- Research article
- Open access
- Published:
Hepatic dysfunction in patients who received acute DeBakey type I aortic dissection repair surgery: incidence, risk factors, and long-term outcomes
Journal of Cardiothoracic Surgery volume 16, Article number: 296 (2021)
Abstract
Background
Hepatic dysfunction (HD) increases the morbidity and mortality rates after cardiac surgery. However, few studies have investigated the association between HD and acute DeBakey type I aortic dissection (ADIAD) surgery. This retrospective study aimed to identify risk factors for developing HD in patients who received acute type I aortic dissection repair and its consequences.
Methods
A total of 830 consecutive patients who received ADIAD surgery from January 2014 to December 2019 at our center were screened for this study. The End-Stage Liver Disease (MELD) score more than 14 was applied to identify postoperative HD. Logistic regression model was applied to identify risk factors for postoperative HD, Kaplan–Meier survival analysis and Cox proportional hazards regression assay were conducted to analyze the association between HD and postoperative long-term survival.
Results
Among 634 patients who eventually enrolled in this study, 401 (63.2%) experienced postoperative HD with a 30-Day mortality of 15.5%. Preoperative plasma fibrinogen level (PFL) [odds ratio (OR): 0.581, 95% confidence interval (CI): 0.362–0.933, P = 0.025], serum creatinine (sCr) on admission (OR: 1.050, 95% CI 1.022–1.079, P < 0.001), cardiopulmonary bypass (CPB) time (OR: 1.017, 95% CI 1.010–1.033, P = 0.039), and postoperative mechanical ventilation (MV) duration (OR: 1.019, 95% CI 1.003–1.035, P = 0.020) were identified as independent risk factors for developing postoperative HD by multivariate analyses. In addition, the Kaplan–Meier analysis indicated that the long-term survival rate was significantly different between patients with or without postoperative HD. However, the hazard ratios of long-term survival for these two groups were not significantly different.
Conclusions
HD was a common complication after ADIAD surgery and associated with an increasing 30-Day mortality rate. Decreased PFL, elevated sCr, prolonged CPB duration, and longer postoperative MV time were independent risk factors for postoperative HD.
Introduction
Acute type A aortic dissection (ATAAD) is a life-threatening condition requires immediate surgical repair. The hourly mortality rate of ATAAD can be as high as 1% to 2% after symptoms onset before surgical intervention [1]. Even though with the advancing techniques, the successful rate of ATAAD surgery has been increasing, the 30-Day mortality is still relatively high with approximately 10% to 20% according to recent comprehensive studies [2, 3]. Acute DeBakey type I aortic dissection (ADIAD) is a severe subset of ATAAD and demands a more challenging surgical procedure [4]. Most ADIAD operation are performed in emergency, and prolonged cardiopulmonary bypass (CPB) time and multiple transfusions are often occurred. What’s more, the short-term malperfusion complications and long-term adverse aortic events arising after surgical treatment of ADIAD are considered to be high because of the wide presence of a false lumen [5, 6].
Hepatic dysfunction (HD) is a common complication after cardiothoracic surgery which often result in increasing mortality. It has been estimated that the incidence of postoperative HD after cardiovascular surgeries ranges from 21.9 to 60.9% [7,8,9]. The most important criteria of HD had been the Child-Turcotte-Pugh (CTP) classification for the past 30Â years which has been challenged recently by the model of End-Stage Liver Disease (MELD) score. Both of these two criteria have been applied to examine the association between HD and ADIAD surgery yet limited by the small cohorts of fewer than 100 patients with a definite diagnoses of liver cirrhosis [10,11,12]. Recently, several reports proved that MELD is a better assessment tool to predict postoperative mortality than CTP in patients received cardiothoracic surgeries, as it does not include subjective variables [8, 13].
Even though multiple studies have been conducted to examine the association between HD and general cardiothoracic surgeries, the association between HD and ADIAD has not been specifically studied. In this retrospective analysis, we applied the MELD criteria to identify the risk factors for postoperative HD and examine its influence on long-term prognosis in a relatively large cohort of ADIAD patients who received aortic dissection surgery.
