Ghafoor Saad, Fan Kimberly, Di Nardo Matteo, Talleur Aimee C, Saini Arun, Potera Renee M, Lehmann Leslie, Annich Gail, Wang Fang, McArthur Jennifer, Sandhu Hitesh
Department of Pediatric Medicine, Division of Critical Care, St. Jude Children's Research Hospital, Memphis, TN, United States.
Division of Pediatric Critical Care, University of Tennessee (IT) Health Science Center, Memphis, TN, United States.
Front Oncol. 2021 Dec 22;11:798236. doi: 10.3389/fonc.2021.798236. eCollection 2021.
Pediatric patients who undergo hematopoietic cell transplant (HCT) or chimeric antigen receptor T-cell (CAR-T) therapy are at high risk for complications leading to organ failure and the need for critical care resources. Extracorporeal membrane oxygenation (ECMO) is a supportive modality that is used for cardiac and respiratory failure refractory to conventional therapies. While the use of ECMO is increasing for patients who receive HCT, candidacy for these patients remains controversial. We therefore surveyed pediatric critical care and HCT providers across North America and Europe to evaluate current provider opinions and decision-making and institutional practices regarding ECMO use for patients treated with HCT or CAR-T.
An electronic twenty-eight question survey was distributed to pediatric critical care and HCT providers practicing in North America (United States and Canada) and Europe through the Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network and individual emails. Responses to the survey were recorded in a REDCap database.
Two-hundred and ten participants completed the survey. Of these, 159 (76%) identified themselves as pediatric critical care physicians and 47 (22%) as pediatric HCT physicians or oncologists. The majority (99.5%) of survey respondents stated that they would consider patients treated with HCT or CAR-T therapy as candidates for ECMO support. However, pediatric critical care physicians identified more absolute and relative contraindications for ECMO than non-pediatric critical care physicians. While only 0.5% of respondents reported that they consider HCT as an absolute contraindication for ECMO, 6% of respondents stated that ECMO is contraindicated in HCT patients within their institution and only 23% have an institutional protocol or policy to guide the evaluation for ECMO candidacy of these patients. Almost half (49.1%) of respondents would accept a survival to hospital discharge of 20-30% for pediatric HCT patients requiring ECMO as adequate.
ECMO use for pediatric patients treated with HCT and CAR-T therapy is generally acceptable amongst physicians. However, there are differences in the evaluation and decision-making regarding ECMO candidacy amongst providers across medical specialties and institutions. Therefore, multidisciplinary collaboration is an essential component in establishing practice guidelines and advancing ECMO outcomes for these patients.
接受造血细胞移植(HCT)或嵌合抗原受体T细胞(CAR-T)治疗的儿科患者发生并发症导致器官衰竭并需要重症监护资源的风险很高。体外膜肺氧合(ECMO)是一种用于常规治疗难治性心脏和呼吸衰竭的支持方式。虽然接受HCT的患者使用ECMO的情况在增加,但这些患者的入选标准仍存在争议。因此,我们对北美和欧洲的儿科重症监护和HCT提供者进行了调查,以评估当前提供者对接受HCT或CAR-T治疗的患者使用ECMO的意见、决策和机构实践。
通过儿科急性肺损伤和脓毒症研究人员(PALISI)网络和个人电子邮件,向在北美(美国和加拿大)和欧洲执业的儿科重症监护和HCT提供者分发了一份包含28个问题的电子调查问卷。调查问卷的回复记录在一个REDCap数据库中。
210名参与者完成了调查。其中,159名(76%)自称是儿科重症监护医生,47名(22%)是儿科HCT医生或肿瘤学家。大多数(99.5%)的调查受访者表示,他们会将接受HCT或CAR-T治疗的患者视为ECMO支持的候选者。然而,儿科重症监护医生确定的ECMO绝对和相对禁忌症比非儿科重症监护医生更多。虽然只有0.5%的受访者报告说他们认为HCT是ECMO的绝对禁忌症,但6%的受访者表示他们所在机构的HCT患者禁忌使用ECMO,只有23%的机构有指导这些患者ECMO候选资格评估的方案或政策。近一半(49.1%)的受访者认为,对于需要ECMO的儿科HCT患者,20%-30%的出院生存率是可以接受的。
医生们普遍接受对接受HCT和CAR-T治疗的儿科患者使用ECMO。然而,不同医学专业和机构的提供者在ECMO候选资格的评估和决策方面存在差异。因此,多学科合作是制定实践指南和改善这些患者ECMO治疗结果的重要组成部分。