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...

Full description

Bibliographic Details
Main Authors: Hong-tian Li, Zhi-hao Cheng, Yong-ying Huang, Xi-lin Lv, Yu-bo Zhou, Erdan Dong, Jian-meng Liu
Format: Article
Language:English
Published: Elsevier 2020-08-01
Series:The Innovation
Online Access:http://www.sciencedirect.com/science/article/pii/S266667582030028X
id doaj-8e07a1bc7b8b4d71a564f84ce9c77fce
record_format Article
spelling 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
work_keys_str_mv AT hongtianli patientsattitudestounproventherapiesintreatingcovid19meritevaluation
AT zhihaocheng patientsattitudestounproventherapiesintreatingcovid19meritevaluation
AT yongyinghuang patientsattitudestounproventherapiesintreatingcovid19meritevaluation
AT xilinlv patientsattitudestounproventherapiesintreatingcovid19meritevaluation
AT yubozhou patientsattitudestounproventherapiesintreatingcovid19meritevaluation
AT erdandong patientsattitudestounproventherapiesintreatingcovid19meritevaluation
AT jianmengliu patientsattitudestounproventherapiesintreatingcovid19meritevaluation
_version_ 1724281929354706944