Abstract
OBJECTIVES
The aim of this study was to perform a meta-analysis of studies reporting outcomes in patients with liver dysfunction addressed by the model of end-stage liver disease and Child–Turcotte–Pugh scores undergoing cardiac surgery.
METHODS
A systematic literature search was conducted to identify contemporary studies reporting short- and long-term outcomes in patients with liver dysfunction compared to patients with no or mild liver dysfunction undergoing cardiac surgery (stratified in high and low score group based on the study cut-offs). Primary outcome was perioperative mortality. Secondary outcomes were perioperative neurological events, prolonged ventilation, sepsis, bleeding and/or need for transfusion, acute kidney injury and long-term mortality.
RESULTS
A total of 33 studies with 48 891 patients were included. Compared with the low score group, being in the high score group was associated with significantly higher risk of perioperative mortality [odds ratio (OR) 3.72, 95% confidence interval (CI) 2.75–5.03, P < 0.001]. High score group was also associated with a significantly higher rate of perioperative neurological events (OR 1.49, 95% CI 1.30–1.71, P < 0.001), prolonged ventilation (OR 2.45, 95% CI 1.94–3.09, P < 0.001), sepsis (OR 3.88, 95% CI 2.07–7.26, P < 0.001), bleeding and/or need for transfusion (OR 1.95, 95% CI 1.43–2.64, P < 0.001), acute kidney injury (OR 3.84, 95% CI 2.12–6.98, P < 0.001) and long-term mortality (incidence risk ratio 1.29, 95% CI 1.14–1.46, P < 0.001)
CONCLUSIONS
The analysis suggests that liver dysfunction in patients undergoing cardiac surgery is independently associated with higher risk of short and long-term mortality and also with an increased occurrence of various perioperative adverse events.
Keywords: Liver dysfunction, MELD score, Child–Turcotte–Pugh score, Open heart surgery
The evaluation of various preoperative risk factors and their association with surgical outcome has become an important aspect of clinical decision-making.
INTRODUCTION
The evaluation of various preoperative risk factors and their association with surgical outcome has become an important aspect of clinical decision-making. In cardiac surgery, large databases have been employed to develop numerous risk scores with the aim to accurately predict surgical risks [1, 2], provide information for patient counselling, assist with evaluation of surgical quality or be used for differentiated financial reimbursement [3].
Liver dysfunction has been recognized early as a critical risk factor [4]. As a result, patients with liver dysfunction are rarely included in these databases, presumably because surgeons have understood this risk and abstained from routinely operating on these patients. With a changing and ageing population, the number of patients with evidence of liver dysfunction has increased in recent years [5, 6] and results suggest that perioperative risks are not appropriately assessed in these cases using the classical risk scores [7, 8].
A thorough assessment of liver dysfunction on mortality and other perioperative complications has not been published, yet. Thus, the only current way to evaluate the impact of liver dysfunction in cardiac surgery in a large number of patients is to evaluate and summarize the existing body of scientific publications. We therefore set out to systematically review the literature and thoroughly assess the effect of liver dysfunction by way of a meta-analysis on clinical outcome after cardiac surgery, with a focus on short- and long-term mortality and all-classic adverse events during the perioperative period.
METHODS
Ethical and IRB approval of this analysis were not required as no human or animal subjects were involved. This review was registered with the National Institute for Health Research International Registry of Systematic Reviews (PROSPERO, CRD42021239043).
Search strategy
A medical librarian (Michelle Demetres) performed a comprehensive literature search to identify contemporary studies reporting short- and long-term outcomes in patients with liver dysfunction compared to patients with no or mild liver dysfunction undergoing open heart surgery. Searches were run on 24 February 2021 in the following databases: Ovid MEDLINE® (ALL; 1946 to present); Ovid EMBASE (1974 to present); and The Cochrane Library (Wiley). The search strategy for Ovid MEDLINE is available in Supplementary Material, Table S1.
