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Background:
Systematic Review

Impact of Perioperative Fluid Strategies on Outcomes in Radical Cystectomy: A Systematic Review

1
Department of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, 85-094 Bydgoszcz, Poland
2
Department of Regenerative Medicine, Collegium Medicum, Nicolaus Copernicus University, 85-094 Bydgoszcz, Poland
*
Authors to whom correspondence should be addressed.
Cancers 2025, 17(11), 1746; https://doi.org/10.3390/cancers17111746
Submission received: 1 April 2025 / Revised: 13 May 2025 / Accepted: 20 May 2025 / Published: 22 May 2025

Simple Summary

Fluid management during bladder cancer surgery can affect how much blood a patient loses, how quickly they recover, and whether complications occur. In this review, we looked at different ways of giving fluids during radical cystectomy, including limited (restrictive) fluids, personalized fluid therapy, and using warmed fluids. Some approaches, like limiting fluids and adjusting them based on the patient’s condition, may help reduce blood loss and complications. However, the studies used different surgical techniques and protocols, which makes it hard to say which method works best. Some patients had robotic surgery, others had open surgery, and some had different ways of reconnecting the urinary system. More high-quality research is needed to better understand which fluid therapy is safest and most effective for patients having this major surgery.

Abstract

Background: Perioperative fluid management plays a critical role in optimizing recovery after radical cystectomy. Various strategies, such as restrictive fluid therapy, goal-directed fluid therapy (GDFT), and warmed fluids, have been studied for their impact on complications and outcomes. However, the optimal approach remains uncertain. Methods: We conducted a systematic review in accordance with PRISMA 2020 guidelines. A PubMed search was performed in January 2025. Eligible studies included randomized controlled trials (RCTs) and observational studies published in English that assessed perioperative fluid strategies in radical cystectomy. Two reviewers independently selected studies, with a third resolving discrepancies. Data were extracted on study characteristics, interventions, and outcomes. Risk of bias was assessed using the Cochrane Risk of Bias Tool. Due to heterogeneity, narrative synthesis was used. Results: Seventeen studies (eight RCTs, nine observational; total n = 3519) were included. Three publications based on a single RCT (n = 167) showed that restrictive fluid therapy with norepinephrine significantly reduced blood loss (p < 0.0001), transfusions (p = 0.0006), complications (p = 0.006), and hospital stay (p = 0.02), with a trend toward fewer 90-day complications (p = 0.12). Six studies (four RCTs, two observational) evaluated GDFT. Doppler- and SVV-based GDFT reduced ileus, nausea, wound infections, and blood loss, although findings on renal function and length of stay were mixed. One RCT showed that warmed fluids reduced transfusion needs (p = 0.028) and hospital stay (p = 0.05). VBFI (Vascular Bed Filling Index)- and aVBFI (adjusted Vascular Bed Filling Index)-guided strategies may lower complications in ileal conduit patients, but evidence remains limited. Conclusions: Restrictive fluid therapy with norepinephrine appears to improve outcomes after radical cystectomy. GDFT and warmed fluids show potential benefits, but findings are inconsistent. Further high-quality trials are needed to define the optimal strategy.

1. Introduction

Radical cystectomy with urinary diversion remains the standard treatment for muscle-invasive bladder cancer. Despite advancements in surgical techniques and perioperative care, the procedure continues to be associated with significant morbidity and complications [1,2,3,4].
Multiple factors influence postoperative complications following radical cystectomy. Even inflammatory and hematological parameters appear to have an impact on surgical outcomes [5]. Perioperative fluid management plays a crucial role in optimizing postoperative recovery and minimizing complications, including postoperative ileus [6]. Some reports suggest that the total perioperative fluid administration should not exceed 3 L within the perioperative period [7]. While various perioperative fluid management approaches during radical cystectomy have been described in the literature, the optimal strategy remains undefined.
Restrictive fluid therapy is a key component of the Enhanced Recovery After Surgery (ERAS) protocol, which was originally developed for general surgery and has since been successfully implemented in urological oncology, including radical cystectomy (RC). Incorporating ERAS elements such as fluid restriction, early mobilization, and minimized surgical stress has been shown to reduce hospital length of stay and improve recovery outcomes [8,9,10]. Meta-analyses further support its benefits in RC, demonstrating lower complication rates and faster return of bowel function [11].
This systematic review aims to evaluate the impact of different perioperative fluid management strategies on surgical outcomes in patients undergoing radical cystectomy. It focuses on key postoperative complications, including ileus, acute kidney injury, and blood transfusion rates. The review follows the PRISMA guidelines to ensure a comprehensive and unbiased synthesis of the available evidence (Supplementary Materials).

2. Materials and Methods

The methodology used in this study adheres to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.
A literature search was conducted in January 2025 using the PubMed database with the following search query:
(“Cystectomy”[Mesh] OR cystectomy OR “RARC” OR “radical cystectomy”) AND (“Perioperative Care”[Mesh] OR “Perioperative Period” OR “ERAS” OR “enhanced recovery after surgery” OR “fluid management” OR “fluid restriction” OR “fluid therapy”) AND (“Postoperative Complications”[Mesh] OR complications OR “acute kidney injury” OR “acute kidney failure” OR “hospital stay” OR “bowel function” OR “analgesic use” OR pain OR readmission OR mortality OR “quality of life” OR “QoL” OR “life quality” OR “surgical site infection” OR “SSI” OR ileus OR “blood transfusion” OR “electrolyte imbalance”) AND (“Urinary Bladder Neoplasms”[Mesh] OR “bladder cancer” OR “bladder neoplasm”). The retrieved studies were subsequently analyzed.
Randomized controlled trials (RCTs) and observational studies published in English, evaluating the impact of different perioperative fluid therapy strategies during radical cystectomy on postoperative outcomes and complications, were included in the review.
The selection process was conducted by two independent reviewers and verified by a third researcher who resolved any discrepancies. Studies without full-text availability were excluded. The selection process is illustrated in the PRISMA flowchart (Figure 1).
Data were extracted regarding authors, year of publication, study type, study population, intervention type, and key outcomes. Study quality was assessed using the Cochrane Risk of Bias Tool (version RoB2). Risk of bias was assessed using the Cochrane Risk of Bias Tool, evaluating domains such as sequence generation, allocation concealment, blinding, completeness of outcome data, and selective reporting. Each domain was classified as having low, high, or unclear risk of bias based on the criteria outlined in the Cochrane Handbook. A narrative synthesis was performed to evaluate significant differences in study designs.
Reporting bias (e.g., publication bias or selective outcome reporting) was not formally assessed due to the narrative nature of the synthesis and the limited number of studies per outcome. Effect measures included mean differences for continuous outcomes (e.g., blood loss and length of stay) and proportions or risk differences for binary outcomes (e.g., complications, transfusions, and AKI). Where available, p-values were reported. Other effect measures, such as odds ratios or confidence intervals, were not consistently provided across studies.
The certainty of evidence for selected key outcomes (acute kidney injury, blood loss and transfusions, postoperative ileus, length of hospital stay, and chronic kidney disease) was assessed using an adapted GRADE approach, taking into account risk of bias, consistency, precision, and directness across studies.
This review was not prospectively registered.

