Pain, Coping and Health Care Utilization in Younger and Older Adults with Sickle Cell Disease

被引:29
|
作者
Sanders, Kathryn A. [1 ,2 ]
Labott, Susan M. [3 ]
Molokie, Robert [3 ,4 ]
Shelby, Sarah R. [3 ]
Desimone, Joseph [3 ,4 ]
机构
[1] VA Connecticut Healthcare Syst, Psychol Serv 116B, West Haven, CT 06516 USA
[2] Yale Univ, Sch Med, New Haven, CT 06520 USA
[3] Univ Illinois, Chicago, IL 60680 USA
[4] Jesse Brown VA Med Ctr, Chicago, IL USA
关键词
coping; health care utilization; pain; sickle cell disease; RECEIVING PRIMARY-CARE; STRATEGIES; ADJUSTMENT; STRESS; DETERMINANTS; LIFE;
D O I
10.1177/1359105309345554
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Sickle cell disease is characterized by acute pain crises. Pain, chronic medical problems, utilization and coping were compared in younger vs older patients using questionnaires and medical record review. Groups reported similar pain intensity and medical conditions. The pattern of utilization differed such that older patients attended outpatient clinic, and younger patients went to the Emergency Department. Younger patients were more likely to cope by ignoring pain, or by using heat, cold or massage. Older patients were more likely to pray and hope. We conclude that age plays an important role in the utilization and coping of sickle cell patients.
引用
收藏
页码:131 / 137
页数:7
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