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. 2014 Mar;15(1):324-30.
doi: 10.1016/j.pmn.2012.10.007. Epub 2013 Jan 21.

Care seeking for pain in young adults with sickle cell disease

Coretta M Jenerette  1 , Cheryl A Brewer  2 , Kenneth I Ataga  3
Affiliations

Care seeking for pain in young adults with sickle cell disease

Coretta M Jenerette et al. Pain Manag Nurs. 2014 Mar.

Abstract

In individuals with sickle cell disease (SCD), recognizing the cues to an acute pain episode and responding appropriately are important. The purpose of this mixed-methods pilot study is to identify preliminary factors that influence care seeking for pain in young adults with SCD. Responses were received from 69 young adults with SCD, age 18-35 years. The majority of respondents (88%) wait until the pain intensity is an average of 8.7 (± 1.2) on a scale of 1 to 10 before seeking care. Prominent themes influencing care seeking for pain include: trying to treat pain at home, avoiding the emergency department because of past treatment experiences, the desire to avoid admission to the hospital, and the importance of time in the lives of the young adults with SCD. Young adults with SCD need additional support from family and healthcare providers in order to make timely, appropriate decisions regarding care seeking.

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Figure 1
Theory of Self-Care Management for Sickle Cell Disease.
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