Evidence map›Paper›PMID 35816301›Full record

Trial reportJAMA network open2022

Development and Validation of a Deep Learning Method to Predict Cerebral Palsy From Spontaneous Movements in Infants at High Risk.

Daniel Groos, Lars Adde, Sindre Aubert, Lynn Boswell, Raye-Ann de Regnier, Toril Fjørtoft, Deborah Gaebler-Spira, Andreas Haukeland, Marianne Loennecken, Michael Msall and 12 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JAMA network open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
26.6field-weighted citation impact, top 1% 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

38 citing papers in PubMed, 76 citations in OpenAlex.

  1. Development of a peripheral blood transcriptomic gene signature to predict bronchopulmonary dysplasia.American journal of physiology. Lung cellular and molecular physiology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 10 institutions in 4 countries.

Daniel GroosDepartment of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway.
Lars AddeDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Sindre AubertDepartment of Computer Science, Norwegian University of Science and Technology, Trondheim, Norway.
Lynn BoswellAnn and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
Raye-Ann de RegnierAnn and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
Toril FjørtoftDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Deborah Gaebler-SpiraNorthwestern University Feinberg School of Medicine, Chicago, Illinois.
Andreas HaukelandDepartment of Computer Science, Norwegian University of Science and Technology, Trondheim, Norway.
Marianne LoenneckenDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Michael MsallSection of Developmental and Behavioral Pediatrics, University of Chicago, Comer Children's Hospital, Chicago, Illinois.
Unn Inger MöinichenDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Aurelie PascalDepartment of Rehabilitation Sciences and Physiotherapy, Ghent University, Ghent, Belgium.
Colleen PeytonNorthwestern University Feinberg School of Medicine, Chicago, Illinois.
Heri RamampiaroDepartment of Computer Science, Norwegian University of Science and Technology, Trondheim, Norway.
Michael D SchreiberDepartment of Pediatrics, University of Chicago, Comer Children's Hospital, Chicago, Illinois.
Inger Elisabeth SilbergDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Nils Thomas SongstadDepartment of Pediatrics and Adolescent Medicine, University Hospital of North Norway, Tromsø, Norway.
Niranjan ThomasDepartment of Neonatology, Christian Medical College Vellore, Vellore, Tamil Nadu, India.
Christine Van den BroeckDepartment of Rehabilitation Sciences and Physiotherapy, Ghent University, Ghent, Belgium.
Gunn Kristin ØbergDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Espen A F IhlenDepartment of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway.
Ragnhild StøenDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Norwegian University of Science and Technology · NOComer Children's Hospital · USOslo University Hospital · NOGhent University · BELurie Children's Hospital · USChristian Medical College & Hospital · INShirley Ryan AbilityLab · USSt Olav's University Hospital · NOUiT The Arctic University of Norway · NOUniversity Hospital of North Norway · NO

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)KL2TR001424 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHARMA, LEENA · 2015 to 2023
$8.1M
NCATS NIH HHS KL2 TR001424
6 · The paper itself

Abstract

Importance: Early identification of cerebral palsy (CP) is important for early intervention, yet expert-based assessments do not permit widespread use, and conventional machine learning alternatives lack validity. Objective: To develop and assess the external validity of a novel deep learning-based method to predict CP based on videos of infants' spontaneous movements at 9 to 18 weeks' corrected age. Design, Setting, and Participants: This prognostic study of a deep learning-based method to predict CP at a corrected age of 12 to 89 months involved 557 infants with a high risk of perinatal brain injury who were enrolled in previous studies conducted at 13 hospitals in Belgium, India, Norway, and the US between September 10, 2001, and October 25, 2018. Analysis was performed between February 11, 2020, and September 23, 2021. Included infants had available video recorded during the fidgety movement period from 9 to 18 weeks' corrected age, available classifications of fidgety movements ascertained by the general movement assessment (GMA) tool, and available data on CP status at 12 months' corrected age or older. A total of 418 infants (75.0%) were randomly assigned to the model development (training and internal validation) sample, and 139 (25.0%) were randomly assigned to the external validation sample (1 test set). Exposure: Video recording of spontaneous movements. Main Outcomes and Measures: The primary outcome was prediction of CP. Deep learning-based prediction of CP was performed automatically from a single video. Secondary outcomes included prediction of associated functional level and CP subtype. Sensitivity, specificity, positive and negative predictive values, and accuracy were assessed. Results: Among 557 infants (310 [55.7%] male), the median (IQR) corrected age was 12 (11-13) weeks at assessment, and 84 infants (15.1%) were diagnosed with CP at a mean (SD) age of 3.4 (1.7) years. Data on race and ethnicity were not reported because previous studies (from which the infant samples were derived) used different study protocols with inconsistent collection of these data. On external validation, the deep learning-based CP prediction method had sensitivity of 71.4% (95% CI, 47.8%-88.7%), specificity of 94.1% (95% CI, 88.2%-97.6%), positive predictive value of 68.2% (95% CI, 45.1%-86.1%), and negative predictive value of 94.9% (95% CI, 89.2%-98.1%). In comparison, the GMA tool had sensitivity of 70.0% (95% CI, 45.7%-88.1%), specificity of 88.7% (95% CI, 81.5%-93.8%), positive predictive value of 51.9% (95% CI, 32.0%-71.3%), and negative predictive value of 94.4% (95% CI, 88.3%-97.9%). The deep learning method achieved higher accuracy than the conventional machine learning method (90.6% [95% CI, 84.5%-94.9%] vs 72.7% [95% CI, 64.5%-79.9%]; P < .001), but no significant improvement in accuracy was observed compared with the GMA tool (85.9%; 95% CI, 78.9%-91.3%; P = .11). The deep learning prediction model had higher sensitivity among infants with nonambulatory CP (100%; 95% CI, 63.1%-100%) vs ambulatory CP (58.3%; 95% CI, 27.7%-84.8%; P = .02) and spastic bilateral CP (92.3%; 95% CI, 64.0%-99.8%) vs spastic unilateral CP (42.9%; 95% CI, 9.9%-81.6%; P < .001). Conclusions and Relevance: In this prognostic study, a deep learning-based method for predicting CP at 9 to 18 weeks' corrected age had predictive accuracy on external validation, which suggests possible avenues for using deep learning-based software to provide objective early detection of CP in clinical settings.

Indexed as

Cerebral PalsyDeep LearningFemaleHumansInfantMaleMovementMuscle SpasticityPredictive Value of TestsPregnancy

Identifiers

PMID35816301
PMCPMC9274325
OpenAlexW4285037000

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.