Zďarská Denisa Janíčková, Brož Jan, Křivská Bohumila, Rušavý Zdeněk, Kvapil Milan
Vnitr Lek. 2014 Sep;60(9):712-9.
To evaluate the safety and efficacy of basal insulin glargine using a basal-bolus regimen in a common clinical practice setting in the Czech Republic.
The LINDA project was a non-interventional, multicenter (n = 255), national, observational project. A total of 4,998 patients with Type 1 and 2 diabetes mellitus (T1DM, T2DM) with predominantly insulin therapy (99,7 %), after switch on insulin glargine at basal-bolus regimen, were enrolled in this project. The patients were followed up for 6 months after initiation of the therapy with insulin glargine. The primary objective of the project was to investigate the incidence of severe hypoglycemic episodes during the treatment with basal insulin analogue glargine (Lantus®) in a common clinical practice setting. The se-condary endpoints were changes in glycosylated hemoglobin (HbA1c) levels, fasting plasma glucose (FPG), body weight, insulin dose, change of number of hypoglycemic episodes in comparison the previous therapy and the frequency of adverse effects.
Severe hypoglycaemia were observed during treatment with insulin glargine at 0.8 % patients. When comparing the incidence of hypoglycemia with the previous therapy, we demonstrated a clinically and statistically significant reduction in their frequencies. The percentage of patients with hypoglycemic episodes (17.6 %), severe hypoglycemia (0.8 %) and severe nocturnal hypoglycemia (0.3 %) over the last month of treatment with insulin glargine using the basal-bolus regimen was consistently lower compared to the last month of treatment before initiation of this therapy (42.5 %, 17.6 %, and 13.8 % of the patients, respectively). In patients with T1DM, the incidence of hypoglycemia decreased from 37.80 ± 15.95 episodes/patient/year to 8.76 ± 4.38 epi-sodes/patient/year (p < 0.001) for all hypoglycemic episodes; from 5.64 ± 3.27 episodes/patient/year to 0.0396 ± 0.012 episodes/patient/year (p < 0.001) for severe hypoglycemia; and from 3.84 ± 2.04 episodes/patient/year to 0.0096 ± 0.003 episodes/patient/year (p < 0.001) for severe nocturnal hypoglycemia. In patients with T2DM, the incidence of hypoglycemia decreased from 12.48 ± 7.57 episodes/patient/year to 1.68 ± 0.78 episodes/patient/year (p < 0.001) for all hypoglycemic episodes; from 2.04 ± 0.94 episodes/patient/year to 0.0132 ± 0.005 episodes/patient/year (p < 0.001) for severe hypoglycemia; and from 1.32 ± 0.77 episodes/patient/year to 0.0048 ± 0.0008 episodes/patient/year (p < 0.001) for severe nocturnal hypoglycemia. A statistically significant improvement in the metabolic control was demonstrated when using insulin glargine. The glycated hemoglobin (HbA1c) decreased from 7.74 ± 1.71 % to 6.43 ± 1.39 % ( -1.31 ± 0.32 %, p < 0.001) in patients with T1DM, and from 8.13 ± 1.56 % to 6.72 ± 1.40 % ( -1.41 ± 0.28 %, p < 0.001) in patients with T2DM. A statistically significant (p < 0.001) increase in the number of patients with HbA1c < 5.4 % was further demonstrated. The decrease in fasting blood glucose (FBG) and 6-point blood sugar profile was also statistically significant in both types of diabetes (p < 0.001). Changes in therapy and subsequent treatment with insulin glargine were perceived positively by both physicians and patients.
In the common clinical practice setting, the initiation of treatment with insulin glargine using the basal-bolus regime in patients with previous insulin therapy resulted in a reduction in the incidence of hypoglycemic events, including severe hypoglycemia and severe nocturnal hypoglycemia, and improved metabolic control in patients with diabetes (reduced glycated hemoglobin, fasting glucose values and 6-point blood glucose profile). Greater satisfaction with the current treatment was reported by both patients and physicians.Key words: basal-bolus regimen - diabetes mellitus - insulin glargine - observational project.
在捷克共和国的普通临床实践环境中,评估使用基础-餐时方案的甘精胰岛素的安全性和有效性。
LINDA项目是一项非干预性、多中心(n = 255)、全国性的观察性项目。共有4998例1型和2型糖尿病(T1DM、T2DM)患者,主要采用胰岛素治疗(99.7%),在改用基础-餐时方案的甘精胰岛素后纳入该项目。患者在开始使用甘精胰岛素治疗后随访6个月。该项目的主要目的是调查在普通临床实践环境中,使用基础胰岛素类似物甘精胰岛素(来得时®)治疗期间严重低血糖事件的发生率。次要终点包括糖化血红蛋白(HbA1c)水平、空腹血糖(FPG)、体重、胰岛素剂量的变化,与先前治疗相比低血糖发作次数的变化以及不良反应的发生频率。
在使用甘精胰岛素治疗期间,0.8%的患者发生了严重低血糖。与先前治疗相比,低血糖发生率在临床和统计学上均有显著降低。使用基础-餐时方案的甘精胰岛素治疗的最后一个月,低血糖发作患者的百分比(17.6%)、严重低血糖(0.8%)和严重夜间低血糖(0.3%)始终低于开始该治疗前的最后一个月(分别为42.5%、17.6%和13.(此处原文有误,推测为13.8%)8%的患者)。在T1DM患者中,所有低血糖发作的发生率从37.80±15.95次/患者/年降至8.76±4.38次/患者/年(p < 0.001);严重低血糖从5.64±3.27次/患者/年降至0.0396±0.012次/患者/年(p < 0.001);严重夜间低血糖从3.84±2.04次/患者/年降至0.0096±0.003次/患者/年(p < 0.001)。在T2DM患者中,所有低血糖发作的发生率从12.48±7.57次/患者/年降至1.68±0.78次/患者/年(p < 0.001);严重低血糖从2.04±0.94次/患者/年降至0.0132±0.005次/患者/年(p < 0.001);严重夜间低血糖从1.32±0.77次/患者/年降至0.0048±0.0008次/患者/年(p < 0.001)。使用甘精胰岛素时,代谢控制有统计学显著改善。T1DM患者的糖化血红蛋白(HbA1c)从7.74±1.71%降至6.43±1.39%(-1.31±0.32%,p < 0.001),T2DM患者从8.13±1.56%降至6.72±1.40%(-1.41±0.28%,p < 0.001)。HbA1c < 5.4%的患者数量也有统计学显著增加(p < 0.001)。空腹血糖(FBG)和六点血糖谱的降低在两种类型的糖尿病中也具有统计学显著性(p < 0.001)。医生和患者对治疗的改变以及随后使用甘精胰岛素的治疗均给予积极评价。
在普通临床实践环境中,先前接受胰岛素治疗的患者开始使用基础-餐时方案的甘精胰岛素治疗,可降低低血糖事件的发生率,包括严重低血糖和严重夜间低血糖,并改善糖尿病患者的代谢控制(降低糖化血红蛋白、空腹血糖值和六点血糖谱)。患者和医生对当前治疗的满意度更高。关键词:基础-餐时方案 - 糖尿病 - 甘精胰岛素 - 观察性项目