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Background:
Systematic Review

Obstructive Sleep Apnea and Outcomes in Cardiac Surgery: A Systematic Review with Meta-Analytic Synthesis (PROSPERO CRD420251049574)

by
Andrei Raul Manzur
1,2,3,
Alina Gabriela Negru
4,*,
Andreea-Roxana Florescu
1,2,*,
Ana Lascu
3,5,6,
Iulia Raluca Munteanu
1,3,
Ramona Cristina Novaconi
3,
Nicoleta Sorina Bertici
2,
Alina Mirela Popa
1,2 and
Stefan Mihaicuta
2
1
Department of Doctoral Studies, “Victor Babes” University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square No. 2, 300041 Timisoara, Romania
2
Department of Pulmonology, Center for Research and Innovation in Precision Medicine of Respiratory Diseases, “Victor Babes” University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square No. 2, 300041 Timisoara, Romania
3
Institute for Cardiovascular Diseases of Timisoara, Clinic of Cardiovascular Surgery, Gheorghe Adam Street, No. 13A, 300310 Timisoara, Romania
4
Department of Cardiology, “Victor Babes” University of Medicine and Pharmacy, Eftimie Murgu Square No. 2, 300041 Timisoara, Romania
5
Department III Functional Sciences—Pathophysiology, “Victor Babes” University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square No. 2, 300041 Timisoara, Romania
6
Centre for Translational Research and Systems Medicine, “Victor Babes” University of Medicine and Pharmacy Timisoara, Eftimie Murgu Square No. 2, 300041 Timisoara, Romania
*
Authors to whom correspondence should be addressed.
Biomedicines 2025, 13(7), 1579; https://doi.org/10.3390/biomedicines13071579 (registering DOI)
Submission received: 12 May 2025 / Revised: 20 June 2025 / Accepted: 23 June 2025 / Published: 27 June 2025

Abstract

Background: Obstructive sleep apnea (OSA) is a prevalent but frequently underdiagnosed comorbidity in patients undergoing cardiac surgery, including coronary artery bypass grafting (CABG), aortic valve replacement (AVR), and mitral valve repair or replacement (MVR). This systematic review and meta-analytic synthesis investigates the relationship between OSA and postoperative morbidity and mortality, with particular attention to the predictive utility of established screening instruments. Methods: A systematic search of the PubMed database was conducted (April 2025), identifying 724 articles published in the last ten years. Seventeen primary studies met the inclusion criteria for qualitative synthesis, and four additional studies were included in the meta-analyses. Outcomes assessed included atrial fibrillation, major adverse cardiac and cerebrovascular events (MACCE), acute kidney injury (AKI), respiratory complications, pneumonia, hospital length of stay (LOS), and mortality. Risk of bias was assessed qualitatively based on study design and reporting limitations. This review was registered in the PROSPERO database under registration number CRD420251049574. Results: Meta-analyses demonstrated significantly elevated odds of atrial fibrillation (OR = 2.44, 95% CI: 1.46–4.07), major adverse cardiac and cerebrovascular events (OR = 2.06, 95% CI: 1.61–2.63), acute kidney injury (OR = 2.24, 95% CI: 1.67–3.01), and respiratory complications (OR = 1.15, 95% CI: 1.05–1.25) among patients with OSA. Additionally, OSA was associated with a significantly prolonged hospital length of stay (standardized mean difference [SMD] = 0.62, 95% CI: 0.46–0.78) and a marginal increase in pneumonia risk (OR = 1.07, 95% CI: 1.00–1.15). Evidence regarding stroke, intensive care unit (ICU) stay, and mortality was inconsistent or underpowered. Conclusions: Across core outcomes, findings were consistent across multiple studies involving a large patient population. Obstructive sleep apnea is a clinically consequential risk factor in cardiac surgery, associated with increased perioperative complications and prolonged hospitalization. These findings support the integration of routine OSA screening into preoperative risk assessment protocols. Further prospective, multicenter trials are warranted to assess the efficacy of perioperative management strategies, including continuous positive airway pressure (CPAP) therapy, in improving surgical outcomes.

1. Introduction

Obstructive sleep apnea is a prevalent yet frequently underdiagnosed disorder among individuals undergoing cardiac surgery [1]. Characterized by recurrent upper airway obstruction during sleep, OSA leads to intermittent hypoxia, cyclical arousals, and sympathetic overactivation, contributing to a cascade of systemic effects, including inflammation, oxidative stress, and endothelial dysfunction [2,3,4,5,6]. These mechanisms are particularly relevant in the context of cardiac surgical interventions, which impose substantial physiologic stress and activate overlapping inflammatory and neurohumoral pathways [7,8,9].
Cardiac surgery encompasses procedures such as coronary artery bypass grafting, aortic and mitral valve repair or replacement, and combined interventions, all of which carry high perioperative risk due to the involvement of cardiopulmonary bypass, ischemia–reperfusion injury, fluid shifts, and hemodynamic instability [10,11,12,13,14,15,16]. The presence of untreated OSA in this setting may amplify the incidence and severity of postoperative complications [17,18,19,20]. These include atrial fibrillation, acute kidney injury, respiratory insufficiency, prolonged mechanical ventilation, and extended intensive care unit and hospital stays [11,21,22,23,24,25,26].
Sleep-disordered breathing exists on a spectrum and is broadly categorized into three subtypes as follows: obstructive sleep apnea, central sleep apnea, and complex sleep apnea [27]. OSA is the most common subtype, resulting from anatomical or functional upper airway collapse [28,29]. Central sleep apnea (CSA) is characterized by impaired central respiratory drive and is frequently observed in patients with heart failure or neurological pathology [30,31,32]. Complex sleep apnea involves elements of both and may emerge during the initiation of positive airway pressure therapy [32,33]. While the present review focuses primarily on OSA, understanding the interplay of all subtypes is essential for a comprehensive perioperative risk assessment.
Given the increasing awareness of OSA as a modifiable risk factor, there is a growing interest in preoperative screening strategies. Tools such as the STOP-Bang and STOP-BAG2 questionnaires offer pragmatic, validated approaches for identifying patients at elevated risk, especially in settings where formal polysomnography is impractical [34,35,36,37,38]. Despite growing observational evidence, the perioperative management of OSA remains inconsistent across institutions, and the impact of interventions such as preoperative or postoperative continuous positive airway pressure therapy remains insufficiently characterized [39,40,41,42,43].
The objective of this systematic review and meta-analysis is to critically evaluate the prevalence, severity, and clinical implications of OSA in patients undergoing cardiac surgery. This includes a synthesis of available data on perioperative complications, an assessment of screening tool utility, and an identification of evidence gaps regarding therapeutic strategies. Through this analysis, we aim to inform clinical practice and guide future research directions in this high-risk patient population [44,45,46].

2. Materials and Methods

This systematic review was conducted in accordance with PRISMA 2020 guidelines. This review was registered in the PROSPERO database under the registration number CRD420251049574. A comprehensive literature search of the PubMed database was performed on 1 April 2025, targeting studies published within the past ten years that examined the association between sleep apnea and postoperative outcomes in cardiac surgery, including coronary artery bypass grafting, aortic valve replacement, and mitral valve procedures. Only PubMed was searched due to its high clinical indexing coverage and relevance for peer-reviewed biomedical literature. While the exclusion of other databases such as Embase or Scopus may have limited comprehensiveness, the strategy was designed for focused retrieval of clinically pertinent studies. Manual screening of reference lists from articles included was also conducted to identify additional eligible publications.
An initial screening of 724 articles was performed by title and abstract. Studies were retained if they explicitly reported on both cardiac surgical procedures and sleep-disordered breathing (obstructive or central sleep apnea). Studies lacking a validated diagnostic methodology for sleep apnea were excluded. After applying inclusion and exclusion criteria, 17 studies, encompassing a combined population of 532,595 adult patients who underwent cardiac surgical procedures, were selected for full qualitative synthesis. The study identification, screening, and inclusion process is illustrated in the PRISMA 2020 flow diagram (Appendix B).
Four additional studies—Wang et al. (2020) [47], Nagappa et al. (2017) [48], Patel et al. (2018) [49], and Javaherforooshzadeh et al. (2022) [50]—were excluded from descriptive synthesis due to their limited reporting scope but were included in outcome-specific meta-analyses. These studies contributed pooled odds ratios (ORs) and standardized mean differences (SMDs) for relevant complications. Studies were grouped into qualitative and quantitative syntheses based on whether they reported extractable data for the meta-analysis of predefined outcomes.
Data extracted from each study included study design, sample size, OSA diagnostic method, presence of central sleep apnea, perioperative outcomes, and screening tool performance metrics. Where available, outcome measures were synthesized using a random-effects model to account for heterogeneity. Effect estimates were pooled for atrial fibrillation, MACCE, AKI, respiratory complications, pneumonia, length of stay, and mortality.
This methodology aimed to integrate both qualitative and quantitative data in a rigorous, clinically meaningful synthesis of sleep apnea-related risk in cardiac surgical populations.

3. Results

The results of this systematic review and meta-analysis focus on the relationship between obstructive sleep apnea and postoperative outcomes in cardiac surgery. Findings are presented in accordance with the PRISMA 2020 guidelines and are organized by study selection, population characteristics, diagnostic methods, outcome measures, and pooled effect estimates where applicable. Comprehensive data extracted from the included studies, including individual outcome measures, diagnostic criteria, and patient characteristics, are presented in Appendix A, providing a detailed summary of the data utilized in the synthesis.

3.1. Study Characteristics

This systematic review included 17 studies, encompassing a combined population of 532,595 adult patients who underwent cardiac surgical procedures. Of these, 12 were prospective cohort studies comprising 4228 patients, and 5 were retrospective cohort analyses accounting for 528,367 patients. The studies reflect a broad international distribution, spanning 11 countries across North America, South America, Europe, Asia, and Oceania.
Prospective studies were conducted in regions including the United States, Brazil, South Korea, Germany, Thailand, China, Sweden, and Japan. Notable examples include Foldvary-Schaefer et al., 2015 [51]; Uchôa et al., 2015 [52]; Koo et al., 2020 [53]; Tafelmeier et al., 2020 [54]; Liamsombut et al., 2021 [55]; and Ding et al., 2016 [56]. These studies typically employed formal diagnostic tools for sleep-disordered breathing, such as full polysomnography or validated clinical screening instruments [57].
Retrospective studies originated primarily from large administrative datasets in countries like the United States, Canada, and Australia. Representative contributions include Gali et al., 2020 [58]; Wolf et al., 2021 [59]; Wong et al., 2015 [60]; and Krishnasamy et al., 2019 [61]. These investigations relied largely on ICD coding and electronic health records for OSA case identification, which may introduce diagnostic variability.
Study sample sizes ranged from 46 to over 500,000 patients, offering both detailed clinical insight and large-scale epidemiologic perspective. Table 1 provides a revised overview of the study characteristics, including design type, sample size, and geographic setting.
Four additional studies (Wang et al., 2020 [47]; Nagappa et al., 2017 [48]; Patel et al., 2018 [49]; and Javaherforooshzadeh et al., 2022 [50]) were not included in the above synthesis of baseline characteristics due to differences in the design or reporting structure but were included in subsequent meta-analyses for relevant postoperative complications.

3.2. Prevalence and Characteristics of Sleep Apnea in Prospective Studies

Among patients undergoing cardiac surgery, the mean prevalence of obstructive sleep apnea, as determined through validated diagnostic or screening modalities, was 63.3%. This high rate highlights the considerable burden of undiagnosed sleep-disordered breathing in this population when systematic evaluation is employed.
Regarding OSA severity, 50.3% of patients had an apnea-hypopnea index (AHI) greater than five events per hour, while moderate-to-severe OSA (AHI > 15) was observed in 31.7% and severe OSA (AHI > 30) in 18.6% of cases. These figures reflect a somewhat lower proportion of severe OSA than initially reported, emphasizing the variability of severity classification across studies.
The average body mass index (BMI) among patients with OSA was 29.15 kg/m2, which falls within the overweight-to-obese range. This slightly elevated BMI suggests a potential contributory role of adiposity to sleep-disordered breathing in this cohort, aligning with established pathophysiological associations.
Male patients constituted 61.1% of the OSA population, compared to 18.6% female representation (noting that sex was unreported in a portion of the sample). This sex disparity, though less extreme than previously noted, is consistent with prior epidemiological data and may reflect both biological predisposition and diagnostic bias.
Central sleep apnea was reported in 136 patients, representing 3.2% of the overall population. However, only a subset of studies (4 out of 12) explicitly documented CSA prevalence, indicating persistent gaps in the comprehensive reporting of sleep-disordered breathing subtypes within cardiac surgical cohorts [54,56,62,63].
Although multiple prospective studies reported high rates of obstructive sleep apnea in patients undergoing cardiac surgery, our independent extraction (Appendix C) and synthesis of raw patient-level data revealed slight numerical inconsistencies. For instance, the overall OSA prevalence calculated across 12 prospective studies was 63.3%, with moderate-to-severe OSA observed in 31.7% and severe OSA in 18.6% of patients. These figures differ from previously reported aggregated summaries which indicated higher values (e.g., 62.5% mean prevalence, 71.6% moderate to severe, 31.0% severe). This divergence likely reflects differences in the denominators, inclusion criteria, and thresholds used to define OSA severity.
Such variations are not necessarily contradictory, but they underscore the heterogeneity in diagnostic methods and data reporting across studies. For example, the use of different types of sleep studies (polysomnography vs. portable monitoring), inconsistent AHI thresholds, and the exclusion of patients with invalid or incomplete tests contribute to the observed differences. Additionally, while some studies reported OSA prevalence based on successfully completed assessments, others included all screened individuals regardless of test quality.
To address this, both the calculated metrics and the previously summarized averages are provided in this section. Together, they offer a more comprehensive and nuanced view of the burden of OSA in cardiac surgical populations, while highlighting the need for standardized definitions and consistent reporting in future research.

3.3. Prevalence and Characteristics of Sleep Apnea in Retrospective Studies

In retrospective analyses, the mean documented prevalence of obstructive sleep apnea among cardiac surgery patients was 21.8%, substantially lower than estimates derived from prospective cohorts. This discrepancy likely reflects underdiagnosis due to the reliance on administrative data, lack of standardized diagnostic protocols, and potential miscoding in retrospective databases.
As shown in Table 2, the average body mass index among OSA-diagnosed patients in retrospective studies was 34.3 kg/m2, categorizing the cohort as obese. This finding aligns with established associations between elevated BMI and OSA, particularly in populations where clinical diagnosis often follows overt symptom presentation.
Male patients accounted for 78.2% of OSA cases, while female representation was limited to 22.6%. The degree of gender disparity was more pronounced than in prospective studies, possibly reflecting gender-related diagnostic bias or differential healthcare-seeking behavior.
Notably, central sleep apnea was not reported in any of the included retrospective studies. This omission underscores the limited clinical granularity inherent to administrative datasets and highlights a critical gap in understanding the full spectrum of sleep-disordered breathing in this patient population.

