Impact on Bisphosphonate Persistence and Compliance: Daily Postprandial Administration
- Abstract
- BACKGROUND: Bisphosphonate (BP) is an effective drug for the prevention and treatment of osteoporosis. However, gastrointestinal distress caused by BP is a well-known side effect for low compliance. The aim of our study was to compare the 1-year persistence, compliance and T-scores between the aperitif medication group and the postprandial medication group. METHODS: Three hundred patients were included in this study to determine their persistence and compliance with the prescribed daily BP (Maxmarvil®, alendronate 5 mg and calcitriol 0.5 µg; YuYu Pharm) following distal radius fractures. Patients in Group 1 (aperitif medication) were asked to adhere to the general guidelines for BPs before breakfast. Patients in Group 2 (postprandial medication) were recommended medication after breakfast. We compared the persistence and compliance of this daily BP therapy using the medication possession ratio (MPR) and T-scores between the 2 groups after 1 year. RESULTS: Bone mineral density in hip and lumbar spine was improved significantly in 2 groups (P<0.001). Significant differences existed between 2 groups, including 73 of 150 patients (48.7%) in Group 1, and 111 of 150 patients (73.3%) in Group 2 for 1-year persistence (P=0.001). The mean MPR is 0.66 in Group 1 (range, 0.50-0.86) and 0.71 in Group 2 (range, 0.54-0.87). A significant difference was detected between the 2 groups (P=0.002). CONCLUSIONS: Postprandial administration improved persistence and compliance with daily BP therapy, resulting in better clinical outcomes.
- All Author(s)
- C. H. Park
; K. J. Jung
; J. H. Nho
; J. H. Kim
; S. H. Won
; D. I. Chun
; D. W. Byun
- Intsitutional Author(s)
- 정기진
- Issued Date
- 2019
- Type
- Article
- Keyword
- Aperitif; Bisphosphonate; Compliance; Daily; Persistence; Postprandial
- Publisher
- 대한골대사학회
대한근감소증학회
Korean Society for Bone and Mineral Research
Korean Society of Sarcopenia
- ISSN
- 2287-6375
- Citation Title
- Journal of Bone Metabolism
- Citation Volume
- 26
- Citation Number
- 1
- Citation Start Page
- 39
- Citation End Page
- 44
- Language(ISO)
- eng
- DOI
- 10.11005/jbm.2019.26.1.39
- URI
- http://schca-ir.schmc.ac.kr/handle/2022.oak/3557
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