A Preliminary Investigation of the Psychometric Properties of PROMIS® Scales in Emerging Adults With Sickle Cell Disease

被引:12
作者
Hildenbrand, Aimee K. [1 ,2 ]
Quinn, Charles T. [3 ,4 ]
Mara, Constance A. [4 ,5 ]
Peugh, James L. [4 ,5 ]
McTate, Emily A. [4 ,5 ]
Britto, Maria T. [4 ,6 ]
Crosby, Lori E. [4 ,5 ]
机构
[1] Nemours Childrens Hlth Syst, Ctr Healthcare Delivery Sci, Rockland Ctr One,Suite 160,1600 Rockland Rd, Wilmington, DE 19803 USA
[2] Nemours Alfred I duPont Hosp Children, Div Behav Hlth, Wilmington, DE USA
[3] Cincinnati Childrens Hosp Med Ctr, Div Hematol, Cincinnati, OH 45229 USA
[4] Univ Cincinnati, Dept Pediat, Coll Med, Storrs, CT USA
[5] Cincinnati Childrens Hosp Med Ctr, Div Behav Med & Clin Psychol, Cincinnati, OH 45229 USA
[6] Cincinnati Childrens Hosp Med Ctr, Ctr Innovat Chron Dis Care, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
sickle cell disease; pain; fatigue; quality of life; young adults; GENERIC CORE SCALES; QUALITY-OF-LIFE; RELIABILITY; FEASIBILITY; CHILDREN; PEDSQL(TM)-4.0; ADOLESCENTS; VALIDITY; CARE;
D O I
10.1037/hea0000696
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: To report preliminary psychometric properties of PROMIS (R) assessments among emerging adults with sickle cell disease (SCD). Method: Forty-five emerging adults with SCD ages 18-24 (M = 20.81, SD = 1.73) completed PROMIS (R) Pain Interference and Fatigue short forms and the Pediatric Quality of Life Inventory (PedsQL). Chart review was used to obtain information regarding SCD complications and health care utilization in the 3 years prior to study enrollment. Multivariate path analysis was used to compare PROMIS (R) scores by disease severity and use of disease-modifying therapies. Cronbach's alpha was used to evaluate internal consistency, and Pearson correlations assessed convergent validity between PROMIS (R) measures and the PedsQL. Results: Internal consistency was excellent for PROMIS (R) Pain Interference (alpha =.95) and good for PROMIS (R) Fatigue (alpha =.85). Associations between PROMIS (R) measures and PedsQL subscales were in the expected direction and large in magnitude (all ps <.001). There were no differences in PROMIS (R) scores based on disease severity or use of disease-modifying therapy (ps =.14-.86). Conclusions: Findings provide preliminary evidence of validity and reliability of the PROMIS (R) Pain Interference and Fatigue short forms among emerging adults with SCD. Additional research is needed to replicate these findings in larger samples and assess sensitivity to change over time .
引用
收藏
页码:386 / 390
页数:5
相关论文
共 50 条
[41]   Health-related quality of life and adherence to hydroxyurea in adolescents and young adults with sickle cell disease [J].
Badawy, Sherif M. ;
Thompson, Alexis A. ;
Lai, Jin-Shei ;
Penedo, Frank J. ;
Rychlik, Karen ;
Liem, Robert I. .
PEDIATRIC BLOOD & CANCER, 2017, 64 (06)
[42]   Measuring Transition Readiness: A Correlational Study of Perceptions of Parent and Adolescents and Young Adults with Sickle Cell Disease [J].
Speller-Brown, Barbara ;
Kelly, Katherine Patterson ;
VanGraafeiland, Brigit ;
Feetham, Suzanne ;
Sill, Anne ;
Darbari, Deepika ;
Meier, Emily R. .
JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES, 2015, 30 (05) :788-796
[43]   Feasibility of Electronic Medication Monitoring Among Adolescents and Emerging Adults with Sickle Cell Disease [J].
Hildenbrand, Aimee K. ;
Kidwell, Katherine M. ;
Mcgrady, Meghan E. ;
Mara, Constance A. ;
Quinn, Charles ;
Crosby, Lori E. .
PATIENT PREFERENCE AND ADHERENCE, 2023, 17 :3167-3171
[44]   The performance of the PedsQL generic core scales in children with sickle cell disease [J].
Panepinto, Julie A. ;
Pajewski, Nicholas M. ;
Foerster, Lisa M. ;
Hoffmann, Raymond G. .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2008, 30 (09) :666-673
[45]   The Kennedy Krieger Independence Scales-Sickle Cell Disease: Executive Components of Transition Readiness [J].
Jones, Kelly E. ;
Jacobson, Lisa A. ;
Tarazi, Reem A. .
REHABILITATION PSYCHOLOGY, 2017, 62 (03) :249-257
[46]   Family caregiving for adults with sickle cell disease and extremely high hospital use [J].
Brown, Shan-Estelle ;
Weisberg, Daniel F. ;
Sledge, William H. .
JOURNAL OF HEALTH PSYCHOLOGY, 2016, 21 (12) :2893-2902
[47]   Subjective Well-being of Adults with Homozygous Sickle Cell Disease in Jamaica [J].
Thomas, J. A. ;
Lipps, G. E. .
WEST INDIAN MEDICAL JOURNAL, 2011, 60 (02) :181-187
[48]   Comparing the Effectiveness of Education Versus Digital Cognitive Behavioral Therapy for Adults With Sickle Cell Disease: Protocol for the Cognitive Behavioral Therapy and Real-time Pain Management Intervention for Sickle Cell via Mobile Applications (CaRISMA) Study [J].
Badawy, Sherif M. ;
Abebe, Kaleab Z. ;
Reichman, Charlotte A. ;
Checo, Grace ;
Hamm, Megan E. ;
Stinson, Jennifer ;
Lalloo, Chitra ;
Carroll, Patrick ;
Saraf, Santosh L. ;
Gordeuk, Victor R. ;
Desai, Payal ;
Shah, Nirmish ;
Liles, Darla ;
Trimnell, Cassandra ;
Jonassaint, Charles R. .
JMIR RESEARCH PROTOCOLS, 2021, 10 (05)
[49]   Stigma and quality of life in adults with sickle cell disease in Jamaica and the United States [J].
Bulgin, Dominique ;
Asnani, Monika ;
Vorderstrasse, Allison ;
Royal, Charmaine ;
Pan, Wei ;
Tanabe, Paula .
PSYCHOLOGY HEALTH & MEDICINE, 2023, 28 (05) :1133-1147
[50]   Cognitive considerations for adults with sickle cell disease completing the brief pain inventory [J].
O'Brien, Julia A. ;
Drake, Jermon A. ;
Bearden, Donald J. ;
Ono, Kim E. ;
Sil, Soumitri ;
Cohen, Lindsey L. ;
Karras, Alana ;
Novelli, Enrico M. ;
Jonassaint, Charles R. .
PAIN REPORTS, 2025, 10 (01)