Evidence map›Paper›PMID 42277181›Full record

ArticlePediatric research2026

Digestive congenital anomalies: a call for equity in global neonatal surgical care.

Mohammad Rahmanian, Mehdi Azizmohammad Looha

Abstract read
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In one paragraph

Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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

2 authors.

Mohammad Rahmanian *Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mehdi Azizmohammad Looha *Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran. mehdi.looha@gmail.com.ORCID http://orcid.org/0000-0002-0700-1431

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global burden of digestive congenital anomalies (DCAs) remains significant, with the recent analysis by Cai et al. highlighting both progress and profound inequities. The disease burden is concentrated in the neonatal period, where the first days of life are a critical window for survival. Optimal outcomes depend on a seamless continuum of care: prenatal diagnosis, delivery at a specialized tertiary center, and immediate postnatal surgery. However, stark disparities in access to this care persist. In high-income countries, multidisciplinary management leads to high survival, while in low- and middle-income countries, delays and limited surgical capacity result in preventable mortality. Beyond treatment, preventive public health measures like maternal nutrition and folate supplementation are crucial. To bridge this equity gap, we must invest in neonatal surgical capacity, integrate DCA care into universal health coverage, and strengthen birth defect surveillance. Ensuring that every newborn with a correctable digestive anomaly has a chance to survive requires coordinated global action to make timely, life-saving surgery accessible to all.

Identifiers

PMID42277181

What OpenQuestion holds

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Registered trials

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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.