3.4. Comparison of Methodological Characteristics of Prospective and Retrospective Studies

Prospective studies offer more accurate prevalence estimates and clinical insights into obstructive sleep apnea in cardiac surgery populations. They employ rigorous diagnostic protocols, such as polysomnography or validated screening tools, allowing for a detailed assessment of sleep-disordered breathing and its direct correlation with perioperative outcomes. These studies also capture relevant clinical variables, including apnea-hypopnea index, body mass index, and comorbidities, thereby enabling nuanced risk stratification.
However, prospective designs are often constrained by limited sample sizes, potential selection bias, and the logistical demands of in-depth physiological assessments. These limitations can restrict their external validity, particularly in representing broader, real-world surgical populations.
In contrast, retrospective studies harness large administrative and clinical databases to evaluate population-level patterns, healthcare utilization, and postoperative outcomes. They facilitate the examination of long-term trends and provide the statistical power necessary to detect less frequent adverse events. Nevertheless, their diagnostic accuracy is frequently compromised by non-standardized or absent criteria for OSA diagnosis, as well as incomplete clinical data. Key variables such as AHI, CSA, and BMI are often missing or imprecisely coded.
As shown in Figure 1, the methodological dichotomy between these study types underscores the need for integrated approaches that balance diagnostic rigor with broad applicability.

3.5. Comparative Diagnostic Performance of Screening Tools

The diagnostic performance of screening instruments for obstructive sleep apnea in cardiac surgical populations varies substantially across studies. Among the evaluated tools, STOP-BAG2 and STOP-Bang questionnaires consistently demonstrated superior predictive accuracy, while the Epworth Sleepiness Scale (ESS) and Berlin Questionnaire yielded suboptimal results, as highlighted in Figure 2.
STOP-BAG2, which integrates components of the STOP-Bang questionnaire with refined risk stratification, achieved the highest area under the curve (AUC) value at 0.66. This level of diagnostic discrimination, while moderate, was consistently observed across retrospective datasets. Importantly, STOP-BAG2 also demonstrated the strongest association with postoperative complications in studies that utilized it.
The STOP-Bang questionnaire, widely adopted due to its ease of administration, exhibited the highest sensitivity (75.8%) among the assessed tools. This makes it a valuable screening instrument, particularly for identifying high-risk individuals prior to surgery. However, its specificity and overall predictive values showed variability across different cohorts, limiting its standalone utility.
In contrast, the ESS performed poorly in terms of sensitivity (6.45%), despite a relatively high specificity (94.87%). Its reliance on subjective symptoms likely contributes to the under-recognition of OSA, especially in patients without overt daytime sleepiness. Similarly, the Berlin Questionnaire demonstrated limited diagnostic value, particularly among patients with high comorbidity burdens, and it has seen declining use in recent clinical research.
These trends reflect a shift toward more balanced and pragmatic instruments capable of integrating anatomical and symptomatic indicators of sleep-disordered breathing.

3.6. Tool-Specific Interpretation and Clinical Relevance

A comparative evaluation of individual screening tools for obstructive sleep apnea (OSA), shown in Table 3 and Table 4, reveals distinct strengths and limitations that influence their clinical utility in the cardiac surgical setting.
-
“STOP-BAG2”: This tool, which builds upon the STOP-Bang framework with additional weighted risk factors, demonstrated the strongest overall performance in retrospective analyses. Its consistent association with adverse outcomes and robust AUC values support its use in population-based screening. However, its limited application in prospective studies and the lack of widespread clinical integration constrain its current practical relevance.
-
“STOP-Bang”: This questionnaire strikes a balance between subjective symptoms and objective risk factors such as BMI, age, and neck circumference. Its high sensitivity and widespread availability make it an attractive choice for preoperative screening, particularly in anesthesia and surgical clinics. Nonetheless, its moderate specificity and lack of validation in certain subgroups warrant caution.
-
“Epworth Sleepiness Scale”: Although easy to administer, the ESS suffers from poor sensitivity, making it unsuitable as a standalone tool. Its reliance on self-reported symptoms limits its effectiveness in detecting asymptomatic or minimally symptomatic OSA, which are common in cardiac patients.
-
“Berlin Questionnaire”: Comprehensive but cumbersome, the Berlin Questionnaire has shown limited discriminative value in surgical populations, particularly those with multiple comorbidities. Its declining clinical use reflects these shortcomings.

3.7. Meta-Analysis Summary

A pooled meta-analysis of studies reporting area under the curve values for screening tools used to identify obstructive sleep apnea in cardiac surgery populations yielded a combined AUC of 0.635 (95% CI: 0.586–0.684). This value suggests moderate diagnostic performance, surpassing random classification but falling short of thresholds typically required for clinical decision making in the absence of confirmatory testing (as shown in Figure 3).
These findings underscore the role of screening instruments as adjunctive tools rather than definitive diagnostics. While tools such as STOP-BAG2 and STOP-Bang have demonstrated promising utility, their optimal application lies in prioritizing patients for further evaluation via polysomnography or portable monitoring.
The variability in performance across studies may be attributed to differences in study populations, comorbidity burden, perioperative contexts, and implementation protocols. Moreover, not all studies reported AUC values or other standardized performance metrics, further complicating direct comparison.
Overall, the meta-analytic estimate supports the cautious but informed integration of validated screening tools into perioperative workflows.
Rationale for Study Exclusion
The study by Wang et al. (2020) [47] was excluded from the tool-specific synthesis due to its methodological limitations. Specifically, the study reported pooled diagnostic metrics without disaggregating results by individual screening tool, introducing the potential for data duplication and confounding. Its inclusion would have undermined the integrity of comparative analyses.

3.8. Postoperative Complications in OSA Groups—Focus on POAF

A targeted meta-analysis was conducted to assess the relationship between obstructive sleep apnea and the incidence of postoperative atrial fibrillation (POAF) in patients undergoing cardiac surgery. In Figure 4, we present data from three independent studies yielded a pooled odds ratio (OR) of 2.44 (95% CI: 1.46–4.07), suggesting that individuals with OSA have more than twice the odds of developing POAF compared to those without OSA. This association was statistically significant and consistent across the included studies.
The observed association is supported by a plausible pathophysiological basis. OSA-related intermittent hypoxia promotes sympathetic activation, oxidative stress, and atrial remodeling—mechanisms known to contribute to atrial arrhythmogenesis. Moreover, fluctuations in intrathoracic pressure and systemic inflammation may further exacerbate electrophysiological instability.
The included studies reported varying effect sizes, with some heterogeneity attributable to differences in study design, diagnostic modalities, and patient characteristics. However, the directionality of association remained consistent, reinforcing the robustness of the pooled estimate.
The clinical implications are substantial. POAF is a common and morbid complication of cardiac surgery, associated with increased stroke risk, prolonged hospitalization, and healthcare costs. Given the modifiable nature of OSA, early identification and perioperative management—potentially including preoperative CPAP therapy—may represent an effective strategy to mitigate this risk.

3.9. Major Adverse Cardiac and Cerebrovascular Events

A meta-analysis evaluating the association between obstructive sleep apnea and major adverse cardiac and cerebrovascular events in cardiac surgery patients demonstrated a pooled odds ratio (OR) of 2.06 (95% CI: 1.61–2.63). This finding indicates that OSA is associated with a twofold increase in the risk of postoperative MACCE, encompassing outcomes such as myocardial infarction, stroke, and cardiovascular mortality.
As shown in Figure 5, the analysis included data from three studies—Nagappa et al. [48], Uchôa et al. [52], and Wang et al. [47]—utilizing both fixed- and random-effects models. The similarity between these models suggests minimal heterogeneity and enhances confidence in the robustness of the findings. While effect sizes varied, all studies demonstrated a consistent direction of association favoring increased risk among OSA patients.
Mechanistically, OSA contributes to MACCE through multiple pathways, including intermittent hypoxia, systemic inflammation, endothelial dysfunction, and increased sympathetic tone. These factors may synergistically exacerbate existing cardiovascular disease or predispose patients to de novo events in the postoperative period.
Clinically, the observed association reinforces the relevance of OSA as a modifiable perioperative risk factor. Incorporating routine OSA screening into preoperative risk assessment protocols may allow for early intervention and improved patient outcomes.

3.10. Ischemic Cardiac Outcomes in OSA Patients

Ischemic cardiac outcomes, including myocardial infarction and unplanned coronary revascularization, have been examined in relation to obstructive sleep apnea in the context of cardiac surgery, yielding mixed findings.
Regarding myocardial infarction, a meta-analysis by Wang et al. (2020) [47] reported no significant association between OSA and postoperative MI. Similarly, Uchôa et al. (2015) [52] observed no statistical difference in MI rates, though the study was likely underpowered. In contrast, Fan et al. (2021) [64] reported a higher incidence of perioperative MI among OSA patients undergoing off-pump coronary artery bypass grafting, potentially driven by increased coronary plaque burden and systemic inflammation as reflected by elevated SYNTAX scores and high-sensitivity C-reactive protein (hs-CRP) levels.
Unplanned revascularization, a surrogate for early graft failure or rapidly progressive coronary disease, exhibited a more robust and consistent association with OSA. Uchôa et al. (2015) [52] reported significantly higher revascularization rates in OSA patients (22% vs. 3%, p = 0.035), and Wang et al. (2020) [47] found a nearly tenfold increased odds of reintervention (OR = 9.47, 95% CI: 2.69–33.33, p < 0.0001) in OSA cohorts.
These findings suggest that while the link between OSA and perioperative MI remains inconclusive, the evidence supporting an association with unplanned revascularization is compelling. Mechanistically, this may reflect the cumulative impact of endothelial dysfunction, inflammation, and sympathetic activation associated with untreated OSA. The cardiac ischemic outcomes in patients with obstructive sleep apnea (OSA) following cardiac surgery are represented in Figure 6.
The data advocate for the proactive screening and management of OSA, particularly in patients undergoing CABG or with known coronary artery disease.

3.11. Acute Kidney Injury in OSA Patients Following Cardiac Surgery

Acute kidney injury is a well-recognized complication following cardiac surgery, contributing to increased morbidity, prolonged hospitalization, and adverse long-term outcomes. Emerging evidence supports a significant association between obstructive sleep apnea and elevated AKI risk in this population.
In a large retrospective cohort study by Gali et al. (2020) [58], the incidence of AKI was significantly higher in OSA patients compared to their non-OSA counterparts (25.2% vs. 19.9%, p < 0.001). This association remained robust after adjustment for relevant covariates, suggesting an independent contribution of OSA to renal vulnerability.
These findings were reinforced by a meta-analysis conducted by Wang et al. (2020) [47], which reported a pooled odds ratio of 2.24 for AKI in patients with OSA as shown in Figure 7. This indicates more than a twofold increase in risk, further substantiating the role of OSA as a modifiable perioperative risk factor.
The bar chart shows a higher AKI rate among OSA patients (25.2%) versus non-OSA patients (19.9%). The meta-analysis reported a pooled odds ratio of 2.24 (95% CI: 1.61–3.13), confirming a significantly elevated AKI risk in the OSA population undergoing cardiac surgery.
Pathophysiological mechanisms underlying this association include intermittent hypoxia, sympathetic overactivity, systemic inflammation, and compromised renal perfusion. In addition, comorbid conditions prevalent among OSA patients—such as hypertension, diabetes mellitus, and reduced left ventricular function—may synergistically amplify renal injury in the postoperative setting.
These data underscore the importance of early identification and potential intervention for OSA in patients undergoing cardiac surgery.

3.12. Stroke Risk in OSA Patients After Cardiac Surgery

Stroke represents a serious postoperative complication in cardiac surgery, with implications for both acute recovery and long-term neurological function. The relationship between obstructive sleep apnea and postoperative stroke, however, remains incompletely defined.
A meta-analysis by Wang et al. (2020) [47] found no statistically significant increase in the risk of stroke or transient ischemic attack (TIA) among OSA patients, suggesting that OSA may not independently elevate cerebrovascular risk in the immediate postoperative period. This finding aligns with other cohort studies that failed to demonstrate a consistent association.
For example, Uchôa et al. (2015) [52] reported three stroke events in the OSA cohort and none in the control group, but the study lacked sufficient power to draw firm conclusions. Similarly, Krishnasamy et al. (2019) [61] noted a single stroke event in the OSA group without formal statistical comparison. All of these findings are presented in Figure 8.
Most included studies did not employ standardized stroke assessment protocols or objective neuroimaging confirmation. This methodological variability, coupled with low event rates, limits the strength of available evidence.
Although current data do not support a definitive link between OSA and postoperative stroke, the potential for increased risk—particularly in subgroups with untreated severe OSA—warrants further investigation. Prospective, adequately powered studies using standardized neurological endpoints are needed to clarify this relationship.

3.13. Postoperative Mortality in OSA Vs. Non-OSA Patients

Postoperative mortality represents a critical endpoint in the evaluation of perioperative risk factors. However, the evidence linking obstructive sleep apnea to increased short-term or in-hospital mortality following cardiac surgery remains inconclusive.
As shown in Figure 9, Wong et al. (2015) [60] reported a significantly elevated odds ratio (OR = 3.82) for in-hospital mortality in OSA patients, most other studies observed either no significant difference or marginal effects. For instance, Gali et al. (2020) [58] reported nearly identical mortality rates between OSA and non-OSA groups (1.7% vs. 1.8%), suggesting no discernible association.
Interpretation of these findings is complicated by several limitations. Many studies lacked adequate sample sizes or were not powered to detect mortality differences. Additionally, reliance on retrospective data and diagnostic coding introduces variability in exposure classification and event adjudication.
Furthermore, potential confounders such as obesity, heart failure, and CPAP adherence are frequently underreported or uncontrolled. These factors may dilute or obscure the true relationship between OSA and surgical mortality.
Although a trend toward increased risk cannot be excluded, especially in untreated or severe OSA, current evidence does not support a definitive causal link. Prospective, well-powered studies with detailed comorbidity adjustment and long-term follow-up are necessary to fully elucidate the impact of OSA on postoperative survival.
While some studies suggest a higher mortality rate in OSA patients, the evidence remains inconsistent. Koo et al. (2020) [53] reported a HR = 1.35 but did not provide event rates, and it thus is excluded from this bar chart.

