Evidence map›Paper›PMID 42411239›Full record

ArticleJournal of Korean medical science2026

Preliminary Report of a Nationwide Prospective Cohort of Congenital Diaphragmatic Hernia in Korea.

Jiyoon Jeong, Byong Sop Lee, Hoseon Eun, Seung Han Shin, So Yoon Ahn, Shin Yun Byun, Eun Song Song, Korean Congenital Diaphragmatic Hernia Cohort

Abstract readMulticenter Study
In one paragraph

Article in Journal of Korean medical science, 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

8 authors.

Jiyoon JeongDepartment of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3363-1162
Byong Sop LeeDepartment of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. mdleebs@amc.seoul.kr.ORCID https://orcid.org/0000-0002-1347-4200
Hoseon EunDepartment of Pediatrics, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-7212-0341
Seung Han ShinDepartment of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7008-4073
So Yoon AhnDepartment of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-1821-3173
Shin Yun ByunDepartment of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Busan, Korea.ORCID https://orcid.org/0000-0002-9034-5533
Eun Song SongDepartment of Pediatrics, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0003-1056-2165
Korean Congenital Diaphragmatic Hernia Cohort

Funding

SNUH Lee Kun-hee Child Cancer & Rare Disease Project 25C-029-0000
6 · The paper itself

Abstract

backgroundMost congenital diaphragmatic hernia (CDH) cases are identified prenatally, enabling early multidisciplinary interventions, including maternal transfer and preparation for extracorporeal membrane oxygenation (ECMO). These strategies may improve the historically stagnant survival rates in Korea. However, multicenter studies on the epidemiology and treatment outcomes of CDH are lacking. This study introduces the Korean CDH cohort (K-CDH), a nationwide prospective registry, and presents interim findings.

methodsThe cohort comprises data from 6 tertiary centers (4 in Seoul and 2 in other regions), all equipped with experienced neonatologists, pediatric surgeons, and ECMO support. Collected data include prenatal characteristics, postnatal management, surgical interventions, and follow-up outcomes. The primary outcome measured was survival to neonatal intensive care unit discharge. Risk factors for mortality or ECMO requirement were also analyzed.

resultsSixty newborns with CDH were enrolled between March 2023 and December 2024. Non-isolated CDH was identified in 16 cases (27%), including three with confirmed genetic syndromes. Sixteen infants (27%) required ECMO, with a mortality rate of 44% among them. In univariate analysis, mortality or ECMO requirement were associated with lower APGAR scores, liver herniation, lower observed-to-expected lung-to-head ratio, and initial PaCO₂, oxygenation index, alveolar-arterial oxygen difference and early severe pulmonary hypertension (PH). Multivariable analysis identified initial PaCO₂ and early severe PH as independent predictors of mortality or ECMO requirement. Among the 57 infants who underwent surgical repair (95%), most had left-sided Bochdalek hernias (n = 47), followed by right-sided (n = 7) and Morgagni-type (n = 3). The median time to surgery of 4 days and 23 (40.4%) required patch repair. Overall, 53% of patients (n = 32) received at least one medication for PH (25 received inhaled nitric oxide and 22 received milrinone). Seven infants were discharged on oral pulmonary vasodilators. The overall survival rate was 85%.

conclusionThe interim analysis of the K-CDH cohort demonstrates improved infant survival rates exceeding international benchmarks and confirm that the initial PaCO₂ and severe PH, consistent with previous studies, are predictors of mortality or ECMO. These findings underscore the importance of standardized perinatal care, early risk stratification, and coordinated efforts across multiple centers.

Indexed as

Hernias, Diaphragmatic, CongenitalExtracorporeal Membrane OxygenationFemaleHumansHypertension, PulmonaryInfant, NewbornMaleProspective StudiesRegistriesRepublic of KoreaRisk FactorsSurvival RateCongenital Diaphragmatic HerniaExtracorporeal Membrane OxygenationKoreaMulticenter Cohort StudyPulmonary Hypertension

Identifiers

PMID42411239
PMCPMC13338470

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.