苏丹儿童镰状细胞病:并发症和管理。

IF 2.2 Q3 HEMATOLOGY Anemia Pub Date : 2022-02-14 eCollection Date: 2022-01-01 DOI:10.1155/2022/3058012
Meysaa Talha, Bashier Osman, Safa Abdalla, Hind Mirghani, Iman Abdoon
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引用次数: 2

摘要

背景:镰状细胞病(SCD)是一种危及生命的遗传性疾病,由于镰状血红蛋白分子(HbS)的形成在缺氧条件下聚合导致SCD相关并发症。不同的方法已被用于SCD的管理,包括症状管理,支持管理和预防管理。目的:评估苏丹喀土穆地区Gaafar Ibnauf转诊医院儿科患者SCD的处理。方法:在Gaafar Ibnauf医院使用数据收集表进行了一项描述性、回顾性、基于医院的研究。该研究包括2018年4月1日至2018年7月1日期间在该医院就诊的SCD儿科患者的所有医疗档案。采用描述性统计和卡方检验对资料进行分析。P < 0.05为差异有统计学意义。结果:207例患儿中,女性占53.1%(平均年龄7.5±3.1岁),男女比例为1.1:1,社会经济地位低。只有4.3%的参与者有医疗保险。苏丹西部的梅塞里亚部落在苏丹部落中发病率最高(11.1%)。血管闭塞危像(33.3%)、感染(13.5%)和神经系统并发症(10.6%)是常规就诊中最常见的并发症。治疗开始后,仅有3.4%的患儿出现溶血危像,1.4%的贫血患者出现脾肿大。100%的患者接受叶酸治疗,73.9%的患者使用羟基脲,69.6%的患者接受输血治疗。15%的患者开具了预防性青霉素处方,41.1%的患者接种了肺炎球菌疫苗(PPSV23)。大多数患者计划每3-6个月随访一次(93.2%)。羟脲和输血可显著降低发热和血管闭塞危象。结论:Gaafar Ibnauf儿童医院的SCD治疗方案包括预防和对症治疗,与国际上实施的SCD治疗方案一致。然而,免疫和预防性青霉素方法是有缺陷的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pediatric Sickle Cell Disease in Sudan: Complications and Management.

Background: Sickle cell disease (SCD) is a life-threatening genetic disorder due to the formation of sickle hemoglobin molecule (HbS) that polymerizes in hypoxic conditions leading to SCD-related complications. Different approaches have been used in the management of SCD including symptomatic management, supportive management, and preventive management.

Objectives: To assess the management of SCD in pediatric patients in Gaafar Ibnauf Referral Hospital in Khartoum locality, Sudan.

Method: A descriptive, retrospective, hospital-based study was conducted in Gaafar Ibnauf Hospital using a data collection sheet. The study included all medical files of pediatric patients with SCD attending the hospital during the period from the first of April 2018 to the first of July 2018. The data were analyzed using descriptive statistics and the chi-square test. P < 0.05 was considered statistically significant.

Results: Out of 207 pediatric patients, 53.1% were females (mean age of 7.5 ± 3.1 years), with a 1.1 : 1 female:male ratio and low socioeconomic status. Only 4.3% of participants had health insurance. The Messeryia tribe in western Sudan had the highest prevalence of the disease among the Sudanese tribes (11.1%). Vaso-occlusive crisis (33.3%), infections (13.5%), and neurological complications (10.6%) were the most frequent complications reported during routine visits. After initiation of management, only 3.4% of pediatric patients had hemolytic crises, and 1.4% of the anemic patients had splenomegaly. 100% of patients received folic acid, 73.9% used hydroxyurea, and 69.6% underwent blood transfusion for the management of SCD. Prophylactic penicillin was prescribed for 15% of patients, and 41.1% were immunized with pneumococcal vaccine (PPSV23). Most patients had been scheduled for planned follow-up visits every 3-6 months (93.2%). Hydroxyurea and blood transfusion significantly reduced fever and vaso-occlusive crisis.

Conclusion: The SCD treatment protocol in Gaafar Ibnauf Children's Hospital, involving preventive and symptomatic therapy, is consistent with the internationally implemented protocols for SCD management. However, immunization and prophylactic penicillin approaches are deficient.

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来源期刊
Anemia
Anemia HEMATOLOGY-
CiteScore
4.80
自引率
3.40%
发文量
11
审稿时长
18 weeks
期刊介绍: Anemia is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies on all types of anemia. Articles focusing on patient care, health systems, epidemiology, and animal models will be considered, among other relevant topics. Affecting roughly one third of the world’s population, anemia is a major public health concern. The journal aims to facilitate the exchange of research addressing global health and mortality relating to anemia and associated diseases.
期刊最新文献
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