Does Extracorporeal Membrane Oxygenation Improve Survival in Pediatric Acute Respiratory Failure?

被引:37
作者
Barbaro, Ryan P. [1 ,2 ]
Xu, Yuejia [3 ]
Borasino, Santiago [4 ]
Truemper, Edward J. [5 ]
Watson, R. Scott [6 ,7 ]
Thiagarajan, Ravi R. [8 ]
Wypij, David [3 ,8 ]
Curley, Martha A. Q. [9 ,10 ,11 ]
机构
[1] Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Child Hlth Evaluat & Res Ctr, Ann Arbor, MI 48109 USA
[3] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
[4] Univ Alabama Birmingham, Dept Pediat, Birmingham, AL USA
[5] Childrens Hosp & Med Ctr Nebraska, Dept Pediat, Omaha, NE USA
[6] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[7] Seattle Childrens Res Inst, Ctr Child Hlth Behav & Dev, Seattle, WA USA
[8] Boston Childrens Hosp, Dept Cardiol, Boston, MA USA
[9] Childrens Hosp Philadelphia, Res Inst, Philadelphia, PA 19104 USA
[10] Univ Penn, Sch Nursing, Dept Family & Community Hlth, Philadelphia, PA 19104 USA
[11] Univ Penn, Perelman Sch Med, Dept Anesthesia & Crit Care, Philadelphia, PA 19104 USA
关键词
extracorporeal membrane oxygenation; pediatric acute respiratory distress syndrome; acute respiratory distress syndrome; extracorporeal life support; propensity score analysis; DISTRESS-SYNDROME PROCEEDINGS; VENTILATORY SUPPORT; CO2; REMOVAL; CHILDREN; MORTALITY; CARE; PRESSURE; SEDATION; THERAPY; VOLUME;
D O I
10.1164/rccm.201709-1893OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Extracorporeal membrane oxygenation (ECMO) has supported gas exchange in children with severe respiratory failure for more than 40 years, without ECMO efficacy studies. Objectives: To compare the mortality and functional status of children with severe acute respiratory failure supported with and without ECMO. Methods: This cohort study compared ECMO-supported children to pair-matched non-ECMO-supported control subjects with severe acute respiratory distress syndrome (ARDS). Both individual case matching and propensity score matching were used. The study sample was selected from children enrolled in the cluster-randomized RESTORE (Randomized Evaluation of Sedation Titration for Respiratory Failure) clinical trial. Detailed demographic and daily physiologic data were used to match patients. The primary endpoint was in-hospital mortality. Secondary outcomes included hospital-free days, ventilator-free days, and change in functional status at hospital discharge. Measurements and Main Results: Of 2,449 children in the RESTORE trial, 879 (35.9%) non-ECMO-supported patients with severe ARDS were eligible to match to 61 (2.5%) ECMO-supported children. When individual case matching was used (60 matched pairs), the in-hospital mortality rate at 90 days was 25% (15 of 60) for both the ECMO-supported and non-ECMO-supported children (P > 0.99). With propensity score matching (61 matched pairs), the ECMO-supported in-hospital mortality rate was 15 of 61 (25%), and the non-ECMO-supported hospital mortality rate was 18 of 61 (30%) (P = 0.70). There was no difference between ECMO-supported and non-ECMO-supported patients in any secondary outcomes. Conclusions: In children with severe ARDS, our results do not demonstrate that ECMO-supported children have superior outcomes compared with non-ECMO-supported children. Definitive answers will require a rigorous multisite randomized controlled trial.
引用
收藏
页码:1177 / 1186
页数:10
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