Evidence map›Paper›PMID 41647306›Full record

ArticleIntestinal Failure (New York, N.Y.)

Incidence, predictors and outcome of neonatal-onset intestinal failure.

Rishi Bolia, Shay McLaren, Sara Alremawi, Looi C Ee

Abstract read
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Article in Intestinal Failure (New York, N.Y.). 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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Rishi BoliaDepartment of Gastroenterology, Hepatology and Liver Transplant, Queensland Children's Hospital, Brisbane, Australia.
Shay McLarenDepartment of Gastroenterology, Hepatology and Liver Transplant, Queensland Children's Hospital, Brisbane, Australia.
Sara AlremawiDepartment of Gastroenterology, Hepatology and Liver Transplant, Queensland Children's Hospital, Brisbane, Australia.
Looi C EeDepartment of Gastroenterology, Hepatology and Liver Transplant, Queensland Children's Hospital, Brisbane, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neonatal-onset Intestinal Failure (IF) and Short Bowel Syndrome (SBS) are associated with significant morbidity. We aimed to estimate incidence, identify predictors and determine outcomes of neonatal IF and SBS. Materials and methods: Retrospective review of children admitted to Queensland Children's Hospital between April, 2018 to March, 2022 who received parenteral nutrition (PN) in the neonatal period. IF was defined as those who required PN> 60 days from a gastrointestinal cause. Population-based estimate of incidence was calculated using census data from the national bureau of statistics. Results: 49 neonatal patients received PN, of which 21 had IF, including 16 with SBS. The population-based incidence of IF and SBS-IF were 13.7(95 % CI 10.0-17.1) and 10.51(95 % CI 5.04-15.59) per 100,000 live-births respectively. Those with IF had lower birth weight [1985(IQR 1321)g vs.3140(IQR778)g, p = 0.001], lower gestational age [34weeks(IQR7.5)vs.38weeks(IQR3),p = 0.001], shorter residual small bowel [45 cm(IQR44)vs.245 cm(IQR50),p = 0.001], more likely to have an enterostomy [17/21vs.10/28,p = 0.003] and no colon [10/21vs.3/28,p = 0.0001] compared to those without IF. On multivariate analysis, residual small bowel length [OR 0.73(95 %CI 0.57-0.93),p = 0.008] and absent colon [OR 0.84(95 %CI 0.69 - 0.92),p = 0.001] were independent predictors of IF. At follow-up, 71 % (15/21) of patients with IF, including 81 % (13/16) with SBS attained enteral autonomy with no mortality. Children who attained enteral autonomy had significantly longer residual bowel [47.5(IQR 33)cm. vs. 26 cm.,p = 0.04] as compared to those who remained on PN. Conclusion: The population-based incidence of IF and SBS-IF in Queensland, Australia was 13.7 and 10.51 per 100,000 live-births respectively. Most children with neonatal IF achieve enteral autonomy with residual small bowel length predictive of it.

Indexed as

Enteral autonomyIntestinal failureParenteral nutritionShort bowel syndrome

Identifiers

PMID41647306
PMCPMC12851332

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