{"title":"Efficacy of Hydroxychloroquine versus Clarithromycin in the Improvement of Dyspnea and Cough in Patients after the Treatment of Acute-Phase COVID-19","authors":"","doi":"10.32592/ircmj.2023.25.4.2080","DOIUrl":null,"url":null,"abstract":"Background: Post-acute COVID-19 syndrome involves the persistence of the patient’s symptoms due to the residual inflammation of the acute phase.\n\nObjectives: In the current study, we aimed to evaluate medication intervention to accelerate the improvement of prolonged respiratory symptoms in this phase.\n\nMethods: Thirty-four patients, aged 20-50 years, in the recovery phase of COVID-19, were enrolled, who still suffered from respiratory problems even two weeks after being discharged from Rasool Akram Hospital, Tehran, Iran. They were divided into three groups based on the type of treatment for eliminating the remaining symptoms: hydroxychloroquine (HCQ, 200 mg twice daily for four weeks), clarithromycin (500 mg twice daily for four weeks), and control (receiving a placebo similar to the last two groups). At the beginning and end of the treatment, patients’ dyspnea and cough were assessed using Medical Research Council and visual analog scale (VAS), respectively, their laboratory tests were checked, and they took a 6-min walk test.\n\nResults: At the end of the treatment, the VAS of cough was 0.74 in the HCQ group, which was higher than that in the clarithromycin group. In addition, dyspnea decreased in the HCQ and clarithromycin groups by 64% and 40%, respectively, compared to the control group. Furthermore, there was a significant relationship between residual dyspnea at the end of the treatment and the severity of initial lung involvement in the acute phase.\n\nConclusion: Based on these findings, it can be concluded that HCQ was more effective in reducing dyspnea, compared to clarithromycin, in the recovery phase, especially in patients with milder lung involvement in the acute phase. Additionally, clarithromycin was found to be more effective in improving coughs.","PeriodicalId":48912,"journal":{"name":"Iranian Red Crescent Medical Journal","volume":null,"pages":null},"PeriodicalIF":0.4000,"publicationDate":"2023-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Red Crescent Medical Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.32592/ircmj.2023.25.4.2080","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Post-acute COVID-19 syndrome involves the persistence of the patient’s symptoms due to the residual inflammation of the acute phase.
Objectives: In the current study, we aimed to evaluate medication intervention to accelerate the improvement of prolonged respiratory symptoms in this phase.
Methods: Thirty-four patients, aged 20-50 years, in the recovery phase of COVID-19, were enrolled, who still suffered from respiratory problems even two weeks after being discharged from Rasool Akram Hospital, Tehran, Iran. They were divided into three groups based on the type of treatment for eliminating the remaining symptoms: hydroxychloroquine (HCQ, 200 mg twice daily for four weeks), clarithromycin (500 mg twice daily for four weeks), and control (receiving a placebo similar to the last two groups). At the beginning and end of the treatment, patients’ dyspnea and cough were assessed using Medical Research Council and visual analog scale (VAS), respectively, their laboratory tests were checked, and they took a 6-min walk test.
Results: At the end of the treatment, the VAS of cough was 0.74 in the HCQ group, which was higher than that in the clarithromycin group. In addition, dyspnea decreased in the HCQ and clarithromycin groups by 64% and 40%, respectively, compared to the control group. Furthermore, there was a significant relationship between residual dyspnea at the end of the treatment and the severity of initial lung involvement in the acute phase.
Conclusion: Based on these findings, it can be concluded that HCQ was more effective in reducing dyspnea, compared to clarithromycin, in the recovery phase, especially in patients with milder lung involvement in the acute phase. Additionally, clarithromycin was found to be more effective in improving coughs.
背景:COVID-19急性后综合征是指由于急性期炎症残留导致患者症状持续存在。目的:在本研究中,我们旨在评估药物干预以加速该阶段延长呼吸道症状的改善。方法:选取34例新冠肺炎恢复期患者,年龄20 ~ 50岁,出院2周后仍有呼吸问题。他们根据消除剩余症状的治疗类型分为三组:羟氯喹(HCQ,每天200毫克两次,持续四周)、克拉霉素(每天500毫克两次,持续四周)和对照组(接受与后两组相似的安慰剂)。在治疗开始和结束时,分别采用医学研究委员会(Medical Research Council)和视觉模拟量表(VAS)评估患者的呼吸困难和咳嗽,检查实验室检查,并进行6分钟步行测试。结果:治疗结束时,HCQ组咳嗽VAS评分为0.74,高于克拉霉素组。此外,与对照组相比,HCQ和克拉霉素组的呼吸困难分别减少了64%和40%。此外,治疗结束时的残余呼吸困难与急性期初始肺部受累的严重程度之间存在显著关系。结论:基于这些发现,与克拉霉素相比,在恢复期,特别是在急性期肺部受累较轻的患者中,HCQ可更有效地减轻呼吸困难。此外,克拉霉素被发现对改善咳嗽更有效。
期刊介绍:
The IRANIAN RED CRESCENT MEDICAL JOURNAL is an international, English language, peer-reviewed journal dealing with general Medicine and Surgery, Disaster Medicine and Health Policy. It is an official Journal of the Iranian Hospital Dubai and is published monthly. The Iranian Red Crescent Medical Journal aims at publishing the high quality materials, both clinical and scientific, on all aspects of Medicine and Surgery