Methods and materials
Study population
This study was approved by the Ethics Committee of the Nanjing Drum Tower Hospital. The individual patient consent was waived considering the nature of this study. A total of 830 medical records of patients who received ADIAD surgery within 14 days of symptom onset at our center between January 2014 and December 2019 were retrospectively screened. Patients who were on renal replacement therapy before surgery (n = 26) were excluded because its influence on serum creatinine (sCr). In addition, patients who died during or within 24 h after surgery (n = 18) were excluded. Patients accompanied with severe alcoholic or viral liver disease (n = 18) were also excluded. Considering that the MELD score includes international normalized ratio (INR) in the formula, patients who received warfarin before or after surgery (n = 129) were excluded from this study. 5 patients with incomplete data were excluded from the study as well. Patients’ general health status was followed up once every year by telephone since 2014. The date and cause of deaths were collected during the follow up if occurred. AKI was defined by the Kidney Disease Improving Global Outcome (KDIGO) classification by the changes in sCr.
Diagnostic criteria for postoperative HD
The MELD score was calculated using the standard formula published by Mayo Clinic College of Medicine: MELD = 11.2 * In (INR) + 3.78* In (total bilirubin [mg/dL]) + 9.57* In (creatinine [mg/dL]) + 6.43* (cause). Where cause equaled 0 for bilious or alcoholic liver disease and 1 for otherwise [14]. Any variable with a value less than 1 was assigned a value of 1 to avoid negative scores. The MELD score was recorded daily for a week after the surgery during which the postoperative HD was determined based on the highest MELD score. Previous studies set the cutoff point as 12 or 13 for HD diagnosis after different surgical procedures [8, 10, 11]. Considering ADIAD surgery is more complicated than other cardiac surgeries, the cutoff value of 14 was selected to define postoperative HD in this study, which was consistent with a previous study [9]. Patients were then classified into HD group (≥ 14) and non-HD group (< 14).
Statistical analysis
Categorical variables were presented as frequencies with percentages. Continuous variables were presented as means ± standard deviation or median with interquartile range (IQR). The χ2 tests or Fisher exact test was applied for categorical variables and the t-test was applied for normally distributed continuous variables whereas the Mann–Whitney U-test was used for non-normally distributed variables. Multivariate logistic regression analysis was conducted to identify independent risk factors for postoperative HD. For regression analysis, all variables with a p-value less than 0.50 in univariate analysis were included in the model. A stepwise enter method was used to introduce variables to the final models. A receiver-operating characteristic (ROC) curve analysis was performed to detect the best cut-off value of the predictors for postoperative HD. Crude survival was estimated with the Kaplan–Meier method. Differences in survival between groups were further analyzed with log-rank tests. Cox proportional hazard analysis was applied to identify independent factors that affect long-term survival. For Cox regression analysis, all variables with a p-value less than 0.20 identified in univariate analysis were included in the model. A stepwise enter procedure was used to introduce variables to the final models. A p value less than 0.05 was considered statistically significant. All analyses were conducted with SPSS version 25.0 (IBM Corp, Armonk, NY, USA).
Results
A total of 634 patients were eventually included in the study with a median age of 52.5 years old (range 24–85 years), and 480 (75.7%) of these patients were men. Our data suggested that a total of 401 patients (63.2%) developed postoperative HD. Patient clinical characteristics and preoperative variables associated with MELD score were presented in Table 1. The time from symptom onset to surgery and liver blood supply condition were similar between HD and non-HD groups. For serum laboratory test results, there were significant differences between patients with or without HD in terms of white blood cell, platelet, fibrinogen, troponin T, D-dimer, albumin, creatinine, blood urine nitrogen, INR, total bilirubin, alanine transaminase, and aspartate transaminase upon admission. For the operative parameters, CPB duration and aortic cross-clamp time were significantly different between the two groups. Furthermore, we discovered that patients with postoperative HD often resulted in unfavorable outcomes, including more frequent dialysis requirement, postoperative acute kidney injury, drainage volume 24 h after surgery, tracheostomy rate, longer intensive care unit stay time, and worse 30-Day mortality (Table 2).