3. Results

3.1. Study Selection and Characteristics

A total of 538 articles were identified in the initial search. After screening, 31 articles were subjected to full-text evaluation. Following a rigorous selection process, 17 articles were included in the systematic review.
These 17 studies focused on comparing perioperative fluid therapy strategies in patients undergoing radical cystectomy with lymphadenectomy and urinary diversion for bladder cancer. Among them, 8 studies were randomized controlled trials (RCTs) with a double-blind design, including 3 articles analyzing the same population, with 1 being a follow-up study. The remaining 9 studies were observational, including 6 retrospective studies, 1 prospective study, and 2 studies comparing retrospective and prospective cohorts.
Regarding the surgical approach, 8 studies analyzed patients undergoing open radical cystectomy (ORC), 1 study assessed patients treated with robot-assisted laparoscopic radical cystectomy (RARC), and 1 study included both RARC and ORC. In 5 studies, the surgical approach was not explicitly defined. Additionally, 8 of the included studies incorporated the ERAS (Enhanced Recovery After Surgery) protocol.
The total patient population analyzed across all included studies comprised 3519 patients. The characteristics of the included studies are presented in Table 1. The risk of bias for the included trials was assessed and is summarized in Table 2, where variability in methodological quality is highlighted as a factor potentially influencing the strength of the evidence. Potential reporting bias was not evaluated.

3.2. Restrictive Fluid Therapy with Norepinephrine Use

The use of norepinephrine infusion combined with restrictive fluid therapy is described in three publications based on a single randomized clinical trial [20,21,22].
A total of 83 patients were included in the study group, and 84 in the control group. The results indicate that the application of restrictive fluid therapy combined with norepinephrine infusion significantly reduces blood loss (800 mL vs. 1200 mL; p < 0.0001) and decreases the need for blood product transfusion (33% vs. 60%; p = 0.0006). This approach also lowers the risk of complications during hospitalization (52% vs. 73%; p = 0.006), including gastrointestinal complications (6% vs. 31%; p < 0.0001) and cardiovascular complications (20% vs. 48% p = 0.0003). Moreover, it shortens the length of hospital stay (15 days vs. 17 days; p = 0.02) and reduces mortality within 90 days postoperatively (0% vs. 4.8%; p = 0.12).

3.3. Goal-Directed Fluid Therapy (GDFT)

Goal-directed fluid therapy refers to individualized fluid administration guided by dynamic hemodynamic parameters to optimize tissue perfusion and avoid fluid overload. The use of GDFT is described in six studies, including four randomized trials [9,10,11,13] and two observational studies [17,28]. The total number of patients in the study groups was 470, while 551 patients were assigned to the control groups. Both observational studies incorporated the ERAS protocol.
Ghoreifi et al. [17] found no significant differences between GDFT and conventional fluid therapy in terms of blood loss (567 mL vs. 580 mL; p = 0.6), eGFR trend (p = 0.85), length of stay (4 days in both groups; p = 0.85), 90-day high-grade complication rate (17.6% vs. 17.2%; p = 0.5), or 90-day readmissions (28.6% vs. 29.7%; p = 0.9). Patel et al. [28] reported a lower intraoperative blood transfusion rate (0.58 vs. 0.97; p ≤ 0.001) and a lower incidence of nausea (3.1% vs. 8.1%; p < 0.05) in the GDFT group. However, no significant differences were observed in length of stay (LOS) (6 days in both groups; p = 0.89), peak pain levels (4.4 vs. 4.4; p = 0.89), or 30- and 90-day readmissions (p = 0.34 and p = 0.14, respectively). The authors noted no differences in time to first flatus or 30- and 90-day complication rates, but p-values were not provided for these variables.
Randomized trials assessing GDFT using Doppler ultrasound demonstrated a lower risk of ileus (22% vs. 53%; p < 0.001), nausea (9% vs. 32% p < 0.01), or time to flatus (3.55 days vs. 5.36 days; p < 0.01 [15]. Wound infection rates were reduced in the study group (1 vs. 8; p < 0.01). Liu et al. [16] demonstrated a lower risk of nausea, vomiting, and hypotension (all p < 0.05). Patients in the intervention groups experienced a faster return of bowel function (2.1 days vs. 3.0 days; p < 0.05); however, the length of hospital stay was shorter in the control group (11.5 days vs. 13.7 days; p < 0.05).
GDFT based on stroke volume variation (SVV) was associated with reduced blood loss (734.3 mL vs. 1096.5 mL; p = 0.019) and a lower transfusion rate (0.5 units vs. 1.9 units; p = 0.005). However, this did not significantly affect gastrointestinal function (p = 0.326, p = 0.4) or length of hospital stay (p = 0.23, p = 0.9) [13].
The data regarding acute kidney injury (AKI) are conflicting. A study with a larger sample size reported a higher risk of AKI in the GDFT group (56% vs. 40%; p = 0.005) [14].
Given the variation in study designs, populations, interventions, and outcome measures, a quantitative synthesis was deemed inappropriate.

