The evaluation of levosimendan in patients with acute myocardial infarction related ventricular septal rupture undergoing cardiac surgery: a prospective observational cohort study with propensity score analysis

被引:6
|
作者
Li, Ze-Shi [1 ,2 ]
Wang, Kuo [3 ]
Pan, Tuo [1 ,2 ]
Sun, Yan-Hua [4 ]
Liu, Chang [5 ]
Cheng, Yong-Qing [5 ]
Zhang, He [1 ,2 ]
Zhang, Hai-Tao [1 ,2 ]
Wang, Dong-Jin [1 ,2 ,3 ,5 ]
Chen, Zu-Jun [6 ]
机构
[1] Peking Union Med Coll, Nanjing Drum Tower Hosp, Dept Cardiothorac Surg, Nanjing 210008, Jiangsu, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll, Grad Sch, Nanjing 210008, Jiangsu, Peoples R China
[3] XuZhou Med Univ, Nanjing Drum Tower Hosp, Dept Cardiothorac Surg, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Univ, Med Sch, Affiliated Hosp, Dept Anesthesia,Nanjing Drum Tower Hosp, Nanjing, Jiangsu, Peoples R China
[5] Nanjing Univ, Med Sch, Dept Cardiothorac Surg, Nanjing Drum Tower Hosp,Affiliated Hosp, Nanjing, Jiangsu, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Dept Intens Care Unite, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Levosimendan; Ventricular septal rupture; Cardiac surgery; Coronary artery bypass grafting; Mortality; Postoperative complication; INTRAAORTIC BALLOON PUMP; RISK-FACTORS; PREOPERATIVE LEVOSIMENDAN; PROPHYLACTIC LEVOSIMENDAN; MECHANICAL COMPLICATIONS; CARDIOPULMONARY BYPASS; CARDIOGENIC-SHOCK; OUTPUT SYNDROME; MORTALITY; SUPPORT;
D O I
10.1186/s12871-022-01663-z
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Study objective The purpose of the present study was to evaluate the efficacy of levosimendan in patients with acute myocardial infarction related ventricular septal rupture (AMI-VSR) underwent cardiac surgery. Design Prospective observational cohort study with propensity score analysis. Patients There were 261 patients with AMI-VSR in our study. After 1:1 propensity matching, 106 patients (53 levosimendan and 53 control) were selected in the matched cohort. Interventions None. Measurements Patients who received levosimendan were assigned to the levosimendan group (n = 164). The patients who were not received were levosimendan assigned to the control group (n = 97). The levosimendan was initiated immediately after cardiopulmonary bypass. Then, it has been maintained during the postoperative 3 days. The poor outcomes were identified as follows: death and postoperative complications (postoperative stroke, low cardiac output syndromeneeded mechanical circulatory support after surgery, acute kidney injury (>= stage III), postoperative infection or septic shock, new developed atrial fibrillation or ventricular arrhythmias). Main results Before matching, the control group had more length of ICU stay (6.69 +/- 3.90 d vs. 5.20 +/- 2.24 d, p < 0.001) and longer mechanical ventilation time (23 h, IQR: 16-53 h vs. 16 h, IQR: 11-23 h, p < 0.001). Other postoperative outcomes have not shown significant differences between two groups. After matching, no significant difference was found between both groups for all postoperative outcomes. The Kaplan-Meier survivul estimate and log-rank test showed that the 90-day survival had no significant differences between two groups before and after matching. Conclusion Our study found that a low-dose infusion of levosimendan in AMI-VSR patients underwent surgical repair did not associated with positively affect to postoperative outcomes.
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页数:10
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