Regional differences in treatment for osteoporosis. The Global Longitudinal Study of Osteoporosis in Women (GLOW)
Identifieur interne : 001486 ( PascalFrancis/Corpus ); précédent : 001485; suivant : 001487Regional differences in treatment for osteoporosis. The Global Longitudinal Study of Osteoporosis in Women (GLOW)
Auteurs : Adolfo Diez-Perez ; Frederick H. Hooven ; Jonathan D. Adachi ; Silvano Adami ; Frederick A. Anderson ; Steven Boonen ; Roland Chapurlat ; Juliet E. Compston ; Cyrus Cooper ; Pierre Delmas ; Susan L. Greenspan ; Andrea Z. Lacroix ; Robert Lindsay ; J. Coen Netelenbos ; Johannes Pfeilschifter ; Christian Roux ; Kenneth G. Saag ; Philip Sambrook ; Stuart Silverman ; Ethel S. Siris ; Nelson B. Watts ; Grigor Nika ; Stephen H. GehlbachSource :
- Bone : (New York, NY) [ 8756-3282 ] ; 2011.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Purpose: To determine if important geographic differences exist in treatment rates for osteoporosis and whether this variation can be explained by regional variation in risk factors. Methods: The Global Longitudinal Study of Osteoporosis in Women is an observational study of women ≥55 years sampled from primary care practices in 10 countries. Self-administered questionnaires were used to collect data on patient characteristics, risk factors for fracture, previous fractures, anti-osteoporosis medication, and health status. Results: Among 58,009 women, current anti-osteoporosis medication use was lowest in Northern Europe (16%) and highest in USA and Australia (32%). Between 48% (USA, Southern Europe) and 68% (Northern Europe) of women aged ≥65 years with a history of spine or hip fracture since age 45 were untreated. Among women with osteoporosis, the percentage of treated cases was lowest in Europe (45-52% versus 62-65% elsewhere). Women with osteopenia and no other risk factors were treated with anti-osteoporosis medication most frequently in USA (31%) and Canada (31%), and least frequently in Southern Europe (12%), Northern Europe (13%), and Australia (16%). After adjusting for risk factors, US women were threefold as likely to be treated with anti-osteoporosis medication as Northern European women (odds ratio 2.8; 95% confidence interval 2.5-3.1 ) and 1.5 times as likely to be treated as Southern European women (1.5, 1.4-1.6). Up to half of women reporting previous hip or spine fracture did not receive treatment. Conclusions: The likelihood of being treated for osteoporosis differed between regions, and cannot be explained by variation in risk factors. Many women at risk of fracture do not receive prophylaxis.
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Format Inist (serveur)
NO : | PASCAL 12-0170990 INIST |
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ET : | Regional differences in treatment for osteoporosis. The Global Longitudinal Study of Osteoporosis in Women (GLOW) |
AU : | DIEZ-PEREZ (Adolfo); HOOVEN (Frederick H.); ADACHI (Jonathan D.); ADAMI (Silvano); ANDERSON (Frederick A.); BOONEN (Steven); CHAPURLAT (Roland); COMPSTON (Juliet E.); COOPER (Cyrus); DELMAS (Pierre); GREENSPAN (Susan L.); LACROIX (Andrea Z.); LINDSAY (Robert); COEN NETELENBOS (J.); PFEILSCHIFTER (Johannes); ROUX (Christian); SAAG (Kenneth G.); SAMBROOK (Philip); SILVERMAN (Stuart); SIRIS (Ethel S.); WATTS (Nelson B.); NIKA (Grigor); GEHLBACH (Stephen H.) |
AF : | Hospital del Mar-IMIM, Autonomous University of Barcelona and RETICEF, Instituto Carlos III/Barcelona/Espagne (1 aut.); Center for Outcomes Research, University of Massachusetts Medical School/Worcester, MA/Etats-Unis (2 aut., 5 aut., 22 aut., 23 aut.); St Joseph's Hospital, McMaster University/Hamilton, ON/Canada (3 aut.); Department of Rheumatology, University of Verona, Ospedale/Verona, Valeggio/Italie (4 aut.); Leuven University Centre for Metabolic Bone Diseases, Division of Geriatric Medicine, Katholieke Universiteit Leuven/Leuven/Belgique (6 aut.); INSERM Research Unit 831, Universite de Lyon, Department of Orthopedics and Rheumatology, Hôpital