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拔管后喘鸣并发新型冠状病毒肺炎相关急性呼吸窘迫综合征:病例系列

Post-Extubation Stridor Complicating COVID-19-Associated Acute Respiratory Distress Syndrome: A Case Series.

作者信息

Moran Joseph V, Godil Sara A, Goldner Breanna, Godil Kareem, Aslam Jonaid

机构信息

Internal Medicine, Lehigh Valley Health Network, Allentown, USA.

Pulmonary and Critical Care Medicine, Lehigh Valley Health Network, Allentown, USA.

出版信息

Cureus. 2020 Sep 16;12(9):e10492. doi: 10.7759/cureus.10492.

Abstract

Post-extubation stridor is a known complication of mechanical ventilation that affects a substantial number of all critical care patients and leads to increased morbidity and mortality. Common risk factors for the development of post-extubation stridor include female gender, older age, and prolonged length of mechanical ventilation. There may be an increased incidence of post-extubation stridor in patients who require mechanical ventilation to manage the respiratory complications of COVID-19. In this case series, we analyzed nine patients from across our institution who were intubated to manage acute respiratory distress syndrome (ARDS) secondary to COVID-19 and subsequently developed post-extubation stridor. The patients were predominantly females with prolonged intubations and multiple days of prone ventilation. While the patients in this case series possessed some of the well-described risk factors for post-extubation stridor, there may be risk factors specific to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection that make these patients more susceptible to the complication. The cuff leak test was performed on the majority of patients in the case series and did not successfully predict successful extubation in this population. Our analysis suggests that prophylactic corticosteroids given in the 24-48 hours prior to elective extubation in female COVID-19 patients who were intubated for more than six days with consecutive days of intermittent prone ventilation may be helpful in reducing the incidence of post-extubation stridor in this population. Overall, this case series elucidates the need for exceptionally close monitoring of COVID-19 patients upon extubation for the development of stridor.

摘要

拔管后喘鸣是机械通气已知的并发症,影响大量重症监护患者,导致发病率和死亡率增加。拔管后喘鸣发生的常见风险因素包括女性、年龄较大以及机械通气时间延长。在需要机械通气来处理新型冠状病毒肺炎(COVID-19)呼吸并发症的患者中,拔管后喘鸣的发生率可能会增加。在本病例系列中,我们分析了我院9例因COVID-19继发急性呼吸窘迫综合征(ARDS)而插管、随后发生拔管后喘鸣的患者。这些患者主要为女性,插管时间延长且进行了多日俯卧位通气。虽然本病例系列中的患者具有一些已被充分描述的拔管后喘鸣风险因素,但可能存在特定于严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的风险因素,使这些患者更容易发生拔管后喘鸣。本病例系列中的大多数患者进行了套囊漏气试验,但该试验未能成功预测该人群的成功拔管。我们的分析表明,对于因COVID-19插管超过6天且连续多日进行间歇性俯卧位通气的女性患者,在择期拔管前24 - 48小时给予预防性皮质类固醇可能有助于降低该人群拔管后喘鸣的发生率。总体而言,本病例系列阐明了对COVID-19患者拔管后发生喘鸣进行密切监测的必要性。

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Prone positioning in severe acute respiratory distress syndrome.俯卧位通气治疗严重急性呼吸窘迫综合征。
N Engl J Med. 2013 Jun 6;368(23):2159-68. doi: 10.1056/NEJMoa1214103. Epub 2013 May 20.

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