Evidence map›Paper›PMID 31045424›Full record

ArticleHealth psychology : official journal of the Division of Health Psychology, American Psychological Association2019

Using PROMIS® to create clinically meaningful profiles of nephrotic syndrome patients.

Jonathan P Troost, Debbie S Gipson, Noelle E Carlozzi, Bryce B Reeve, Patrick H Nachman, Rasheed Gbadegesin, Jichuan Wang, Frank Modersitzki, Susan Massengill, John D Mahan and 5 more

Abstract read
In one paragraph

Article in Health psychology : official journal of the Division of Health Psychology, American Psychological Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
–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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

15 authors.

Jonathan P TroostDivision of Nephrology, Department of Pediatrics and Communicable Diseases, C. S. Mott Children's Hospital, University of Michigan.ORCID 0000-0002-1183-8330
Debbie S GipsonDivision of Nephrology, Department of Pediatrics and Communicable Diseases, C. S. Mott Children's Hospital, University of Michigan.
Noelle E CarlozziDepartment of Physical Medicine and Rehabilitation, University of Michigan.
Bryce B ReeveDepartment of Health Policy and Management, University of North Carolina at Chapel Hill.
Patrick H NachmanDepartment of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill.
Rasheed GbadegesinDepartment of Pediatrics, Division of Nephrology, Duke University Medical Center.
Jichuan WangCenter for Translational Science, The Children's Research Institute, Children's National Health System.
Frank ModersitzkiDepartment of Medicine, Division of Nephrology, New York University Langone Medical Center.ORCID 0000-0002-5461-8637
Susan MassengillDivision of Pediatric Nephrology, Levine Children's Hospital.
John D MahanDepartment of Pediatrics, Division of Pediatric Nephrology, Nationwide Children's Hospital, The Ohio State University College of Medicine.
Yang LiuSchool of Social Sciences, Humanities and Arts, University of California, Merced.
Howard TrachtmanDepartment of Pediatrics, Division of Nephrology, New York University Langone Medical Center.ORCID 0000-0001-7447-9489
Emily G HerreshoffDivision of Nephrology, Department of Pediatrics and Communicable Diseases, C. S. Mott Children's Hospital, University of Michigan.
Darren A DeWaltDivision of General Medicine & Clinical Epidemiology, Department of Medicine, University of North Carolina at Chapel Hill.
David T SelewskiDivision of Nephrology, Department of Pediatrics and Communicable Diseases, C. S. Mott Children's Hospital, University of Michigan.

