Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment
Richard Derman1, Joseph D Kohles2, Ann Babbitt31Department of Obstetrics and Gynecology, Christiana Hospital, Newark, DE, USA; 2Roche, Nutley, NJ, USA; 3Greater Portland Bone and Joint Specialists, Portland, ME, USAAbstract: Data from two open-label trials (PRIOR and CURRENT) of women with postmenop...
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Dove Medical Press
2009
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oai:doaj.org-article:0de30185bf0e4187965286a0d57c2d8c2021-12-02T02:46:15ZGastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment1178-1998https://doaj.org/article/0de30185bf0e4187965286a0d57c2d8c2009-09-01T00:00:00Zhttps://www.dovepress.com/gastrointestinal-tolerability-with-ibandronate-after-previous-weekly-b-peer-reviewed-article-CIAhttps://doaj.org/toc/1178-1998Richard Derman1, Joseph D Kohles2, Ann Babbitt31Department of Obstetrics and Gynecology, Christiana Hospital, Newark, DE, USA; 2Roche, Nutley, NJ, USA; 3Greater Portland Bone and Joint Specialists, Portland, ME, USAAbstract: Data from two open-label trials (PRIOR and CURRENT) of women with postmenopausal osteoporosis or osteopenia were evaluated to assess whether monthly oral and quarterly intravenous (IV) ibandronate dosing improved self-reported gastrointestinal (GI) tolerability for patients who had previously experienced GI irritation with bisphosphonate (BP) use. In PRIOR, women who had discontinued daily or weekly BP treatment due to GI intolerance received monthly oral or quarterly IV ibandronate for 12 months. The CURRENT subanalysis included women receiving weekly BP treatment who switched to monthly oral ibandronate for six months. GI symptom severity and frequency were assessed using the Osteoporosis Patient Satisfaction Questionnaire™. In PRIOR, mean GI tolerability scores increased significantly at month 1 from screening for both treatment groups (oral: 79.3 versus 54.1; IV: 84.4 versus 51.0; p < 0.001 for both). Most patients reported improvement in GI symptom severity and frequency from baseline at all post-screening assessments (>90% at Month 10). In the CURRENT subanalysis >60% of patients reported improvements in heartburn or acid reflux and >70% indicated improvement in other stomach upset at month 6. Postmenopausal women with GI irritability with daily or weekly BPs experienced improvement in symptoms with extended dosing monthly or quarterly ibandronate compared with baseline.Keywords: ibandronate, osteoporosis, bisphosphonate, gastrointestinalRichard DermanJoseph D KohlesAnn BabbittDove Medical PressarticleosteoporosisbisphosphonateibandronategastrointestinaltolerabilityGeriatricsRC952-954.6ENClinical Interventions in Aging, Vol Volume 4, Pp 357-365 (2009) |
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osteoporosis bisphosphonate ibandronate gastrointestinal tolerability Geriatrics RC952-954.6 |
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osteoporosis bisphosphonate ibandronate gastrointestinal tolerability Geriatrics RC952-954.6 Richard Derman Joseph D Kohles Ann Babbitt Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
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Richard Derman1, Joseph D Kohles2, Ann Babbitt31Department of Obstetrics and Gynecology, Christiana Hospital, Newark, DE, USA; 2Roche, Nutley, NJ, USA; 3Greater Portland Bone and Joint Specialists, Portland, ME, USAAbstract: Data from two open-label trials (PRIOR and CURRENT) of women with postmenopausal osteoporosis or osteopenia were evaluated to assess whether monthly oral and quarterly intravenous (IV) ibandronate dosing improved self-reported gastrointestinal (GI) tolerability for patients who had previously experienced GI irritation with bisphosphonate (BP) use. In PRIOR, women who had discontinued daily or weekly BP treatment due to GI intolerance received monthly oral or quarterly IV ibandronate for 12 months. The CURRENT subanalysis included women receiving weekly BP treatment who switched to monthly oral ibandronate for six months. GI symptom severity and frequency were assessed using the Osteoporosis Patient Satisfaction Questionnaire™. In PRIOR, mean GI tolerability scores increased significantly at month 1 from screening for both treatment groups (oral: 79.3 versus 54.1; IV: 84.4 versus 51.0; p < 0.001 for both). Most patients reported improvement in GI symptom severity and frequency from baseline at all post-screening assessments (>90% at Month 10). In the CURRENT subanalysis >60% of patients reported improvements in heartburn or acid reflux and >70% indicated improvement in other stomach upset at month 6. Postmenopausal women with GI irritability with daily or weekly BPs experienced improvement in symptoms with extended dosing monthly or quarterly ibandronate compared with baseline.Keywords: ibandronate, osteoporosis, bisphosphonate, gastrointestinal |
format |
article |
author |
Richard Derman Joseph D Kohles Ann Babbitt |
author_facet |
Richard Derman Joseph D Kohles Ann Babbitt |
author_sort |
Richard Derman |
title |
Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
title_short |
Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
title_full |
Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
title_fullStr |
Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
title_full_unstemmed |
Gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
title_sort |
gastrointestinal tolerability with ibandronate after previous weekly bisphosphonate treatment |
publisher |
Dove Medical Press |
publishDate |
2009 |
url |
https://doaj.org/article/0de30185bf0e4187965286a0d57c2d8c |
work_keys_str_mv |
AT richardderman gastrointestinaltolerabilitywithibandronateafterpreviousweeklybisphosphonatetreatment AT josephdkohles gastrointestinaltolerabilitywithibandronateafterpreviousweeklybisphosphonatetreatment AT annbabbitt gastrointestinaltolerabilitywithibandronateafterpreviousweeklybisphosphonatetreatment |
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1718402143876022272 |