Department of Internal Medicine, VieCuri Medical Center, Tegelseweg 210, 5912 BL, Venlo, the Netherlands.
Department of Internal Medicine, Maastricht University, Maastricht, the Netherlands.
Osteoporos Int. 2019 Sep;30(9):1837-1844. doi: 10.1007/s00198-019-05052-0. Epub 2019 Jul 18.
This study evaluated the 2-year persistence with teriparatide in the Netherlands. Analyses showed that the risk of non-persistence was 28% lower in patients who were followed according to an additional educational and motivational support program.
Until recently, teriparatide (TPTD) was a third-line treatment option for severe osteoporosis in the Netherlands, which could only be prescribed by medical specialists based on a specific medical statement. We aimed to determine whether an educational and motivational support program (EMSP) increased 2-year treatment persistence with TPTD in patients with severe osteoporosis.
We evaluated persistence in 1573 Dutch patients treated with TPTD from January 2013 until January 2018. From January 2013 onwards, all patients received a basic support program (BSP) consisting of an educational home visit to initiate TPTD treatment and phone calls (at 1, 2.5 and 8 weeks). Since May 2015, all patients received the EMSP consisting of the BSP extended with evaluation of medication adherence during phone calls, an additional phone call (at 12 months), and motivational letters at 9 and 14 months.
The EMSP showed a statistically significantly higher 2-year persistence (78%) with TPTD as compared with the BSP (72%). Reasons for treatment discontinuation were comparable between groups, except for the proportion of patients who had stopped TPTD administration due to side effects, which was significantly lower in the EMSP group (8% vs. 15% in BSP, p < 0.001). Overall, the risk of non-persistence was 28% lower in the EMSP compared with the BSP group (HR: 0.72; 95% CI: 0.55-0.93).
The introduction of the EMSP has demonstrated to improve the persistence with TPTD, resulting in 78% of the patients being persistent with TPTD during the 2-year treatment period.
本研究评估了荷兰特立帕肽的 2 年持续性。分析表明,在接受额外教育和激励支持计划随访的患者中,非持续性风险降低了 28%。
直到最近,特立帕肽(TPTD)在荷兰是一种三线治疗严重骨质疏松症的药物,只能由医学专家根据特定的医学声明开处。我们旨在确定教育和激励支持计划(EMSP)是否能提高严重骨质疏松症患者使用特立帕肽的 2 年治疗持续性。
我们评估了 2013 年 1 月至 2018 年 1 月期间在荷兰接受特立帕肽治疗的 1573 名患者的持续性。从 2013 年 1 月起,所有患者接受了基本支持计划(BSP),包括一次家庭教育访问以启动特立帕肽治疗和电话随访(第 1、2.5 和 8 周)。自 2015 年 5 月起,所有患者都接受了 EMSP,包括 BSP 扩展,包括电话随访中评估药物依从性、一次额外的电话随访(第 12 个月)和第 9 和 14 个月的激励信。
与 BSP(72%)相比,EMSP 显示出统计学上更高的 2 年持续性(78%)。两组停药原因相似,但因副作用停止特立帕肽治疗的患者比例在 EMSP 组明显较低(8%对 BSP 组的 15%,p<0.001)。总体而言,与 BSP 组相比,EMSP 组非持续性的风险降低了 28%(HR:0.72;95%CI:0.55-0.93)。
引入 EMSP 已被证明可以提高特立帕肽的持续性,使 78%的患者在 2 年治疗期间持续使用特立帕肽。