Evidence map›Paper›PMID 40432859›Full record

ArticleJournal of the Pediatric Orthopaedic Society of North America2025

Congenital Muscular Torticollis: Clinical Risk Factors and Rates of Surgery.

Akshitha Adhiyaman, Emilie Lijesen, Olivia C Tracey, Ruth H Jones, Keza E Levine, Shevaun M Doyle

Abstract read
In one paragraph

Article in Journal of the Pediatric Orthopaedic Society of North America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

6 authors.

Akshitha AdhiyamanHospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.
Emilie LijesenHospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.
Olivia C TraceyHospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.
Ruth H JonesHospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.
Keza E LevineHospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.
Shevaun M DoyleHospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Congenital muscular torticollis (CMT) is a rare shortening of the sternocleidomastoid muscle leading to lateral flexion and rotation of the cervical spine. Nonoperative treatment is most common; however, failure of contracture resolution may result in surgery. The aim of this study was to determine the clinical risk factors for CMT, exploring surgical correction rates, resolution rates, and cervical range of motion surrounding various treatment paths. Methods: This retrospective study reviewed all patients diagnosed with CMT at a single institution from January 1, 2016, to July 31, 2023. Patient demographics, risk factors, and clinical notes were collected. Two analyses were performed, separated by sufficiency of the clinical note. Results: A total of 171 patients were included in the final evaluation. Mean age was 5.0 ± 8.7 months at initial visit, 52% were female and 51.1% of patients had right-sided CMT. Of the 171 patients included in the initial analysis, 47.3% of patients had no other medical history prior to diagnosis of CMT, 12.3% had a history of developmental dysplasia of the hip (DDH), and 20.5% had plagiocephaly. Of all, 40.9% of patients were delivered via Cesarean section and 41.5% via normal spontaneous vaginal delivery. For the 110 patients included in treatment and range of motion (ROM) analysis, the mean follow-up time was 9.6 ± 13.0 months. Average lateral flexion improvement was 11.6 ± 20.4° ( Conclusions: Most infants with CMT who are healthy otherwise will improve rapidly and not undergo surgery. Meanwhile, for patients with longer treatment and/or surgical intervention, this study demonstrates favorable outcomes. Key Concepts: (1)History of developmental dysplasia of the hip and plagiocephaly were common in patients diagnosed with congenital muscular torticollis (CMT).(2)Rarely, infants with long treatment regimens for CMT will need surgical intervention, but, if indicated, the outcomes are favorable with no complications.(3)Overall, parents and caregivers can be reassured that most infants who have CMT are healthy children without significant risk factors that improve rapidly. Level of Evidence: III.

Indexed as

Congenital muscular torticollisDevelopmental dysplasia of the hipRange of motion

Identifiers

PMID40432859
PMCPMC12088285

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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.