3.4. Warming Fluid Transfusion

A randomized clinical trial by Luo et al. indicates that perioperative fluid therapy using warmed fluids at 38–42 °C in patients undergoing robot-assisted radical cystectomy (RARC) reduces fluid transfusions (1903 mL vs. 2153 mL; p = 0.028) and shortens the length of hospital stay (16 days vs. 20 days; p = 0.05). However, it does not affect blood loss, the need for reoperation, or bowel function [12].

3.5. Vascular Bed Filling Index

In another study of ours, we proposed the use of the Vascular Bed Filling Index (VBFI) and the adjusted Vascular Bed Filling Index (aVBFI) to determine the optimal volume of perioperatively administered fluids [23]. These indices are based on blood loss, the volume of perioperatively administered fluids, and the duration of the surgical procedure. The results suggest that fluid therapy guided by these indices may reduce the severity of complications after radical cystectomy, particularly in patients undergoing urinary diversion using an ileal conduit (VBFI = between 0 and 8; p = 0.011 for VBFI; p = 0.005 for aVBFI). Although the VBFI/aVBFI-guided approach showed a reduction in complications in patients undergoing ileal conduit diversion, it should be considered exploratory and hypothesis-generating, as it is based on a single retrospective study from the authors’ institution.

3.6. Anesthetist Impact

A retrospective study evaluated the impact of anesthesiologist experience on the outcomes of radical cystectomy. The study indicates that greater anesthesiologist experience (>10 cases) is associated with reduced blood loss (600 mL vs. 800 mL, p < 0.001) and a lower transfusion rate (7.2% vs. 22%, p = 0.001). However, it does not affect mortality or the need for rehospitalization [27].

3.7. Impact on Specific Complications

3.7.1. Acute Kidney Injury

Based on assessments of four studies (included two randomized trials and two retrospective observational studies), the relationship between perioperative fluid therapy and acute kidney injury (AKI) was analyzed. Both randomized trials compared the effects of goal-directed fluid therapy (GDFT) with control groups.
In the randomized studies, a total of 165 patients were included in the intervention groups, and 164 patients in the control groups. In both studies, the risk of AKI was higher in the intervention group. In a study by Kong et al. [13], 8 patients (34%) in the GDFT group and 6 patients (26%) in the control group developed AKI (p = 0.522). However, these numbers did not reach statistical significance, likely due to the small sample size. In contrast, Arslan-Carlon et al. [14] analyzed a larger cohort, where the risk of AKI was significantly higher in the restrictive fluid therapy group (56% vs. 40%, p = 0.005).
The results of observational studies are inconsistent. One observational study also indicates a higher risk of AKI in patients who received <5 mL/kg/h of perioperative fluids (p = 0.043, Citation 15). Conversely, Furrer et al. suggests that the administration of >2527 mL of crystalloids intraoperatively is associated with an increased risk of AKI (p = 0.3) [22].

3.7.2. Blood Loss and Transfusions

The results of four randomized clinical trials assessed perioperative blood loss and transfusion rates. Two studies investigated goal-directed fluid therapy (GDFT), one examined warming fluid transfusion, and one evaluated norepinephrine-assisted restrictive fluid therapy.
Restrictive fluid therapy with norepinephrine significantly reduced intraoperative transfusion rates (8% vs. 31%; p < 0.001) and postoperative transfusion requirements (28% vs. 48%, p = 0.0006) [25].
The findings regarding GDFT were inconsistent. Kong et al. [15] demonstrated that stroke volume variation (SVV) monitoring for fluid optimization significantly reduced blood loss (734 mL vs. 1096 mL; p < 0.001) and the number of transfusions (0.5–0.8 units vs. 1.9–2.2 units; p = 0.005) [13]. Conversely, Pillai et al. [15] found that Doppler ultrasound-based fluid therapy had no significant impact on blood loss (p = 0.6) or red blood cell transfusion requirements (p = 0.82). However, both of these studies had small sample sizes, with 23 vs. 23 and 32 vs. 34 patients in the study and control groups, respectively.
Additionally, warming fluid transfusion at 43 °C during cystectomy did not significantly affect blood loss (p = 0.19) [12].

3.7.3. Postoperative Ileus

Postoperative ileus is a significant concern in patients undergoing radical cystectomy. This issue was addressed in four clinical studies, with a total of 334 patients in the intervention groups and 337 patients in the control groups.
The use of low-dose norepinephrine was associated with a significant reduction in the risk of ileus (6% vs. 37%; p = 0.007) and gastrointestinal complications (6% vs. 31%; p < 0.0001) [24].
The remaining findings regarding various GDFT strategies were inconsistent. Most data indicate no significant effect of GDFT on the incidence of postoperative ileus (p = 0.4–(14); p = 0.3–(13)).
Only Pillai et al. [15] demonstrated a positive impact of GDFT on postoperative ileus (p < 0.001), bowel motility (p = 0.01), and time to first bowel movement (p = 0.02); however, this study had a small sample size.

3.8. Length of Stay

The findings regarding hospital length of stay (LOS) are as follows: Restrictive fluid therapy combined with norepinephrine infusion significantly reduced hospital stay (15 days vs. 17 days; p = 0.01) [24]. In contrast, GDFT did not impact LOS (7 days vs. 7 days; p = 0.9) [14], while warming fluid transfusion at 38–42 °C was associated with a shorter hospital stay (16 days vs. 20 days; p = 0.05) [12].
All of the above findings are derived from randomized clinical trials; however, it is noteworthy that significant differences were observed only in studies where the average hospital stay exceeded several days.
Additionally, an observational study using SVV-based GDFT found no difference in LOS between groups (4 days vs. 4 days; p = 0.85) [17].

