Key Components of Pain Management for Children and Adults with Sickle Cell Disease

被引：44

作者：

Brandow, Amanda M. ^{[1
]}

DeBaun, Michael R. ^{[2
]}

机构：

[1] Med Coll Wisconsin, MFRC, Dept Pediat, Sect Pediat Hematol Oncol, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA

[2] Vanderbilt Univ, Sch Med, Med Ctr, Dept Pediat, 2200 Childrens Way,Ste 11101, Nashville, TN 37232 USA

来源：

HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA | 2018年 / 32卷 / 03期

基金：

美国国家卫生研究院;

关键词：

Sickle cell disease; Acute pain; Chronic pain syndrome; Opioids; Depression; Anxiety; Sleep; PATIENT-CONTROLLED ANALGESIA; RANDOMIZED CONTROLLED-TRIAL; CARE UTILIZATION; DEPRESSION; QUESTIONNAIRE; VALIDATION; INVENTORY; OUTCOMES; SCALE; SEVERITY;

D O I：

10.1016/j.hoc.2018.01.014

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Sickle cell disease pain manifests as severe acute pain episodes and a debilitating chronic pain syndrome. Acute pain episodes are the most common reason for health care use; however, acute pain episodes are also frequently managed at home. Chronic pain syndrome develops in 30% to 40% of individuals with sickle cell disease, with an increasing incidence and severity with age. The authors review the critical aspects of pain management that are integral to the comprehensive approach to sickle cell disease pain and are rooted in the biopsychosocial model. The article focuses on opioid pharmacology and psychosocial comorbidities.

引用

页码：535 / +

页数：17

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