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Descriptive Epidemiology of Hemophilia and Other Coagulation Disorders in Mansoura Egypt: Retrospective Analysis.

机译:埃及曼苏拉血友病和其他凝血障碍的描述性流行病学:回顾性分析。

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摘要

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 <1% of normal.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)的近亲结婚频率很高,因此常染色体隐性凝血功能障碍的患病率比其他许多国家更高。本研究的主要目的是描述埃及曼苏拉血友病的流行病学情况,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。第二个目标是评估这些患者的骨科并发症和丙型肝炎的发生率,并将此状况与研究之前接受的替代治疗类型相关联该研究包括2000年至2008年在MUCH注册的72例血液学疾病患儿。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正常水平的6-30%,则严重程度分类为轻度;如果正常水平为1%-5%,则严重度分类为中度;如果严重度<1%,则严重度分类为严重。严重程度占大多数的占76.7%,其次是中等严重度,占17.2%。最常见的IBD为A型血友病,影响44例患者,其次是B型血友病,影响15例患者。稀有类型为XI因子缺乏症,V因子缺乏症,VII因子缺乏症以及FVIII,FIX和FX合并缺乏症。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年幼儿童中发现IBDs可以预防关节病。适当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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