At Least One Cyclic Teriparatide Administration Can Be Helpful to Delay Initial Onset of a New Osteoporotic Vertebral Compression Fracture

被引:2
|
作者
Suk, Kyung Soo [1 ]
Lee, Hwan Mo [1 ]
Moon, Seong-Hwan [1 ]
Kim, Hee June [1 ]
Kim, Hak Sun [1 ]
Park, Jin-Oh [1 ]
Lee, Byung Ho [2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Orthopaed Surg, Seoul, South Korea
[2] Catholic Kwandong Univ, Coll Med, Dept Orthopaed Surg, Int St Marys Hosp, Inchon 404834, South Korea
关键词
Osteoporosis; teriparatide; duration; vertebral compression fracture; PARATHYROID-HORMONE; 1-34; POSTMENOPAUSAL WOMEN; RANDOMIZED-TRIAL; COST-EFFECTIVENESS; VERTEBROPLASTY; RISK; ALENDRONATE; PREVENTION; REDUCTION; UTILITY;
D O I
10.3349/ymj.2014.55.6.1576
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Teiiparatide markedly increases bone formation and strength, while reducing the incidence of new-onset osteoporotic vertebral compression fractures (OVCFs). In some countries, expenses for teriparatide use are covered by medical insurance for up to 6 months; however, the national medical insurance of the authors' country does not cover these expenses. This retrospective cohort study compared the therapeutic effects of teriparatide on the initial onset of a new OVCF after treatment of osteoporosis and/or related OVCFs with regard to therapeutic durations of longer than 3 months (LT3M) or shorter than 3 months (ST3M). Materials and Methods: From May 2007 to February 2012, 404 patients who were prescribed and administered teriparatide and who could be followed-up for longer than 12 months were enrolled. They were divided into two groups depending on teriparatide duration: LT3M (n=132) and ST3M (n=272). Results: The group with the teriparatide duration of LT3M showed significantly less development of an initial OVCF within 1 year (p=0.004, chi-square). Duration of teriparatide use, body mass index, pre-teriparatide lowest spinal bone mineral density, and severity of osteoporosis significantly affected multiple regression analysis results (p<0.05). Survival analysis of first new-onset OVCFs demonstrated a significantly better survival rate for the LT3M group (log rank, p=0.005). Also, the ST3M group showed a higher odds ratio of 54.00 for development of an initial OVCF during follow-up than the LT3M group (Mantel-Haenzel common odds ratio, p=0.006). Conclusion: At least one cyclic teriparatide administration is recommended to provide a protective effect against the initial onset of a new OVCF for up to one year after therapy.
引用
收藏
页码:1576 / 1583
页数:8
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