strategies such as reducing intraoperative blood loss, optimizing anastomotic techniques, and minimizing the use of unnecessary prophylactics have been linked to improved outcomes [60,66,72]. For instance, experienced surgeons have adopted refined techniques such as pancreatojejunostomy over pancreaticogastrostomy, omitted the use of octreotide, and minimized intraoperative blood loss to improve outcomes in high-risk cases [60]. Similarly, center-level standardization of duct-to-mucosa anastomosis and tailored gland-specific strategies have shown a reduction in postoperative pancreatic fistula and mortality [72]. Furthermore, intraoperative hemorrhage and transfusion volume have been identified as independent predictors of FTR, reinforcing the importance of refined surgical technique and close anesthesiology collaboration to mitigate against excessive bleeding [60,86].
The focus of innovation in surgical technique has therefore shifted from mere technical feasibility to the development of safe, team-based, and context-appropriate implementation strategies. Meaningfully reducing FTR, requiresthe evolution of surgical techniques andalso how these techniques are embedded within systems of training, clinical governance, deploying a culture of deep team learning, and multidisciplinary collaboration [53,70,84].

3.3.3. Improvements in Perioperative Management

Optimizing perioperative management is a critical component to reducing Failure to Rescue (FTR) after pancreatic surgery. Evidence supports a multifaceted approach combining clinical vigilance, structured protocols, and multidisciplinary coordination [23,26,53]. Timely recognition and intervention remain central. The adoption of early warning systems (EWS), real-time monitoring tools, and structured daily briefings can enhance situational awareness and prompt escalation of care [41,47,50]. Simulation-based training may also help frontline staff recognize subtle signs of deterioration and respond effectively [26,43]. Enhanced recovery protocols (ERAS)—including fluid management, early mobilization, and multimodal analgesia—have been shown to reduce postoperative complications and promote physiological resilience [39,56,70,87]. These system-based learning elements support earlier recovery and help prevent the progression of complications into life-threatening events. Daily multidisciplinary rounds involving surgeons, anesthesiologists, nurses, critical care physicians, and allied health professionals ensure alignment of care plans and facilitate proactive responses to complications [25,53]. Moreover, establishing explicit escalation pathways—with predefined thresholds and responsible role clarity—can enable rapid coordination during clinical deterioration [5,47].
Institutional implementation of standardized algorithms, morbidity and mortality (M&M) conferences, and benchmark tracking further strengthens accountability and shared learning [36,63,81]. When embedded into standard clinical practice, these strategies collectively foster a safety-oriented perioperative culture that mitigates the risks of FTR [20,23,50]. Several studies affirm these principles. Timely reoperation in deteriorating patients has been shown to be potentially lifesaving [50]. Improved rescue rates have also been associated with increased postoperative vigilance, early diagnostic imaging, and the preferential use of interventional radiology over reoperation in the management of complications [20,47,81]. Relevant process measures—such as time to diagnostic imaging or interventional radiology and documentation of escalation plans—have been proposed as practical quality indicators to evaluate the quality of the perioperative rescue.

3.3.4. Consideration of Patient-Related Factors

Individual patient factors—such as frailty, nutritional status, comorbidities, and psychological resilience—profoundly influence postoperative outcomes and the likelihood of successful rescue in the event of complications [4,51,56,60]. Proactive risk stratification and personalized optimization planned and co-designed with patients and their caregivers are therefore essential components of any effective strategy to reduce FTR. Preoperative assessment tools, including prehabilitation programs as part of enhanced recovery after surgery (ERAS), should be employed to evaluate frailty, cardiopulmonary function, sarcopenia, and nutritional deficiencies [88]. Tailored interventions—such as exercise training to address functional deficits, nutritional supplementation, psychological support, and coaching toward healthier behaviors—can improve surgical readiness and physiological resilience [43,70,72]. Shared decision-making is particularly critical for high-risk patients. Involving patients and their families in discussions of operative risk, expected recovery, and potential complications not only supports informed consent but also sets realistic expectations and promotes engagement in perioperative care [25,58]. Multidisciplinary teams must develop individualized perioperative plans based on comprehensive risk profiles. Coordination with patients, informed by input from surgeons, anesthesiologists, nutritionists, physiotherapists, and psychosocial staff, ensures holistic management before and after surgery. These teams should also establish contingency strategies for high-risk individuals, including early access to intensive care and interventional radiology [18,43]., Aligning perioperative care with patient-specific vulnerabilities enhances resilience, facilitates timely rescue, and improves outcomes in pancreatic surgery [89]. As surgical candidates become increasingly complex, these personalized strategies become ever more vital to delivering safe and effective care [43,57,72].

3.3.5. Emphasis on Non-Technical Skills (NTSs)

A closer synthesis of the reviewed literature reveals frequent references to elements such as communication, coordination, escalation of care, and teamwork. These appear primarily within broader discussions of institutional functioning and complication management. Although the term Non-Technical Skills (NTSs) was not used in any of the studies included in this systematic review, many of the descriptions align closely with what is recognized in the patient safety literature as NTS [90]. It is likely that the authors were not consciously framing their observations within the established NTS taxonomy.

3.4. Role of Non-Technical Skills (NTSs) in Reducing FTR

This section organizes the relevant findings according to the seven-domain framework proposed by Flin et al.: decision-making, situational awareness, communication, teamwork, leadership, managing stress, and coping with fatigue [91]. For each domain, we highlight how the reviewed literature—while not explicitly framed as NTS—offers insights into behaviors, structures, and practices that support timely rescue and safe perioperative care. Notably, among these domains, stress and fatigue management were not addressed in any of the 52 included studies, representing a critical gap in the current evidence.
An overview of the seven NTS categories, their subcomponents, and representative examples in the context of pancreatic surgery is summarized in Table 4.

3.4.1. Decision-Making

Effective decision-making plays a central role in facilitating timely and appropriate responses to postoperative deterioration [92]. Several studies identified that failures in rescue were not primarily due to recognition or communication delays, but rather to delayed clinical action in response to deterioration, often stemming from insufficient escalation mechanisms [25,44,61]. Timeliness in decision-making can be supported by structured tools and protocols. Institutionalized clinical pathways such as “sepsis bundles” and time-outs have been suggested to help standardize responses to deterioration [37]. Predefined escalation protocols and clear systems of senior support are also considered essential to empower junior staff to act promptly when complications arise [25,44]. In the preoperative phase, aligning surgical strategies with individual risk profiles and patient preferences through shared decision-making is another approach to optimize outcomes [59]. Taken together, these insights indicate that improving decision-making capacity depends not only on individual clinical judgment, but also on embedding structured institutional strategies and decision-support tools throughout the surgical care continuum [93].

3.4.2. Situational Awareness

Timely detection of postoperative deterioration is a critical prerequisite for effective rescue. Evidence suggests that failures to rescue are often influenced by the adequacy of situational awareness, including the ability to recognize early signs of physiological decline and initiate appropriate responses without delay. Structured monitoring systems such as Early Warning Scores (EWS) and continuous physiologic surveillance supported by electronic health records have been introduced to support early recognition of deterioration, particularly in patients who initially appear clinically stable [61]. Conditions such as postoperative shock, renal failure, and unplanned intubation have been identified as key triggers requiring immediate vigilance and diagnostic escalation [41,47]. Distributed monitoring responsibilities, especially among nursing staff, play a substantial role in enhancing situational awareness. More favorable nurse staffing (e.g., lower patient-to-nurse ratios) and attentive bedside observation have been associated with earlier detection of complications and more timely interventions [23,50]. Institutional readiness—including real-time access to radiology, intensive care, and experienced clinical personnel—also contributes to effective recognition and response. Facilities with well-coordinated multidisciplinary teams and clearly defined escalation pathways appear better equipped to detect and act upon early signs of severe postoperative complications [18,44,52,53,60,65].
Together, these findings suggest that situational awareness in the postoperative setting depends on the presense of a culture of patient safety supported by a combination of technological infrastructure, organizational design, and consistent clinical vigilance [94].

3.4.3. Communication

Only a limited number of studies (n = 8) have explicitly addressed communication as a contributing factor in failure to rescue. Reported elements include escalation frameworks requiring direct notification of senior physicians [25,44], structured communication interventions such as technology-based systems [25], improved patient handovers using templated communication and interdisciplinary communication during critical moments [23,47,60]. Interestingly, one study reported that communication itself was not the limiting factor, as patient deterioration was recognized and conveyed but not acted upon promptly [61]. Additional studies addressed institutional communication strategies such as sharing outcomes transparently [63] and preoperative counseling [59].
Although the evidence is limited, these studies suggest that communication—across the institution and among clinical service members and especially between trainees—can influence rescue capacity through multiple pathways [95].

3.4.4. Teamwork

Effective teamwork requires the integration of multidisciplinary expertise throughout the preoperative, intraoperative, and postoperative phases. Structured collaboration involving anesthesiologists, interventional radiologists, endoscopists, intensivists, and infection control professionals contributes to improved detection and management of complications, potentially reducing FTR [18,53,65]. Formal multidisciplinary team (MDT) meetings have been implemented at institutional and regional levels to enhance patient selection and care coordination across the surgical and cancer patient journey [63,78]. In settings with limited case volume, videoconference-based MDTs have been used to access external expert guidance and facilitate consistent perioperative standards. These practices reflect a broader shift toward team-based clinical governance and shared accountability in complex surgical patient management.

3.4.5. Leadership

Leadership in complex surgical settings supports timely decision-making and effective team coordination. Among the 52 studies reviewed, only nine provided direct or indirect references to leadership-related factors, indicating a relative underrepresentation of this domain within the FTR literature. Identified barriers—such as hierarchical rigidity, lack of escalation protocols, and insufficient senior support—were found to impair complication response, underscoring the need for structured and responsive leadership that facilitates timely action and empowers clinical teams [25,44]. Furthermore, institutional strategies such as structured mentoring and expert supervision, particularly in the implementation of advanced procedures like robotic pancreaticoduodenectomy, reflect leadership investment in surgical safety and capacity-building [66,69].

3.4.6. Stress and Fatigue

Stress and fatigue are known to degrade decision-making and undermine effective surgical teams. However, among the seven domains of non-technical skills (NTS) defined by Flin et al. [91], no study included in this review explicitly addressed stress management or fatigue management in the context of failure to rescue (FTR) after pancreatic surgery. Across the 52 reviewed studies, there were no references to interventions, assessments, or institutional strategies directly related to psychological stress, provider workload, fatigue, or duty-hour limitations as factors associated with rescue failure. This absence represents a notable gap in the literature.

4. Discussion

4.1. Statement of Main Findings

Three key messages emerge in reviewing the lead 52 studies on failure to rescue (FTR) after pancreatic surgery. First, reported FTR rates are not directly comparable because definitions vary widely by the observation window (in-hospital vs. 30 vs. 90-day), severity threshold (e.g., Clavien–Dindo ≥III/Iiia vs. any-complication denominators), and data sources—choices that alter both numerators and denominators and bias cross-study comparisons. Second, several structural and technical levers—regional centralization to high-volume centers, safe adoption and refinement of operative technique, and structured perioperative pathways with explicit escalation—are consistently associated with lower FTR. Third, the largest prospective opportunity to further reduce FTR lies in strengthening non-technical skills (NTS) in surgical teams—decision-making, situational awareness, communication, teamwork, and leadership—across the perioperative continuum. Given substantial heterogeneity and our descriptive synthesis (no formal meta-analysis), these conclusions are contextual and hypothesis-generating; see Section 5 for methodological limitations.

4.2. Strengthening Non-Technical Skills (NTS) to Reduce FTR: The Central Insight

4.2.1. Why NTS Matters for Rescue

The most salient insight emerging from this narrative review is that strengthening non-technical skills (NTS) and enhancing medical team performance constitute a critical yet underdeveloped opportunity and a key strategy for reducing failure to rescue (FTR) after pancreatic surgery. While structural and technical domains such as centralization, surgical technique, and perioperative protocols have received substantial attention, timely recognition and coordinated response to deterioration are often compromised by breakdowns in decision-making, communication, and leadership. FTR is not solely a function of complication severity or surgical complexity—it frequently results from cognitive, behavioral, and team-based failures that delay or obstruct rescue. This reframes FTR mitigation as not only a matter of infrastructure but also of behavioral and organizational cultural dynamics within clinical teams. In the context of medical safety, insufficient team coordination, ambiguous leadership, and reluctance to speak up have been identified as frequent contributors to adverse outcomes, even in technically advanced environments [96]. These issues reflect deeply rooted deficits in present medical training in NTS, which are rarely addressed through standard quality improvement initiatives [97,98].
Failure to rescue a patient often unfolds during moments of clinical uncertainty—subtle physiological deviations, ambiguous signs, or shifting care priorities—when rapid interpretation of evolving risks, role clarity, coordinated interdisciplinary action, and confident escalation are required. In such situations, it is not technical expertise but vigilance, situational awareness, collaborative sense-making, and assertive decision-making that prove decisive. While the importance of non-technical skills (NTS) has been widely recognized in the intraoperative setting, with structured systems such as the Non-Technical Skills for Surgeons (NOTSS) formalizing decision-making, communication, and leadership within the operating theater [99], similar capacities are equally critical in the postoperative phase. Rescue failure often occurs not because a complication is undetectable, but because teams fail to recognize or respond to it on time.
Conceptual frameworks describing team-based vigilance, shared mental models, and adaptive expertise provide compelling justification for extending NTS principles beyond the operating room [100]. However, structured frameworks alone are insufficient. Their successful application depends on the environment in which they are enacted. In actual clinical settings, the execution of NTS is often hindered by latent organizational human factors that impair team functioning [101]. Rigid hierarchies, ambiguous role expectations, and suppressed speaking-up behaviors—common in high-stakes medical environments—can prevent even well-trained teams from taking timely and appropriate action [102,103]. These barriers are not merely operational; they are deeply rooted in medical clinical disciplines and institutional cultures. Foundational work in safety science, notably by Leape (1994), Reason (1997), and Vaughn (1997), has described how normalization of deviance and diffusion of responsibility can allow latent hazards to persist undetected until they culminate in harm [104,105,106]. These dynamics are particularly dangerous when time is critical, as they impair the team’s ability to make sense of the impending FTR and mount an effective rescue to transform manageable complications into preventable deaths.