As suggested in Table 3, the multivariate analysis indicated that preoperative plasma fibrinogen level (PFL) [odds ratio (OR): 0.581, 95% confidence interval (CI): 0.362–0.933, P = 0.025], preoperative sCr (OR: 1.050, 95% CI 1.022–1.079, P < 0.001), CPB time (OR: 1.017, 95% CI 1.010–1.033, P = 0.039), and postoperative mechanical ventilation (MV) duration (OR: 1.019, 95% CI 1.003–1.035, P = 0.020) were independent risk factors for developing postoperative HD.
In addition, to better determine the predictive value of PFL and sCr. The ROC curves were plotted and the cutoff values of PFL and sCr levels upon admission for preoperative HD were 2.25 g/L and 88.85 μmol/L, respectively. These values were associated with a sensitivity of 57.7% and a specificity of 60.9% for PFL and of 58.1% and 86.7% for sCr, respectively. In addition, the AUC for PFL was 0.606 (95% CI 0.561–0.651, P < 0.001) and 0.772 (95% CI 0.737–0.807, P < 0.001) for sCr, respectively (Fig. 1).
65 patients (16.2%) in the HD group and 7 patients (3.0%) in the non-HD group died during the hospitalization period. By December 2020, 562 patients had been followed up with a median of 20 months. 38 of 562 (6.8%) patients were lost from the cohort and excluded from the survival analysis. A total of 6 patients dead in the non-HD group and 24 in the HD group during follow-up period. A significant overall difference was indicated between two groups by the Kaplan–Meier survival curves (Fig. 2; P = 0.025 by log-rank test), whereas after adjusting for confounders, the hazard ratios for postoperative HD (1.150, 95% CI 0.295 to 4.481, P = 0.841) was not significantly different compared to non-HD patients (Table 4).
Discussion
In this study, we examined the incidence and risk factors of developing postoperative HD in patients who received ADIAD surgery. Our data suggested that among all enrolled 634 patients, 401 patients (63.2%) developed postoperative HD. Multivariate logistic regression analysis revealed that decreased PFL and elevated sCr on admission, longer CPB duration, and longer MV time were independent risk factors for postoperative HD. The present study also indicated a clear trend that patients with postoperative HD had a lower survival rate, although the hazard ratios was not significantly different compared to patients without HD. The strength of the present study is that this was the first study aimed to identify the risk factors for and long-term outcomes of postoperative HD in a relatively large cohort which also excluded the influence of warfarin treatment.
The incidence of postoperative HD in our study was similar to that found in a previous study [9] which showed a incidence of HD of 60.9% among 215 patients who received ATAAD surgery with deep hypothermic circulatory arrest. Liu and colleagues [15] reported that early postoperative HD incidence was 8.7% after ATAAD surgery, while another study showed an HD incidence of 1.5% postoperatively among patients with descending thoracic and thoracoabdominal aortic dissection [16]. However, these studies relied on biochemical markers to evaluate liver function rather than a comprehensive evaluation.
Our data suggested that the 30-Day mortality in patients with HD was 15.5% (62 of 401 patients), which was comparable to a previous study focused on thoracic aortic surgery (16.8%) [9]. It has been known that postoperative HD is associated with worse disease outcomes such as 30-Day mortality, morbidity, and increasing cost [7, 8]. However, these studies did not examine the association between postoperative HD and long-term survival. The present study showed that patients with postoperative HD have a significantly lower long-term survival rate compared to patients without HD. However, after adjusting for confounders, the hazard ratios for postoperative HD was not significantly higher compared to patients without HD. It might be that the HD occurred after surgery was temporary and did not result in chronic liver disease. Therefore, identifying risk factors and preventing postoperative HD is critical in improving short-term prognosis. For long-term survival, more studies and longer follow-up are needed to confirm the reproducibility of these results.
