接受 ECMO 和/或挥发性麻醉剂作为哮喘状态抢救疗法的患者的疗效

Kavipriya Komeswaran, Deanna Todd Tzanetos, Tiffany Wright, Jamie M. Furlong-Dillard
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引用次数: 0

摘要

背景:在肯塔基州,许多哮喘(SA)患者需要在儿科重症监护室(PICU)接受治疗,其中一部分患者可能会接受吸入性挥发性麻醉剂(IVA)和/或体外膜氧合(ECMO)的 "抢救疗法"。我们的目的是比较接受这两种疗法的患者的临床参数。方法:对 2014 年 1 月至 2020 年 7 月期间入住我院 PICU 的 2-18 岁 SA 患儿进行回顾性分析,将其分为:1)仅接受 IVA 的患者;2)接受 IVA 后又接受 ECMO 的患者;3)仅接受 ECMO 的患者。结果:共发现 1,772 例 SA 病例,其中 13 例死亡。 7 名 SA 患儿接受了 IVA、ECMO 或两种治疗。1 名患者仅接受了 IVA,5 名同时接受了 IVA 和 ECMO,1 名仅接受了 ECMO。 在升级治疗前,所有患者都接受了类固醇、阿布特罗、硫酸镁和氨茶碱等标准哮喘治疗。七名难治性 SA 患者中有六名接受了 IVA,其中五名(83%)随后升级为 ECMO。在 ECMO 插管后的 24 小时内,患者的吸气峰值压力从平均 30 降至 18。没有出现与 ECMO 置入相关的其他并发症。结论:虽然由于样本较少,我们无法从我们的研究中得出任何决定性结论,但我们注意到,在 ECMO 之前使用 IVA 对我们的患者没有明显优势。大多数接受 IVA 的患者都升级到了 ECMO,这表明早期 ECMO 插管可能是有益的。鉴于两者的高昂费用和潜在并发症,有必要为 PICU 重症 SA 的管理制定明确的指南。
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Outcomes in patients who received ECMO and/or volatile anesthetics as rescue therapies for status asthmaticus
Background: In the state of Kentucky many status asthmaticus (SA) patients require care in the Pediatric Intensive Care Unit (PICU) and a fraction of these patients may receive “rescue therapies” with inhaled volatile anesthetics (IVA) and/or Extracorporeal Membrane Oxygenation (ECMO). Our objective was to compare the clinical parameters of individual patients who received either or both therapies.   Methods: Children between 2-18 years of age admitted to our PICU from January 2014- July 2020 with SA were reviewed categorized as 1) patients who received IVA alone 2) patients who received IVA and then subsequently ECMO and 3) patients on ECMO alone.   Results: 1772 children with SA episodes were identified with a mortality of 13 patients.  7 children with SA were identified who received either IVA, ECMO or both. One patient received only IVA, 5 received both IVA and ECMO and one received only ECMO.  All received standard asthma therapies of steroids, albuterol, magnesium sulphate and aminophylline prior to escalation. Six out of seven refractory SA received IVA, and five (83%) of those were subsequently escalated to ECMO. pCO2 levels had no improvement after IVA administration but decreased by an average of 20 points after ECMO. Patients peak inspiratory pressures decreased within the 1 st 24 hours of ECMO cannulation from a mean of 30 to 18. There were no other complications related to ECMO placement.   Conclusion: While we cannot decisively draw any conclusions from our study due to small sample, it was noted that there was no clear advantage of using IVA prior to ECMO in our patients. Most patients who received IVA were escalated to ECMO indicating that early ECMO cannulation may be beneficial. Given the high cost and potential complications of both, there is a need for the development of well-defined guidelines for severe SA management in the PICU.
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