Schmidt Matthieu, Schellongowski Peter, Patroniti Nicolò, Taccone Fabio Silvio, Reis Miranda Dinis, Reuter Jean, Prodanovic Helène, Pierrot Marc, Dorget Amandine, Park Sunghoon, Balik Martin, Demoule Alexandre, Crippa Ilaria Alice, Mercat Alain, Wohlfarth Philipp, Sonneville Romain, Combes Alain
Sorbonne Universités, UPMC University Paris 06, INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
Medical Intensive Care Unit, Hôpital de la Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Am J Respir Crit Care Med. 2018 May 15;197(10):1297-1307. doi: 10.1164/rccm.201708-1761OC.
Because encouraging rates for hospital and long-term survival of immunocompromised patients in ICUs have been described, these patients are more likely to receive invasive therapies, like extracorporeal membrane oxygenation (ECMO). To report outcomes of immunocompromised patients treated with ECMO for severe acute respiratory distress syndrome (ARDS) and to identify their pre-ECMO predictors of 6-month mortality and main ECMO-related complications. Retrospective multicenter study in 10 international ICUs with high volumes of ECMO cases. Immunocompromised patients, defined as having hematological malignancies, active solid tumor, solid-organ transplant, acquired immunodeficiency syndrome, or long-term or high-dose corticosteroid or immunosuppressant use, and severe ECMO-treated ARDS, from 2008 to 2015 were included. We collected demographics, clinical data, ECMO-related complications, and ICU- and 6 month-outcome data for 203 patients (median Acute Physiology and Chronic Health Evaluation II score, 28 [25th-75th percentile, 20-33]; age, 51 [38-59] yr; Pa/Fi, 60 [50-82] mm Hg before ECMO) who fulfilled our inclusion criteria. Six-month survival was only 30%, with a respective median ECMO duration and ICU stay of 8 (5-14) and 25 (16-50) days. Patients with hematological malignancies had significantly poorer outcomes than others (log-rank = 0.02). ECMO-related major bleeding, cannula infection, and ventilator-associated pneumonia were frequent (36%, 10%, and 50%, respectively). Multivariate analyses retained fewer than 30 days between immunodeficiency diagnosis and ECMO cannulation as being associated with lower 6-month mortality (odds ratio, 0.32 [95% confidence interval, 0.16-0.66]; = 0.002), and lower platelet count, higher Pco, age, and driving pressure as independent pre-ECMO predictors of 6-month mortality. Recently diagnosed immunodeficiency is associated with a much better prognosis in ECMO-treated severe ARDS. However, low 6-month survival of our large cohort of immunocompromised patients supports restricting ECMO to patients with realistic oncological/therapeutic prognoses, acceptable functional status, and few pre-ECMO mortality-risk factors.
由于已有关于重症监护病房(ICU)免疫功能低下患者的医院生存率和长期生存率的报道,这些患者更有可能接受侵入性治疗,如体外膜肺氧合(ECMO)。报告接受ECMO治疗的重症急性呼吸窘迫综合征(ARDS)免疫功能低下患者的结局,并确定其ECMO前6个月死亡率的预测因素以及主要的ECMO相关并发症。对10个拥有大量ECMO病例的国际ICU进行回顾性多中心研究。纳入2008年至2015年期间被定义为患有血液系统恶性肿瘤、活动性实体瘤、实体器官移植、获得性免疫缺陷综合征或长期或大剂量使用皮质类固醇或免疫抑制剂且接受ECMO治疗的重症ARDS的免疫功能低下患者。我们收集了符合纳入标准的203例患者的人口统计学资料、临床数据、ECMO相关并发症以及ICU结局和6个月结局数据(急性生理与慢性健康状况评分II中位数,28[第25 - 75百分位数,20 - 33];年龄,51[38 - 59]岁;ECMO前动脉血氧分压/吸入氧浓度比值,60[50 - 82]mmHg)。6个月生存率仅为30%,ECMO持续时间中位数和ICU住院时间分别为8(5 - 14)天和25(16 - 50)天。血液系统恶性肿瘤患者的结局明显比其他患者差(对数秩检验P = 0.02)。ECMO相关的大出血、插管感染和呼吸机相关性肺炎很常见(分别为36%、10%和50%)。多变量分析显示,免疫缺陷诊断与ECMO插管之间间隔少于30天与较低的6个月死亡率相关(比值比,0.32[95%置信区间,0.16 - 0.66];P = 0.002),较低的血小板计数、较高的二氧化碳分压、年龄和驱动压是ECMO前6个月死亡率的独立预测因素。最近诊断出的免疫缺陷与接受ECMO治疗的重症ARDS患者预后明显较好相关。然而,我们大量免疫功能低下患者队列的6个月低生存率支持将ECMO限制应用于具有现实肿瘤学/治疗预后、可接受的功能状态且ECMO前死亡风险因素较少的患者。