The results of this study demonstrated that preoperative sCr was a risk factor for postoperative HD, which implied that presence of impaired renal function contributed to developing deranged liver function tests. As the OR for preoperative sCr to predict postoperative HD is only 1.050, which imply that preoperative renal function is not a strong risk factor that affect postoperative HD. A previous study showed that preoperative sCr > 133 μmol/L was a risk factor for postoperative HD in patients undergoing ATAAD operations [15], which was consistent with our results. Acute liver dysfunction is associated with renal insufficiency, whose mechanism may be related to activation of the hepatorenal reflex [17, 18].
The logistic regression model identified lower PFL as an independent risk factor for developing HD. Decreased fibrinogen level upon hospital admission within 24Â h after symptom onset has been demonstrated as a powerful predictor of mortality in patients with ATAAD [19, 20], as fibrinogen is a very common substance in the coagulation system and could lead to activation of the coagulation cascade [21]. It has been proved that low PFL is a risk factor for postoperative blood loss [22, 23]. Several possible mechanisms might explain the association between low fibrinogen level and postoperative HD. Fibrinogen is synthesized and secreted by the liver and participates in the thrombosis. Previous studies indicated that the level of coagulation and fibrinolytic activation was proportionally related to the anatomic extent of the dissection [24]. Intimal tearing in aortic dissection induces subendothelial element exposure and tissue factor release which further activates the coagulation cascade. This process consumes large amounts of fibrinogen and results in a decreased serum level. It has been hypothesized that lower PFL indicates greater extent injury of the aorta and more severely impaired liver function. On the other hand, it has been proposed that PFL as a surrogate marker for consumption coagulopathy in patients with dissecting aorta which is associated with increasing risk of transfusion, complications, and fatality [25]. Large prospective cohort studies should be performed to further explore the role of fibrinogen in TAAD treatment.
In addition to fibrinogen level, longer CPB duration was identified as another risk factor for HD, as has been demonstrated previously [15]. It has been reported that the blood volume in liver arteries decreases by 20–25% during CPB [26]. The decreased liver perfusion often results in liver damage. Furthermore, surgical procedure and CPB could induce the release of inflammatory cytokines and endotoxins, which influences the hemodynamics, coagulation system, immune system, vascular resistance and permeability as well as platelet concentration and function [27]. Furthermore, hypothermia and nonpulsatile circulation during CPB are thought to contribute to hemodynamic deterioration that often lead to overwhelming protective mechanisms and synergistically exacerbate hypoxic liver damage [28]. However, another study reported that the aortic cross-clamp time, rather than CPB time, was associated with the developing of HD [9]. These controversies might be attributed to confounding factors in heterogeneous patient cohorts.
The postoperative MV time was identified as another risk factor for postoperative HD. Prolonged MV duration indicated an extended postoperative respiratory dysfunction. Previous study showed that the incidence of prolonged MV (≥ 48 h) was up to 44.5% after ADIAD surgery [29]. Previous studies identified that prolonged extubation substantially increased the risk of developing postoperative acute kidney injury in cardiac surgical patients [6, 30, 31]. Our findings suggested that the duration of postoperative positive pressure ventilation was an important and previously under estimated risk factor for developing HD after ADIAD surgery that was consistent with a previous study which identified postoperative respiratory dysfunction as a risk factor for HD in patients who received ATAAD surgery [9]. MV can reduce cardiac output, blood pressure, effective circulating blood volume, and ultimately liver perfusion. It is believed that prolonged MV time not only induces hemodynamic disturbance but also aggravates systemic inflammatory reaction through mechanical damage to the lung [32]. It has been well known that MV is an important risk factor of causing and aggravating hepatic function damage in critical ill patients even after successful resuscitation [33].
