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枸橼酸钠和普通肝素钠在严重高脂血症产妇连续性肾脏替代治疗抗凝时的安全性和疗效比较 被引量:2
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作者 尤德源 孙旭日 洪思白 《海峡药学》 2020年第8期108-110,共3页
目的比较枸橼酸钠与普通肝素钠在严重高脂血症产妇连续性肾脏替代治疗(Continuous renal replacement therapy,CRRT)时抗凝的安全性和疗效。方法回顾性分析福建医科大学附属第二医院重症医学科因严重高脂血症而行CRRT治疗的27名产妇,其... 目的比较枸橼酸钠与普通肝素钠在严重高脂血症产妇连续性肾脏替代治疗(Continuous renal replacement therapy,CRRT)时抗凝的安全性和疗效。方法回顾性分析福建医科大学附属第二医院重症医学科因严重高脂血症而行CRRT治疗的27名产妇,其中枸橼酸钠抗凝组(13例)和普通肝素钠组抗凝(14例)。通过对比滤器使用寿命、出血事件等因素来评价两者安全性,对比血脂下降程度来评价其疗效。结果在滤器使用寿命上,枸橼酸钠组与普通肝素钠组差异无统计学意义(P> 0.05)。出血事件发生率上,普通肝素钠组高于枸橼酸钠组,差异具有统计学意义(P <0.05)。在血脂下降程度上,枸橼酸钠钠组与普通肝素钠组差异无统计学意义(P> 0.05)。结论严重高脂血症产妇在CRRT治疗中,枸橼酸钠抗凝与普通肝素钠抗凝具有相同的疗效,但在安全性上,枸橼酸钠优于普通肝素钠,故建议在严重高脂血症产妇进行CRRT时采用枸橼酸钠进行抗凝。 展开更多
关键词 严重高脂血症 产妇 连续性肾脏替代治疗 枸橼酸钠 普通肝素钠 安全性和疗效
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全子宫切除术与广泛性子宫切除术治疗Ⅱ期子宫内膜癌的临床效果比较
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作者 邢新 刘祝泉 +2 位作者 王毛毛 赵冰冰 张洁清 《医药前沿》 2024年第30期74-77,共4页
目的:比较全子宫切除术(TH)与广泛性子宫切除术(RH)治疗Ⅱ期子宫内膜癌的临床效果.方法:回顾性分析2014年1月—2021年12月在广西医科大学附属肿瘤医院接受手术治疗的81例Ⅱ期子宫内膜癌患者的临床资料,依据手术方式不同分为RH组(n=53)... 目的:比较全子宫切除术(TH)与广泛性子宫切除术(RH)治疗Ⅱ期子宫内膜癌的临床效果.方法:回顾性分析2014年1月—2021年12月在广西医科大学附属肿瘤医院接受手术治疗的81例Ⅱ期子宫内膜癌患者的临床资料,依据手术方式不同分为RH组(n=53)与TH组(n=28).比较两组患者手术时间、术中出血量、术中输血率、术后肛门恢复排气时间、术中及术后并发症等.结果:RH组手术时间、留置尿管时间长于TH组,差异有统计学意义(P<0.05);两组术中出血量、术后血红蛋白下降程度、盆腔淋巴结清扫数量及腹主动脉旁淋巴结清扫数量、留置腹腔引流管时间、术后排气时间及住院时间比较,差异无统计学意义(P>0.05).TH组术后并发症总发生率低于RH组,差异有统计学意义(P<0.05).结论:Ⅱ期子宫内膜癌的手术方式可选择TH,也可选择RH,但TH安全性优于RH,可考虑作为治疗的首选. 展开更多
关键词 Ⅱ期子宫内膜癌 广泛性子宫切除 全子宫切除 安全性和疗效
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Cynergy双波长激光治疗鲜红斑痣临床应用
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作者 杨彩云 吴彩风 +1 位作者 盛旭东 王少华 《中国医疗美容》 2014年第5期95-95,99,共2页
目的:观察Cynergy双波长激光治疗仪治疗鲜红斑痣的临床疗效。方法:选取鲜红斑痣患者67例,排除禁忌症后应用Cynergy脉冲燃料激光治疗,随访3~6个月后观察其临床治疗效果。结果:本组67例患者治疗3~4次治疗后,治愈21例,有效41例,无效5例... 目的:观察Cynergy双波长激光治疗仪治疗鲜红斑痣的临床疗效。方法:选取鲜红斑痣患者67例,排除禁忌症后应用Cynergy脉冲燃料激光治疗,随访3~6个月后观察其临床治疗效果。结果:本组67例患者治疗3~4次治疗后,治愈21例,有效41例,无效5例,总有效率92.5%,本组中11例出现小水泡,一周后自然消退;8例出现暂时性色素沉着,半年后均消退。结论:Cynergy双波长治疗鲜红色斑痣疗效肯定,且不良反应轻,无严重并发症,值得临床推广。 展开更多
关键词 Cynergy双波长激光 鲜红斑痣 安全性和疗效
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Chiglitazar monotherapy with sitagliptin as an active comparator in patients with type 2 diabetes:a randomized,double-blind,phase 3 trial(CMAS) 被引量:15
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作者 Weiping Jia Jianhua Ma +36 位作者 Heng Miao Changjiang Wang Xiaoyue Wang Quanmin Li Weiping Lu Jialin Yang Lihui Zhang Jinkui Yang Guixia Wang Xiuzhen Zhang Min Zhang Li Sun Xuefeng Yu Jianling Du Bingyin Shi Changqing Xiao Dalong Zhu Hong Liu Liyong Zhong Chun Xu Qi Xu Ganxiong Liang Ying Zhang Guangwei Li Mingyu Gu Jun Liu Guoyue Yuan Zhaoli Yan Dewen Yan Shandong Ye Fan Zhang Zhiqiang Ning Haixiang Cao Desi Pan He Yao Xianping Lu Linong Ji 《Science Bulletin》 SCIE EI CSCD 2021年第15期1581-1590,M0004,共11页
Chiglitazar(Carfloglitazar)is a novel peroxisome proliferator-activated receptor(PPAR)pan-agonist that has shown promising effects on glycemic control and lipid regulation in patients with type 2 diabetes.In this rand... Chiglitazar(Carfloglitazar)is a novel peroxisome proliferator-activated receptor(PPAR)pan-agonist that has shown promising effects on glycemic control and lipid regulation in patients with type 2 diabetes.In this randomized phase 3 trial,we compared the efficacy and safety of chiglitazar with sitagliptin in patients with type 2 diabetes who had insufficient glycemic control despite a strict diet and exercise regimen.Eligible patients were randomized(1:1:1)to receive chiglitazar 32 mg(n=245),chiglitazar 48 mg(n=246),or sitagliptin 100 mg(n=248)once daily for 24 weeks.The primary endpoint was the change in glycosylated hemoglobin A_(1C)(HbA_(1c))from baseline at week 24 with the non-inferiority of chiglitazar over sitagliptin.Both chiglitazar and sitagliptin significantly reduced