Caregiver factors related to emergency department utilization for youth with sickle cell disease

被引：8

作者：

Pantaleao, Ashley ^{[1
]}

DiPlacido, Joanne ^{[2
]}

Guite, Jessica W. ^{[3
]}

Zempsky, William T. ^{[4
]}

机构：

[1] Univ Maryland, Sch Publ Hlth, Dept Family Sci, College Pk, MD 20742 USA

[2] Cent Connecticut State Univ, Dept Psychol Sci, New Britain, CT 06050 USA

[3] Connecticut Childrens Med Ctr, Ctr Behav Hlth, Hartford, CT USA

[4] Connecticut Childrens Med Ctr, Div Pain & Palliat Med, Hartford, CT USA

来源：

CHILDRENS HEALTH CARE | 2019年 / 48卷 / 01期

关键词：

HEALTH-CARE; PARENT EXPERIENCE; PAIN; CHILDREN; ADOLESCENTS; BURDEN; VALIDATION; COMMUNICATION; PERSPECTIVES; STRATEGIES;

D O I：

10.1080/02739615.2018.1454838

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

This study addressed caregivers' stress, adjustment, and mechanisms related to treatment-seeking for children (age 6 to 16) with sickle cell disease (SCD). We hypothesized cues to action (i.e., perceived pain burden) would mediate relationships between psychosocial factors (i.e., stress, adjustment) and emergency department (ED) utilization. Perceived pain burden mediated relationships between stress that caregivers experience (a) communicating about SCD to their child and/or medical providers and (b) providing medical care for their child with ED utilization. Results suggest caregivers of children with SCD could benefit from interventions that enhance stress-management and communication skills with their child and health care providers.

引用

页码：59 / 74

页数：16

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