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Clinical effect of Diltiazem combined with Digoxin in the treatment of rheumatic heart disease complicated with rapid atrial fibrillation |
SUN Liang-zhen, FANG Zhen |
Department of Cardiovascular Medicine,People′s Hospital of Yudu County,Jiangxi Province,Yudu 342300,China |
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Abstract Objective To observe the clinical effect of Diltiazem combined with Digoxin in the treatment of rheumatic heart disease with rapid atrial fibrillation.Methods Forty patients with rheumatic heart disease and rapid atrial fibrillation admitted into our hospital from January 15th,2016 to March 12th,2017 were selected in this study.They were evenly divided into two groups in random,observation group was treated by Diltiazem combined with Digoxin,and control group was only treated by Digoxin.The total clinical effective rate,quality of life,incidence of adverse reactions,and improvement of cardiac function were observed in the two groups.Results The total clinical effective rate was 95.00% in the observation group,much higher than that in the control group accounting for 60.00% (P<0.05).In the observation group,the scores of quality of life including physiological function,social function,psychological function,and material life were (91.44±6.33),(90.26±6.25),(88.43±5.45) points,and (90.35±6.30) points respectively,was higher than that in the control group [(72.45±4.25),(70.15±4.20),(71.21±4.22),(75.34±4.30) points] (P<0.05).The incidence of adverse reactions in the observation group was 5.00%,lower than that in the control group accounting for 35.00% (P<0.05).The improvement of cardiac function in the observation group was 8 cases in grade Ⅰ and 12 cases in grade Ⅱ,which was superior to those in the control group,5 cases in grade Ⅰ and 15 cases in grade Ⅱ(P<0.05).Conclusion Diltiazem combined with Digoxin in the treatment of rheumatic heart disease complicated with rapid atrial fibrillation obtains a remarkable clinical effect,not only ensures the therapeutic effect,but also reduces the incidence of adverse reactions,which has a value for clinical promotion.
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Received: 27 June 2017
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