Evidence map›Paper›PMID 29936975›Full record

ArticleThe Journal of surgical research2018

Impaired growth outcomes in children with congenital colorectal diseases.

Laura V Veras, Pranit N Chotai, Andrew Z Tumen, Ankush Gosain

Abstract read
In one paragraph

Article in The Journal of surgical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Review
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

4 authors at 1 institution in 1 country.

Laura V VerasDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee.
Pranit N ChotaiDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee.
Andrew Z TumenDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee.
Ankush GosainDivision of Pediatric Surgery, Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee; Children's Foundation Research Institute, Le Bonheur Children's Hospital, Memphis, Tennessee. Electronic address: agosain@uthsc.edu.
University of Tennessee Health Science Center · US

Funding

Gastrointestinal Mucosal Immune Defects in Hirschsprungs DiseaseK08DK098271 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GOSAIN, ANKUSH · 2014 to 2018
$815k
Validating Intestinal Enteroids to Study Hirschsprung's Associated EnterocolitisR03DK114543 · NIDDK · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GOSAIN, ANKUSH · 2017 to 2018
$152k
NIDDK NIH HHS K08 DK098271NIDDK NIH HHS R03 DK114543
6 · The paper itself

Abstract

backgroundCloaca, Hirschsprung disease, and anorectal malformations (CHARM) are congenital anomalies of the hindgut. Small series have suggested that children suffering from one of these anomalies may be at risk for growth impairment. We sought to expand on these findings in a comprehensive cohort, hypothesizing that patients with Medicaid insurance or African-American (AA) race would be at higher risk for poor growth.

methodsFollowing Institutional Review Board (IRB) approval, single-institution retrospective review of children with CHARM anomalies was performed (2009-2016). Body mass index (BMI) value Z-scores were obtained using the 2006 World Health Organization (age 0-24 mo) and 2000 Centers for Disease Control (CDC) (age >2 y) growth charts and calculators (statistical analysis system). Patient factors and BMI Z-scores were analyzed with descriptive statistics and Fisher's exact test.

resultsOne hundred sixty-six patients (Cloaca n = 16, Hirschsprung disease [HD] n = 71, anorectal malformation [ARM] n = 79) were identified. The BMI Z-score distribution for the entire CHARM cohort was lower than controls (P < 0.0001). HD and ARM BMI Z-scores were also lower versus controls (P < 0.0007, P < 0.0037). Requiring more or less than the average number of surgeries did not impact BMI Z-score [P = non-significant (NS)]. Patients with Medicaid had lower Z-scores versus private or commercial insurance (P < 0.0001). AA race BMI Z-score distribution was lower than controls (P < 0.0002), but there was no statistical difference in BMI Z-scores when comparing AA versus non-AA CHARM patients (P = NS).

conclusionsPatients born with CHARM anomalies are at risk for impaired growth. Furthermore study is warranted to identify modifiable risk factors contributing to this impairment. Longitudinal follow-up should include interventions to mitigate these risks.

Indexed as

Health Status DisparitiesAdolescentAnorectal MalformationsBlack or African AmericanBody Mass IndexBody WeightChildChild DevelopmentChild, PreschoolCloacaElectronic Health RecordsFemaleFollow-Up StudiesHirschsprung DiseaseHumansInfantAnorectal malformationCloacaCongenitalDevelopmentGrowthHirschsprung

Identifiers

PMID29936975
PMCPMC6020164
OpenAlexW2802869481

What OpenQuestion holds

Textmetadata
LicenceTDM
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.