Study selection and data extraction
The study selection followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) strategy. After de-duplication, records were screened by 2 independent reviewers (Tulio Caldonazo and Hristo Kirov). Any discrepancies and disagreements were resolved by a third author (Torsten Doenst). Titles and abstracts were reviewed against pre-defined inclusion and exclusion criteria. Studies were considered for inclusion if they were written in English and reported direct comparison between patients with liver dysfunction and patients with no or mild liver dysfunction undergoing open heart surgery. The severity of liver dysfunction was evaluated with preoperative model for end-stage liver disease (MELD) score and/or Child–Turcotte–Pugh (CTP) score. Patients were stratified in the high score group (with liver dysfunction) and the low score group (no or mild liver dysfunction) based on the cutoffs proposed by each study as previously published [9–11]. Animal studies, abstracts, case reports, commentaries, editorials, expert opinions, conference presentations and studies not reporting the outcomes of interest were excluded. The full text was pulled for the selected studies for a second round of eligibility screening. References for articles selected were also reviewed for relevant studies not captured by the original search.
The quality of the included studies was assessed using the Newcastle-Ottawa Scale for observational studies (Supplementary Material, Table S2).
Two reviewers (Tulio Caldonazo and Hristo Kirov) independently performed data extraction, and the accuracy was verified by a third author (Torsten Doenst). The variables included were: study characteristics (publication year, country, sample size and type of surgery), patient demographics (age, sex, left ventricular ejection fraction, hypertension, diabetes mellitus, prior cerebrovascular accident, prior myocardial infarction and chronic renal failure) and postoperative characteristics [perioperative mortality, perioperative neurological events, prolonged ventilation, sepsis, bleeding and/or need for transfusion, acute kidney injury (AKI) and long-term mortality]. For studies that categorized patients using both the MELD and CTP score, all available data were used for the analysis.
Outcomes
The primary outcome was perioperative mortality. The secondary outcomes were perioperative neurological events, prolonged ventilation, sepsis, bleeding and/or need for transfusion, AKI and long-term mortality. Perioperative outcomes were defined as in-hospital and 30-day events. Individual study definitions were used for all outcomes (Supplementary Material, Table S3). Subgroup analyses were performed for studies in which liver dysfunction was evaluated with the MELD score only and for studies in which it was evaluated with the CTP score only.
Score definitions
Prognostic models are important tools for estimating disease severity and survival. Therefore, they serve as helpful medical decision-making tools for guiding patient care. These models were developed using statistical methodologies associated with the effects of variables of interest (e.g. demographics, clinical data and laboratory values). The MELD score was a prospectively developed and validated chronic liver disease severity scoring system that uses patient laboratory values (serum bilirubin, creatinine, sodium and the international normalized ratio for prothrombin time) to predict 3-month survival [12]. The CTP score involves the presence of ascites and hepatic encephalopathy and the serum albumin and international normalized ratio [13].
Statistical analysis
Short-term binary outcomes were reported as odds ratios (ORs) with 95% confidence intervals (CIs) using the generic inverse variance method. For long-term mortality, incidence rate ratio (IRR) with its 95% CIs was reported using generic inverse variance method. IRR was estimated through several means based on the available study data. When hazard ratios were provided, the natural logarithm of the hazard ratio was used, otherwise IRR was estimated through the reported events and accumulated group-specific person-years of follow-up. Random effect meta-analysis was performed using ‘metafor’ and ‘meta’ packages. Publication bias was assessed by funnel plot (using the trim and fill method) and Egger test. Heterogeneity was reported as low (I2 = 0–25%), moderate (I2 = 26–50%) or high (I2 > 50%). Leave-one-out analyses for the primary outcome was performed to assess the robustness of the obtained estimate. P-value for interaction was used to ascertain subgroup differences.
All statistical analyses were performed using R (version 3.3.3, R Project for Statistical Computing) within RStudio.
RESULTS
Study and patient characteristics
A total of 7563 studies were retrieved from the systematic search, of which 33 met the criteria for inclusion in the final analysis. The PRISMA flowchart for study selection is provided in Supplementary Material, Fig. S1. Included studies were published between 1998 and 2020, all were observational cohort studies and 4 were multicentre. Eleven originated from the USA, 8 from Japan, 4 from Germany and the remaining from other countries. Sixteen studies used the CTP score to classify the severity of the liver dysfunction, 13 used the MELD score and 4 used both. Details of the included studies are provided in Table 1.