E Herriot/Lyon/France (7 aut.); University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital/Cambridge/Royaume-Uni (8 aut.); MRC Epidemiology Resource Centre, University of Southampton, Southampton General Hospital and Norman Collisson Chair of Musculoskeletal Sciences, University of Oxford/Oxford/Royaume-Uni (9 aut.); Hôpital Edouard Herriot/Lyon/France (10 aut.); University of Pittsburgh/PA/Etats-Unis (11 aut.); Fred Hutchinson Cancer Research Center/Seattle, WA/Etats-Unis (12 aut.); Regional Bone Center, Helen Hayes Hospital/West Haverstraw, NY/Etats-Unis (13 aut.); Department of Endocrinology, VU University Medical Center/Amsterdam/Pays-Bas (14 aut.); Alfried Krupp Krankenhaus, Department of Internal Medicine III/Essen/Allemagne (15 aut.); Paris Descartes University, Cochin Hospital/Paris/France (16 aut.); University of Alabama-Birmingham, Division of Clinical Immunology and Rheumatology/Birmingham, AL/Etats-Unis (17 aut.); University of Sydney-Royal North Shore Hospital, St. Leonards/Sydney, NSW/Australie (18 aut.); Cedars-Sinai Medical Center/Los Angeles, CA/Etats-Unis (19 aut.); Columbia University Medical Center/New York, NY/Etats-Unis (20 aut.); Bone Health and Osteoporosis Center, University of Cincinnati/Cincinnati, OH/Etats-Unis (21 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Bone : (New York, NY); ISSN 8756-3282; Pays-Bas; Da. 2011; Vol. 49; No. 3; Pp. 493-498; Bibl. 26 ref. |
LA : | Anglais |
EA : | Purpose: To determine if important geographic differences exist in treatment rates for osteoporosis and whether this variation can be explained by regional variation in risk factors. Methods: The Global Longitudinal Study of Osteoporosis in Women is an observational study of women ≥55 years sampled from primary care practices in 10 countries. Self-administered questionnaires were used to collect data on patient characteristics, risk factors for fracture, previous fractures, anti-osteoporosis medication, and health status. Results: Among 58,009 women, current anti-osteoporosis medication use was lowest in Northern Europe (16%) and highest in USA and Australia (32%). Between 48% (USA, Southern Europe) and 68% (Northern Europe) of women aged ≥65 years with a history of spine or hip fracture since age 45 were untreated. Among women with osteoporosis, the percentage of treated cases was lowest in Europe (45-52% versus 62-65% elsewhere). Women with osteopenia and no other risk factors were treated with anti-osteoporosis medication most frequently in USA (31%) and Canada (31%), and least frequently in Southern Europe (12%), Northern Europe (13%), and Australia (16%). After adjusting for risk factors, US women were threefold as likely to be treated with anti-osteoporosis medication as Northern European women (odds ratio 2.8; 95% confidence interval 2.5-3.1 ) and 1.5 times as likely to be treated as Southern European women (1.5, 1.4-1.6). Up to half of women reporting previous hip or spine fracture did not receive treatment. Conclusions: The likelihood of being treated for osteoporosis differed between regions, and cannot be explained by variation in risk factors. Many women at risk of fracture do not receive prophylaxis. |
CC : | 002A16; 002B15A; 002B16H |
FD : | Traitement régional; Ostéoporose; Femme; Fracture; Facteur risque; Prévention; Morphologie |
FG : | Homme; Pathologie du système ostéoarticulaire; Traumatisme |
ED : | Regional treatment; Osteoporosis; Woman; Fracture; Risk factor; Prevention; Morphology |
EG : | Human; Diseases of the osteoarticular system; Trauma |
SD : | Tratamiento regional; Osteoporosis; Mujer; Fractura; Factor riesgo; Prevención; Morfología |
LO : | INIST-19041.354000194653440220 |
ID : | 12-0170990 |
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Regional differences in treatment for osteoporosis. The Global Longitudinal Study of Osteoporosis in Women (GLOW)</title>
<author><name sortKey="Diez Perez, Adolfo" sort="Diez Perez, Adolfo" uniqKey="Diez Perez A" first="Adolfo" last="Diez-Perez">Adolfo Diez-Perez</name>