3.14. Respiratory Complications and Prolonged Ventilation in OSA Patients

Respiratory complications constitute a significant concern in patients with obstructive sleep apnea undergoing cardiac surgery. The anatomical and physiological vulnerabilities associated with OSA—including upper airway collapsibility, opioid sensitivity, and impaired arousal response—predispose this population to postoperative respiratory failure, prolonged mechanical ventilation, and increased need for non-invasive ventilatory support.
As shown in Figure 10, several cohort studies have documented these risks. Krishnasamy et al. (2019) [61] reported a 2.3-fold increase in the likelihood of requiring postoperative non-invasive ventilation among OSA patients. Tafelmeier et al. (2020) [54] noted elevated rates of prolonged mechanical ventilation in central sleep apnea (CSA) patients, with similar though less pronounced trends observed in OSA cohorts. Fan et al. (2021) [64] described a higher incidence of perioperative hypoxemia and ventilation-associated complications in patients undergoing off-pump coronary artery bypass grafting.
A pooled meta-analysis incorporating data from these studies yielded a statistically significant odds ratio of 1.15 (95% CI: 1.05–1.25) for respiratory complications in OSA patients, confirming a modest but consistent elevation in risk.
Despite heterogeneity in outcome definitions and baseline characteristics, the consistency of results underscores the clinical importance of recognizing and addressing respiratory vulnerability in this population. The judicious use of opioids, early extubation protocols, and the preemptive application of non-invasive ventilation may be beneficial strategies.

3.15. Hospital Length of Stay (LOS) in OSA Patients

Hospital length of stay serves as an important indicator of postoperative recovery, healthcare resource utilization, and complication burden. Obstructive sleep apnea, due to its systemic pathophysiological effects, has been associated with prolonged LOS in patients undergoing cardiac surgery. A meta-analysis pooling data from three studies—Gali et al. (2020) [58], Teo et al. (2021) [66], and Wolf et al. (2021) [59]—calculated a standardized mean difference (SMD) of 0.62 (95% CI: 0.46–0.78), indicating a moderate and statistically significant prolongation of hospital stay in OSA patients compared to non-OSA counterparts is shown in Figure 11.
The observed extension in LOS may reflect increased perioperative complications, slower recovery trajectories, or the need for more intensive monitoring and intervention. This is particularly relevant in patients with moderate-to-severe OSA or those with poorly controlled comorbidities such as obesity, hypertension, or diabetes mellitus.
These findings emphasize the value of preoperative OSA screening and multidisciplinary perioperative planning. Early identification and targeted management may not only improve clinical outcomes but also reduce postoperative length of stay and associated healthcare costs.

3.16. Pneumonia in OSA Patients Following Cardiac Surgery

Pneumonia is a notable postoperative complication in patients undergoing cardiac surgery, particularly in those with impaired respiratory mechanics such as those with obstructive sleep apnea. The association between OSA and postoperative pneumonia has been explored across several observational studies [65,69,70,71,72].
A pooled analysis reported an odds ratio of 1.07 (95% CI: 1.00–1.15) is presented in Figure 12, indicating a borderline but statistically marginal increase in pneumonia risk among OSA patients. While the effect size is modest, the consistent directionality across studies suggests a clinically relevant trend.
Mechanistically, OSA contributes to pneumonia risk via impaired cough reflex, aspiration due to nocturnal hypoventilation, and the residual effects of sedation and opioids. These factors may be further compounded by prolonged intubation or delayed extubation protocols often necessitated by perioperative respiratory instability.
Although the absolute increase in pneumonia incidence is small, even marginal gains in risk are important in high-risk cardiac surgery populations. Preventive strategies—including early mobilization, pulmonary hygiene, and the selective use of non-invasive ventilation—may mitigate these risks.

3.17. ICU Length of Stay

Intensive care unit length of stay serves as a surrogate marker for postoperative acuity and recovery trajectory following cardiac surgery. While the relationship between obstructive sleep apnea and ICU LOS has been explored in several studies, the evidence remains limited and inconsistent.
Many studies failed to report ICU LOS as a primary outcome or lacked group-specific mean and standard deviation data. In several cases, ICU LOS was embedded within multivariable regression models or described solely for the OSA cohort, precluding direct comparison. The absence of standardized reporting criteria further contributes to the interpretative challenge.
Despite these limitations, a qualitative synthesis suggests a possible trend toward prolonged ICU stay in patients with OSA, particularly those with moderate-to-severe disease. This may reflect increased perioperative complications, extended ventilatory support requirements, or heightened monitoring needs.
Given the high costs and resource demands associated with ICU care, future studies should aim to quantify the impact of OSA on ICU LOS using uniform definitions and robust statistical models. Such analyses would enhance our understanding of the healthcare burden imposed by untreated or unrecognized sleep-disordered breathing in cardiac surgical populations.

4. Discussion

This systematic review provides a comprehensive synthesis of the current literature examining the association between obstructive sleep apnea and postoperative outcomes in cardiac surgery. Seventeen primary studies were included in the qualitative synthesis, with four additional studies contributing data to meta-analyses of specific outcomes. Collectively, these studies offer robust evidence that OSA constitutes a significant and potentially modifiable perioperative risk factor in patients undergoing procedures such as coronary artery bypass grafting (CABG), aortic valve replacement, and mitral valve surgery [47,48,49,50,51,52,54,55,56,58,59,60,61,62,63,64,65,66,67,68,72].
Among the prospective studies, the prevalence of OSA exceeded 60%, with moderate-to-severe disease (AHI > 15) affecting over 70% of patients. These figures underscore the underappreciated diagnostic burden of OSA when active screening or polysomnography is implemented. In contrast, retrospective datasets relying on administrative codes reported substantially lower prevalence estimates (~22%), highlighting the diagnostic gap associated with passive or indirect case identification [51,52,54,55,56,62,63,64,65,66,68,72]
The findings also confirm that OSA is associated with a higher risk of several clinically meaningful outcomes. Meta-analyses demonstrated increased odds for postoperative atrial fibrillation (OR = 2.44), major adverse cardiac and cerebrovascular events (MACCE) (OR = 2.06), acute kidney injury (AKI) (OR = 2.24), and respiratory complications (OR = 1.15). Hospital length of stay was also prolonged (SMD = 0.62), and pneumonia risk was marginally increased (OR = 1.07). In contrast, findings regarding stroke, ICU length of stay, and mortality were less consistent and did not meet statistical thresholds across pooled analyses [47,48,49,50,55].
These results support the assertion that OSA exerts a clinically significant impact on perioperative morbidity. Importantly, many of the complications associated with OSA are potentially preventable or modifiable through preoperative risk stratification, use of positive airway pressure (PAP) therapy, intraoperative management strategies, and enhanced postoperative monitoring [73,74,75,76].
This review also highlights the need for standardized diagnostic criteria and consistent reporting of sleep metrics and surgical outcomes. Prospective studies utilizing validated tools, objective endpoints, and multicenter designs are essential to further elucidate the mechanisms by which OSA contributes to adverse surgical outcomes and to assess the efficacy of targeted interventions.

4.1. Mechanistic Insights

The pathophysiological mechanisms underlying the association between obstructive sleep apnea and adverse surgical outcomes are multifactorial and increasingly well characterized. OSA is typified by repetitive upper airway collapse during sleep, resulting in intermittent hypoxia, hypercapnia, and frequent arousals from sleep. These physiological disturbances trigger a cascade of systemic responses that negatively influence perioperative stability and postoperative recovery [77,78,79].
Intermittent hypoxia activates sympathetic nervous system pathways, leading to elevated catecholamine levels, increased blood pressure, and heightened myocardial oxygen demand [18,80,81,82,83,84]. These changes contribute to arrhythmogenicity and may explain the observed association between OSA and postoperative atrial fibrillation [85]. Hypoxia also induces oxidative stress and systemic inflammation, both of which have been implicated in endothelial dysfunction and plaque instability, potentially elevating the risk of ischemic events and acute kidney injury [86,87,88,89,90,91,92].
In terms of respiratory complications, OSA is associated with impaired ventilatory control, increased upper airway resistance, and heightened opioid sensitivity. These factors elevate the risk of postoperative hypoventilation, prolonged intubation, and pneumonia. Additionally, the disruption of normal sleep architecture may impair immune function and tissue healing [93,94,95,96,97,98,99,100,101].
Neurohumoral activation, endothelial damage, and microvascular dysfunction are other plausible mechanisms by which OSA may exacerbate perioperative morbidity. These systemic effects are particularly relevant in the context of cardiac surgery, where inflammatory burden, ischemia–reperfusion injury, and hemodynamic shifts are already pronounced [102,103,104,105,106,107,108,109].
Collectively, these mechanisms offer a plausible explanation for the range of complications observed in patients with untreated or inadequately managed OSA undergoing cardiac surgery [43,48,58,110,111]. Further mechanistic studies, including biomarker-based and hemodynamic monitoring investigations, are warranted to refine our understanding and inform targeted therapeutic strategies [112,113].

4.2. Comparison to the Previous Literature

The findings of this systematic review are broadly consistent with earlier research highlighting the adverse impact of obstructive sleep apnea on perioperative outcomes in cardiac surgery. Prior studies have identified OSA as a risk factor for postoperative complications, particularly atrial fibrillation, respiratory insufficiency, and prolonged hospitalization [114,115].
Meta-analyses by Wang et al. (2020) [47] and Nagappa et al. (2017) [48] similarly reported elevated odds for major adverse cardiac and cerebrovascular events and atrial fibrillation in OSA populations. The present review confirms these findings and extends them by disaggregating outcomes such as acute kidney injury, pneumonia, and length of stay. This additional granularity strengthens the case for routine OSA screening and perioperative management.
In contrast, several studies including Patel et al. (2018) [49] and Javaherforooshzadeh et al. (2022) [50] have underscored methodological inconsistencies in the literature, particularly concerning OSA diagnosis and outcome reporting. This review acknowledges these limitations and attempts to address them by stratifying findings by study design, screening method, and population characteristics.
Notably, the association between OSA and mortality or stroke was less pronounced in the current analysis compared to earlier reports [72,116,117,118,119]. This discrepancy may reflect improved perioperative care, advancements in surgical techniques, and increased awareness of OSA as a comorbidity. Alternatively, it may be attributable to methodological limitations such as small sample sizes, low event rates, and inadequate follow-up durations.
Overall, this review supports and extends the existing literature while emphasizing the need for greater standardization in future research. The convergence of findings across studies reinforces the role of OSA as a clinically meaningful, yet often underappreciated, risk factor in the cardiac surgical setting.

4.3. Clinical Implications

The findings of this review carry important implications for the perioperative management of patients undergoing cardiac surgery. Given the high prevalence of obstructive sleep apnea in this population and its consistent association with adverse outcomes, routine preoperative screening should be strongly considered. Instruments such as the STOP-Bang and STOP-BAG2 questionnaires offer pragmatic and clinically validated tools for identifying high-risk individuals, particularly when resources for polysomnography are limited [38,120,121]. Their integration into anesthesia preoperative evaluations or cardiology-driven risk stratification pathways could improve early detection and perioperative planning.
For patients identified with moderate-to-severe OSA, the initiation or reinforcement of continuous positive airway pressure therapy prior to surgery may mitigate risks related to arrhythmias, respiratory complications, and prolonged recovery. However, a significant limitation of the current evidence base is the paucity of data on CPAP adherence and perioperative implementation. Most studies included in this review did not document whether patients received or complied with OSA treatment, limiting the ability to determine the direct effect of intervention on surgical outcomes. This gap is particularly relevant given that therapy adherence likely mediates many of the complications observed in OSA cohorts [122].
In the postoperative setting, enhanced respiratory monitoring, early mobilization, opioid-sparing analgesia, and careful fluid management may be particularly beneficial in OSA patients [123,124]. Institutions should consider embedding OSA screening within enhanced recovery after surgery (ERAS) protocols or developing formal perioperative care bundles. Importantly, the implementation of such pathways will require interdisciplinary coordination among anesthesiologists, sleep medicine specialists, cardiologists, and surgical teams. The modifiable nature of OSA and the feasibility of targeted interventions make it a compelling focus for improving outcomes in high-risk surgical populations [125].
To promote standardization in future research and enhance the comparability of findings across studies, we propose a structured framework for the classification, analysis, and reporting of patients with OSA in the context of cardiac surgery.
(Figure 13). This protocol includes stratification by OSA severity and treatment status, incorporation of key surgical and clinical variables, standardized outcome definitions, and follow-up parameters. Adopting such an approach may facilitate meta-analytic synthesis, improve reporting transparency, and ultimately support more tailored perioperative care strategies.

4.4. Limitations and Future Directions

Despite the comprehensive nature of this systematic review and meta-analysis, several limitations warrant consideration. First, substantial heterogeneity was present among the included studies, particularly with respect to the methods used for diagnosing obstructive sleep apnea. While some studies employed gold-standard polysomnography, others relied on screening questionnaires or administrative coding, introducing potential classification bias and limiting the comparability of findings. Moreover, inconsistencies in the application of apnea–hypopnea index thresholds further complicate direct comparisons across studies.
Second, many studies lacked granular clinical data, including OSA severity, continuous positive airway pressure adherence, and the timing of perioperative interventions. These omissions hindered efforts to stratify patients by risk level and assess the true impact of therapeutic measures. Given that CPAP use is a key modifiable factor, its underreporting represents a critical gap in the current evidence base.
Third, several important clinical outcomes—such as intensive care unit length of stay, stroke, and mortality—were either inconsistently reported or underpowered, precluding robust meta-analytic synthesis. The absence of standardized outcome definitions and limited subgroup analyses further constrained interpretability. Additionally, the inclusion of studies with overlapping patient populations in both qualitative and quantitative syntheses may have introduced an element of duplication bias, despite efforts to avoid this.
Fourth, the predominance of observational study designs limits causal inference. Confoundments by comorbidities such as obesity, hypertension, and heart failure may have influenced outcome estimates, even in studies that attempted multivariable adjustment.
Future research should prioritize large-scale, prospective, multicenter trials with clearly defined diagnostic criteria and standardized outcome reporting. Particular attention should be paid to quantifying CPAP adherence and perioperative implementation, as well as exploring the impact of OSA treatment on clinically meaningful endpoints. Additionally, efforts to harmonize definitions for perioperative complications and integrate sleep-disordered breathing into risk stratification models are necessary to translate observational findings into actionable clinical practice.
The narrative risk of bias assessment, as outlined in the PROSPERO protocol, identified potential sources of bias related to selection criteria, diagnostic heterogeneity, and outcome reporting. These limitations should be considered when interpreting the findings, particularly regarding the strength of evidence for pooled effect estimates.

4.5. Gaps in the Current Literature on OSA and Cardiac Surgery

Despite growing evidence linking obstructive sleep apnea (OSA) to adverse cardiovascular and surgical outcomes, several key gaps persist in the current literature as follows:
-
“Lack of uniform OSA diagnosis and severity stratification”: Many studies rely on administrative codes, screening questionnaires (e.g., STOP-Bang), or self-reported history rather than gold-standard polysomnography. The inconsistent application of apnea-hypopnea index (AHI) thresholds—such as ≥5, ≥15, or ≥30 events per hour—limits comparability across studies and hinders pooled data analysis.
-
“Heterogeneity in outcome reporting”: Definitions and metrics for outcomes such as atrial fibrillation, myocardial infarction, acute kidney injury (AKI), and ICU length of stay vary widely. This inconsistency impairs direct comparisons and undermines the strength of cumulative evidence.
-
“Limited focus on treatment effects”: Few studies explicitly evaluate the impact of therapeutic interventions, such as preoperative or perioperative CPAP use. The modifiability of OSA-related risk remains largely speculative in the absence of controlled trials.
-
“Dominance of underpowered or retrospective designs”: A majority of studies are single-center and observational, limiting statistical power and increasing susceptibility to selection and information bias. This contributes to equivocal findings for key endpoints such as stroke and mortality.
-
“Insufficient integration into perioperative protocols”: Despite strong evidence of risk, OSA is infrequently incorporated into formal risk assessment tools or clinical pathways for cardiac surgery. Current guidelines do not include OSA as a standard component of preoperative evaluation, highlighting a disconnect between evidence and practice.
Addressing these gaps through standardized diagnostic protocols, prospective multicenter designs, and trials evaluating therapeutic interventions will be essential to fully realize the clinical relevance of OSA in cardiac surgery.

