首页> 外文期刊>Journal of cardiovascular electrophysiology >Sentinel symptoms in patients with unexplained cardiac arrest: From the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER)
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Sentinel symptoms in patients with unexplained cardiac arrest: From the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER)

机译:原因不明的心脏骤停患者的前哨症状:保留射血分数的心脏骤停幸存者(CASPER)

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Sentinel Symptoms in Unexplained Cardiac Arrest. Background: Warning symptoms may provide an opportunity to diagnose genetic disorders leading to preventative therapy. We explored the symptom history of patients with apparently unexplained cardiac arrest to determine the frequency of sentinel symptoms. Methods: Patients with apparently unexplained cardiac arrest and no evident cardiac disease underwent systematic clinical evaluation. Patients and first-degree relatives were interviewed to determine the presence of cardiac symptoms, and those with syncope underwent 2 structured Calgary Syncope Score questionnaires to determine the probable mechanism of syncope. Results: One hundred consecutive cardiac arrest patients (age 43.0 ± 13.4 years, 60% male) and 63 first-degree relatives (age 37.6 ± 16.3 years, 54% female) were enrolled. Previous cardiac symptoms were present in 69% of cardiac arrest patients compared to 43% of family members (P = 0.001). Prior syncope was present in 26% of cardiac arrest patients, compared to 22% of family members (P = 0.59). Twenty-four of 25 cardiac arrest patients who completed the syncope questionnaires had a syncope versus seizure score <1 favoring syncope. The area under the receiver operator curve (ROC) for the syncope mechanism score was 0.79 for identifying patients with subsequent cardiac arrest (95% CI, 0.6328-0.9395, P = 0.004). A score of ≤-2 had a sensitivity of 68% and specificity of 85%. Thirty percent of patients with a proven genetic cause had preceding syncope versus 19% in patients with noninherited or idiopathic causes (P = 0.032). Conclusions: Syncope that may represent a sentinel event is present in a modest proportion of patients and family members, and is often suggestive of an arrhythmia.
机译:无法解释的心脏骤停的前哨症状。背景:警告症状可能为诊断导致预防性治疗的遗传性疾病提供机会。我们探讨了明显原因不明的心脏骤停患者的症状史,以确定前哨症状的发生频率。方法:对明显无法解释的心脏骤停且无明显心脏病的患者进行系统的临床评估。采访患者和一级亲属以确定是否存在心脏症状,患有晕厥的患者接受2份结构化的卡尔加里Syncope Score问卷调查以确定晕厥的可能机制。结果:入选了100例连续性心脏骤停患者(年龄43.0±13.4岁,男性60%)和63名一级亲属(年龄37.6±16.3岁,女性54%)。 69%的心脏骤停患者出现过以前的心脏症状,而家庭成员中这一比例为43%(P = 0.001)。心脏骤停患者中有26%曾发生晕厥,而家庭成员中有22%(P = 0.59)。在完成晕厥问卷调查的25名心脏骤停患者中,有24名的晕厥与癫痫发作评分<1有利于晕厥。晕厥机制评分的接受者操作员曲线(ROC)下的面积为0.79,用于识别随后的心脏骤停患者(95%CI,0.6328-0.9395,P = 0.004)。分数≤-2的敏感性为68%,特异性为85%。遗传原因被证实的患者中有30%曾患有晕厥,而非遗传性或特发性原因中有19%曾患有晕厥(P = 0.032)。结论:可能代表前哨事件的晕厥存在于适度的患者和家属中,并且通常提示心律不齐。

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