Literature DB >> 31710671

Patient-Reported and Parent Proxy-Reported Outcomes in Pediatric Medical Specialty Clinical Settings: A Systematic Review of Implementation.

Lindsay M Anderson1, Jaclyn L Papadakis1, Anthony T Vesco1,2, Jenna B Shapiro3, Marissa A Feldman4, Meredyth A Evans1,2, Jill Weissberg-Benchell1,2.   

Abstract

OBJECTIVE: Youth with chronic illness are at higher risk for psychosocial difficulties, leading to a call for screening via patient-reported outcomes (PROs). The purpose of the current review is to summarize PRO implementation in pediatric medical specialty settings. A literature review of PRO implementation in these settings, conceptual issues, value and approach, legal and ethical concerns, as well as a case example of PROA in type 1 diabetes are presented.
METHODS: A systematic review was conducted to identify relevant articles published since the most recent Journal of Pediatric Psychology Special Issue on Evidence-Based Assessment in Pediatric Psychology (2008).
RESULTS: Thirty-two articles were identified and reviewed. The majority of studies reported that PROA was feasible, did not disrupt clinic flow, identified psychosocial issues warranting intervention, and was acceptable to families and providers. Response to elevated scores and impact on behavioral health referrals varied.
CONCLUSION: While many evidenced-based assessment measures are well-validated within pediatric chronic illness groups, the literature regarding implementation of PROs is still emerging. Research findings are promising, with PROs being feasible, acceptable, and leading to increased discussion of psychosocial issues when integrated into pediatric medical settings. Additional research is needed to evaluate the longitudinal impact of PROs and the optimal manner of responding to assessment data, particularly when clinically-elevated. Ultimately, identifying psychosocial issues in pediatric medical settings can promote optimal health and well-being of youth with chronic illness and their families.
© The Author(s) 2019. Published by Oxford University Press on behalf of the Society of Pediatric Psychology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  patient-reported outcomes; pediatric chronic illness; psychosocial screening

Year:  2020        PMID: 31710671     DOI: 10.1093/jpepsy/jsz082

Source DB:  PubMed          Journal:  J Pediatr Psychol        ISSN: 0146-8693


  8 in total

1.  Measuring PROMIS® Physical Activity and Sleep Problems in Early Childhood.

Authors:  Jin-Shei Lai; Courtney K Blackwell; Carole A Tucker; Sally E Jensen; David Cella
Journal:  J Pediatr Psychol       Date:  2022-05-13

2.  Documentation of Psychosocial Distress and Its Antecedents in Children with Rare or Life-Limiting Chronic Conditions.

Authors:  Sarah R McCarthy; Elizabeth H Golembiewski; Derek L Gravholt; Jennifer E Clark; Jeannie Clark; Caree Fischer; Hannah Mulholland; Kristina Babcock; Victor M Montori; Amie Jones
Journal:  Children (Basel)       Date:  2022-05-05

3.  Uptake of an Integrated Electronic Questionnaire System in Community Pediatric Clinics.

Authors:  Janel Hanmer; Kristin N Ray; Polly McCracken; Lorraine Ferrante; Sharon Wardlaw; Lauren Fleischman; David Wolfson
Journal:  Appl Clin Inform       Date:  2021-04-14       Impact factor: 2.342

4.  Ready or not? Greater readiness for independent self-care predicts better self-management but not HbA1c in teens with type 1 diabetes.

Authors:  Eveline R Goethals; Lisa K Volkening; Liane Tinsley; Lori M Laffel
Journal:  Diabet Med       Date:  2021-02-17       Impact factor: 4.359

5.  Who should we ask about mental health symptoms in adolescents with CFS/ME? Parent-child agreement on the revised children's anxiety and depression scale.

Authors:  Teona Serafimova; Maria Loades; Daisy Gaunt; Esther Crawley
Journal:  Clin Child Psychol Psychiatry       Date:  2021-02-15       Impact factor: 2.544

6.  Innovative features and functionalities of an artificial pancreas system: What do youth and parents want?

Authors:  Persis V Commissariat; Lisa K Volkening; Deborah A Butler; Eyal Dassau; Stuart A Weinzimer; Lori M Laffel
Journal:  Diabet Med       Date:  2021-01-20       Impact factor: 4.213

7.  Effectiveness-implementation hybrid-2 randomised trial of a collaborative Shared Care Model for Detecting Neurodevelopmental Impairments after Critical Illness in Young Children (DAISY): pilot study protocol.

Authors:  Debbie Long; Kristen Gibbons; Belinda Dow; James Best; Kerri-Lyn Webb; Helen G Liley; Christian Stocker; Debra Thoms; Luregn J Schlapbach; Carolyn Wharton; Paula Lister; Lori Matuschka; Maria Isabel Castillo; Zephanie Tyack; Samudragupta Bora
Journal:  BMJ Open       Date:  2022-07-15       Impact factor: 3.006

Review 8.  Using Person-Reported Outcomes (PROs) to Motivate Young People with Diabetes.

Authors:  Maartje de Wit; Judith Versloot; Ian Zenlea; Eveline R Goethals
Journal:  Curr Diab Rep       Date:  2020-05-16       Impact factor: 4.810

  8 in total

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