Outcomes of heparinized adult veno-arterial extracorporeal membrane oxygenation patients managed with low and high activated partial thromboplastin time targets: A systematic review and meta-analysis

医学 部分凝血活酶时间 体外膜肺氧合 并发症 血栓形成 随机对照试验 荟萃分析 外科 麻醉 入射(几何) 内科学 凝结 光学 物理
作者
Michael Mazzeffi,Dora Lin,Alberto Gonzalez-Almada,D Keegan Stombaugh,Jonathan Curley,Venkat Mangunta,Nicholas R. Teman,Leora T. Yarboro,Robert H. Thiele
出处
期刊:Perfusion [SAGE Publishing]
卷期号:39 (3): 525-535 被引量:5
标识
DOI:10.1177/02676591221150880
摘要

Introduction There are no randomized controlled trials comparing low and high activated partial thromboplastin time (aPTT) targets in heparinized adult veno-arterial (VA) extracorporeal membrane oxygenation (ECMO) patients. Our systematic review and meta-analysis summarized complication rates in adult VA ECMO patients treated with low and high aPTT targets. Methods Studies published from January 2000 to May 2022 were identified using Pubmed, Embase, Cochrane Library, and LILACS (Latin American and Caribbean Health Sciences Literature). Studies were included if aPTT was primarily used to guide heparin anticoagulation. For the low aPTT group, we included studies where aPTT goal was ≤60 seconds and for the high aPTT group, we included studies where aPTT goal was ≥60 seconds. Proportional meta-analysis with a random effects model was used to calculate pooled complication rates for patients in the two aPTT groups. Results Twelve studies met inclusion criteria (5 in the low aPTT group and 7 in the high aPTT group). The pooled bleeding complication incidence for low aPTT studies was 53.6% (95% CI = 37.4%–69.4%, I 2 = 60.8%) and for high aPTT studies was 43.8% (95% CI = 21.7%–67.1%, I 2 = 91.8%). No studies in the low aPTT group reported overall thrombosis incidence, while three studies in the high aPTT group reported overall thrombosis incidence. The pooled thrombosis incidence for high aPTT studies was 16.1% (95% CI = 9.0%–24.5%, I 2 = 13.1%). Conclusions Adult ECMO patients managed with low and high aPTT goals appeared to have similar bleeding and other complication rates further highlighting the need for a randomized controlled trial.
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