Evidence map›Paper›PMID 41647304›Full record

ArticleIntestinal Failure (New York, N.Y.)

Measuring disease-specific quality of life in pediatric intestinal failure: Development and validation of the PIF-QoL.

Marie L Neumann, Amy Ladner, Jessica Y Allen, Swapna Kakani, Meghan H Rauen, David F Mercer

Abstract read
In one paragraph

Article in Intestinal Failure (New York, N.Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

6 authors.

Marie L NeumannDepartment of Surgery, Division of Transplant Surgery, University of Nebraska Medical Center, Omaha, NE, USA.
Amy LadnerThe Gutsy Perspective, Huntsville, AL, USA.
Jessica Y AllenThe Gutsy Perspective, Huntsville, AL, USA.
Swapna KakaniThe Gutsy Perspective, Huntsville, AL, USA.
Meghan H RauenThe Gutsy Perspective, Huntsville, AL, USA.
David F MercerDepartment of Surgery, Division of Transplant Surgery, University of Nebraska Medical Center, Omaha, NE, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Research suggests pediatric intestinal failure (PIF) patients experience impaired quality of life (QoL), but no disease-specific instrument has been available to assess this patient population. The aim of this study was to develop and validate a PIF-specific QoL assessment tool. Methods: Our team of patient-, caregiver-, and clinician researchers developed a questionnaire to assess self- and proxy-reported QoL in PIF using a community-driven study design that included a literature review and exploratory study, review by content experts, focus groups and cognitive interviews with children, and the tool's implementation at a large U.S.-based PIF center. An initial psychometric evaluation was conducted to assess validity and reliability. Results: A total of 181 caregivers of children (ages 4-18) with a history of PIF and 70 patients (ages 8-18) with a history of PIF completed the caregiver and child versions of the PIF-QoL, respectively, and were included in the internal consistency assessment. Test-retest reliability was assessed with a sample of 30 caregivers and 21 children who completed the questionnaires at two timepoints. Across both PIF-QoL versions, results suggest acceptable to good internal consistency and test-retest reliability for individual domains. One exception was the "Food and Eating" domain, which may warrant future refinement. Instrument internal consistency and test-retest reliability were excellent (Caregiver: α≥ 0.89, ICC= 0.90; Child: α≥ 0.83, ICC= 0.92). Conclusion: Initial empirical testing and psychometric evaluation of the PIF-QoL support its use as a practical, valid, and reliable tool for assessing self- and proxy-reported QoL of patients with PIF.

Indexed as

AssessmentIntestinal failurePatient-reported outcomes measure (PROM)PediatricQuality of lifeQuestionnaireShort bowel syndrome

Identifiers

PMID41647304
PMCPMC12851342

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LicenceCC BY-NC-ND
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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.