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Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study
BACKGROUND: Since the COVID-19 pandemic, several therapeutic agents have been used in COVID-19 management. However, the results were controversial. Here, we aimed to evaluate the efficacy and safety of hydroxychloroquine (HCQ)/chloroquine (CQ) in COVID-19. METHODS: We retrospectively reviewed the me...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358550/ https://www.ncbi.nlm.nih.gov/pubmed/34384388 http://dx.doi.org/10.1186/s12879-021-06477-x |
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author | Chen, Zhe Liu, Aihua Cheng, Yongjing Wang, Xutao Xu, Xiaomao Huang, Jia Ma, Yuqing Gao, Ming Huang, Cibo |
author_facet | Chen, Zhe Liu, Aihua Cheng, Yongjing Wang, Xutao Xu, Xiaomao Huang, Jia Ma, Yuqing Gao, Ming Huang, Cibo |
author_sort | Chen, Zhe |
collection | PubMed |
description | BACKGROUND: Since the COVID-19 pandemic, several therapeutic agents have been used in COVID-19 management. However, the results were controversial. Here, we aimed to evaluate the efficacy and safety of hydroxychloroquine (HCQ)/chloroquine (CQ) in COVID-19. METHODS: We retrospectively reviewed the medical charts of patients with COVID-19 admitted to an inpatient ward in Wuhan from 2020/Feb/08 to 2020/Mar/05. Patients with HCQ/CQ and age, gender, disease severity matched ones without HCQ/CQ were selected at a 1:2 ratio. The clinical, laboratory and imaging findings were compared between these two groups. The multivariate linear regression analysis was performed to identify the factors that might influence patients’ virus shedding periods (VSPs). RESULTS: A total of 14 patients with HCQ/CQ and 21 matched ones were analyzed. The HCQ/CQ treatment lasted for an average of 10.36 ± 3.12 days. The mean VSPs were longer in the HCQ/CQ treatment group (26.57 ± 10.35 days vs. 19.10 ± 7.80 days, P = 0.020). There were 3 patients deceased during inpatient period, two patients were with HCQ/CQ treatment (P = 0.551). In the multivariate linear regression analysis, disease durations at admission (t = 3.643, P = 0.001) and HCQ/CQ treatment (t = 2.637, P = 0.013) were independent parameters for patients’ VSPs. One patient with CQ had recurrent first-degree atrioventricular block (AVB) and obvious QTc elongation, another one complained about dizziness and blurred vision which disappeared after CQ discontinuation. One patient with HCQ had transient AVB. CONCLUSIONS: In summary, we identify that the HCQ/CQ administration is not related to less mortality cases at later phase of COVID-19. More studies are needed to explore whether HCQ/CQ treatment would lead to SARS-Cov-2 RNA clearance delay or not. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06477-x. |
format | Online Article Text |
id | pubmed-8358550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83585502021-08-12 Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study Chen, Zhe Liu, Aihua Cheng, Yongjing Wang, Xutao Xu, Xiaomao Huang, Jia Ma, Yuqing Gao, Ming Huang, Cibo BMC Infect Dis Research Article BACKGROUND: Since the COVID-19 pandemic, several therapeutic agents have been used in COVID-19 management. However, the results were controversial. Here, we aimed to evaluate the efficacy and safety of hydroxychloroquine (HCQ)/chloroquine (CQ) in COVID-19. METHODS: We retrospectively reviewed the medical charts of patients with COVID-19 admitted to an inpatient ward in Wuhan from 2020/Feb/08 to 2020/Mar/05. Patients with HCQ/CQ and age, gender, disease severity matched ones without HCQ/CQ were selected at a 1:2 ratio. The clinical, laboratory and imaging findings were compared between these two groups. The multivariate linear regression analysis was performed to identify the factors that might influence patients’ virus shedding periods (VSPs). RESULTS: A total of 14 patients with HCQ/CQ and 21 matched ones were analyzed. The HCQ/CQ treatment lasted for an average of 10.36 ± 3.12 days. The mean VSPs were longer in the HCQ/CQ treatment group (26.57 ± 10.35 days vs. 19.10 ± 7.80 days, P = 0.020). There were 3 patients deceased during inpatient period, two patients were with HCQ/CQ treatment (P = 0.551). In the multivariate linear regression analysis, disease durations at admission (t = 3.643, P = 0.001) and HCQ/CQ treatment (t = 2.637, P = 0.013) were independent parameters for patients’ VSPs. One patient with CQ had recurrent first-degree atrioventricular block (AVB) and obvious QTc elongation, another one complained about dizziness and blurred vision which disappeared after CQ discontinuation. One patient with HCQ had transient AVB. CONCLUSIONS: In summary, we identify that the HCQ/CQ administration is not related to less mortality cases at later phase of COVID-19. More studies are needed to explore whether HCQ/CQ treatment would lead to SARS-Cov-2 RNA clearance delay or not. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06477-x. BioMed Central 2021-08-12 /pmc/articles/PMC8358550/ /pubmed/34384388 http://dx.doi.org/10.1186/s12879-021-06477-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Chen, Zhe Liu, Aihua Cheng, Yongjing Wang, Xutao Xu, Xiaomao Huang, Jia Ma, Yuqing Gao, Ming Huang, Cibo Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study |
title | Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study |
title_full | Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study |
title_fullStr | Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study |
title_full_unstemmed | Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study |
title_short | Hydroxychloroquine/chloroquine in patients with COVID-19 in Wuhan, China: a retrospective cohort study |
title_sort | hydroxychloroquine/chloroquine in patients with covid-19 in wuhan, china: a retrospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358550/ https://www.ncbi.nlm.nih.gov/pubmed/34384388 http://dx.doi.org/10.1186/s12879-021-06477-x |
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