4.2.2. Evidence Gap in the Current Literature

Despite widespread recognition of the importance of non-technical skills (NTS) in ensuring patient safety, their integration into surgical outcomes research—especially in the context of failure to rescue (FTR)—remains markedly limited. In this systematic review A few studies in this systematic review explicitly examin how cognitive and behavioral processes such as decision-making, escalation of care, situational awareness, or communication influenced the progression from time of surgical complication to mortality. This omission reveals a critical blind spot in the current literature, which continues to emphasize structural factors over behavioral dynamics. Most FTR studies still focus on institutional metrics such as hospital volume, ICU staffing, or surgical expertise, while largely neglecting how interprofessional teams function and learn in real time under duress during episodes of patient deterioration [80]. Even when adverse events are reported, the root causes related to human performance—such as delayed recognition, lack of role clarity, communication breakdowns, or poor team coordination—are rarely acknowledged or analyzed in a systematic fashion. Frameworks developed to assess NTS, such as the Non-Technical Skills for Surgeons (NOTSS) taxonomy [99], have largely been restricted to intraoperative or simulation environments, with minimal application to the postoperative settings where most FTR events arise. Similarly, observant clinical studies of real-world team behaviors in clinical care have revealed that latent threats and communication failures often go undetected in routine practice, yet these findings remain poorly integrated into the FTR research. In addition, foundational safety science work by Vincent et al. (2004) has emphasized that outcomes are shaped not only by systems and protocols but also by shared mental models, coordination, and adaptability—core components of NTS [100]. The lack of behavioral monitoring and team-based evaluation in the postoperative phase thus represents a missed opportunity to intervene before failure occurs. Bridging this evidence gap requires intentional study designs that can capture real-time team interactions, cognitive load, and communication flow during the critical window between complication and rescue and translate these domains into measurable and auditable quality indicators. Only by incorporating these human factors can future research move toward a more comprehensive and actionable model of perioperative surgical safety. Notably, none of the reviewed studies addressed stress or fatigue management, despite their established relevance to cognitive performance, clinical vigilance, and decision-making under pressure [107]. These omissions highlight a critical blind spot in the behavioral dimensions of rescue that remains unexplored in current surgical literature.

4.3. Current Landscape and Definition-Driven Limitations of FTR

4.3.1. Definition Heterogeneity and Interpretability

As detailed in the Results section (see Table 2), estimates of failure to rescue (FTR) vary systematically with the observation window (in-hospital vs. 30 vs. 90 days), the severity threshold (e.g., CD ≥ III/Iiia vs. broader “any-complication” denominators), and the data source (clinical registries, NSQIP, administrative claims). The directional signal is consistent across definition groups (G1–G8): wider time windows and higher severity thresholds yield higher—and clinically tighter—FTR estimates. These definitional choices are not neutral; they embed ascertainment biases that can alter cross-center or cross-country comparisons and may even invert comparative statements if definitions differ. Because the FTR is a ratio among patients with complications, broad denominators (e.g., “any complication”) dilute the ratio, whereas restricting to intervention-requiring events (CD ≥ III/IIIa) tightens attribution to genuine “rescue” opportunities [23,37,47,75]. NSQIP commonly anchors 30-day follow-up; administrative claims often lack validated severity mapping; and registry designs differ in post-discharge capture. For interpretability and comparability, definition elements must be declared up front and held constant in primary analyses.

4.3.2. Studies Not Reporting FTR and Why It Matters

Missing a severity threshold (R1) prevents anchoring the denominator to CD ≥ III; an unspecified time window (R2) makes the numerator scope (in-hospital vs. 30 vs. 90-day mortality) non-comparable; and absent counts (R6) preclude calculating n/N even when a percentage is provided. Because our standardized FTR relies on 90-day deaths among CD ≥ III, any one of these deficits can invalidate re-tabulation; in this subset, they were present in every study (often jointly). When the complication cohort is undefined or mixed (R4), “rescue” is diluted or inflated depending on whether minor or organ-specific endpoints are included. In-hospital-only follow-up (R3) systematically underestimates FTR by missing post-discharge deaths—precisely where delayed deterioration and the need for effective rescue are most apparent. A minority of studies either did not use the FTR construct (R5) or mixed PD/DP/TP without stratification (R7). These are structural rather than reporting problems: even with perfect counts, such designs would remain ill-suited for comparative FTR benchmarking.
Examples include specialty-restricted denominators (e.g., POPF grade B/C only) or time windows that could not be uniquely identified from the text/tables. These choices make the reported “FTR-like” numbers non-mappable to 90 d × CD ≥ III.

4.3.3. The Persistent Blind Spot: Post-Discharge Rescue

Many studies rely on in-hospital ascertainment, omitting deaths that occur soon after discharge. This decision point disproportionately skews evaluation of team-based detection and escalation, because recognition, early re-intervention, and safe readmission pathways operate close to the discharge boundary. Routine incorporation of post-discharge status via national registries, cross-system EHR linkages, or prospective 90-day follow-up is essential [42,52,74,108].

4.3.4. A Reference Definition: 90-Day FTR Among CD ≥ III Complications

The Clavien–Dindo classification provides an internationally adopted, behaviorally meaningful threshold at grade III/IIIa, i.e., complications that mandate procedural or operative intervention—the precise domain in which “rescue” is actionable [109]. This aligns naturally with contemporary pancreas-specific taxonomies: the ISGPS 2016 update re-grounded POPF as clinically relevant (CR-POPF B/C), explicitly tying definition to therapeutic consequence and resource mobilization, conceptually congruent with CD ≥ III [110]. Where legacy datasets use alternative scales, the Accordion severity grading system offers a defensible cross-walk to CD, enabling harmonization without distorting the rescue construct [111].
Pancreatectomy mortality accrues materially after 30 days; restricting ascertainment to in-hospital or 30-day endpoints systematically misses deaths that are tightly coupled to postoperative complications and their rescue pathways. Evidence from oncology pancreatectomy shows that 90-day mortality substantially exceeds 30-day mortality, underscoring the clinical relevance of a longer window [112]. More broadly, health-services analyses demonstrate that including post-discharge deaths changes hospital performance signals, reinforcing that shorter windows underestimate failure to rescue impact [108]. Contemporary international practice is converging on this standard: a recent 67-country prospective snapshot of pancreatic surgery proposed and operationalized modern outcome definitions with extended follow-up, illustrating feasibility and global face validity [49].
FTR is not merely “mortality per complication”; it sits within goals-of-care decisions and cultural norms around escalation [113]. Given these definition-driven constraints, our synthesis is descriptive and hypothesis-generating; see Section 5 for methodological limitations.

4.4. Practical Implementation Strategies for Embedding NTS in Surgical Practice

Strengthening NTS requires translating conceptual frameworks into measurable and auditable process indicators:
(a)
Decision-making
Implementation of structured tools such as early warning scores, SBAR communication protocols, escalation checklists, and predefined contingency plans reduces ambiguity and inertia during deteriorating situations. These cognitive aids support timely escalation and mitigate delay-related FTR [105,114]. Simulation-based training has also been shown to improve decision fluency in complex scenarios [115].
Indicators: EWS compliance rates, SBAR utilization, time from abnormality to escalation, senior review documentation, simulation participation and performance.
(b)
Situational awareness tools
Maintaining shared situational awareness is essential for early recognition of patient deterioration. Team huddles, risk dashboards, and cross-disciplinary briefings can enhance team alignment and vigilance across shifts and roles [97]. These mechanisms prevent fragmented monitoring and promote anticipatory care.
Indicators: Huddle implementation rates, frequency of nursing observations, dashboard review adherence, and time from warning sign to escalation.
(c)
Structured communication frameworks
Miscommunication remains one of the leading contributors to preventable harm in surgery. Standardized handover protocols, such as SBAR, and the adoption of closed-loop communication practices reduce misunderstanding and information loss during crises [116,117,118]. These approaches enhance clarity, especially under stress.
Indicators: Handover completeness, closed-loop adherence, and documentation of calls escalated to senior staff.
(d)
Team training and simulation
High-fidelity simulation and scenario-based team training build collective reflexes, support shared mental models, and foster environments where team members can speak up regardless of hierarchy [115]. TeamSTEPPS, developed by the Agency for Healthcare Research and Quality (AHRQ), provides evidence-based tools and strategies to enhance team performance and patient safety [119]. Its implementation in clinical settings has demonstrated improvements in patient outcomes, underpinned by improved communication, leadership behaviors, and mutual support across diverse surgical environments [120].
Indicators: Frequency of MDT meetings, staff participation rates, simulation training uptake, and TeamSTEPPS implementation audits.
(e)
Leadership and role of clarity
Clear definition of escalation roles, responsibility handoffs, and leadership expectations during critical phases improves coordination and response speed [95].
Ambiguity in team structure and leadership has been shown to contribute to confusion, duplication, and diffusion of responsibility [97,105]. In the context of anesthesia and critical care, poor role delineation was associated with delayed or inappropriate actions during crises [121]. Regular reinforcement of shared accountability norms is essential to overcome these latent system failures.
Despite their relatively low cost and strong theoretical foundation, NTS strategies are rarely implemented in a structured, system-wide manner within surgical practice. To reduce preventable mortality after complex procedures, NTS must be treated not as soft skills but as critical, trainable, and measurable competencies embedded in clinical routines, protocols, and institutional culture.
Indicators: Presence of written escalation protocols, chain-of-command documentation, and leadership training participation rates.
(f)
Stress and fatigue
Individual and team stress levels and fatigue levels domains are critical to cognitive performance although absent from the reviewed studies.
Indicators: Monitoring duty hours, compliance with rest breaks, stress evaluation tool completion, and institutional fatigue management systems.

4.5. Future Directions for Research and Implementation

Future research and implementation efforts must address several critical gaps to effectively translate non-technical skills (NTS) into measurable improvements in surgical outcomes, especially in the high-risk context of pancreatic cancer surgery. First, the field must prioritize the establishment of standardized and universally accepted definitions of FTR, including consistent thresholds for timing, severity, and complication types. The current heterogeneity across studies limits comparability and precludes effective benchmarking. Consensus definitions would enable robust cross-institutional and cross-national research, including in low- and middle-income settings where surgical infrastructure and rescue capabilities are limited and vary widely in quality. Second, prospective multicenter studies and international collaborative registries using standardized definitions are urgently needed. These initiatives should capture not only structural variables and outcomes but also process- and organizational context-level data on team behavior, escalation practices, and communication flow [122]. Given the complexity and high complication burden of pancreatic procedures, the creation of a global registry focused on FTR after pancreatic surgery could provide critical insights into modifiable contributors to mortality. Third, targeted investigations into the specific, quantifiable impact of non-technical skills on FTR reduction are warranted. Rather than reiterating individual process indicators, future studies should focus on validating surgery-specific NTS measures and determining their association with rescue outcomes. Fourth, the development and validation of standardized NTS metrics is essential to enable benchmarking across healthcare institutions and countries. These measures should be piloted and refined in high-risk units such as hepato-biliary-pancreatic surgery services. Fifth, simulation-based research can serve as a powerful modality for testing team interventions in safe, controlled environments. High-fidelity simulations of common postoperative complications—such as delayed hemorrhage, anastomotic leak, or intra-abdominal sepsis—can be used to evaluate escalation reflexes, speaking-up behavior, and leadership role clarity under pressure. These simulations can also inform training program design and system-level improvements. Sixth, dedicated applications of implementation science methodologies and tools are necessary to ensure that NTS-based strategies are sustainably integrated into real-world surgical practice. Barriers such as hierarchical culture, unclear role expectations, and resistance to change must be identified and addressed. In pancreatic surgery, where care is delivered across multiple disciplines and settings, successful implementation requires institution-wide coordination and cultural adaptation. Seventh, surgical training and accreditation frameworks must evolve to include formal NTS training not only in the operating room but throughout the perioperative continuum. In addition to technical mastery, trainees must develop fluency in recognizing clinical deterioration, initiating timely escalation, team engagement and support, and learning to lead coordinated team-based responses. These competencies should be assessed early and longitudinally and treated as core qualifications for independent surgical practice. Finally, emerging technologies, including continuous physiological monitoring, machine learning algorithms, and predictive analytics, have potential for enhancing early detection and guiding rescue efforts [123]. However, their deployment must be rigorously evaluated through prospective trials to determine their safety, effectiveness, integration feasibility, and cost–benefit balance—particularly in the complex environment of postoperative pancreatic care. Ultimately, reducing FTR in pancreatic surgery requires a paradigm shift, from viewing mortality as an inevitable outcome of technical complexity to understanding it as a preventable system’s failure of recognition, team coordination, and effectively mounted responses.

