Successful outcome using Tocilizumab in COVID-19 pneumonia with respiratory failure on a ward level

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
B. Morărașu, Aida Basirat, M. Kooblall, S. Lane
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Abstract

Abstract We describe the case of a 40-year-old man of Asian ethnicity, who presented with one week history of shortness of breath, productive cough, intermittent hemoptysis, temperature, and systemic symptoms. He had a positive nasopharyngeal swab for SARS-CoV-2, standard COVID panel admission blood tests, a chest X-ray and a CT Pulmonary Angiogram. Significant bilateral infiltrates and no pulmonary embolism were identified. The patient received standard COVID-19 treatment. After 36 hours, he deteriorated requiring initiation of non-invasive ventilatory (NIV) support. In the context of worsening clinical status, the patient received Tocilizumab as a single dose with good clinical response. Early Tocilizumab intervention in appropriately selected patients should improve the outcome and length of hospitalization in COVID-19 pneumonia. It can be used as an intensive therapy unit sparing agent allowing management of critically ill patients on a ward-based level. This may further contribute to prevention of intensive therapy unit related complications and increased mortality.
Tocilizumab治疗病房级别的新冠肺炎肺炎伴呼吸衰竭的成功结果
摘要我们描述了一名40岁的亚裔男子的病例,他有一周的呼吸急促、生产性咳嗽、间歇性咳血、体温和全身症状病史。他的鼻咽拭子检测出严重急性呼吸系统综合征冠状病毒2型呈阳性,标准的新冠肺炎专家组入院血液测试、胸部X光片和CT肺血管造影呈阳性。双侧明显浸润,无肺栓塞。患者接受了标准的新冠肺炎治疗。36小时后,病情恶化,需要启动无创通气(NIV)支持。在临床状况恶化的情况下,患者接受了托奇利珠单抗单剂量治疗,临床反应良好。对适当选择的患者进行托奇利珠单抗早期干预应能改善新冠肺炎肺炎的结果和住院时间。它可以用作重症监护病房的备用药剂,从而在病房级别上管理危重患者。这可能进一步有助于预防重症监护室相关并发症和增加死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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