Management of Acute Complications of Sickle Cell Disease.

IF 1.1 4区 医学 Q3 PEDIATRICS Pediatric Annals Pub Date : 2024-02-01 DOI:10.3928/19382359-20231205-03
Sabina Shamayeva, Perry Morocco
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Abstract

Sickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. This leads to varied acute and chronic complications for patients with SCD. Here, we review some of the acute complications of SCD with focus on diagnosis and management. [Pediatr Ann. 2024;53(2):e47-e51.].

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镰状细胞病急性并发症的处理。
镰状细胞病(SCD)是一组影响血红蛋白结构的常染色体隐性遗传疾病。血红蛋白 S 这种变异形式的存在会导致细胞形状异常("镰刀形")。这些镰状红细胞会导致小血管中的血流中断,并引发多种并发症。这种疾病的特点是疼痛难忍且难以预测。此外,许多器官都会受到影响,包括但不限于大脑、肾脏、骨骼和肺部。这导致 SCD 患者出现各种急性和慢性并发症。在此,我们回顾了 SCD 的一些急性并发症,重点是诊断和处理。[2024; 53(2):e47-e51.].
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来源期刊
Pediatric Annals
Pediatric Annals 医学-小儿科
CiteScore
1.80
自引率
0.00%
发文量
104
审稿时长
2 months
期刊介绍: Published for more than 40 years, Pediatric Annals is an online-only, monthly medical review journal dedicated to providing pediatricians and other clinicians with the latest practical information on the diagnosis and treatment of pediatric diseases and disorders. Begin to explore the Journal and all of its great benefits such as: -Single-topic summary reviews of important trends in pediatric medicine -Access to current articles, as well as several years of archived content -Columns including Healthy Baby/Healthy Child and Case Challenges
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