<affiliation><inist:fA14 i1="01"><s1>Hospital del Mar-IMIM, Autonomous University of Barcelona and RETICEF, Instituto Carlos III</s1>
<s2>Barcelona</s2>
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</inist:fA14>
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<author><name sortKey="Hooven, Frederick H" sort="Hooven, Frederick H" uniqKey="Hooven F" first="Frederick H." last="Hooven">Frederick H. Hooven</name>
<affiliation><inist:fA14 i1="02"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1>
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<author><name sortKey="Adachi, Jonathan D" sort="Adachi, Jonathan D" uniqKey="Adachi J" first="Jonathan D." last="Adachi">Jonathan D. Adachi</name>
<affiliation><inist:fA14 i1="03"><s1>St Joseph's Hospital, McMaster University</s1>
<s2>Hamilton, ON</s2>
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<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Adami, Silvano" sort="Adami, Silvano" uniqKey="Adami S" first="Silvano" last="Adami">Silvano Adami</name>
<affiliation><inist:fA14 i1="04"><s1>Department of Rheumatology, University of Verona, Ospedale</s1>
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<s3>ITA</s3>
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</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Anderson, Frederick A" sort="Anderson, Frederick A" uniqKey="Anderson F" first="Frederick A." last="Anderson">Frederick A. Anderson</name>
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<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
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</author>
<author><name sortKey="Boonen, Steven" sort="Boonen, Steven" uniqKey="Boonen S" first="Steven" last="Boonen">Steven Boonen</name>
<affiliation><inist:fA14 i1="05"><s1>Leuven University Centre for Metabolic Bone Diseases, Division of Geriatric Medicine, Katholieke Universiteit Leuven</s1>
<s2>Leuven</s2>
<s3>BEL</s3>
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</affiliation>
</author>
<author><name sortKey="Chapurlat, Roland" sort="Chapurlat, Roland" uniqKey="Chapurlat R" first="Roland" last="Chapurlat">Roland Chapurlat</name>
<affiliation><inist:fA14 i1="06"><s1>INSERM Research Unit 831, Universite de Lyon, Department of Orthopedics and Rheumatology, Hôpital E Herriot</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
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</affiliation>
</author>
<author><name sortKey="Compston, Juliet E" sort="Compston, Juliet E" uniqKey="Compston J" first="Juliet E." last="Compston">Juliet E. Compston</name>
<affiliation><inist:fA14 i1="07"><s1>University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital</s1>
<s2>Cambridge</s2>
<s3>GBR</s3>
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</affiliation>
</author>
<author><name sortKey="Cooper, Cyrus" sort="Cooper, Cyrus" uniqKey="Cooper C" first="Cyrus" last="Cooper">Cyrus Cooper</name>
<affiliation><inist:fA14 i1="08"><s1>MRC Epidemiology Resource Centre, University of Southampton, Southampton General Hospital and Norman Collisson Chair of Musculoskeletal Sciences, University of Oxford</s1>
<s2>Oxford</s2>
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<author><name sortKey="Delmas, Pierre" sort="Delmas, Pierre" uniqKey="Delmas P" first="Pierre" last="Delmas">Pierre Delmas</name>
<affiliation><inist:fA14 i1="09"><s1>Hôpital Edouard Herriot</s1>
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<author><name sortKey="Greenspan, Susan L" sort="Greenspan, Susan L" uniqKey="Greenspan S" first="Susan L." last="Greenspan">Susan L. Greenspan</name>
<affiliation><inist:fA14 i1="10"><s1>University of Pittsburgh</s1>
<s2>PA</s2>
<s3>USA</s3>
<sZ>11 aut.</sZ>
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</author>
<author><name sortKey="Lacroix, Andrea Z" sort="Lacroix, Andrea Z" uniqKey="Lacroix A" first="Andrea Z." last="Lacroix">Andrea Z. Lacroix</name>
<affiliation><inist:fA14 i1="11"><s1>Fred Hutchinson Cancer Research Center</s1>