5. Limitations

This systematic review with narrative synthesis has several limitations that merit acknowledgment. First, although we followed a PRISMA-based search and selection [35], we did not preregister a protocol (e.g., PROSPERO) [124] and we did not perform a formal risk-of-bias assessment (e.g., ROBINS-I for nonrandomized studies [125], RoB 2 for randomized trials [126]). In conjunction with the substantial heterogeneity in FTR definitions, outcomes, and study designs across the included studies, these omissions limit the certainty of our findings and constrain their generalizability. Nonetheless, the use of predefined inclusion/exclusion criteria, independent dual screening, and consensus-based data extraction helped mitigate these risks. Second, our literature search was limited to the PubMed database, which may have omitted relevant studies indexed elsewhere or in the gray literature, introducing the possibility of publication bias [127]. Third, restricting the search to English-language publications may have introduced language bias by excluding relevant studies published in other languages [128]. Fourth, the included studies exhibited substantial heterogeneity in terms of FTR definitions (time frames and severity thresholds), limiting comparability across studies. Accordingly, we did not conduct a formal meta-analysis; while we report a small number of exploratory pooled estimates generated in Excel, these are descriptive only, and our conclusions primarily reflect qualitative (narrative) synthesis [129]. We therefore could not quantify between-study inconsistency or examine small-study effects, further constraining the precision and generalizability of the results [21,130]. Fifth, most included studies were conducted in high-income countries and large academic centers, limiting generalizability to settings with different healthcare resources and infrastructures [131]. Sixth, the majority of the included studies used retrospective, observational designs, thereby limiting data accuracy, raising concerns about unmeasured confounding, and restricting causal inference [132]. In particular, selection and information biases (e.g., inconsistent case capture and variable FTR definitions) could have inflated apparent benefits of centralization or specific techniques, while residual data confounding at the hospital level may partially account for observed between-center differences in FTR. Seventh, although non-technical skills (NTS) have emerged as critical to reducing FTR, the variability in their measurement methods and definitions across studies prevents objective quantification and synthesis of their effectiveness; moreover, core NTS domains such as stress and fatigue were seldom measured, precluding any quantitative assessment of their impact, although the success of NTS implementation and team training in other surgical domains demonstrates their potential [133,134]. Finally, we did not assess the certainty of evidence using formal approaches such as GRADE [135], which further limits the strength of inference. Taken together, the absence of a formal quality appraisal and our decision not to undertake a formal meta-analysis because of study heterogeneity are limitations that affect the strength and generalizability of our conclusions; accordingly, our findings should be interpreted as contextual and hypothesis-generating rather than definitive.

6. Conclusions

Failure to rescue (FTR) remains a critical vulnerability in pancreatic surgery, reflecting persistent challenges in the timely recognition and coordinated management of major postoperative complications. We observed across 52 studies, substantial heterogeneity in how FTR is defined and measured and, consequently, wide variation in reported rates. Convergent signals nevertheless point to actionable safety opportunities: regional centralization to high-volume centers; safe adoption and refinement of surgical technique; structured perioperative management with explicit escalation pathways; patient-specific risk stratification and prehabilitation; and deliberate integration of non-technical skills (decision-making, situational awareness, communication, teamwork, and leadership) among surgical teams and across the care continuum.
We strongly recommend to enable fair benchmarking and reduce reporting variability, a pancreas-specific operational definition of FTR—numerator: all-cause 90-day mortality; denominator: patients with major complications (Clavien–Dindo ≥ III/IIIa). Given the heterogeneity across studies and the absence of a formal quality assessment and meta-analysis in our review, our synthesis should be interpreted as descriptive. To make this definition actionable and auditable, centers should report a concise set of standardized, process-level rescue indicators that capture the timeliness of recognition, escalation, and definitive treatments. Examples include time to diagnostic imaging, time to interventional radiology or reoperation, and adherence to predefined escalation protocols.
Embedding new measurements and training of non-technical skills within routine quality programs—and evaluating these strategies across diverse resource settings and referral networks—should be prioritized. Building reliable patient rescue systems in which deterioration is detected early, escalation is unequivocal, and definitive treatment is delivered without delay offers the most credible path to lowering FTR and improving survival after pancreatic surgery.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/cancers17193259/s1. Table S1: Reasons studies could not be standardized to the reference FTR definition.

Author Contributions

Conceptualization, M.U., Y.F. and Y.N.; methodology, M.U., Y.F. and Y.N.; formal analysis, M.U., H.O., M.M. and Y.N.; investigation, M.U., H.O., M.M. and Y.F.; writing—original draft preparation, M.U., P.B. and Y.N.; writing—review and editing, M.U., Y.F., P.B. and Y.N.; visualization, M.U.; supervision, P.B. and Y.F.; project administration, M.U. and Y.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable. This study is a systematic review with narrative synthesis based on previously published literature and does not involve new data collection from humans or animals.

Informed Consent Statement

Not applicable. This study is a systematic review with narrative synthesis based on previously published literature and does not involve new data collection from humans.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

We thank Guest Editor Atsushi Masamune for his kind recommendation and support in the submission process.

Conflicts of Interest

The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Abbreviations

The following abbreviations are used in this manuscript:
PDPancreatoduodenectomy
POPFPostoperative Pancreatic Fistula
PPHPostpancreatectomy Hemorrhage
FTRFailure to Rescue
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
HBPHepato-Biliary-Pancreatic
NSQIPNational Surgical Quality Improvement Program
RNRetrospective Analyses of National Registries
RSRetrospective Single-Center Studies
RMRetrospective Multicenter Studies
RIRetrospective International Multicenter Studies
PNProspective National Registry Studies
PMProspective Multicenter Domestic Studies
PIProspective International Multicenter Studies
NISNationwide Inpatient Sample
HCUPHealthcare Cost and Utilization Project
AHRQAgency for Healthcare Research and Quality
AHAAmerican Hospital Association (Annual Survey)
PUFParticipant-Use File
MSQCMichigan Surgical Quality Collaborative
MEDPARMedicare Provider Analysis and Review
PMSIProgramme de Médicalisation des Systèmes d’Information
DRGDiagnosis-Related Group
RDCResearch Data Center
DPCADutch Pancreatic Cancer Audit.
OSHPDOffice of Statewide Health Planning and Development
SNPPCRSwedish National Pancreatic & Periampullary Cancer Registry
StuDoQStuDoQ|Pancreas registry
DGAVGerman Society for General and Visceral Surgery
NCDNational Clinical Database
JSHBPSJapanese Society of Hepato-Biliary-Pancreatic Surgery
MPOGMulticenter Perioperative Outcomes Group
DICADutch Institute for Clinical Auditing
DHBADutch Hepato-Biliary Audit
PORSCHDutch Stepped-Wedge “Algorithm-Based Care” Program/Trial After PD
CRFCase Report Form
EPJElectronic Patient Journal
ISGPSInternational Study Group of Pancreatic Surgery
ICDInternational Classification of Diseases
HV/IV/LVHigh/Intermediate/Low Volume
PPPylorus-Preserving Pancreaticoduodenectomy
PRPDPylorus-Resecting Pancreaticoduodenectomy
DPDistal Pancreatectomy
TPTotal Pancreatectomy
CPCentral Pancreatectomy
LPLaparoscopic
RbRobotic
MISMinimally Invasive Surgery
RAMPS:Radical Antegrade Modular Pancreatosple-Nectomy
AAAAbdominal Aortic Aneurysm
CABGCoronary Artery Bypass Grafting
HPDhepatopancreatoduodenectomy
ICUIntensive Care Unit
EWSEarly Warning Score/System
ERASEnhanced Recovery After Surgery
IRInterventional Radiology
MDTMultidisciplinary Team
EHRElectronic Health Record
SBARSituation, Background, Assessment, Recommendation
NTSNon-Technical Skills
NOTSSNon-Technical Skills for Surgeons
PROSPEROInternational Prospective Register of Systematic Reviews
ROBINS-IRisk of Bias in Non-randomized Studies of Interventions
RoB 2Risk of Bias 2
GRADEGrading of Recommendations Assessment, Development and Evaluation

