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对家族性蛛网膜下腔出血家族中的动脉瘤进行初始筛查和随访筛查。

Initial and follow-up screening for aneurysms in families with familial subarachnoid hemorrhage.

作者信息

Raaymakers T W, Rinkel G J, Ramos L M

机构信息

Department of Neurology, University Hospital Utrecht, The Netherlands.

出版信息

Neurology. 1998 Oct;51(4):1125-30. doi: 10.1212/wnl.51.4.1125.

Abstract

BACKGROUND AND OBJECTIVE

In families with two or more relatives with subarachnoid hemorrhage (SAH), other first-degree relatives have an increased risk of SAH. We studied the presence of unruptured intracranial aneurysms in 125 members of 23 families with familial SAH, defined as two or more affected first-degree relatives, in a cross-sectional design.

METHODS

MR angiography was performed in 116 relatives; CT angiography was performed in the remaining 9 relatives because they had been treated for intracranial aneurysms in the past.

RESULTS

Overall, we found 16 aneurysms in 10 of 125 relatives (8%; 95% CI, 4 to 14%). Of the nine patients with previous surgery for ruptured or unruptured intracranial aneurysms, three had new aneurysms. Two factors were associated with a significantly higher risk of intracranial aneurysms: 1) a history of treatment for ruptured or unruptured intracranial aneurysms (relative risk 5.5; 95% CI, 1.7 to 17.8) and 2) having three or more affected relatives (relative risk 3.3; 95% CI, 1.0 to 10.6). Siblings tended to have a higher risk of intracranial aneurysms than did children of SAH patients, although the difference was not significant.

CONCLUSIONS

Because the yield is high, screening is recommended in first-degree members of families with familial SAH. Repeated screening should be considered in relatives who have been treated for familial intracranial aneurysms.

摘要

背景与目的

在有两名或更多亲属患蛛网膜下腔出血(SAH)的家庭中,其他一级亲属患SAH的风险增加。我们采用横断面设计,研究了23个家族性SAH家庭(定义为两名或更多受影响的一级亲属)的125名成员中未破裂颅内动脉瘤的情况。

方法

对116名亲属进行了磁共振血管造影;其余9名亲属因过去曾接受过颅内动脉瘤治疗而进行了CT血管造影。

结果

总体而言,我们在125名亲属中的10名(8%;95%可信区间,4%至14%)中发现了16个动脉瘤。在9名曾因破裂或未破裂颅内动脉瘤接受手术的患者中,3名有新的动脉瘤。有两个因素与颅内动脉瘤风险显著较高相关:1)有破裂或未破裂颅内动脉瘤的治疗史(相对风险5.5;95%可信区间,1.7至17.8)和2)有三名或更多受影响的亲属(相对风险3.3;95%可信区间,1.0至10.6)。SAH患者的兄弟姐妹患颅内动脉瘤的风险往往高于其子女,尽管差异不显著。

结论

由于筛查阳性率高,建议对家族性SAH家庭的一级成员进行筛查。对于接受过家族性颅内动脉瘤治疗的亲属,应考虑重复筛查。

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