The right to withdraw from controlled human infection studies: Justifications and avoidance. (24th January 2020)

• Record Type: Journal Article
• Authors: Fernandez Lynch, Holly
• Other Names: Shah Seema K. guestEditor.; Rid Annette guestEditor.
• Is Part Of: Bioethics. Volume 34:Number 8(2020)
• Page Start: 833
• Page End: 848
• Publication Date: 2020-01-24
• Subjects: bystander -- completion bonus -- consent -- controlled human infection study -- human challenge trial -- penalty -- right to withdraw; Bioethics -- Periodicals; 174.957
• DOI: 10.1111/bioe.12704
• Languages: English
• ISSNs: 0269-9702

Abstract

Abstract: The right to withdraw from research without penalty is well established around the world. However, it has been challenged in some corners of bioethics based on concerns about various harms—to participants, to scientific integrity, and to research bystanders—that may stem from withdrawal. These concerns have become particularly salient in emerging debates about the ethics of controlled human infection (CHI) studies in which participants are intentionally infected with pathogens, often in inpatient settings with extensive follow‐up. In this article, I provide support for preserving the right to withdraw from research without penalty and demonstrate that it is also typically justified in the specific context of CHI studies. The right is well aligned with individual freedoms outside the research setting, where autonomous individuals are permitted to engage in behaviors that will foreseeably cause them harm; where they cannot be compelled to satisfy contracts for their services, nor penalized for failure to do so; and where their behavior is not constrained by public health authorities except in extreme circumstances. These freedoms are supported by U.S. law, as well as by ethical analysis that is more globally relevant. The problems associated with the right to withdraw, however, remain. The best approach to addressing them is not to restrict the right but rather to avoid initiating research when withdrawal would be especially problematic. If research proceeds, steps can still be taken to minimize participant withdrawal without infringing the right. Investigators can avoid participant surprise through informed consent focused on a study's most burdensome aspects and promote study completion through financial incentives. Should participants nonetheless seek to withdraw, investigators may attempt to persuade them not to do so by encouraging consideration of the range of potential harms that may result. Researchers conducting CHI studies and other research from which withdrawal might be especially problematic should prepare for the possibility of participant withdrawal, respect participant requests to withdraw without penalty, and incorporate various measures to avoid such requests.