Zhong Huaping, Yin Xiaoshu
Department of Cardiovascular Medicine, The First Affiliated Hospital of Gannan Medical University Ganzhou 341000, Jiangxi, China.
Department of Cardiovascular Medicine, Ganzhou People's Hospital Ganzhou 341000, Jiangxi, China.
Am J Transl Res. 2023 May 15;15(5):3539-3547. eCollection 2023.
To compare the efficacy and safety of nicorandil monotherapy and nicorandil-clopidogrel combination therapy on cardiac function in patients with coronary heart disease (CHD).
The clinical data of 200 patients with CHD were retrospectively analyzed. The patients were divided into two groups according to different treatment methods. Group A (n = 100) received nicorandil-clopidogrel combination therapy (intravenously injected with 25 mg of nicorandil and orally administered 300 mg of clopidogrel for 3 months), and Group B (n = 100) received nicorandil monotherapy (intravenously injected with 25 mg of nicorandil for 3 months). The primary endpoints included cardiac function indices and ST-segment behavior on electrocardiogram (ECG) before and after treatment. The secondary endpoints included adverse reactions, clinical efficacy, platelet aggregation, activated partial thromboplastin time (APTT), high-sensitivity cardiac troponin T (hs-cTnT), and creatine kinase isoenzyme MB (CK-MB) levels after treatment. Multivariate regression analyses were used to assess the contribution of a single drug to the ultimate outcome.
After treatment, both groups exhibited significant decreases in brain natriuretic peptide (BNP) and N-terminal pro-hormone BNP levels compared with before treatment, with the levels significantly lower in Group A than in Group B ( < 0.05). After treatment, left ventricular ejection fraction was significantly increased in both groups compared with before treatment, and that was much higher in Group A than in Group B ( < 0.05). After treatment, the frequency and duration of ST-segment depression were decreased in both groups compared with before treatment, and they were much lower in Group A than in Group B (all < 0.05). The total incidence of adverse reactions in Group A (4.00%) was slightly lower than that in Group B (7.00%), with no significant difference ( > 0.05). Group A (92.00%) had a higher overall response rate than Group B (81.00%) ( < 0.05).
Nicorandil-clopidogrel combination therapy exhibited enhanced clinical efficacy in patients with CHD. In addition, the combination therapy regulated hs-cTnT and CK-MB levels, which may suggest a better patient prognosis.
比较尼可地尔单药治疗与尼可地尔-氯吡格雷联合治疗对冠心病(CHD)患者心功能的疗效和安全性。
回顾性分析200例CHD患者的临床资料。根据不同治疗方法将患者分为两组。A组(n = 100)接受尼可地尔-氯吡格雷联合治疗(静脉注射25 mg尼可地尔,口服300 mg氯吡格雷,持续3个月),B组(n = 100)接受尼可地尔单药治疗(静脉注射25 mg尼可地尔,持续3个月)。主要终点包括治疗前后的心功能指标和心电图(ECG)上的ST段表现。次要终点包括治疗后的不良反应、临床疗效、血小板聚集、活化部分凝血活酶时间(APTT)、高敏心肌肌钙蛋白T(hs-cTnT)和肌酸激酶同工酶MB(CK-MB)水平。采用多变量回归分析评估单一药物对最终结局的贡献。
治疗后,两组脑钠肽(BNP)和N末端前体脑钠肽水平均较治疗前显著降低,且A组水平显著低于B组(<0.05)。治疗后,两组左心室射血分数均较治疗前显著升高,且A组升高幅度远高于B组(<0.05)。治疗后,两组ST段压低的频率和持续时间均较治疗前降低,且A组降低幅度远低于B组(均<0.05)。A组不良反应总发生率(4.00%)略低于B组(7.00%),差异无统计学意义(>0.05)。A组总有效率(92.00%)高于B组(81.00%)(<0.05)。
尼可地尔-氯吡格雷联合治疗对CHD患者显示出增强的临床疗效。此外,联合治疗可调节hs-cTnT和CK-MB水平,这可能提示患者预后较好。