3.9. Chronic Kidney Disease

A randomized clinical trial comparing conventional fluid therapy with restrictive fluid therapy combined with norepinephrine infusion found no significant differences in kidney function between groups after 7 days (p = 0.37) and at 3, 6, and 12 months after discharge (p = 0.49; p = 0.197; and p = 0.78, respectively) [26].
However, the study identified independent risk factors for kidney function deterioration, including diabetes (p = 0.002), preoperative eGFR (p = 0.007), and age (p = 0.038).

3.10. Certainty of Evidence (GRADE Assessment)

The overall certainty of evidence for outcomes was low to moderate. Certainty ratings were based on study design, consistency of results, precision of estimates, and risk of bias, following the GRADE framework. According to the GRADE assessment, the evidence was rated as low for acute kidney injury, postoperative ileus, and length of stay due to inconsistency and imprecision across studies. Moderate certainty was assigned to outcomes such as blood loss and transfusions and chronic kidney disease based on consistent findings and lower risk of bias. Detailed ratings are presented in Table 3.

4. Discussion

This systematic review assessed the impact of various perioperative fluid therapy strategies in patients undergoing radical cystectomy with lymphadenectomy and urinary diversion due to bladder cancer. The analyzed studies exhibit significant heterogeneity, and some contain methodological limitations, making direct comparisons between studies challenging. It is important to note that radical cystectomy and its postoperative complications vary significantly depending on the type of urinary diversion used [29]. This factor further complicates direct comparisons between studies.
The results of the current systematic review suggest that the most optimal approach involves restrictive fluid therapy combined with low-dose norepinephrine infusion or goal-directed fluid therapy (GDFT) using stroke volume variation (SVV) for fluid administration. The administration of pre-warmed fluids also appears to be a noteworthy strategy.
However, it is essential to consider that the Enhanced Recovery After Surgery (ERAS) protocol is actively implemented during radical cystectomy, contributing to reduced postoperative complications and faster recovery [26,27,28,29,30]. Since all components of the ERAS protocol work synergistically, evaluating fluid therapy in isolation from the protocol may be controversial. In this review, the ERAS protocol was applied in eight studies, but the methodologies of these studies do not allow for direct comparisons.
Restrictive fluid therapy with norepinephrine during radical cystectomy appears to be a promising strategy; however, ERAS was not implemented in these studies [20,21,22]. This approach has also been investigated in other surgical fields, including liver surgery [31], thoracic surgery [32], and head and neck oncological surgery [33], showing favorable outcomes.
The GDFT strategy, based on stroke volume variation or transesophageal Doppler monitoring, also appears to be a beneficial approach. However, randomized controlled trials evaluating these techniques included small sample sizes and did not involve concurrent ERAS protocol implementation [9,11,12].
Fluid therapy with pre-warmed fluids at approximately 41 °C may also be a valuable strategy. Although the total population of studies investigating this method during radical cystectomy is relatively small, this approach has demonstrated efficacy in other surgical procedures, including in elderly patients [33,34,35,36].
Differences in surgical approach (robotic vs. open) and urinary diversion technique (intracorporeal vs. extracorporeal) may influence key perioperative outcomes such as bleeding, postoperative ileus, and length of stay, and should therefore be taken into account when evaluating the effects of fluid management strategies [37,38].
The studies included in this review also differ in terms of surgical technique. It is important to emphasize that a significant proportion of radical cystectomies are now performed using laparoscopic or robot-assisted techniques. Robot-assisted surgery is associated with a longer operative time but a lower need for blood transfusion [37,38]. Based on these findings, the optimal fluid therapy strategy should also be considered in conjunction with the surgical approach.
The use of the Vascular Bed Filling Index and adjusted Vascular Bed Filling Index is based on a single retrospective study and requires further research to draw definitive conclusions.
This review was not prospectively registered, and only one database (PubMed) was searched, which may have led to selection bias. Only English-language publications were included, potentially omitting relevant evidence. Although study selection was conducted by two independent reviewers, data extraction and bias assessment were not independently duplicated. Reporting bias was not assessed, and certainty of evidence was evaluated only for selected outcomes. The included studies exhibited substantial heterogeneity in terms of design, population, surgical approach, and outcome reporting. A significant proportion of studies were observational and retrospective, with potential confounding and variable implementation of ERAS protocols. Additionally, the lack of standardized definitions for key outcomes, such as postoperative ileus or complications, limits comparability across studies. The presence of high or unclear risk of bias in multiple studies highlights the need for cautious interpretation of the findings and underlines the importance of high-quality randomized trials in this field.
Based on current evidence, restrictive fluid therapy with norepinephrine may reduce perioperative complications and blood loss, and could be considered as part of perioperative strategies in radical cystectomy, especially where ERAS protocols are not fully implemented. GDFT shows potential for reducing gastrointestinal complications and improving recovery, although findings on renal outcomes are inconsistent and warrant caution.
Future research should focus on direct comparisons of fluid therapy strategies in conjunction with the ERAS protocol and modern surgical techniques, with particular emphasis on the type of urinary diversion used.

5. Conclusions

Restrictive therapy with norepinephrine reduces blood loss and complications, while goal-directed fluid therapy improves hemodynamics but has mixed effects on complications and hospital stay. Warming fluids lower transfusions, and Vascular Bed Filling Index–based management may reduce complications, though evidence is limited. Further research is needed to determine the optimal approach.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cancers17111746/s1, PRISMA 2020 Checklist.

Author Contributions

Conceptualization, P.L. and A.O.; methodology, A.O. and P.L.; software, F.K.; validation, J.A., P.L. and T.D.; formal analysis, P.L. and K.J.; investigation, P.L.; resources, P.L.; data curation, P.L. and F.K; writing—original draft preparation, P.L.; writing—review and editing, A.O., K.J. and J.A.; visualization, P.L. and A.O.; supervision, K.J. and T.D.; project administration, K.J.; funding acquisition, K.J. 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.

Informed Consent Statement

Not applicable.