Table 1:
Summary of included studies [references (superscript numbers) are reported in the Supplementary Material)
Study | Year | Country | Study period | Type of surgery | No patients with CTP or MELD score | No patients per arm |
---|---|---|---|---|---|---|
Part 1 | ||||||
Liver dysfunction score used: CTP and MELD | ||||||
Garatti et al.1 | 2020 | Italy | 2000–2017 | CABG, valve surgery | 144 |
|
Morimoto et al.2 | 2013 | Japan | 1999–2009 | CABG, valve surgery, aortic surgery | 32 |
|
Thielmann et al.3 | 2010 | Germany | 1998–2008 | CABG, valve surgery, other | 57 |
|
Vanhuyse et al.4 | 2012 | France | 1996–2010 | CABG, valve surgery, aortic surgery, other | 34 |
|
Liver dysfunction score used: CTP only | ||||||
An et al.5 | 2007 | China | 1996–2005 | CABG, valve surgery, aortic surgery, pericardiectomy, other | 24 |
|
Arif et al.6 | 2012 | Germany | 2001–2011 | CABG, valve surgery, aortic surgery, heart transplants, LVAD implantation, other | 109 |
|
Bizouarn et al.7 | 1999 | France | 1995–1997 | CABG, valve surgery, aortic surgery, heart transplants, LVAD implantation, other | 12 |
|
Filsoufi et al.8 | 2007 | USA | 1998–2004 | CABG, valve surgery, aortic surgery, pericardiectomy | 27 |
|
Hayashida et al.9 | 2004 | Japan | 1989–2003 | CABG, valve surgery, aortic surgery, pericardiectomy, other | 18 |
|
Kaplan et al.10 | 2002 | Turkey | 1996–2000 | CABG, valve surgery | 10 |
|
Klemperer et al.11 | 1998 | USA | 1990–1996 | CABG, valve surgery | 13 |
|
Komoda et al.12 | 2013 | Germany | 1996–2011 | Pericardiectomy | 64 |
|
Lin et al.13 | 2014 | Taiwan | 1993–2012 | CABG, valve surgery | 55 |
|
Part 2 | ||||||
Liver dysfunction score used: CTP only | ||||||
Lopez-Delgado et al.14 | 2012 | Spain | 2004–2009 | CABG, valve surgery | 58 |
|
Macaron et al.15 | 2012 | USA | 1992–2009 | CABG, valve surgery | 54 |
|
Morisaki et al.16 | 2010 | Japan | 1991–2009 | CABG, valve surgery, aortic surgery | 42 |
|
Murashita et al.17 | 2009 | Japan | 2002–2006 | CABG, valve surgery | 12 |
|
Sugimura et al.18 | 2012 | Japan | 2001–2010 | CABG, valve surgery, aortic surgery, pericardiectomy, other | 13 |
|
Suman et al.19 | 2004 | USA | 1992–2002 | CABG, valve surgery, pericardiectomy | 44 |
|
Yamane et al.20 | 2008 | Japan | 1999–2007 | CABG, valve surgery, pericardiectomy, other | 21 |
|
Liver dysfunction score used: MELD only | ||||||
Ailawadi et al.21 | 2009 | USA | 1994–2008 | Valve surgery | 168 |
|
Chokshi et al.22 | 2012 | USA | 1998–2008 | Heart transplant | 617 |
|
Deo et al.23 | 2013 | USA | 2007–2011 | LVAD implantation | 68 |
|
Grimm et al.24 | 2015 | USA | 2000–2012 | Heart transplant | 22 597 |
|
Hawkins et al.25 | 2019 | USA | 2011–2016 | CABG, valve surgery, aortic surgery | 21 272 |
|
Part 3 | ||||||
Liver dysfunction score used: MELD only | ||||||
Loforte et al.26 | 2019 | Italy | 2000–2018 | Heart transplant | 425 |
|
Murata et al.27 | 2016 | Japan | 2008–2013 | CABG, valve surgery, other | 1856 |
|
Ortiz-Bautista et al.28 | 2018 | Spain | 2005–2015 | Heart transplant | 190 |
|
Radakovic et al.29 | 2018 | Germany | 2009–2016 | Pericardiectomy | 79 |
|
Tsuda et al.30 | 2013 | Japan | 1991–2011 | CABG, valve surgery, pericardiectomy, other | 168 |
|
Woolley et al.31 | 2015 | USA | 2001–2011 | LVAD implantation | 63 |
|
Yalcin et al.32 | 2020 | Netherlands | 2004–2017 | LVAD implantation | 290 |
|
Yang et al.33 | 2012 | USA | 2000–2010 | LVAD implantation | 255 |
|
CABG: coronary artery bypass grafting; CTP: Child–Turcotte–Pugh; MELD: model for end-stage liver disease; LVAD: left ventricular assist device.