<s2>Seattle, WA</s2>
<s3>USA</s3>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lindsay, Robert" sort="Lindsay, Robert" uniqKey="Lindsay R" first="Robert" last="Lindsay">Robert Lindsay</name>
<affiliation><inist:fA14 i1="12"><s1>Regional Bone Center, Helen Hayes Hospital</s1>
<s2>West Haverstraw, NY</s2>
<s3>USA</s3>
<sZ>13 aut.</sZ>
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</author>
<author><name sortKey="Coen Netelenbos, J" sort="Coen Netelenbos, J" uniqKey="Coen Netelenbos J" first="J." last="Coen Netelenbos">J. Coen Netelenbos</name>
<affiliation><inist:fA14 i1="13"><s1>Department of Endocrinology, VU University Medical Center</s1>
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<s3>NLD</s3>
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<author><name sortKey="Pfeilschifter, Johannes" sort="Pfeilschifter, Johannes" uniqKey="Pfeilschifter J" first="Johannes" last="Pfeilschifter">Johannes Pfeilschifter</name>
<affiliation><inist:fA14 i1="14"><s1>Alfried Krupp Krankenhaus, Department of Internal Medicine III</s1>
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<sZ>15 aut.</sZ>
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</affiliation>
</author>
<author><name sortKey="Roux, Christian" sort="Roux, Christian" uniqKey="Roux C" first="Christian" last="Roux">Christian Roux</name>
<affiliation><inist:fA14 i1="15"><s1>Paris Descartes University, Cochin Hospital</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>16 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Saag, Kenneth G" sort="Saag, Kenneth G" uniqKey="Saag K" first="Kenneth G." last="Saag">Kenneth G. Saag</name>
<affiliation><inist:fA14 i1="16"><s1>University of Alabama-Birmingham, Division of Clinical Immunology and Rheumatology</s1>
<s2>Birmingham, AL</s2>
<s3>USA</s3>
<sZ>17 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Sambrook, Philip" sort="Sambrook, Philip" uniqKey="Sambrook P" first="Philip" last="Sambrook">Philip Sambrook</name>
<affiliation><inist:fA14 i1="17"><s1>University of Sydney-Royal North Shore Hospital, St. Leonards</s1>
<s2>Sydney, NSW</s2>
<s3>AUS</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Silverman, Stuart" sort="Silverman, Stuart" uniqKey="Silverman S" first="Stuart" last="Silverman">Stuart Silverman</name>
<affiliation><inist:fA14 i1="18"><s1>Cedars-Sinai Medical Center</s1>
<s2>Los Angeles, CA</s2>
<s3>USA</s3>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Siris, Ethel S" sort="Siris, Ethel S" uniqKey="Siris E" first="Ethel S." last="Siris">Ethel S. Siris</name>
<affiliation><inist:fA14 i1="19"><s1>Columbia University Medical Center</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Watts, Nelson B" sort="Watts, Nelson B" uniqKey="Watts N" first="Nelson B." last="Watts">Nelson B. Watts</name>
<affiliation><inist:fA14 i1="20"><s1>Bone Health and Osteoporosis Center, University of Cincinnati</s1>
<s2>Cincinnati, OH</s2>
<s3>USA</s3>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Nika, Grigor" sort="Nika, Grigor" uniqKey="Nika G" first="Grigor" last="Nika">Grigor Nika</name>
<affiliation><inist:fA14 i1="02"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1>
<s2>Worcester, MA</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Gehlbach, Stephen H" sort="Gehlbach, Stephen H" uniqKey="Gehlbach S" first="Stephen H." last="Gehlbach">Stephen H. Gehlbach</name>
<affiliation><inist:fA14 i1="02"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1>
<s2>Worcester, MA</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Bone : (New York, NY)</title>
<title level="j" type="abbreviated">Bone : (NY NY)</title>
<idno type="ISSN">8756-3282</idno>
<imprint><date when="2011">2011</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Bone : (New York, NY)</title>
<title level="j" type="abbreviated">Bone : (NY NY)</title>
<idno type="ISSN">8756-3282</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Fracture</term>
<term>Morphology</term>
<term>Osteoporosis</term>
<term>Prevention</term>