Data Availability Statement

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

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Maibom, S.L.; Joensen, U.N.; Poulsen, A.M.; Kehlet, H.; Brasso, K.; Røder, M.A. Short-term morbidity and mortality following radical cystectomy: A systematic review. BMJ Open 2021, 11, e043266. [Google Scholar] [CrossRef] [PubMed]
  2. Duquesne, I.; Benamran, D.; Masson-Lecomte, A.; De La Taille, A.; Peyromaure, M.; Rouprêt, M.; Delongchamps, N.B. Intraoperative complication of radical cystectomy for muscle-invasive bladder cancer: Does the surgical approach matter? A retrospective multicenter study using the EAUiaiC classification. World J. Urol. 2023, 41, 1061–1067. [Google Scholar] [CrossRef] [PubMed]
  3. van Ginkel, N.; Meijer, D.; Boormans, J.L.; Mertens, L.S.; van Beek, S.C.; Vis, A.N. The Dutch Cystectomy Snapshot Research Group Predictors of Major Complications and the Association with Oncological Outcomes After Radical Cystectomy for Bladder Cancer: A Nationwide Registry Study. Med. Res. Arch. 2023, 11. [Google Scholar] [CrossRef]
  4. Katsimperis, S.; Tzelves, L.; Tandogdu, Z.; Ta, A.; Geraghty, R.; Bellos, T.; Manolitsis, I.; Pyrgidis, N.; Schulz, G.B.; Sridhar, A.; et al. Complications After Radical Cystectomy: A Systematic Review and Meta-analysis of Randomized Controlled Trials with a Meta-regression Analysis. Eur. Urol. Focus 2023, 9, 920–929. [Google Scholar] [CrossRef]
  5. Ślusarczyk, A.; Pustuła, P.; Garbas, K.; Zapała, Ł.; Radziszewski, P. Mean platelet volume to lymphocyte ratio as an inflammatory marker associated with high-grade recurrence and progression of non-muscle-invasive bladder cancer treated with Bacillus Calmette-Guérin. Cent. Eur. J. Urol. 2024, 77, 599–611. [Google Scholar]
  6. Gómez-Izquierdo, J.C.; Feldman, L.S.; Carli, F.; Baldini, G. Meta-analysis of the effect of goal-directed therapy on bowel function after abdominal surgery. Br. J. Surg. 2015, 102, 577–589. [Google Scholar] [CrossRef]
  7. Schwenk, W.; Flemming, S.; Girona-Johannkämper, M.; Wendt, W.; Darwich, I.; Strey, C. Structured implementation of fast-track pathways to enhance recovery after elective colorectal resection: First results from five German hospitals. Chirurgie 2024, 95, 148–156. [Google Scholar] [CrossRef]
  8. Daneshmand, S.; Ahmadi, H.; Schuckman, A.K.; Mitra, A.P.; Cai, J.; Miranda, G.; Djaladat, H. Enhanced recovery protocol after radical cystectomy for bladder cancer. J. Urol. 2014, 192, 50–56. [Google Scholar] [CrossRef]
  9. Frees, S.K.; Aning, J.; Black, P.; Struss, W.; Bell, R.; Chavez-Munoz, C.; Gleave, M.; So, A.I. A prospective randomized pilot study evaluating an ERAS protocol versus a standard protocol for patients treated with radical cystectomy and urinary diversion for bladder cancer. World J. Urol. 2018, 36, 215–220. [Google Scholar] [CrossRef]
  10. Persson, B.; Carringer, M.; Andrén, O.; Andersson, S.-O.; Carlsson, J.; Ljungqvist, O. Initial experiences with the enhanced recovery after surgery (ERAS®) protocol in open radical cystectomy. Scand. J. Urol. 2015, 49, 302–307. [Google Scholar] [CrossRef]
  11. Tyson, M.D.; Chang, S.S. Enhanced Recovery Pathways Versus Standard Care After Cystectomy: A Meta-analysis of the Effect on Perioperative Outcomes. Eur. Urol. 2016, 70, 995–1003. [Google Scholar] [CrossRef] [PubMed]
  12. Luo, J.; Zhou, L.; Lin, S.; Yan, W.; Huang, L.; Liang, S. Beneficial effect of fluid warming in elderly patients with bladder cancer undergoing Da Vinci robotic-assisted laparoscopic radical cystectomy. Clinics 2020, 75, e1639. [Google Scholar] [CrossRef]
  13. Kong, Y.-G.; Kim, J.Y.; Yu, J.; Lim, J.; Hwang, J.-H.; Kim, Y.-K. Efficacy and safety of stroke volume variation-guided fluid therapy for reducing blood loss and transfusion requirements during radical cystectomy: A randomized clinical trial. Medicine 2016, 95, e3685. [Google Scholar] [CrossRef]
  14. Arslan-Carlon, V.; Tan, K.S.; Dalbagni, G.; Pedoto, A.C.; Herr, H.W.; Bochner, B.H.; Cha, E.K.; Donahue, T.F.; Fischer, M.; Donat, S.M. Goal-directed versus standard fluid therapy to decrease ileus after open radical cystectomy: A prospective randomized controlled trial. Anesthesiology 2020, 133, 293–303. [Google Scholar] [CrossRef]
  15. Pillai, P.; McEleavy, I.; Gaughan, M.; Snowden, C.; Nesbitt, I.; Durkan, G.; Johnson, M.; Cosgrove, J.; Thorpe, A. A double-blind randomized controlled clinical trial to assess the effect of doppler optimized intraoperative fluid management on outcome following radical cystectomy. J. Urol. 2011, 186, 2201–2206. [Google Scholar] [CrossRef]
  16. Liu, T.-J.; Zhang, J.-C.; Gao, X.-Z.; Tan, Z.-B.; Wang, J.-J.; Zhang, P.-P.; Cheng, A.-B.; Zhang, S.-B. Clinical research of goal-directed fluid therapy in elderly patients with radical resection of bladder cancer. J. Cancer Res. Ther. 2018, 14, S173–S179. [Google Scholar] [CrossRef]
