Goal-Directed Osteoporosis Treatment: ASBMR/BHOF Task Force Position Statement 2024
The overarching goal of osteoporosis management is to prevent fractures. A goal-directed approach to long-term management of fracture risk helps ensure that the most appropriate initial treatment and treatment sequence is selected for individual patients. Goal-directed treatment decisions require as...
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Veröffentlicht in: | Journal of bone and mineral research 2024-09, Vol.39 (10), p.1393-1405 |
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creator | Cosman, Felicia Lewiecki, E Michael Eastell, Richard Ebeling, Peter R De Beur, Suzanne Jan Langdahl, Bente Rhee, Yumie Fuleihan, Ghada El-Hajj Kiel, Douglas P Schousboe, John T Borges, Joao Lindolfo Cheung, Angela M Diez-Perez, Adolfo Hadji, Peyman Tanaka, Sakae Thomasius, Friederike Xia, Weibo Cummings, Steven R |
description | The overarching goal of osteoporosis management is to prevent fractures. A goal-directed approach to long-term management of fracture risk helps ensure that the most appropriate initial treatment and treatment sequence is selected for individual patients. Goal-directed treatment decisions require assessment of clinical fracture history, vertebral fracture identification (using vertebral imaging as appropriate), measurement of bone mineral density (BMD) and consideration of other major clinical risk factors. Treatment targets should be tailored to each patient's individual risk profile and based on the specific indication for beginning treatment, including recency, site, number and severity of prior fractures, and BMD levels at the total hip, femoral neck, and lumbar spine. Instead of first-line bisphosphonate treatment for all patients, selection of initial treatment should focus on reducing fracture risk rapidly for patients at very high and imminent risk, such as in those with recent fractures. Initial treatment selection should also consider the probability that a BMD treatment target can be attained within a reasonable period of time and the differential magnitude of fracture risk reduction and BMD impact with osteoanabolic versus antiresorptive therapy. This position statement of the ASBMR/BHOF Task Force on Goal-Directed Osteoporosis Treatment provides an overall summary of the major clinical recommendations about treatment targets and strategies to achieve those targets based on the best evidence available, derived primarily from studies in older postmenopausal women of European ancestry. |
doi_str_mv | 10.1093/jbmr/zjae119 |
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A goal-directed approach to long-term management of fracture risk helps ensure that the most appropriate initial treatment and treatment sequence is selected for individual patients. Goal-directed treatment decisions require assessment of clinical fracture history, vertebral fracture identification (using vertebral imaging as appropriate), measurement of bone mineral density (BMD) and consideration of other major clinical risk factors. Treatment targets should be tailored to each patient's individual risk profile and based on the specific indication for beginning treatment, including recency, site, number and severity of prior fractures, and BMD levels at the total hip, femoral neck, and lumbar spine. Instead of first-line bisphosphonate treatment for all patients, selection of initial treatment should focus on reducing fracture risk rapidly for patients at very high and imminent risk, such as in those with recent fractures. Initial treatment selection should also consider the probability that a BMD treatment target can be attained within a reasonable period of time and the differential magnitude of fracture risk reduction and BMD impact with osteoanabolic versus antiresorptive therapy. This position statement of the ASBMR/BHOF Task Force on Goal-Directed Osteoporosis Treatment provides an overall summary of the major clinical recommendations about treatment targets and strategies to achieve those targets based on the best evidence available, derived primarily from studies in older postmenopausal women of European ancestry.</description><identifier>ISSN: 0884-0431</identifier><identifier>ISSN: 1523-4681</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1093/jbmr/zjae119</identifier><identifier>PMID: 39073912</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Review</subject><ispartof>Journal of bone and mineral research, 2024-09, Vol.39 (10), p.1393-1405</ispartof><rights>The Author(s) [2024]. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research.</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research.