The Potential Impact of Inducing a Restriction in Reimbursement Criteria on Vitamin D Supplementation in Osteoporotic Patients with or without Fractures

  • Nutrients. 2022 Apr 29;14(9):1877. doi: 10.3390/nu14091877.
Luca Degli Esposti  1 Valentina Perrone  1 Stefania Sella  2 Gaetano Arcidiacono  2 Francesco Bertoldo  3 Andrea Giustina  4 Salvatore Minisola  5 Nicola Napoli  6 Giovanni Passeri  7 Maurizio Rossini  8 Sandro Giannini  2 LHU Study Group
Affiliations
  • 1. CliCon Srl Società Benefit Health Economics and Outcome Research, 40137 Bologna, Italy.
  • 2. Clinica Medica 1, Department of Medicine, University of Padova, 35128 Padova, Italy.
  • 3. Internal Medicine, Department of Medicine, University Hospital AOUI, 37134 Verona, Italy.
  • 4. Institute of Endocrine and Metabolic Sciences, Instituto di Ricovero e Cura a Carattere Scientifico (IRCSS) San Raffaele Hospital, San Raffaele Vita-Salute University, 20132 Milan, Italy.
  • 5. Department of Clinical, Internal, Anaesthesiology, and Cardiovascular Sciences Sapienza University of Rome, 00185 Rome, Italy.
  • 6. Division of Endocrinology and Diabetes, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.
  • 7. Unit of Clinica e Terapia Medica, Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
  • 8. Rheumatology Unit, Department of Medicine, University of Verona, 37134 Verona, Italy.
Abstract

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.

Keywords
clinical setting; osteoporosis; refracture risk; regulatory restriction; vitamin D supplementation.