Funding

Training Program in Clinical & Translationa Research in Human Glomerular DiseaseU54DK083912 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KRETZLER, MATTHIAS · 2009 to 2023
$20.3M
NIH PROMIS Statistical Coordinating Center(RMI)U01AR052177 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CELLA, DAVID · 2004 to 2010
$10.6M
Validating and Extending the PROMIS Sexual Function Measure for Clinical ResearchU01AR052186 · NIAMS · DUKE UNIVERSITY · PI WEINFURT, KEVIN P · 2004 to 2013
$9.5M
PROMIS Pediatrics: Longitudinal Validation and Linking Pediatric and Adult Item BU01AR052181 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI REEVE, BRYCE B · 2004 to 2013
$9.1M
Patient reported outcomes in routine clinical care of patients infected with HIVU01AR057954 · NIAMS · UNIVERSITY OF WASHINGTON · PI CRANE, HEIDI M., CRANE, PAUL K · 2009 to 2013
$7.8M
Validation and domain development in mental health and sleep-wake functionU01AR052155 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PILKONIS, PAUL A · 2004 to 2013
$6.0M
Validation of PROMIS in Diverse Cancer PopulationsU01AR057971 · NIAMS · GEORGETOWN UNIVERSITY · PI MOINPOUR, CAROL M, POTOSKY, ARNOLD L · 2009 to 2013
$5.7M
Improving Assessment of Physical Function and Drug Safety in Health and DiseaseU01AR052158 · NIAMS · STANFORD UNIVERSITY · PI KRISHNAN, ESWAR · 2004 to 2013
$5.6M
PROMIS Technical CenterU54AR057943 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GERSHON, RICHARD · 2009 to 2013
$5.3M
UW Center on Outcomes Research in Rehabilitation(RMI)U01AR052171 · NIAMS · UNIVERSITY OF WASHINGTON · PI AMTMANN, DAGMAR · 2004 to 2008
$5.0M
Pediatric PROMIS: Advancing the Measurement and Conceptualizaiton of Child HealthU01AR057956 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI FORREST, CHRISTOPHER B · 2009 to 2014
$4.9M
Ecolog validity- patient-reported chronic disease*(RMI)U01AR052170 · NIAMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI STONE, ARTHUR A · 2004 to 2008
$3.8M
American Institutes for ResearchBoston UniversityChildren's Hospital Medical Center, CincinnatiChildren's Hospital of PhiladelphiaDuke UniversityGeorgetown UniversityHalpin FoundationNational Center for Advancing Translational SciencesNational Institute of Diabetes and Digestive and Kidney DiseasesNational Institutes of Health; Common Fund InitiativeNephCure Kidney InternationalNIAMS NIH HHS U01 AR052155NIAMS NIH HHS U01 AR052158NIAMS NIH HHS U01 AR052170NIAMS NIH HHS U01 AR052171NIAMS NIH HHS U01 AR052177NIAMS NIH HHS U01 AR052181NIAMS NIH HHS U01 AR052186NIAMS NIH HHS U01 AR057929NIAMS NIH HHS U01 AR057936NIAMS NIH HHS U01 AR057940NIAMS NIH HHS U01 AR057948NIAMS NIH HHS U01 AR057954NIAMS NIH HHS U01 AR057956NIAMS NIH HHS U01 AR057967NIAMS NIH HHS U01 AR057971NIAMS NIH HHS U54 AR057926NIAMS NIH HHS U54 AR057943NIAMS NIH HHS U54 AR057951NIDDK NIH HHS U54 DK083912Northwestern UniversityOffice of Rare Diseases ResearchStanford UniversityState University of New York, Stony BrookUniversity of California, Los AngelesUniversity of Maryland, BaltimoreUniversity of MichiganUniversity of North Carolina at Chapel HillUniversity of PittsburghUniversity of Washington, Seattle
6 · The paper itself

Abstract

objectiveNephrotic syndrome (NS) is a kidney disease known to adversely impact health-related quality of life (HRQOL). Patient-reported outcome (PRO) measures are commonly used to characterize HRQOL and the patient disease experience. This study aims to improve the interpretability and clinical utility of the Patient-Reported Outcomes Measurement Information System® (PROMIS®) by identifying distinct meaningful HRQOL profiles in children and adults with NS.

methodPatients were from 2 prospective NS cohort studies (PROMIS-II®: 121 children; NEPTUNE: 40 children and 219 adults) with data from 6 PROMIS® domains. Latent Profile Analysis was used to identify subgroups of patients based on PROMIS® score patterns. A 3-step analysis of latent profile predictors was used to determine how clinical parameters predicted HRQOL profile membership.

resultsWe identified 3 HRQOL profiles (Good, Average, and Poor) with strong indicators of membership classification (entropy >0.86). Complete proteinuria remission, reduction in symptoms, and shorter disease duration, were significant predictors of better HRQOL profile membership.

conclusionsPatients with NS can be classified by HRQOL into clinically meaningful categories. Integrating this approach into clinic may help in the identification of individuals with poor HRQOL will help clinicians better manage their symptoms and researchers study the causes and possible interventions for these patients. PROMIS® HRQOL profiles were reproducible in replication cohorts. (PsycINFO Database Record (c) 2019 APA, all rights reserved).

Indexed as

Patient Reported Outcome MeasuresAdolescentAdultChildCohort StudiesFemaleHumansLongitudinal StudiesMaleNephrotic SyndromeQuality of LifeYoung Adult

Identifiers

PMID31045424
PMCPMC6499490

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.