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[甘精胰岛素与门冬胰岛素基础-餐时治疗方案对2型糖尿病患者的疗效——基于药物报销视角的分析]

[Effectiveness of one-year insulin glargine and insulin glulisine basal-bolus treatment in people with type 2 diabetes. An analysis from drug reimbursement perspective].

作者信息

Jermendy György, Kovács Gábor

机构信息

Bajcsy-Zsilinszky Kórház és Rendelőintézet Budapest.

Medico-Pharmecon Kft. Budapest, Madarász V. u. 13., 1. ép. 5. em. 85., 1131.

出版信息

Orv Hetil. 2018 Dec;159(50):2122-2128. doi: 10.1556/650.2018.31214.

Abstract

INTRODUCTION

Being entitled for no patient co-payment, the Hungarian reimbursement condition of analogue insulins as part of basal-bolus treatment in type 2 diabetes mellitus (T2DM) requires that two HbA levels should achieve <8.0% target value within 12 months (measured two months apart) after switching from treatment with human insulins. Achieving this target, the treatment should be considered effective from drug reimbursement perspective.

AIM

The aims of the study were to investigate the effectiveness of insulin glargine + insulin glulisine basal-bolus regimen from the payer's perspective and to investigate the ability to maintain the achieved glycaemic control in previously uncontrolled T2DM patients (HbA >9.0%).

METHOD

This one-year, non-interventional study included patients with T2DM inadequately controlled (HbA >9.0%) on previous human basal-bolus treatment. The main outcomes were the proportion of patients who achieved the adequate glycaemic control (defined by the reimbursement rules) and the proportion of patients who achieved reimbursement rules defined HbA <8.0% target value by the 6 months after switch and could maintain this glycaemic control for upcoming further 6 months. As safety outcome, the hypoglycaemic events were recorded.

RESULTS

Out of the 557 patients enrolled, 287 had available data to be included in the efficacy analysis. Out of the 287 efficacy analysis patients, 169 (58.9%) achieved the reimbursement rules defined glycaemic control. At 6 months, 167 patients had HbA value <8.0% and 152 (91.0%) remained in this target range until the end of the 12-month observational period. Overall, 1221 non-severe and 6 severe hypoglycaemic events were reported.

CONCLUSIONS

More than half of the patients with T2DM who were newly switched to insulin glargine + glulisine basal-bolus treatment could achieve the reimbursement rule criteria requiring for prescription of the analogue insulins with no co-payment beyond 1 year of treatment in Hungary. However, the results revealed that glycaemic control assessment with HbA measurements had not met the reimbursement requirements in a significant part of patients. Orv Hetil. 2018; 159(50): 2122-2128.

摘要

引言

匈牙利将预混胰岛素作为2型糖尿病(T2DM)基础-餐时治疗一部分的报销条件是,在从人胰岛素治疗转换后12个月内(间隔两个月测量),两次糖化血红蛋白(HbA)水平应达到<8.0%的目标值。达到该目标后,从药物报销角度来看,该治疗应被视为有效。

目的

本研究的目的是从支付方的角度调查甘精胰岛素+赖脯胰岛素基础-餐时方案的有效性,并调查在先前未得到控制的T2DM患者(HbA>9.0%)中维持所达到的血糖控制的能力。

方法

这项为期一年的非干预性研究纳入了先前接受人胰岛素基础-餐时治疗但控制不佳(HbA>9.0%)的T2DM患者。主要结局是达到血糖充分控制(根据报销规则定义)的患者比例,以及在转换后6个月内达到报销规则定义的HbA<8.0%目标值并能在接下来的6个月内维持该血糖控制的患者比例。作为安全性结局,记录低血糖事件。

结果

在纳入的557例患者中,287例有可用于疗效分析的数据。在这287例进行疗效分析的患者中,169例(58.9%)达到了报销规则定义的血糖控制。在6个月时,167例患者的HbA值<8.0%,152例(91.0%)在12个月观察期结束时仍处于该目标范围内。总体而言,报告了1221次非严重低血糖事件和6次严重低血糖事件。

结论

新转换为甘精胰岛素+赖脯胰岛素基础-餐时治疗的T2DM患者中,超过一半能够达到匈牙利胰岛素类似物无自付费用处方超过1年治疗所需的报销规则标准。然而,结果显示,在很大一部分患者中,用HbA测量进行的血糖控制评估未达到报销要求。《匈牙利医学周报》。2018年;159(50): 2122 - 2128。

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