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双语推荐:诺和锐30

目的:观察比较诺和锐30和诺和灵30R治疗2型糖尿病( T2DM)的临床疗效。方法58例T2DM患者随机分为诺和锐30组和诺和灵30R组,治疗12周,观察治疗前后患者的空腹血糖( FPG)、餐后2 h 血糖(2 h PG)、糖化血红蛋白(HbA1c)、低血糖发生率及体质量指数变化。结果治疗12周后,诺和锐30治疗组的FBG、HbA1c、2 h PG 控制明显优于诺和灵30R 组,诺和锐30组的低血糖发生率明显低于诺和灵30R 组( P ﹤0.05),两组体质量指数比较差异无统计学意义(P﹥0.05)。结论诺和锐30和诺和灵30R均可安全有效地降低血糖,诺和锐30控制餐后血糖更具优势,低血糖事件发生率较低。
Objective To observe and compare the clinical curative effect of novorapid 30 and novolin 30R on type 2 diabetes mellitus. Methods Fifty-eight cases of T2DM were randomly divided into novorapid 30 group and novolin 30R group,the treatment lasted for 12 weeks. Fasting blood glucose(FPG),2 h postprandial blood glucose(2hPG),glycosylated hemoglobin(HbA1c),the rate of hypoglycemia and weight index were observed before and after treatment. Results After 12 weeks of treatment,the FBG,HbA1c,2hPG in novorapid 30 group were better than that in novolin 30R group,the hypo-glycemia incidence of novorapid 30 group was significantly lower than that of novolin 30R group(P﹤0. 05). There was no significant difference in body mass index between the two groups(P﹥0. 05). Conclusions Novorapid 30 and novolin 30R can safely and effectively reduce the blood glucose,novorapid 30 has more advantage in controlling postprandial blood glu-cose,and the incidence of hypoglycemia is low.

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目的探讨诺和锐30与诺和灵30R对于住院初诊的2型糖尿病患者的治疗效果。方法回顾性分析2010年5月一2012年9月我院收治的60例初诊T2DM患者,根据患者当时接受的治疗方法分为诺和锐30组与诺和灵30R组,各30例,两组患者分别以诺和锐30和诺和灵30R进行治疗,在经过一段时间治疗以后对患者的疗效进行观察对比。结果两组患者相对于接受治疗前,空腹血糖(FPG)、糖化血糖蛋白(HbAlC)以及餐后2h血糖(2hPBG)均有明显的下降,但是诺和锐30组的患者在HbAlC以及2hPBG方面下降更为显著(P〈0.01;P〈0.05);对血糖进行控制的前提上诺和锐30剂量相对于诺和灵30R少很多(P〈0.05);诺和锐30组患者出现低血糖概率相对于诺和灵30R组别患者要低(P〈O.05)。结论诺和锐30以及诺和灵30R均有着降低血糖指数的效果,但与诺和灵30R相比,诺和锐30对于T2DM患者在血糖水平及低血糖反应方面有着更加突出的优越性。
Objective To explore and analyze the clinical efficacy of Novomix30 and pre-mixed30R in the treatment of type 2 diabetes mellitus (T2DM). Methods 60 cases with T2DM in our hospital from May 2010 to September 2012 were selected and retrospectively analyzed,the patients were divided into Novomix30 group and pre-mixed30R group according to the treatment they received,each group had 30 cases, the two groups were treated by Novomix30 and pre-mixed30R respectively.Observed and compared the efficacy of the two groups after a period of treatment. Results compared with before the treatment, FPG,HbA1C and 2hPBG of the two groups had both decreased significantly,but HbA1C and 2hPBG in Novomix30 group decreased more significantly(P<0.01;P<0.05),hypoglycemia probability in Novomix30 group was lower than that in pre-mixed30R group(P < 0.05). Conclusion Novomix30 and pre-mixed30R both can reduce glycemic index,but compare with pre-mixed30R,Novomix30 in blood sugar levels and hypoglycemia reaction for