<term>Regional treatment</term>
<term>Risk factor</term>
<term>Woman</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Traitement régional</term>
<term>Ostéoporose</term>
<term>Femme</term>
<term>Fracture</term>
<term>Facteur risque</term>
<term>Prévention</term>
<term>Morphologie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Purpose: To determine if important geographic differences exist in treatment rates for osteoporosis and whether this variation can be explained by regional variation in risk factors. Methods: The Global Longitudinal Study of Osteoporosis in Women is an observational study of women ≥55 years sampled from primary care practices in 10 countries. Self-administered questionnaires were used to collect data on patient characteristics, risk factors for fracture, previous fractures, anti-osteoporosis medication, and health status. Results: Among 58,009 women, current anti-osteoporosis medication use was lowest in Northern Europe (16%) and highest in USA and Australia (32%). Between 48% (USA, Southern Europe) and 68% (Northern Europe) of women aged ≥65 years with a history of spine or hip fracture since age 45 were untreated. Among women with osteoporosis, the percentage of treated cases was lowest in Europe (45-52% versus 62-65% elsewhere). Women with osteopenia and no other risk factors were treated with anti-osteoporosis medication most frequently in USA (31%) and Canada (31%), and least frequently in Southern Europe (12%), Northern Europe (13%), and Australia (16%). After adjusting for risk factors, US women were threefold as likely to be treated with anti-osteoporosis medication as Northern European women (odds ratio 2.8; 95% confidence interval 2.5-3.1 ) and 1.5 times as likely to be treated as Southern European women (1.5, 1.4-1.6). Up to half of women reporting previous hip or spine fracture did not receive treatment. Conclusions: The likelihood of being treated for osteoporosis differed between regions, and cannot be explained by variation in risk factors. Many women at risk of fracture do not receive prophylaxis.</div>
</front>
</TEI>
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</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Regional differences in treatment for osteoporosis. The Global Longitudinal Study of Osteoporosis in Women (GLOW)</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>DIEZ-PEREZ (Adolfo)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>HOOVEN (Frederick H.)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>ADACHI (Jonathan D.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>ADAMI (Silvano)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>ANDERSON (Frederick A.)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>BOONEN (Steven)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>CHAPURLAT (Roland)</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>COMPSTON (Juliet E.)</s1>
</fA11>
<fA11 i1="09" i2="1"><s1>COOPER (Cyrus)</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>DELMAS (Pierre)</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>GREENSPAN (Susan L.)</s1>
</fA11>
<fA11 i1="12" i2="1"><s1>LACROIX (Andrea Z.)</s1>
</fA11>
<fA11 i1="13" i2="1"><s1>LINDSAY (Robert)</s1>
</fA11>
<fA11 i1="14" i2="1"><s1>COEN NETELENBOS (J.)</s1>
</fA11>
<fA11 i1="15" i2="1"><s1>PFEILSCHIFTER (Johannes)</s1>
</fA11>
<fA11 i1="16" i2="1"><s1>ROUX (Christian)</s1>
</fA11>
<fA11 i1="17" i2="1"><s1>SAAG (Kenneth G.)</s1>
</fA11>
<fA11 i1="18" i2="1"><s1>SAMBROOK (Philip)</s1>
</fA11>
<fA11 i1="19" i2="1"><s1>SILVERMAN (Stuart)</s1>
</fA11>
<fA11 i1="20" i2="1"><s1>SIRIS (Ethel S.)</s1>
</fA11>
<fA11 i1="21" i2="1"><s1>WATTS (Nelson B.)</s1>
</fA11>
<fA11 i1="22" i2="1"><s1>NIKA (Grigor)</s1>
</fA11>
<fA11 i1="23" i2="1"><s1>GEHLBACH (Stephen H.)</s1>
</fA11>
<fA14 i1="01"><s1>Hospital del Mar-IMIM, Autonomous University of Barcelona and RETICEF, Instituto Carlos III</s1>
<s2>Barcelona</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1>
