Parental information, motivation, and adherence behaviors among children with sickle cell disease

医学 社会心理的 心理干预 疾病 家庭医学 社会支持 医疗保健 可能性 有序逻辑 病历 临床心理学 逻辑回归 精神科 心理学 机器学习 计算机科学 内科学 经济 心理治疗师 经济增长 病理 放射科
作者
Jean L. Raphael,Ashley M. Butler,Tiffany L. Rattler,Marc Kowalkowski,Brigitta U. Mueller,Thomas P. Giordano
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:60 (7): 1204-1210 被引量:18
标识
DOI:10.1002/pbc.24466
摘要

Abstract Background Identification of psychosocial correlates of health care utilization has become an important strategy in improving clinical care. The objective of the study was to examine the fit of the Information‐Motivation‐Behavioral Skills (IMB) model, applied to health care utilization among children with sickle cell disease (SCD). Procedure Participants were parents of 150 children, ages 1–17 years, receiving care in a sickle cell center. Parents completed questionnaires assessing information, motivation, adherence behaviors, and other factors with respect to SCD management. Data regarding health care utilization in the previous 12 months were obtained from parent report and electronic medical records. Stepwise multiple regression analysis was conducted to determine associations between IMB factors and health care use. Results Parents rated highly in the domains of information, motivation, and adherence behaviors for managing their child's SCD. Children of parents reporting higher satisfaction with social supports had higher odds (OR 1.49, 95% CI 1.03–2.15) of two or more routine hematology visits in the previous 12 months. Neither information nor adherence behavior was associated with urgent or routine care use. Among other variables measured, high parental illness‐related stress and child health status reported as fair/poor were the strongest predictors of urgent care use while private insurance type was the strongest predictor of routine care use. Conclusions Among IMB factors, social support was associated with routine health care utilization. Social support and parental illness‐related stress may serve as important, modifiable targets in interventions to allocate needed resources to families and reduce unnecessary medical care. Pediatr Blood Cancer 2013; 60: 1204–1210. © 2013 Wiley Periodicals, Inc.
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