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芪苈强心胶囊联合沙库巴曲缬沙坦治疗慢性心力衰竭的临床效果。

Clinical Effect of Qili Qiangxin Capsule Combined with Sacubitril-Valsartan in Patients with Chronic Heart Failure.

机构信息

Department of Cardiology, The First People's Hospital, Affiliated to Huzhou Normal College, Huzhou 313000, China.

Department of Nephrology, Central Hospital, Huzhou 313000, China.

出版信息

J Healthc Eng. 2022 Mar 23;2022:8598806. doi: 10.1155/2022/8598806. eCollection 2022.

Abstract

The clinical effect of Qili Qiangxin capsule combined with sacubitril-valsartan on patients with chronic heart failure was studied. We selected 108 patients with chronic heart failure in our hospital from March 2016 to January 2020 and divided them into a control group and a study group according to the random table method, with 54 cases in each. The control group took sacubitril and valsartan orally, and the study group took Qili Qiangxin pill on the basis of sacubitril and valsartan. The course of the treatment for 2 groups is 4 weeks. We compared the total effective rate of the treatment of the 2 groups for 4 weeks, cardiac function (left ventricular end-systolic volume (LVESV), left ventricular end-diastolic volume (LVEDV), and left ventricular ejection fraction (LVEF)) before and after 4 weeks of treatment, 6 min walking distance (6MWT), changes in cTnI and NT-proBNP levels, and adverse reactions. The total effective rate in the study group (90.74%) is higher than that in the control group (72.22%) (<0.05). After 4 weeks of treatment, the study group LVESV (45.23 ± 2.98 mm) and LVEDV (43.38 ± 4.01 mm) are lower than those of the control group ((49.98 ± 2.56 mm) and (50.75 ± 3.49 mm), respectively), while LVEF (47.38 ± 2.78%) is higher than that in the control group (42.08 ± 3.24%) ( < 0.05). After 4 weeks of treatment, the study group 6MWT (476.58 ± 31.25 ) of patients with chronic heart failure is higher than that of the control group (396.52 ± 24.52 ) (P <0.05). After 4 weeks of treatment, the study group serum cTnI (0.36 ± 0.12 g/L) and NT-proBNP (276.91 ± 30.12 pg/ml) of patients with chronic heart failure are lower than those in the control group (0.87 ± 0.25 g/L) and (367.48 ± 48.57 pg/ml) (<0.05). There is no significant difference between the adverse reactions in the two groups ( > 0.05). Conclusion: Xinbao pills combined with sacubitril and valsartan have a good effect on patients with chronic heart failure, which can improve the heart function and exercise endurance and reduce serum cTnI and NT-proBNP levels.

摘要

研究了芪苈强心胶囊联合沙库巴曲缬沙坦治疗慢性心力衰竭的临床效果。我们选取了 2016 年 3 月至 2020 年 1 月我院收治的 108 例慢性心力衰竭患者,按照随机表法分为对照组和观察组,各 54 例。对照组采用沙库巴曲缬沙坦口服治疗,观察组在沙库巴曲缬沙坦基础上加用芪苈强心胶囊治疗。两组疗程均为 4 周。比较两组治疗 4 周的总有效率,治疗前后 4 周的左心室收缩末期容积(LVESV)、左心室舒张末期容积(LVEDV)、左心室射血分数(LVEF),6 分钟步行距离(6MWT),cTnI 和 NT-proBNP 水平变化及不良反应。观察组总有效率(90.74%)高于对照组(72.22%)(<0.05)。治疗 4 周后,观察组 LVESV(45.23±2.98mm)和 LVEDV(43.38±4.01mm)低于对照组((49.98±2.56mm)和(50.75±3.49mm)),LVEF(47.38±2.78%)高于对照组(42.08±3.24%)(<0.05)。治疗 4 周后,观察组慢性心力衰竭患者 6MWT(476.58±31.25)高于对照组(396.52±24.52)(P<0.05)。治疗 4 周后,观察组慢性心力衰竭患者血清 cTnI(0.36±0.12g/L)和 NT-proBNP(276.91±30.12pg/ml)低于对照组(0.87±0.25g/L)和(367.48±48.57pg/ml)(<0.05)。两组不良反应发生率无统计学差异(>0.05)。结论:芪苈强心胶囊联合沙库巴曲缬沙坦治疗慢性心力衰竭效果较好,可改善心功能和运动耐力,降低血清 cTnI 和 NT-proBNP 水平。

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