5. Conclusions

This systematic review and meta-analysis demonstrate that obstructive sleep apnea is a prevalent and clinically impactful comorbidity in patients undergoing cardiac surgery. The presence of OSA was consistently associated with an increased risk of major perioperative complications, including atrial fibrillation, major adverse cardiac and cerebrovascular events, acute kidney injury, respiratory complications, and prolonged hospital length of stay. Although associations with stroke, ICU length of stay, and postoperative mortality were less consistent, the overall pattern of findings suggests a substantive and potentially modifiable risk profile.
Importantly, many of the adverse outcomes linked to OSA may be mitigated through early identification and targeted perioperative management, such as the use of continuous positive airway pressure therapy. However, current evidence is limited by the heterogeneity in diagnostic methods, underreporting of treatment adherence, and inconsistent outcome definitions.
These findings underscore the need for routine OSA screening as part of preoperative risk assessment in cardiac surgery candidates. Future prospective, multicenter trials incorporating standardized diagnostic criteria, clearly defined endpoints, and interventional strategies are essential to determine the clinical benefit of structured OSA management. Addressing these gaps represents a critical opportunity to improve perioperative outcomes and inform evidence-based guidelines for this high-risk surgical population.

Author Contributions

Conceptualization, A.R.M. and A.-R.F.; methodology, S.M. and N.S.B.; software, I.R.M.; validation, A.G.N., N.S.B. and A.L.; formal analysis, R.C.N.; investigation, A.R.M., A.M.P.; resources, R.C.N.; data curation, A.L. and I.R.M.; writing—original draft preparation, A.R.M.; writing—review and editing, A.G.N.; visualization, A.-R.F.; supervision, S.M.; project administration, A.R.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding. We would like to acknowledge Victor Babes University of Medicine and Pharmacy Timisoara for their support in covering the costs of publication for this research paper.

Data Availability Statement

The protocol for this review is publicly accessible via the PROSPERO database under the registration number CRD420251049574. The original contributions presented in this study are included in the article. Further inquiries can be directed to the corresponding authors.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
AHIApnea-Hypopnea Index
AKIAcute Kidney Injury
ASAAmerican Society of Anesthesiologists
AUCArea Under the Curve
AVRAortic Valve Replacement
BMIBody Mass Index
CABGCoronary Artery Bypass Grafting
CIConfidence Interval
CPAPContinuous Positive Airway Pressure
CSACentral Sleep Apnea
ERASEnhanced Recovery After Surgery
ESSEpworth Sleepiness Scale
FFemale
hs-CRPHigh-Sensitivity C-Reactive Protein
ICDInternational Classification of Diseases
ICUIntensive Care Unit
LOSLength of Stay
M Male
MACCEMajor Adverse Cardiac and Cerebrovascular Events
MIMyocardial Infarction
MVRMitral Valve Repair or Replacement
nsNot Specified
OROdds Ratios
OSAObstructive Sleep Apnea
PAPPositive Airway Pressure
POAFPostoperative Atrial Fibrillation
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
PSGPolysomnography
SA-SDQSleep Apnea-Specific Distress Questionnaire
SMDStandardized Mean Difference
STOP-BAG2Screening Tool for Obstructive Sleep Apnea—Modified Version 2
STOP-BangSnoring, Tiredness, Observed Apnea, Blood Pressure, BMI, Age, Neck circumference, Gender
TIATransient Ischemic Attack

Appendix A

Overview of Recent Publications on Sleep Apnea associated with Cardiac Surgery (2015–2025).
NumberArticle NameStudy TypeNumber of PatientsAge (Years) OSAMale OSAFemale OSA
1Foldvary-Schaefer et al., 2015 [51]Prospective10769.7 ± 12.5nsns
2Gali et al., 2020 [58]Retrospective861265.32001635
3Wolf et al., 2021 [59]Retrospective12,50565.41245310
4Nagappa et al., 2017 [48]
5Wong et al., 2015 [60]Retrospective54567.8 ± 10.25715
6Uchôa et al., 2015 [52]Prospective6759.0 ± 7.9316
7Koo et al., 2020 [53]Prospective10076244271
8Tafelmeier et al., 2020 [54]Prospective25067.9 ± 7.711215
9Liamsombut et al., 2021 [55]Prospective10769.7 ± 12.53318
10Javaherforooshzadeh et al., 2022 [50]
11Krishnasamy et al., 2019 [61]Retrospective10160 ± 84915
12Wang et al. (2020) [47]
13Patel et al. (2018) [49]
14Ding et al., 2016 [56]Prospective29055.20 ± 9.056154
15Keymel et al., 2015 [62]Prospective4881 ± 8nsns
16Oldham et al., 2024 [63]Prospective4667.13114
17Fan et al., 2021 [64]Prospective14762.9 ± 8.24715
18Peker et al., 2022 [65]Prospective14766.5 ± 7.5nsns
19Teo et al., 2021 [66]Prospective10076244271
20Feng et al., 2019 [67]Retrospective506,60464.5 ± 10.524,9777568
21Sezai et al., 2016 [68]Prospective100569.3 ± 10.3519259
NumberEpworth Sleeping ScaleQuestionnairesBerlinSTOPSTOPBANG2
1yesyesyesnsns
2nsnsnsnsns
3nsnsnsnsns
4
5nsnsnsnsns
6nsnsnsnsns
7yes > 10 in 69 patientsyes239 patients with high risknsns
8nsnsnsnsns
9yes > 10 in 35 patientsyes49 patients with high risk≥2 in 72 de patientsIt differentiated patients with AHI greater or lower than 15.
10
11yes > 10 in 4 patientsyesnsns≥3: 47 of the OSA group
12
13
14nsnsnsnsns
15nsnsnsnsns
16yes > 10 in 7 patientsPittsburgh Sleep Quality Index > 5 la 34 patients, Patient Health Questionnaire-9nsnsns
17nsnsnsnsns
18yes > 10 in 18 patientsnsnsnsns
19yes < 10 in all groupsyesyesnsns
20nsnsnsnsns
21nsnsnsnsns
NumberSAS Scale of Sleep Disorder QuestionnaireOSACSAAHI < 5AHI > 5AHI > 15AHI > 30Mean AHISpO2 < 90%Pre-Op PAP TherapyBMI OSA
1ns79ns28282229nsnsno26.8 ± 6.4
2ns2636nsnsnsnsnsnsnsns33.8
3ns1555nsnsnsnsnsnsnsns34.8
4
5ns72nsnsnsnsnsnsns32ns
6ns37nsnsns37ns36.4 ± 18.828ns29.1 ± 4.4
7ns513nsnsns513ns30.1385ns25.9
8ns5968nsns127ns15.250ns30.1 ± 4.6
9≥ 32 for women and ≥ 36 for men corelated with OSA diagnosis77ns302651nsnsnsno26.5 ± 6.6
10
11ns62ns3935131425.8 ± 4.3nsnons
12
13
14ns5461175115nsnsnsnsno23.85 ± 3.7
15ns361113718nsns28no26 ± 5
16ns3961151812ns35no32.4
17ns62nsnsns62ns26.2nsno25.2 ± 3.7
18ns141ns6215367ns37ns28.0 ± 4.5
19ns800ns207287254259nsnsnons
20ns32,545nsnsnsnsnsnsnsnsns
21ns778ns227361260157ns no24.3 ± 3.8
NumberBMI CSABMI AHI < 15BMI AHI > 15EF in AHI > 15EF < 30EF: 30–50EF < 40EF < 45EF > 45EF: 50EF < 55Mean EF
1ns26.3 ± 6.826.8 ± 6.4ns 7226nsns43.6 ± 15.4
2nsnsnsns nsnsnsnsns
3nsnsnsnsnsns153nsnsnsnsns
4
5nsnsnsnsnsnsnsnsnsns18ns
6nsns29.1 ± 4.4nsnsnsnsnsnsnsns49.2 ± 14.2
7nsns25.9ns84158nsnsns223nsns
828.5 ± 4.1nsnsnsnsnsnsnsnsns4151.8 ± 13
9ns26.3 ± 6.826.8 ± 6.443.6 ± 15.4nsnsnsnsnsnsnsns
10
11nsnsnsnsnsnsnsnsnsnsnsns
12
13
1423.32 ± 3.04nsnsnsnsnsnsnsnsnsns58.97 ± 8.27
15ns26 ± 626 ± 552 ± 10nsnsnsnsnsnsnsns
16ns27.432.4nsnsnsns
17nsns25.2 ± 3.756.8 ± 10.2nsnsnsnsnsnsnsns
18nsnsnsnsnsnsnsnsnsnsnsns
19nsnsnsnsnsnsnsnsnsnsnsns
20nsnsnsnsnsnsnsnsnsnsnsns
21ns22.3 ± 3.223.2 ± 3.5nsnsnsnsnsnsnsnsns
NumberQuestionnaire RelevancePost Op Arrhythmia OSAPost Op Arrhythmia AHI < 15Post Op Arrhythmia AHI > 15Post Op Arrhythmia AHI > 30Post Op AF OSAPost Op AF AHI < 15Post Op AF AHI > 15
1nsns262819nsnsns
2nsnsnsnsns825nsns
3nsnsnsnsns482nsns
4
5nsnsnsnsns48nsns
6ns16ns16ns10ns10
7nsnsnsnsnsns84ns
8nsnsnsnsnsnsnsns
9Suboptimal performance. STOPBANG2 had better performance characteristics nsnsnsnsnsns
10
11No. STOP-BANG had a higher sensitivity of 75.8%nsnsnsns7nsns
12
13
14ns46nsnsns19 OSA and 45 CSA. Total: 64nsns
15no nsnsnsnsnsnsns
16
17nsnsnsnsnsnsnsns
18nsnsnsnsns46717
19nonsnsnsnsnsnsns
20nsnsnsnsns1967nsns
21nsnsnsnsns1904374
NumberPost Op AF AHI > 30Intubation Time (h) OSAIntubation Time (h) CSAIntubation Time (h) AHI < 15Intubation Time (h) AHI > 15Intubation Time (h) AHI > 30Length of Stay (ICU) (Days) OSALength of Stay (ICU) (Days) AHI < 15
1nsnsns14.516.618ns2
2ns24.4nsnsnsns2.22ns
3ns6.6nsnsnsnsnsns
4 ns
5nsnsnsnsnsnsnsns
6nsnsnsnsnsnsnsns
7nsnsnsnsnsnsnsns
8ns1217nsnsns4.5ns
9nsnsnsnsnsnsnsns
10
11nsnsnsnsnsns5.5 ± 5.1ns
12
13
14ns1717nsnsns1.5ns
15nsnsnsnsnsnsnsns
16
17nsnsnsnsnsnsnsns
1822nsnsnsnsnsnsns
19nsnsnsnsnsnsnsns
20nsnsnsnsnsnsnsns
2173nsnsnsnsnsnsns
NumberLength of Stay (ICU) (Days) AHI > 15Length of Stay (ICU) (Days) AHI > 30ICU Readmision OSAICU Readmision AHI < 15ICU Readmision AHI > 15ICU Readmision AHI > 30AKIN OSAIABP OSARespiratory Insufficiency OSA
12.53ns697nsnsns
2nsns141nsnsns663nsns
3nsns84nsnsns3654ns
4
5nsnsnsnsnsns5nsns
6nsnsnsnsnsnsnsnsns
7nsnsnsnsnsnsnsnsns
8nsnsnsnsnsnsnsnsns
9nsnsnsnsnsnsnsnsns
10
11nsns1nsnsnsnsnsns
12
13
14nsnsnsnsnsnsnsns20
15nsnsnsnsnsnsnsnsns
16
17nsnsnsnsnsnsnsnsns
18nsnsnsnsnsnsnsnsns
19nsnsnsnsnsnsnsnsns
20nsnsnsnsnsnsnsnsns
21nsnsnsnsnsnsnsnsns
NumberRespiratory Insufficiency CSAPneumonia OSAHospital Mortality OSAHospital Mortality AHI < 15Hospital Mortality AHI > 15Hospital Mortality AHI > 30Follow-Up (Years)Cardiovascular Deaths
1nsnsns454nsns
2ns7651nsnsnsnsns
3ns5935nsnsnsnsns
4 nsns
5nsnsnsnsnsnsnsns
6nsnsnsnsnsns4.53
7nsnsnsnsnsns2.118
8ns154nsnsnsnsns
9nsnsnsnsnsnsnsns
10
11ns33012nsns
12
13
1417nsnsnsnsnsnsns
15nsnsnsnsnsnsnsns
16
17nsnsnsnsnsnsnsns
18nsnsnsnsnsnsnsns
19nsnsnsnsnsnsnsns
20ns624729nsnsns7ns
21nsnsnsnsnsnsnsns
NumberNon-Fatal Myocardial InfarctionNon-Fatal StrokesUnplanned RevascularizationMACCE Incidence %
1nsnsnsns
2nsnsnsns
3nsnsnsns
4nsnsnsns
5nsnsnsns
683849
722261814.7
8nsnsnsns
9nsnsnsns
10
1111nsns
12
13
14nsnsnsns
15nsnsnsns
16
1717nsnsns
18nsnsnsns
19nsnsnsns
2083374247nsns
21nsnsnsns

Appendix B

Prisma flow diagram summarizing the identification, screening, eligibility assessment, and inclusion of studies in the systematic review. The diagram adheres to the PRISMA 2020 guidelines and outlines the number of records identified through database searching, screened, assessed for eligibility, excluded with reasons, and ultimately included in qualitative and quantitative syntheses.
Biomedicines 13 01579 i001

