Osteoporosis in the Women’s Health Initiative: Another Treatment Gap?

Abstract Background Osteoporotic fractures are associated with high morbidity, mortality, and cost. Methods We performed a post hoc analysis of the Women’s Health Initiative (WHI) clinical trials (CT) data to assess osteoporosis treatment and identify participant characteristics associated with util...

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Veröffentlicht in:The American journal of medicine 2017-08, Vol.130 (8), p.937-948
Hauptverfasser: Sattari, Maryam, MD, MS, Cauley, Jane A., DrPH, Garvan, Cynthia, PhD, Johnson, Karen C., MD, MPH, LaMonte, Michael J., PhD MPH, Li, Wenjun, PhD, Limacher, Marian, MD, Manini, Todd, PhD, Sarto, Gloria E., MD, PhD, Sullivan, Shannon D., MD, PhD, Wactawski-Wende, Jean, PhD, Beyth, Rebecca J., MD, MSc
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container_end_page 948
container_issue 8
container_start_page 937
container_title The American journal of medicine
container_volume 130
creator Sattari, Maryam, MD, MS
Cauley, Jane A., DrPH
Garvan, Cynthia, PhD
Johnson, Karen C., MD, MPH
LaMonte, Michael J., PhD MPH
Li, Wenjun, PhD
Limacher, Marian, MD
Manini, Todd, PhD
Sarto, Gloria E., MD, PhD
Sullivan, Shannon D., MD, PhD
Wactawski-Wende, Jean, PhD
Beyth, Rebecca J., MD, MSc
description Abstract Background Osteoporotic fractures are associated with high morbidity, mortality, and cost. Methods We performed a post hoc analysis of the Women’s Health Initiative (WHI) clinical trials (CT) data to assess osteoporosis treatment and identify participant characteristics associated with utilization of osteoporosis medication(s) after new diagnoses of osteoporosis and/or fracture. Information from visits prior to and immediately subsequent to the first fracture event or osteoporosis diagnosis were evaluated for medication use. A full logistic regression model was used to identify factors predictive of osteoporosis medication use after a fracture and/or a diagnosis of osteoporosis. Results The median length of follow-up from enrollment to the last WHI clinic visit for the study cohort was 13.9 years. Among the 13,990 women who reported new diagnoses of osteoporosis and/or fracture between enrollment and their final WHI visit, and also had medication data available, 21.6% reported taking an osteoporosis medication other than estrogen. Higher daily calcium intake, diagnosis of osteoporosis alone or both osteoporosis and fracture (compared to diagnosis of fracture alone), Asian or Pacific Islander race/ethnicity (compared to white/Caucasian), higher income, and hormone therapy use (past or present) were associated with significantly higher likelihood of osteoporosis pharmacotherapy. Women with black/African-American race/ethnicity (compared to white/Caucasian), BMI > 30 (compared to BMI of 18.5-24.9), current tobacco use (compared to past use or lifetime nonusers), and history of arthritis were less likely to use osteoporosis treatment. Conclusion Despite well-established treatment guidelines in postmenopausal women with osteoporosis and/or history of fractures, pharmacotherapy use was suboptimal in this study. Initiation of osteoporosis treatment after fragility fracture may represent an opportunity to improve later outcomes in these high-risk women. Specific attention needs to be paid to increasing treatment among women with fragility fractures, obesity, current tobacco use, history of arthritis or of black race/ethnicity.