</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c272t-f4e31ffd69c62b8b538543aecb95d79a56da782e6993d064e33a8c88e9879ee63</cites><orcidid>0000-0002-0323-3366 ; 0000-0001-8474-0310 ; 0000-0001-9210-9414 ; 0000-0003-4554-6616 ; 0000-0003-4227-5638</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39073912$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cosman, Felicia</creatorcontrib><creatorcontrib>Lewiecki, E Michael</creatorcontrib><creatorcontrib>Eastell, Richard</creatorcontrib><creatorcontrib>Ebeling, Peter R</creatorcontrib><creatorcontrib>De Beur, Suzanne Jan</creatorcontrib><creatorcontrib>Langdahl, Bente</creatorcontrib><creatorcontrib>Rhee, Yumie</creatorcontrib><creatorcontrib>Fuleihan, Ghada El-Hajj</creatorcontrib><creatorcontrib>Kiel, Douglas P</creatorcontrib><creatorcontrib>Schousboe, John T</creatorcontrib><creatorcontrib>Borges, Joao Lindolfo</creatorcontrib><creatorcontrib>Cheung, Angela M</creatorcontrib><creatorcontrib>Diez-Perez, Adolfo</creatorcontrib><creatorcontrib>Hadji, Peyman</creatorcontrib><creatorcontrib>Tanaka, Sakae</creatorcontrib><creatorcontrib>Thomasius, Friederike</creatorcontrib><creatorcontrib>Xia, Weibo</creatorcontrib><creatorcontrib>Cummings, Steven R</creatorcontrib><title>Goal-Directed Osteoporosis Treatment: ASBMR/BHOF Task Force Position Statement 2024</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>The overarching goal of osteoporosis management is to prevent fractures. A goal-directed approach to long-term management of fracture risk helps ensure that the most appropriate initial treatment and treatment sequence is selected for individual patients. Goal-directed treatment decisions require assessment of clinical fracture history, vertebral fracture identification (using vertebral imaging as appropriate), measurement of bone mineral density (BMD) and consideration of other major clinical risk factors. Treatment targets should be tailored to each patient's individual risk profile and based on the specific indication for beginning treatment, including recency, site, number and severity of prior fractures, and BMD levels at the total hip, femoral neck, and lumbar spine. Instead of first-line bisphosphonate treatment for all patients, selection of initial treatment should focus on reducing fracture risk rapidly for patients at very high and imminent risk, such as in those with recent fractures. Initial treatment selection should also consider the probability that a BMD treatment target can be attained within a reasonable period of time and the differential magnitude of fracture risk reduction and BMD impact with osteoanabolic versus antiresorptive therapy. This position statement of the ASBMR/BHOF Task Force on Goal-Directed Osteoporosis Treatment provides an overall summary of the major clinical recommendations about treatment targets and strategies to achieve those targets based on the best evidence available, derived primarily from studies in older postmenopausal women of European ancestry.</description><subject>Review</subject><issn>0884-0431</issn><issn>1523-4681</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVkb1PwzAUxC0EoqWwMaOMDIT6I3FsFtQCpUigIlpmy3FeICWpi-0iwV9PKkoF0xvup7unO4SOCT4nWLL-PG9c_2uugRC5g7okpSxOuCC7qIuFSGKcMNJBB97PMcY85XwfdZjEGZOEdtH01uo6vq4cmABFNPEB7NI66ysfzRzo0MAiXESD6fDhqT8cT0bRTPu3aGSdgeixxUJlF9E06ABrMqKYJodor9S1h6PN7aHn0c3sahzfT27vrgb3saEZDXGZACNlWXBpOM1FnjKRJkyDyWVaZFKnvNCZoMClZAXmLc20MEKAFJkE4KyHLn98l6u8gcK0-U7XaumqRrtPZXWl_iuL6lW92A9FSELTDLPW4XTj4Oz7CnxQTeUN1LVegF15xbDgmGOZ4BY9-0FNW453UG5zCFbrIdR6CLUZosVP_v62hX-bZ99GzIWE</recordid><startdate>20240926</startdate><enddate>20240926</enddate><creator>Cosman, Felicia</creator><creator>Lewiecki, E Michael</creator><creator>Eastell, Richard</creator><creator>Ebeling, Peter R</creator><creator>De Beur, Suzanne Jan</creator><creator>Langdahl, Bente</creator><creator>Rhee, Yumie</creator><creator>Fuleihan, Ghada El-Hajj</creator><creator>Kiel, Douglas P</creator><creator>Schousboe, John T</creator><creator>Borges, Joao Lindolfo</creator><creator>Cheung, Angela M</creator><creator>Diez-Perez, Adolfo</creator><creator>Hadji, Peyman</creator><creator>Tanaka, Sakae</creator><creator>Thomasius, Friederike</creator><creator>Xia, Weibo</creator><creator>Cummings, Steven R</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0323-3366</orcidid><orcidid>https://orcid.org/0000-0001-8474-0310</orcidid><orcidid>https://orcid.org/0000-0001-9210-9414</orcidid><orcidid>https://orcid.org/0000-0003-4554-6616</orcidid><orcidid>https://orcid.org/0000-0003-4227-5638</orcidid></search><sort><creationdate>20240926</creationdate><title>Goal-Directed Osteoporosis Treatment: ASBMR/BHOF Task Force Position Statement 2024</title><author>Cosman, Felicia ; 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A goal-directed approach to long-term management of fracture risk helps ensure that the most appropriate initial treatment and treatment sequence is selected for individual patients. Goal-directed treatment decisions require assessment of clinical fracture history, vertebral fracture identification (using vertebral imaging as appropriate), measurement of bone mineral density (BMD) and consideration of other major clinical risk factors. Treatment targets should be tailored to each patient's individual risk profile and based on the specific indication for beginning treatment, including recency, site, number and severity of prior fractures, and BMD levels at the total hip, femoral neck, and lumbar spine. Instead of first-line bisphosphonate treatment for all patients, selection of initial treatment should focus on reducing fracture risk rapidly for patients at very high and imminent risk, such as in those with recent fractures. Initial treatment selection should also consider the probability that a BMD treatment target can be attained within a reasonable period of time and the differential magnitude of fracture risk reduction and BMD impact with osteoanabolic versus antiresorptive therapy. 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source | Oxford University Press Journals All Titles (1996-Current); Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Review |
title | Goal-Directed Osteoporosis Treatment: ASBMR/BHOF Task Force Position Statement 2024 |
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