Affiliation(s)
1. School of Law, University of Papua New Guinea, Waigani, PO Box 126, National Capital District, Papua New Guinea
2. Institute of Statistics, College of Arts and Sciences, University of the Philippines Los Baños, Laguna 4031, Philippines
3. Townsville Hospital, Townsville, PO Box 670, Townsville Queensland 4810, Australia
ABSTRACT
This work is based on an
on-going research on medical informed consent in Papua New Guinea (PNG) with 19
doctors from hospitals, health care centers and private medical establishments
in the National Capital District and Central Province who voluntarily participated
in the study. The authors conducted an examination of doctors’ understanding of
informed consent for medical procedures through a qualitative interview study
and we describe our findings. We saw a need to involved patients in
decision-making about their care, ethical imperative and concerns about
litigation and their complaints highlighted the issue of informed consent. In
order for the patients to make an informed decision about medical procedure,
the doctors involved in the proposed treatment should conduct the informed
consent discussion. The discussion should include the treatment, the risks and
benefits of treatment, and alternative therapies with associated risks and
benefits. We studied doctors’
perspectives of gaining informed consent for routine medical procedures. We
used qualitative study methods using structured interviews selected by
purposive sampling. The data collected were entered into a data base and were
analyzed thematically. The discussion is based on review of legal decisions,
commentaries and our personal experience in studying medical malpractice cases.
We have utilized case reports and several informative writings that have
appeared in the world
literature, as well as selections from vast amounts of material available in
USA, UK, Australia, India and PNG. The current informed consent processes do not
appear to be ideal for many doctors in PNG. In particular, there are inhibiting
factors that affect patients from making medical informed decisions, doctors
find time not enough to run discussions on informed consent, Department of
Health does not have a standard informed consent form, patients complain about
no consent form, and they have not signed consent forms. These are but some
issues that affect patients when trying to make informed decisions. We say that informed
consent process flows from the relationship between doctor and patient, however
when this does not occur, serious legal and ethical consequences may result. This report is not
intended to be specific advice on any private legal matter.
KEYWORDS
Health care professionals,
qualitative study, consent form, medical procedure, litigation.
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References