Sickle cell disease: A primary care update

被引：24

作者：

Onimoe, Grace ^{[1
,2
]}

Rotz, Seth ^{[3
,4
,5
]}

机构：

[1] Metrohlth Hosp, Dept Pediat, Cleveland, OH USA

[2] Case Western Reserve Univ, Cleveland, OH 44106 USA

[3] Cleveland Clin, Dept Pediat Hematol & Oncol, Cleveland, OH 44195 USA

[4] Cleveland Clin, Blood & Marrow Transplant Program, Cleveland, OH 44195 USA

[5] Case Western Reserve Univ, Cleveland Clin Lerner Coll Med, Cleveland, OH 44106 USA

来源：

CLEVELAND CLINIC JOURNAL OF MEDICINE | 2020年 / 87卷 / 01期

关键词：

BONE-MARROW-TRANSPLANTATION; SILENT CEREBRAL INFARCTS; VENOUS THROMBOEMBOLISM; PULMONARY-HYPERTENSION; ADULTS; MANAGEMENT; CHILDREN; PAIN; SURVIVAL; THERAPY;

D O I：

10.3949/ccjm.87a.18051

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Sickle cell disease (SCD) is the most common hemoglobinopathy in the United States and causes significant disease-related morbidity including multiorgan damage, chronic anemia, and debilitating pain crises. Primary care physicians play a key role in the medical home model of care for adults with SCD. This review focuses on current recommendations for health maintenance and provides a brief summary of disease complications and current updates.

引用

页码：19 / 27

页数：9

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