Cost-effectiveness of Multifaceted Evidence Implementation Programs for the Prevention of Glucocorticoid-induced Osteoporosis
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Orthopedics
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Summary: Using a computer simulation model, we determined that an intervention aimed at improving the management of glucocorticoid-induced osteoporosis is likely to be cost-effective to third-party health insurers only if it focuses on individuals with very high fracture risk and the proportion of prescriptions for generic bisphosphonates increases substantially.
Introduction: The purpose of this study is to determine whether an evidence implementation program (intervention) focused on increasing appropriate management of glucocorticoid-induced osteoporosis (GIOP) might be cost-effective compared with current practice (no intervention) from the perspective of a third-party health insurer.
Methods: We developed a Markov microsimulation model to determine the cost-effectiveness of the intervention. The hypothetical patient cohort was of current chronic glucocorticoid users 50-65 years old and 70% female. Model parameters were derived from published literature, and sensitivity analyses were performed.
Results: The intervention resulted in incremental cost-effectiveness ratios (ICERs) of $298,000 per quality adjusted life year (QALY) and $206,000 per hip fracture averted. If the cohort's baseline risk of fracture was increased by 50% (10-year cumulative incidence of hip fracture of 14%), the ICERs improved significantly: $105,000 per QALY and $137,000 per hip fracture averted. The ICERs improved significantly if the proportion of prescriptions for generic bisphosphonates was increased to 75%, with $113,000 per QALY and $77,900 per hip fracture averted.
Conclusions: Evidence implementation programs for the management of GIOP are likely to be cost-effective to third-party health insurers only if they are targeted at individuals with a very high risk of fracture and the proportion of prescriptions for less expensive generic bisphosphonates increases substantially.
Laurent M, Goemaere S, Verroken C, Bergmann P, Body J, Bruyere O Front Endocrinol (Lausanne). 2022; 13:908727.
PMID: 35757436 PMC: 9219603. DOI: 10.3389/fendo.2022.908727.
Glucocorticoid-induced osteoporosis: 2019 concise clinical review.
Adami G, Saag K Osteoporos Int. 2019; 30(6):1145-1156.
PMID: 30805679 DOI: 10.1007/s00198-019-04906-x.
Moriwaki K, Fukuda H Osteoporos Int. 2019; 30(2):299-310.
PMID: 30610244 DOI: 10.1007/s00198-018-4798-9.
Du X, Li M, Zhu P, Wang J, Hou L, Li J PLoS One. 2018; 13(8):e0200807.
PMID: 30133454 PMC: 6104919. DOI: 10.1371/journal.pone.0200807.
Thomas T, Horlait S, Ringe J, Abelson A, Gold D, Atlan P Osteoporos Int. 2012; 24(1):263-9.
PMID: 22736069 DOI: 10.1007/s00198-012-2060-4.