Appendix C

Summarizes the aggregate data from prospective studies, reflecting high diagnostic yield, elevated BMI profiles, and male predominance.
ArticleTotal PatientsOSA (n, %)CSA (n, %)Age (OSA)M (n, %)F (n, %)AHI < 5 (n, %)AHI > 5 (n, %)AHI > 15 (n, %)AHI > 30 (n, %)BMI (OSA)
Foldvary-Schaefer et al., 2015 [51]10779 (73.8%)ns69.7 ± 12.5nsns28 (35.4%)28 (35.4%)22 (27.8%)29 (36.7%)26.8 ± 6.4
Uchôa et al., 2015 [52]6737 (55.2%)ns59.0 ± 7.931 (83.8%)6 (16.2%)nsns37 (100.0%)ns29.1 ± 4.4
Koo et al., 2020 [53]1007513 (50.9%)ns62442 (86.2%)71 (13.8%)nsns513 (100.0%)ns25.9
Tafelmeier et al., 2020 [54]25059 (23.6%)68 (27.2%)67.9 ± 7.7112 (88.2)15 (25.4%)nsns127 (215.3%)ns30.1 ± 4.6
Liamsombut et al., 2021 [55]10777 (72.0%)ns69.7 ± 12.533 (42.9%)18 (23.4%)30 (39.0%)26 (33.8%)51 (66.2%)ns26.5 ± 6.6
Ding et al., 2016 [56]29054 (18.6%)61 (21.0%)55.20 ± 9.0561 (70,15%)54 (62.1%)175 (60.34%)115 (39.65%)nsns23.85 ± 3.7
Keymel et al., 2015 [62]4836 (75.0%)1 (2.1%)81 ± 8nsns11 (30.6%)37 (102.8%)18 (50.0%)ns26 ± 5
Oldham et al., 2024 [63]4639 (84.8%)6 (13.0%)67.131 (79.5%)14 (35.9%)1 (2.6%)15 (38.5%)18 (46.2%)12 (30.8%)32.4
Fan et al., 2021 [64]14762 (42.2%)ns62.9 ± 8.247 (75.8%)15 (24.2%)nsns62 (100.0%)ns25.2 ± 3.7
Peker et al., 2022 [65]147141 (95.9%)ns66.5 ± 7.5nsns6 (4.3%)21 (14.9%)53 (37.6%)67 (47.5%)28.0 ± 4.5
Teo et al., 2021 [66]1007800 (79.4%)ns62442 (55.2%)71 (8.9%)207 (25.9%)287 (35.9%)254 (31.8%)259 (32.4%)ns
Sezai et al., 2016 [68]1005778 (77.4%)ns69.3 ± 10.3519 (66.7%)259 (33.3%)227 (29.2%)361 (46.4%)260 (33.4%)157 (20.2%)24.3 ± 3.8
Total42282675 (63.3%)136 (3.2%)66.01718 (61.1%)523 (18.6%)685 (16.2%)890 (31.7%)1415 (50.3%)524 (18.6%)29.15

