Health-Related Quality of Life after Knee Replacement: Results of the Knee Replacement Patient Outcomes Research Team Study
A cross-sectional, community-based survey of a random sample of 1750 of 242,311 Medicare recipients was performed. The patients were at least sixty-five years old and had had a primary or revision knee replacement (either unilaterally or bilaterally) between 1985 and 1989. Three samples were surveye...
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Published in | Journal of bone and joint surgery. American volume Vol. 80; no. 2; pp. 163 - 173 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Boston, MA
Copyright by The Journal of Bone and Joint Surgery, Incorporated
01.02.1998
Journal of Bone and Joint Surgery Incorporated |
Subjects | |
Online Access | Get full text |
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Abstract | A cross-sectional, community-based survey of a random sample of 1750 of 242,311 Medicare recipients was performed. The patients were at least sixty-five years old and had had a primary or revision knee replacement (either unilaterally or bilaterally) between 1985 and 1989. Three samples were surveyed separatelya national sample (to reflect the United States as a whole) and samples from Indiana and the western part of Pennsylvania (sites chosen for convenience to assess the validity of the findings for the national sample on a regional level). Each sample was stratified by race, age, residence (urban or rural), and the year of the procedure. Valid and reliable questionnaires were used to elicit the participants' assessments of pain, physical function, and satisfaction two to seven years after the knee replacement.Of the 1486 patients who were eligible for inclusion in the survey, 1193 (80.3 per cent) responded. The mean age of the respondents was 72.6 years. Eight hundred and forty-nine respondents (71.2 per cent) were white, and 849 (71.2 per cent) were women.The participants reported that they had little or no pain in the knee at the time of the survey, regardless of the age at the time of the knee replacement, the body-mass index, or the length of time since the knee replacement. After adjustment for potential confounding variables, predictors of better physical function after the replacement were an absence of problems with the contralateral knee, primary knee replacement (rather than revision) (Indiana sample only), and a lower body-mass index (Indiana and western Pennsylvania samples). Four hundred and fifteen (85.2 per cent) of the 487 patients in the national sample were satisfied with the result of the knee replacement.In what we believe to be the first community-based study of the outcome of knee replacement, patients reported having significant (p = 0.0001) and persistent relief of pain, improved physical function, and satisfaction with the result two to seven years postoperatively. The findings of the present study suggest that age and obesity do not have a negative impact on patient-relevant outcomes (pain and physical function). Dissemination of these findings has the potential to increase appropriate referrals for knee replacement and thereby reduce the pain and functional disability due to osteoarthrosis of the knee. |
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AbstractList | A cross-sectional, community-based survey of a random sample of 1750 of 242,311 Medicare recipients was performed. The patients were at least sixty-five years old and had had a primary or revision knee replacement (either unilaterally or bilaterally) between 1985 and 1989. Three samples were surveyed separatelya national sample (to reflect the United States as a whole) and samples from Indiana and the western part of Pennsylvania (sites chosen for convenience to assess the validity of the findings for the national sample on a regional level). Each sample was stratified by race, age, residence (urban or rural), and the year of the procedure. Valid and reliable questionnaires were used to elicit the participants' assessments of pain, physical function, and satisfaction two to seven years after the knee replacement.Of the 1486 patients who were eligible for inclusion in the survey, 1193 (80.3 per cent) responded. The mean age of the respondents was 72.6 years. Eight hundred and forty-nine respondents (71.2 per cent) were white, and 849 (71.2 per cent) were women.The participants reported that they had little or no pain in the knee at the time of the survey, regardless of the age at the time of the knee replacement, the body-mass index, or the length of time since the knee