Abstract
Objectives Bisphosphonates are central to osteoporosis management, but prolonged use may not be needed in some individuals, and/or increase the risk of rare adverse events.[1] Deprescribing guidance could support safe discontinuation decisions, including for individuals initiated on bisphosphonates to prevent glucocorticoid-induced osteoporosis (GIOP). This rapid scoping review examined deprescribing, drug holiday, and treatment duration recommendations within osteoporosis guidelines to inform decision support for rheumatologists and other clinicians.
Methods We conducted a rapid scoping review searching PubMed, Embase, MEDLINE, and gray literature. Leveraging a prior systematic review of guidelines published 2012-2022,[2] we updated the search to June 10, 2025, and expanded the scope to include GIOP and other secondary osteoporosis. Eligible guidelines contained ≥1 deprescribing recommendation for adults receiving bisphosphonates. One reviewer screened all records, with independent verification of selected records by a second reviewer. We extracted deprescribing criteria, considerations for monitoring and re-prescribing, and evidence grading.
Results We identified 291 records, reviewed 104 in full, and included 41 guidance documents from 23 countries (7 new, 34 retained from the original review.[2] Two-thirds (66%, n=27) relied on expert consensus without structured evidence grading, while 34% (n=14) used formal evidence appraisal methods including the GRADE framework (17%, n=7). All recommendations focused on deprescribing in individuals with initial indications for therapy. Most (93%, n=38) framed deprescribing as a drug holiday and generally recommended consideration after ≥5 years of oral or ≥3 years of intravenous bisphosphonate exposure in individuals without high fracture risk (34%, n=14), without prior or incident fractures on treatment (34%, n = 14), and/or with bone mineral density (BMD) T-score > −2.5 (29%, n=12). Three (7%) recommended deprescribing in other settings, including after glucocorticoid withdrawal in the setting of low fracture risk (n=1). Few incorporated individualized factors including life expectancy (5%, n=2), overall health (3%, n=1), or patient preferences (18%, n = 7). The majority (73%, n = 30) outlined when deprescribing should be avoided. Suggested drug holiday durations ranged 1-5 years. About half (44%, n = 18) advised BMD or fracture monitoring after deprescribing, and 29% (n = 12) recommended restarting therapy if BMD declined or a new fracture occurred.
Conclusion Most guidelines framed bisphosphonate deprescribing as drug holidays in postmenopausal osteoporosis, implying that future re-prescribing will be necessary. Recommendations were largely consensus-based. Practical guidance regarding deprescribing in patients who started bisphosphonates to prevent GIOP was scarce. Our results can inform decision support to guide safe deprescribing.
References [1.] Eastell R. J Bone Miner Res 2019;34:7-10. [2.] Jepsen DB. Eur Geriatr Med 2023;14:747-60.
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