Service de Médecine Intensive-Réanimation, Institut de Cardiologie, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, Paris, France; Collège de France, Centre of Interdisciplinary Research in Biology, CNRS UMR7241, INSERM U1050, Paris, France.
Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié Salpêtrière-Charles Foix, Département Biostatistique Santé Publique et Information Médicale, Centre de Pharmacoépidémiologie (Cephepi), Paris, France.
Lancet. 2020 Aug 22;396(10250):545-552. doi: 10.1016/S0140-6736(20)30733-9.
Patients with sepsis-induced cardiomyopathy with cardiogenic shock have a high mortality. This study assessed venoarterial extracorporeal membrane oxygenation (VA-ECMO) support for sepsis-induced cardiogenic shock refractory to conventional treatments.
In this retrospective, multicentre, international cohort study, we compared outcomes of 82 patients (aged ≥18 years) with septic shock who received VA-ECMO at five academic ECMO centres, with 130 controls (not receiving ECMO) obtained from three large databases of septic shock. All patients had severe myocardial dysfunction (cardiac index 3 L/min per m or less or left ventricular ejection fraction [LVEF] 35% or less) and severe haemodynamic compromise (inotrope score at least 75 μg/kg per min or lactic acidaemia at least 4 mmol/L) at time of inclusion. The primary endpoint was survival at 90 days. A propensity score-weighted analysis was done to control for confounders.
At baseline, patients treated with VA-ECMO had more severe myocardial dysfunction (mean cardiac index 1·5 L/min per mvs 2·2 L/min per m, LVEF 17% vs 27%), more severe haemodynamic impairment (inotrope score 279 μg/kg per min vs 145 μg/kg per min, lactataemia 8·9 mmol/L vs 6·5 mmol/L), and more severe organ failure (Sequential Organ Failure Assessment score 17 vs 13) than did controls, with p<0·0001 for each comparison. Survival at 90 days for patients treated with VA-ECMO was significantly higher than for controls (60% vs 25%, risk ratio [RR] for mortality 0·54, 95% CI [0·40-0·70]; p<0·0001). After propensity score weighting, ECMO remained associated with improved survival (51% vs 14%, adjusted RR for mortality 0·57, 95% CI [0·35-0·93]; p=0·0029). Lactate and catecholamine clearance were also significantly enhanced in patients treated with ECMO. Among the 49 survivors treated with ECMO, 32 who had been treated at the largest centre reported satisfactory Short Form-36 evaluated health-related quality of life at 1-year follow-up.
Patients with severe sepsis-induced cardiogenic shock treated with VA-ECMO had a large and significant improvement in survival compared with controls not receiving ECMO. However, despite the careful propensity-weighted analysis, we cannot rule out unmeasured confounders.
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脓毒症性心肌病合并心源性休克的患者死亡率较高。本研究评估了体外膜肺氧合(VA-ECMO)对常规治疗无效的脓毒性心源性休克的支持作用。
在这项回顾性、多中心、国际队列研究中,我们比较了在 5 个学术 ECMO 中心接受 VA-ECMO 治疗的 82 名(年龄≥18 岁)脓毒性休克患者的结局与来自 3 个大型脓毒性休克数据库的 130 名对照(未接受 ECMO)的结局。所有患者在纳入时均有严重的心肌功能障碍(心指数 3 L/min/m 或更低或左心室射血分数 [LVEF] 35%或更低)和严重的血液动力学障碍(正性肌力药评分至少 75μg/kg/min 或乳酸酸中毒至少 4mmol/L)。主要终点为 90 天的生存率。采用倾向评分加权分析控制混杂因素。
在基线时,接受 VA-ECMO 治疗的患者的心肌功能障碍更严重(平均心指数 1.5 L/min/m 与 2.2 L/min/m,LVEF 17%与 27%),血液动力学损害更严重(正性肌力药评分 279μg/kg/min 与 145μg/kg/min,乳酸血症 8.9mmol/L 与 6.5mmol/L),器官衰竭更严重(序贯器官衰竭评估评分 17 与 13),每项比较的 p 值均<0.0001。接受 VA-ECMO 治疗的患者 90 天的生存率显著高于对照组(60%与 25%,死亡率的风险比 [RR]为 0.54,95%CI [0.40-0.70];p<0.0001)。在进行倾向评分加权后,ECMO 仍与生存率的提高相关(51%与 14%,死亡率的调整 RR 为 0.57,95%CI [0.35-0.93];p=0.0029)。接受 ECMO 治疗的患者的乳酸和儿茶酚胺清除率也显著提高。在接受 ECMO 治疗的 49 名幸存者中,在最大中心接受治疗的 32 名患者在 1 年随访时报告了满意的健康相关生活质量(SF-36 短表评估)。
与未接受 ECMO 治疗的对照组相比,接受 VA-ECMO 治疗的严重脓毒症性心肌病合并心源性休克患者的生存率有显著提高。然而,尽管进行了仔细的倾向评分加权分析,我们仍不能排除未测量的混杂因素。
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