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患有青紫型先天性心脏病的成年患者的脑血管事件

Cerebrovascular events in adult patients with cyanotic congenital heart disease.

作者信息

Ammash N, Warnes C A

机构信息

Division of Cardiovascular Diseases and Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

J Am Coll Cardiol. 1996 Sep;28(3):768-72. doi: 10.1016/0735-1097(96)00196-9.

Abstract

OBJECTIVES

We sought to determine the frequency of spontaneous cerebrovascular events in adult patients with cyanotic congenital heart disease and to evaluate any contributing factors.

BACKGROUND

Cerebrovascular events are a serious complication of cyanotic congenital heart disease in infants and children but are said to be uncommon in adults.

METHODS

Between 1988 and 1995, 162 patients with cyanotic congenital heart disease (mean age 37 years, range 19 to 70) were retrospectively evaluated for any well documented cerebrovascular events that occurred at > or = 18 years of age. Events related to procedures, endocarditis or brain abscess were excluded.

RESULTS

Twenty-two patients (13.6%) had 29 cerebrovascular events (1/100 patient-years). There was no significant difference between those with and without a cerebrovascular event in terms of age, smoking history, degree of erythrocytosis, ejection fraction or use of aspirin or warfarin (Coumadin). Patients who had a cerebrovascular event had a significantly increased tendency to develop hypertension, atrial fibrillation, microcytosis (mean corpuscular volume < 82) and history of phlebotomy (p < 0.05). Even when patients with hypertension or atrial fibrillation were excluded, there was an increased risk of cerebrovascular events associated with microcytosis (p < 0.01).

CONCLUSIONS

Adults with cyanotic congenital heart disease are at risk of having cerebrovascular events. This risk is increased in the presence of hypertension, atrial fibrillation, history of phlebotomy and microcytosis, the latter condition having the strongest significance (p < 0.005). This finding leads us to endorse a more conservative approach toward phlebotomy and a more aggressive approach toward treating microcytosis in adults with cyanotic congenital heart disease.

摘要

目的

我们试图确定成年紫绀型先天性心脏病患者自发性脑血管事件的发生率,并评估相关因素。

背景

脑血管事件是婴幼儿紫绀型先天性心脏病的严重并发症,但据说在成年人中并不常见。

方法

回顾性评估1988年至1995年间162例紫绀型先天性心脏病患者(平均年龄37岁,范围19至70岁)在18岁及以上发生的任何有充分记录的脑血管事件。排除与手术、心内膜炎或脑脓肿相关的事件。

结果

22例患者(13.6%)发生了29次脑血管事件(每100患者年1次)。有脑血管事件和无脑血管事件的患者在年龄、吸烟史、红细胞增多程度、射血分数或使用阿司匹林或华法林(香豆素)方面无显著差异。发生脑血管事件的患者患高血压、房颤、小红细胞症(平均红细胞体积<82)和放血史的倾向显著增加(p<0.05)。即使排除高血压或房颤患者,小红细胞症仍与脑血管事件风险增加相关(p<0.01)。

结论

成年紫绀型先天性心脏病患者有发生脑血管事件的风险。在存在高血压、房颤、放血史和小红细胞症的情况下,这种风险会增加,后一种情况意义最为显著(p<0.005)。这一发现使我们赞同对成年紫绀型先天性心脏病患者放血采取更保守的方法,对治疗小红细胞症采取更积极的方法。

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