<s2>Worcester, MA</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
<sZ>23 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>St Joseph's Hospital, McMaster University</s1>
<s2>Hamilton, ON</s2>
<s3>CAN</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Department of Rheumatology, University of Verona, Ospedale</s1>
<s2>Verona, Valeggio</s2>
<s3>ITA</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="05"><s1>Leuven University Centre for Metabolic Bone Diseases, Division of Geriatric Medicine, Katholieke Universiteit Leuven</s1>
<s2>Leuven</s2>
<s3>BEL</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="06"><s1>INSERM Research Unit 831, Universite de Lyon, Department of Orthopedics and Rheumatology, Hôpital E Herriot</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="07"><s1>University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital</s1>
<s2>Cambridge</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="08"><s1>MRC Epidemiology Resource Centre, University of Southampton, Southampton General Hospital and Norman Collisson Chair of Musculoskeletal Sciences, University of Oxford</s1>
<s2>Oxford</s2>
<s3>GBR</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="09"><s1>Hôpital Edouard Herriot</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>10 aut.</sZ>
</fA14>
<fA14 i1="10"><s1>University of Pittsburgh</s1>
<s2>PA</s2>
<s3>USA</s3>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="11"><s1>Fred Hutchinson Cancer Research Center</s1>
<s2>Seattle, WA</s2>
<s3>USA</s3>
<sZ>12 aut.</sZ>
</fA14>
<fA14 i1="12"><s1>Regional Bone Center, Helen Hayes Hospital</s1>
<s2>West Haverstraw, NY</s2>
<s3>USA</s3>
<sZ>13 aut.</sZ>
</fA14>
<fA14 i1="13"><s1>Department of Endocrinology, VU University Medical Center</s1>
<s2>Amsterdam</s2>
<s3>NLD</s3>
<sZ>14 aut.</sZ>
</fA14>
<fA14 i1="14"><s1>Alfried Krupp Krankenhaus, Department of Internal Medicine III</s1>
<s2>Essen</s2>
<s3>DEU</s3>
<sZ>15 aut.</sZ>
</fA14>
<fA14 i1="15"><s1>Paris Descartes University, Cochin Hospital</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>16 aut.</sZ>
</fA14>
<fA14 i1="16"><s1>University of Alabama-Birmingham, Division of Clinical Immunology and Rheumatology</s1>
<s2>Birmingham, AL</s2>
<s3>USA</s3>
<sZ>17 aut.</sZ>
</fA14>
<fA14 i1="17"><s1>University of Sydney-Royal North Shore Hospital, St. Leonards</s1>
<s2>Sydney, NSW</s2>
<s3>AUS</s3>
<sZ>18 aut.</sZ>
</fA14>
<fA14 i1="18"><s1>Cedars-Sinai Medical Center</s1>
<s2>Los Angeles, CA</s2>
<s3>USA</s3>
<sZ>19 aut.</sZ>
</fA14>
<fA14 i1="19"><s1>Columbia University Medical Center</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>20 aut.</sZ>
</fA14>
<fA14 i1="20"><s1>Bone Health and Osteoporosis Center, University of Cincinnati</s1>
<s2>Cincinnati, OH</s2>
<s3>USA</s3>
<sZ>21 aut.</sZ>
</fA14>
<fA20><s1>493-498</s1>
</fA20>
<fA21><s1>2011</s1>
</fA21>
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<s5>354000194653440220</s5>
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<fA44><s0>0000</s0>
<s1>© 2012 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>26 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>12-0170990</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Bone : (New York, NY)</s0>
</fA64>
<fA66 i1="01"><s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Purpose: To determine if important geographic differences exist in treatment rates for osteoporosis and whether this variation can be explained by regional variation in risk factors. Methods: The Global Longitudinal Study of Osteoporosis in Women is an observational study of women ≥55 years sampled from primary care practices in 10 countries. Self-administered questionnaires were used to collect data on patient characteristics, risk factors for fracture, previous fractures, anti-osteoporosis medication, and health status. Results: Among 58,009 women, current anti-osteoporosis medication use was lowest in Northern Europe (16%) and highest in USA and Australia (32%). Between 48% (USA, Southern Europe) and 68% (Northern Europe) of