Department of Family Practice Education, Mercy Health Saint Mary's, Grand Rapids, Michigan.
Department of Pharmacy Services, Mercy Health Saint Mary's, Grand Rapids, Michigan.
Pharmacotherapy. 2020 Jun;40(6):592-598. doi: 10.1002/phar.2403. Epub 2020 May 20.
We present a case of late initiation of remdesivir antiviral therapy in the successful treatment of a patient with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a mixed medical intensive care unit of a community teaching hospital. A previously healthy 40-year-old man was admitted to the hospital 3 days after the onset of coronavirus disease 2019 (COVID-19) symptoms including dry cough, fever, and shortness of breath progressing to intubation and increased mechanical ventilator support. A request for compassionate use remdesivir was submitted on the same hospital day as the positive COVID-19 polymerase chain reaction result. Supportive measures, in addition to a 5-day course of hydroxychloroquine, were maintained until remdesivir could be supplied on day 9 of hospitalization, 13 days after symptom onset. Sixty hours after initiating remdesivir, the patient was successfully extubated and able to transition to room air within 24 hours of extubation. Late initiation of remdesivir may be effective in treating SARS-CoV-2, unlike antivirals utilized for different disease states, such as oseltamivir, that are most effective when started as soon as possible following symptom onset. Urgent action is needed by regulatory agencies to work with drug manufacturers to expedite the study and approval of investigational agents targeting SARS-CoV-2 as well as to meet manufacturing demands.
我们报告了 1 例在社区教学医院综合重症监护病房中成功治疗严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的患者,该患者延迟开始使用瑞德西韦抗病毒治疗。一名 40 岁的既往健康男性,在出现新型冠状病毒病 2019(COVID-19)症状后 3 天被收入院,这些症状包括干咳、发热和呼吸急促,病情进展为需要插管和增加机械通气支持。在 COVID-19 聚合酶链反应结果阳性的同一天提交了同情使用瑞德西韦的申请。除了羟氯喹 5 天疗程外,还维持了支持性措施,直到住院第 9 天(发病后第 13 天)才能供应瑞德西韦。在开始使用瑞德西韦后 60 小时,患者成功拔管,并在拔管后 24 小时内能够过渡到室内空气。与用于不同疾病状态的抗病毒药物(如奥司他韦)不同,瑞德西韦延迟使用可能对治疗 SARS-CoV-2 有效,这些抗病毒药物在症状出现后尽快开始使用效果最佳。监管机构需要采取紧急行动,与药物制造商合作,加快针对 SARS-CoV-2 的研究和批准调查性药物,并满足制造需求。