References

  1. Harnoss, J.C.; Ulrich, A.B.; Harnoss, J.M.; Diener, M.K.; Büchler, M.W.; Welsch, T. Use and results of consensus definitions in pancreatic surgery: A systematic review. Surgery 2014, 155, 47–57. [Google Scholar] [CrossRef] [PubMed]
  2. Okano, K.; Hirao, T.; Unno, M.; Fujii, T.; Yoshitomi, H.; Suzuki, S.; Satoi, S.; Takahashi, S.; Kainuma, O.; Suzuki, Y. Postoperative infectious complications after pancreatic resection. Br. J. Surg. 2015, 102, 1551–1560. [Google Scholar] [CrossRef] [PubMed]
  3. Pugalenthi, A.; Protic, M.; Gonen, M.; Kingham, T.P.; D’Angelica, M.I.; Dematteo, R.P.; Fong, Y.; Jarnagin, W.R.; Allen, P.J. Postoperative complications and overall survival after pancreaticoduodenectomy for pancreatic ductal adenocarcinoma. J. Surg. Oncol. 2016, 113, 188–193. [Google Scholar] [CrossRef] [PubMed]
  4. El Amrani, M.; Clement, G.; Lenne, X.; Farges, O.; Delpero, J.R.; Theis, D.; Pruvot, F.R.; Truant, S. Failure-to-rescue in patients undergoing pancreatectomy: Is hospital volume a standard for quality improvement programs? Nationwide analysis of 12,333 patients. Ann. Surg. 2018, 268, 799–807. [Google Scholar] [CrossRef] [PubMed]
  5. Sánchez-Velázquez, P.; Muller, X.; Malleo, G.; Park, J.S.; Hwang, H.K.; Napoli, N.; Javed, A.A.; Inoue, Y.; Beghdadi, N.; Kalisvaart, M.; et al. Benchmarks in pancreatic surgery: A novel tool for unbiased outcome comparisons. Ann. Surg. 2019, 270, 211–218. [Google Scholar] [CrossRef] [PubMed]
  6. Smits, F.J.; Henry, A.C.; Besselink, M.G.; Busch, O.R.; van Eijck, C.H.; Arntz, M.; Bollen, T.L.; van Delden, O.M.; van den Heuvel, D.; van der Leij, C.; et al. Algorithm-based care versus usual care for the early recognition and management of complications after pancreatic resection in the Netherlands: An open-label, nationwide, stepped-wedge cluster-randomised trial. Lancet 2022, 399, 1867–1875. [Google Scholar] [CrossRef] [PubMed]
  7. Bloomfield, G.C.; Shoucair, S.; Nigam, A.; Park, B.U.; Fishbein, T.M.; Radkani, P.; Winslow, E.R. The utility of axial imaging among selected patients in the early postoperative period after pancreatectomy. Surgery 2024, 176, 1171–1178. [Google Scholar] [CrossRef] [PubMed]
  8. Krautz, C.; Nimptsch, U.; Weber, G.F.; Mansky, T.; Grützmann, R. Effect of hospital volume on in-hospital morbidity and mortality following pancreatic surgery in Germany. Ann. Surg. 2018, 267, 411–417. [Google Scholar] [CrossRef] [PubMed]
  9. Uttinger, K.L.; Diers, J.; Baum, P.; Pietryga, S.; Baumann, N.; Hankir, M.; Germer, C.T.; Wiegering, A. Mortality, complications and failure to rescue after surgery for esophageal, gastric, pancreatic and liver cancer patients based on minimum caseloads set by the German Cancer Society. Eur. J. Surg. Oncol. 2022, 48, 924–932. [Google Scholar] [CrossRef] [PubMed]
  10. Baum, P.; Diers, J.; Lichthardt, S.; Kastner, C.; Schlegel, N.; Germer, C.T.; Wiegering, A. Mortality and complications following visceral surgery: A nationwide analysis based on the diagnostic categories used in German hospital invoicing data. Dtsch. Arztebl. Int. 2019, 116, 739–746. [Google Scholar] [CrossRef] [PubMed]
  11. Bassi, C.; Dervenis, C.; Butturini, G.; Fingerhut, A.; Yeo, C.; Izbicki, J.; Neoptolemos, J.; Sarr, M.; Traverso, W.; Buchler, M. Postoperative pancreatic fistula: An international study group (ISGPF) definition. Surgery 2005, 138, 8–13. [Google Scholar] [CrossRef] [PubMed]
  12. Welsch, T.; Müssle, B.; Korn, S.; Sturm, D.; Bork, U.; Distler, M.; Grählert, X.; Klimova, A.; Trebesius, N.; Kleespies, A.; et al. Pancreatoduodenectomy with or without prophylactic falciform ligament wrap around the hepatic artery for prevention of postpancreatectomy haemorrhage: Randomized clinical trial (PANDA trial). Br. J. Surg. 2021, 109, 37–45. Available online: https://academic.oup.com/bjs/article/109/1/37/6422748 (accessed on 1 October 2025). [PubMed]
  13. Augustinus, S.; Mackay, T.M.; Andersson, B.; Beane, J.D.; Busch, O.R.; Gleeson, E.M.; Koerkamp, B.G.; Keck, T.; van Santvoort, H.C.; Tingstedt, B.; et al. Ideal outcome after pancreatoduodenectomy: A transatlantic evaluation of a harmonized composite outcome measure. Ann. Surg. 2023, 278, 740–747. [Google Scholar] [CrossRef] [PubMed]
  14. Mackay, T.M.; Wellner, U.F.; van Rijssen, L.B.; Stoop, T.F.; Busch, O.R.; Groot Koerkamp, B.; Bausch, D.; Petrova, E.; Besselink, M.G.; Keck, T.; et al. Variation in pancreatoduodenectomy as delivered in two national audits. Br. J. Surg. 2019, 106, 747–755. [Google Scholar] [CrossRef] [PubMed]
  15. Wente, M.N.; Veit, J.A.; Bassi, C.; Dervenis, C.; Fingerhut, A.; Gouma, D.J.; Izbicki, J.R.; Neoptolemos, J.P.; Padbury, R.T.; Sarr, M.G.; et al. Postpancreatectomy hemorrhage (PPH): An international study group of pancreatic surgery (ISGPS) definition. Surgery 2007, 142, 20–25. [Google Scholar] [CrossRef] [PubMed]
  16. Giuliani, T.; Marchegiani, G.; Di Gioia, A.; Amadori, B.; Perri, G.; Salvia, R.; Bassi, C. Patterns of mortality after pancreatoduodenectomy: A root cause, day-to-day analysis. Surgery 2022, 172, 329–335. [Google Scholar] [CrossRef] [PubMed]
  17. Beugniez, C.; Sauvanet, A.; Sulpice, L.; Gaujoux, S.; Turrini, O.; Truant, S.; Schwarz, L.; Piessen, G.; Regimbeau, J.M.; Muscari, F.; et al. Root-cause analysis of mortality after pancreatic resection (CARE study): A multicenter cohort study. Ann. Surg. 2021, 274, 789–796. [Google Scholar] [CrossRef] [PubMed]
  18. El Amrani, M.; Lenne, X.; Clément, G.; Turrini, O.; Theis, D.; Pruvot, F.R.; Bruandet, A.; Truant, S. Referring patients to expert centers after pancreatectomy is too late to improve outcome. Inter-hospital transfer analysis in nationwide study of 19,938 patients. Ann. Surg. 2020, 272, 723–730. [Google Scholar] [CrossRef] [PubMed]
  19. Silber, J.H.; Williams, S.V.; Krakauer, H.; Schwartz, J.S. Hospital and patient characteristics associated with death after surgery. A study of adverse occurrence and failure to rescue. Med. Care. 1992, 30, 615–629. [Google Scholar] [CrossRef] [PubMed]
  20. Gleeson, E.M.; Pitt, H.A.; Mackay, T.M.; Wellner, U.F.; Williamsson, C.; Busch, O.R.; Koerkamp, B.G.; Keck, T.; van Santvoort, H.C.; Tingstedt, B.; et al. Failure to rescue after pancreatoduodenectomy: A transatlantic analysis. Ann. Surg. 2021, 274, 459–466. [Google Scholar] [CrossRef] [PubMed]
  21. Ghaferi, A.A.; Dimick, J.B. Variation in mortality after high-risk cancer surgery: Failure to rescue. Surg. Oncol. Clin. N. Am. 2012, 21, 389–395. Available online: https://www.surgonc.theclinics.com/article/S1055-3207(12)00024-5/abstract (accessed on 1 October 2025). [CrossRef] [PubMed]
  22. Portuondo, J.I.; Shah, S.R.; Singh, H.; Massarweh, N.N. Failure to rescue as a surgical quality indicator: Current concepts and future directions for improving surgical outcomes. Anesthesiology 2019, 131, 426–437. [Google Scholar] [CrossRef] [PubMed]
  23. Ghaferi, A.A.; Osborne, N.H.; Birkmeyer, J.D.; Dimick, J.B. Hospital characteristics associated with failure to rescue from complications after pancreatectomy. J. Am. Coll. Surg. 2010, 211, 325–330. [Google Scholar] [CrossRef] [PubMed]
  24. Sheetz, K.H.; Krell, R.W.; Englesbe, M.J.; Birkmeyer, J.D.; Campbell, D.A., Jr.; Ghaferi, A.A. The importance of the first complication: Understanding failure to rescue after emergent surgery in the elderly. J. Am. Coll. Surg. 2014, 219, 365–370. [Google Scholar] [CrossRef] [PubMed]
  25. Tamirisa, N.P.; Parmar, A.D.; Vargas, G.M.; Mehta, H.B.; Kilbane, E.M.; Hall, B.L.; Pitt, H.A.; Riall, T.S. Relative contributions of complications and failure to rescue on mortality in older patients undergoing pancreatectomy. Ann. Surg. 2016, 263, 385–391. [Google Scholar] [CrossRef] [PubMed]
  26. Capretti, G.; Balzano, G.; Gianotti, L.; Stella, M.; Ferrari, G.; Baccari, P.; Zuliani, W.; Braga, M.; Zerbi, A. Management and outcomes of pancreatic resections performed in high-volume referral and low-volume community hospitals led by surgeons who shared the same mentor: The importance of training. Dig. Surg. 2018, 35, 42–48. [Google Scholar] [CrossRef] [PubMed]
  27. Smits, F.J.; Molenaar, I.Q.; Besselink, M.G.; Borel Rinkes, I.H.M.; van Eijck, C.H.J.; Busch, O.R.; van Santvoort, H.C.; Dutch Pancreatic Cancer Group. Early recognition of clinically relevant postoperative pancreatic fistula: A systematic review. HPB (Oxford) 2020, 22, 1–11. [Google Scholar] [CrossRef] [PubMed]
  28. Mazzola, M.; Calcagno, P.; Giani, A.; Maspero, M.; Bertoglio, C.L.; De Martini, P.; Magistro, C.; Sgrazzutti, C.; Vanzulli, A.; Ferrari, G. Is routine CT scan after pancreaticoduodenectomy a useful tool in the early detection of complications? A single center retrospective analysis. Langenbecks Arch. Surg. 2022, 407, 2801–2810. [Google Scholar] [CrossRef] [PubMed]
  29. Uchida, Y.; Masui, T.; Nakano, K.; Yogo, A.; Yoh, T.; Nagai, K.; Anazawa, T.; Takaori, K.; Uemoto, S. Combination of postoperative C-reactive protein value and computed tomography imaging can predict severe pancreatic fistula after pancreatoduodenectomy. HPB (Oxford) 2020, 22, 282–288. [Google Scholar] [CrossRef] [PubMed]
  30. Augustin, T.; Burstein, M.D.; Schneider, E.B.; Morris-Stiff, G.; Wey, J.; Chalikonda, S.; Walsh, R.M. Frailty predicts risk of life-threatening complications and mortality after pancreatic resections. Surgery 2016, 160, 987–996. Available online: https://www.surgjournal.com/article/S0039-6060(16)30342-7/fulltext (accessed on 1 October 2025). [CrossRef] [PubMed]
  31. Berkel, A.E.M.; Bongers, B.C.; Kotte, H.; Weltevreden, P.; de Jongh, F.H.C.; Eijsvogel, M.M.M.; Wymenga, M.; Bigirwamungu-Bargeman, M.; van der Palen, J.; van Det, M.J.; et al. Effects of community-based exercise prehabilitation for patients scheduled for colorectal surgery with high risk for postoperative complications: Results of a randomized clinical trial. Ann. Surg. 2022, 275, e299–e306. [Google Scholar] [CrossRef] [PubMed]
  32. van Hilst, J.; de Rooij, T.; Bosscha, K.; Brinkman, D.J.; van Dieren, S.; Dijkgraaf, M.G.; Gerhards, M.F.; de Hingh, I.H.J.T.; Karsten, T.M.; Lips, D.J.; et al. Laparoscopic versus open pancreatoduodenectomy for pancreatic or periampullary tumours (LEOPARD-2): A multicentre, patient-blinded, randomised controlled phase 2/3 trial. Lancet Gastroenterol. Hepatol. 2019, 4, 199–207. [Google Scholar] [CrossRef] [PubMed]
  33. Zureikat, A.H.; Beane, J.D.; Zenati, M.S.; Al Abbas, M.I.; Boone, B.A.; Moser, A.J.; Bartlett, D.L.; Hogg, M.E.; Zeh, H.J., 3rd. 500 minimally invasive robotic pancreatoduodenectomies: One decade of optimizing performance. Ann. Surg. 2021, 273, 966–972. [Google Scholar] [CrossRef] [PubMed]
  34. Kinny-Köster, B.; Habib, J.R.; Javed, A.A.; Shoucair, S.; van Oosten, A.F.; Fishman, E.K.; Lafaro, K.J.; Wolfgang, C.L.; Hackert, T.; He, J. Technical progress in robotic pancreatoduodenectomy: TRIANGLE and periadventitial dissection for retropancreatic nerve plexus resection. Langenbecks Arch. Surg. 2021, 406, 2527–2534. [Google Scholar] [CrossRef] [PubMed]
  35. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
  36. Haigh, P.I.; Bilimoria, K.Y.; DiFronzo, L.A. Early postoperative outcomes after pancreaticoduodenectomy in the elderly. Arch. Surg. 2011, 146, 715–723. [Google Scholar] [CrossRef] [PubMed]
  37. Amini, N.; Spolverato, G.; Kim, Y.; Pawlik, T.M. Trends in hospital volume and failure to rescue for pancreatic surgery. J. Gastrointest. Surg. 2015, 19, 1581–1592. [Google Scholar] [CrossRef] [PubMed]
  38. Healy, M.A.; Krell, R.W.; Abdelsattar, Z.M.; McCahill, L.E.; Kwon, D.; Frankel, T.L.; Hendren, S.; Campbell, D.A., Jr.; Wong, S.L. Pancreatic resection results in a statewide surgical collaborative. Ann. Surg. Oncol. 2015, 22, 2468–2474. [Google Scholar] [CrossRef] [PubMed]
  39. Carr, R.A.; Chung, C.W.; Schmidt, C.M.; Jester, A.; Kilbane, M.E.; House, M.G.; Zyromski, N.J.; Nakeeb, A.; Schmidt, C.M.; Ceppa, E.P. Impact of fellow versus resident assistance on outcomes following pancreatoduodenectomy. J. Gastrointest. Surg. 2017, 21, 1025–1030. [Google Scholar] [CrossRef] [PubMed]
  40. Gani, F.; Johnston, F.M.; Nelson-Williams, H.; Cerullo, M.; Dillhoff, M.E.; Schmidt, C.R.; Pawlik, T.M. Hospital volume and the costs associated with surgery for pancreatic cancer. J. Gastrointest. Surg. 2017, 21, 1411–1419. [Google Scholar] [CrossRef] [PubMed]
  41. Varley, P.R.; Geller, D.A.; Tsung, A. Factors influencing failure to rescue after pancreaticoduodenectomy: A National Surgical Quality Improvement Project perspective. J. Surg. Res. 2017, 214, 131–139. [Google Scholar] [CrossRef] [PubMed]
  42. Chen, Q.; Merath, K.; Bagante, F.; Akgul, O.; Dillhoff, M.; Cloyd, J.; Pawlik, T.M. A comparison of open and minimally invasive surgery for hepatic and pancreatic resections among the Medicare population. J. Gastrointest. Surg. 2018, 22, 2088–2096. [Google Scholar] [CrossRef] [PubMed]
  43. Pecorelli, N.; Capretti, G.; Sandini, M.; Damascelli, A.; Cristel, G.; De Cobelli, F.; Gianotti, L.; Zerbi, A.; Braga, M. Impact of sarcopenic obesity on failure to rescue from major complications following pancreaticoduodenectomy for cancer: Results from a multicenter study. Ann. Surg. Oncol. 2018, 25, 308–317. [Google Scholar] [CrossRef] [PubMed]
  44. van Rijssen, L.B.; Zwart, M.J.; van Dieren, S.; de Rooij, T.; Bonsing, B.A.; Bosscha, K.; van Dam, R.M.; van Eijck, C.H.; Gerhards, M.F.; Gerritsen, J.J.; et al. Variation in hospital mortality after pancreatoduodenectomy is related to failure to rescue rather than major complications: A nationwide audit. HPB (Oxford) 2018, 20, 759–767. [Google Scholar] [CrossRef] [PubMed]
  45. Cerullo, M.; Gani, F.; Chen, S.Y.; Canner, J.K.; Dillhoff, M.; Cloyd, J.; Pawlik, T.M. Routine intensive care unit admission among patients undergoing major pancreatic surgery for cancer: No effect on failure to rescue. Surgery 2019, 165, 741–746. [Google Scholar] [CrossRef] [PubMed]
  46. Diaz, A.; Burns, S.; Paredes, A.Z.; Pawlik, T.M. Accessing surgical care for pancreaticoduodenectomy: Patient variation in travel distance and choice to bypass hospitals to reach higher volume centers. J. Surg. Oncol. 2019, 120, 1318–1326. [Google Scholar] [CrossRef] [PubMed]
  47. Gleeson, E.M.; Clarke, J.R.; Morano, W.F.; Shaikh, M.F.; Bowne, W.B.; Pitt, H.A. Patient-specific predictors of failure to rescue after pancreaticoduodenectomy. HPB (Oxford) 2019, 21, 283–290. [Google Scholar] [CrossRef] [PubMed]
