临床医学工程
臨床醫學工程
림상의학공정
Clinical Medical & Engineering
2015年
11期
1459-1460
,共2页
顽固性心力衰竭%心肾综合征%新活素
頑固性心力衰竭%心腎綜閤徵%新活素
완고성심력쇠갈%심신종합정%신활소
Refractory heart failure%Cardiorenal syndrome%Xinhuosu
目的 探讨应用新活素治疗心肾综合征顽固性心力衰竭的效果. 方法 选择我院收治的心肾综合征顽固性心力衰竭患者92作为研究对象并进行分组治疗. 对照组予以血液透析等常规治疗, 研究组在常规治疗的基础上实施新活素治疗. 比较两组患者治疗后的临床表现以及心肾功能改善情况. 结果 研究组临床治疗有效率为95.65%, 显著高于对照组的82.61% (P <0.05). 经过治疗后, 两组患者的血浆BNP前体 (NT-pro-BNP) 浓度均显著降低 (P<0.05), 研究组降低幅度显著大于对照组(P<0.05); 两组血肌酐 (Cr) 均显著降低 (P<0.05), 但组间无显著差异 (P>0.05); 两组左室射血分数 (LVEF) 均显著升高(P<0.05), 研究组升高幅度显著大于对照组 (P<0.05). 治疗过程中, 两组患者均未发现药物过敏、 低血压及其他的严重不良反应. 结论 应用新活素治疗心肾综合征顽固性心力衰竭效果显著, 安全性高, 具有极大的推广应用价值.
目的 探討應用新活素治療心腎綜閤徵頑固性心力衰竭的效果. 方法 選擇我院收治的心腎綜閤徵頑固性心力衰竭患者92作為研究對象併進行分組治療. 對照組予以血液透析等常規治療, 研究組在常規治療的基礎上實施新活素治療. 比較兩組患者治療後的臨床錶現以及心腎功能改善情況. 結果 研究組臨床治療有效率為95.65%, 顯著高于對照組的82.61% (P <0.05). 經過治療後, 兩組患者的血漿BNP前體 (NT-pro-BNP) 濃度均顯著降低 (P<0.05), 研究組降低幅度顯著大于對照組(P<0.05); 兩組血肌酐 (Cr) 均顯著降低 (P<0.05), 但組間無顯著差異 (P>0.05); 兩組左室射血分數 (LVEF) 均顯著升高(P<0.05), 研究組升高幅度顯著大于對照組 (P<0.05). 治療過程中, 兩組患者均未髮現藥物過敏、 低血壓及其他的嚴重不良反應. 結論 應用新活素治療心腎綜閤徵頑固性心力衰竭效果顯著, 安全性高, 具有極大的推廣應用價值.
목적 탐토응용신활소치료심신종합정완고성심력쇠갈적효과. 방법 선택아원수치적심신종합정완고성심력쇠갈환자92작위연구대상병진행분조치료. 대조조여이혈액투석등상규치료, 연구조재상규치료적기출상실시신활소치료. 비교량조환자치료후적림상표현이급심신공능개선정황. 결과 연구조림상치료유효솔위95.65%, 현저고우대조조적82.61% (P <0.05). 경과치료후, 량조환자적혈장BNP전체 (NT-pro-BNP) 농도균현저강저 (P<0.05), 연구조강저폭도현저대우대조조(P<0.05); 량조혈기항 (Cr) 균현저강저 (P<0.05), 단조간무현저차이 (P>0.05); 량조좌실사혈분수 (LVEF) 균현저승고(P<0.05), 연구조승고폭도현저대우대조조 (P<0.05). 치료과정중, 량조환자균미발현약물과민、 저혈압급기타적엄중불량반응. 결론 응용신활소치료심신종합정완고성심력쇠갈효과현저, 안전성고, 구유겁대적추엄응용개치.
Objective To explore the clinical effect of Xinhuosu for the treatment of patients with refractory heart failure complicated with cardiorenal syndrome. Methods 92 patients with refractory heart failure complicated with cardiorenal syndrome were divided into two groups equally. The control group was given routine therapy, while the research group was given Xinhuosu therapy on the basis of routine therapy. The clinical manifestations and improvement situations of cardiorenal function after therapy were compared. Results The clinical effective rate of research group was 95.65%, significantly higher than 82.61% of control group (P <0.05). After therapy, the level of NT-pro-BNP decreased significantly in both groups (P<0.05), and the research group decreased more significantly than the control group (P<0.05). The level of Cr decreased significantly in both groups (P<0.05), and the declines of two groups had no statistical difference (P>0.05). The level of LVEF increased significantly in both groups (P<0.05), and the research group increased more significantly than the control group (P<0.05). No drug allergy, hypotension, or other serious adverse reaction was found in both groups during therapy. Conclusions Xinhuosu has significant efficacy and safety for the treatment of patients with refractory heart failure complicated with cardiorenal syndrome.