doi_str_mv 10.1016/j.amjmed.2017.02.042
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Methods We performed a post hoc analysis of the Women’s Health Initiative (WHI) clinical trials (CT) data to assess osteoporosis treatment and identify participant characteristics associated with utilization of osteoporosis medication(s) after new diagnoses of osteoporosis and/or fracture. Information from visits prior to and immediately subsequent to the first fracture event or osteoporosis diagnosis were evaluated for medication use. A full logistic regression model was used to identify factors predictive of osteoporosis medication use after a fracture and/or a diagnosis of osteoporosis. Results The median length of follow-up from enrollment to the last WHI clinic visit for the study cohort was 13.9 years. Among the 13,990 women who reported new diagnoses of osteoporosis and/or fracture between enrollment and their final WHI visit, and also had medication data available, 21.6% reported taking an osteoporosis medication other than estrogen. Higher daily calcium intake, diagnosis of osteoporosis alone or both osteoporosis and fracture (compared to diagnosis of fracture alone), Asian or Pacific Islander race/ethnicity (compared to white/Caucasian), higher income, and hormone therapy use (past or present) were associated with significantly higher likelihood of osteoporosis pharmacotherapy. Women with black/African-American race/ethnicity (compared to white/Caucasian), BMI &gt; 30 (compared to BMI of 18.5-24.9), current tobacco use (compared to past use or lifetime nonusers), and history of arthritis were less likely to use osteoporosis treatment. Conclusion Despite well-established treatment guidelines in postmenopausal women with osteoporosis and/or history of fractures, pharmacotherapy use was suboptimal in this study. Initiation of osteoporosis treatment after fragility fracture may represent an opportunity to improve later outcomes in these high-risk women. Specific attention needs to be paid to increasing treatment among women with fragility fractures, obesity, current tobacco use, history of arthritis or of black race/ethnicity.</description><identifier>ISSN: 0002-9343</identifier><identifier>EISSN: 1555-7162</identifier><identifier>DOI: 10.1016/j.amjmed.2017.02.042</identifier><identifier>PMID: 28366425</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Bone Density Conservation Agents - therapeutic use ; Calcium - therapeutic use ; Disparity ; Educational Status ; Female ; Forecasting ; Fracture ; Humans ; Internal Medicine ; Logistic Models ; Longitudinal Studies ; Middle Aged ; Multicenter Studies as Topic ; Osteoporosis ; Osteoporosis - complications ; Osteoporosis - drug therapy ; Osteoporosis - epidemiology ; Osteoporotic Fractures - epidemiology ; Osteoporotic Fractures - prevention &amp; control ; Patient Acceptance of Health Care - statistics &amp; numerical data ; Social Class ; Treatment ; United States - epidemiology ; Vitamin D - therapeutic use ; Women's Health - statistics &amp; numerical data</subject><ispartof>The American journal of medicine, 2017-08, Vol.130 (8), p.937-948</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-2fc45df34a3163dce0b512ffe2a271a75e949ab0379f0ecdb1120e0aeb339eca3</citedby><cites>FETCH-LOGICAL-c463t-2fc45df34a3163dce0b512ffe2a271a75e949ab0379f0ecdb1120e0aeb339eca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.amjmed.2017.02.042$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28366425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sattari, Maryam, MD, MS</creatorcontrib><creatorcontrib>Cauley, Jane A., DrPH</creatorcontrib><creatorcontrib>Garvan, Cynthia, PhD</creatorcontrib><creatorcontrib>Johnson, Karen C., MD, MPH</creatorcontrib><creatorcontrib>LaMonte, Michael J., PhD MPH</creatorcontrib><creatorcontrib>Li, Wenjun, PhD</creatorcontrib><creatorcontrib>Limacher, Marian, MD</creatorcontrib><creatorcontrib>Manini, Todd, PhD</creatorcontrib><creatorcontrib>Sarto, Gloria E., MD, PhD</creatorcontrib><creatorcontrib>Sullivan, Shannon D., MD, PhD</creatorcontrib><creatorcontrib>Wactawski-Wende, Jean, PhD</creatorcontrib><creatorcontrib>Beyth, Rebecca J., MD, MSc</creatorcontrib><title>Osteoporosis in the Women’s Health Initiative: Another Treatment Gap?