HbA1c at week 24 with values of-1.40%,-1.47%,and-1.39%for chiglitazar 32 mg,chiglitazar 48 mg,and sitagliptin 100 mg,respectively.Chiglitazar 32 and 48 mg were both non-inferior to sitagliptin 100 mg,with mean differences of-0.04%(95%confidential interval(Cl)-0.22 to 0.15)and-0.08%(95%Cl-0.27 to 0.10),respectively.Compared with sitagliptin,greater reduction in fasting and 2-h postprandial plasma glucose and fasting insulin was observed with chiglitazar.Overall adverse event rates were similar between the groups.A small increase in mild edema in the chiglitazar 48 mg group and slight weight gain in both chiglitazar groups were reported.The overall results demonstrated that chiglitazar possesses good efficacy and safety profile in patients with type 2 diabetes inadequately controlled with lifestyle interventions,thereby providing adequate supporting evidence for using this PPAR pan-agonist as a treatment option for type 2 diabetes. 展开更多
关键词 Chiglitazar PPAR pan-agonist Type 2 diabetes Glycemic control Insulin resistance
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Efficacy and safety of chiglitazar,a novel peroxisome proliferatoractivated receptor pan-agonist,in patients with type 2 diabetes:a randomized,double-blind,placebo-controlled,phase 3 trial(CMAP) 被引量:19
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作者 Linong Ji Weihong Song +29 位作者 Hui Fang Wei Li Jianlin Geng Yangang Wang Lian Guo Hanqing Cai Tao Yang Hongmei Li Gangyi Yang Qifu Li Kuanzhi Liu Shuying Li Yanjun Liu Fuyan Shi Xinsheng Li Xin Gao Haoming Tian Qiuhe Ji Qing Su Zhiguang Zhou Wenbo Wang Zunhai Zhou Xuejun Li Yancheng Xu Zhiqiang Ning Haixiang Cao Desi Pan He Yao Xianping Lu Weiping Jia 《Science Bulletin》 SCIE EI CSCD 2021年第15期1571-1580,M0004,共11页
Chiglitazar(Carfloglitazar)is a novel non-thiazolidinedione(TZD)structured peroxisome proliferatoractivated receptor(PPAR)pan-agonist that has shown promising effects on glycemic control and lipid regulation in patien... Chiglitazar(Carfloglitazar)is a novel non-thiazolidinedione(TZD)structured peroxisome proliferatoractivated receptor(PPAR)pan-agonist that has shown promising effects on glycemic control and lipid regulation in patients with type 2 diabetes in previous clinical studies.This randomized phase 3 trial aimed to compare the efficacy and safety of chiglitazar with placebo in patients with type 2 diabetes with insufficient glycemic control by strict diet and exercise alone.Eligible patients were randomly assigned to receive chiglitazar 32 mg(n=167),chiglitazar 48 mg(n=166),or placebo(n=202)once daily.The primary endpoint was the change in glycosylated hemoglobin A_(1c)(HbA_(1c))at week 24 with superiority of chiglitazar over placebo.The results showed that both chiglitazar 32 and 48 mg resulted in significant and clinically meaningful reductions in HbA_(1c),and placebo-adjusted estimated treatment differences at week 24 for chiglitazar 32 and 48 mg were-0.87%(95%confidential interval(CI):-1.10 to-0.65;P<0.0001)and-1.05%(95%CI:-1.29 to-0.81;P<0.0001),respectively.Secondary efficacy parameters including glycemic control,insulin sensitivity and triglyceride reduction were also significantly improved in the chiglitazar groups.The overall frequency of adverse events and study discontinuation attributable to adverse events were similar among the groups.Low incidences of mild edema and body weight gain were reported in the chiglitazar dose groups.The results from this phase 3 trial demonstrated that the PPAR pan-agonist chiglitazar possesses an overall good efficacy and safety profile in patients with type 2 diabetes inadequately controlled with lifestyle interventions,thereby providing adequate supporting evidence for using this PPAR pan-agonist as a treatment option for type 2 diabetes. 展开更多
关键词 Chiglitazar Carfloglitazar PPAR pan-agonist
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