Evidence map›Paper›PMID 26539543›Full record

ArticleBioMed research international2015

Contribution of Electronic Medical Records to the Management of Rare Diseases.

Dominique Bremond-Gignac, Elisabeth Lewandowski, Henri Copin

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The National Hospital Care Survey Is a Unique Source of Data on Rare Diseases.Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research · 2022
    Article
  5. Review
  6. Leveraging unstructured data to identify hereditary angioedema patients in electronic medical records.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2021
    Article
  7. EMR in Eye Units.Romanian journal of ophthalmology
    Review
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

3 authors at 3 institutions in 1 country.

Dominique Bremond-GignacOphthalmology Department, Amiens University Medical Center, University of Picardie Jules Verne, 80054 Amiens, France ; Ophthalmology Department, University Medical Center Necker Enfants Malades, APHP and CNRS Unit FR3636, Paris V University, 75015 Paris, France.
Elisabeth LewandowskiDepartment of Medical Information, Amiens University Medical Center, 80054 Amiens, France.
Henri CopinCytogenetics and Reproduction Biology, Amiens University Medical Center, University of Picardie Jules Verne, 80054 Amiens, France ; EA Hervy, 80000 Amiens, France.
Assistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire Amiens-Picardie · FRUniversité de Picardie Jules Verne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeElectronic health record systems provide great opportunity to study most diseases. Objective of this study was to determine whether electronic medical records (EMR) in ophthalmology contribute to management of rare eye diseases, isolated or in syndromes. Study was designed to identify and collect patients' data with ophthalmology-specific EMR.

methodsOphthalmology-specific EMR software (Softalmo software Corilus) was used to acquire ophthalmological ocular consultation data from patients with five rare eye diseases. The rare eye diseases and data were selected and collected regarding expertise of eye center.

resultsA total of 135,206 outpatient consultations were performed between 2011 and 2014 in our medical center specialized in rare eye diseases. The search software identified 29 congenital aniridia, 6 Axenfeld/Rieger syndrome, 11 BEPS, 3 Nanophthalmos, and 3 Rubinstein-Taybi syndrome. DISCUSSION: EMR provides advantages for medical care. The use of ophthalmology-specific EMR is reliable and can contribute to a comprehensive ocular visual phenotype useful for clinical research.

conclusionRoutinely EMR acquired with specific software dedicated to ophthalmology provides sufficient detail for rare diseases. These software-collected data appear useful for creating patient cohorts and recording ocular examination, avoiding the time-consuming analysis of paper records and investigation, in a University Hospital linked to a National Reference Rare Center Disease.

Indexed as

Electronic Health RecordsEye DiseasesHumansMedical InformaticsModels, TheoreticalRare DiseasesUser-Computer Interface

Identifiers

PMID26539543
PMCPMC4619907
OpenAlexW2119144066

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.