  48. Merath, K.; Chen, Q.; Bagante, F.; Sun, S.; Akgul, O.; Idrees, J.J.; Dillhoff, M.; Schmidt, C.; Cloyd, J.; Pawlik, T.M. Variation in the cost-of-rescue among Medicare patients with complications following hepatopancreatic surgery. HPB (Oxford) 2019, 21, 310–318. [Google Scholar] [CrossRef] [PubMed]
  49. van Roessel, S.; Mackay, T.M.; Tol, J.A.M.G.; van Delden, O.M.; van Lienden, K.P.; Nio, C.Y.N.; Phoa, S.K.S.; Fockens, P.; van Hooft, J.E.; Verheij, J.; et al. Impact of expanding indications on surgical and oncological outcome in 1434 consecutive pancreatoduodenectomies. HPB (Oxford) 2019, 21, 865–875. [Google Scholar] [CrossRef] [PubMed]
  50. Wroński, M.; Cebulski, W.; Witkowski, B.; Guzel, T.; Karkocha, D.; Lech, G.; Słodkowski, M. Surgical management of the grade C pancreatic fistula after pancreatoduodenectomy. HPB (Oxford) 2019, 21, 1166–1174. [Google Scholar] [CrossRef] [PubMed]
  51. Bhatti, A.B.H.; Jafri, R.Z.; Khan, N.A. Best achievable results need territorial familiarity: Impact of living donor liver transplant experience on outcomes after pancreaticoduodenectomy. Ann. Med. Surg. (Lond) 2020, 55, 213–218. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  52. Nymo, L.S.; Kleive, D.; Waardal, K.; Bringeland, E.A.; Søreide, J.A.; Labori, K.J.; Mortensen, K.E.; Søreide, K.; Lassen, K. Centralizing a national pancreatoduodenectomy service: Striking the right balance. BJS Open. 2020, 4, 904–913. [Google Scholar] [CrossRef] [PubMed]
  53. Endo, I.; Hirahara, N.; Miyata, H.; Yamamoto, H.; Matsuyama, R.; Kumamoto, T.; Homma, Y.; Mori, M.; Seto, Y.; Wakabayashi, G.; et al. Mortality, morbidity, and failure to rescue in hepatopancreatoduodenectomy: An analysis of patients registered in the National Clinical Database in Japan. J. Hepatobiliary Pancreat. Sci. 2021, 28, 305–316. [Google Scholar] [CrossRef] [PubMed]
  54. Lequeu, J.B.; Cottenet, J.; Facy, O.; Perrin, T.; Bernard, A.; Quantin, C. Failure to rescue in patients with distal pancreatectomy: A nationwide analysis of 10,632 patients. HPB (Oxford) 2021, 23, 1410–1417. [Google Scholar] [CrossRef] [PubMed]
  55. Pastrana Del Valle, J.; Mahvi, D.A.; Fairweather, M.; Wang, J.; Clancy, T.E.; Ashley, S.W.; Urman, R.D.; Whang, E.E.; Gold, J.S. The improvement in post-operative mortality following pancreaticoduodenectomy between 2006 and 2016 is associated with an improvement in the ability to rescue patients after major morbidity, not in the rate of major morbidity. HPB (Oxford) 2021, 23, 434–443. [Google Scholar] [CrossRef] [PubMed]
  56. Bassi, C.; Marchegiani, G.; Giuliani, T.; Di Gioia, A.; Andrianello, S.; Zingaretti, C.C.; Brentegani, G.; De Pastena, M.; Fontana, M.; Pea, A.; et al. Pancreatoduodenectomy at the Verona Pancreas Institute: The evolution of indications, surgical techniques, and outcomes: A retrospective analysis of 3000 consecutive cases. Ann Surg. 2022, 276, 1029–1038. [Google Scholar] [CrossRef] [PubMed]
  57. Di Gioia, A.; Giuliani, T.; Marchegiani, G.; Andrianello, S.; Bonamini, D.; Secchettin, E.; Esposito, A.; Bassi, C.; Salvia, R. Pancreatoduodenectomy in obese patients: Surgery for nonmalignant tumors might be deferred. HPB (Oxford). 2022, 24, 885–892. [Google Scholar] [CrossRef] [PubMed]
  58. Sutton, T.L.; Potter, K.C.; O’Grady, J.; Aziz, M.; Mayo, S.C.; Pommier, R.; Gilbert, E.W.; Rocha, F.; Sheppard, B.C. Intensive Care Unit Observation after Pancreatectomy: Treating the Patient or the Surgeon? J. Surg. Oncol. 2022, 125, 847–855. Available online: https://onlinelibrary.wiley.com/doi/10.1002/jso.26800 (accessed on 1 October 2025). [CrossRef] [PubMed]
  59. van Beek, D.J.; Takkenkamp, T.J.; Wong-Lun-Hing, E.M.; de Kleine, R.J.; Walenkamp, A.M.E.; Klaase, J.M.; Nijkamp, M.W.; Valk, G.D.; Molenaar, I.Q.; Hagendoorn, J.; et al. Risk factors for complications after surgery for pancreatic neuroendocrine tumors. Surgery 2022, 172, 127–136. [Google Scholar] [CrossRef] [PubMed]
  60. Fukada, M.; Murase, K.; Higashi, T.; Yasufuku, I.; Sato, Y.; Tajima, J.Y.; Kiyama, S.; Tanaka, Y.; Okumura, N.; Matsuhashi, N. Perioperative predictive factors of failure to rescue following highly advanced hepatobiliary-pancreatic surgery: A single-institution retrospective study. World J. Surg. Oncol. 2023, 21, 365. [Google Scholar] [CrossRef] [PubMed]
  61. Li, V.; Serrano, P.E. Prediction of postoperative mortality in patients with organ failure following pancreaticoduodenectomy. Am. Surg. 2023, 89, 1519–1526. [Google Scholar] [CrossRef] [PubMed]
  62. Moazzam, Z.; Lima, H.A.; Alaimo, L.; Endo, Y.; Ejaz, A.; Beane, J.; Dillhoff, M.; Cloyd, J.; Pawlik, T.M. Hepatopancreatic surgeons versus pancreatic surgeons: Does surgical subspecialization impact patient care and outcomes? J. Gastrointest. Surg. 2023, 27, 750–759. [Google Scholar] [CrossRef] [PubMed]
  63. Suurmeijer, J.A.; Henry, A.C.; Bonsing, B.A.; Bosscha, K.; van Dam, R.M.; van Eijck, C.H.; Gerhards, M.F.; van der Harst, E.; de Hingh, I.H.; Intven, M.P.; et al. Outcome of pancreatic surgery during the first 6 years of a mandatory audit within the Dutch Pancreatic Cancer Group. Ann. Surg. 2023, 278, 260–266. [Google Scholar] [CrossRef] [PubMed]
  64. Theijse, R.T.; Stoop, T.F.; Hendriks, T.E.; Suurmeijer, J.A.; Smits, F.J.; Bonsing, B.A.; Lips, D.J.; Manusama, E.; van der Harst, E.; Patijn, G.A.; et al. Nationwide outcome after pancreatoduodenectomy in patients at very high risk (ISGPS-D) for postoperative pancreatic fistula. Ann. Surg. 2023, 281, 322–328. [Google Scholar] [CrossRef] [PubMed]
  65. Vawter, K.; Kuhn, S.; Pitt, H.; Wells, A.; Jensen, H.K.; Mavros, M.N. Complications and failure-to-rescue after pancreatectomy and hospital participation in the targeted American College of Surgeons National Surgical Quality Improvement Program registry. Surgery 2023, 174, 1235–1240. [Google Scholar] [CrossRef] [PubMed]
  66. Cannas, S.; Casciani, F.; Vollmer, C.M.; Pancreas Fistula Study Group. Extending quality improvement for pancreatoduodenectomy within the high-volume setting: The experience factor. Ann. Surg. 2024, 279, 1036–1045. [Google Scholar] [CrossRef] [PubMed]
  67. de Graaff, M.R.; Hendriks, T.E.; Wouters, M.; Nielen, M.; de Hingh, I.H.J.T.; Koerkamp, B.G.; van Santvoort, H.C.; Busch, O.R.; den Dulk, M.; Klaase, J.M.; et al. Assessing quality of hepato-pancreato-biliary surgery: Nationwide benchmarking. Br. J. Surg. 2024, 111, znae119. [Google Scholar] [CrossRef] [PubMed]
  68. Duclos, C.; Durin, T.; Marchese, U.; Sauvanet, A.; Laurent, C.; Ayav, A.; Turrini, O.; Sulpice, L.; Addeo, P.; Souche, F.R.; et al. Management and outcomes of hemorrhage after distal pancreatectomy: A multicenter study at high volume centers. HPB (Oxford) 2024, 26, 234–240. [Google Scholar] [CrossRef] [PubMed]
  69. Heckman, J.T.; Martinez, A.E.; Keim, R.L.; Mazzaferro, S.E.; Mir, K.S.; Gorman, M.A.; Shah, U.S. Implementation of robotic pancreaticoduodenectomy at a community tertiary care hospital utilizing a comprehensive curriculum. Am. J. Surg. 2024, 228, 83–87. [Google Scholar] [CrossRef] [PubMed]
  70. Henry, A.C.; Smits, F.J.; Daamen, L.A.; Busch, O.R.; Bosscha, K.; van Dam, R.M.; van Dam, C.J.L.; van Eijck, C.H.; Festen, S.; van der Harst, E.; et al. Root-cause analysis of mortality after pancreatic resection in a nationwide cohort. HPB (Oxford) 2025, 27, 461–469. [Google Scholar] [CrossRef] [PubMed]
  71. Khalid, A.; Pasha, S.A.; Demyan, L.; Standring, O.; King, D.A.; Newman, E.; DePeralta, D.; Gholami, S.; Weiss, M.J.; Melis, M. Evaluating the association of area deprivation index (ADI) on postoperative outcomes in pancreatic adenocarcinoma. J. Surg. Oncol. 2025, 131, 637–645. [Google Scholar] [CrossRef] [PubMed]
  72. Kinny-Köster, B.; Halm, D.; Tran, D.; Kaiser, J.; Heckler, M.; Hank, T.; Hinz, U.; Berchtold, C.; Al-Saeedi, M.; Roth, S.; et al. Who do we fail to rescue after pancreatoduodenectomy? Outcomes among >4000 procedures expose windows of opportunity. Ann. Surg. 2024. epub ahead of print. [Google Scholar] [CrossRef] [PubMed]
  73. Leech, N.; Krige, J.E.J.; Sobnach, S.; Kloppers, J.C.; Bernon, M.M.; Burmeister, S.; Jonas, E.G. Does the textbook outcome in pancreatic surgery score after pancreaticoduodenectomy for ampullary carcinoma have prognostic value? S Afr. J. Surg. 2024, 62, 33–38. Available online: https://journals.co.za/doi/10.36303/SAJS.00414 (accessed on 1 October 2025). [CrossRef] [PubMed]
  74. PancreasGroup.org Collaborative. Pancreatic surgery outcomes: Multicentre prospective snapshot study in 67 countries. Br. J. Surg. 2024, 111, znad330. [Google Scholar] [CrossRef] [PubMed]
  75. Patel, P.B.; Anyanwu, A.; Gross, C.R.; Adams, D.H.; Varghese, R. The intra-aortic balloon pump as a rescue device: Do we need to shift our strategy for cardiogenic shock rescue after cardiac surgery? J. Thorac. Cardiovasc. Surg. 2025, 170, 618–627. [Google Scholar] [CrossRef] [PubMed]
  76. Wang, X.; Liang, X.; Wang, S.; Zhang, C.S. The impact of body mass index on multiple complications, respiratory complications, failure to rescue and in-hospital mortality after laparoscopic pancreaticoduodenectomy: A single-center retrospective study. J. Laparoendosc. Adv. Surg. Technol. A. 2024, 34, 497–504. [Google Scholar] [CrossRef] [PubMed]
  77. Capretti, G.; Ricci, C.; Langella, S.; Nicolini, D.; Pacilio, C.A.; Aymerito, F.; Ingaldi, C.; Mocchegiani, F.; Russolillo, N.; Ferrero, F.; et al. Outcomes after pancreatoduodenectomy and total pancreatectomy in patients with a high-risk pancreatic anastomosis: An entropy balance analysis. Surgery 2025, 181, 109277. [Google Scholar] [CrossRef] [PubMed]
  78. Tschaidse, T.; Hofmann, F.O.; Renz, B.; Hungbauer, M.; Klinger, C.; Buhr, H.J.; Uhl, W.; Mees, S.T.; Keck, T.; Reissfelder, C.; et al. Perioperative outcomes in an age-adapted analysis of the German StuDoQ|Pancreas registry for PDAC. BMC Surg. 2025, 25, 4. [Google Scholar] [CrossRef] [PubMed]
  79. Uttinger, K.; Niezold, A.; Weimann, L.; Plum, P.S.; Baum, P.; Diers, J.; Brunotte, M.; Rademacher, S.; Germer, C.T.; Seehofer, D.; et al. Weekday effect of surgery on in-hospital outcome in pancreatic surgery: A population-based study. Langenbecks Arch. Surg. 2024, 410, 4. [Google Scholar] [CrossRef] [PubMed]
  80. Ghaferi, A.A.; Birkmeyer, J.D.; Dimick, J.B. Complications, failure to rescue, and mortality with major inpatient surgery in Medicare patients. Ann. Surg. 2009, 250, 1029–1034. [Google Scholar] [CrossRef] [PubMed]
  81. Gleeson, E.M.; Pitt, H.A. Failure to rescue after the Whipple: What do we know? Adv. Surg. 2022, 56, 1–11. [Google Scholar] [CrossRef] [PubMed]
  82. Belghiti, J.; Sauvanet, A. Ancient and modern history of pancreatic surgery. Pancreas 2025. epub ahead of print. [Google Scholar] [CrossRef] [PubMed]
  83. Chen, Q.; Beal, E.W.; Kimbrough, C.W.; Bagante, F.; Merath, K.; Dillhoff, M.; Schmidt, C.; White, S.; Cloyd, J.; Pawlik, T.M. Perioperative complications and the cost of rescue or failure to rescue in hepato-pancreato-biliary surgery. HPB (Oxford). 2018, 20, 854–864. [Google Scholar] [CrossRef] [PubMed]
  84. Cassin, B.R.; Barach, P.R. Making sense of root cause analysis investigations of surgery-related adverse events. Surg. Clin. North. Am. 2012, 92, 101–115. [Google Scholar] [CrossRef] [PubMed]
  85. Muthu, S.; Ramasubramanian, S.; Jeyaraman, M.; Hartl, R.; Tavakoli, J.; Cho, S.K.; Scaramuzzo, L.; Singh, H.; Louie, P.K.; Demetriades, A.K.; et al. Framework for adoption of enabling technologies for improved outcomes in spine surgery. Global Spine, J. 2025, 15, 2977–2985. [Google Scholar] [CrossRef] [PubMed]
  86. Hallet, J.; Jerath, A.; Perez d’Empaire, P.; Carrier, F.M.; Turgeon, A.F.; McIsaac, D.I.; Idestrup, C.; Lorello, G.; Flexman, A.; Kidane, B.; et al. Familiarity of the Surgeon-Anesthesiologist Dyad and Major Morbidity After High-Risk Elective Surgery. JAMA Surg. 2025, 160, 772–781. Available online: https://jamanetwork.com/journals/jamasurgery/fullarticle/2834597 (accessed on 1 October 2025). [CrossRef] [PubMed]
  87. De Bie, A.J.R.; Subbe, C.P.; Bezemer, R.; Cooksley, T.; Kellett, J.G.; Holland, M.; Bouwman, R.A.; Bindels, A.J.G.H.; Korsten, H.H.M. Differences in identification of patients’ deterioration may hamper the success of clinical escalation protocols. QJM 2019, 112, 497–504. [Google Scholar] [CrossRef] [PubMed]
  88. Ramaswamy, R.; Barach, P.R. Toward a learning system for ERAS: Embedding implementation and learning evaluation. In Enhanced Recovery After Surgery: A Complete Guide to Optimizing Outcomes; Ljungvist, O., Urman, R.D., Francis, N.K., Eds.; Springer International Publishing: Cham, Switzerland, 2020; pp. 361–372. [Google Scholar] [CrossRef]
  89. Hanson, C.C.; Barach, P. Improving cardiac care quality and safety through partnerships with patients and their families. Prog. Pediatr. Cardiol. 2012, 33, 73–79. [Google Scholar] [CrossRef]
  90. Baker, D.P.; Salas, E.; King, H.; Battles, J.; Barach, P. The role of teamwork in the professional education of physicians: Current status and assessment recommendations. Jt. Comm. J. Qual. Patient Saf. 2005, 31, 185–202. [Google Scholar] [CrossRef] [PubMed]
  91. Flin, R.; Martin, L.; Goeters, K.M.; Hörmann, H.J.; Amalberti, R.; Valot, C.; Nijhuis, H. Development of the NOTECHS (non-technical skills) system for assessing pilots’ CRM skills. Hum. Factors Aerosp. Saf. 2003, 3, 95–117. [Google Scholar]
  92. Barach, P.; Weinger, M.B. Trauma team performance. In Trauma: Critical Care; Wilson, W.C., Grande, C.M., Hoyt, D.B., Eds.; Marcel Dekker: New York, NY, USA, 2003; pp. 101–113. [Google Scholar] [CrossRef]
  93. Barach, P.; Johnson, J.K. Understanding the complexity of redesigning care around the clinical microsystem. Qual. Saf. Health Care. 2006, 15, i10–i16. [Google Scholar] [CrossRef] [PubMed]
  94. Bognár, A.; Barach, P.; Johnson, J.K.; Duncan, R.C.; Birnbach, D.; Woods, D.; Holl, J.L.; Bacha, E.A. Errors and the burden of errors: Attitudes, perceptions, and the culture of safety in pediatric cardiac surgical teams. Ann. Thorac. Surg. 2008, 85, 1374–1381. [Google Scholar] [CrossRef] [PubMed]
  95. Rattray, N.A.; Flanagan, M.E.; Militello, L.G.; Barach, P.; Franks, Z.; Ebright, P.; Rehman, S.U.; Gordon, H.S.; Frankel, R.M. “Do you know what I know?”: How communication norms and recipient design shape the content and effectiveness of patient handoffs. J. Gen. Intern. Med. 2019, 34, 264–271. [Google Scholar] [CrossRef] [PubMed]
