Mandatory reporting obligations within the context of health research: Grappling with some of the ethical-legal complexities

JurisdictionSouth Africa
Date01 April 2023
Pages4-8
AuthorA Strode,C Badul
Published date01 April 2023
DOI10.7196/SAJBL.2023.v16i1.e824
4 April 2023, Vol. 16, No. 1 SAJBL
ARTICLE ARTICLE
Mandatory reporting is aimed at the early detection of abuse and
neglect to facilitate the identification of persons in need of care
and/or protection and then to ensure state intervention.[1,2] Globally,
it has been in place since the 1960s.[3] Initially only doctors had a
legal duty to report suspicions of child abuse under mandatory
reporting laws.[4] Later, further obligations were added to require
reporting by other professionals, and the circumstances in which
information should be reported were extended.[5]
In some instances, researchers and other members of the study
team may encounter reportable information. This issue must be
considered in the design, implementation and review of health
research. There are complexities involved because of the differing
approaches of the law and ethical guidelines. The law requires
mandatory reporting and in most cases there is limited discretion
regarding not complying with this obligation. However, ethical
guidelines advocate a more nuanced approach, allowing in some
instances non-compliance with the law. This creates an ethical
dilemma of whether to report information or not. There is also
the unanswered question of how to establish when it would be
ethically justified not to comply with the law. This article builds on
earlier work.[6-8] Its main objectives are to describe the mandatory
reporting obligations in South African (SA) law; to discuss the
ways in which these provisions apply within the context of health
research; and to propose some factors which could be used to
determine whether it is ethical to not report information.
Mandatory reporting in SA law
There are two main clusters of reporting obligations in SA law.
The first relates to special protections for three vulnerable groups:
children, the mentally disabled and the elderly. The second relates
to knowledge of crimes that have been committed.
Reporting aimed at protecting members of
vulnerable groups
Reporting in terms of the Children’s Act of 2005
There are several mandatory reporting obligations regarding children.
They relate to certain harmful behaviours by adults or other children and
to some circumstances in which children require protection. S110(1) and
(2) of the Children’s Act use mandatory reporting obligations to facilitate
the identification of and the providing of assistance to vulnerable
children to protect them from further harm.[9]
S110(1) of the Act lists persons who must make such reports, including
for example, medical practitioners, nurses, psychologists, social service
professionals and social workers.[9] There is also a broader category of
voluntary reporting in s110(2) where ‘any person who on reasonable
grounds believes that a child is in need of care and protection’ may report
such a belief.[9] The use of the word ‘may’ implies that such persons are not
compelled to report.
In terms of s110(3)(a) the reportable information must be submitted
to the provincial Department of Social Development, a designated child
protection organisation such as Child Welfare or the police for further
investigation.[9] If the reporter acts in good faith, they are protected from
civil liability in terms of s110(3)(b) of the Act.[9] In other words, even if the
information later turns out to be inaccurate or false, they cannot be held
liable. Against this background the following are reportable:
(a) Physical, sexual and emotional abuse
Abuse is defined very broadly in s1 of the Children’s Act as any
form of harm or ill-treatment deliberately inflicted on a child,
This open-access article is distributed under
Creative Commons licence CC-BY-NC 4.0.
Mandatory reporting obligations within the context of
health research: Grappling with some of the ethical-legal
complexities
A Strode, PhD; C Badul, PhD
School of Law, University of KwaZulu-Natal, Durban, South Africa
Corresponding author: A Strode (harwooda@ukzn.ac.za; strodea@ukzn.ac.za)
Mandatory reporting of various forms of abuse, from violence to corruption, is an attempt by the state to intervene in circumstances where there
is a public or a private interest that ought to be protected. This intrusion of the state into what is often a very personal space, such as the home, is
largely justified on the basis of the need to provide protection to prevent further harm, and in services to vulnerable populations such as children,
the disabled or the elderly. In some instances, researchers and other members of the study team may encounter reportable information requiring
the consideration of mandatory reporting in the design, implementation and review of health research. This is not simple. There are complex and
competing interests at play, particularly as there are differing approaches in law and ethical guidelines. This article aims to describe the mandatory
reporting obligations in South African law, discussing the ways in which these provisions apply within the context of health research, and to propose
some factors that could be used to determine whether it is ethical or not to report information.
S Afr J Bioethics Law 2023;16(1):e824. https://doi.org/10.7196/SAJBL.2023.v16i1.e824

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