Evidence map›Paper›PMID 34356566›Full record

ArticleChildren (Basel, Switzerland)2021

Patient-Reported Outcome Measures and Clinical Outcomes in Children with Foregut Anomalies.

Isabel I Sreeram, Chantal A Ten Kate, Joost van Rosmalen, Johannes M Schnater, Saskia J Gischler, René M H Wijnen, Hanneke IJsselstijn, André B Rietman

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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
  3. Article
  4. Article
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 at 2 institutions in 1 country.

Isabel I SreeramDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.ORCID 0000-0002-0016-7121
Chantal A Ten KateDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.ORCID 0000-0001-9921-7776
Joost van RosmalenDepartment of Biostatistics, Erasmus University Medical Centre, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.
Johannes M SchnaterDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.ORCID 0000-0003-4910-8293
Saskia J GischlerDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.
René M H WijnenDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.
Hanneke IJsselstijnDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.
André B RietmanDepartment of Pediatric Surgery and Intensive Care, Erasmus MC Sophia Children's Hospital, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands.
Erasmus MC - Sophia Children’s Hospital · NLErasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing numbers of children and adults with chronic disease status highlight the need for a value-based healthcare system. Patient-reported outcome measures (PROMs) are essential to value-based healthcare, yet it remains unclear how they relate to clinical outcomes such as health and daily functioning. We aimed to assess the added value of self-reported PROMs for health status (HS) and quality of life (QoL) in the long-term follow-up of children with foregut anomalies. We evaluated data of PROMs for HS and/or QoL among eight-year-olds born with congenital diaphragmatic hernia (CDH), esophageal atresia (EA), or congenital lung malformations (CLM), collected within the infrastructure of a multidisciplinary, longitudinal follow-up program. Clinical outcomes were categorized into different outcome domains, and their relationships with self-reported HS and QoL were assessed through multivariable linear regression analyses. A total of 220 children completed HS and/or QoL self-reports. In children with CDH and EA, lower cognition was significantly associated with lower self-reported HS. Due to the low number of cases, multivariable linear regression analysis was not possible in children with CLM. HS, QoL, and clinical outcomes represent different aspects of a child's wellbeing and should be measured simultaneously to facilitate a more holistic approach to clinical decision making.

Indexed as

clinical decision-makingcongenital diaphragmatic herniacongenital lung malformationsesophageal atresiavalue-based healthcare

Identifiers

PMID34356566
PMCPMC8307606
OpenAlexW3181083862

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.