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心尖肥厚型心肌病患者的心律失常特點研究

2019-05-28 11:32:42秦淑娟
中外醫療 2019年5期

秦淑娟

[摘要] 目的 從生化指標表達、超聲心動圖表現及預后3方面分析心尖肥厚型心肌病患者合并發生心律失常后的特點。 方法 方便選取2013年4月—2015年10月期間北京阜外醫院/成都市第三人民醫院收治的87例心尖肥厚型心肌病患者作為研究對象,根據是否合并心律失常將87例患者分為觀察組(合并心律失常)和對照組(未合并心律失常),收集兩組患者生化指標檢測結果、超聲心動圖檢查結果、臨床治療及預后資料,進行數據統計分析,從上述3個方面總結心尖肥厚型心肌病患者的心律失常特點。 結果 觀察組合并心律失常的類型包括心房撲動、竇性心動過緩、心房顫動、室性心律失常、房室傳導阻滯。生化指標,觀察組患者的TG為(1.53±0.35)mmol/L,低于對照組的為(2.30±0.39)mmol/L(t=6.571;P<0.05),NT-pro BNP為(2.93±0.35)pmol/L,高于對照組的(2.26±0.41)pmol/L(t=5.558;P<0.05),其他生化指標檢測結果比較差異無統計學意義(P>0.05)。超聲心動圖檢查結果,觀察組中心律失常組類型為心房顫動的患者左心房前后徑為(40.05±5.02)mm,大于對照組患者的(34.91±4.88)mm(t=3.283;P<0.05)。其他參數比較差異無統計學意義(P>0.05)。觀察組患者隨訪期間的心臟不良事件發生率為8.16%、死亡率為4.08%,與對照組患者的5.26%、2.63%比較差異無統計學意義(χ2=0.713、0.135,P>0.05)。 結論 心律失常作為心尖肥厚型心肌病患者的常見臨床表現,類型較多,包括心房撲動、竇性心動過緩、室性心律失常等,但合并發生后并不會出現較多特異性表現,對患者預后無明顯影響。

[關鍵詞] 心尖肥厚型心肌病;超聲心動圖;生化指標

[中圖分類號] R542.2 [文獻標識碼] A [文章編號] 1674-0742(2019)02(b)-0025-03

Arrhythmia Characteristics in Patients with Apical Hypertrophic Cardiomyopathy

QIN Shu-juan

Institute of Cardiovascular Diseases, Chengdu Third People's Hospital, Chengdu, Sichuan Province, 610031 China

[Abstract] Objective To analyze the characteristics of arrhythmia patients with apical hypertrophic cardiomyopathy after biochemical index expression, echocardiographic findings and prognosis. Methods From April 2013 to October 2015, 87 patients with apical hypertrophic cardiomyopathy admitted to Beijing Fuwai Hospital/Chengdu Third People's Hospital were convenient included in the study. 87 patients were divided into observation group according to whether or not they had arrhythmia combined arrhythmia and control group (without arrhythmia), biochemical indicators, echocardiography, clinical treatment and prognosis data were collected from two groups, and statistical analysis was performed. The apical hypertrophic myocardium was summarized from the above three aspects. Arrhythmia characteristics of patients. Results The types of combined arrhythmias were observed including atrial flutter, sinus bradycardia, atrial fibrillation, ventricular arrhythmia, and atrioventricular block. The TG of the observation group was (1.53±0.35) mmol/L, which was lower than that of the control group (2.30±0.39) mmol/L (t=6.571; P<0.05), and NT-pro BNP was (2.93±0.35) pmol/L, which was higher than that of the control group (2.26±0.41) pmol/L (t=5.558; P<0.05). There was no significant difference between the other biochemical indicators (P>0.05). According to the results of echocardiography, the left atrial anteroposterior diameter of the patients with atrial fibrillation in the observation group was (40.05±5.02) mm, which was greater than that of the control group (34.91±4.88) mm (t=3.283; P<0.05). There were no significant differences in other parameters (P>0.05). The incidence of cardiac adverse events during the follow-up period was 8.16% and the mortality rate was 4.08%. There was no significant difference between the control group of (5.26%, 2.63%) (χ2=0.713, 0.135, P>0.05). Conclusion Arrhythmia is a common clinical manifestation of patients with apical hypertrophic cardiomyopathy. There are many types, including atrial flutter, sinus bradycardia, ventricular arrhythmia, etc., but there will be no more specific manifestations after the merger. There is no significant effect on the prognosis of patients.

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