women aged ≥65 years with a history of spine or hip fracture since age 45 were untreated. Among women with osteoporosis, the percentage of treated cases was lowest in Europe (45-52% versus 62-65% elsewhere). Women with osteopenia and no other risk factors were treated with anti-osteoporosis medication most frequently in USA (31%) and Canada (31%), and least frequently in Southern Europe (12%), Northern Europe (13%), and Australia (16%). After adjusting for risk factors, US women were threefold as likely to be treated with anti-osteoporosis medication as Northern European women (odds ratio 2.8; 95% confidence interval 2.5-3.1 ) and 1.5 times as likely to be treated as Southern European women (1.5, 1.4-1.6). Up to half of women reporting previous hip or spine fracture did not receive treatment. Conclusions: The likelihood of being treated for osteoporosis differed between regions, and cannot be explained by variation in risk factors. Many women at risk of fracture do not receive prophylaxis.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002A16</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B15A</s0>
</fC02>
<fC02 i1="03" i2="X"><s0>002B16H</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Traitement régional</s0>
<s5>07</s5>
</fC03>
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<s5>07</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Tratamiento regional</s0>
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<s5>09</s5>
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<fC03 i1="03" i2="X" l="ENG"><s0>Woman</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Mujer</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Fracture</s0>
<s5>14</s5>
</fC03>
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<s5>14</s5>
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<s5>14</s5>
</fC03>
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<s5>15</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Risk factor</s0>
<s5>15</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Factor riesgo</s0>
<s5>15</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Prévention</s0>
<s5>16</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Prevention</s0>
<s5>16</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Prevención</s0>
<s5>16</s5>
</fC03>
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<s5>17</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Morphology</s0>
<s5>17</s5>
</fC03>
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<s5>17</s5>
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<s5>37</s5>
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<s5>37</s5>
</fC07>
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<s5>37</s5>
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<s5>38</s5>
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<s5>38</s5>
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<fN21><s1>129</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 12-0170990 INIST</NO>
<ET>Regional differences in treatment for osteoporosis. The Global Longitudinal Study of Osteoporosis in Women (GLOW)</ET>
<AU>DIEZ-PEREZ (Adolfo); HOOVEN (Frederick H.); ADACHI (Jonathan D.); ADAMI (Silvano); ANDERSON (Frederick A.); BOONEN (Steven); CHAPURLAT (Roland); COMPSTON (Juliet E.); COOPER (Cyrus); DELMAS (Pierre); GREENSPAN (Susan L.); LACROIX (Andrea Z.); LINDSAY (Robert); COEN NETELENBOS (J.); PFEILSCHIFTER (Johannes); ROUX (Christian); SAAG (Kenneth G.); SAMBROOK (Philip); SILVERMAN (Stuart); SIRIS (Ethel S.); WATTS (Nelson B.); NIKA (Grigor); GEHLBACH (Stephen H.)</AU>
