Evidence map›Paper›PMID 37474849›Full record

ArticleQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2023

The early years: hirschsprung disease and health-related quality of life.

Fern Ee Caryn Koo, Man Ching Esther Chan, Sebastian K King, Misel Trajanovska

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Article in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

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  9. A Narrative Review of Patient-Reported Outcome Measures and Their Application in Recent Pediatric Surgical Research: Advancing Knowledge and Offering New Perspectives to the Field.European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie · 2024
    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 2 institutions in 1 country.

Fern Ee Caryn KooMelbourne Graduate School of Education, The University of Melbourne, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0002-6758-1538
Man Ching Esther ChanMelbourne Graduate School of Education, The University of Melbourne, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0001-6066-0738
Sebastian K KingClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0001-5396-0265
Misel TrajanovskaClinical Sciences, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, Australia. misel.trajanovska@mcri.edu.au.ORCID http://orcid.org/0000-0001-6983-0166
The University of Melbourne · AURoyal Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeChronic diseases are notorious in the way that they interfere with many aspects of a child's development, and this holds true for children with Hirschsprung disease (HD). The present research aims to (1) determine whether the health-related quality of life (HRQoL) of HD children differs from healthy paediatric populations; and (2) explore the relationship between HD children's HRQoL and psychosocial outcomes of parents.

methodsUsing a cross-sectional survey study design, children's HRQoL was assessed using the Pediatric Quality of Life Inventory (PedsQL), while parental psychosocial outcomes were measured using the Patient-Reported Outcomes Measurement Information System (PROMIS) anxiety and depression short-forms, Family Management Measure (FaMM), and Parent Experience of Child Illness. Surveys were administered over telephone to parents of 48 Australian children treated for HD (87.5% male, median age 4.5 years) during the period May to November 2021.

resultsWhile postoperative HRQoL of HD children was comparable to that of healthy age-matched controls, psychosocial quality of life of HD children was significantly poorer (mean difference = 3.40, CI [0.05, 6.76]). All parental outcome measures were significantly correlated with the PedsQL (r = - 0.77-0.67, p < 0.05) in expected directions, with FaMM subscales (except parent mutuality) demonstrating the most variation (R

conclusionDespite overall positive results for children, parents reported elevated symptoms of anxiety. This study highlights the importance of long-term follow-up care for HD patients and their families.

Indexed as

Hirschsprung DiseaseQuality of LifeAustraliaChildChild, PreschoolCross-Sectional StudiesCutaneous Malignant MelanomaFemaleHumansMaleParentsSurveys and QuestionnairesCongenital malformationHealth-related quality of lifeHirschsprung diseaseParental psychosocial outcomes

Identifiers

PMID37474849
OpenAlexW4384924033

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.