Evidence map›Paper›PMID 40906172›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2025

The relationship between osteoporosis treatment history and receipt of a second zoledronic acid dose.

Natalia Konstantelos, Sandra Kim, Angela M Cheung, Andrea M Burden, Paul Grootendorst, Suzanne M Cadarette

Abstract read
In one paragraph

Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Natalia KonstantelosLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada. natalia.konstantelos@gmail.com.ORCID http://orcid.org/0000-0003-4100-8650
Sandra KimLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Angela M CheungDalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Andrea M BurdenLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Paul GrootendorstLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Suzanne M CadaretteLeslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.

Funding

Benefits and Harms of Long-term Osteoporosis Pharmacotherapy: Impact of Treatment Length, Type, Switching, and HolidaysR01AG078759 · NIA · BROWN UNIVERSITY · PI CADARETTE, SUZANNE, HAYES, KALEEN NICOLE · 2022 to 2025
$2.5M
NIA NIH HHS R01 AG078759NIA NIH HHS R01AG078759
6 · The paper itself

Abstract

We examined characteristics of patients in Ontario, Canada, initiating publicly funded zoledronic acid for osteoporosis from 2006 to 2021. Most patients had prior osteoporosis treatments, with those previously using oral bisphosphonates more likely to receive a second dose. Understanding treatment decisions and patient beliefs is key for future research. PURPOSE: Zoledronic acid is a once-yearly intravenous bisphosphonate and is considered a second-line osteoporosis therapy in Ontario, Canada. This regimen was approved using evidence from clinical trials of treatment-naïve patients. However, many patients initiating zoledronic acid have used other osteoporosis medications prior, which may influence the frequency of dosing. We describe the characteristics of patients initiating zoledronic acid and identify if previous osteoporosis pharmacotherapy impacts the receipt of a second dose.

methodsHealthcare administrative data in Ontario were used to identify older patients initiating publicly funded zoledronic acid from 10/2006 to 10/2021 and followed until 10/2022. Patients were categorized based on 5-year osteoporosis treatment look back history in mutually exclusive groups: (1) no history, (2) denosumab, (3) oral bisphosphonates, and (4) other osteoporosis medications. Cox proportional hazards models were used to compare receipt of a second zoledronic acid infusion between patients in treatment history groups.

resultsWe identified 3308 patients initiating zoledronic acid; median age = 77, 81% female, 31% received a second infusion of zoledronic acid. Half (49%) had a history of oral bisphosphonates, 37% no history, 11% denosumab, and 3% other medications. Overall, patients having history of oral bisphosphonates were 1.5 times more likely to receive a second dose relative to no history (HR, 95%CI: 1.50 [1.31-1.71]).

conclusionIn contrast to patients in pivotal trials, most patients receiving zoledronic acid had prior osteoporosis pharmacotherapy. Patients with prior oral bisphosphonate use had higher rates of receiving a second dose. Better understanding of treatment decisions and patient beliefs around receiving a second infusion of zoledronic acid should be further investigated.

Indexed as

Bone Density Conservation AgentsOsteoporosisZoledronic AcidAdministration, OralAgedAged, 80 and overDenosumabDrug Administration ScheduleFemaleHumansMaleOntarioOsteoporotic FracturesBone Density Conservation AgentsDenosumabZoledronic AcidBisphosphonateDenosumabOsteoporosisZoledronic acid

Identifiers

PMID40906172
PMCPMC12433616

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.