Limitations
This study had some limitations. Firstly, although the number of patients was relatively large compared with other studies, this study was conducted in a single center and might not be representable for the general population. Secondly, because of the emergent nature of the disease, complete demographic data were absent for some patients. Finally, our surgical technique has been advanced over the study period, and the results in this study might be influenced by the involvement of different techniques and surgeons. Therefore, additional prospective multicenter studies are warranted to assess the prognostic significance of HD and establish the most effective strategies to prevent and treat postoperative HD in patients who received ADIAD surgery.
Conclusions
In conclusion, our data confirmed that the HD was a common complication among patients who received ADIAD surgery. The decreased PFL, elevated sCr, increased CPB duration, and prolonged MV time were identified as independent risk factors for postoperative HD.
Availability of data and materials
Data sharing in the current study are available from the corresponding author on reasonable request.
Abbreviations
- HD:
-
Hepatic dysfunction
- ADIAD:
-
Acute DeBakey type I aortic dissection
- MELD:
-
Model of end-stage liver disease
- PFL:
-
Preoperative fibrinogen level
- CPB:
-
Cardiopulmonary bypass
- MV:
-
Mechanical ventilation
- OR:
-
Odds ratio
- CI:
-
Confidence interval
References
Wang D, Wang ZY, Wang JF, Zhang LL, Zhu JM, Yuan ZX, et al. Values of aortic dissection detection risk score combined with ascending aorta diameter >40 mm for the early identification of type A acute aortic dissection. J Thorac Dis. 2018;10(3):1815–24. https://doi.org/10.21037/jtd.2018.02.42.
Stevens LM, Madsen JC, Isselbacher EM, Khairy P, MacGillivray TE, Hilgenberg AD, et al. Surgical management and long-term outcomes for acute ascending aortic dissection. J Thorac Cardiovasc Surg. 2009;138(6):1349–57. https://doi.org/10.1016/j.jtcvs.2009.01.030.
Bekkers JA, Raap GB, Takkenberg JJ, Bogers AJ. Acute type A aortic dissection: long-term results and reoperations. Eur J Cardiothorac Surg. 2013;43(2):389–96. https://doi.org/10.1093/ejcts/ezs342.
Wu Q, Wang Z, Qiu Z, Shen Y, Chen X, Chen X, et al. Mid-term outcomes of modified valve-sparing aortic root replacement versus the Bentall procedure for middle-aged Chinese patients with acute DeBakey I aortic dissection: a single-center retrospective study. BMC Cardiovasc Disord. 2021;21(1):196. https://doi.org/10.1186/s12872-021-02014-5.
Omura A, Miyahara S, Yamanaka K, Sakamoto T, Matsumori M, Okada K, et al. Early and late outcomes of repaired acute DeBakey type I aortic dissection after graft replacement. J Thorac Cardiovasc Surg. 2016;151(2):341–8. https://doi.org/10.1016/j.jtcvs.2015.03.068.
Wang Z, Ge M, Chen T, Chen C, Zong Q, Lu L, et al. Acute kidney injury in patients operated on for type A acute aortic dissection: incidence, risk factors and short-term outcomes. Interact Cardiovasc Thorac Surg. 2020;31(5):697–703. https://doi.org/10.1093/icvts/ivaa164 (PubMed PMID: 32851399).
Araujo L, Dombrovskiy V, Kamran W, Lemaire A, Chiricolo A, Lee LY, et al. The effect of preoperative liver dysfunction on cardiac surgery outcomes. J Cardiothorac Surg. 2017;12(1):73. https://doi.org/10.1186/s13019-017-0636-y.
Murata M, Kato TS, Kuwaki K, Yamamoto T, Dohi S, Amano A. Preoperative hepatic dysfunction could predict postoperative mortality and morbidity in patients undergoing cardiac surgery: Utilization of the MELD scoring system. Int J Cardiol. 2016;203:682–9. https://doi.org/10.1016/j.ijcard.2015.10.181.
Zhou W, Wang G, Liu Y, Tao Y, Du Z, Tang Y, et al. Outcomes and risk factors of postoperative hepatic dysfunction in patients undergoing acute type A aortic dissection surgery. J Thorac Dis. 2019;11(8):3225–33. https://doi.org/10.21037/jtd.2019.08.72.