  17. Ghoreifi, A.; Basin, M.F.; Ghodoussipour, S.; Bazargani, S.T.; Amini, E.; Aslzare, M.; Cai, J.; Miranda, G.; Sugeir, S.; Bhanvadia, S.; et al. Perioperative outcomes of goal-directed versus conventional fluid therapy in radical cystectomy with enhanced recovery protocol. Int. Urol. Nephrol. 2021, 53, 1827–1833. [Google Scholar] [CrossRef]
  18. Wei, C.; Wan, F.; Zhao, H.; Ma, J.; Gao, Z.; Lin, C. Application of enhanced recovery after surgery in patients undergoing radical cystectomy. J. Int. Med. Res. 2018, 46, 5011–5018. [Google Scholar] [CrossRef]
  19. Bazargani, S.T.; Ghodoussipour, S.; Tse, B.; Miranda, G.; Cai, J.; Schuckman, A.; Daneshmand, S.; Djaladat, H. The association between intraoperative fluid intake and postoperative complications in patients undergoing radical cystectomy with an enhanced recovery protocol. World J. Urol. 2018, 36, 401–407. [Google Scholar] [CrossRef]
  20. Dobé, T.-R.; Belhadj, Y.; Michel, C.; Djouadou, M.; Bouchardi, A.; Liron, C.; Bento, C.; Aregui, A.; Meria, P.; Thevenot, A.; et al. Perioperative results of radical cystectomy after neoadjuvant chemotherapy according to the implementation of ERAS pathway. Progres Urol. 2022, 32, 401–409. [Google Scholar] [CrossRef]
  21. Marques, M.; Tezier, M.; Tourret, M.; Cazenave, L.; Brun, C.; Duong, L.N.; Cambon, S.; Pouliquen, C.; Ettori, F.; Sannini, A.; et al. Risk factors for postoperative acute kidney injury after radical cystectomy for bladder cancer in the era of ERAS protocols: A retrospective observational study. PLoS ONE 2024, 19, e0309549. [Google Scholar] [CrossRef] [PubMed]
  22. Furrer, M.A.; Schneider, M.P.; Löffel, L.M.; Burkhard, F.C.; Wuethrich, P.Y. Impact of intra-operative fluid and noradrenaline administration on early postoperative renal function after cystectomy and urinary diversion. Eur. J. Anaesthesiol. 2018, 35, 641–649. [Google Scholar] [CrossRef] [PubMed]
  23. Lipowski, P.; Ostrowski, A.; Adamowicz, J.; Jasiewicz, P.; Kowalski, F.; Drewa, T.; Juszczak, K. Does the Administration of Intravenous Fluid Matter in the Context of the Incidence of Postoperative Complications After Radical Cystectomy? Cancers 2024, 17, 102. [Google Scholar] [CrossRef]
  24. Wüthrich, P.Y.; Burkhard, F.C.; Thalmann, G.; Stueber, F.; Studer, U. Restrictive Deferred Hydration Combined with Preemptive Norepinephrine Infusion During Radical Cystectomy Reduces Postoperative Complications and Hospitalization Time: A Randomized Clinical Trial. Anesthesiology 2014, 120, 365–377. [Google Scholar] [CrossRef]
  25. Wuethrich, P.Y.; Studer, U.E.; Thalmann, G.N.; Burkhard, F.C. intraoperative continuous norepinephrine infusion combined with restrictive deferred hydration significantly reduces the need for blood transfusion in patients undergoing open radical cystectomy: Results of a prospective randomised trial. Eur. Urol. 2014, 66, 352–360. [Google Scholar] [CrossRef]
  26. Wu, F.M.W.; Burkhard, F.; Turri, F.; Furrer, M.; Loeffel, L.; Thalmann, G.; Wuethrich, P. Renal outcome after radical cystectomy and urinary diversion performed with restrictive hydration and vasopressor administration in the frame of an enhanced recovery program: A follow-up study of a randomized clinical trial. Urol. Oncol. Semin. Orig. Investig. 2017, 35, 602.e11–602.e17. [Google Scholar] [CrossRef]
  27. Jubber, I.; Pang, K.H.; Groves, R.; Reed, O.; Noon, A.P.; Catto, J.W.; Cumberbatch, M.G. Impact of Anaesthetist Volume on Radical Cystectomy Outcomes. Eur. Urol. Focus 2021, 7, 117–123. [Google Scholar] [CrossRef]
  28. Patel, S.Y.; Getting, R.E.G.; Alford, B.; Hussein, K.; Schaible, B.J.; Boulware, D.; Lee, J.K.; Gilbert, S.M.; Powsang, J.M.; Sexton, W.J.; et al. Improved Outcomes of Enhanced Recovery After Surgery (ERAS) Protocol for Radical Cystectomy with Addition of a Multidisciplinary Care Process in a US Comprehensive Cancer Care Center. World J. Surg. 2018, 42, 2701–2707. [Google Scholar] [CrossRef]
  29. Tappero, S.; Dell’Oglio, P.; Cerruto, M.A.; Salas, R.S.; Rueda, O.B.; Simone, G.; Hendricksen, K.; Soria, F.; Umari, P.; Antonelli, A.; et al. Ileal Conduit Versus Orthotopic Neobladder Urinary Diversion in Robot-assisted Radical Cystectomy: Results from a Multi-institutional Series. Eur. Urol. Open Sci. 2023, 50, 47–56. [Google Scholar] [CrossRef]
  30. Crettenand, F.; M’baya, O.; Grilo, N.; Valerio, M.; Dartiguenave, F.B.; Cerantola, Y.; Roth, B.; Rouvé, J.-D.; Blanc, C.; Lucca, I. ERAS® protocol improves survival after radical cystectomy: A single-center cohort study. Medicine 2022, 101, e30258. [Google Scholar] [CrossRef]
  31. Coeckelenbergh, S.; Soucy-Proulx, M.; Van der Linden, P.; Roullet, S.; Moussa, M.; Kato, H.; Toubal, L.; Naili, S.; Rinehart, J.; Grogan, T.; et al. Restrictive versus Decision Support Guided Fluid Therapy during Major Hepatic Resection Surgery: A Randomized Controlled Trial. Anesthesiology 2024, 141, 881–890. [Google Scholar] [CrossRef] [PubMed]