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目的比较精蛋白重组人胰岛素注射液(诺和灵30R)与门冬胰岛素30注射液(诺和锐30)治疗2型糖尿病(T2DM)的有效性及安全性。方法入选72例血糖控制不达标的T2DM患者,随机分为诺和灵30R组(n=35)与诺和锐30组(n=37),治疗前和24周后测定糖化血红蛋白(HbA1c)、空腹血糖(FPG)、餐后2小时血糖(2hPG)水平、血脂、体重、体脂含量和BMI值变化,记录不良事件和低血糖事件发生率。结果治疗24周后,两组患者HbA1c、FPG和2hPG水平均明显降低(P0.01),诺和锐30组2hPG水平明显低于诺和灵30R组。诺和灵30R治疗后体重和BMI值有显著增加,而诺和锐30组体重及BMI值治疗前后差异无统计学意义。结论在治疗T2DM有效性及安全性方面,诺和锐30要优于诺和灵30R。
Objective To compare the efficacy and safety of protamine recombinant human insulin injection (Novolin 30R) and insulin aspart 30 injection (NovoMix 30) in the treatment of type 2 diabetes mellitus (T2DM). Methods 72 patients with T2DM were randomly divided into Novolin 30R group (n=35) and NovoMix 30 group (n=37), to measure HbA1c, FPG, 2hPG, lipids, body weight, body fat, and BMI, and to record the adverse events and hypoglycemia incidence. Results The HbA1C, FPG and 2hPG levels decreased significantly in both groups compared with the baseline levels (all P<0.01). The 2hPG level in NovoMix 30 group was significantly lower than that in Novolin 30R group after 24 weeks of treatment. The body weight and BMI values increased significantly in Novolin 30R group after treatment. Conclusions NovoMix 30 is more safe and effective than Novolin 30R in the treatment of type 2 diabetes mellitus.

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目的:混合门冬胰岛素302次/d注射(诺和锐30)与预混人胰岛素(诺和灵30R 30R)在2型糖尿病患者治疗的安全性的疗效。方法68例口服降糖药控制不佳的2型糖尿病患者随机分为两组,诺和锐30治疗组与诺和灵30R治疗组,分别,每日早餐前晚餐前诺和锐30与诺和灵30R注射。观察12 w。比较两组患者的糖化血红蛋白(HbAlc),血糖,低血糖的频率等。结果早期诺和锐30治疗组。餐后血糖显著低于诺和灵30R治疗组(P<0.01);门冬胰岛素30治疗组低血糖比诺和灵30R治疗组少,但差异无统计学意义(P>0.05),门冬胰岛素治疗组无严重低血糖。结论2型糖尿病患者。2次/d注射门冬胰岛素30比诺和灵30R显著降低餐后血糖,降低低血糖风险,易为患者接受。
Objective Mixed insulin aspart 302 infusions of /d (Nuo Herui 30) mixed human insulin (Novolin 30R and pre 30R) on the ef icacy and safety of treatment of type 2 diabetic patients. Methods 68 cases of oral antidiabetic drug control in type 2 diabetic patients were randomly divided into two groups of poor, insulin aspart 30 in treatment group and Nuo Heling 30R treatment group, respectively, every morning before breakfast before supper insulin aspart 30 and Nuo Heling 30R injection. Observation of 12 W. Comparing the two groups of patients with glycosylated hemoglobin (HbAlc), blood glucose, and frequency of hypoglycemia etc. Results The early insulin aspart 30 in the treatment group. Postprandial blood glucose was significantly lower than that of Novolin 30R treated group (P 0.05), insulin aspart treatment group without severe hypoglycemia. Conclusion Patients with type 2 diabetes mel itus. The 2 /d injection of insulin aspart 30 Noir and spirit of 30R significantly decreased the postp

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目的探讨优泌乐25及诺和锐30在治疗2型糖尿病中的疗效。方法60例经VI服降糖药治疗效果不佳的2型糖尿病患者分为优泌乐25治疗组及诺和锐30治疗组,在继续服用原有降糖药的基础上,分别采用每日2次注射上述两种胰岛素降糖12周后,对两组患者的空腹血糖、早餐后2h的血糖、糖化血红蛋白、胰岛素日均用量和低血糖情况进行比较。结果(1)治疗后两组患者的空腹血糖、早餐后2h的血糖、糖化血红蛋白均较治疗前明显下降(P〈0.05)。(2)治疗后两组患者的胰岛素日均用量及低血糖发生率差别无统计学意义。(3)优泌乐25组空腹血糖水平低于诺和锐30组空腹血糖水平(P〈0.05),而诺和锐30组早餐后2h血糖水平低于优泌乐25组(P〈0.05),差异有统计学意义。结论对于2型糖尿病患者而言,使用优泌乐25及诺和锐30均能较好的控制血糖且稳定,不易发生低血糖反应,使用优泌乐25能较好的控制空腹血糖,而诺和锐30能较好地控制早餐后2h血糖。
Objective To investigate the effects of twice subcutaneous injections of mixed insulin analogue lilymix25 and mixed insulin analogue novomix30 on treating type 2 diabetes. Methods 60 cases of DM2 patients who lost the effectiveness of oral medicines were divided into two groups, given mixed insulin analogue lilymix25 and novomix30 respectively,based on continued to take the oral medicines,and observed for 12weeks. Results (1)The fasting blood-glucose,the postprandial blood-glucose 2 hours after the breakfast and HbAlC of both two groups were lower than before treating, the difference has statistical significance(P < 0.05).(2)The average daily dose of insulin and the incidence of low blood-glucose in both two groups has no significant differences.(3)The fasting blood-glucose levels in group A was less than group B,the difference has statistical significance(P < 0.05).And the postprandial blood-glucose 2 hours after the meal in group B was less than group A, the difference has statistica

