Frequently Asked Questions by Hospitalists Managing Pain in Adults With Sickle Cell Disease

被引：18

作者：

Smith, Wally R. ^{[1
]}

Jordan, Lanetta B. ^{[2
]}

Hassell, Kathryn L. ^{[3
]}

机构：

[1] Virginia Commonwealth Univ, Div Gen Internal Med, Adult Sickle Cell Program, Dept Internal Med, Richmond, VA 23298 USA

[2] Sickle Cell Dis Assoc Amer Inc, Sickle Cell Serv, S Broward Hosp Dist, Mem Hlth Care Syst, Hollywood, FL USA

[3] Univ Colorado Denver, Hlth Sci Ctr, Colorado Sickle Cell Treatment & Res Ctr, Aurora, CO USA

来源：

JOURNAL OF HOSPITAL MEDICINE | 2011年 / 6卷 / 05期

关键词：

hematology; pain; multidisciplinary care; quality improvement; sickle cell disease; PATIENT-CONTROLLED ANALGESIA; MANAGEMENT; CHILDREN; ANEMIA; TRANSFUSIONS; PERCEPTIONS; HYDROXYUREA; LIMITATIONS; PATTERNS; INFUSION;

D O I：

10.1002/jhm.933

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Pain is the predominant medical presentation to hospitalists for patients with sickle cell disease (SCD). Dramatic treatment gains of SCD in childhood have resulted in more adults now requiring hospitalization than children. This has created new challenges to improve the quality of hospital care for SCD. The evidence base for pain management in SCD is lacking. We therefore offer some evidence and our informed opinion to answer frequently asked questions (FAQs) about pain management by hospitalists caring for adults with SCD. The most common questions center around defining a crisis; selecting and managing opioids; distinguishing between opioid tolerance, physical dependence, and addiction or misuse; determining appropriateness of discharge; and avoiding lengthy or recurrent hospitalizations. Journal of Hospital Medicine 2011;6:297-303. (C) 2011 Society of Hospital Medicine.

引用

页码：297 / 303

页数：7

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