CliCon Srl Società Benefit Health Economics and Outcome Research, 40137 Bologna, Italy.
Clinica Medica 1, Department of Medicine, University of Padova, 35128 Padova, Italy.
Nutrients. 2022 Apr 29;14(9):1877. doi: 10.3390/nu14091877.
In October 2019, the Italian Drug Agency (AIFA) restricted reimbursement criteria for vitamin D (VD) use outside the osteoporosis setting (Note 96). However, whether this restriction could also have involved patients at risk for or with osteoporotic fractures has not yet been investigated. We retrospectively analyzed databases from five Italian Local Health Units. Patients aged ≥50 years with either at least one prescription for osteoporosis treatment or with fragility fractures and evidence of osteoporosis from 2011 to 2020 were included. The proportion of subjects with an interruption in VD treatment before and after the introduction of the new reimbursement criteria and predictors of this interruption were analyzed. A total of 94,505 patients (aged 69.4 years) were included. Following the introduction of Note 96, a 2-fold (OR 1.98, 95% CI: 1.92-2.04) increased risk of VD discontinuation was observed. These findings were independent of seasonal variation, osteoporosis treatment patterns, as well as other confounding variables. However, a higher rate of interruption was observed in patients without vertebral/femur fracture (37.8%) vs. those with fracture (32.9%). Rheumatoid arthritis, dyslipidemia and previous fracture were associated with a lower risk of VD interruption, while stroke increased the risk of VD interruption. Our results highlight that a possible misinterpretation of newly introduced criteria for reimbursement restrictions in VD outside of osteoporosis have resulted in an inadequate level of VD supplementation in patients with osteoporosis. This undertreatment could reduce the effect of osteoporosis therapies leading to increased risk of negative outcome.
2019 年 10 月,意大利药品管理局(AIFA)限制了维生素 D(VD)在骨质疏松症治疗以外的报销标准(注 96)。然而,这种限制是否也涉及到有骨质疏松症骨折风险或已经发生骨质疏松症骨折的患者,尚未进行研究。我们对来自意大利五个地方卫生单位的数据库进行了回顾性分析。纳入年龄≥50 岁的患者,其至少有一种骨质疏松症治疗药物的处方,或有脆性骨折和骨质疏松症证据,且在 2011 年至 2020 年期间。分析了在引入新的报销标准前后中断 VD 治疗的患者比例以及中断治疗的预测因素。共纳入 94505 例患者(年龄 69.4 岁)。在引入注 96 后,VD 停药的风险增加了 2 倍(OR 1.98,95%CI:1.92-2.04)。这些发现与季节性变化、骨质疏松症治疗模式以及其他混杂因素无关。然而,在没有椎体/股骨骨折的患者(37.8%)中,中断治疗的发生率高于有骨折的患者(32.9%)。类风湿关节炎、血脂异常和既往骨折与 VD 中断风险较低相关,而中风则增加了 VD 中断的风险。我们的结果表明,对 VD 骨质疏松症以外的新引入的报销限制标准可能存在错误解读,导致骨质疏松症患者的 VD 补充不足。这种治疗不足可能会降低骨质疏松症治疗的效果,导致不良后果的风险增加。