  32. Gao, Y.; Ji, D.; Fang, Q.; Li, Y.; Wang, K.; Liu, J.; Wang, L.; Gu, E.; Zhang, L.; Chen, L. Effect of low-dose norepinephrine combined with goal-directed fluid therapy on postoperative pulmonary complications in lung surgery: A prospective randomized controlled trial. J. Clin. Anesthesia 2024, 99, 111645. [Google Scholar] [CrossRef] [PubMed]
  33. Al Saied, G.; Almutairi, H.M.; Alharbi, Y.; Almohanna, M.; Almutairi, A. Comparison Between the Impact of Vasopressors and Goal-Directed Fluid Therapy on the Management of Free Flap Reconstruction of Head and Neck and Monitoring in ICU. Cureus 2020, 12, e12108. [Google Scholar] [CrossRef]
  34. Simegn, G.D.; Bayable, S.D.; Fetene, M.B. Prevention and management of perioperative hypothermia in adult elective surgical patients: A systematic review. Ann. Med. Surg. 2021, 72, 103059. [Google Scholar] [CrossRef]
  35. Roshan, M.B.A.; Jafarpoor, H.; Shamsalinia, A.; Fotokian, Z.; Hamidi, S.H. Effects of a forced-air warming system and warmed intravenous fluids on hemodynamic parameters, shivering, and time to awakening in elderly patients undergoing open cardiac surgery. Ann. Card. Anaesth. 2023, 26, 386–392. [Google Scholar] [CrossRef]
  36. Camus, Y.; Delva, E.; Cohen, S.; Lienhart, A. The effects of warming intravenous fluids on intraoperative hypothermia and postoperative shivering during prolonged abdominal surgery. Acta Anaesthesiol. Scand. 1996, 40, 779–782. [Google Scholar] [CrossRef]
  37. Cella, L.; Basile, G.; Moretto, S.; Paciotti, M.; Hurle, R.; Lughezzani, G.; Avolio, P.P.; Piccolini, A.; Mancon, S.; Lazzeri, M.; et al. Robotic assisted vs open radical cystectomy: An updated systematic review and meta-analysis. J. Robot. Surg. 2024, 18, 277. [Google Scholar] [CrossRef]
  38. Mastroianni, R.; Tuderti, G.; Ferriero, M.; Anceschi, U.; Bove, A.M.; Brassetti, A.; D’Annunzio, S.; Misuraca, L.; Torregiani, G.; Covotta, M.; et al. Robot-assisted Radical Cystectomy with Totally Intracorporeal Urinary Diversion Versus Open Radical Cystectomy: 3-Year Outcomes from a Randomised Controlled Trial. Eur. Urol. 2024, 85, 422–430. [Google Scholar] [CrossRef]
Figure 1. PRISMA flowchart of the study selection process.
Figure 1. PRISMA flowchart of the study selection process.
Cancers 17 01746 g001
Table 1. Characteristics of included studies.
Table 1. Characteristics of included studies.
No.Author (Year)Study DesignParticipants
(Study Group vs. Control Group)
InterventionOutcomes
1Luo J. (2020) [12]RCT53 vs. 55Pre-warm fluid infusion use↓ transfusion, ↓ LOS
2Kong Y. (2016) [13]RCT23 vs. 23Fluid infusion based on stroke volume variation (SVV) 10–20% vs. <10%↓ transfusion, ↓ blood loss. ↔ complications,
↔ AKI, ↔ LOS
3Arslan-Carlon V. (2020) [14]RCT142 vs. 141Goal-directed stroke volume (SV) vs. standard fluid therapy↑ 30-day complications,
↑ acute kidney injury
↔ ileus, ↔LOS
4Pillai P. (2011) [15]RCT32 vs. 34Doppler-guided vs. standard fluid therapy↓ ileus, ↓ nausea, ↓ vomiting. ↓wound infection.
5Liu T. (2016)
[16]
RCT38 vs. 38Goal-directed SVV vs. routine fluid therapy↑ cardiac output index,
↑ MAP, ↑ central venous pressure. Better metabolic index. ↓ nausea, ↓ vomiting, ↓ hypotension.
6Ghoreifi A. (2021) [17]Retrospective cohort119 vs. 192Goal-directed SVV vs. convectional fluid therapy↔ kidney function,
↔ LOS, ↔ blood loss, ↔ transfusions, and readmissions.
7Wei C. (2018) [18]Retrospective cohort91 vs. 101ERAS (less fluids) vs. no ERAS↓ blood loss, ↓ transfusions, ↓ readmissions, and ↓ complications.
↓ bowel complications.
8Bazargani T.
(2018) [19]
Prospective cohort180Total intraoperative fluid volume, type of fluid impact↔ 30 -, 90-day complications, ↔ in LOS.
9Dobe T. (2022) [20]Prospective vs. retrospective control group29 vs. 50ERAS (less fluids + vasopressive drugs) vs. no ERAS↔ blood loss, ↔ transfusions, ↔ ileus, ↔ complications rate. ↓ LOS.
10Marques M. (2024) [21]Retrospective cohort51 vs. 71No AKI vs. AKI↑ AKI if restrictive intraoperative vascular filling, female sex, postoperative sepsis, day 1 SOFA score, creatinin D1.
11Furrer M. (2018) [22]Retrospective cohort100 vs. 812AKI vs. no AKI↑ AKI if surgery time >400 min, male, obesity, high blood loss, blood transfusion, more crystalloids.
12Lipowski P. (2024) [23]Retrospective cohort48 vs. 240Ileal conduit (IC) vs. ureterocutaneostomy (UCS), Vascular Bed Filling Index (VBFI),
adjusted Vascular Bed Filling Index (aVBFI)
VBFI, aVBFI:
< 8–UCS ↓ complications;
= 8–IC = UCS;
>8–IC ↑ complications.
13Wuethrich P. (2013) [24]RCT83 vs. 84Low volume + noradrenaline vs. balanced Ringer’s solution↓ hospital complications, ↓ gastrointestinal, ↓ cardiac, ↓ 90 days complications. ↓ LOS.
14Wuethrich P. (2013) [25]RCT83 vs. 84Low volume + noradrenaline vs. balanced Ringer’s solution↓ blood loss, ↓ transfusions.
15Mei Wen Wu F. (2013) [26]RCT83 vs. 84Low volume + noradrenaline vs. balanced Ringer’s solution↔ in renal function
7 days, 3, 6, and 12 months after surgery.
16Jubber I. (2019) [27]Retrospective cohort430High-volume anesthetist vs. low-volume anesthetist↓ LOS, ↓ blood loss,
