首页> 外文期刊>Quality of life research: An international journal of quality of life aspects of treatment, care and rehabilitation >The effect of prandial glucose regulation with repaglinide on treatment satisfaction, wellbeing and health status in patients with pharmacotherapy naive Type 2 diabetes: a placebo-controlled, multicentre study.
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The effect of prandial glucose regulation with repaglinide on treatment satisfaction, wellbeing and health status in patients with pharmacotherapy naive Type 2 diabetes: a placebo-controlled, multicentre study.

机译:瑞格列奈对餐前血糖的调节对初治2型糖尿病药物治疗患者的治疗满意度,幸福感和健康状况的影响:一项安慰剂对照的多中心研究。

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This prospective, 16-week, randomised, double-blind, parallel-group study assessed the differential impact of the prandial glucose regulating oral hypoglycaemic drug, repaglinide, and placebo upon perceptions of quality of life (QoL) and treatment satisfaction in pharmacotherapy-naive patients with Type 2 diabetes. In addition, the study assessed whether these outcomes were influenced by the patients' level of glycaemic control. A total of 253 patients were randomised in a 2:1 ratio of repaglinide: placebo, with doses taken flexibly with main meals (2-4 per day), whenever they were eaten. Repaglinide was initiated at 0.5 mg per meal, increased to 1 mg after 4 weeks if fasting plasma glucose exceeded 7.8 mmol/l. QoL and treatment satisfaction outcomes were compared using generic and disease-specific self-assessment measures, previously applied in diabetes: the WHO Wellbeing Questionnaire (WHO-WBQ), WHO Diabetes Treatment Satisfaction Questionnaire (WHO-DTSQ) and EuroQoL EQ-5D. Over the trial period, repaglinide-treated patients reported a significant 9% improvement in (WHO-DTSQ) treatment satisfaction score (p < 0.05). No significant increase was associated with placebo. The correlation between decrease in glycated haemoglobin (HbA1c) and increase in treatment satisfaction (WHO-DTSQ) was -0.22 (p < 0.01). Scores obtained with the other measures did not change significantly during the trial in either group, but the cohort exhibited only a slight reduction in wellbeing (WHO-WBQ) and health status (EQ-5D) at baseline compared with the background population. In conclusion, flexible mealtime dosing with oral medication appears to be well accepted by pharmacotherapy-naive patients with Type 2 diabetes. The results suggest that repaglinide provides a higher level of treatment satisfaction than placebo, and this may in part relate to improved glycaemic control.
机译:这项前瞻性,为期16周,随机,双盲,平行分组的研究评估了餐后血糖调节口服降血糖药,瑞格列奈和安慰剂对初次药物治疗对生活质量(QoL)和治疗满意度的影响的差异。 2型糖尿病患者。此外,该研究评估了这些结局是否受到患者血糖控制水平的影响。总共253名患者被随机分配为瑞格列奈:安慰剂2:1的比例,每顿饭时随主餐灵活服用剂量(每天2-4次)。瑞格列奈开始时为每餐0.5 mg,如果空腹血糖超过7.8 mmol / l,则在4周后增加至1 mg。使用之前在糖尿病中使用的通用和针对疾病的自我评估方法,对生活质量和治疗满意度结果进行了比较:世卫组织幸福感问卷(WHO-WBQ),世卫组织糖尿病治疗满意度问卷(WHO-DTSQ)和EuroQoL EQ-5D。在试验期间,瑞格列奈治疗的患者报告(WHO-DTSQ)治疗满意度得分显着提高9%(p <0.05)。安慰剂无明显增加。糖化血红蛋白减少(HbA1c)与治疗满意度增加(WHO-DTSQ)之间的相关性为-0.22(p <0.01)。在两组中,其他方法获得的分数在试验期间均无显着变化,但与背景人群相比,该人群在基线时的健康状况(WHO-WBQ)和健康状况(EQ-5D)仅略有降低。总之,灵活的进餐时间口服药物似乎已被纯药物治疗的2型糖尿病患者很好地接受。结果表明瑞格列奈比安慰剂提供更高的治疗满意度,这可能部分与改善血糖控制有关。

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