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目的探讨来得时联合拜唐苹和诺和锐30治疗高龄(80岁以上)2型糖尿病(T2DM)患者血糖、糖化血红蛋白(HbAlC)变化,低血糖事件发生率及临床意义。方法将120例口服降糖药物疗效较差的高龄T2DM患者随机分为来得时联合拜唐苹组和诺和锐30组(每组60例)。来得时联合拜唐苹组每日早餐前注射1次来得时加三餐中口服拜唐苹,诺和锐30组早晚餐前各皮下注射1次,共16周,比较两组患者空腹血糖(FBG)及餐后2小时血糖(2hPBG)、甘油三酯(TG)、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C),高密度脂蛋白胆固醇(HDL.C)、HbAlc的下降情况,低血糖事件发生率。结果两组治疗前后血糖、TG、TC、LDL.C、HbAlc下降明显,其中来得时联合拜唐苹组HbA1c从(8.8%±2.0%)下降至(7.1%±1.2%);诺和锐30组HbA1c从(8.9%±2.4%)下降到(7.0%±1.2%);治疗后两组之间差异无统计学意义(P〉0.05);来得时联合拜唐苹组低血糖事件发生率明显低于诺和锐30组(3.3%vs13.3%,P〈0.01)。结论来得时联合拜唐苹组和诺和锐30组都具有明显降低FBG、2hPBG、TG、TC、LDL.C、HbAlc的作用,来得时联合拜唐苹组低血糖事件发生率明显低于诺和锐30组。
Objective To investigate the changes of blood glucose, HbA1c, and incidence of hypoglycemia in the very old patients (over 80 years) with type 2 diabetes mellitus (T2DM) after the treatment of lantus with glucobay or Novomix 30, and the clinical significance. Methods A total of 120 very old T2DM patients poorly controlled with oral hypoglycemic drugs admitted in our department from July 2011 to June 2012 were subjected in this study. They were randomly divided into lantus with glucobay group and Novomix 30 group (n=60 in each group). Lantus was injected before breakfast, and glucobay was taken with meals, while Novomix 30 was injected before morning and evening meals for total 16 weeks. Fasting blood glucose (FBG) and 2-hour postprandial blood glucose (2hPBG), triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), the decrease of HbA1c, and the incidence of hypoglycemia were compared between the two groups.

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目的观察阿卡波糖联合诺和锐30治疗肝源性糖尿病的疗效。方法肝源性糖尿病患者46例,随机分为两组,每组23例,治疗组在早、晚餐前30 min皮下注射诺和锐30(12-40 U/d)及口服阿卡波糖片50 mg,1-3次/d;对照组仅给予诺和锐30治疗,用法与治疗组相同。比较两组空腹血糖(FBG)、餐后2 h血糖(2hPG)及糖化血红蛋白(HbA1c)水平。结果两组患者治疗后FBG、2hPG及HbA1c水平与治疗前相比均明显下降(P〈0.05);治疗后两组FBG水平比较,差异无统计学意义(P〉0.05);治疗后,治疗组2hPG及HbA1c水平均明显低于对照组(P均〈0.05)。结论阿卡波糖联合诺和锐30治疗肝源性糖尿病,可以有效降低患者的2hPG、HbA1c水平。
Objective To observe the effect of acarbose combined with insulin aspart 30 on hepatogenic diabetes . Methods Forty-six patients with hepatogenic diabetes were randomly divided into two groups ,with 23 cases in each group.The treatment group was given subcutaneous injection of insulin aspart 30(12-40 U/d) and oral acarbose tablet (50 mg) 30 minutes before breakfast and dinner ,one to three times a day .The control group was given insulin aspart 30 alone,the method of medication was as same as that conducted in the treatment group .The levels of fast blood glucose (FBG),2 hours plasma glucose(2hPG) and hemoglobin A1c(HbA1c) were compared between two groups .Results The levels of FBG,2hPG and HbA1 c decreased significantly in both groups after treatment in contrast with those before treatment (P 0.05).The levels of 2hPG and HbA1 c in the treatment group were significantly lower than those in the control group after treatment ( all P<0 .05 ) . Conclusion Acarbose combined with insulin asp

