Literature DB >> 26853841

Responsiveness of PROMIS® Pediatric Measures to Hospitalizations for Sickle Pain and Subsequent Recovery.

Carlton Dampier1,2, Byron Jaeger3, Heather E Gross4, Vaughn Barry1,2, Lloyd Edwards3, Yang Lui5, Darren A DeWalt4,6, Bryce B Reeve4,7.   

Abstract

BACKGROUND: The Patient-Reported Outcomes Measurement Information System(®) (PROMIS(®) ) created pediatric self-report scales measuring a variety of health attributes (domains), but their responsiveness to changes in health status has not yet been determined in children with sickle cell disease (SCD). PROCEDURE: A convenience cohort of symptomatic SCD children, aged 8-17 years, was asked to complete PROMIS pediatric scales at an initial clinic visit, at the end of a subsequent hospitalization for sickle pain, at a subsequent clinic visit or at home 2-3 weeks after hospitalization, and at a clinic visit 1-2 years after their initial assessment.
RESULTS: A total of 121 participants (mean age 12.5 ± 3.1 years, 56.2% female) participated in the study. Pain interference and fatigue domain scores were elevated at baseline, increased substantially during hospitalization, and largely returned to baseline by the recovery period, whereas the depressive symptoms, anger, and anxiety domain scores displayed a less pronounced elevation during hospitalizations and a slower return to baseline levels. The two physical functioning scales showed a substantial decline in response to hospitalization, but only modest improvements at the recovery assessment, likely representing incomplete recovery.
CONCLUSIONS: Several PROMIS pediatric measures were responsive to changes in health status associated with occurrence and resolution of acute vaso-occlusive pain requiring hospitalization. The substantial differences in these domains during SCD-related pain exacerbations support their potential usefulness in clinical research or in clinical practice. Further studies to characterize variations in symptom patterns over time may provide insights into strategies for more effective management of sickle pain.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  PROMIS; health-related quality of life; sickle cell disease

Mesh:

Year:  2016        PMID: 26853841      PMCID: PMC5055833          DOI: 10.1002/pbc.25931

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  33 in total

1.  Sampling plan and patient characteristics of the PROMIS pediatrics large-scale survey.

Authors:  Debra E Irwin; Brian D Stucky; David Thissen; Esi Morgan Dewitt; Jin Shei Lai; Karin Yeatts; James W Varni; Darren A DeWalt
Journal:  Qual Life Res       Date:  2010-03-05       Impact factor: 4.147

Review 2.  Health-related quality of life in sickle cell disease: past, present, and future.

Authors:  Julie A Panepinto; Melanie Bonner
Journal:  Pediatr Blood Cancer       Date:  2012-04-22       Impact factor: 3.167

3.  Prevalence and characteristics of moderate to severe fatigue: a multicenter study in cancer patients and survivors.

Authors:  Xin Shelley Wang; Fengmin Zhao; Michael J Fisch; Ann M O'Mara; David Cella; Tito R Mendoza; Charles S Cleeland
Journal:  Cancer       Date:  2014-02-01       Impact factor: 6.860

4.  The relationships between asthma control, daytime sleepiness, and quality of life among children with asthma: a path analysis.

Authors:  Zheng Li; I-Chan Huang; Lindsay Thompson; Sanjeev Tuli; Shih-Wen Huang; Darren DeWalt; Dennis Revicki; Elizabeth Shenkman
Journal:  Sleep Med       Date:  2013-05-16       Impact factor: 3.492

5.  Feasibility and acceptability of the patient-reported outcomes measurement information system measures in children and adolescents in active cancer treatment and survivorship.

Authors:  Johanna C Menard; Pamela S Hinds; Shana S Jacobs; Katie Cranston; Jichuan Wang; Darren A DeWalt; Heather E Gross
Journal:  Cancer Nurs       Date:  2014 Jan-Feb       Impact factor: 2.592

6.  PedsQL™ Multidimensional Fatigue Scale in sickle cell disease: feasibility, reliability, and validity.

Authors:  Julie A Panepinto; Sylvia Torres; Cristiane B Bendo; Timothy L McCavit; Bogdan Dinu; Sandra Sherman-Bien; Christy Bemrich-Stolz; James W Varni
Journal:  Pediatr Blood Cancer       Date:  2013-09-13       Impact factor: 3.167

7.  The performance of the PedsQL generic core scales in children with sickle cell disease.

Authors:  Julie A Panepinto; Nicholas M Pajewski; Lisa M Foerster; Raymond G Hoffmann
Journal:  J Pediatr Hematol Oncol       Date:  2008-09       Impact factor: 1.289

8.  Psychometric properties of the PROMIS ® pediatric scales: precision, stability, and comparison of different scoring and administration options.