</title><title>The American journal of medicine</title><addtitle>Am J Med</addtitle><description>Abstract Background Osteoporotic fractures are associated with high morbidity, mortality, and cost. Methods We performed a post hoc analysis of the Women’s Health Initiative (WHI) clinical trials (CT) data to assess osteoporosis treatment and identify participant characteristics associated with utilization of osteoporosis medication(s) after new diagnoses of osteoporosis and/or fracture. Information from visits prior to and immediately subsequent to the first fracture event or osteoporosis diagnosis were evaluated for medication use. A full logistic regression model was used to identify factors predictive of osteoporosis medication use after a fracture and/or a diagnosis of osteoporosis. Results The median length of follow-up from enrollment to the last WHI clinic visit for the study cohort was 13.9 years. Among the 13,990 women who reported new diagnoses of osteoporosis and/or fracture between enrollment and their final WHI visit, and also had medication data available, 21.6% reported taking an osteoporosis medication other than estrogen. Higher daily calcium intake, diagnosis of osteoporosis alone or both osteoporosis and fracture (compared to diagnosis of fracture alone), Asian or Pacific Islander race/ethnicity (compared to white/Caucasian), higher income, and hormone therapy use (past or present) were associated with significantly higher likelihood of osteoporosis pharmacotherapy. Women with black/African-American race/ethnicity (compared to white/Caucasian), BMI &gt; 30 (compared to BMI of 18.5-24.9), current tobacco use (compared to past use or lifetime nonusers), and history of arthritis were less likely to use osteoporosis treatment. Conclusion Despite well-established treatment guidelines in postmenopausal women with osteoporosis and/or history of fractures, pharmacotherapy use was suboptimal in this study. Initiation of osteoporosis treatment after fragility fracture may represent an opportunity to improve later outcomes in these high-risk women. 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numerical data</subject><subject>Social Class</subject><subject>Treatment</subject><subject>United States - epidemiology</subject><subject>Vitamin D - therapeutic use</subject><subject>Women's Health - statistics &amp; numerical data</subject><issn>0002-9343</issn><issn>1555-7162</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFO3DAQhi1UVLa0b4CqHHtJOh47yYZDK4TogoTEAVCPluNMhNMkXmwvEre-Rl-PJ6mjhUsvPVkjf_-M5hvGTjgUHHj1dSj0NEzUFQi8LgALkHjAVrwsy7zmFb5jKwDAvBFSHLEPIQyphKas3rMjXIuqkliu2OYmRHJb512wIbNzFh8o--kmml9-_wnZJekxPmRXs41WR_tEp9nZ7BLjsztPOiYuZhu9_f6RHfZ6DPTp9T1m9z8u7s4v8-ubzdX52XVuZCVijr2RZdcLqQWvRGcI2pJj3xNqrLmuS2pko1sQddMDma7lHIFAUytEQ0aLY_Zl33fr3eOOQlSTDYbGUc_kdkHx9VqsJUdsEir3qEnLBU-92no7af-sOKhFoRrUXqFaFCpAlRSm2OfXCbt2-XsLvTlLwLc9QGnPJ0teBWNpNtRZTyaqztn_Tfi3gRntbI0ef9EzhcHt_JwcKq5CCqjb5YzLFXktQCBK8ReVEJmL</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Sattari, Maryam, MD, MS</creator><creator>Cauley, Jane A., DrPH</creator><creator>Garvan, Cynthia, PhD</creator><creator>Johnson, Karen C., MD, MPH</creator><creator>LaMonte, Michael J., PhD MPH</creator><creator>Li, Wenjun, PhD</creator><creator>Limacher, Marian, MD</creator><creator>Manini, Todd, PhD</creator><creator>Sarto, Gloria E., MD, PhD</creator><creator>Sullivan, Shannon D., MD, PhD</creator><creator>Wactawski-Wende, Jean, PhD</creator><creator>Beyth, Rebecca J., MD, MSc</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170801</creationdate><title>Osteoporosis in the Women’s Health Initiative: Another Treatment Gap?</title><author>Sattari, Maryam, MD, MS ; 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control</topic><topic>Patient Acceptance of Health Care - statistics &amp; numerical data</topic><topic>Social Class</topic><topic>Treatment</topic><topic>United States - epidemiology</topic><topic>Vitamin D - therapeutic use</topic><topic>Women's Health - statistics &amp; numerical data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sattari, Maryam, MD, MS</creatorcontrib><creatorcontrib>Cauley, Jane A., DrPH</creatorcontrib><creatorcontrib>Garvan, Cynthia, PhD</creatorcontrib><creatorcontrib>Johnson, Karen C., MD, MPH</creatorcontrib><creatorcontrib>LaMonte, Michael