Evidence map›Paper›PMID 40463918›Full record

ArticleEplasty2024

Statewide Prevalence of Congenital Hand Anomalies: A 6-Year Review of Patients Presenting to Mississippi's Only Children's Hospital.

Brittany N Corder, Katherine C Benedict, Hannah G Buie, Reagan M Moak, Martin G McCandless, Marc E Walker

Abstract read
In one paragraph

Article in Eplasty, 2024. 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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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Brittany N CorderUniversity of Mississippi Medical Center, Division of Plastic and Reconstructive Surgery, Jackson, Mississippi.
Katherine C BenedictUniversity of Mississippi Medical Center, Division of Plastic and Reconstructive Surgery, Jackson, Mississippi.
Hannah G BuieUniversity of Mississippi Medical Center, Division of Plastic and Reconstructive Surgery, Jackson, Mississippi.
Reagan M MoakUniversity of Mississippi Medical Center, Division of Plastic and Reconstructive Surgery, Jackson, Mississippi.
Martin G McCandlessUniversity of Mississippi Medical Center, Division of Plastic and Reconstructive Surgery, Jackson, Mississippi.
Marc E WalkerUniversity of Mississippi Medical Center, Division of Plastic and Reconstructive Surgery, Jackson, Mississippi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Incidence and prevalence data for congenital upper extremity anomalies in the literature are scarce due to lack of reporting requirements, absence of a centralized database, and insufficient referral networks. As the state's only pediatric hospital and congenital hand clinic, the University of Mississippi Medical Center (UMMC) is uniquely positioned to report the per capita rate of congenital upper extremity anomalies. Methods: Pediatric patients presenting from 2015 to 2020 were identified using International Classification of Diseases codes in the UMMC electronic medical record. Exclusion criteria included age older than 18 years at presentation and defects secondary to trauma. Diagnoses included polydactyly, syndactyly, reduction defects, club hand malformations, and syndromes with upper limb anomalies. Demographic data were collected including age, race, sex, maternal age, family history of extremity anomalies, geographic location, and insurance status. Geographic trends were identified, and results were presented in incidence of disease per 10,000 births. Results: A total of 477 pediatric patients presented with a congenital upper extremity anomaly from 2015 to 2020. The average rate of congenital upper extremity anomalies in Mississippi was 21.5 per 10,000 births. The 3 most common upper extremity anomalies were polydactyly (13.1 per 10,000 births), congenital trigger thumb (2.67 per 10,000 births), and syndactyly (1.66 per 10,000 births). The polydactyly group was further divided into preaxial (1.98 per 10,000 births) and postaxial (10.9 per 10,000 births) polydactyly. There was a male predominance in presentation with 60.4% (n = 288) of patients being male. Conclusions: In the past 5 years, only New York State has published similar findings delineating the incidence of congenital hand anomalies through their Birth Defect Registry. The prevalence of upper extremity defects presenting to UMMC from 2015 to 2020 was 21.5 per 10,000 births; however, 5 specific counties had a significantly higher prevalence, ranging from 53.65 to 63.97 per 10,000 births. To develop effective programs to comprehensively treat these pediatric patients, accurate reporting and data collection mechanisms are critical.

Indexed as

Birth DefectCongenital Hand AnomalyPolydactylyRegistrySyndactyly

Identifiers

PMID40463918
PMCPMC12132596

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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.