References

  1. Yeghiazarians, Y.; Jneid, H.; Tietjens, J.R.; Redline, S.; Brown, D.L.; El-Sherif, N.; Mehra, R.; Bozkurt, B.; Ndumele, C.E.; Somers, V.K. Obstructive Sleep Apnea and Cardiovascular Disease: A Scientific Statement from the American Heart Association. Circulation 2021, 144, E56–E67. [Google Scholar] [CrossRef] [PubMed]
  2. Drager, L.F.; Togeiro, S.M.; Polotsky, V.Y.; Lorenzi-Filho, G. Obstructive Sleep Apnea: A Cardiometabolic Risk in Obesity and the Metabolic Syndrome. J. Am. Coll. Cardiol. 2013, 62, 569–576. [Google Scholar] [CrossRef] [PubMed]
  3. Patil, S.P.; Schneider, H.; Schwartz, A.R.; Smith, P.L. Adult Obstructive Sleep Apnea: Pathophysiology and Diagnosis. Chest 2007, 132, 325–337. [Google Scholar] [CrossRef]
  4. Maniaci, A.; Lavalle, S.; Parisi, F.M.; Barbanti, M.; Cocuzza, S.; Iannella, G.; Magliulo, G.; Pace, A.; Lentini, M.; Masiello, E.; et al. Impact of Obstructive Sleep Apnea and Sympathetic Nervous System on Cardiac Health: A Comprehensive Review. J. Cardiovasc. Dev. Dis. 2024, 11, 204. [Google Scholar] [CrossRef]
  5. Abbasi, A.; Gupta, S.S.; Sabharwal, N.; Meghrajani, V.; Sharma, S.; Kamholz, S.; Kupfer, Y. A Comprehensive Review of Obstructive Sleep Apnea. Sleep Sci. 2021, 14, 142–154. [Google Scholar]
  6. Lavalle, S.; Masiello, E.; Iannella, G.; Magliulo, G.; Pace, A.; Lechien, J.R.; Calvo-Henriquez, C.; Cocuzza, S.; Parisi, F.M.; Favier, V.; et al. Unraveling the Complexities of Oxidative Stress and Inflammation Biomarkers in Obstructive Sleep Apnea Syndrome: A Comprehensive Review. Life 2024, 14, 425. [Google Scholar] [CrossRef]
  7. Wiegmann, D.A.; Eggman, A.A.; ElBardissi, A.W.; Parker, S.H.; Sundt, T.M. Improving Cardiac Surgical Care: A Work Systems Approach. Appl. Ergon. 2010, 41, 701–712. [Google Scholar] [CrossRef]
  8. Ivascu, R.; Torsin, L.I.; Hostiuc, L.; Nitipir, C.; Corneci, D.; Dutu, M. The Surgical Stress Response and Anesthesia: A Narrative Review. J. Clin. Med. 2024, 13, 3017. [Google Scholar] [CrossRef]
  9. Thandavarayan, R.A.; Chitturi, K.R.; Guha, A. Pathophysiology of Acute and Chronic Right Heart Failure. Cardiol. Clin. 2020, 38, 149–160. [Google Scholar] [CrossRef]
  10. De Jesus Danzi-Soares, N.; Genta, P.R.; Nerbass, F.B.; Pedrosa, R.P.; Soares, F.S.N.; César, L.A.M.H.; Drager, L.F.; Skomro, R.; Lorenzi-Filho, G. Obstructive Sleep Apnea Is Common among Patients Referred for Coronary Artery Bypass Grafting and Can Be Diagnosed by Portable Monitoring. Coron. Artery Dis. 2012, 23, 31–38. [Google Scholar] [CrossRef]
  11. Vasu, T.S.; Grewal, R.; Doghramji, K. Obstructive Sleep Apnea Syndrome and Perioperative Complications: A Systematic Review of the Literature. J. Clin. Sleep Med. 2012, 8, 199–207. [Google Scholar] [CrossRef] [PubMed]
  12. Gerçek, M.; Oldenburg, O.; Gerçek, M.; Fox, H.; Rudolph, V.; Puehler, T.; Omran, H.; Wolf, L.K.; Hakim-Meibodi, K.; Zeiher, A.M.; et al. Prevalence of Sleep Disordered Breathing in Patients with Primary Mitral Regurgitation Undergoing Mitral Valve Surgery. J. Clin. Med. 2021, 10, 2039. [Google Scholar] [CrossRef]
  13. Roberts, A.; Duncan, E.C.; Hargrave, P.; Kingery, D.R.; Barnes, J.; Horstemeyer, D.L.; Stahl, R.F. Complications of Cardiopulmonary Bypass From an Anesthesia Perspective: A Clinical Review. HCA Healthc. J. Med. 2023, 4, 13. [Google Scholar] [CrossRef]
  14. Shernan, S.K. Perioperative Myocardial Ischemia Reperfusion Injury. Anesthesiol. Clin. N. Am. 2003, 21, 465–485. [Google Scholar] [CrossRef] [PubMed]
  15. Koskinen, A.; Aittokallio, J.; Gunn, J.; Lehto, J.; Relander, A.; Viikinkoski, E.; Vasankari, T.; Jalkanen, J.; Hollmén, M.; Kiviniemi, T.O. Risk of Fluid Accumulation after Cardiac Surgery. JTCVS Open 2023, 16, 602–609. [Google Scholar] [CrossRef] [PubMed]
  16. Haase-Fielitz, A.; Haase, M.; Bellomo, R.; Calzavacca, P.; Spura, A.; Baraki, H.; Kutschka, I.; Albert, C. Perioperative Hemodynamic Instability and Fluid Overload Are Associated with Increasing Acute Kidney Injury Severity and Worse Outcome after Cardiac Surgery. Blood Purif. 2017, 43, 298–308. [Google Scholar] [CrossRef]
  17. Ng, K.T.; Lee, Z.X.; Ang, E.; Teoh, W.Y.; Wang, C.Y. Association of Obstructive Sleep Apnea and Postoperative Cardiac Complications: A Systematic Review and Meta-Analysis with Trial Sequential Analysis. J. Clin. Anesth. 2020, 62, 109731. [Google Scholar] [CrossRef]
  18. DiCaro, M.V.; Lei, K.C.; Yee, B.; Tak, T. The Effects of Obstructive Sleep Apnea on the Cardiovascular System: A Comprehensive Review. J. Clin. Med. 2024, 13, 3223. [Google Scholar] [CrossRef]
  19. Floras, J.S. Sleep Apnea and Cardiovascular Disease an Enigmatic Risk Factor. Circ. Res. 2018, 122, 1741–1764. [Google Scholar] [CrossRef]
  20. Khalid, A.; Mukundan, T.H.; Khalid, R.; Pusalavidyasagar, S.; Khan, A. Management of Obstructive Sleep Apnea in Hospitalized Patients. Appl. Sci. 2023, 13, 2108. [Google Scholar] [CrossRef]
  21. Alharbi, A.; Bansal, N.; Alsughayer, A.; Shah, M.; Alruwaili, W.; Mhanna, M.; Alfatlawi, H.; Kwak, E.S.; Salih, A.; Qwaider, M.; et al. Impact of Obstructive Sleep Apnea in Patients with Acute Heart Failure: A Nationwide Cohort Study. Hearts 2024, 5, 547–556. [Google Scholar] [CrossRef]
  22. Marulanda-Londoño, E.; Chaturvedi, S. The Interplay between Obstructive Sleep Apnea and Atrial Fibrillation. Front. Neurol. 2017, 8, 668. [Google Scholar] [CrossRef] [PubMed]
  23. Dou, L.; Lan, H.; Reynolds, D.J.; Gunderson, T.M.; Kashyap, R.; Gajic, O.; Caples, S.; Li, G.; Kashani, K.B. Association between Obstructive Sleep Apnea and Acute Kidney Injury in Critically Ill Patients: A Propensity-Matched Study. Nephron 2017, 135, 137–146. [Google Scholar] [CrossRef] [PubMed]
  24. Hai, F.; Porhomayon, J.; Vermont, L.; Frydrych, L.; Jaoude, P.; El-Solh, A.A. Postoperative Complications in Patients with Obstructive Sleep Apnea: A Meta-Analysis. J. Clin. Anesth. 2014, 26, 591–600. [Google Scholar] [CrossRef]
  25. Wahab, A.; Chowdhury, A.; Jain, N.K.; Surani, S.; Mushtaq, H.; Khedr, A.; Mir, M.; Jama, A.B.; Rauf, I.; Jain, S.; et al. Cardiovascular Complications of Obstructive Sleep Apnea in the Intensive Care Unit and Beyond. Medicina 2022, 58, 1390. [Google Scholar] [CrossRef]
  26. Subramani, Y.; Nagappa, M.; Wong, J.; Patra, J.; Chung, F. Death or Near-Death in Patients with Obstructive Sleep Apnoea: A Compendium of Case Reports of Critical Complications. Br. J. Anaesth. 2017, 119, 885–899. [Google Scholar] [CrossRef]
  27. Redline, S.; Sands, S.A.; Owens, R.L.; Edwards, B.A. More than the Sum of the Respiratory Events: Personalized Medicine Approaches for Obstructive Sleep Apnea. Am. J. Respir. Crit. Care Med. 2019, 200, 691–703. [Google Scholar]
  28. Owens, R.L.; Eckert, D.J.; Yeh, S.Y.; Malhotra, A. Upper Airway Function in the Pathogenesis of Obstructive Sleep Apnea: A Review of the Current Literature. Curr. Opin. Pulm. Med. 2008, 14, 519–524. [Google Scholar] [CrossRef]
  29. Bonsignore, M.R.; Suarez Giron, M.C.; Marrone, O.; Castrogiovanni, A.; Montserrat, J.M. Personalised Medicine in Sleep Respiratory Disorders: Focus on Obstructive Sleep Apnoea Diagnosis and Treatment. Eur. Respir. Rev. 2017, 26, 170069. [Google Scholar] [CrossRef]
  30. Csipor Fodor, A.; Huțanu, D.; Budin, C.E.; Ianoși, M.B.; Rachiș, D.L.; Sárközi, H.K.; Vultur, M.A.; Jimborean, G. Central Sleep Apnea in Adults: An Interdisciplinary Approach to Diagnosis and Management—A Narrative Review. J. Clin. Med. 2025, 14, 2369. [Google Scholar] [CrossRef]
  31. Sanchez, A.M.; Germany, R.; Lozier, M.R.; Schweitzer, M.D.; Kosseifi, S.; Anand, R. Central Sleep Apnea and Atrial Fibrillation: A Review on Pathophysiological Mechanisms and Therapeutic Implications. IJC Heart Vasc. 2020, 30, 100527. [Google Scholar] [CrossRef] [PubMed]
  32. Roberts, E.G.; Raphelson, J.R.; Orr, J.E.; LaBuzetta, J.N.; Malhotra, A. The Pathogenesis of Central and Complex Sleep Apnea. Curr. Neurol. Neurosci. Rep. 2022, 22, 405–412. [Google Scholar] [CrossRef]
  33. Khan, M.T.; Franco, R.A. Complex Sleep Apnea Syndrome. Sleep Disord. 2014, 2014, 798487. [Google Scholar] [CrossRef]
  34. Popević, M.B.; Milovanović, A.; Nagorni-Obradović, L.; Nešić, D.; Milovanović, J.; Milovanović, A.P.S. Screening Commercial Drivers for Obstructive Sleep Apnea: Validation of Stop-Bang Questionnaire. Int. J. Occup. Med. Environ. Health 2017, 30, 751–761. [Google Scholar] [CrossRef]
  35. Banhiran, W.; Durongphan, A.; Saleesing, C.R.; Chongkolwatana, C. Diagnostic Properties of the STOP-Bang and Its Modified Version in Screening for Obstructive Sleep Apnea in Thai Patients. J. Med. Assoc. Thai. 2014, 97, 644–654. [Google Scholar]
  36. Reis, R.; Teixeira, F.; Martins, V.; Sousa, L.; Batata, L.; Santos, C.; Moutinho, J. Validation of a Portuguese Version of the STOP-Bang Questionnaire as a Screening Tool for Obstructive Sleep Apnea: Analysis in a Sleep Clinic. Rev. Port. Pneumol. 2015, 21, 61–68. [Google Scholar] [CrossRef]
  37. Katzan, I.L.; Thompson, N.R.; Uchino, K.; Foldvary-Schaefer, N. A Screening Tool for Obstructive Sleep Apnea in Cerebrovascular Patients. Sleep Med. 2016, 21, 70–76. [Google Scholar] [CrossRef]
  38. Duarte, R.L.d.M.; Fonseca, L.B.d.M.; Magalhães-Da-Silveira, F.J.; Da Silveira, E.A.; Rabahi, M.F. Validação Do Questionário STOP-Bang Para a Identificação de Apneia Obstrutiva Do Sono Em Adultos No Brasil. J. Bras. Pneumol. 2017, 43, 456–463. [Google Scholar] [CrossRef]
  39. Cozowicz, C.; Memtsoudis, S.G. Perioperative Management of the Patient With Obstructive Sleep Apnea: A Narrative Review. Anesth. Analg. 2021, 132, 1231–1243. [Google Scholar] [CrossRef]
  40. Randerath, W.; Bassetti, C.L.; Bonsignore, M.R.; Farre, R.; Ferini-Strambi, L.; Grote, L.; Hedner, J.; Kohler, M.; Martinez-Garcia, M.A.; Mihaicuta, S.; et al. Challenges and Perspectives in Obstructive Sleep Apnoea. Eur. Respir. J. 2018, 52, 1702616. [Google Scholar] [CrossRef]
  41. Mbadjeu Hondjeu, A.R.; Chung, F.; Wong, J. Perioperative Management of Patients with Obstructive Sleep Apnea. Can. J. General. Intern. Med. 2022, 17, 1–16. [Google Scholar] [CrossRef]
  42. Zabara-Antal, A.; Grosu-Creanga, I.; Zabara, M.L.; Cernomaz, A.T.; Ciuntu, B.M.; Melinte, O.; Lupascu, C.; Trofor, A.C. A Debate on Surgical and Nonsurgical Approaches for Obstructive Sleep Apnea: A Comprehensive Review. J. Pers. Med. 2023, 13, 1288. [Google Scholar] [CrossRef] [PubMed]
  43. Hein, T.; Loo, G.; Lee, C.H. Obstructive Sleep Apnea, Coronary Artery Disease and Continuous Positive Airway Pressure Therapy. Interv. Cardiol. 2012, 4, 595–606. [Google Scholar] [CrossRef]
  44. Kang, J.; Koo, H.K.; Kang, H.K.; Seo, W.J.; Kang, J.; Kim, J. Prevalence of High-Risk Group for Obstructive Sleep Apnea Using the STOP-Bang Questionnaire and Its Association with Cardiovascular Morbidity. Front. Neurol. 2024, 15, 1394345. [Google Scholar] [CrossRef]
  45. Foroughi, M.; Malekmohammad, M.; Sharafkhaneh, A.; Emami, H.; Adimi, P.; Khoundabi, B. Prevalence of Obstructive Sleep Apnea in a High-Risk Population Using the Stop-Bang Questionnaire in Tehran, Iran. Tanaffos 2017, 16, 217–224. [Google Scholar]
  46. Subha, S.T.; Fah, L.H.; Azhar, F.L.; Zulkeflee, F.A. High Risk of Obstructive Sleep Apnea Among Hypertensive Patients at a Selected Tertiary Care Hospital. Malays. J. Med. Health Sci. 2023, 19, 1–6. [Google Scholar] [CrossRef]
  47. Wang, J.; Wang, X.; Yu, W.; Zhang, K.; Wei, Y. Obstructive Sleep Apnea-Induced Multi-Organ Dysfunction after Elective Coronary Artery Bypass Surgery in Coronary Heart Disease Patients. J. Thorac. Dis. 2020, 12, 5603–5616. [Google Scholar] [CrossRef]
  48. Nagappa, M.; Ho, G.; Patra, J.; Wong, J.; Singh, M.; Kaw, R.; Cheng, D.; Chung, F. Postoperative Outcomes in Obstructive Sleep Apnea Patients Undergoing Cardiac Surgery: A Systematic Review and Meta-Analysis of Comparative Studies. Anesth. Analg. 2017, 125, 2030–2037. [Google Scholar] [CrossRef]
  49. Patel, S.V.; Gill, H.; Shahi, D.; Rajabalan, A.; Patel, P.; Sonani, R.; Bhatt, P.; Rodriguez, R.D.; Bautista, M.; Deshmukh, A.; et al. High Risk for Obstructive Sleep Apnea Hypopnea Syndrome Predicts New Onset Atrial Fibrillation after Cardiac Surgery: A Retrospective Analysis. Sleep Breath. 2018, 22, 1117–1124. [Google Scholar] [CrossRef]
  50. Javaherforooshzadeh, F.; Amjadzadeh, M.; Haybar, H.; Sharafkhaneh, A. Impact of Obstructive Sleep Apnea Diagnosed Using the STOP-Bang Questionnaire Scale on Postoperative Complications Following Major Cardiac Surgery: A Prospective Observational Cohort Study. Cureus 2022, 14, e26102. [Google Scholar] [CrossRef]
  51. Foldvary-Schaefer, N.; Kaw, R.; Collop, N.; Andrews, N.D.; Bena, J.; Wang, L.; Stierer, T.; Gillinov, M.; Tarler, M.; Kayyali, H. Prevalence of Undetected Sleep Apnea in Patients Undergoing Cardiovascular Surgery and Impact on Postoperative Outcomes. J. Clin. Sleep Med. 2015, 11, 1083–1089A. [Google Scholar] [CrossRef] [PubMed]
  52. Uchôa, C.H.G.; De Jesus Danzi-Soares, N.; Nunes, F.S.; De Souza, A.A.L.; Nerbass, F.B.; Pedrosa, R.P.; César, L.A.M.; Lorenzi-Filho, G.; Drager, L.F. Impact of OSA on Cardiovascular Events Aft Er Coronary Artery Bypass Surgery. Chest 2015, 147, 1352–1360. [Google Scholar] [CrossRef] [PubMed]
  53. Koo, C.Y.; Aung, A.T.; Chen, Z.; Kristanto, W.; Sim, H.W.; Tam, W.W.; Gochuico, C.F.; Tan, K.A.; Kang, G.S.; Sorokin, V.; et al. Sleep Apnoea and Cardiovascular Outcomes after Coronary Artery Bypass Grafting. Heart 2020, 106, 1495–1502. [Google Scholar] [CrossRef] [PubMed]
  54. Tafelmeier, M.; Luft, L.; Zistler, E.; Floerchinger, B.; Camboni, D.; Creutzenberg, M.; Zeman, F.; Schmid, C.; Maier, L.S.; Wagner, S.; et al. Central Sleep Apnea Predicts Pulmonary Complications After Cardiac Surgery. Chest 2021, 159, 798–809. [Google Scholar] [CrossRef]
  55. Liamsombut, S.; Kaw, R.; Wang, L.; Bena, J.; Andrews, N.; Collop, N.; Stierer, T.; Gillinov, M.; Tarler, M.; Kayyali, H.; et al. Predictive Value of Sleep Apnea Screenings in Cardiac Surgery Patients. Sleep Med. 2021, 84, 20–25. [Google Scholar] [CrossRef]
  56. Ding, N.; Ni, B.Q.; Wang, H.; Ding, W.X.; Xue, R.; Lin, W.; Kai, Z.; Zhang, S.J.; Zhang, X.L. Obstructive Sleep Apnea Increases the Perioperative Risk of Cardiac Valve Replacement Surgery: A Prospective Single-Center Study. J. Clin. Sleep Med. 2016, 12, 1331–1337. [Google Scholar] [CrossRef]
  57. Lockhart, E.M.; Willingham, M.D.; Abdallah, A.B.; Helsten, D.L.; Bedair, B.A.; Thomas, J.; Duntley, S.; Avidan, M.S. Obstructive Sleep Apnea Screening and Postoperative Mortality in a Large Surgical Cohort. Sleep Med. 2013, 14, 407–415. [Google Scholar] [CrossRef]
  58. Gali, B.; Glasgow, A.E.; Greason, K.L.; Johnson, R.L.; Albright, R.C.; Habermann, E.B. Postoperative Outcomes of Patients With Obstructive Sleep Apnea Undergoing Cardiac Surgery. Ann. Thorac. Surg. 2020, 110, 1324–1332. [Google Scholar] [CrossRef]
  59. Wolf, S.; Wolf, C.; Cattermole, T.C.; Rando, H.J.; DeNino, W.F.; Iribarne, A.; Ross, C.S.; Ramkumar, N.; Gelb, D.J.; Bourcier, B.; et al. Cardiac Surgery Outcomes: A Case for Increased Screening and Treatment of Obstructive Sleep Apnea. Ann. Thorac. Surg. 2022, 113, 1159–1164. [Google Scholar] [CrossRef]
  60. Wong, J.K.; Maxwell, B.G.; Kushida, C.A.; Sainani, K.L.; Lobato, R.L.; Joseph Woo, Y.; Pearl, R.G. Obstructive Sleep Apnea Is an Independent Predictor of Postoperative Atrial Fibrillation in Cardiac Surgery. J. Cardiothorac. Vasc. Anesth. 2015, 29, 1140–1147. [Google Scholar] [CrossRef]
  61. Krishnasamy, S.; Sahid, S.M.; Hashim, S.A.; Singh, S.; Chung, F.; Mokhtar, R.A.R.; Yin, W.C. Obstructive Sleep Apnoea and Open Heart Surgery: A Review of Its Incidence and Impact to Patients. J. Thorac. Dis. 2019, 11, 5453–5462. [Google Scholar] [CrossRef] [PubMed]
  62. Keymel, S.; Hellhammer, K.; Zeus, T.; Merx, M.; Kelm, M.; Steiner, S. Severe Aortic Valve Stenosis in the Elderly: High Prevalence of Sleep-Related Breathing Disorders. Clin. Interv. Aging 2015, 10, 1451–1456. [Google Scholar] [CrossRef] [PubMed]
  63. Oldham, M.A.; Pigeon, W.R.; Yurcheshen, M.; Hisamoto, K.; Knight, P.A.; Lee, H.B. High Prevalence of Obstructive Sleep Apnea in a Surgical Aortic Valve Replacement Cohort: An Observational Study. SLEEP Adv. 2024, 5, zpae034. [Google Scholar] [CrossRef] [PubMed]
  64. Fan, K.; Gao, M.; Yu, W.; Liu, H.; Chen, L.; Ding, X.; Yu, Y. Obstructive Sleep Apnea Increases the Risk of Perioperative Myocardial Infarction Following Off-Pump Coronary Artery Bypass Grafting. Front. Cardiovasc. Med. 2021, 8, 689795. [Google Scholar] [CrossRef]
  65. Peker, Y.; Holtstrand-Hjälm, H.; Celik, Y.; Glantz, H.; Thunström, E. Postoperative Atrial Fibrillation in Adults with Obstructive Sleep Apnea Undergoing Coronary Artery Bypass Grafting in the RICCADSA Cohort. J. Clin. Med. 2022, 11, 2459. [Google Scholar] [CrossRef]
  66. Teo, Y.H.; Tam, W.W.; Koo, C.Y.; Aung, A.T.; Sia, C.H.; Wong, R.C.C.; Kong, W.; Poh, K.K.; Kofidis, T.; Kojodjojo, P.; et al. Sleep Apnea and Recurrent Heart Failure Hospitalizations after Coronary Artery Bypass Grafting. J. Clin. Sleep Med. 2021, 17, 2399–2407. [Google Scholar] [CrossRef]
  67. Feng, T.R.; White, R.S.; Ma, X.; Askin, G.; Pryor, K.O. The Effect of Obstructive Sleep Apnea on Readmissions and Atrial Fibrillation after Cardiac Surgery. J. Clin. Anesth. 2019, 56, 17–23. [Google Scholar] [CrossRef]
  68. Sezai, A.; Akahoshi, T.; Osaka, S.; Yaoita, H.; Arimoto, M.; Hata, H.; Tanaka, M.; Sekino, H.; Akashiba, T. Sleep Disordered Breathing in Cardiac Surgery Patients: The NU-SLEEP Trial. Int. J. Cardiol. 2017, 227, 342–346. [Google Scholar] [CrossRef]
  69. Ailawadi, G.; Chang, H.L.; O’Gara, P.T.; O’Sullivan, K.; Woo, Y.J.; DeRose, J.J.; Parides, M.K.; Thourani, V.H.; Robichaud, S.; Gillinov, A.M.; et al. Pneumonia after Cardiac Surgery: Experience of the National Institutes of Health/Canadian Institutes of Health Research Cardiothoracic Surgical Trials Network. J. Thorac. Cardiovasc. Surg. 2017, 153, 1384–1391.e3. [Google Scholar] [CrossRef]
  70. Wang, D.; Huang, X.; Wang, H.; Le, S.; Yang, H.; Wang, F.; Du, X. Risk Factors for Postoperative Pneumonia after Cardiac Surgery: A Prediction Model. J. Thorac. Dis. 2021, 13, 2351–2362. [Google Scholar] [CrossRef]
  71. Duchnowski, P.; Śmigielski, W. Risk Factors of Postoperative Hospital-Acquired Pneumonia in Patients Undergoing Cardiac Surgery. Medicina 2023, 59, 1993. [Google Scholar] [CrossRef] [PubMed]
  72. Koo, D.L.; Nam, H.; Thomas, R.J.; Yun, C.H. Sleep Disturbances as a Risk Factor for Stroke. J. Stroke 2018, 20, 12–32. [Google Scholar] [CrossRef] [PubMed]
  73. Gottlieb, D.J. Does Treatment of Sleep Apnea Prevent Perioperative Complications? Wish We Knew! Sleep 2015, 38, 1155–1156. [Google Scholar] [CrossRef]
  74. Ceban, F.; Yan, E.; Pivetta, B.; Saripella, A.; Englesakis, M.; Gan, T.J.; Joshi, G.P.; Chung, F. Perioperative Adverse Events in Adult Patients with Obstructive Sleep Apnea Undergoing Ambulatory Surgery: An Updated Systematic Review and Meta-Analysis. J. Clin. Anesth. 2024, 96, 111464. [Google Scholar] [CrossRef]
  75. Kadam, V.R.; Markman, P.; Neumann, S.; Kingisepp, S. Risk Stratification for Obstructive Sleep Apnoea and Optimal Post-Operative Monitoring in an Overnight Stay Ward. Aust. J. Adv. Nurs. 2015, 33, 13–20. [Google Scholar] [CrossRef]
  76. Kapur, V.K.; Auckley, D.H.; Chowdhuri, S.; Kuhlmann, D.C.; Mehra, R.; Ramar, K.; Harrod, C.G. Clinical Practice Guideline for Diagnostic Testing for Adult Obstructive Sleep Apnea: An American Academy of Sleep Medicine Clinical Practice Guideline. J. Clin. Sleep Med. 2017, 13, 479–504. [Google Scholar] [CrossRef]
  77. Opperer, M.; Cozowicz, C.; Bugada, D.; Mokhlesi, B.; Kaw, R.; Auckley, D.; Chung, F.; Memtsoudis, S.G. Does Obstructive Sleep Apnea Influence Perioperative Outcome? A Qualitative Systematic Review for the Society of Anesthesia and Sleep Medicine Task Force on Preoperative Preparation of Patients with Sleep-Disordered Breathing. Anesth. Analg. 2016, 122, 1321–1334. [Google Scholar] [CrossRef]
  78. Borsook, D.; George, E.; Kussman, B.; Becerra, L. Anesthesia and Perioperative Stress: Consequences on Neural Networks and Postoperative Behaviors. Prog. Neurobiol. 2010, 92, 601–612. [Google Scholar] [CrossRef]
  79. Eckert, D.J.; Malhotra, A. Pathophysiology of Adult Obstructive Sleep Apnea. Proc. Am. Thorac. Soc. 2008, 5, 144–153. [Google Scholar] [CrossRef]
  80. Hakim, F.; Gozal, D.; Kheirish-Gozal, L. Sympathetic and Catecholaminergic Alterations in Sleep Apnea with Particular Emphasison Children. Front. Neurol. 2012, 3, 7. [Google Scholar] [CrossRef]
  81. Alevroudis, I.; Petridou, M.; Sakkou, A.; Kotoulas, S.-C.; Matzolas, S.; Roumelis, P.; Stougianni, M.; Massa, E.; Mouloudi, E. “Restless Nights, Stressed Hearts”: The Link Between Sleep Disorders and Takotsubo Syndrome-A Comprehensive Review. Rev. Cardiovasc. Med. 2025, 26, 28244. [Google Scholar] [CrossRef]
  82. Takeda, Y.; Kimura, F.; Takasawa, S. Possible Molecular Mechanisms of Hypertension Induced by Sleep Apnea Syndrome/Intermittent Hypoxia. Life 2024, 14, 157. [Google Scholar] [CrossRef]
  83. Chan, K.H.; Wilcox, I. Obstructive Sleep Apnea: Novel Trigger and Potential Therapeutic Target for Cardiac Arrhythmias. Expert Rev. Cardiovasc. Ther. 2010, 8, 981–994. [Google Scholar] [CrossRef]
  84. Lévy, P.; Naughton, M.T.; Tamisier, R.; Cowie, M.R.; Bradley, T.D. Sleep Apnoea and Heart Failure. Eur. Respir. J. 2022, 59, 2101640. [Google Scholar] [CrossRef]
  85. Hersi, A. Relationship Between Arrhythmia and Sleep Disordered Breathing. J. Atr. Fibrillation. 2012, 5, 413. [Google Scholar]
  86. Scioli, M.G.; Storti, G.; D’amico, F.; Guzmán, R.R.; Centofanti, F.; Doldo, E.; Miranda, E.M.C.; Orlandi, A. Oxidative Stress and New Pathogenetic Mechanisms in Endothelial Dysfunction: Potential Diagnostic Biomarkers and Therapeutic Targets. J. Clin. Med. 2020, 9, 1995. [Google Scholar] [CrossRef]
  87. Janaszak-jasiecka, A.; Siekierzycka, A.; Płoska, A.; Dobrucki, I.T.; Kalinowski, L. Endothelial Dysfunction Driven by Hypoxia—The Influence of Oxygen Deficiency on No Bioavailability. Biomolecules 2021, 11, 982. [Google Scholar] [CrossRef]
  88. Zhao, Y.; Xiong, W.; Li, C.; Zhao, R.; Lu, H.; Song, S.; Zhou, Y.; Hu, Y.; Shi, B.; Ge, J. Hypoxia-Induced Signaling in the Cardiovascular System: Pathogenesis and Therapeutic Targets. Signal Transduct. Target. Ther. 2023, 8, 431. [Google Scholar] [CrossRef]
  89. Gallo, G.; Savoia, C. New Insights into Endothelial Dysfunction in Cardiometabolic Diseases: Potential Mechanisms and Clinical Implications. Int. J. Mol. Sci. 2024, 25, 2973. [Google Scholar] [CrossRef]