Authors:  James W Varni; Brooke Magnus; Brian D Stucky; Yang Liu; Hally Quinn; David Thissen; Heather E Gross; I-Chan Huang; Darren A DeWalt
Journal:  Qual Life Res       Date:  2013-10-02       Impact factor: 4.147

9.  Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks.

Authors:  San D Keller; Manshu Yang; Marsha J Treadwell; Ellen M Werner; Kathryn L Hassell
Journal:  Health Qual Life Outcomes       Date:  2014-08-22       Impact factor: 3.186

10.  Promising insights into the health related quality of life for children with severe obesity.

Authors:  David T Selewski; David N Collier; Jackie MacHardy; Heather E Gross; Edward M Pickens; Alan W Cooper; Selam Bullock; Marian F Earls; Keeley J Pratt; Kelli Scanlon; Jonathan D McNeill; Kassandra L Messer; Yee Lu; David Thissen; Darren A DeWalt; Debbie S Gipson
Journal:  Health Qual Life Outcomes       Date:  2013-03-01       Impact factor: 3.186

View more
  23 in total

1.  Brief Screening Measures Identify Risk for Psychological Difficulties Among Children with Sickle Cell Disease.

Authors:  Anna M Hood; Ilana Reife; Allison A King; Desiree A White
Journal:  J Clin Psychol Med Settings       Date:  2020-12

Review 2.  Rigorous and practical quality indicators in sickle cell disease care.

Authors:  Suzette O Oyeku; Elissa Z Faro
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

3.  Vitamin D Supplementation Improves Health-Related Quality of Life and Physical Performance in Children with Sickle Cell Disease and in Healthy Children.

Authors:  Kelly A Dougherty; Joan I Schall; Chiara Bertolaso; Kim Smith-Whitley; Virginia A Stallings
Journal:  J Pediatr Health Care       Date:  2020-06-05       Impact factor: 1.812

Review 4.  Pain-measurement tools in sickle cell disease: where are we now?

Authors:  Deepika S Darbari; Amanda M Brandow
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

5.  A preliminary investigation of the psychometric properties of PROMIS® scales in emerging adults with sickle cell disease.

Authors:  Aimee K Hildenbrand; Charles T Quinn; Constance A Mara; James L Peugh; Emily A McTate; Maria T Britto; Lori E Crosby
Journal:  Health Psychol       Date:  2019-05       Impact factor: 4.267

Review 6.  Responsiveness of Patient-Reported Outcome Measurement Information System (PROMIS) pain domains and disease-specific patient-reported outcome measures in children and adults with sickle cell disease.

Authors:  Susanna Curtis; Amanda M Brandow
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 7.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

8.  Clinical meaning of PROMIS pain domains for children with sickle cell disease.

Authors:  Ashima Singh; Julie A Panepinto
Journal:  Blood Adv       Date:  2019-08-13

9.  End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain.

Authors:  Ann T Farrell; Julie Panepinto; C Patrick Carroll; Deepika S Darbari; Ankit A Desai; Allison A King; Robert J Adams; Tabitha D Barber; Amanda M Brandow; Michael R DeBaun; Manus J Donahue; Kalpna Gupta; Jane S Hankins; Michelle Kameka; Fenella J Kirkham; Harvey Luksenburg; Shirley Miller; Patricia Ann Oneal; David C Rees; Rosanna Setse; Vivien A Sheehan; John Strouse; Cheryl L Stucky; Ellen M Werner; John C Wood; William T Zempsky
Journal:  Blood Adv       Date:  2019-12-10

Review 10.  Key Components of Pain Management for Children and Adults with Sickle Cell Disease.

Authors:  Amanda M Brandow; Michael R DeBaun
Journal:  Hematol Oncol Clin North Am       Date:  2018-06       Impact factor: 3.722

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.