A total of 48 891 patients were included in the final analysis, and the number of patients in each study ranged from 10 to 22 597. Twenty-nine thousand nine hundred twelve patients were included in the low score group and 18 979 in the high score group. Demographic data of the patient population in each study are summarized in Supplementary Material, Table S4. The mean age ranged from 47.0 to 70.1 years in the low score group and from 48.5 to 71.0 in the high score group. Percentage of male patients ranged from 25.0% to 87.5% in the low score group and from 33.3% to 88.0% in the high score group. The prevalence of hypertension ranged from 8.0% to 82.6% in the low score group and 16.0% to 89.0% in the high score group. The prevalence of diabetes mellitus ranged from 3.5% to 60.0% in the low score group and 8.0% to 50.5% in the high score group.
Meta-analysis
Primary outcome
Compared with low score, high score was associated with significantly higher perioperative mortality (OR 3.72, 95% CI 2.75–5.03, P < 0.001) (Fig. 1 and Table 2). Leave-one-out analysis confirmed the robustness of the main analysis (Supplementary Material, Fig. S2). Publication bias assessment is provided in Supplementary Fig. S3.
Figure 1:
Forest plot for the primary outcome of perioperative mortality. CI: confidence interval; CTP: Child–Turcotte–Pugh; MELD: model of end-stage liver disease; OR: odds ratio.
Table 2:
Outcomes summary
Outcome | Number of studies | Measured estimate | Effect estimate (95% CI) | Higher in |
---|---|---|---|---|
Perioperative mortality (primary) | 32 | OR | 3.72 [2.75; 5.03], P < 0.001 | High score |
|
20 | OR | 5.43 [2.96; 9.96] | High score |
|
12 | OR | 3.18 [2.25; 4.50] | High score |
Perioperative neurological events | 12 | OR | 1.49 [1.30; 1.71], P < 0.001 | High score |
|
8 | OR | 1.49 [1.30; 1.70] | High score |
|
4 | OR | 3.17 [0.66; 15.13] | High score |
Prolonged ventilation | 15 | OR | 2.45 [1.94; 3.09], P < 0.001 | High score |
|
8 | OR | 3.31 [1.54; 7.11] | High score |
|
7 | OR | 2.38 [1.79; 3.16] | High score |
Sepsis | 10 | OR | 3.88 [2.07; 7.26], P < 0.001 | High score |
|
4 | OR | 4.01 [1.76; 9.13] | High score |
|
6 | OR | 3.70 [1.40; 9.76] | High score |
Bleeding and/or need for transfusion | 16 | OR | 1.95 [1.43; 2.64], P < 0.001 | High score |
|
5 | OR | 2.12 [1.45; 3.10] | High score |
|
11 | OR | 1.84 [1.02; 3.34] | High score |
Acute Kidney Injury | 17 | OR | 3.84 [2.12; 6.98], P < 0.001 | High score |
|
9 | OR | 3.18 [1.61; 6.28] | High score |
|
8 | OR | 4.08 [1.87; 8.87] | High score |
Long-term mortality | 16 | IRR | 1.29 [1.14; 1.46], P < 0.001 | High score |
|
8 | IRR | 1.74 [1.20; 2.53] | High score |
|
8 | IRR | 1.21 [1.07; 1.37] | High score |
CI: confidence interval; CTP: Child–Turcotte–Pugh; IRR: incidence rate ratio; MELD: model for end-stage liver disease; OR: odds ratios.
Subgroup analysis of the primary outcome
The results of the subgroup analyses were consistent with the primary analysis. The OR for perioperative mortality was 3.18 (95% CI 2.25–4.50) for studies in which the MELD score was used and 5.43 (95% CI 2.96–9.96) for studies in with the CTP score was used (P for interaction: 0.13) (Fig. 2).
Figure 2:
Subgroup analysis for perioperative mortality for studies using the MELD score versus the CTP score. CI: confidence interval; CTP: Child–Turcotte–Pugh; MELD: model of end-stage liver disease; OR: odds ratio.
Secondary outcomes
Compared with low score, high score was associated with a significantly higher rate of perioperative neurological events (OR 1.49, 95% CI 1.30–1.71, P < 0.001), prolonged ventilation (OR 2.45, 95% CI 1.94–3.09, P < 0.001), sepsis (OR 3.88, 95% CI 2.07–7.26, P < 0.001), bleeding and/or need for transfusion (OR 1.95, 95% CI 1.43–2.64, P < 0.001), AKI (OR 3.84, 95% CI 2.12–6.98, P < 0.001) and long-term mortality (IRR 1.29, 95% CI 1.14–1.46, P < 0.001) (Table 2).
