首页> 外文期刊>European Journal of Haematology >Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)
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Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)

机译:在漫长的连续观察期(23.5年)中,因X因子缺乏症(主要针对FX Friuli)而导致的128位杂合子的出血表现与128位未受影响的家庭成员相匹配

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Objectives: The main objective of the study was to evaluate the incidence of bleeding manifestations in heterozygotes for FX deficiency vs. unaffected family members. Secondary objective was to compare the prevalence of arterial or venous diseases found in the two groups. Patients and methods: A total of 128 heterozygote patients for FX deficiency were investigated. A total of 102 patients had FX Friuli; 26 patients had other forms of FX deficiency. At time of diagnosis, each patient was paired with an unaffected family member, matched by gender and age (+/-5). Patients and their normal counterparts were checked every 12 yr for a mean period of 23.5 yr. The occurrence of bleeding manifestations was recorded and scored. The occurrence of arterial diseases and venous thrombosis was also recorded as a secondary finding. Results: A total of 38 heterozygote patients (29.7%) had one or more than one bleeding manifestation. The most frequent one was bleeding after tooth extraction or surgery. On the contrary, only three control subjects (2.3%) had documented hemorrhagic symptoms. There was a good correlation between bleeding and FX levels. Arterial disease (acute coronary syndromes, ischemic stroke, stable angina, peripheral arteries disease) was found in eight patients (6.3%) with FX deficiency and in seven unaffected subjects (5.5%). On the contrary, no venous thrombosis was seen in the affected group, whereas three cases (2.3%) of documented venous thrombosis were observed in the control group (two deep veins and one superficial vein). Conclusions: Heterozygotes FX deficiency may be accompanied by a mild bleeding tendency. This has important implications to assure a safe FX level in case of surgery or invasive procedures. Furthermore, mild FX deficiency seems to have no protective effect on arterial disease but does seem to protect from venous thrombosis.
机译:目的:该研究的主要目的是评估与缺乏影响的家庭成员相比,FX缺乏的杂合子出血表现的发生率。次要目的是比较两组中发现的动脉或静脉疾病的患病率。患者和方法:共调查了128名FX缺乏的杂合子患者。共有102名患者患有FX Friuli病; 26名患者患有其他形式的FX缺乏症。在诊断时,每位患者均与一个未受影响的家庭成员配对,并按性别和年龄(+/- 5)进行匹配。每12年检查一次患者及其正常的同伴,平均时间为23.5年。记录并记录出血表现的发生。动脉疾病和静脉血栓形成的发生也被记录为次要发现。结果:总共38例杂合子患者(29.7%)有一种或多种出血表现。最常见的是拔牙或手术后出血。相反,只有三个对照组(2.3%)有出血症状的记录。出血和FX水平之间存在良好的相关性。在八名FX缺乏的患者(6.3%)和七名未受影响的受试者(5.5%)中发现了动脉疾病(急性冠状动脉综合征,缺血性中风,稳定型心绞痛,外周动脉疾病)。相反,在患病组中未观察到静脉血栓形成,而在对照组中观察到三例(2.3%)已记录的静脉血栓形成(两条深静脉和一条浅静脉)。结论:杂合子FX缺乏可能伴有轻度出血倾向。这对于确保在外科手术或侵入性手术的情况下确保安全的FX水平具有重要意义。此外,轻度FX缺乏似乎对动脉疾病没有保护作用,但似乎可以预防静脉血栓形成。

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