Literature DB >> 20064892

Pain, coping and health care utilization in younger and older adults with sickle cell disease.

Kathryn A Sanders1, Susan M Labott, Robert Molokie, Sarah R Shelby, Joseph Desimone.   

Abstract

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.

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Year:  2010        PMID: 20064892     DOI: 10.1177/1359105309345554

Source DB:  PubMed          Journal:  J Health Psychol        ISSN: 1359-1053


  13 in total

1.  Outpatient pain predicts subsequent one-year acute health care utilization among adults with sickle cell disease.

Authors:  Miriam O Ezenwa; Robert E Molokie; Zaijie Jim Wang; Yingwei Yao; Marie L Suarez; Veronica Angulo; Diana J Wilkie
Journal:  J Pain Symptom Manage       Date:  2014-03-15       Impact factor: 3.612

2.  Bodily pain and coping styles among four geriatric age groups of women.

Authors:  Luciana Laganà; Christina Marie Hassija
Journal:  J Health Psychol       Date:  2011-09-26

3.  Perceived injustice predicts stress and pain in adults with sickle cell disease.

Authors:  Miriam O Ezenwa; Robert E Molokie; Diana J Wilkie; Marie L Suarez; Yingwei Yao
Journal:  Pain Manag Nurs       Date:  2014-10-31       Impact factor: 1.929

4.  Sickle cell disease in adults: developing an appropriate care plan.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  Clin J Oncol Nurs       Date:  2015-10       Impact factor: 1.027

5.  Acceptability and Feasibility of a Mindfulness-Based Intervention for Pain Catastrophizing among Persons with Sickle Cell Disease.

Authors:  Leigh Ann Simmons; Hants Williams; Susan Silva; Francis Keefe; Paula Tanabe
Journal:  Pain Manag Nurs       Date:  2019-05-10       Impact factor: 1.929

6.  The association of optimism and perceived discrimination with health care utilization in adults with sickle cell disease.

Authors:  Michael V Stanton; Charles R Jonassaint; Frederick B Bartholomew; Christopher Edwards; Laura Richman; Laura DeCastro; Redford Williams
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

7.  Health-related stigma in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

8.  Voices of Adults Living with Sickle Cell Disease Pain.

Authors:  Maxine A Adegbola; Donelle M Barnes; Jakki G Opollo; Keela Herr; Jennifer Gray; Ann Marie McCarthy
Journal:  J Natl Black Nurses Assoc       Date:  2012-12

9.  Coping with Pain in the Face of Healthcare Injustice in Patients with Sickle Cell Disease.

Authors:  Miriam O Ezenwa; Yingwei Yao; Robert E Molokie; Zaijie Jim Wang; Molly W Mandernach; Marie L Suarez; Diana J Wilkie
Journal:  J Immigr Minor Health       Date:  2017-12

10.  Self-care recommendations of middle-aged and older adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer; Ashley N Leak
Journal:  Nurs Res Pract       Date:  2011-08-15
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