Evidence map›Paper›PMID 35962389›Full record

ArticleBMC health services research2022

On the universality of medical device regulations: the case of Benin.

A Maccaro, D Piaggio, S Leesurakarn, N Husen, S Sekalala, S Rai, L Pecchia

Abstract read
In one paragraph

Article in BMC health services research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

A Maccaro *Applied Biomedical Signal Processing Intelligent eHealth Lab, School of Engineering, University of Warwick, Coventry, CV47AL, UK. alessia.maccaro@warwick.ac.uk.ORCID http://orcid.org/0000-0001-9338-9884
D Piaggio *Applied Biomedical Signal Processing Intelligent eHealth Lab, School of Engineering, University of Warwick, Coventry, CV47AL, UK.ORCID http://orcid.org/0000-0001-5408-9360
S LeesurakarnThe Warwick Interdisciplinary Research Centre for International Development (WICID), University of Warwick, Coventry, CV47AL, UK.
N HusenNekemte Zonal Health Organization, Oromia, Ethiopia.
S SekalalaThe Warwick Interdisciplinary Research Centre for International Development (WICID), University of Warwick, Coventry, CV47AL, UK.
S RaiThe Warwick Interdisciplinary Research Centre for International Development (WICID), University of Warwick, Coventry, CV47AL, UK.
L PecchiaApplied Biomedical Signal Processing Intelligent eHealth Lab, School of Engineering, University of Warwick, Coventry, CV47AL, UK.ORCID http://orcid.org/0000-0002-7900-5415

Funding

EPSRC Impact Accelerator Award EP/K503848/1Marie Sklodowska-Curie Actions WIRL COFUND
6 · The paper itself

Abstract

backgroundRegulatory frameworks surrounding medical devices (MDs) and medical locations are of utter importance for safeguarding patients and users, and for granting a universal access to healthcare. Currently, as the main existing regulatory frameworks are drafted by high-income countries, they pretend to be general and applicable globally, but fail to understand particular contexts, specifically those in low-resource settings (LRSs), resulting, therefore, inapplicable. In particular, LRSs present a varied situation, with legal transplants of guidelines from their previous colonial regimes. This apparently theoretical issue, is, effectively, a tangible and rising matter of concern, given the ever-increasing number of MD patent applications per year, as well as the appearance of low- and middle-income countries (LMICs) on the MD market itself. This article will focus on the European Regulation on MDs 745/2017 and its applicability in LRSs, specifically presenting the case of Benin, a Sub-Saharan African country.

methodsThis work is based on a field study conducted in 2019 in Benin, which is particularly exemplar to show the complexity of the "legal transplantation" concept. A multidisciplinary approach, comprising the standard tools and methods of ethics, law, and biomedical engineering, was used to draft a heuristic hermeneutic framework, and to analyse related bioethical issues concerning Medical Device Regulations (MDRs) in LRSs, the role of Maintenance, and other sociological questions; as well as the rural population's perception on MDs and health technologies, and the role of ethics in the hospitals of LRSs.

resultsThe definition of these themes helped approach the local perspective and define the research questions. Downstream of the analysis of the Medical Devices Regulations, the Maintenance and other bioethical issues in Benin, the heuristic hermeneutic framework was created to guide a shift in the paradigm of law and regulation making, so as to make them more contextualised and inclusive, globally.

conclusionThis article proposes a framework that will help policymakers take into account the particularism of each context, especially those of the most vulnerable countries, when drafting and issuing regulatory frameworks, promoting an ever-evolving model of universalism.

Indexed as

Bioethical IssuesMedical Device LegislationBeninDelivery of Health CareHumansBioethics by designFrugal regulationHermeneutic heuristic frameworkLegal transplantationLow-resource settingsMedical device regulations

Identifiers

PMID35962389
PMCPMC9375389

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.