Management of sickle cell pain crisis in the emergency department at teaching hospitals

被引:22
作者
Silbergleit, R
Jancis, MO
McNamara, RM
机构
[1] Univ Michigan, Sect Emergency Med, Dept Surg, Ann Arbor, MI 48109 USA
[2] MCP Hahnemann Univ, Dept Emergency Med, Philadelphia, PA USA
[3] Temple Univ, Dept Med, Sect Emergency Med, Philadelphia, PA 19122 USA
关键词
sickle cell anemia; pain crisis; emergency department; survey;
D O I
10.1016/S0736-4679(99)00050-5
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The purpose of this study is to determine the frequency and variety of strategies being used in the Emergency Department (ED) management of sickle cell pain crisis (SCPC), One thousand randomly selected academic emergency physicians received a multiple choice survey; 549 (55%) completed the survey. Forty-five percent of respondents treat patients with SCPC every week or almost every shift. Twenty percent use protocols for management of SCPC. Respondents consider pain refractory to outpatient treatment if it is persistent after two (23%) or three (53%) doses of parenteral analgesic. Meperidine or morphine is the most common initial analgesic. In the routine management of uncomplicated SCPC, i.v. analgesics, i.v. hydration, oxygen therapy, and complete blood counts are often or always used by 67, 71, 66, and 82% of respondents, respectively. Same patterns in the diagnostic and therapeutic management of patients with SCPC in the ED are identified, but overall practice is highly variable. Some popular elements of care are divergent from those suggested by the scientific Literature. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:625 / 630
页数:6
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