DISCUSSION
Our analysis suggests that liver dysfunction in patients after cardiac surgery is associated with higher short- and long-term mortality and increased occurrence of most perioperative adverse events. Specifically, the high MELD or CTP score was associated with significantly increased perioperative mortality, higher rate of perioperative neurological events, prolonged ventilation, sepsis, bleeding and/or need for transfusion and AKI.
Although the findings of liver dysfunction being associated with worse outcome may not be surprising, or relevant because it appears to affect only a small number of patients. While this impression may be true for patients with preoperatively diagnosed liver cirrhosis, it is not for all patients with liver dysfunction per se. Patients with liver cirrhosis reflect <1% of all patients in the STS database [14]. However, if one assumes that the liver does not function normally anymore at a MELD score above 9, 27% of all patients in the STS database would be affected [7]. Thus, this recent database analysis demonstrates that the number of patients with evidence for liver dysfunction in the cardiac surgical population is much higher than currently expected. In fact, it is at least comparable to the number of patients developing new-onset postoperative atrial fibrillation. Several publications out of the STS database have shown an incidence of postoperative atrial fibrillation of 19% (for all cardiac surgeries) [15] or 29% for isolated coronary bypass surgery [16]. Interestingly, the literature reveals only half as many publications addressing liver dysfunction than postoperative atrial fibrillation having analysed only one-fifth of patients [17] compared to postoperative atrial fibrillation studies.
It is therefore highly important to systematically review the negative effects of liver dysfunction on classic short and long-term cardiovascular adverse events. This meta-analysis provides important information for clinical decision-making and patient information. Appropriately assessing preoperative risk is most important for the patient, specifically if the requirement for cardiac surgery is free of alternatives (e.g. infective endocarditis). For instance, we demonstrated in a cohort of patients requiring surgery for infective endocarditis that preoperative liver dysfunction was a tremendous risk factor for death. However, we also showed that those patients who survived the hospital stay, had similar 5-year survival and quality of life to those patients not affected by pre- or perioperative liver dysfunction [18].
In such cases where surgery is without alternatives, being aware of the increased risk (reflected by increased MELD scores for instance) may help with defining a suitable operative strategy. Gopaldas et al. [14] identified in over 3 million patients from the STS database that the use of cardiopulmonary bypass is an independent risk factor for mortality in patients with liver cirrhosis undergoing coronary artery bypass grafting. Use of cardiopulmonary bypass increased the odds for mortality 4.6-fold [14]. When performed off-pump, the presence of cirrhosis did not affect mortality or morbidity unless there was severe liver dysfunction [14]. Therefore, the avoidance of cardiopulmonary bypass and cardioplegia at least in isolated coronary cases might be a successful strategy in patients with liver dysfunction. However, the evidence in support of this conclusion by Gopaldas et al. does not exist, yet.
Although there seems to be a clear association between liver dysfunction and adverse events after cardiac surgery, some of the most commonly used risk evaluation models do not take it into consideration [1], and other seem not to adequately assess the risks [7]. The results of our analysis provide a previously unknown quantification of dimensions of these relationships. The association of liver dysfunction not only with mortality, but also with neurological events, prolonged ventilation, sepsis, bleeding and/or need for transfusion and AKI may help in preoperative patient counselling, and even estimating individually varying financial investments. Furthermore, the results of our work suggest that routine evaluation of liver scores might be helpful for preoperative evaluation of patients in cardiac surgery and may assist identifying high-risk patients in cases when classic surgical scores fail. Therefore, we believe that this work will contribute to raising the awareness of the importance of properly assessing for liver dysfunction in patients undergoing open cardiac surgery.
To the best of our knowledge, this comprehensive meta-analysis is the first to include studies with both CTP and MELD scores and provide a broad overview of various clinical outcomes and their association with liver dysfunction after cardiac surgery. The findings are relevant because an increasing number of patients undergoing cardiac surgery have liver dysfunction [6].