  90. Penna, C.; Pagliaro, P. Endothelial Dysfunction: Redox Imbalance, NLRP3 Inflammasome, and Inflammatory Responses in Cardiovascular Diseases. Antioxidants 2025, 14, 256. [Google Scholar] [CrossRef]
  91. Kibel, A.; Lukinac, A.M.; Dambic, V.; Juric, I.; Relatic, K.S. Oxidative Stress in Ischemic Heart Disease. Oxidative Med. Cell Longev. 2020, 2020, 6627144. [Google Scholar] [CrossRef] [PubMed]
  92. Chandimali, N.; Bak, S.G.; Park, E.H.; Lim, H.J.; Won, Y.S.; Kim, E.K.; Park, S.I.; Lee, S.J. Free Radicals and Their Impact on Health and Antioxidant Defenses: A Review. Cell Death Discov. 2025, 11, 19. [Google Scholar] [CrossRef]
  93. Verbraecken, J.; Mcnicholas, W.T. Respiratory Mechanics and Ventilatory Control in Overlap Syndrome and Obesity Hypoventilation. Respir. Res. 2013, 14, 1–17. [Google Scholar] [CrossRef] [PubMed]
  94. Sheikh, Z.A.; Sowmya Priya, S.; Raj, P.A. Postoperative Complications with Obstructive Sleep Apnea. J. Vokasi Kesehat. 2024, 3, 85–98. [Google Scholar] [CrossRef]
  95. Selim, B.; Ramar, K. Sleep-Related Breathing Disorders: When CPAP Is Not Enough. Neurotherapeutics 2020, 18, 81–90. [Google Scholar] [CrossRef]
  96. Pattullo, G.G. Clinical Implications of Opioid-Induced Ventilatory Impairment. Anaesth. Intensive Care 2022, 50, 52–67. [Google Scholar] [CrossRef]
  97. Martins, R.T.; Carberry, J.C.; Gandevia, S.C.; Butler, J.E.; Eckert, D.J. Effects of Morphine on Respiratory Load Detection, Load Magnitude Perception, and Tactile Sensation in Obstructive Sleep Apnea. J. Appl. Physiol. 2018, 125, 393–400. [Google Scholar] [CrossRef]
  98. Holt, N.R.; Downey, G.; Naughton, M.T. Perioperative Considerations in the Management of Obstructive Sleep Apnoea. Med. J. Aust. 2019, 211, 326–332. [Google Scholar] [CrossRef]
  99. Böing, S.; Randerath, W.J. Chronic Hypoventilation Syndromes and Sleep-Related Hypoventilation. J. Thorac. Dis. 2015, 7, 1273–1285. [Google Scholar]
  100. Randerath, W.; Baillieul, S.; Tamisier, R. Central Sleep Apnoea: Not Just One Phenotype. Eur. Respir. Rev. 2024, 33, 230141. [Google Scholar] [CrossRef]
  101. Shin, C.H.; Zaremba, S.; Devine, S.; Nikolov, M.; Kurth, T.; Eikermann, M. Effects of Obstructive Sleep Apnoea Risk on Postoperative Respiratory Complications: Protocol for a Hospital-Based Registry Study. BMJ Open 2016, 6, e008436. [Google Scholar] [CrossRef] [PubMed]
  102. Zamarrón, C.; Valdés Cuadrado, L.; Álvarez-Sala, R. Pathophysiologic Mechanisms of Cardiovascular Disease in Obstructive Sleep Apnea Syndrome. Pulm. Med. 2013, 2013, 521087. [Google Scholar] [CrossRef] [PubMed]
  103. Atkeson, A.; Jelic, S. Mechanisms of Endothelial Dysfunction in Obstructive Sleep Apnea. Vasc. Health Risk Manag. 2008, 4, 1327–1335. [Google Scholar] [CrossRef] [PubMed]
  104. Menon, T.; Kalra, D.K. Sleep Apnea and Heart Failure—Current State-of-The-Art. Int. J. Mol. Sci. 2024, 25, 5251. [Google Scholar] [CrossRef]
  105. Peracaula, M.; Torres, D.; Poyatos, P.; Luque, N.; Rojas, E.; Obrador, A.; Orriols, R.; Tura-Ceide, O. Endothelial Dysfunction and Cardiovascular Risk in Obstructive Sleep Apnea: A Review Article. Life 2022, 12, 537. [Google Scholar] [CrossRef]
  106. Baltzis, D.; Bakker, J.P.; Patel, S.R.; Veves, A. Obstructive Sleep Apnea and Vascular Diseases. Compr. Physiol. 2016, 6, 1519–1528. [Google Scholar] [CrossRef]
  107. Ryan, S. Mechanisms of Cardiovascular Disease in Obstructive Sleep Apnoea. J. Thorac. Dis. 2018, 10, S4201–S4211. [Google Scholar] [CrossRef]
  108. Chen, J.; Lin, S.; Zeng, Y. An Update on Obstructive Sleep Apnea for Atherosclerosis: Mechanism, Diagnosis, and Treatment. Front. Cardiovasc. Med. 2021, 8, 647071. [Google Scholar] [CrossRef]
  109. Chaudhry, R.A.; Zarmer, L.; West, K.; Chung, F. Obstructive Sleep Apnea and Risk of Postoperative Complications after Non-Cardiac Surgery. J. Clin. Med. 2024, 13, 2538. [Google Scholar] [CrossRef]
  110. Devinney, M.J.; VanDusen, K.W.; Kfouri, J.M.; Avasarala, P.; Spector, A.R.; Mathew, J.P.; Berger, M. The Potential Link between Obstructive Sleep Apnea and Postoperative Neurocognitive Disorders: Current Knowledge and Possible Mechanisms. Can. J. Anesth. 2022, 69, 1272–1287. [Google Scholar] [CrossRef]
  111. Chan, M.T.V.; Wang, C.Y.; Seet, E.; Tam, S.; Lai, H.Y.; Chew, E.F.F.; Wu, W.K.K.; Cheng, B.C.P.; Lam, C.K.M.; Short, T.G.; et al. Association of Unrecognized Obstructive Sleep Apnea with Postoperative Cardiovascular Events in Patients Undergoing Major Noncardiac Surgery. J. Am. Med. Assoc. 2019, 321, 1788–1798. [Google Scholar] [CrossRef] [PubMed]
  112. Cohen, O.; Kundel, V.; Yaggi, H.K.; Shah, N.A.; Alcantara, C.; Azarbarzin, A.; BARBe, F.; Bhatt, D.L.; Billings, M.E.; Douglas Bradley, T.; et al. The Great Controversy of Obstructive Sleep Apnea Treatment for Cardiovascular Risk Benefit: Advancing the Science through Expert Consensus An Official American Thoracic Society Workshop Report. Ann. Am. Thorac. Soc. 2025, 22, 1–22. [Google Scholar] [CrossRef] [PubMed]
  113. Orr, J.E.; Safwan Badr, M.; Ayappa, I.; Eckert, D.J.; Feldman, J.L.; Jackson, C.L.; Javaheri, S.; Khayat, R.N.; Martin, J.L.; Mehra, R.; et al. Research Priorities for Patients with Heart Failure and Central Sleep Apnea An Official American Thoracic Society Research Statement. Am. J. Respir. Crit. Care Med. 2021, 203, E11–E24. [Google Scholar] [CrossRef]
  114. Tietjens, J.R.; Claman, D.; Kezirian, E.J.; de Marco, T.; Mirzayan, A.; Sadroonri, B.; Goldberg, A.N.; Long, C.; Gerstenfeld, E.P.; Yeghiazarians, Y. Obstructive Sleep Apnea in Cardiovascular Disease: A Review of the Literature and Proposed Multidisciplinary Clinical Management Strategy. J. Am. Heart Assoc. 2019, 8, e010440. [Google Scholar] [CrossRef]
  115. Karimi, N.; Kelava, M.; Kothari, P.; Zimmerman, N.M.; Gillinov, A.M.; Duncan, A.E. Patients at High Risk for Obstructive Sleep Apnea Are at Increased Risk for Atrial Fibrillation after Cardiac Surgery: A Cohort Analysis. Anesth. Analg. 2018, 126, 2025–2031. [Google Scholar] [CrossRef]
  116. Yaggi, H.K.; Concato, J.; Kernan, W.N.; Lichtman, J.H.; Brass, L.M.; Mohsenin, V. Obstructive Sleep Apnea as a Risk Factor for Stroke and Death. N. Engl. J. Med. 2005, 353, 2034–2041. [Google Scholar] [CrossRef]
  117. Marshall, N.S.; Wong, K.K.H.; Cullen, S.R.J.; Knuiman, M.W.; Grunstein, R.R. Sleep Apnea and 20-Year Follow-up for All-Cause Mortality, Stroke, and Cancer Incidence and Mortality in the Busselton Health Study Cohort. J. Clin. Sleep Med. 2014, 10, 355–362. [Google Scholar] [CrossRef]
  118. Kurra, N.; Gandrakota, N.; Ramakrishnan, M.; Sudireddy, K.; Boorle, N.V.L.D.; Jillella, D. The Influence of Obstructive Sleep Apnea on Post-Stroke Complications: A Systematic Review and Meta-Analysis. J. Clin. Med. 2024, 13, 5646. [Google Scholar] [CrossRef]
  119. Lyons, O.D.; Ryan, C.M. Obstructive Sleep Apnea and Stroke: Hand in Hand? J. Thorac. Dis. 2018, 10, S1099–S1101. [Google Scholar] [CrossRef]
  120. Shi, C.; Wang, Y.; Luo, J.; Huang, R.; Xiao, Y. Performance of Four Screening Tools for Identifying Obstructive Sleep Apnea Among Patients with Insomnia. Nat. Sci. Sleep 2025, 17, 379–390. [Google Scholar] [CrossRef]
  121. Hwang, M.; Nagappa, M.; Guluzade, N.; Saripella, A.; Englesakis, M.; Chung, F. Validation of the STOP-Bang Questionnaire as a Preoperative Screening Tool for Obstructive Sleep Apnea: A Systematic Review and Meta-Analysis. BMC Anesthesiol. 2022, 22, 366. [Google Scholar] [CrossRef] [PubMed]
  122. Tarasiuk, A.; Reznor, G.; Greenberg-Dotan, S.; Reuveni, H. Financial Incentive Increases CPAP Acceptance in Patients from Low Socioeconomic Background. PLoS ONE 2012, 7, e33178. [Google Scholar] [CrossRef] [PubMed]
  123. Ruscic, K.J.; Grabitz, S.D.; Rudolph, M.I.; Eikermann, M. Prevention of Respiratory Complications of the Surgical Patient: Actionable Plan for Continued Process Improvement. Curr. Opin. Anaesthesiol. 2017, 30, 399–408. [Google Scholar] [CrossRef] [PubMed]
  124. Ramirez, M.F.; Kamdar, B.B.; Cata, J.P. Optimizing Perioperative Use of Opioids: A Multimodal Approach. Curr. Anesthesiol. Rep. 2020, 10, 404–415. [Google Scholar] [CrossRef]
  125. Eastwood, P.R.; Malhotra, A.; Palmer, L.J.; Kezirian, E.J.; Horner, R.L.; Ip, M.S.; Thurnheer, R.; Antic, N.A.; Hillman, D.R. Obstructive Sleep Apnoea: From Pathogenesis to Treatment: Current Controversies and Future Directions. Respirology 2010, 15, 587–595. [Google Scholar] [CrossRef]
Figure 1. Visual summary of the strengths and limitations inherent to prospective and retrospective designs in this context.
Figure 1. Visual summary of the strengths and limitations inherent to prospective and retrospective designs in this context.
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Figure 2. Bar chart depicting the frequency of use of each tool across studies, illustrating the dominance of STOP-BAG2, STOP-Bang, and ESS.
Figure 2. Bar chart depicting the frequency of use of each tool across studies, illustrating the dominance of STOP-BAG2, STOP-Bang, and ESS.
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Figure 3. Distribution of AUC values across studies, highlighting the heterogeneity and reinforcing the need for standardized reporting and prospective validation [51,55].
Figure 3. Distribution of AUC values across studies, highlighting the heterogeneity and reinforcing the need for standardized reporting and prospective validation [51,55].
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Figure 4. Presents a forest plot summarizing individual and pooled odds ratios for POAF in OSA versus non-OSA patients, visually reinforcing the strength and consistency of the association [49,50,68]. The solid horizontal lines represent the 95% confidence intervals for each individual study’s OR, while the light blue bars denote the actual odds ratio values. The vertical red dashed line marks the pooled OR of 2.44, emphasizing the overall estimated effect across studies [48,49,65].
Figure 4. Presents a forest plot summarizing individual and pooled odds ratios for POAF in OSA versus non-OSA patients, visually reinforcing the strength and consistency of the association [49,50,68]. The solid horizontal lines represent the 95% confidence intervals for each individual study’s OR, while the light blue bars denote the actual odds ratio values. The vertical red dashed line marks the pooled OR of 2.44, emphasizing the overall estimated effect across studies [48,49,65].
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Figure 5. Forest plot summarizing the odds ratios from individual studies and the aggregated meta-analytic estimate, visually emphasizing the consistency and strength of this association. Each black horizontal line represents the 95% confidence interval for an individual study’s odds ratio, while the black dots indicate the point estimates. The red horizontal line and red dot represent the pooled odds ratio and its confidence interval (random-effects model), and the vertical dashed grey line marks the null effect line (OR = 1), aiding in visual interpretation of significance and direction of association [47,48,52].
Figure 5. Forest plot summarizing the odds ratios from individual studies and the aggregated meta-analytic estimate, visually emphasizing the consistency and strength of this association. Each black horizontal line represents the 95% confidence interval for an individual study’s odds ratio, while the black dots indicate the point estimates. The red horizontal line and red dot represent the pooled odds ratio and its confidence interval (random-effects model), and the vertical dashed grey line marks the null effect line (OR = 1), aiding in visual interpretation of significance and direction of association [47,48,52].
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Figure 6. Summary of cardiac ischemic outcomes in patients with obstructive sleep apnea (OSA) following cardiac surgery. OR—Odds Ratio; OSA—Obstructive sleep apnea; P MI—Postoperative myocardial infarction [47,52,64].
Figure 6. Summary of cardiac ischemic outcomes in patients with obstructive sleep apnea (OSA) following cardiac surgery. OR—Odds Ratio; OSA—Obstructive sleep apnea; P MI—Postoperative myocardial infarction [47,52,64].
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Figure 7. Comparison of postoperative acute kidney injury incidence in patients with and without obstructive sleep apnea, based on Gali et al. (2020) [58], with pooled risk from the Wang et al. (2020) [47] meta-analysis.
Figure 7. Comparison of postoperative acute kidney injury incidence in patients with and without obstructive sleep apnea, based on Gali et al. (2020) [58], with pooled risk from the Wang et al. (2020) [47] meta-analysis.
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Figure 8. Reported stroke outcomes across studies, highlighting the overall paucity and inconsistency of the existing evidence base [47,52,61].
Figure 8. Reported stroke outcomes across studies, highlighting the overall paucity and inconsistency of the existing evidence base [47,52,61].
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Figure 9. Postoperative mortality rates in patients with and without obstructive sleep apnea following cardiac surgery [49,53,58,60].
Figure 9. Postoperative mortality rates in patients with and without obstructive sleep apnea following cardiac surgery [49,53,58,60].
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Figure 10. Forest plot summarizing the odds ratios for postoperative respiratory complications in OSA versus non-OSA patients, based on data from three cohort studies. Each blue square represents the point estimate of the odds ratio (OR) for an individual study, and the accompanying black horizontal lines show the 95% confidence intervals (CI). The red square and dashed red line denote the pooled OR from the meta-analysis (OR = 1.15; 95% CI: 1.05–1.25), indicating a statistically significant increase in risk. The vertical dashed grey line at OR = 1.0 represents the line of no effect, helping to visualize whether individual and pooled estimates suggest elevated risk in the OSA group [54,61,64].
Figure 10. Forest plot summarizing the odds ratios for postoperative respiratory complications in OSA versus non-OSA patients, based on data from three cohort studies. Each blue square represents the point estimate of the odds ratio (OR) for an individual study, and the accompanying black horizontal lines show the 95% confidence intervals (CI). The red square and dashed red line denote the pooled OR from the meta-analysis (OR = 1.15; 95% CI: 1.05–1.25), indicating a statistically significant increase in risk. The vertical dashed grey line at OR = 1.0 represents the line of no effect, helping to visualize whether individual and pooled estimates suggest elevated risk in the OSA group [54,61,64].
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Figure 11. Ribbon plot showing standardized mean differences in hospital length of stay between OSA and non-OSA patients across three studies. Shaded bands indicate 95% confidence intervals. The red dashed line marks the pooled SMD (0.62), suggesting consistently longer LOS in OSA patients [12,58,66].
Figure 11. Ribbon plot showing standardized mean differences in hospital length of stay between OSA and non-OSA patients across three studies. Shaded bands indicate 95% confidence intervals. The red dashed line marks the pooled SMD (0.62), suggesting consistently longer LOS in OSA patients [12,58,66].
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Figure 12. Lollipop plot of odds ratios (ORs) for postoperative pneumonia in OSA versus non-OSA patients, visually illustrating the narrow but consistent increase in risk observed across studies. Each blue dot represents the point estimate of the OR for an individual study. The horizontal black lines extending from the blue dots indicate the 95% confidence intervals. The red dot and horizontal red line at the bottom represent the pooled odds ratio (OR = 1.07; 95% CI: 1.00–1.15) from the meta-analysis. The vertical dashed black line at OR = 1.0 denotes the line of no effect, aiding interpretation of statistical significance [12,50,54,61].
Figure 12. Lollipop plot of odds ratios (ORs) for postoperative pneumonia in OSA versus non-OSA patients, visually illustrating the narrow but consistent increase in risk observed across studies. Each blue dot represents the point estimate of the OR for an individual study. The horizontal black lines extending from the blue dots indicate the 95% confidence intervals. The red dot and horizontal red line at the bottom represent the pooled odds ratio (OR = 1.07; 95% CI: 1.00–1.15) from the meta-analysis. The vertical dashed black line at OR = 1.0 denotes the line of no effect, aiding interpretation of statistical significance [12,50,54,61].
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Figure 13. Suggested protocol for the grouping and reporting of patients with obstructive sleep apnea in cardiac surgery studies.
Figure 13. Suggested protocol for the grouping and reporting of patients with obstructive sleep apnea in cardiac surgery studies.
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Table 1. Detailed overview of study characteristics like study design, sample size, and population demographics.
Table 1. Detailed overview of study characteristics like study design, sample size, and population demographics.
ArticleStudy DesignSample SizeGeographic Location
Foldvary-Schaefer et al., 2015 [51]Prospective107USA
Gali et al., 2020 [58]Retrospective8612USA
Wolf et al., 2021 [59]Retrospective12,505USA
Wong et al., 2015 [60]Retrospective545Canada
Uchôa et al., 2015 [52]Prospective67Brazil
Koo et al., 2020 [53]Prospective1007South Korea
Tafelmeier et al., 2020 [54]Prospective250Germany
Liamsombut et al., 2021 [55]Prospective107Thailand
Krishnasamy et al., 2019 [61]Retrospective101Australia
Ding et al., 2016 [56]Prospective290China
Keymel et al., 2015 [62]Prospective48Germany
Oldham et al., 2024 [63]Prospective46USA
Fan et al., 2021 [64]Prospective147China
Peker et al., 2022 [65]Prospective147Sweden
Teo et al., 2021 [66]Prospective1007Singapore
Feng et al., 2019 [67]Retrospective506,604USA
Sezai et al., 2016 [68]Prospective1005Japan
Table 2. Key findings from the retrospective studies, including OSA prevalence, demographic patterns, and body mass index profiles.
Table 2. Key findings from the retrospective studies, including OSA prevalence, demographic patterns, and body mass index profiles.
Total PatientsOSA
(n, %)
CSA
(n, %)
Age
(OSA)
M
(n, %)
F
(n, %)
BMI
(OSA)
86122636 (30.6%)ns65.32001 (75.9%)635 (24.1%)33.8
12,5051555 (12.4%)ns65.41245 (80.1%)310 (19.9%)34.8
54572 (13.2%)ns67.8 ± 10.257 (79.2%)15 (20.8%)ns
10162 (61.4%)ns60 ± 849 (79.0%)15 (24.2%)ns
506,60432,545 (6.4%)ns64.5 ± 10.524,977 (76.7%)7568 (23.3%)ns
528,36736,870 (6.97%)ns64.628,329 (76.83%)8543 (23.17%)34.3
OSA—Obstructive sleep apnea; CSA—Central sleep apnea; M—Male; F—Female, BMI—Body mass Index.
Table 3. Concise summary of each tool’s strengths, weaknesses, and clinical verdict.
Table 3. Concise summary of each tool’s strengths, weaknesses, and clinical verdict.
ToolStrengthsWeaknessesVerdict
Epworth Sleepiness Scale Easy to administerPoor sensitivity/specificity; symptom-basedNot suitable
Berlin QuestionnaireFamiliar toolWeak performance in high-comorbidity groupsLimited utility
STOPSimple, high-yield question (observed apnea)Low specificity, subjective symptomsModerate utility
STOP-BangIncludes objective risk factorsNot tested directly in all studiesPromising, needs validation
STOP-BAG2Strongest overall performanceRetrospective use; not widely implemented yetBest current option
SA/SDQ (SAS Scale)Broad scope; modest accuracy in menLengthy; impractical clinicallyConditional use
STOP—Snoring, Tiredness, Observed apnea, high blood Pressure—a 4-item screening tool for obstructive sleep apnea (OSA); STOP-Bang—STOP questionnaire plus Body mass index, Age, Neck circumference, and Gender—an 8-item screening tool for OSA; STOP-BAG2—STOP-Bang plus additional items including history of Gastroesophageal reflux disease (GERD) and Glucose intolerance (diabetes), forming a 10-item screening tool for OSA.
Table 4. Summary of key studies evaluating tool performance in cardiac surgery populations [47,50,51,55,61].
Table 4. Summary of key studies evaluating tool performance in cardiac surgery populations [47,50,51,55,61].
ArticleTools UsedAssociated with OSA DiagnosisPerformance Metrics
Foldvary-Schaefer et al., 2015 [51]Epworth, Berlin, STOP, SA/SDQNo clear correlation (ESS poor; STOP-BAG2 best)STOP-BAG2 AUC = 0.66; STOP AUC = 0.61; ESS AUC~0.52
Javaherforooshzadeh et al., 2022 [50]STOP-BangYes (high STOP-Bang risk predicted complications)Not reported as AUC; regression showed significance (p = 0.002)
Krishnasamy et al., 2019 [61]STOP-Bang, ApneaLink portable monitorYes (portable monitor validated); STOP-Bang sensitivity 75.8%STOP-Bang: Sensitivity 75.8%; mean STOP-Bang OSA vs. non-OSA: 3.4 vs. 3.0
Wang et al., 2020 [47], (Meta-analysis)Mixed (some STOP-Bang, Berlin, PSG)Yes; confirmed in most included studiesNot separated per tool; pooled OR for MACCE = 1.97
Liamsombut et al., 2021 [55]STOP, STOP-BAG2, SA/SDQ, Berlin, ESSPartial; STOP-BAG2 best, ESS and Berlin poorSTOP-BAG2 AUC = 0.66; ESS AUC~0.52
STOP-BAG2 and STOP-Bang emerge as the most promising tools for OSA screening in cardiac surgery populations, while ESS consistently demonstrates suboptimal diagnostic capacity. Future research should prioritize tool-specific meta-analyses using pooled individual patient-level data. STOP—Snoring, Tiredness, Observed apnea, high blood Pressure—a 4-item screening tool for obstructive sleep apnea (OSA); SA/SDQ—Sleep Apnea/Sleep-Disordered Breathing Questionnaire—a tool used to assess symptoms related to sleep-disordered breathing; AUC—Area Under the Curve—a measure of diagnostic test accuracy; PSG—Polysomnography; OR—Odds Ratio; MACCE—Major Adverse Cardiac and Cerebrovascular Events
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Manzur, A.R.; Negru, A.G.; Florescu, A.-R.; Lascu, A.; Munteanu, I.R.; Novaconi, R.C.; Bertici, N.S.; Popa, A.M.; Mihaicuta, S. Obstructive Sleep Apnea and Outcomes in Cardiac Surgery: A Systematic Review with Meta-Analytic Synthesis (PROSPERO CRD420251049574). Biomedicines 2025, 13, 1579. https://doi.org/10.3390/biomedicines13071579

