肺移植术后早期原发性移植物功能丧失的危险因素分析及预后评价

Analysis of risk factors and prognostic evaluation of early primary graft dysfunction after lung transplantation

  • 摘要:
    目的 探讨肺移植术后早期原发性移植物功能丧失(PGD)的危险因素,分析冷缺血时间与PGD严重程度的剂量-效应关系,评价PGD对患者近期及远期预后的影响。
    方法 回顾性分析2020年1月—2024年12月在本院接受肺移植手术的156例患者的临床资料。根据术后72 h内PGD发生情况,将患者分为PGD组(n=42)和非PGD组(n=114)。收集患者的供体特征、受体基线资料、手术相关指标及术后并发症等数据; 采用单因素分析和多因素Logistic回归模型筛选PGD发生的独立危险因素; 通过Kaplan-Meier法绘制生存曲线,采用Log-rank检验比较2组患者的生存率,并采用Cox比例风险回归模型分析PGD对患者预后的影响。
    结果 156例患者中, PGD发生率为26.9%(42/156)。单因素分析显示,供体年龄>55岁、供体吸烟史≥20包/年、供体氧合指数 < 300 mmHg、受体术前慢性阻塞性肺疾病(COPD)病史、受体术前肌酐>110 μmol/L、冷缺血时间>6 h、手术时间>4 h、体外循环(CPB)使用是PGD发生的潜在危险因素(P < 0.05)。多因素Logistic回归分析显示,供体年龄>55岁(OR=3.215, 95%CI: 1.423~7.241, P=0.005)、冷缺血时间>6 h(OR=2.897, 95%CI: 1.268~6.614, P=0.012)、受体术前肌酐>110 μmol/L(OR=2.534, 95%CI: 1.098~5.827, P=0.030)、CPB使用(OR=3.012, 95%CI: 1.305~6.928, P=0.010)是PGD发生的独立危险因素。生存分析显示, PGD组患者术后30 d、1年、3年生存率分别为71.4%、52.4%、38.1%, 显著低于非PGD组的92.1%、83.3%、75.4%(Log-rank χ2=28.643, P < 0.001)。Cox回归分析显示, PGD是患者术后死亡的独立危险因素(HR=3.125, 95%CI: 1.876~5.198, P < 0.001)。
    结论 供体年龄>55岁、冷缺血时间>6 h、受体术前肾功能不全(肌酐>110 μmol/L)及CPB使用是肺移植术后早期PGD发生的独立危险因素。PGD显著降低患者的短期及长期生存率, 临床需针对性优化供体选择、缩短冷缺血时间、改善受体术前肾功能及谨慎使用CPB, 以降低PGD发生率并改善患者预后。

     

    Abstract:
    Objective To explore the risk factors for early primary graft dysfunction (PGD) after lung transplantation, analyze the dose-effect relationship between cold ischemia time and PGD severity, and evaluate the impact of PGD on patient's short-term and long-term prognosis.
    Methods A retrospective analysis was conducted on the clinical data of 156 patients who underwent lung transplantation in the hospital from January 2020 to December 2024. Based on the occurrence of PGD within 72 h after surgery, patients were divided into PGD group (n=42) and non-PGD group (n=114). Data on donor characteristics, recipient baseline information, surgery-related indicators, and postoperative complications were collected. Univariate analysis and multivariate Logistic regression models were used to screen independent risk factors for PGD occurrence. Survival curves were plotted using the Kaplan-Meier method, and the Log-rank test was employed to compare the survival rates between the two groups. Additionally, the Cox proportional hazards regression model was used to analyze the impact of PGD on patient's prognosis.
    Results Among the 156 patients, the incidence rate of PGD was 26.9% (42/156). Univariate analysis revealed that donor age >55 years, donor smoking history ≥20 packs per year, donor oxygenation index < 300 mmHg, recipient preoperative history of chronic obstructive pulmonary disease (COPD), recipient preoperative creatinine >110 μmol/L, cold ischemia time >6 h, surgery time >4 h, and the use of cardiopulmonary bypass (CPB) were potential risk factors for PGD occurrence (P < 0.05). Multivariate Logistic regression analysis showed that donor age >55 years (OR=3.215, 95%CI, 1.423 to 7.241, P=0.005), cold ischemia time >6 h (OR=2.897, 95%CI, 1.268 to 6.614, P=0.012), recipient preoperative creatinine >110 μmol/L (OR=2.534, 95%CI, 1.098 to 5.827, P=0.030), and CPB use (OR=3.012, 95%CI, 1.305 to 6.928, P=0.010) were independent risk factors for PGD occurrence. Survival analysis indicated that the 30-day, 1-year, and 3-year survival rates of patients in the PGD group were 71.4%, 52.4% and 38.1% respectively, which were significantly lower than 92.1%, 83.3% and 75.4% respectively in the non-PGD group (Log-rank χ2=28.643, P < 0.001). Cox regression analysis demonstrated that PGD was an independent risk factor for postoperative death in patients (HR=3.125, 95%CI, 1.876 to 5.198, P < 0.001).
    Conclusion Donor age >55 years, cold ischemia time >6 h, recipient preoperative renal insufficiency (creatinine >110 μmol/L), and CPB use are independent risk factors for early PGD after lung transplantation. PGD significantly reduces patient's short-term and long-term survival rates. Clinically, it is necessary to optimize donor selection, shorten cold ischemia time, improve recipient preoperative renal function, and use CPB cautiously to reduce the incidence rate of PGD and improve patient's prognosis.

     

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