  96. Uramatsu, M.; Fujisawa, Y.; Mizuno, S.; Souma, T.; Komatsubara, A.; Miki, T. Do failures in non-technical skills contribute to fatal medical accidents in Japan? A review of the 2010–2013 national accident reports. BMJ Open. 2017, 7, e013678. [Google Scholar] [CrossRef] [PubMed]
  97. Flin, R.; O’Connor, P. Safety at the Sharp End: A Guide to Non-Technical Skills; CRC Press: London, UK, 2008; p. 330. [Google Scholar] [CrossRef]
  98. Reason, J. Patient Safety; Wiley-Blackwell: Chichester, UK, 2010. [Google Scholar]
  99. Yule, S.; Flin, R.; Paterson-Brown, S.; Maran, N.; Rowley, D. Development of a rating system for surgeons’ non-technical skills. Med. Educ. 2006, 40, 1098–1104. [Google Scholar] [CrossRef] [PubMed]
  100. Vincent, C.; Moorthy, K.; Sarker, S.K.; Chang, A.; Darzi, A. Systems approaches to surgical quality and safety: From concept to measurement. Ann. Surg. 2004, 239, 475–482. [Google Scholar] [CrossRef] [PubMed]
  101. Arulampalam, T.; Barach, P. Human factors in surgery: Optimal surgical team proficiency and decision making. Bull. R. Coll. Surg. Engl. 2023, 105, 128–133. Available online: https://publishing.rcseng.ac.uk/doi/10.1308/rcsbull.2023.45 (accessed on 1 October 2025). [CrossRef]
  102. Edmondson, A.C. Psychological Safety and Learning Behavior in Work Teams. Adm. Sci. Q. 1999, 44, 350–383. [Google Scholar] [CrossRef]
  103. Sutcliffe, K.M.; Lewton, E.; Rosenthal, M.M. Communication failures: An insidious contributor to medical mishaps. Acad. Med. 2004, 79, 186–194. [Google Scholar] [CrossRef] [PubMed]
  104. Leape, L.L. Error in medicine. JAMA. 1994, 272, 1851–1857. Available online: https://jamanetwork.com/journals/jama/article-abstract/384554 (accessed on 1 October 2025). [CrossRef] [PubMed]
  105. Reason, J. Managing the Risks of Organizational Accidents; Routledge: London, UK, 1997; p. 272. [Google Scholar] [CrossRef]
  106. Vaughan, D. The Challenger Launch Decision: Risky Technology, Culture, and Deviance at NASA, Enlarged ed.; University of Chicago Press: Chicago, IL, USA, 1996. [Google Scholar]
  107. Wong, L.R.; Flynn-Evans, E.; Ruskin, K. Fatigue Risk Management: The Impact of Anesthesiology Residents’ Work Schedules on Job Performance and a Review of Potential Countermeasures. Anesth. Analg. 2018, 126, 1340–1348. Available online: https://journals.lww.com/anesthesia-analgesia/fulltext/2018/04000/fatigue_risk_management__the_impact_of.38.aspx (accessed on 1 October 2025). [CrossRef] [PubMed]
  108. Pouw, M.E.; Peelen, L.M.; Moons, K.G.M.; Kalkman, C.J.; Lingsma, H.F. Including post-discharge mortality in calculation of hospital standardised mortality ratios: Retrospective analysis of hospital episode statistics. BMJ 2013, 347, f5913. Available online: https://www.bmj.com/content/347/bmj.f5913 (accessed on 1 October 2025). [CrossRef] [PubMed]
  109. Dindo, D.; Demartines, N.; Clavien, P.A. Classification of surgical complications: A new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann. Surg. 2004, 240, 205–213. Available online: https://journals.lww.com/annalsofsurgery/fulltext/2004/08000/classification_of_surgical_complications__a_new.3.aspx (accessed on 1 October 2025). [CrossRef] [PubMed]
  110. Bassi, C.; Marchegiani, G.; Dervenis, C.; Sarr, M.; Hilal, M.A.; Adham, M.; PAllen, P.; Andersson, R.; Asbun, H.J.; Besselink, M.G. The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 Years After. Surgery 2017, 161, 584–591. Available online: https://www.surgjournal.com/article/S0039-6060(16)30757-7/fulltext (accessed on 1 October 2025). [CrossRef] [PubMed]
  111. Strasberg, S.M.; Linehan, D.C.; Hawkins, W.G. The accordion severity grading system of surgical complications. Ann. Surg. 2009, 250, 177–186. Available online: https://journals.lww.com/annalsofsurgery/fulltext/2009/08000/the_accordion_severity_grading_system_of_surgical.1.aspx (accessed on 1 October 2025). [CrossRef] [PubMed]
  112. Swanson, R.S.; Pezzi, C.M.; Mallin, K.; Loomis, A.M.; Winchester, D.P. The 90-day mortality after pancreatectomy for cancer is double the 30-day mortality: More than 20,000 resections from the national cancer data base. Ann. Surg. Oncol. 2014, 21, 4059–4067. Available online: https://link.springer.com/article/10.1245/s10434-014-4036-4 (accessed on 1 October 2025). [CrossRef] [PubMed]
  113. Ellis, D.I.; Altan, D.; Chang, D.C. Failure and Rescue in Surgery—Surgical Covenant, Palliative Care, and Reimagining Quality. JAMA Surg. 2022. Online ahead of print. Available online: https://jamanetwork.com/journals/jamasurgery/fullarticle/2796288 (accessed on 1 October 2025). [PubMed]
  114. Agha, R.A.; Fowler, A.J.; Sevdalis, N. The role of non-technical skills in surgery. Ann. Med. Surg. (Lond) 2015, 4, 422–427. [Google Scholar] [CrossRef] [PubMed]
  115. Blum, R.H.; Raemer, D.B.; Carroll, J.S.; Sunder, N.; Felstein, D.M.; Cooper, J.B. Crisis resource management training for an anaesthesia faculty: A new approach to continuing education. Med. Educ. 2004, 38, 45–55. [Google Scholar] [CrossRef] [PubMed]
  116. Leonard, M.; Graham, S.; Bonacum, D. The human factor: The critical importance of effective teamwork and communication in providing safe care. Qual. Saf. Health Care. 2004, 13, i85–i90. [Google Scholar] [CrossRef] [PubMed]
  117. Greenberg, C.C.; Regenbogen, S.E.; Studdert, D.M.; Lipsitz, S.R.; Rogers, S.O.; Zinner, M.J.; Gawande, A.A. Patterns of communication breakdowns resulting in injury to surgical patients. J. Am. Coll. Surg. 2007, 204, 533–540. [Google Scholar] [CrossRef] [PubMed]
  118. Lingard, L.; Espin, S.; Whyte, S.; Regehr, G.; Baker, G.R.; Reznick, R.; Bohnen, J.; Orser, B.; Doran, D.; Grober, E. Communication failures in the operating room: An observational classification of recurrent types and effects. Qual. Saf. Health Care. 2004, 13, 330–334. [Google Scholar] [CrossRef] [PubMed]
  119. Agency for Healthcare Research and Quality. TeamSTEPPS®: National Implementation. Available online: https://www.ahrq.gov/teamstepps/index.html (accessed on 9 August 2025).
  120. King, H.B.; Battles, J.; Baker, D.P.; Alonso, A.; Salas, E.; Webster, J.; Toomey, L.; Salisbury, M. TeamSTEPPS™: Team Strategies and Tools to Enhance Performance and Patient Safety. In Advances in Patient Safety: New Directions and Alternative Approaches (Vol. 3: Performance and Tools); Henriksen, K., Battles, J.B., Keyes, M.A., Grady, M.L., Eds.; Agency for Healthcare Research and Quality: Rockville, MD, USA, 2008. Available online: https://www.ncbi.nlm.nih.gov/books/NBK43686/ (accessed on 9 August 2025). [PubMed]
  121. Fletcher, G.C.L.; McGeorge, P.; Flin, R.H.; Glavin, R.J.; Maran, N.J. The role of non-technical skills in anaesthesia: A review of current literature. Br. J. Anaesth. 2002, 88, 418–429. [Google Scholar] [CrossRef] [PubMed]
  122. Chejfec-Ciociano, J.M.; Barach, P.; Gelb, A.W. Operationalising perioperative safety: Learning to walk the talk. Br. J. Anaesth. 2025, 135, 538–543. [Google Scholar] [CrossRef] [PubMed]
  123. Taha, A.; Taha-Mehlitz, S.; Ortlieb, N.; Ochs, V.; Honaker, M.D.; Rosenberg, R.; Lock, J.F.; Bolli, M.; Cattin, P.C.C. Machine learning in pancreas surgery, what is new? literature review. Front. Surg. 2023, 10, 1142585. [Google Scholar] [CrossRef] [PubMed]
  124. Booth, A.; Clarke, M.; Dooley, G.; Ghersi, D.; Moher, D.; Petticrew, M.; Stewart, L. The nuts and bolts of PROSPERO: An international prospective register of systematic reviews. Syst. Rev. 2012, 1, 2. [Google Scholar] [CrossRef] [PubMed]
  125. Sterne, J.A.; Hernán, M.A.; Reeves, B.C.; Savović, J.; Berkman, N.D.; Viswanathan, M.; Henry, D.; Altman, D.G.; Ansari, M.T.; Boutron, I.; et al. ROBINS-I: A tool for assessing risk of bias in non-randomised studies of interventions. BMJ 2016, 355, i4919. [Google Scholar] [CrossRef] [PubMed]
  126. Sterne, J.A.C.; Savović, J.; Page, M.J.; Elbers, R.G.; Blencowe, N.S.; Boutron, I.; Cates, C.J.; Cheng, H.Y.; Corbett, M.S.; Eldridge, S.M.; et al. RoB 2: A revised tool for assessing risk of bias in randomised trials. BMJ 2019, 366, l4898. Available online: https://www.bmj.com/content/366/bmj.l4898 (accessed on 1 October 2025). [CrossRef] [PubMed]
  127. Higgins, J.P.T.; Thomas, J.; Chandler, J.; Cumpston, M.; Li, T.; Page, M.J.; Welch, V.A. (Eds.) Cochrane Handbook for Systematic Reviews of Interventions, 2nd ed.; Wiley-Blackwell: Chichester, UK, 2019. [Google Scholar] [CrossRef]
  128. Morrison, A.; Polisena, J.; Husereau, D.; Moulton, K.; Clark, M.; Fiander, M.; Mierzwinski-Urban, M.; Clifford, T.; Hutton, B.; Rabb, D. The effect of English-language restriction on systematic review-based meta-analyses: A systematic review of empirical studies. Int. J. Technol. Assess. Health Care. 2012, 28, 138–144. [Google Scholar] [CrossRef] [PubMed]
  129. Yuan, Y.; Hunt, R.H. Systematic reviews: The good, the bad, and the ugly. Am. J. Gastroenterol. 2009, 104, 1086–1092. [Google Scholar] [CrossRef] [PubMed]
  130. Portuondo, J.; Shah, S.R.; Raval, M.V.; Pan, I.W.; Zhu, H.; Fallon, S.C.; Harris, A.H.; Singh, H.; Massarweh, N.N. Complications and failure to rescue after inpatient pediatric surgery. Ann. Surg. 2022, 276, e239–e246. [Google Scholar] [CrossRef] [PubMed]
  131. Biccard, B.M.; Madiba, T.E.; South African Surgical Outcomes Study Investigators. The South African Surgical Outcomes Study: A 7-day prospective observational cohort study. S Afr. Med, J. 2015, 105, 465–475. Available online: https://www.sajaa.co.za/index.php/sajaa/article/view/1590 (accessed on 1 October 2025). [CrossRef] [PubMed]
  132. Glance, L.G.; Osler, T.M.; Mukamel, D.B.; Dick, A.W. Effect of complications on mortality after coronary artery bypass grafting surgery: Evidence from New York State. J. Thorac. Cardiovasc. Surg. 2007, 134, 53–58. Available online: https://www.jtcvs.org/article/S0022-5223(07)00543-0/fulltext (accessed on 1 October 2025). [CrossRef] [PubMed]
  133. Hull, L.; Arora, S.; Aggarwal, R.; Darzi, A.; Vincent, C.; Sevdalis, N. The impact of nontechnical skills on technical performance in surgery: A systematic review. J. Am. Coll. Surg. 2012, 214, 214–230. [Google Scholar] [CrossRef] [PubMed]
  134. Neily, J.; Mills, P.D.; Young-Xu, Y.; Carney, B.T.; West, P.; Berger, D.H.; Mazzia, L.; Paull, D.E.; Bagian, J.P. Association between implementation of a medical team training program and surgical mortality. JAMA 2010, 304, 1693–1700. Available online: https://jamanetwork.com/journals/jama/fullarticle/186748 (accessed on 1 October 2025). [CrossRef] [PubMed]
  135. Guyatt, G.H.; Oxman, A.D.; Vist, G.E.; Kunz, R.; Falck-Ytter, Y.; Alonso-Coello, P.; Schünemann, H.J.; GRADE Working Group. GRADE: An emerging consensus on rating quality of evidence and strength of recommendations. BMJ 2008, 336, 924–926. [Google Scholar] [CrossRef] [PubMed]
Figure 1. PRISMA 2020 flow diagram of study selection for this systematic review with narrative synthesis on failure to rescue (FTR) after pancreatic surgery. Studies were sequentially excluded if they were unrelated to hepato-biliary-pancreatic surgery, lacked specific reference to FTR, or did not include data on pancreatic surgery.
Figure 1. PRISMA 2020 flow diagram of study selection for this systematic review with narrative synthesis on failure to rescue (FTR) after pancreatic surgery. Studies were sequentially excluded if they were unrelated to hepato-biliary-pancreatic surgery, lacked specific reference to FTR, or did not include data on pancreatic surgery.
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Table 1. Summary of key failure to rescue (FTR) studies: Authors, year, design, study period, number of institutions, number of patients, data source, and procedure mix.
Table 1. Summary of key failure to rescue (FTR) studies: Authors, year, design, study period, number of institutions, number of patients, data source, and procedure mix.
AuthorsYearDesignDurationNo. of
Institutions
No. of PatientsData SourceProcedure Mix (PD/DP/TP) & Approach
Ghaferi et al. [23]2010RN2000–20066728862NIS (HCUP-AHRQ) + AHA Annual SurveyNR (identified by pancreatectomy ICD-9-CM codes; PD/DP/TP breakdown not reported)
Haigh et al. [36]2011RN2005–20071832610ACS NSQIP participant-use filesPD 100% (classic or pylorus-preserving)
Amini et al. [37]2015RN2000–2011180235,986HCUP Nationwide Inpatient SamplePD 51.7%; DP 33.3%; TP 5.6% (Others 9.4%) (Open 94.9%; MIS 5.1%)
Healy et al. [38]2015RM2008–2013191007Michigan Surgical Quality Collaborative (MSQC)PD 62.1% (Whipple 48.1% + PP-Whipple 14.0%); DP 34.1%; TP 1.8% (Open 100%)
Tamirisa et al. [25]2016RM2011–2012372694ACS NSQIP Pancreatectomy Demonstration ProjectPD 64.4%; DP 30.7%; TP 3.0%
Carr et al. [39]2017RS2013–20151254ACS NSQIP (QITI) + institutional PD databasePD 100%
Gani et al. [40]2017RN2002–2011~183411,081HCUP Nationwide Inpatient Sample (AHRQ)PD 65.8%; DP 24.6%; TP 3.7% (Open 95%; MIS 5.0%)
Varley et al. [41]2017RN2005–2012NR4514ACS NSQIP PUFPD 100%
Capretti et al. [26]2018RM2010–20137856Prospectively collected hospital databases, centrally merged at HumanitasPD 61.8%; DP 28.2%; TP 10.0% (LP 10.7%)
Chen et al. [42]2018RN2013–2015NR15,140 MEDPAR Inpatient Files + Denominator FilePD/DP/TP breakdown NR (Open 90.6%; MIS 9.4%)
El Amrani et al. [4]2018RN2012–2015NR (exact count not specified)12,333PMSI (ICD-10 + French procedure classification; linked administrative data)PD 68.9%; DP 26.9%; TP 3.2%; central 1.0%
Krautz et al. [8]2018RN2009–2014~65460,858Nationwide DRG statistics (Federal Statistical Office & Länder RDC)PD (proximal) 60.3%; DP 26.5%; TP 8.0% (remaining: segmental 2.8%; other partial 2.4%)
Pecorelli et al. [43]2018RM2008–20153120Institutional prospective databases at three university-affiliated high-volume centers; preoperative CT assessed centrallyPD 100%; DP 0%; TP 0%
van Rijssen et al. [44]2018PN2014–2015181342Dutch Pancreatic Cancer Audit (DPCA)PD 100%
Cerullo et al. [45]2019RN2010–2014NR3280Truven Health Analytics MarketScan Commercial Claims & EncountersPD 93.3%; TP 6.7%
Diaz et al. [46]2019RM2005–201618923,014California OSHPD hospital discharge databasePD 100%
Gleeson et al. [47]2019RN2005–2012NR5027ACS NSQIP PUFPD 100%; DP 0%; TP 0%
Merath et al. [48]2019RN2013–201573713,873MEDPAR Inpatient Files linked with Denominator File; AHA Survey; Medicare cost reports (wage index)NR
Sánchez-Velázquez et al. [5]2019RI2012–2015232375Prospective databases from each center centrally pooled (whipplebenchmarks.org)PD 100% (Open 100%)
van Roessel et al. [49]2019RS1992–201711434Institutional prospective database; survival from National Cancer RegistryPD 100% (PPPD 81.9%; Whipple 18.1%) (Open 96.4%; LP 3.6%)