↓ transfusion rate.
17Patel S. (2018) [28]Retrospective cohort116 vs. 143Multidisciplinary ERAS (goal-directed fluid therapy) vs. surgical ERAS↓ intraoperative transfusions, ↓ nausea. ↔ in bowel function, ↔ LOS, ↔ 30 and 90 days complications, ↔ readmissions.
Abbreviations: LOS—length of stay; AKI—acute kidney injury; VBFI—Vascular Bed Filling Index; aVBFI—adjusted Vascular Bed Filling Index; ERAS—Enhanced Recovery After Surgery; ↓—significant reduction (favorable effect); ↑—significant increase (unfavorable effect); ↔—no significant difference.
Table 2. Cochrane Risk of Bias (risk (high/low/unclear).
Table 2. Cochrane Risk of Bias (risk (high/low/unclear).
No.Author (Year)Random Sequence GenerationAllocation ConcealmentBlinding of Participants and PersonnelBlinding of Outcome AssessmentIncomplete DataSelective ReportingMain Limitations/Quality Considerations
1Luo J. (2020) [12]UnclearUnclearUnclearUnclearLowLowRandomization and blinding procedures poorly described, potential risk of bias.
2Kong Y. (2016) [13]LowLowLowLowLowLowGood methodology but small sample size (risk of imprecise estimates).
3Arslan-Carlon V. (2020) [14]LowLowLowLowLowLowGood methodology, large sample size, low risk of bias.
4Pillai P. (2011)
[15]
HighUnclearUnclearUnclearLowLowSmall sample size, unclear, randomization and blinding procedures, high risk of bias.
5Liu T. (2016)
[16]
HighUnclearUnclearUnclearLowLowSmall sample size, unclear randomization details, moderate risk of bias.
6Ghoreifi A. (2021)
[17]
HighHighHighHighLowLowRetrospective observational design, possible selection and confounding biases.
7Wei C. (2018)
[18]
HighHighHighHighLowUnclearRetrospective, observational study design, risk of selection and confounding biases.
8Bazargani T.
(2018)
[19]
HighHighHighHighLowLowObservational design without clear control group, potential confounding bias.
9Dobe T. (2022)
[20]
HighHighHighHighLowLowSmall sample size, mixed prospective-retrospective groups, risk of confounding and selection bias.
10Marques M. (2024)
[21]
HighHighHighHighLowLowRetrospective design, limited to AKI risk factors, potential confounding bias.
11Furrer M. (2018)
[22]
HighHighHighHighLowLowRetrospective design, large population but significant confounding risks.
12Lipowski P. (2024)
[23]
HighHighHighHighLowLowSingle-center, retrospective, exploratory and hypothesis generating.
13Wuethrich P. (2013)
[24]
LowLowLowLowLowLowStrong methodology, single population, limited external validity.
14Wuethrich P. (2013)
[25]
LowLowLowLowLowLowStrong methodology, single population, limited external validity
15Mei Wen Wu F. (2013)
[26]
LowLowLowLowLowLowStrong methodology, single population, limited external validity
16Jubber I. (2019)
[27]
HighHighHighHighUnclearLowRetrospective design, high-volume anesthetist group limited to few providers, risk of bias.
17Patel S. (2018)
[28]
HighHighHighHighLowLowRetrospective design, historical control group, significant selection and confounding biases.
Table 3. Grade summary table.
Table 3. Grade summary table.
OutcomeNo. of StudiesConsistencyPrecisionRisk of BiasCertainty (GRADE)
Acute Kidney Injury (AKI)4 (2 RCTs, 2 obs.)InconsistentImprecise (small N, some p > 0.05)Moderate to high (obs. studies, limited blinding)Low
Blood Loss and Transfusions4 RCTsPartially consistentModerate (some large effects)Low to moderate (RCTs well reported)Moderate
Postoperative Ileus4 studies (mixed)Mixed resultsLow (small N in key studies)High in some studiesLow
Length of Hospital Stay4 RCTs + obs.InconsistentLow (heterogeneity of LOS reporting)ModerateLow
Chronic Kidney Disease1 RCTConsistentModerateLowModerate
Reporting bias was not formally evaluated, and no results related to publication bias are available.
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Lipowski, P.; Ostrowski, A.; Adamowicz, J.; Kowalski, F.; Drewa, T.; Juszczak, K. Impact of Perioperative Fluid Strategies on Outcomes in Radical Cystectomy: A Systematic Review. Cancers 2025, 17, 1746. https://doi.org/10.3390/cancers17111746

AMA Style

Lipowski P, Ostrowski A, Adamowicz J, Kowalski F, Drewa T, Juszczak K. Impact of Perioperative Fluid Strategies on Outcomes in Radical Cystectomy: A Systematic Review. Cancers. 2025; 17(11):1746. https://doi.org/10.3390/cancers17111746

Chicago/Turabian Style

Lipowski, Paweł, Adam Ostrowski, Jan Adamowicz, Filip Kowalski, Tomasz Drewa, and Kajetan Juszczak. 2025. "Impact of Perioperative Fluid Strategies on Outcomes in Radical Cystectomy: A Systematic Review" Cancers 17, no. 11: 1746. https://doi.org/10.3390/cancers17111746

APA Style

Lipowski, P., Ostrowski, A., Adamowicz, J., Kowalski, F., Drewa, T., & Juszczak, K. (2025). Impact of Perioperative Fluid Strategies on Outcomes in Radical Cystectomy: A Systematic Review. Cancers, 17(11), 1746. https://doi.org/10.3390/cancers17111746

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