Evidence map›Paper›PMID 33980506›Full record

ArticleThe British journal of ophthalmology2022

Development and validation of a new clinical decision support tool to optimize screening for retinopathy of prematurity.

Aldina Pivodic, Helena Johansson, Lois E H Smith, Anna-Lena Hård, Chatarina Löfqvist, Bradley A Yoder, M Elizabeth Hartnett, Carolyn Wu, Marie-Christine Bründer, Wolf A Lagrèze and 12 more

Abstract read
In one paragraph

Article in The British journal of ophthalmology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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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

22 authors.

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
Helena JohanssonMary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, Victoria, Australia.
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.
Bradley A YoderDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
M Elizabeth HartnettDepartment of Ophthalmology, John A Moran Eye Center, University of Utah, Salt Lake City, Utah, USA.
Carolyn WuDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Marie-Christine BründerDepartment of Ophthalmology, University Medicine Greifswald, Greifswald, Germany.
Wolf A LagrèzeDepartment of Ophthalmology, Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Andreas StahlDepartment of Ophthalmology, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0002-8013-7597
Abbas Al-HawasiDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Eva LarssonDepartment of Neuroscience/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
Lotta GränseDepartment of Clinical Sciences, Ophthalmology, Skåne University Hospital, Lund University, Lund, Sweden.
Birgitta SunnqvistLänssjukhuset Ryhov, Jönköping, Sweden.
Kristina TornqvistDepartment of Clinical Sciences, Ophthalmology, Skåne University Hospital, Lund University, Lund, Sweden.
Agneta WallinSt. Erik Eye Hospital, Stockholm, Sweden.
Gerd HolmströmDepartment of Neuroscience/Ophthalmology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-5600-7186
Kerstin Albertsson-WiklandDepartment of Physiology/Endocrinology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Staffan NilssonMathematical Sciences, Chalmers University of Technology, Gothenburg, Sweden.
Ann HellströmDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-9259-1244

Funding

Dietary control of angiogenesis in retinopathy modelsR01EY017017 · NEI · BOSTON CHILDREN'S HOSPITAL · PI Zhongjie Fu, Lois Smith · 2006 to 2026
$11.8M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI STEVENS, BETH ANN · 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 P50 HD105351NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

BACKGROUND/

aimsPrematurely born infants undergo costly, stressful eye examinations to uncover the small fraction with retinopathy of prematurity (ROP) that needs treatment to prevent blindness. The aim was to develop a prediction tool (DIGIROP-Screen) with 100% sensitivity and high specificity to safely reduce screening of those infants not needing treatment. DIGIROP-Screen was compared with four other ROP models based on longitudinal weights.

methodsData, including infants born at 24-30 weeks of gestational age (GA), for DIGIROP-Screen development (DevGroup, N=6991) originate from the Swedish National Registry for ROP. Three international cohorts comprised the external validation groups (ValGroups, N=1241). Multivariable logistic regressions, over postnatal ages (PNAs) 6-14 weeks, were validated. Predictors were birth characteristics, status and age at first diagnosed ROP and essential interactions.

resultsROP treatment was required in 287 (4.1%)/6991 infants in DevGroup and 49 (3.9%)/1241 in ValGroups. To allow 100% sensitivity in DevGroup, specificity at birth was 53.1% and cumulatively 60.5% at PNA 8 weeks. Applying the same cut-offs in ValGroups, specificities were similar (46.3% and 53.5%). One infant with severe malformations in ValGroups was incorrectly classified as not needing screening. For all other infants, at PNA 6-14 weeks, sensitivity was 100%. In other published models, sensitivity ranged from 88.5% to 100% and specificity ranged from 9.6% to 45.2%.

conclusionsDIGIROP-Screen, a clinical decision support tool using readily available birth and ROP screening data for infants born GA 24-30 weeks, in the European and North American populations tested can safely identify infants not needing ROP screening. DIGIROP-Screen had equal or higher sensitivity and specificity compared with other models. DIGIROP-Screen should be tested in any new cohort for validation and if not validated it can be modified using the same statistical approaches applied to a specific clinical setting.

Indexed as

Decision Support Systems, ClinicalPeptide Nucleic AcidsRetinopathy of PrematurityBirth WeightGestational AgeHumansInfantInfant, NewbornNeonatal ScreeningRetrospective StudiesRisk FactorsPeptide Nucleic Acidsclinical decision support tooldiagnostic tests/Investigationneovascularisationoptimized screeningprediction modelpretermretinopathy of prematurityROP screening

Identifiers

PMID33980506
PMCPMC8627649

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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.