Wroński et al. [50]2019RS2003–2017143Single institution (Medical University of Warsaw)PD 100%; DP 0%
Bhatti et al. [51]2020RS2011–20181116Single-institution hospital recordsPD 100% (standard PD 70%; PPPD 19%; PD + organ resection 11%; vascular resection 12%)
El Amrani et al. [18]2020RN2012–2018NR (nationwide; all hospitals)19,938PMSI (ICD-10 diagnoses + CCAM procedures)PD 75.0%; DP 23.9%; CP 0.7%; TP 0.4%
Nymo et al. [52]2020RN2015–20165394NoRGast national quality registry + EPJ cross-check; deaths via National Registry linkagePD 100%
Endo et al. [53]2021RN2011–2014≈4000422National Clinical Database (NCD)HPD (which includes PD as a component) 100%; Major HPD (60%); Minor HPD (40%)
Gleeson et al. [20]2021RI2014–2017≈22422,983ACS NSQIP; DPCA; SNPPCR; DGAV StuDoQ PancreasPD 100% (MIS 6.0%)
Lequeu et al. [54]2021RN2009–201863110,632PMSI (Programme de Médicalisation des Systèmes d’Information)DP 100% (Open 77.0%; LP 23.0%)
Pastrana et al. [55]2021RN2006–2016~121–68032,165ACS NSQIP PUFPD 100%
Bassi et al. [56]2022RS2000–201912989Institutional database (prospectively collected; retrospectively analyzed)PD 100% (PPPD 86.0%; Whipple 14.0%)
Di Gioia et al. [57]2022RS2010–201911865University of Verona Hospital Trust (Pancreas Institute) prospective database; retrospectively analyzedPD 100%
Sutton et al. [58]2022RS2013–20201637Institutional NSQIP (100% capture of pancreatectomies); MPOG (intra-op); hospital cost administrative data (USD)Whipple/Total pancreatectomy 63%; DP/RAMPS 37% (Open 81.5%; MIS 18.5% by back-calculatin)
van Beek et al. [59]2022RM2008–20192123Hospital surgical databases & histopathology archives; electronic patient recordsPD/PPPD 41.5%; DP 40.7%; TP 4.9% (enucleation 9.8%; combined 3.3%) (Open 66.7%; LP 13.0%; Rb 20.3%)
Fukada et al. [60]2023RS2010–20221177Single-institution hospital dataset (JSHBPS-certified training institution)NR (mixed HPB procedures; PD/DP/TP distribution unclear)
Li et al. [61]2023RS2011–2020158Single-center HPB prospective registry + retrospective chart completionPD 100%
Moazzam et al. [62]2023RN2013–201767719,625100% Medicare Standard Analytic Files (SAFs)NR
Suurmeijer et al. [63]2023PN2014–201918 → 165345Dutch Pancreatic Cancer Audit (DPCA; DPCG)PD 79%; DP 21%
Theijse et al. [64]2023RN2014–2021NR (all national DPCG centers)1402 Dutch Pancreatic Cancer Audit (DPCA)PD 100% (PPPD 48.2%; PRPD 12.6%; Classic Whipple 39.2%) (Open 74.6%; Rb 20.3%; LP 5.11%)
Vawter et al. [65]2023RN2014–2019NR45,157ACS NSQIP standard & pancreas-targeted registriesPD 67%; DP 33%
Cannas et al. [66]2024RI2003–2023188189Pancreas Fistula Study Group datasetPD 100% (MIS 3.8%)
de Graaff et al. [67]2024RN2014–2021247365DHBA, DPCA (managed by DICA)PD 78.9%; DP 21.1% (Open 68.8%; LP 26.8%; 4.4%, minor variable-level missingness remains)
Duclos et al. [68]2024RM2014–201821118821 high-volume centers (data collected at each site)DP 100% (Open 52.8%; LP 41.4%; Rb 5.8%)
Heckman et al. [69]2024RS2016–2022165Prospectively maintained institutional database + ACS NSQIPPD 100% (Rb 100%)
Henry et al. [70]2024RN2014–201917149Dutch Pancreatic Cancer Audit (DPCA); PORSCH PD 82%; DP 11%; TP 7% (Open 88%; LP 7%; Rb 6%)
Khalid et al. [71]2024RM2014–2023NR (multicenter health-system EHR registry) 314Northwell Health multicenter pancreatic cancer database (EHR abstracted to REDCap)PD (classical; PPPD; LP; Rb;); DP (open; LP; Rb); TP
Kinny-Köster et al. [72]2024RS2003–20211156Prospective institutional pancreatectomy registryPD 100% (Open 96.8%; Rb 3.2%)
Leech et al. [73]2024RS1999–2023179Pancreatic resection registry (UCT/Groote Schuur)PD 100% (PPPD 98.7%; Classical 1.3%)
PancreasGroup.org Collaborative [74]2024PI20213544223PancreasGroup.org electronic CRF (mandatory outcome fields)PD 59.3%; DP 24.5%; TP 6.9%; Enucleation 1.5%; Other 5.2% (percentages may not sum to 100%) (Open 83.9%; LP 11.6%; Rb 4.5%)
Patel et al. [75]2024RN2014–2020NR (multicenter NSQIP)15,790ACS NSQIP Pancreatectomy TargetedPD/DP/TP (PD/DP/TP distribution unclear)
Wang et al. [76]2024RS2015–20221995Single hospital database (The First Hospital of Jilin University)PD 100% (LP 100%)
Capretti et al. [77]2025PM2016–20225277Prospectively collected data from participating centersPD 72.9%; TP 27.1%
Tschaidse et al. [78]2023RN2014–2019~603011StuDoQ|Pancreas (DGAV) registryPD 80.1%; DP 19.9% (Open 94%; LP 5.7%)
Uttinger et al. [79]2025RN2010–202093994,661German DRG billing data (Federal Statistical Office)PD 61.2%; DP 26.6%; TP 9.9%
PD: pancreatoduodenectomy (Whipple); PP: pylorus-preserving; PRPD: pylorus-resecting PD; DP: distal pancreatectomy; TP: total pancreatectomy; CP: central pancreatectomy. LP: laparoscopic; Rb: robotic; MIS: minimally invasive surgery; RAMPS: radical antegrade modular pancreatosplenectomy; HPD: hepatopancreatoduodenectomy. NR: not reported; “–” = not applicable/excluded. ACS NSQIP, DPCA, DPCG, PMSI, MEDPAR, NoRGast, DGAV, DICA, OSHPD, AHRQ follow their standard registry/agency names.
Table 2. The literature explicitly defining and reporting failure to rescue (FTR) metrics.
Table 2. The literature explicitly defining and reporting failure to rescue (FTR) metrics.
AuthorsYearDefinitionTime WindowSeverity ThresholdDenominatorReported FTR (n/N, %)Post-Discharge Capture
Capretti et al. (PD) [77] 202590-CD3 [G1]90 daysCD ≥ III (≥IIIa)CD ≥ III complication15/73 (20.5%)Yes (90-day follow-up; method NR)
Capretti et al. (TP) [77] 202590-CD3 [G1]90 daysCD ≥ III (≥IIIa)CD ≥ III complication3/19 (15.8%)Yes (90-day follow-up; method NR)
Lequeu et al. [54]202190-CD3 [G1]90 daysCD ≥ IIICD ≥ III complication355/3153 (11.2%)Unclear (national in/outpatient linkage, external death ascertainment NR)
Nymo et al. [52]202090-Acc3 [G1]90 daysAccordion ≥ 3 (re-anchored to CD ≥ III)Major complication (Accordion ≥ 3)17/125 (13.6%)Yes (national registry linkage incl. cross-regional EPJ)
PancreasGroup.org Collaborative (PD) [74]202490-CD3a [G1]90 daysCD ≥ IIIaMajor-complication (CD ≥ IIIa)157/717 (21.9%)Yes (prospective 90-day follow-up via CRF; ascertainment method NR)
PancreasGroup.org Collaborative (DP) [74]202490-CD3a [G1]90 daysCD ≥ IIIaMajor-complication (CD ≥ IIIa)20/203 (10.0%)Yes (prospective 90-day follow-up via CRF; ascertainment method NR)
Pecorelli et al. [43]201890-CD3 [G1]90 daysCD ≥ III (III–IV)CD ≥ III complication23/120 (19.2%)Yes (90-day mortality; method NR)
van Beek et al. [59]202290-CD3 [G1]90 daysCD ≥ IIICD ≥ III complication1/51 (2.0%)Unclear (90-day mortality adopted; ascertainment NR)
Bassi et al. [56]2022H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)70/597 (11.7%)No (in-hospital only)
de Graaff et al. (PD) [67]2024H/30-CD3a [G3]In-hospital/30 daysCD ≥ IIIaMajor complications (CD ≥ IIIa)7.5% (1.6–28.5%)No (in-hospital/30 d)
de Graaff et al. (DP) [67]2024H/30-CD3a [G3]In-hospital/30 daysCD ≥ IIIaMajor complications (CD ≥ IIIa)3.1% (0–14.9%)No (in-hospital/30 d)
Di Gioia et al. [57]2022H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)57/404 (14.1%)No (in-hospital only)
Fukada et al. [60]2023H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)9/177 (5.1%)No (in-hospital only)
Leech et al. [73]2024H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)3/21 (14.3%)No (in-hospital only)
Suurmeijer et al. [63]2023H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)PD 54/404 > 46/426 > 34/462 (13.4 > 10.8 > 7.4%); DP 5/57 > 6/84 > 5/85 (8.8 > 7.1 > 5.9%)No (in-hospital/30 d; 90 d not obtained)
Theijse et al. [64]2023H-CD3a [G3]In-hospitalCD ≥ IIIaMajor complications (CD ≥ IIIa)57/642 (8.9%)No (DPCA −30 d only)
van Rijssen et al. [44]2018H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)56/391 (14.3%)No (in-hospital only)
van Roessel et al. [49]2019H-CD3 [G3]In-hospitalCD ≥ IIIMajor complications (CD ≥ III)31/463 (6.7%)No (in-hospital only)
Gleeson et al. [20]2021H-CD3-Mix [G3]In-hospitalCD ≥ III or ISGPS POPF B/C (mixed)CD ≥ III or POPF B/C (mixed)8.20%No (in-hospital only)
Chen et al. [42]201890-Any-Admin [G4]90 daysAny (administrative)Any complicationPancreas Open 19.4%, MIS 13.4%Yes (Medicare denominator file)
Carr et al. [39]2017H/30-Any [G5]30 d/In-hospitalAny (non-CD)Any complicationFellow 6%, Resident 4%Unclear (30 d and in-hospital mixed)
Haigh et al. [36]201130-Any-NSQIP [G5]30 daysNSQIP “≥1 morbidity”“≥1 morbidity”older 10.1% vs. younger 4.1%Yes (NSQIP 30 d)
Amini et al. [37]2015H-Any-Admin [G6]In-hospitalOther (ICD-9 “major”)Any complication (ICD-9 “major”)All 9.0%; LV 12.0%; IV 8.5%; HV 6.4%No (in-hospital only; NIS)
Cerullo et al. [45]2019H-Any-Admin [G6]In-hospitalOther (claims “major”)Major complications (claims)27/920 (2.9%)No (in-hospital only)
El Amrani et al. [18]2020H-Any-Admin [G6]In-hospitalOther (administrative “major”)≥1 major complications940/10,758 (8.7%)No (in-hospital only)
Gani et al. [40]2017H-Any-Admin [G6]In-hospitalAny (AHRQ)Any complicationLV 11.1%, IV 7.1%, HV5.4%No (in-hospital only)
Ghaferi et al. [23]2010H-Any-Admin [G6]In-hospitalOther (ICD-9 “major”)Major complications
(ICD-9)
Quintile of hospital mortality (6.4–40.0)No (in-hospital only)
Tamirisa et al. [25]2016H-Any-NSQIP [G6]In-hospitalAny (NSQIP events)Any complication34/1111 (3.1%)No (in-hospital only)
Uttinger et al. [79]2025H-Any-Admin [G6]In-hospitalAny (administrative/registry)Any complication8040/64,029 (12.6%)No (in-hospital only)
Varley et al. [41]2017H-Any-NSQIP [G6]In-hospitalAny (NSQIP major/minor)Any complication312/4514 (6.9%)No (in-hospital only)
Duclos et al. [68]202490-Spec [G7]90 daysISGPS CR-PPH B/C and/or CR-POPF B/CSpecific complications (CR-PPH n = 65; CR-POPF n = 202)CR-PPH 9/65 (13.8%); CR-POPF 1.3% (n NR)Yes (90-day outcome capture; method NR)
Cannas et al. [66]202490-Acc3-Alt [G8]90 daysAccordion ≥3Severe complications (Accordion ≥ 3)182/1533 (11.9%)Yes (90-day follow-up)
Gleeson et al. [47]201930-NSser-NSQIP [G8]30 daysNSQIP serious/majorSerious/major morbidity361/5027 (7.2%)Yes (NSQIP 30 d)
Healy et al. [38]201530-Alt [G8]30 daysMSQC major (non-Clavien)Major complications (MSQC)LV 21.8%, HV 14.9%Yes (registry 30 d)
Li et al. [61]2023H + 90-CD4 [G8]In-hospital + 90 daysCD IVCD IV patients19/58 (33.0%)Unclear (90 d capture; method NR)
Pastrana Del Valle et al. [55]202130-NSmaj-NSQIP [G8]30 daysNSQIP major morbidityMajor morbidityYearly % 9.8→4.1 (2006→2016)Yes (NSQIP 30 d)
Patel et al. [75]202430-CD3-NSQIP [G8]30 daysCD ≥ III (NSQIP mapped)Major complications (CD ≥ III)245/4623 (5.3%)Yes (NSQIP 30 d)
Vawter et al. [65]202330-NSser-NSQIP [G8]30 daysNSQIP serious morbiditySerious morbidityStandard NSQIP: PD 184/1720 (10.7%); DP 47/578 (8.1%); Pancreas-targeted NSQIP: PD 400/5871 (6.8%); DP 94/1681 (5.6%)Yes (NSQIP 30 d)
Wang et al. [76]2024H-Any-Alt [G8]In-hospitalOther (enumerated “major”)“Major complications” (denominator NR)24 (2.4%)No (in-hospital only)
Endo et al. [53]2021Comp-Any [G8]Composite (in-hospital ≤90 days + 30 days post-discharge)Any (non-CD)Any complication33.3%/17.0%/9.3% (22/66; 8/47; 18/193)Partial (composite window)
Definitions: G1: FTR90—Clavien–Dindo grade ≥III, G2: FTR30—Clavien–Dindo grade ≥III, G3: In-hospital—Clavien–Dindo grade ≥III, G4: FTR90—Any complication, G5: FTR30—Any complication, G6: In-hospital—Any complication, G7: Specific complication (e.g., POPF grade B/C as the index event), G8: Alternative/Non-comparable definitions, Severity threshold: CD: Clavien–Dindo; ISGPS: International Study Group of Pancreatic Surgery; NSQIP: National Quality Improvement Project; ICD: International Classification of Diseases; Agency for Healthcare Research and Quality; MSQC: Michigan Surgical Quality Collaborative; Reported FTR (n/N, %): PD: pancreatoduodenectomy (Whipple); DP: distal pancreatectomy; MIS: minimally invasive surgery; LV: low volume; IV: intermediate volume; HV: high volume; CR: clinically relevant; PPH: postpancreatectomy hemorrhage; POPF: postoperative pancreatic fistula, Post-discharge capture: NR: not reported; EPJ: electronic patient journal; CRF: cade report form; DPCA: Dutch Pancreatic Cancer Audit; NIS: Nationwide Inpatient Sample.
Table 3. Summary of intervention strategies identified for reducing failure to rescue (FTR) in pancreatic surgery.
Table 3. Summary of intervention strategies identified for reducing failure to rescue (FTR) in pancreatic surgery.
AuthorsOrganizational/Institutional FactorsSurgical
Technique
Perioperative ManagementPatient-
Related
Factors
Non-Technical Skills (NTS)
Ghaferi et al. [23]
Haigh et al. [36]
Amini et al. [37]
Healy et al. [38]
Tamirisa et al. [25]
Carr et al. [39]
Gani et al. [40]
Varley et al. [41]
Capretti et al. [26]
Chen et al. [42]
El Amrani et al. [4]
Krautz et al. [8]
Pecorelli et al. [43]
van Rijssen et al. [44]
Cerullo et al. [45]
Diaz et al. [46]
Gleeson et al. [47]
Merath et al. [48]
Sánchez-Velázquez et al. [5]
van Roessel et al. [49]
Wroński et al. [50]
Bhatti et al. [51]
El Amrani et al. [68]
Nymo et al. [52]
Endo et al. [53]
Gleeson et al. [20]
Lequeu et al. [54]
Pastrana et al. [55]
Bassi et al. [56]
Di Gioia et al. [57]
Sutton et al. [58]
van Beek et al. [59]
Fukada et al. [60]
Li et al. [61]
Moazzam et al. [62]
Suurmeijer et al. [63]
Theijse et al. [64]
Vawter et al. [65]
Cannas et al. [66]
de Graaff et al. [67]
Duclos et al. [68]
Heckman et al. [69]
Henry et al. [70]
Khalid et al. [71]
Kinny-Köster et al. [72]
Leech et al. [73]
Patel et al. [75]
Uttinger et al. [79]
Wang et al. [76]
PancreasGroup.org Collaborative [74]
Capretti et al. [77]
Tschaidse et al. [78]
Table 4. Main categories and elements of non-technical skills.
Table 4. Main categories and elements of non-technical skills.
CategoryElements
Situation awareness Gathering information
Interpreting information
Anticipating future states
Decision-making Defining the problem
Considering options
Selecting and implementing an option
Outcome review
CommunicationSending information clearly and concisely
Including context and intent during information exchange
Receiving information, especially by listening
Identifying and addressing barriers to communication
Team workingSupporting others
Solving conflicts
Exchanging information
Coordinating activities
Leadership Using authority
Maintaining standards
Planning and prioritizing
Managing workload and resources
Managing stress Identifying the symptoms of stress
Recognizing the effects of stress
Implementing coping strategies
Coping with fatigue Identifying the symptoms of fatigue
Recognizing the effects of fatigue
Implementing coping strategies
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MDPI and ACS Style