<AF>Hospital del Mar-IMIM, Autonomous University of Barcelona and RETICEF, Instituto Carlos III/Barcelona/Espagne (1 aut.); Center for Outcomes Research, University of Massachusetts Medical School/Worcester, MA/Etats-Unis (2 aut., 5 aut., 22 aut., 23 aut.); St Joseph's Hospital, McMaster University/Hamilton, ON/Canada (3 aut.); Department of Rheumatology, University of Verona, Ospedale/Verona, Valeggio/Italie (4 aut.); Leuven University Centre for Metabolic Bone Diseases, Division of Geriatric Medicine, Katholieke Universiteit Leuven/Leuven/Belgique (6 aut.); INSERM Research Unit 831, Universite de Lyon, Department of Orthopedics and Rheumatology, Hôpital E Herriot/Lyon/France (7 aut.); University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital/Cambridge/Royaume-Uni (8 aut.); MRC Epidemiology Resource Centre, University of Southampton, Southampton General Hospital and Norman Collisson Chair of Musculoskeletal Sciences, University of Oxford/Oxford/Royaume-Uni (9 aut.); Hôpital Edouard Herriot/Lyon/France (10 aut.); University of Pittsburgh/PA/Etats-Unis (11 aut.); Fred Hutchinson Cancer Research Center/Seattle, WA/Etats-Unis (12 aut.); Regional Bone Center, Helen Hayes Hospital/West Haverstraw, NY/Etats-Unis (13 aut.); Department of Endocrinology, VU University Medical Center/Amsterdam/Pays-Bas (14 aut.); Alfried Krupp Krankenhaus, Department of Internal Medicine III/Essen/Allemagne (15 aut.); Paris Descartes University, Cochin Hospital/Paris/France (16 aut.); University of Alabama-Birmingham, Division of Clinical Immunology and Rheumatology/Birmingham, AL/Etats-Unis (17 aut.); University of Sydney-Royal North Shore Hospital, St. Leonards/Sydney, NSW/Australie (18 aut.); Cedars-Sinai Medical Center/Los Angeles, CA/Etats-Unis (19 aut.); Columbia University Medical Center/New York, NY/Etats-Unis (20 aut.); Bone Health and Osteoporosis Center, University of Cincinnati/Cincinnati, OH/Etats-Unis (21 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Bone : (New York, NY); ISSN 8756-3282; Pays-Bas; Da. 2011; Vol. 49; No. 3; Pp. 493-498; Bibl. 26 ref.</SO>
<LA>Anglais</LA>
<EA>Purpose: To determine if important geographic differences exist in treatment rates for osteoporosis and whether this variation can be explained by regional variation in risk factors. Methods: The Global Longitudinal Study of Osteoporosis in Women is an observational study of women ≥55 years sampled from primary care practices in 10 countries. Self-administered questionnaires were used to collect data on patient characteristics, risk factors for fracture, previous fractures, anti-osteoporosis medication, and health status. Results: Among 58,009 women, current anti-osteoporosis medication use was lowest in Northern Europe (16%) and highest in USA and Australia (32%). Between 48% (USA, Southern Europe) and 68% (Northern Europe) of women aged ≥65 years with a history of spine or hip fracture since age 45 were untreated. Among women with osteoporosis, the percentage of treated cases was lowest in Europe (45-52% versus 62-65% elsewhere). Women with osteopenia and no other risk factors were treated with anti-osteoporosis medication most frequently in USA (31%) and Canada (31%), and least frequently in Southern Europe (12%), Northern Europe (13%), and Australia (16%). After adjusting for risk factors, US women were threefold as likely to be treated with anti-osteoporosis medication as Northern European women (odds ratio 2.8; 95% confidence interval 2.5-3.1 ) and 1.5 times as likely to be treated as Southern European women (1.5, 1.4-1.6). Up to half of women reporting previous hip or spine fracture did not receive treatment. Conclusions: The likelihood of being treated for osteoporosis differed between regions, and cannot be explained by variation in risk factors. Many women at risk of fracture do not receive prophylaxis.</EA>
<CC>002A16; 002B15A; 002B16H</CC>
<FD>Traitement régional; Ostéoporose; Femme; Fracture; Facteur risque; Prévention; Morphologie</FD>
<FG>Homme; Pathologie du système ostéoarticulaire; Traumatisme</FG>
<ED>Regional treatment; Osteoporosis; Woman; Fracture; Risk factor; Prevention; Morphology</ED>
<EG>Human; Diseases of the osteoarticular system; Trauma</EG>
<SD>Tratamiento regional; Osteoporosis; Mujer; Fractura; Factor riesgo; Prevención; Morfología</SD>
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<ID>12-0170990</ID>
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