Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation
Since the outbreak of COVID-19, many randomized controlled trials have been launched to test the efficacy of promising treatments. These trials will offer great promise for future treatment. However, a public health emergency calls for a balance between gathering sound evidence and granting therapeu...
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doaj-8e07a1bc7b8b4d71a564f84ce9c77fce2021-02-07T04:25:45ZengElsevierThe Innovation2666-67582020-08-0112100028Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit EvaluationHong-tian Li0Zhi-hao Cheng1Yong-ying Huang2Xi-lin Lv3Yu-bo Zhou4Erdan Dong5Jian-meng Liu6Institute of Reproductive and Child Health, National Health Commission Key Laboratory of Reproductive Health, Peking University Health Science Center, No 38, Xueyuan Road, Haidian District, Beijing 100191, China; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, ChinaInstitute of Reproductive and Child Health, National Health Commission Key Laboratory of Reproductive Health, Peking University Health Science Center, No 38, Xueyuan Road, Haidian District, Beijing 100191, China; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, ChinaInstitute of Reproductive and Child Health, National Health Commission Key Laboratory of Reproductive Health, Peking University Health Science Center, No 38, Xueyuan Road, Haidian District, Beijing 100191, China; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, ChinaInstitute of Reproductive and Child Health, National Health Commission Key Laboratory of Reproductive Health, Peking University Health Science Center, No 38, Xueyuan Road, Haidian District, Beijing 100191, China; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, ChinaInstitute of Reproductive and Child Health, National Health Commission Key Laboratory of Reproductive Health, Peking University Health Science Center, No 38, Xueyuan Road, Haidian District, Beijing 100191, China; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, ChinaDepartment of Cardiology and Institute of Vascular Medicine, Peking University Third Hospital, Beijing 100191, China; National Health Commission Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Peking University Third Hospital, Beijing 100191, China; Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Cardiovascular Receptors Research, Peking University Third Hospital, Beijing 100191, ChinaInstitute of Reproductive and Child Health, National Health Commission Key Laboratory of Reproductive Health, Peking University Health Science Center, No 38, Xueyuan Road, Haidian District, Beijing 100191, China; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing 100191, China; Corresponding authorSince the outbreak of COVID-19, many randomized controlled trials have been launched to test the efficacy of promising treatments. These trials will offer great promise for future treatment. However, a public health emergency calls for a balance between gathering sound evidence and granting therapeutic access to promising trial drugs as widely as possible. In an electronic survey, we found that 3.9% of the participants preferred to receive an unproven trial drug directly in the hypothetical scenario of mild COVID-19 infection. This percentage increased drastically to 31.1% and 54.2% in the hypothetical scenario of severe and extremely severe infection, respectively. Our survey indicates a likelihood of substantial receptivity of trial drugs among actual patients in severe conditions. From the perspective of deontological ethics, a trial can only be approved when potential benefits of the investigational treatment are presumed to outweigh risks, so compassionate or off-label use of investigational therapies merits evaluation.http://www.sciencedirect.com/science/article/pii/S266667582030028X |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hong-tian Li Zhi-hao Cheng Yong-ying Huang Xi-lin Lv Yu-bo Zhou Erdan Dong Jian-meng Liu |
spellingShingle |
Hong-tian Li Zhi-hao Cheng Yong-ying Huang Xi-lin Lv Yu-bo Zhou Erdan Dong Jian-meng Liu Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation The Innovation |
author_facet |
Hong-tian Li Zhi-hao Cheng Yong-ying Huang Xi-lin Lv Yu-bo Zhou Erdan Dong Jian-meng Liu |
author_sort |
Hong-tian Li |
title |
Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation |
title_short |
Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation |
title_full |
Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation |
title_fullStr |
Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation |
title_full_unstemmed |
Patients' Attitudes to Unproven Therapies in Treating COVID-19 Merit Evaluation |
title_sort |
patients' attitudes to unproven therapies in treating covid-19 merit evaluation |
publisher |
Elsevier |
series |
The Innovation |
issn |
2666-6758 |
publishDate |
2020-08-01 |
description |
Since the outbreak of COVID-19, many randomized controlled trials have been launched to test the efficacy of promising treatments. These trials will offer great promise for future treatment. However, a public health emergency calls for a balance between gathering sound evidence and granting therapeutic access to promising trial drugs as widely as possible. In an electronic survey, we found that 3.9% of the participants preferred to receive an unproven trial drug directly in the hypothetical scenario of mild COVID-19 infection. This percentage increased drastically to 31.1% and 54.2% in the hypothetical scenario of severe and extremely severe infection, respectively. Our survey indicates a likelihood of substantial receptivity of trial drugs among actual patients in severe conditions. From the perspective of deontological ethics, a trial can only be approved when potential benefits of the investigational treatment are presumed to outweigh risks, so compassionate or off-label use of investigational therapies merits evaluation. |
url |
http://www.sciencedirect.com/science/article/pii/S266667582030028X |
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