PMID- 32303862 OWN - NLM STAT- MEDLINE DCOM- 20200916 LR - 20201211 IS - 1862-3514 (Electronic) IS - 1862-3522 (Print) VI - 15 IP - 1 DP - 2020 Apr 17 TI - Adherence to and persistence with zoledronic acid treatment for osteoporosis-reasons for early discontinuation. PG - 58 LID - 10.1007/s11657-020-00733-4 [doi] LID - 58 AB - This retrospective study reports 81% long-term (> 3 years) adherence to and 77% persistence with zoledronic acid (ZA) treatment in osteoporosis patients, with ZA being costfree for patients. Eight percent of patients discontinued treatment because of adverse events (AEs), with a tendency of higher discontinuation rate in older patients. PURPOSE: This study investigated (1) long-term adherence to and persistence with ZA treatment in a real-world setting, (2) extent to which an adverse reaction to ZA impacted on adherence and persistence, and (3) whether there were sex or age differences in patients that had early treatment termination (ETT) due to AEs and those who adhered to the regimen. METHODS: All patients treated with ZA at the Endocrinology Department at Linkoping University Hospital, Linkoping, Sweden between 2012 and 2017 were included. ETT was defined as < 3 ZA infusions, which was confirmed from patients' medical records. RESULTS: A total of 414 patients were treated with ZA, with 81% receiving > 3 ZA infusions. Three-year persistence was 77% for a treatment window of 365 days +/- 90 days (75% with 365 days +/- 60 days window). The most common reason for ETT was AEs (8%), followed by medical conditions (5%), biological aging (3%), and other (e.g., lost to follow-up [3%]). Most patients who discontinued treatment because of AEs reported symptoms of acute-phase reaction, and tended to be older than those who adhered to treatment (74 +/- 9 vs 70 +/- 13 years, p = 0.064). There was no difference in sex ratio between the 2 groups (85% vs 90% females, p = 0.367). CONCLUSION: Rates of long-term adherence to and persistence with ZA treatment were high with a pre-scheduled 3-year treatment regimen in the tax-financed Swedish healthcare system. AEs-mainly acute-phase reaction-were the most common reason for ETT, occurring in nearly 1 out of 10 patients. FAU - Spangeus, Anna AU - Spangeus A AUID- ORCID: 0000-0002-7130-9158 AD - Department of Acute Internal Medicine and Geriatrics, Linkoping University Hospital, Linkoping, Sweden. anna.spangeus@liu.se. AD - Division of Diagnostics and Specialist Medicine, Department of Health, Medicine and Caring Sciences, Linkoping University, Linkoping, Sweden. anna.spangeus@liu.se. FAU - Johansson, Simon AU - Johansson S AD - Division of Diagnostics and Specialist Medicine, Department of Health, Medicine and Caring Sciences, Linkoping University, Linkoping, Sweden. FAU - Woisetschlager, Mischa AU - Woisetschlager M AUID- ORCID: 0000-0003-0066-4985 AD - Division of Diagnostics and Specialist Medicine, Department of Health, Medicine and Caring Sciences, Linkoping University, Linkoping, Sweden. AD - Department of Radiology, Linkoping University Hospital, Linkoping, Sweden. LA - eng PT - Evaluation Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20200417 PL - England TA - Arch Osteoporos JT - Archives of osteoporosis JID - 101318988 RN - 0 (Bone Density Conservation Agents) RN - 6XC1PAD3KF (Zoledronic Acid) SB - IM MH - Aged MH - Bone Density Conservation Agents/*administration & dosage/adverse effects MH - Female MH - Humans MH - Male MH - Medication Adherence/*statistics & numerical data MH - Middle Aged MH - Osteoporosis/*drug therapy MH - Retrospective Studies MH - Sweden MH - Time Factors MH - Withholding Treatment/*statistics & numerical data MH - Zoledronic Acid/*administration & dosage/adverse effects PMC - PMC7165128 OTO - NOTNLM OT - Adherence OT - Adverse event OT - Bisphosphonate OT - Discontinuation OT - Osteoporosis OT - Zoledronic acid COIS- Anna Spangeus has received lecture fees from Amgen Inc., Renapharma, and Mylan. Simon Johansson and Mischa Woisetschlager declare that they have no conflict of interest. EDAT- 2020/04/19 06:00 MHDA- 2020/09/17 06:00 PMCR- 2020/04/17 CRDT- 2020/04/19 06:00 PHST- 2020/02/24 00:00 [received] PHST- 2020/04/07 00:00 [accepted] PHST- 2020/04/19 06:00 [entrez] PHST- 2020/04/19 06:00 [pubmed] PHST- 2020/09/17 06:00 [medline] PHST- 2020/04/17 00:00 [pmc-release] AID - 10.1007/s11657-020-00733-4 [pii] AID - 733 [pii] AID - 10.1007/s11657-020-00733-4 [doi] PST - epublish SO - Arch Osteoporos. 2020 Apr 17;15(1):58. doi: 10.1007/s11657-020-00733-4.