Evidence map›Paper›PMID 40099291›Full record

ArticleRevista de salud publica (Bogota, Colombia)2023

[Identification of barriers in medical care service for children eith congenital defects detected in the AIVA program].

Alba Ibáñez-Morantes, Karen Sarmiento-Acuña, Fernando Suárez-Obando, Ignacio Zarante

Abstract readEnglish Abstract
In one paragraph

Article in Revista de salud publica (Bogota, Colombia), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Alba Ibáñez-MorantesAI: MD. Residente de Patología. Instituto de Genética Humana. Facultad de Medicina, Pontificia Universidad Javeriana. Bogotá, Colombia. aciml217@hotmail.com Pontificia Universidad Javeriana Instituto de Genética Humana Facultad de Medicina Pontificia Universidad Javeriana Bogotá Colombia.
Karen Sarmiento-AcuñaKS: MD. M.SC. Toxicología. Esp. Gerencia en Salud y Salud en el Trabajo. Departamento de Ciencias Fisiológicas. Facultad de Medicina, Pontificia Universidad Javeriana. Bogotá, Colombia. ksarmiento@javeriana.edu.co Pontificia Universidad Javeriana Departamento de Ciencias Fisiológicas Facultad de Medicina Pontificia Universidad Javeriana Bogotá Colombia ksarmiento@javeriana.edu.co.
Fernando Suárez-ObandoFS: MD. Esp. Genética. Ph.D. Genética. Instituto de Genética Humana. Facultad de Medicina, Pontificia Universidad Javeriana. Bogotá, Colombia. fernando.suarez@javeriana.edu.co Pontificia Universidad Javeriana Instituto de Genética Humana Facultad de Medicina Pontificia Universidad Javeriana Bogotá Colombia.
Ignacio ZaranteIZ: MD. M. Sc. Ciencias Biológicas. Ph.D. Genética. Instituto de Genética Humana. Hospital Universitario San Ignacio. Facultad de Medicina, Pontificia Universidad Javeriana. Bogotá, Colombia. izarante@javeriana.edu.co Pontificia Universidad Javeriana Hospital Universitario San Ignacio Facultad de Medicina Pontificia Universidad Javeriana Bogotá Colombia izarante@javeriana.edu.co.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To identify the barriers in health care in patients with visual and auditory congenital defects (CD) treated through the Comprehensive Care Program for Families with Orphan Diseases with Visual and/or Auditory Compromise (AIVA), in Bogotá D. C., Colombia. Materials and Methods: Cross-sectional study carried out in 58 children diagnosed with CD with possible visual or auditory compromise. The study population was selected from the AIVA program database, and to obtain the data, parents or legal representatives were asked to take the children for an initial medical evaluation and answer an interview. The barriers were classified according to Tanahashi's effective coverage model and the data were analyzed using descriptive statistics; absolute and relative frequencies were calculated for the qualitative variables, and means and standard deviations or medians and interquartile ranges (according to the distribution of the data determined with the Shapiro-Wilk test) for the quantitative variables. Results: 81.03% of parents or legal representatives expressed at least one barrier, the most frequent being availability (49.38%), followed by accessibility (32.24%), acceptability (11.83%) and contact (6.53%). Conclusion: The majority of parents or legal representatives interviewed reported barriers to accessing health services. Given that these have a negative impact on the health of children with CI, joint interventions are required to reduce them and thus guarantee better health conditions in children with CI and auditory or visual impairment.

Indexed as

Access to health servicescongenital abnormalities (source: MeSH, NLM)hearing lossloss of visionquality of life disabled children

Identifiers

PMID40099291
PMCPMC11648372

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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.