首页> 外文期刊>Mediterranean Journal of Hematology and Infectious Diseases >DESCRIPTIVE EPIDEMIOLOGY OF HEMOPHILIA AND OTHER COAGULATION DISORDERS IN MANSOURA , EGYPT
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DESCRIPTIVE EPIDEMIOLOGY OF HEMOPHILIA AND OTHER COAGULATION DISORDERS IN MANSOURA , EGYPT

机译:埃及曼苏拉的血友病和其他凝血障碍的描述性流行病学

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Hemophilia represent the most severe inherited bleeding disorder (INB) , it’s thought to affect inviduals from all geographical areas in equal frequency. In Egypt which has a population of approximately (80million) consanguineous marriage are frequent, therefore autosomal recessive coagulation disorders reach a higher prevalence than in many other countries. The primary aim of this study was to describe the epidemiological situation of hemophilia in Mansoura, Egypt ,as based on retrospective analysis of clinical records Mansoura University Children Hospital between years 2000 and 2008. The second aim was to assess the orthopedic complications and occurrence of hepatitis C in those patients and relate this status to the type of replacement therapy received prior to the study. The study included 72 children with hematological disorders registered from 2000 to 2008 in MUCH. The hemophilic patient was defined as a person with physician-diagnosed hemophilia A or B and a measured factor VIII or IX activity level of 30% or less. Persons with acquired inhibitors of FVIII or FIX excluded. Severity level was categorized as mild if the factor activity level was 6–30%, moderate if 1–5% and severe if The severe presentation represents the majority in 76.7% followed by moderate severity in 17.2%.The commonest IBDs was hemophilia A affecting 44 patients, followed by Hemophilia B affecting 15 patients. The rare types were Factor XI deficiency, Factor V deficiency, Factor VII deficiency and combined FVIII, FIX and FX deficiency. The commonest orthopedic manifestation needing therapy was found among hemophilia A representing 8.3%. Hepatitis C viremia detected by PCR was found in 11.1% of patients. The bleeding complications as hematoma or hemarthrosis were the common complications. Nevertheless, 44.4% of patients had no complications, From this study we can conclude that the most common IBDs in our locality is hemophilia A followed by hemophilia B. The common presenting symptom was bleeding following male circumcision. Hepatitis C infection and arthropathy represented the main complications. The discovery of IBDs in young age children with proper supportive therapy could prevent arthropathy. Proper screening of blood and blood products reduce the risk of viral hepatitis and HIV acquisition.
机译:血友病是最严重的遗传性出血性疾病(INB),据认为它会以相同的频率影响所有地理区域的个体。在埃及(约有8000万)人口,近亲结婚很频繁,因此常染色体隐性凝血障碍的患病率高于许多其他国家。这项研究的主要目的是基于对Mansoura大学儿童医院2000年至2008年之间临床记录的回顾性分析,描述埃及曼苏拉血友病的流行病学情况。第二个目的是评估骨科并发症和肝炎的发生C在这些患者中并将这种状态与研究前接受的替代治疗的类型相关联。该研究纳入了2000年至2008年在MUCH注册的72名血液学疾病患儿。血友病患者定义为经医生诊断为血友病A或B且测得的VIII或IX因子活性水平为30%或以下的人。排除获得性FVIII或FIX抑制剂的人。如果因子活性水平为6–30%,则严重程度为轻度;如果为1–5%,则程度为重度;如果严重程度为76.7%,则为严重;其次为中等程度,为17.2%。最常见的IBD是A型血友病44例患者,其次为B血友病患者,影响15例患者。稀有类型是XI因子缺乏,V因子缺乏,VII因子缺乏以及FVIII,FIX和FX合并缺乏。在血友病A中发现需要治疗的最常见的骨科表现,占8.3%。通过PCR检测到的丙型肝炎病毒血症在11.1%的患者中被发现。出血并发症为血肿或血栓形成是常见的并发症。尽管如此,仍有44.4%的患者没有并发症。根据这项研究,我们可以得出结论,我们所在地区最常见的IBD是血友病A,其次是血友病B。男性包皮环切术后常见的症状是出血。丙型肝炎感染和关节炎是主要并发症。在接受适当支持治疗的幼儿中发现IBDs可以预防关节病。正确筛查血液和血液制品可降低病毒性肝炎和HIV感染的风险。

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