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目的比较地特胰岛素联合格列齐特缓释片与诺和锐30治疗2型糖尿病患者的疗效。方法选择80例继发性磺脲类降糖药失效的2型糖尿病患者,随机分为地特胰岛素联合格列齐特缓释片组和诺和锐30治疗组。观察两组治疗前后血糖及HbA1c变化,以及低血糖发生率。结果两组各监测点血糖及HbA1c治疗后与治疗前比较均明显下降(P 0.05)。结论地特胰岛素联合格列齐特缓释片与诺和锐30均能有效控制血糖,两组低血糖发生率低且相近。
Objective To study the therapeutic effects of insulin detemir combined with gliclazide sustained-release tablets and insulin aspart30 in treating type 2 diabetes melitus. Methods 80 type 2 diabetes patients with secondary failure to sulfonylureas(SFS) were grouped randomly by insulin detemir combined with gliclazide sustained-release tablets ,insulin aspart30 for 3 months. The blood glucose and HbA1c before and after treatment were observed. And the incidence of hypoglycemia were compared. Result There were statisticaly significant differences in blood glucose at various points in 24 hours and in HbA1c between the two groups before and after treatment (P 0.05) .Conclusion The above two treatments can reduce the blood glucose and HbA1c effectively. The incidence of hypoglycemia in insulin detemir combined with gliclazide sustained-release tablets was as low as in insulin aspart30.

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目的比较单用门冬胰岛素(诺和锐30血糖控制差的2型糖尿病患者加用阿卡波糖后和其改用四次胰岛素皮下注射方案的有效性、安全性。方法将医院60例单用诺和锐30血糖控制差的2型糖尿病患者随机分为2组,对照组30例采用诺和锐30 3次皮下注射同时3餐嚼服阿卡波糖;研究组30例采用4次胰岛素皮下注射(生物合成人胰岛素R+地特胰岛素)。根据血糖调整胰岛素剂量,连续治疗12周后比较2组空腹血糖、餐后血糖、糖化血红蛋白(HbA1c)、胰岛素使用剂量及低血糖发生情况。结果 2组空腹血糖,餐后血糖,HbA1c都较前明显下降(P〈0.05),但2组之间3项指标无明显统计学差异(P〉0.05);对照组胰岛素用量明显减少,且低血糖发生率低,差异均有统计学意义(P〈0.05)。结论诺和锐30+阿卡波糖较4次胰岛素注射使血糖达标时所用的胰岛素量减少,并具有更少的低血糖发生率。
Objective To compare the efficacy and safety between insulin aspart 30 injection( NovoMix 30)com-bined with acarbose and four-times-insulin subcutaneous injection in patients with poorly-controlled type 2 diabetes(T2DM) by alone NovoMix 30. Methods 60 cases of patients with poorly-controlled type 2 diabetes(T2DM)by alone NovoMix 30 were randomly divided into 2 groups. The control group was given NovoMix 30 subcutaneous injections,three times Daily,at the same time plus acarbose;the research group was given four subcutaneous insulin injections including biosynthetic human insu-lin injection(Novolin R)+ insulin detemir injection(Levemir). Adjust the dose of insulin according to the blood sugar. After 12 weeks of continuous treatment,the fasting blood sugar( FBS),postprandial blood glucose,glycosylated hemoglobin (HbA1c),the dose of insulin for daily use,and frequency of hypoglycemia of 2 groups were compared. Results The FBS, 2hPG,HbA1c of 2 groups were obviously decreased(P 0.
目的:探究与分析诺和锐30联合维格列汀治疗初诊重度2型糖尿病的临床疗效。方法选取本院自2012年12月~2013年11月收治的初诊重度2型糖尿病患者60例,将其作为临床研究对象,采取随机数字表法分为对照组和观察组,每组各30例,对照组给予诺和锐30治疗,观察组在其基础上加用维格列汀治疗,观察与对比两组患者的临床疗效。结果两组患者治疗后空腹血糖、餐后血糖、HbA1c、甘油三酯、总胆固醇、低密度脂蛋白胆固醇较治疗前显著降低,差异有统计学意义(P<0.05),观察组较对照组降低显著, P<0.05,差异具有统计学意义。结论诺和锐30联合维格列汀治疗初诊重度2型糖尿病的临床疗效显著,能够全面降低患者血糖,不良反应少,低血糖发生率低。
Objective To explore and analyze clinical effect of aspart 30 combined with vildagliptin in the treatment of newly diagnosed severe type 2 diabetes. Methods From December 2012 to November 2013, 60 cases of newly diagnosed severe type 2 diabetic patients were randomly divided into control group and observation group, 30 cases for each group, control group were given aspart treatment, observation group received vildagliptin treatment on its basis, and clinical efficacy of two groups was compared. Results After treatment, levels of fasting plasma glucose, postprandial glucose, HbA1c, TG, TC and LDL-C in observation group decreased significantly compared with control group, P<0.05, statistically significant. Conclusion Aspart 30 combined with vildagliptin therapy can significantly decrease blood sugar of newly severe diagnosed type 2 diabetes with less adverse reaction and low rates of hypoglycemia.

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