Evidence map›Paper›PMID 35885763›Full record

ArticleHealthcare (Basel, Switzerland)2022

Genetic Testing on Patients with Developmental Delay: A Preliminary Study from the Perspective of Physicians.

Gwanwook Bang, Sook Joung Lee, Bomyee Lee, Minji Park, So-Youn Park

Open access · goldAbstract read
In one paragraph

Article in Healthcare (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 20% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 2 countries.

Gwanwook BangDepartment of Medical Education and Humanities, School of Medicine, Kyung Hee University, Seoul 02447, Korea.ORCID 0000-0002-9998-0226
Sook Joung LeeDepartment of Physical Medicine & Rehabilitation, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Bomyee LeeKorea National Institute for Bioethics Policy, Seoul 04522, Korea.
Minji ParkDepartment of Medical Education and Humanities, School of Medicine, Kyung Hee University, Seoul 02447, Korea.ORCID 0000-0002-7843-8163
So-Youn ParkDepartment of Medical Education and Humanities, School of Medicine, Kyung Hee University, Seoul 02447, Korea.
Kyung Hee University Medical Center · KRSt. Mary's Hospital · US

Funding

National Research Foundation of Korea NRF-2019S1A5A2A03051412
6 · The paper itself

Abstract

This study aimed to discover and propose solutions to various decision-making problems, including obtaining consent, encountered by physicians when administering genetic testing to patients with disabilities. A preliminary survey and focus group interviews (FGIs) were conducted with 27 specialists who had 5-25 years of clinical experience in rehabilitation medicine, pediatrics, and obstetrics and gynecology, regarding their experience in providing genetic testing to people with developmental disabilities. This included the "role of medical staff in the patient's decision-making process", "difficulty of the consent process for genetic testing", and so forth. Some limitations were identified in the genetic testing communication process for patients with disabilities. Although providing information corresponding to the level of understanding of each person and accurately evaluating the correct consenting ability is important, the usage rate of auxiliary tools, such as booklets and videos, was only 50.0%. Additionally, there were concerns regarding the marriage prospects of people with disabilities. For people with developmental disabilities to provide consent for genetic testing, legal consent forms and explanation aids that consider individual characteristics are necessary. Moreover, education on disability awareness throughout society, including cost support, is needed.

Indexed as

clinical decision-makingdisabilitygenetic testinginformed consentmedical communication

Identifiers

PMID35885763
PMCPMC9317730
OpenAlexW4283768863

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.