机构地区:[1]秦皇岛市第一医院心血管内科,河北秦皇岛066000
出 处:《中华老年多器官疾病杂志》2023年第7期492-496,共5页Chinese Journal of Multiple Organ Diseases in the Elderly
基 金:秦皇岛市重点研发计划(201805A042);河北省重点研发计划(182777235)。
摘 要:目的观察沙库巴曲缬沙坦对合并肾功能不全的慢性心力衰竭(简称心衰)患者肾功能的影响。方法连续纳入2020年12月至2022年3月秦皇岛市第一医院慢性心衰合并肾功能不全患者84例,分为沙库巴曲缬沙坦组(n=48)和对照组(n=36)。沙库巴曲缬沙坦组接受沙库巴曲缬沙坦治疗,对照组接受单一的缬沙坦治疗。观察2组患者服药后6个月和12个月肌酐、估算的肾小球滤过率(eGFR)、尿素氮、尿酸、肾功能恶化(WRF)指标的变化情况。采用SPSS 22.0软件进行数据分析。根据数据类型,组间比较分别采用t检验、非参数秩和检验、非参数检验、Mann-Whitney U检验及χ2检验。结果服药后6个月,对比基线水平,沙库巴曲缬沙坦组肌酐、eGFR的变化值与对照组比较无明显差异;尿素氮及尿酸下降值显著高于对照组[-2.62(1.83,3.90)和0.45(0.29,0.70)mmol/L,P<0.01;-137.00(-92.30,-201.13)和-9.65(49.00,-79.80)μmol/L,P=0.000];与对照组比较,沙库巴曲缬沙坦降低了患者的收缩压及舒张压[(132±17)和(133±24)mmHg(1 mmHg=0.133 kPa),P=0.824;(81±14)和(82±12)mmHg,P=0.732],但尚无统计学差异,NYHA分级明显改善(Z=-2.150,P=0.032)。服药后12个月,对比基线水平,沙库巴曲缬沙坦组eGFR下降值明显低于对照组[-2.21(1.33,3.49)和-22.11(12.32,29.67)ml/(min·1.73m 2),P=0.023];肌酐升高值明显低于对照组[1.50(0.98,2.07)和31.65(22.77,42.53)μmol/L,P=0.043];尿素氮及尿酸下降值也显著高于对照组[-2.80(2.01,4.23)和0.80(0.58,1.14)mmol/L,P<0.01;-141.00(-96.40,-200.25)和-8.45(45.00,-77.70)μmol/L,P=0.000];沙库巴曲缬沙坦组收缩压及舒张压降幅、NYHA分级均显著优于对照组[(123±14)和(130±17)mmHg,P=0.042;(76±11)和(81±11)mmHg,P=0.042;Z=-2.200,P=0.028]。服药后6个月,沙库巴曲缬沙坦组WRF发生率与对照组相比无明显统计学差异[3(6.25%)和7(19.44%),P=0.132];服药后12个月,沙库巴曲缬沙坦组WRF发生率显著低于对照组[4(8.33%)和9(25.00%),P=0.03Objective To observe the effect of sacubitril/valsartan on renal function in patients with chronic heart failure(CHF)and renal insufficiency.Methods A total of 84 consecutive CHF patients with renal insufficiency who visited the First Hospital of Qinhuangdao form December 2020 to March 2022 were enrolled and divided into sacubitril/valsartan group(n=48)and control group(n=36).The sacubitril/valsartan group received sacubitril/valsartan and the control group received single valsartan.The two groups were observed for the changes in serum creatinine,estimated glomerular filtration rate(eGFR),urea nitrogen,uric acid,and worsening renal function(WRF)at 6 and 12 months after medication.SPSS statistics 22.0 was used for statistical analysis.Data comparison between two groups was perfomed using t test,non-parametric rank sum test,non-parametric test,Mann-Whitney U test orχ2 test depending on data type.Results At 6 months,there were no significant differences in serum creatinine(P=0.254)and eGFR(P=0.061)in comparison with the baseline between the two groups.The decreased values of urea nitrogen[-2.62(1.83,3.90)vs 0.45(0.29,0.70)mmol/L;P<0.01]and uric acid[-137.00(-92.30,-201.13)vs-9.65(49.00,-79.80)μmol/L;P=0.000]were significantly higher in the sacubitril/valsartan group than those in the control group.Compared with the control group,sacubitril/valsartan reduced systolic blood pressure[(132±17)vs(133±24)mmHg(1 mmHg=0.133 kPa);P=0.824]and diastolic blood pressure[(81±14)vs(82±12)mmHg;P=0.732],but there was no statistical differences.NYHA classification was significantly improved between two groups(Z=-2.150;P=0.032).Compared with the baseline at,12 months,the decline of eGFR was lower in the sacubitril/valsartan group than the control group[-2.21(1.33,3.49)vs-22.11(12.32,29.67)ml/(min·1.73 m 2);P=0.023];the increase in serum creatinine was significantly lower in the sacubitril/valsartan group than in the control group[1.50(0.98,2.07)vs 31.65(22.77,42.53)μmol/L;P=0.043];the decreases in urea nitrogen[-2.80(2.01,4.23
关 键 词:慢性心力衰竭 肾功能不全 沙库巴曲缬沙坦 肾功能恶化
分 类 号:R541.61[医药卫生—心血管疾病]
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