School of Public Health, ICMR-National Institute of Epidemiology, Chennai, Tamil Nadu, India.
ICMR-National Institute of Epidemiology, Chennai, Tamil Nadu, India.
Indian J Med Res. 2020;151(2 & 3):184-189. doi: 10.4103/ijmr.IJMR_502_20.
As of February 29, 2020, more than 85,000 cases of coronavirus disease 2019 (COVID-19) have been reported from China and 53 other countries with 2,924 deaths. On January 30, 2020, the first laboratory-confirmed case of COVID was reported from Kerala, India. In view of the earlier evidence about effectiveness of repurposed lopinavir/ritonavir against severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) coronavirus (CoV), as well as preliminary docking studies conducted by the ICMR-National Institute of Virology, Pune, the Central Drugs Standard Control Organization approved the restricted public health use of lopinavir/ritonavir combination amongst symptomatic COVID-19 patients detected in the country. Hospitalized adult patients with laboratory-confirmed SARS-CoV-2 infection with any one of the following criteria will be eligible to receive lopinavir/ritonavir for 14 days after obtaining written informed consent: (i) respiratory distress with respiratory rate ≥22/min or SpOof <94 per cent; (ii) lung parenchymal infiltrates on chest X-ray; (iii) hypotension defined as systolic blood pressure <90 mmHg or need for vasopressor/inotropic medication; (iv) new-onset organ dysfunction; and (v) high-risk groups - age >60 yr, diabetes mellitus, renal failure, chronic lung disease and immunocompromised persons. Patients will be monitored to document clinical (hospital length of stay and mortality at 14, 28 and 90 days), laboratory (presence of viral RNA in serial throat swab samples) and safety (adverse events and serious adverse events) outcomes. Treatment outcomes amongst initial cases would be useful in providing guidance about the clinical management of patients with COVID-19. If found useful in managing initial SARS-CoV-2-infected patients, further evaluation using a randomized control trial design is warranted to guide future therapeutic use of this combination.
截至 2020 年 2 月 29 日,中国和其他 53 个国家报告了超过 85000 例 2019 年冠状病毒病(COVID-19)病例,并有 2924 人死亡。2020 年 1 月 30 日,印度喀拉拉邦报告了首例实验室确诊的 COVID 病例。鉴于先前关于洛匹那韦/利托那韦对严重急性呼吸综合征(SARS)和中东呼吸综合征(MERS)冠状病毒(CoV)有效性的证据,以及浦那印度医学研究理事会-国家病毒学研究所进行的初步对接研究,中央药物标准控制组织批准在该国发现的有症状 COVID-19 患者中限制公共卫生使用洛匹那韦/利托那韦组合。符合以下任何一项标准的住院成年 SARS-CoV-2 感染患者将有资格接受洛匹那韦/利托那韦治疗 14 天,前提是获得书面知情同意:(i)呼吸急促,呼吸频率≥22/分钟或 SpOof <94%;(ii)胸部 X 光片上有肺实质浸润;(iii)血压定义为收缩压<90mmHg 或需要血管加压药/正性肌力药物;(iv)新发器官功能障碍;和(v)高危人群 - 年龄>60 岁、糖尿病、肾功能衰竭、慢性肺病和免疫功能低下者。将对患者进行监测,以记录临床(住院时间和 14、28 和 90 天的死亡率)、实验室(连续咽喉拭子样本中病毒 RNA 的存在)和安全性(不良事件和严重不良事件)结果。初始病例的治疗结果将有助于为 COVID-19 患者的临床管理提供指导。如果在管理初始 SARS-CoV-2 感染患者方面有用,使用随机对照试验设计进行进一步评估是合理的,以指导这种组合的未来治疗用途。