2017年沙特阿拉伯Makkah Al-Mukaramah地区镰状细胞病并发症患病率调查

Mohammad M. Alkot, Walaa A Almaghrabi, Noura A. Al-Najdi, Mohammad Al-Otaibi, M. Shatla, H. Abdelbaki
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引用次数: 14

摘要

背景:对中东阿拉伯人的研究发现,镰状细胞病(SCD)在世界人口快速增长和近亲婚姻增加的地区更为普遍存在特定的危险因素。尽管如此,在Makkah Al-Mukarramah甚至在沙特阿拉伯(KSA)的所有地区都没有进行过关于SCD并发症及其相关危险因素的研究。目的:确定2017年沙特阿拉伯Makkah Al-Mukaramah儿童SCD的入院模式并估计其不同并发症的患病率。患者和方法:在沙特阿拉伯的Makkah Al- Mukaramah进行了一项回顾性、分析性、非介入性队列研究,为期6个月(2017年6月1日至2017年12月底)。该研究回顾了在给定时间内所有被相关医院儿科收治的病情较重的患者的医疗档案。合并地中海贫血和/或葡萄糖6磷酸脱氢酶缺乏症(G6PD)的患者被排除在研究之外。所需要的数据是通过使用设计良好、半结构化、有效和可靠的核对表的硬拷贝来收集的。结果:本研究纳入145例小儿SCD患者的医疗档案。年龄1 ~ 14岁,平均±SD为7±3.6岁。其中男性占54.5%。几乎三分之二的患者(67.6%)是沙特人。所有居住在麦加以外的病例(n=5)均被诊断为镰状细胞性贫血合并血管闭塞危象(VOC),而居住在麦加的患者中有47.1%在入院时被诊断为VOC。最常见的并发症是VOC(55.9%),其次是感染(9%)。总体而言,41.4%的SCA儿科患者入院一次,而25.5%的患者入院超过5次。在3.1%的沙特患者中报告了急性脾隔离危机,而非沙特患者的这一比例为12.8%。这一差异具有统计学意义。其他并发症与患者国籍无显著相关性。结论:SCD最常见的并发症是VOC。SCD急性并发症的初级预防应基于具有SCD专业知识的卫生保健提供者,最好是血液科医生。除了通过在新生儿时期开始使用青霉素预防并发症、适当的免疫接种和对有中风危险的人输血来预防并发症外。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of Complications of Sickle Cell Disease at Makkah Al-Mukaramah, Saudi Arabia, 2017
Background: The studies in the Middle East Arabs have found that there are specific risk factors making Sickle cell disease (SCD) more prevalent in that part of the world, which has the fast growing in the population and the increase in consanguinity marriage. Despite of that, there are no studies conducted in Makkah Al-Mukarramah or even in all Saudi Arabia (KSA) regions that, focusing on the complications of SCD and its related risk factors. Objectives: To determine the pattern of admission and estimate the prevalence of different complications of SCD among children in Makkah Al-Mukaramah, KSA, 2017. Patients and methods: A retrospective, analytic, noninterventional cohort study was carried out in Makkah Al- Mukaramah, KSA over a 6 months period (from first of June 2017 to end of December 2017). The study reviewed the medical files of all sickler patients who have been admitted to the pediatric departments of the involved hospitals in the given time. Records of patients having combined thalassemia disease and/or Glucose 6 Phosphate Dehydrogenase Deficiency (G6PD) were excluded from the study. The required data were collected by using hard copies of a well-designed, semi-structured, valid and reliable checklist. Results: The study included 145 medical files of pediatric patients with SCD. Their age ranged between one day to 14 years with a Mean ± SD of 7 ± 3.6 years. Males represent 54.5% of them. Almost two-thirds of patients (67.6%) were Saudis. All cases live outside Makkah (n=5) were diagnosed as Sickle cell anemia with Vaso-occlusive crisis (VOC) whereas 47.1% of those live in Makkah were diagnosed by VOC at admission. The most frequent complication was VOC (55.9%), followed by infection (9%). Overall, 41.4% of SCA pediatric patients were admitted once whereas 25.5% were admitted more than 5 times. Acute splenic sequestration crisis was reported among 3.1% of Saudi patients compared to 12.8% of non-Saudi patients. This difference was statistically significant. Other complications were not significantly related to patients` nationality. Conclusion: The most frequent complication of SCD was VOC. Primary prevention of the acute complications of SCD should base on health care provider with expertise in SCD, preferably hematologist. In addition to prevention of complications through the use of penicillin prophylaxis started in the newborn period, appropriate immunizations, and blood transfusions for those at risk for stroke.
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