Kyung Soo Suk1, Hwan Mo Lee1, Seong-Hwan Moon1, Hee June Kim1, Hak Sun Kim1, Jin-Oh Park1, Byung Ho Lee2. 1. Department of Orthopaedic Surgery, Yonsei University College of Medicine, Seoul, Korea. 2. Department of Orthopaedic Surgery, International St. Mary's Hospital, Catholic Kwandong University College of Medicine, Incheon, Korea. 144667@daum.net.
Abstract
PURPOSE: Teriparatide 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.
PURPOSE:Teriparatide 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.
Authors: J A Kanis; D Black; C Cooper; P Dargent; B Dawson-Hughes; C De Laet; P Delmas; J Eisman; O Johnell; B Jonsson; L Melton; A Oden; S Papapoulos; H Pols; R Rizzoli; A Silman; A Tenenhouse Journal: Osteoporos Int Date: 2002-07 Impact factor: 4.507
Authors: Michael R McClung; Javier San Martin; Paul D Miller; Roberto Civitelli; Francisco Bandeira; Molly Omizo; David W Donley; Gail P Dalsky; Erik F Eriksen Journal: Arch Intern Med Date: 2005 Aug 8-22
Authors: P Ravn; G Cizza; N H Bjarnason; D Thompson; M Daley; R D Wasnich; M McClung; D Hosking; A J Yates; C Christiansen Journal: J Bone Miner Res Date: 1999-09 Impact factor: 6.741
Authors: D W Dempster; F Cosman; E S Kurland; H Zhou; J Nieves; L Woelfert; E Shane; K Plavetić; R Müller; J Bilezikian; R Lindsay Journal: J Bone Miner Res Date: 2001-10 Impact factor: 6.741
Authors: B Ettinger; D M Black; B H Mitlak; R K Knickerbocker; T Nickelsen; H K Genant; C Christiansen; P D Delmas; J R Zanchetta; J Stakkestad; C C Glüer; K Krueger; F J Cohen; S Eckert; K E Ensrud; L V Avioli; P Lips; S R Cummings Journal: JAMA Date: 1999-08-18 Impact factor: 56.272
Authors: D M Black; S R Cummings; D B Karpf; J A Cauley; D E Thompson; M C Nevitt; D C Bauer; H K Genant; W L Haskell; R Marcus; S M Ott; J C Torner; S A Quandt; T F Reiss; K E Ensrud Journal: Lancet Date: 1996-12-07 Impact factor: 79.321
Authors: Yebin Jiang; Jenny J Zhao; Bruce H Mitlak; Ouhong Wang; Harry K Genant; Erik F Eriksen Journal: J Bone Miner Res Date: 2003-11 Impact factor: 6.741
Authors: Jean-Jacques Body; Gregory A Gaich; Wim H Scheele; Pandurang M Kulkarni; Paul D Miller; Anne Peretz; Robin K Dore; Ricardo Correa-Rotter; Alexandra Papaioannou; David C Cumming; Anthony B Hodsman Journal: J Clin Endocrinol Metab Date: 2002-10 Impact factor: 5.958
Authors: D-C Chan; C H-C Chang; L-C Lim; A J M Brnabic; J-Y Tsauo; R Burge; F-Y Hsiao; L Jin; S Gürbüz; R-S Yang Journal: Osteoporos Int Date: 2016-05-12 Impact factor: 4.507