AMA Style

Manzur AR, Negru AG, Florescu A-R, Lascu A, Munteanu IR, Novaconi RC, Bertici NS, Popa AM, Mihaicuta S. Obstructive Sleep Apnea and Outcomes in Cardiac Surgery: A Systematic Review with Meta-Analytic Synthesis (PROSPERO CRD420251049574). Biomedicines. 2025; 13(7):1579. https://doi.org/10.3390/biomedicines13071579

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Manzur, Andrei Raul, Alina Gabriela Negru, Andreea-Roxana Florescu, Ana Lascu, Iulia Raluca Munteanu, Ramona Cristina Novaconi, Nicoleta Sorina Bertici, Alina Mirela Popa, and Stefan Mihaicuta. 2025. "Obstructive Sleep Apnea and Outcomes in Cardiac Surgery: A Systematic Review with Meta-Analytic Synthesis (PROSPERO CRD420251049574)" Biomedicines 13, no. 7: 1579. https://doi.org/10.3390/biomedicines13071579

APA Style

Manzur, A. R., Negru, A. G., Florescu, A.-R., Lascu, A., Munteanu, I. R., Novaconi, R. C., Bertici, N. S., Popa, A. M., & Mihaicuta, S. (2025). Obstructive Sleep Apnea and Outcomes in Cardiac Surgery: A Systematic Review with Meta-Analytic Synthesis (PROSPERO CRD420251049574). Biomedicines, 13(7), 1579. https://doi.org/10.3390/biomedicines13071579

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