Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00198-021-05907-5
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dc.titleAlendronate use in older patients with reduced renal function: challenges and opportunities in clinical practice
dc.contributor.authorNaganathar, N
dc.contributor.authorYau, WP
dc.contributor.authorMok, ZH
dc.contributor.authorTan, ZYF
dc.contributor.authorChew, STH
dc.date.accessioned2023-03-09T00:50:42Z
dc.date.available2023-03-09T00:50:42Z
dc.date.issued2021-10-01
dc.identifier.citationNaganathar, N, Yau, WP, Mok, ZH, Tan, ZYF, Chew, STH (2021-10-01). Alendronate use in older patients with reduced renal function: challenges and opportunities in clinical practice. Osteoporosis International 32 (10) : 1981-1988. ScholarBank@NUS Repository. https://doi.org/10.1007/s00198-021-05907-5
dc.identifier.issn0937-941X
dc.identifier.issn1433-2965
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/237958
dc.description.abstractSummary: In this retrospective cohort study, alendronate use among older osteoporosis patients (age>65 years) with reduced renal function (creatinine clearance<35ml/min) was not associated with significant deterioration in renal function from baseline nor increased incidence of osteoporotic fractures or acute kidney injury, compared with patients conservatively managed with only calcium/vitamin D supplementation. Introduction: Oral bisphosphonates are not recommended in patients with creatinine clearance (CrCl) <35ml/min, although this is not supported by post hoc analyses of pivotal oral bisphosphonate studies. As both osteoporosis and renal insufficiency are more prevalent with advancing age, it is important to determine the safety and efficacy of oral bisphosphonates among these patients. Methods: Patients with CrCl <35ml/min on alendronate (group A, n=98), with CrCl <35ml/min conservatively managed (group B, n=96), and with CrCl ≥35ml/min on alendronate (group C, n=96) were followed up to 22 months. Primary outcomes were mean change in CrCl from baseline in group A compared with groups B and C, respectively. Secondary outcomes were the incidence of osteoporotic fractures and adverse events between groups. Results: There was no significant change in CrCl from baseline when comparing group A (−1.53±6.83ml/min) with group B (0.59±5.17ml/min) (p=0.075), and group A with group C (−3.71±7.54ml/min) (p=0.163). There was no significant increase in incidences of osteoporotic fractures in group A compared with group B (adjusted relative risk (aRR) 2.02, 95% confidence interval (CI) 0.64–6.37) and group A compared with group C (aRR 1.15, 95% CI 0.46–2.89). There was no significant difference in incidences of acute kidney injury (AKI) in group A compared with group B (aRR 0.48, 95% CI 0.20–1.12). Although statistically non-significant, there was an increase in AKI incidence in group A compared with group C (RR 7.84, 95% CI 0.98–62.66). Conclusion: Among patients with CrCl <35ml/min, alendronate therapy was not associated with significant deterioration in renal function from baseline. Although not powered for secondary outcomes, there were no statistically significant differences in osteoporotic fracture or AKI incidence between the groups.
dc.publisherSpringer Science and Business Media LLC
dc.sourceElements
dc.subjectAlendronate
dc.subjectBisphosphonates
dc.subjectElderly
dc.subjectOsteoporosis
dc.subjectRenal impairment
dc.subjectAged
dc.subjectAlendronate
dc.subjectDiphosphonates
dc.subjectHumans
dc.subjectKidney
dc.subjectRenal Insufficiency
dc.subjectRetrospective Studies
dc.typeArticle
dc.date.updated2023-03-08T09:31:04Z
dc.contributor.departmentMEDICINE
dc.contributor.departmentPHARMACY
dc.description.doi10.1007/s00198-021-05907-5
dc.description.sourcetitleOsteoporosis International
dc.description.volume32
dc.description.issue10
dc.description.page1981-1988
dc.published.statePublished
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