J., PhD MPH</creatorcontrib><creatorcontrib>Li, Wenjun, PhD</creatorcontrib><creatorcontrib>Limacher, Marian, MD</creatorcontrib><creatorcontrib>Manini, Todd, PhD</creatorcontrib><creatorcontrib>Sarto, Gloria E., MD, PhD</creatorcontrib><creatorcontrib>Sullivan, Shannon D., MD, PhD</creatorcontrib><creatorcontrib>Wactawski-Wende, Jean, PhD</creatorcontrib><creatorcontrib>Beyth, Rebecca J., MD, MSc</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sattari, Maryam, MD, MS</au><au>Cauley, Jane A., DrPH</au><au>Garvan, Cynthia, PhD</au><au>Johnson, Karen C., MD, MPH</au><au>LaMonte, Michael J., PhD MPH</au><au>Li, Wenjun, PhD</au><au>Limacher, Marian, MD</au><au>Manini, Todd, PhD</au><au>Sarto, Gloria E., MD, PhD</au><au>Sullivan, Shannon D., MD, PhD</au><au>Wactawski-Wende, Jean, PhD</au><au>Beyth, Rebecca J., MD, MSc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteoporosis in the Women’s Health Initiative: Another Treatment Gap?</atitle><jtitle>The American journal of medicine</jtitle><addtitle>Am J Med</addtitle><date>2017-08-01</date><risdate>2017</risdate><volume>130</volume><issue>8</issue><spage>937</spage><epage>948</epage><pages>937-948</pages><issn>0002-9343</issn><eissn>1555-7162</eissn><abstract>Abstract Background Osteoporotic fractures are associated with high morbidity, mortality, and cost. Methods We performed a post hoc analysis of the Women’s Health Initiative (WHI) clinical trials (CT) data to assess osteoporosis treatment and identify participant characteristics associated with utilization of osteoporosis medication(s) after new diagnoses of osteoporosis and/or fracture. Information from visits prior to and immediately subsequent to the first fracture event or osteoporosis diagnosis were evaluated for medication use. A full logistic regression model was used to identify factors predictive of osteoporosis medication use after a fracture and/or a diagnosis of osteoporosis. Results The median length of follow-up from enrollment to the last WHI clinic visit for the study cohort was 13.9 years. Among the 13,990 women who reported new diagnoses of osteoporosis and/or fracture between enrollment and their final WHI visit, and also had medication data available, 21.6% reported taking an osteoporosis medication other than estrogen. Higher daily calcium intake, diagnosis of osteoporosis alone or both osteoporosis and fracture (compared to diagnosis of fracture alone), Asian or Pacific Islander race/ethnicity (compared to white/Caucasian), higher income, and hormone therapy use (past or present) were associated with significantly higher likelihood of osteoporosis pharmacotherapy. Women with black/African-American race/ethnicity (compared to white/Caucasian), BMI &gt; 30 (compared to BMI of 18.5-24.9), current tobacco use (compared to past use or lifetime nonusers), and history of arthritis were less likely to use osteoporosis treatment. Conclusion Despite well-established treatment guidelines in postmenopausal women with osteoporosis and/or history of fractures, pharmacotherapy use was suboptimal in this study. Initiation of osteoporosis treatment after fragility fracture may represent an opportunity to improve later outcomes in these high-risk women. Specific attention needs to be paid to increasing treatment among women with fragility fractures, obesity, current tobacco use, history of arthritis or of black race/ethnicity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28366425</pmid><doi>10.1016/j.amjmed.2017.02.042</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Bone Density Conservation Agents - therapeutic use
Calcium - therapeutic use
Disparity
Educational Status
Female
Forecasting
Fracture
Humans
Internal Medicine
Logistic Models
Longitudinal Studies
Middle Aged
Multicenter Studies as Topic
Osteoporosis
Osteoporosis - complications
Osteoporosis - drug therapy
Osteoporosis - epidemiology
Osteoporotic Fractures - epidemiology
Osteoporotic Fractures - prevention & control
Patient Acceptance of Health Care - statistics & numerical data
Social Class
Treatment
United States - epidemiology
Vitamin D - therapeutic use
Women's Health - statistics & numerical data
title Osteoporosis in the Women’s Health Initiative: Another Treatment Gap?
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