Michael Dorsey MD , Katherine Phillips MD , Les James MD , Emily Kelley BSN, RN , Erica Duff MSN, RN , Tyler Lewis PharmD, BCCCP , Cristian Merchan PharmD, BCCCP , Neil Menghani MS , Justin Chan MD , Stephanie Chang MD , Travis Geraci MD , Nader Moazami MD , Deane Smith MD
{"title":"Decreased bleeding and thrombotic complications on extracorporeal membrane oxygenation support following an updated anticoagulation protocol","authors":"Michael Dorsey MD , Katherine Phillips MD , Les James MD , Emily Kelley BSN, RN , Erica Duff MSN, RN , Tyler Lewis PharmD, BCCCP , Cristian Merchan PharmD, BCCCP , Neil Menghani MS , Justin Chan MD , Stephanie Chang MD , Travis Geraci MD , Nader Moazami MD , Deane Smith MD","doi":"10.1016/j.xjon.2024.11.019","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>Anticoagulation monitoring in patients supported on extracorporeal membrane oxygenation is challenging given the risks of both bleeding and thrombotic complications. Based on our early clinical experience, we revised our heparin protocol by reducing our target anti-factor Xa assay from 0.3 to 0.7 U/mL to 0.15 to 0.5 U/mL, while instituting a partial thromboplastin time cutoff of 70 seconds. We evaluated the impact of this change on bleeding/thrombotic complications.</div></div><div><h3>Methods</h3><div>A single-center retrospective study of adult patients on extracorporeal membrane oxygenation support was conducted from January 2015 to August 2022. Patients were stratified into groups based on protocol revision: Pre-Revision (2015-2018) or Post-Revision (2019-2022). Our primary end point was the incidence of bleeding/thrombotic complications. Time in therapeutic range was calculated to determine protocol adherence. Poisson regression was performed to correlate time in therapeutic range with the likelihood of complication.</div></div><div><h3>Results</h3><div>A total of 302 patients were supported on extracorporeal membrane oxygenation during the study period: 67 Pre-Revision and 235 Post-Revision, median age 57 years. Post-Revision, patients experienced longer extracorporeal membrane oxygenation durations with an increase in the percentage of venovenous extracorporeal membrane oxygenation configurations. The incidence of bleeding complications decreased for all categories, reaching significance for surgical site bleeds (5% vs 14%, <em>P = .</em>013) and gastrointestinal hemorrhage (2% vs 6%, <em>P = .</em>049). Likewise, thrombotic complications decreased for all categories except fasciotomy, which was unchanged. Time in therapeutic range for anti-factor Xa assay and partial thromboplastin time were similar across time periods. On Poisson regression, the Post-Revision anti-factor Xa assay range significantly correlated with decreases in bleeding (<em>P = .</em>023) and a composite of bleeding/thrombotic complications (<em>P = .</em>008).</div></div><div><h3>Conclusions</h3><div>A modified heparin monitoring protocol defined by a lower therapeutic anti-factor Xa assay target and a set partial thromboplastin time cutoff correlated with decreases in bleeding/thrombotic complications in patients on extracorporeal membrane oxygenation.</div></div>","PeriodicalId":74032,"journal":{"name":"JTCVS open","volume":"23 ","pages":"Pages 199-209"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JTCVS open","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666273624004352","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
Anticoagulation monitoring in patients supported on extracorporeal membrane oxygenation is challenging given the risks of both bleeding and thrombotic complications. Based on our early clinical experience, we revised our heparin protocol by reducing our target anti-factor Xa assay from 0.3 to 0.7 U/mL to 0.15 to 0.5 U/mL, while instituting a partial thromboplastin time cutoff of 70 seconds. We evaluated the impact of this change on bleeding/thrombotic complications.
Methods
A single-center retrospective study of adult patients on extracorporeal membrane oxygenation support was conducted from January 2015 to August 2022. Patients were stratified into groups based on protocol revision: Pre-Revision (2015-2018) or Post-Revision (2019-2022). Our primary end point was the incidence of bleeding/thrombotic complications. Time in therapeutic range was calculated to determine protocol adherence. Poisson regression was performed to correlate time in therapeutic range with the likelihood of complication.
Results
A total of 302 patients were supported on extracorporeal membrane oxygenation during the study period: 67 Pre-Revision and 235 Post-Revision, median age 57 years. Post-Revision, patients experienced longer extracorporeal membrane oxygenation durations with an increase in the percentage of venovenous extracorporeal membrane oxygenation configurations. The incidence of bleeding complications decreased for all categories, reaching significance for surgical site bleeds (5% vs 14%, P = .013) and gastrointestinal hemorrhage (2% vs 6%, P = .049). Likewise, thrombotic complications decreased for all categories except fasciotomy, which was unchanged. Time in therapeutic range for anti-factor Xa assay and partial thromboplastin time were similar across time periods. On Poisson regression, the Post-Revision anti-factor Xa assay range significantly correlated with decreases in bleeding (P = .023) and a composite of bleeding/thrombotic complications (P = .008).
Conclusions
A modified heparin monitoring protocol defined by a lower therapeutic anti-factor Xa assay target and a set partial thromboplastin time cutoff correlated with decreases in bleeding/thrombotic complications in patients on extracorporeal membrane oxygenation.
目的考虑到出血和血栓并发症的风险,体外膜氧合支持患者的抗凝监测具有挑战性。基于我们的早期临床经验,我们修改了我们的肝素方案,将我们的目标抗因子Xa测定从0.3至0.7 U/mL降低到0.15至0.5 U/mL,同时设置了部分凝血活素时间截止时间为70秒。我们评估了这一变化对出血/血栓并发症的影响。方法对2015年1月至2022年8月接受体外膜氧合支持的成人患者进行单中心回顾性研究。根据方案修订将患者分为修订前(2015-2018)和修订后(2019-2022)两组。我们的主要终点是出血/血栓并发症的发生率。计算治疗范围内的时间以确定方案的依从性。泊松回归将治疗范围内的时间与并发症发生的可能性联系起来。结果在研究期间,共有302例患者接受体外膜氧合治疗:翻修前67例,翻修后235例,中位年龄57岁。翻修后,随着静脉-静脉体外膜氧合配置百分比的增加,患者经历了更长的体外膜氧合持续时间。所有类别的出血并发症发生率均下降,手术部位出血(5% vs 14%, P = 0.013)和胃肠道出血(2% vs 6%, P = 0.049)达到显著性。同样,除筋膜切开术外,所有类别的血栓性并发症均有所减少。抗Xa因子测定的治疗范围时间和部分凝血活酶时间在不同的时间段是相似的。在泊松回归中,修订后的抗因子Xa检测范围与出血的减少(P = 0.023)和出血/血栓并发症的复合(P = 0.008)显著相关。结论采用较低的治疗性抗Xa因子检测靶点和设定的部分凝血活酶时间截止点来确定改良肝素监测方案与体外膜氧合患者出血/血栓并发症的减少相关。