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Patient-reported outcome measures can advance population health, but is access to instruments and use equitable?
Patient reported outcome measures (PROM) can engage patients and clinicians to improve health outcomes. Their population health impact may be limited by systematic barriers inhibiting access to completion. In this analysis we evaluated the association between individual parent/child characteristics...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622997/ https://www.ncbi.nlm.nih.gov/pubmed/36330368 http://dx.doi.org/10.3389/fped.2022.892947 |
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author | McCabe, Carolyn F. Wood, G. Craig Franceschelli-Hosterman, Jennifer Cochran, William J. Savage, Jennifer S. Bailey-Davis, Lisa |
author_facet | McCabe, Carolyn F. Wood, G. Craig Franceschelli-Hosterman, Jennifer Cochran, William J. Savage, Jennifer S. Bailey-Davis, Lisa |
author_sort | McCabe, Carolyn F. |
collection | PubMed |
description | Patient reported outcome measures (PROM) can engage patients and clinicians to improve health outcomes. Their population health impact may be limited by systematic barriers inhibiting access to completion. In this analysis we evaluated the association between individual parent/child characteristics and clinic factors with parental completion of a locally developed PROM, the Early Healthy Lifestyles (EHL) questionnaire. Participants included parent-child dyads who presented at 14 pediatric clinics for regularly scheduled well-child visits (WCV) prior to age 26 months. EHL items include feeding practices, diet, play time, screen exposure, and sleep. Completion was categorized at patient- (i.e., parent-child dyad) and clinic-levels. Parents completed the 15-item EHL in the patient portal before arrival or in the clinic; ninety-three percent of EHL questionnaires were completed in the clinic vs. 7% in the patient portal. High-completers completed EHL for half of WCVs; low-completers completed at least once; and non-completers never completed. Clinics were classified by EHL adoption level (% high completion): High-adoption: >50%; Moderate-adoption: 10%–50%; and Low-adoption: <10%. Individual-level factors had negligible impact on EHL completion within moderate/low EHL adoption sites; high-adoption sites were used to evaluate infant and maternal factors in association with EHL completion using hierarchical logistic regression. Noncompletion of EHL was significantly associated (p < 0.05) with infant use of public insurance (OR = 1.92 [1.42, 2.59]), >1 clinic site for WCV (OR = 1.83 [1.34, 2.50]), non-White birth mother (OR = 1.78 [1.28, 2.47]), and body weight <2,500 grams or gestational age <34 weeks (OR = 1.74 [1.05, 2.90]). The number of WCVs, a proxy for clinic size, was evaluated but was not associated with completion. Findings indicate potential disparities between populations exposed to, completing, and benefitting from these tools. |
format | Online Article Text |
id | pubmed-9622997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96229972022-11-02 Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? McCabe, Carolyn F. Wood, G. Craig Franceschelli-Hosterman, Jennifer Cochran, William J. Savage, Jennifer S. Bailey-Davis, Lisa Front Pediatr Pediatrics Patient reported outcome measures (PROM) can engage patients and clinicians to improve health outcomes. Their population health impact may be limited by systematic barriers inhibiting access to completion. In this analysis we evaluated the association between individual parent/child characteristics and clinic factors with parental completion of a locally developed PROM, the Early Healthy Lifestyles (EHL) questionnaire. Participants included parent-child dyads who presented at 14 pediatric clinics for regularly scheduled well-child visits (WCV) prior to age 26 months. EHL items include feeding practices, diet, play time, screen exposure, and sleep. Completion was categorized at patient- (i.e., parent-child dyad) and clinic-levels. Parents completed the 15-item EHL in the patient portal before arrival or in the clinic; ninety-three percent of EHL questionnaires were completed in the clinic vs. 7% in the patient portal. High-completers completed EHL for half of WCVs; low-completers completed at least once; and non-completers never completed. Clinics were classified by EHL adoption level (% high completion): High-adoption: >50%; Moderate-adoption: 10%–50%; and Low-adoption: <10%. Individual-level factors had negligible impact on EHL completion within moderate/low EHL adoption sites; high-adoption sites were used to evaluate infant and maternal factors in association with EHL completion using hierarchical logistic regression. Noncompletion of EHL was significantly associated (p < 0.05) with infant use of public insurance (OR = 1.92 [1.42, 2.59]), >1 clinic site for WCV (OR = 1.83 [1.34, 2.50]), non-White birth mother (OR = 1.78 [1.28, 2.47]), and body weight <2,500 grams or gestational age <34 weeks (OR = 1.74 [1.05, 2.90]). The number of WCVs, a proxy for clinic size, was evaluated but was not associated with completion. Findings indicate potential disparities between populations exposed to, completing, and benefitting from these tools. Frontiers Media S.A. 2022-10-18 /pmc/articles/PMC9622997/ /pubmed/36330368 http://dx.doi.org/10.3389/fped.2022.892947 Text en © 2022 McCabe, Wood, Franceschelli-Hosterman, Cochran, Savage and Bailey-Davis. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics McCabe, Carolyn F. Wood, G. Craig Franceschelli-Hosterman, Jennifer Cochran, William J. Savage, Jennifer S. Bailey-Davis, Lisa Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
title | Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
title_full | Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
title_fullStr | Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
title_full_unstemmed | Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
title_short | Patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
title_sort | patient-reported outcome measures can advance population health, but is access to instruments and use equitable? |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622997/ https://www.ncbi.nlm.nih.gov/pubmed/36330368 http://dx.doi.org/10.3389/fped.2022.892947 |
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