Limitations
This work has the intrinsic limitations of trial-level meta-analyses of observational series, including the risk of methodological heterogeneity of the included studies. Studies have included different numbers of patients with 2 studies including the majority of them. Furthermore, patient management among included studies was performed according to individual centre strategy or protocol, with heterogeneous approaches and diverse indications, which may limit data pooling or the definitive value of the conclusions.
CONCLUSION
This analysis suggests that liver dysfunction in patients undergoing cardiac surgery is associated with the higher risk of short- and long-term mortality and also with an increased occurrence of various perioperative adverse events.
Supplementary Material
ACKNOWLEDGEMENTS
We thank Mr. Benjamin May for his editorial assistance. Tulio Caldonazo is supported by the Clinical Scientist Program (Jena University Hospital) and Mudathir Ibrahim is supported by Maimonides research fellowship grant.
Glossary
ABBREVIATIONS
- AKI
Acute kidney injury
- CI
Confidence interval
- CTP
Child–Turcotte–Pugh
- IRR
Incidence rate ratio
- MELD
Model of end-stage liver disease
- OR
Odds ratio
Contributor Information
Hristo Kirov, Department of Cardiothoracic Surgery, Friedrich-Schiller-University Jena, Germany.
Tulio Caldonazo, Department of Cardiothoracic Surgery, Friedrich-Schiller-University Jena, Germany.
Katia Audisio, Department of Cardiothoracic Surgery at New York Presbyterian, Weill Cornell Medical Center, USA.
Mohamed Rahouma, Department of Cardiothoracic Surgery at New York Presbyterian, Weill Cornell Medical Center, USA.
N Bryce Robinson, Department of Cardiothoracic Surgery at New York Presbyterian, Weill Cornell Medical Center, USA.
Gianmarco Cancelli, Department of Cardiothoracic Surgery at New York Presbyterian, Weill Cornell Medical Center, USA.
Giovanni J Soletti, Department of Cardiothoracic Surgery at New York Presbyterian, Weill Cornell Medical Center, USA.
Michelle Demetres, Samuel J. Wood Library and C.V. Starr Biomedical Information Center, Weill Cornell Medicine, New York, NY, USA.
Mudathir Ibrahim, Department of General Surgery, Maimonides Medical Center, Brooklyn, NY, USA; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
Gloria Faerber, Department of Cardiothoracic Surgery, Friedrich-Schiller-University Jena, Germany.
Mario Gaudino, Department of Cardiothoracic Surgery at New York Presbyterian, Weill Cornell Medical Center, USA.
Torsten Doenst, Department of Cardiothoracic Surgery, Friedrich-Schiller-University Jena, Germany.
SUPPLEMENTARY MATERIAL
Supplementary material is available at ICVTS online.
Funding
Tulio Caldonazo was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) Clinician Scientist Program OrganAge funding number 413668513 and by the Interdisciplinary Center of Clinical Research of the Medical Faculty Jena.
Conflict of interest: none declared.
Data Availability
The data underlying this article are available in the article and in its online supplementary material.
Author contributions
Hristo Kirov: Conceptualization; Data curation; Formal analysis; Methodology; Writing—original draft; Writing—review & editing. Tulio Caldonazo: Conceptualization; Data curation; Formal analysis; Methodology; Writing—original draft; Writing—review & editing. Katia Audisio: Formal analysis; Methodology; Validation. Mohamed Rahouma: Data curation; Methodology. N. Bryce Robinson: Data curation; Formal analysis; Methodology; Supervision. Gianmarco Cancelli: Data curation; Methodology; Validation. Giovanni J. Soletti: Data curation; Formal analysis; Investigation. Michelle Demetres: Data curation; Formal analysis; Investigation; Methodology. Mudathir Ibrahim: Data curation; Formal analysis; Investigation; Methodology; Writing—original draft; Writing—review & editing. Gloria Faerber: Conceptualization; Supervision; Validation; Writing—original draft; Writing—review & editing. Mario Gaudino: Conceptualization; Investigation; Supervision; Validation; Writing—original draft; Writing—review & editing. Torsten Doenst: Conceptualization; Formal analysis; Methodology; Supervision; Validation; Writing—original draft; Writing—review & editing.
Reviewer information
Interactive CardioVascular and Thoracic Surgery thanks Roman Gottardi, Tomislav Kopjar and the other, anonymous reviewer(s) for their contribution to the peer review process of this article.
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Associated Data
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Supplementary Materials
Data Availability Statement
The data underlying this article are available in the article and in its online supplementary material.