Morisaki A, Hosono M, Sasaki Y, Kubo S, Hirai H, Suehiro S, et al. Risk factor analysis in patients with liver cirrhosis undergoing cardiovascular operations. Ann Thorac Surg. 2010;89(3):811–7. https://doi.org/10.1016/j.athoracsur.2009.12.021.
Filsoufi F, Salzberg SP, Rahmanian PB, Schiano TD, Elsiesy H, Squire A, et al. Early and late outcome of cardiac surgery in patients with liver cirrhosis. Liver Transpl. 2007;13(7):990–5. https://doi.org/10.1002/lt.21075.
Vanhuyse F, Maureira P, Portocarrero E, Laurent N, Lekehal M, Carteaux JP, et al. Cardiac surgery in cirrhotic patients: results and evaluation of risk factors. Eur J Cardiothorac Surg. 2012;42(2):293–9. https://doi.org/10.1093/ejcts/ezr320.
Dimarakis I, Grant S, Corless R, Velissaris T, Prince M, Bridgewater B, et al. Impact of hepatic cirrhosis on outcome in adult cardiac surgery. Thorac Cardiovasc Surg. 2015;63(1):58–66. https://doi.org/10.1055/s-0034-1389084.
Kamath PS, Wiesner RH, Malinchoc M, Kremers W, Therneau TM, Kosberg CL, et al. A model to predict survival in patients with end-stage liver disease. Hepatology. 2001;33(2):464–70. https://doi.org/10.1053/jhep.2001.22172.
Liu N, Sun LZ, Chang Q. The relative risk factors analysis of hepatic dysfunction following aortic dissection repair. Zhonghua Wai Ke Za Zhi. 2010;48(15):1154–7.
Achouh PE, Madsen K, Miller CC 3rd, Estrera AL, Azizzadeh A, Dhareshwar J, et al. Gastrointestinal complications after descending thoracic and thoracoabdominal aortic repairs: a 14-year experience. J Vasc Surg. 2006;44(3):442–6. https://doi.org/10.1016/j.jvs.2006.05.018.
Akriviadis E, Botla R, Briggs W, Han S, Reynolds T, Shakil O. Pentoxifylline improves short-term survival in severe acute alcoholic hepatitis: a double-blind, placebo-controlled trial. Gastroenterology. 2000;119(6):1637–48. https://doi.org/10.1053/gast.2000.20189.
Ming Z, Fan YJ, Yang X, Lautt WW. Contribution of hepatic adenosine A1 receptors to renal dysfunction associated with acute liver injury in rats. Hepatology. 2006;44(4):813–22. https://doi.org/10.1002/hep.21336.
Yang S, Xue Y, Liu J, Zhang H, Jiang W. Is fibrinogen plasma level a risk factor for the first 24-hour death of medically treated acute type A aortic dissection patients? Ann Transl Med. 2020;8(16):1015. https://doi.org/10.21037/atm-20-5466.
Liu J, Sun LL, Wang J, Ji G. The relationship between fibrinogen and in-hospital mortality in patients with type A acute aortic dissection. Am J Emerg Med. 2018;36(5):741–4. https://doi.org/10.1016/j.ajem.2017.10.001.
Sorensen B, Larsen OH, Rea CJ, Tang M, Foley JH, Fenger-Eriksen C. Fibrinogen as a hemostatic agent. Semin Thromb Hemost. 2012;38(3):268–73. https://doi.org/10.1055/s-0032-1309287.
Walden K, Jeppsson A, Nasic S, Backlund E, Karlsson M. Low preoperative fibrinogen plasma concentration is associated with excessive bleeding after cardiac operations. Ann Thorac Surg. 2014;97(4):1199–206. https://doi.org/10.1016/j.athoracsur.2013.11.064.