Uramatsu, M.; Fujisawa, Y.; Barach, P.; Osakabe, H.; Matsumoto, M.; Nagakawa, Y. Failure to Rescue After Surgery for Pancreatic Cancer: A Systematic Review and Narrative Synthesis of Risk Factors and Safety Strategies. Cancers 2025, 17, 3259. https://doi.org/10.3390/cancers17193259

AMA Style

Uramatsu M, Fujisawa Y, Barach P, Osakabe H, Matsumoto M, Nagakawa Y. Failure to Rescue After Surgery for Pancreatic Cancer: A Systematic Review and Narrative Synthesis of Risk Factors and Safety Strategies. Cancers. 2025; 17(19):3259. https://doi.org/10.3390/cancers17193259

Chicago/Turabian Style

Uramatsu, Masashi, Yoshikazu Fujisawa, Paul Barach, Hiroaki Osakabe, Moe Matsumoto, and Yuichi Nagakawa. 2025. "Failure to Rescue After Surgery for Pancreatic Cancer: A Systematic Review and Narrative Synthesis of Risk Factors and Safety Strategies" Cancers 17, no. 19: 3259. https://doi.org/10.3390/cancers17193259

APA Style

Uramatsu, M., Fujisawa, Y., Barach, P., Osakabe, H., Matsumoto, M., & Nagakawa, Y. (2025). Failure to Rescue After Surgery for Pancreatic Cancer: A Systematic Review and Narrative Synthesis of Risk Factors and Safety Strategies. Cancers, 17(19), 3259. https://doi.org/10.3390/cancers17193259

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