Evidence map›Paper›PMID 35277395›Full record

ArticleThe British journal of ophthalmology2023

Validation of DIGIROP models and decision support tool for prediction of treatment for retinopathy of prematurity on a contemporary Swedish cohort.

Aldina Pivodic, Lois E H Smith, Anna-Lena Hård, Chatarina Löfqvist, Ana Catarina Almeida, Abbas Al-Hawasi, Eva Larsson, Pia Lundgren, Birgitta Sunnqvist, Kristina Tornqvist and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The British journal of ophthalmology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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

13 authors at 8 institutions in 3 countries.

Aldina PivodicDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden aldina.pivodic@gu.se.ORCID 0000-0002-2224-3236
Lois E H SmithDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Anna-Lena HårdDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Chatarina LöfqvistDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Ana Catarina AlmeidaDepartment of Ophthalmology, Hospital Beatriz Angelo, Loures, Portugal.ORCID 0000-0002-8015-9606
Abbas Al-HawasiDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Eva LarssonDepartment of Surgical Sciences/Ophthalmology, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-9674-0094
Pia LundgrenDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-7731-1988
Birgitta SunnqvistLänssjukhuset Ryhov, Jönköping, Sweden.
Kristina TornqvistDepartment of Clinical Sciences, Ophthalmology, Skane University Hospital, Lund University, Lund, Sweden.
Agneta WallinSt. Erik Eye Hospital, Stockholm, Sweden.
Gerd HolmstromDepartment of Surgical Sciences/Ophthalmology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-5600-7186
Lotta GränseDepartment of Clinical Sciences, Ophthalmology, Skane University Hospital, Lund University, Lund, Sweden.
University of Gothenburg · SELund University · SEUppsala University · SEBoston Children's Hospital · USCentro Hospitalar de Lisboa Ocidental · PTLinköping University · SERegion Jönköpings län · SES:t Eriks Ögonsjukhus · SE

Funding

Dietary control of angiogenesis in retinopathy modelsR01EY017017 · NEI · BOSTON CHILDREN'S HOSPITAL · PI Zhongjie Fu, Lois Smith · 2006 to 2026
$11.8M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI WOOLF, CLIFFORD J · 2016 to 2020
$5.2M
Glucose/lipid metabolism and vessel development in phase I ROPR01EY030904 · NEI · BOSTON CHILDREN'S HOSPITAL · PI SMITH, LOIS · 2020 to 2023
$1.7M
NEI NIH HHS R01 EY017017NEI NIH HHS R01 EY030904NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

BACKGROUND/

aimsRetinopathy of prematurity (ROP) is currently diagnosed through repeated eye examinations to find the low percentage of infants that fulfil treatment criteria to reduce vision loss. A prediction model for severe ROP requiring treatment that might sensitively and specifically identify infants that develop severe ROP, DIGIROP-Birth, was developed using birth characteristics. DIGIROP-Screen additionally incorporates first signs of ROP in different models over time. The aim was to validate DIGIROP-Birth, DIGIROP-Screen and their decision support tool on a contemporary Swedish cohort.

methodsData were retrieved from the Swedish national registry for ROP (2018-2019) and two Swedish regions (2020), including 1082 infants born at gestational age (GA) 24 to <31 weeks. The predictors were GA at birth, sex, standardised birth weight and age at the first sign of ROP. The outcome was ROP treatment. Sensitivity, specificity and area under the receiver operating characteristic curve (AUC) with 95% CI were described.

resultsFor DIGIROP-Birth, the AUC was 0.93 (95% CI 0.90 to 0.95); for DIGIROP-Screen, it ranged between 0.93 and 0.97. The specificity was 49.9% (95% CI 46.7 to 53.0) and the sensitivity was 96.5% (95% CI 87.9 to 99.6) for the tool applied at birth. For DIGIROP-Screen, the cumulative specificity ranged between 50.0% and 78.7%. One infant with Beckwith-Wiedemann syndrome who fulfilled criteria for ROP treatment and had no missed/incomplete examinations was incorrectly flagged as not needing screening.

conclusionsDIGIROP-Birth and DIGIROP-Screen showed high predictive ability in a contemporary Swedish cohort. At birth, 50% of the infants born at 24 to <31 weeks of gestation were predicted to have low risk of severe ROP and could potentially be released from ROP screening examinations. All routinely screened treated infants, excluding those screened for clinical indications of severe illness, were correctly flagged as needing ROP screening.

Indexed as

Retinopathy of PrematurityBirth WeightFemaleGestational AgeHumansInfantInfant, NewbornInfant, PrematureMaleNeonatal ScreeningRetrospective StudiesRisk FactorsSwedendiagnostic tests/investigationretina

Identifiers

PMID35277395
PMCPMC10359565
OpenAlexW4220664738

What OpenQuestion holds

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LicenceCC BY
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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.