Gielen C, Dekkers O, Stijnen T, Schoones J, Brand A, Klautz R, et al. The effects of pre- and postoperative fibrinogen levels on blood loss after cardiac surgery: a systematic review and meta-analysis. Interact Cardiovasc Thorac Surg. 2014;18(3):292–8. https://doi.org/10.1093/icvts/ivt506.
Ohlmann P, Faure A, Morel O, Petit H, Kabbaj H, Meyer N, et al. Diagnostic and prognostic value of circulating D-Dimers in patients with acute aortic dissection. Crit Care Med. 2006;34(5):1358–64. https://doi.org/10.1097/01.CCM.0000216686.72457.EC.
Paparella D, Rotunno C, Guida P, Malvindi PG, Scrascia G, De Palo M, et al. Hemostasis alterations in patients with acute aortic dissection. Ann Thorac Surg. 2011;91(5):1364–9. https://doi.org/10.1016/j.athoracsur.2011.01.058.
Mathie RT. Hepatic blood flow during cardiopulmonary bypass. Crit Care Med. 1993;21(2 Suppl):S72–6. https://doi.org/10.1097/00003246-199302001-00013.
Paparella D, Yau TM, Young E. Cardiopulmonary bypass induced inflammation: pathophysiology and treatment. An Update Eur J Cardiothorac Surg. 2002;21(2):232–44. https://doi.org/10.1016/s1010-7940(01)01099-5.
Laribi S, Mebazaa A. Cardiohepatic syndrome: liver injury in decompensated heart failure. Curr Heart Fail Rep. 2014;11(3):236–40. https://doi.org/10.1007/s11897-014-0206-8.
Ge M, Wang Z, Chen T, Cheng Y, Ye J, Lu L, et al. Risk factors for and outcomes of prolonged mechanical ventilation in patients received DeBakey type I aortic dissection repairment. J Thorac Dis. 2021;13(2):735–42. https://doi.org/10.21037/jtd-20-2736.
Heringlake M, Nowak Y, Schon J, Trautmann J, Berggreen AE, Charitos EI, et al. Postoperative intubation time is associated with acute kidney injury in cardiac surgical patients. Crit Care. 2014;18(5):547. https://doi.org/10.1186/s13054-014-0547-4.
Nemati MH, Astaneh B. The effects of preoperative statins on the incidence of postoperative acute kidney injury in patients undergoing cardiac surgeries. Interact Cardiovasc Thorac Surg. 2015;21(4):493–8. https://doi.org/10.1093/icvts/ivv194.
Lellouche F, Dionne S, Simard S, Bussieres J, Dagenais F. High tidal volumes in mechanically ventilated patients increase organ dysfunction after cardiac surgery. Anesthesiology. 2012;116(5):1072–82. https://doi.org/10.1097/ALN.0b013e3182522df5.
Ferreira FL, Bota DP, Bross A, Melot C, Vincent JL. Serial evaluation of the SOFA score to predict outcome in critically ill patients. JAMA. 2001;286(14):1754–8. https://doi.org/10.1001/jama.286.14.1754.
Acknowledgements
Not applicable.
Funding
Not applicable.
Author information
Authors and Affiliations
Contributions
DJW and ZGW designed the study; CC and LCL collected the data; ZGW and MG analyzed the data; MG and LFZ analyzed and interpreted the results; DJW support and encourage the study; All the authors wrote this article; All the authors have read and reviewed this manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Ethical approval was obtained from Nanjing Drum Tower Hospital ethics committee. This retrospective study was conducted without informed consent for some objective reasons and was approved by the ethics committee. All procedures performed in studies were in accordance with the Declaration of Helsinki.
Consent for publication
Not applicable.
Competing interests
The authors have declared that they have no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Wang, Z., Ge, M., Chen, C. et al. Hepatic dysfunction in patients who received acute DeBakey type I aortic dissection repair surgery: incidence, risk factors, and long-term outcomes. J Cardiothorac Surg 16, 296 (2021). https://doi.org/10.1186/s13019-021-01676-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s13019-021-01676-8