Research: Disease severity impacts perceived quality of life in congenital diaphragmatic hernia: a prospective observational study

Arch Dis Child

. 2024 Apr 8:archdischild-2024-326906.

 doi: 10.1136/archdischild-2024-326906. Online ahead of print. https://pubmed.ncbi.nlm.nih.gov/38589198/

Disease severity impacts perceived quality of life in congenital diaphragmatic hernia: a prospective observational study

Alexandra Dimmer 1Madison Meehan 2Sabrina Beauseigle 1Louise Koclas 2Katryn Paquette 2Carolina Michel Macias 2Shiran S Moore 3Ana Sant’Anna 2Adam Shapiro 4Jessica Simoneau 2Daniela Villegas Martinez 2Gabriel Altit 2Pramod Puligandla 5

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Abstract

Background: While research indicates comparable quality of life (QOL) in congenital diaphragmatic hernia (CDH) and healthy populations, the effect of CDH severity on patients’ health perceptions remains unexplored. We aimed to assess QOL perception in CDH, hypothesising a decline correlated with increased disease severity.

Methods: In this prospective observational study, we analysed patients with CDH aged 5 years and above participating in a longitudinal outpatient programme. We excluded bilateral CDH, genetic/syndromic conditions, prematurity and late diagnosis. Participants self-administered the age-adapted Pediatric Quality of Life Inventory (PedsQL) survey, covering four domains (physical, emotional, social, school). After enrolment, data were collected blind to severity status (larger defects denoting significant/’severe’ disease). Repeated measurements were managed using a random mixed-effects model.

Results: Of 34 participants (50% males) who completed the PedsQL, 10 provided measurements at two visits. Eight required a patch (type C), while 26 had primary repairs (type A=8; type B=18). Age at first evaluation was comparable across groups (no patch: median 11 (7-16), patch: 13 (8-15) years, p=0.78). Severe CDH correlated significantly with lower PedsQL scores (adjusted β: -18%, 95% CI -28%; -7%, adjusted for age at visit and sex). Lower scores specifically occurred in walking, exercising, social and academic functioning.

Conclusion: Severe CDH significantly lowers QOL. This finding is crucial for resource allocation in long-term CDH health surveillance and advocates for regular inclusion of patient experiences in quality improvement efforts.

Keywords: Child Development; Child Health; Follow-Up Studies; Infant Development; Paediatrics.

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