ArticleBMC medical ethics2026
The informed consent process for surgical procedures: perspectives of patients and next-of-kins in a lower middle-income country.
Article in BMC medical ethics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
backgroundThe informed consent process is a mandatory requirement for surgical procedures that enables patients to exercise autonomy and make informed decisions concerning their medical care, fully aware of the consequences. However, emerging evidence suggests inconsistent adherence to this requirement.
aimThis study investigated patients' and next-of-kins perspectives and experiences of the informed consent process following the completion of a surgical procedure.
methodsUsing a qualitative approach, patients and next-of-kins who had consented or offered proxy consent on behalf of a patient to undergo surgical procedures at a teaching hospital's surgical departments in Ghana were purposively recruited. We audio-recorded and transcribed 30 semi-structured interviews with 15 patients and 15 next-of-kins. Two members of the team conducted an independent thematic analysis of the data, guided by Braun and Clarke's six-step approach.
resultsThe data analysis generated four key themes related to the context, key elements, influencing factors, perceptions, and experiences of the informed consent process. The informed consent process took place in varied hospital settings, largely in the presence of next-of-kins and typically facilitated by a team of medical professionals, under private conditions where possible. Family opinion, doctors' paternalism and trust in the doctor's expertise seemed to be major factors that influenced the decision-making process. However, when conflicts emerged, the patient's choice and best interest remained paramount in the final decision. The consent process often involved discussions regarding the medical condition, treatment options, and potential risks; participant experiences of these deliberations showed variability. Issues of time constraints, poor doctor-client communication, and language barriers often complicated the informed consent experience.
conclusionPatient experiences of the informed consent process varied, which points to the importance of standardized guidelines and a more patient-centered approach. This approach should encourage continued collaboration and effective communication between medical professionals and patients/next-of-kins, while upholding the patient's right to make an informed surgical decision.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.