rhBNP联合Sacubitril/Valsartan序贯治疗肺心病肺动脉高压所致心力衰竭的疗效分析

    Analysis of the efficacy of rhBNP combined with Sacubitril/Valsartan sequential treatment for heart failure caused by pulmonary hypertension and pulmonary heart disease

    • 摘要: 目的:评价重组人脑利钠肽(rhBNP)联合沙库巴曲缬沙坦钠(Sacubitril/Valsartan)序贯治疗肺心病肺动脉高压所致心力衰竭的临床疗效。方法:收集继发性肺动脉高压合并肺心病所致心力衰竭病人170例临床资料,根据治疗方式分为观察组和对照组,各85例。对照组给予Sacubitril/Valsartan,观察组采用rhBNP联合Sacubitril/Valsartan序贯治疗,2组疗程均为6个月。比较2组病人临床疗效和症状体征改善情况,比较2组治疗前后肺功能指标第1秒用力呼气量(FEV1)、FEV1占用力肺活量百分比(FEV1/FVC)、肺动脉平均压、心功能指标左心室射血分数(LVEF)、左心室收缩末期内径(LVESD)、左心室舒张末期内径(LVEDD)和血清心肌标志物全血氨基末端脑钠肽前体(NT-proBNP)、血管紧张素转换酶2(ACE2)、心肌肌钙蛋白I(cTnI)变化情况。结果:观察组治疗总有效率为91.76%(78/85),明显高于对照组的75.29%(64/85)(P<0.01)。观察组咳嗽、水肿、发绀、啰音等症状体征消失时间和痰液恢复时间均明显短于对照组(P<0.01)。治疗后,观察组FEV1、FEV1/FVC、LVEF均明显高于对照组(P<0.01),肺动脉平均压、LVESD、LVEDD均明显低于对照组(P<0.01),心肌损伤标志物NT-proBNP、ACE2水平均明显高于对照组,cTnI明显低于对照组(P<0.01)。观察组不良反应发生率为7.06%(6/85),低于对照组的17.65%(15/85)(P<0.05)。结论:rhBNP联合Sacubitril/Valsartan序贯治疗继发性肺动脉高压合并肺心病所致心力衰竭的临床效果显著,有效提升心功能,减轻心肌损害,降低肺动脉压力,且安全可靠,值得进一步临床推广。

       

      Abstract: Objective: To evaluate the clinical efficacy of recombinant human brain natriuretic peptide(rhBNP) combined with Sacubitril/Valsartan in the sequential treatment of heart failure caused by pulmonary hypertension due to pulmonary heart disease. Methods: The clinical data of 170 patients with heart failure caused by secondary pulmonary hypertension complicated with pulmonary heart disease were collected.The patients were divided into the observation group and control group according to the treatment methods(85 cases in each group).The control group was treated with Sacubitril/Valsartan,while the observation group was treated with rhBNP combined with Sacubitril/Valsartan sequentially.The treatment course in two groups was 6 months.The clinical efficacy and improvement of symptoms and signs were compared between two groups.The pulmonary function indicatorsforced expiratory volume in one second(FEV1),percentage of FEV1 to forced vital capacity(FEV1/FVC),mean pulmonary artery pressure,cardiac function indicatorsleft ventricular ejection fraction(LVEF),left ventricular end-systolic diameter(LVESD),left ventricular end-diastolic diameter(LVEDD) and serum myocardium markerswhole blood N-terminal pro-brain natriuretic peptide(NT-proBNP),angiotensin-converting enzyme 2(ACE2) and cardiac troponin I(cTnI) before and after treatment were compared between two groups. Results: The total effective rate of treatment in the observation group was 91.76% (78/85),which was significantly higher than that in control group75.29%(64/85)(P<0.01).The disappearance time of symptoms and signs such as cough,edema,cyanosis and rales,and recovery time of sputum in the observation group were significantly shorter than those in control group(P<0.01).After treatment,the FEV1,FEV1/FVC and LVEF in the observation group were significantly higher than those in control group(P<0.01),the mean pulmonary artery pressure,LVESD and LVEDD were significantly lower than those in control group(P<0.01),the levels of myocardial injury markers NT-proBNP and ACE2 were significantly higher than those in control group,and the cTnI was significantly lower than that in control group(P<0.01).The incidence of adverse reactions in the observation group was 7.06%(6/85),which was lower than 17.65%(15/85) in the control group(P<0.05). Conclusions: The sequential treatment of rhBNP combined with Sacubitril/Valsartan for heart failure caused by secondary pulmonary hypertension complicated with pulmonary heart disease has a significant clinical effect.It can effectively improve the cardiac function,reduce the myocardial damage and lower the pulmonary artery pressure,and is safe and reliable.It is worthy of further clinical promotion.

       

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