replacement. After adjustment for potential confounding variables, predictors of better physical function after the replacement were an absence of problems with the contralateral knee, primary knee replacement (rather than revision) (Indiana sample only), and a lower body-mass index (Indiana and western Pennsylvania samples). Four hundred and fifteen (85.2 per cent) of the 487 patients in the national sample were satisfied with the result of the knee replacement.In what we believe to be the first community-based study of the outcome of knee replacement, patients reported having significant (p = 0.0001) and persistent relief of pain, improved physical function, and satisfaction with the result two to seven years postoperatively. The findings of the present study suggest that age and obesity do not have a negative impact on patient-relevant outcomes (pain and physical function). Dissemination of these findings has the potential to increase appropriate referrals for knee replacement and thereby reduce the pain and functional disability due to osteoarthrosis of the knee. |
Author | BOMBARDIER, CLAIRE HECK, DAVID CROXFORD, RUTH DITTUS, ROBERT KATZ, BARRY FREUND, DEBORAH PAUL, JOHN HAWKER, GILLIAN COYTE, PETER WRIGHT, JAMES |
AuthorAffiliation | TORONTO (HAWKER, WRIGHT, COYTE); RESEARCH TRIANGLE PARK, NORTH CAROLINA (PAUL); INDIANAPOLIS (DITTUS); TORONTO (CROXFORD); INDIANAPOLIS (KATZ); TORONTO, ONTARIO, CANADA (BOMBARDIER); INDIANAPOLIS, INDIANA (HECK, FREUND). Investigation performed at the Departments of Medicine, Surgery, Statistics, and Health Administration, University of Toronto, Toronto; Institute for Policy Analysis, Toronto; the Departments of Medicine, Regenstrief Institute for Health Care, Bowen Research Centre, and School of Public and Environmental Affairs, Indiana University, Indianapolis; and Research Triangle Institute and Glaxo Wellcome, Research Triangle Park. No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. Funds were received in total or partial support of the research or clinical study presented in this article. The funding sources were Grant 06432 of the Agency for Health Care Policy and Research to India |
AuthorAffiliation_xml | – name: TORONTO (HAWKER, WRIGHT, COYTE); RESEARCH TRIANGLE PARK, NORTH CAROLINA (PAUL); INDIANAPOLIS (DITTUS); TORONTO (CROXFORD); INDIANAPOLIS (KATZ); TORONTO, ONTARIO, CANADA (BOMBARDIER); INDIANAPOLIS, INDIANA (HECK, FREUND). Investigation performed at the Departments of Medicine, Surgery, Statistics, and Health Administration, University of Toronto, Toronto; Institute for Policy Analysis, Toronto; the Departments of Medicine, Regenstrief Institute for Health Care, Bowen Research Centre, and School of Public and Environmental Affairs, Indiana University, Indianapolis; and Research Triangle Institute and Glaxo Wellcome, Research Triangle Park. No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. Funds were received in total or partial support of the research or clinical study presented in this article. The funding sources were Grant 06432 of the Agency for Health Care Policy and Research to Indiana University and subgrantees (University of Toronto, Research Triangle Institute, Pittsburgh Research Institute, and University of Indiana) and Medical Research Council Scholarships (G. H. and J. W.). (HAWKER) Women's College Hospital, Burton Hall, Room 416, 60 Grosvenor Street, Toronto, Ontario M5S 1B6, Canada. (WRIGHT) Division of Orthopaedic Surgery, The Hospital for Sick Children, 555 University Avenue, Room S107, Toronto, Ontario M5G 1X8, Canada. (COYTE) Department of Health Administration, University of Toronto, McMurrich Building, Second Floor, 12 Queen's Park West, Toronto, Ontario M5S 1A8, Canada. (PAUL) Care Management Division, Clinical Economics Outcomes Assessment, Glaxo Wellcome, 5 Moore Drive, Research Triangle Park, North Carolina 27709. (DITTUS) Vanderbilt Medical Center, Seventh Floor, Medical Center East, Nashville, Tennessee 37232. (CROXFORD) Sunnybrook Health Science Centre, Institute for Clinical Evaluative Science, G Wing, 2075 Bayview Avenue, North York, Ontario M4N 3M5, Canada. (KATZ) Division of Biostatistics, Indiana University School of Medicine, 699 West Drive, Riley Research Wing, Room 135, Indianapolis, Indiana 46202-5200. (BOMBARDIER) Institute for Work and Health, 250 Bloor Street East, Suite 702, Toronto, Ontario M4W 1E6, Canada. (HECK) 541 Clinical Drive, Room 600, Indianapolis, Indiana 46202-5111. (FREUND) Office of Academic Affairs, Bryan Hall, Room 109, Indiana University, Bloomington, Indiana 47405 |
Author_xml | – sequence: 1 givenname: GILLIAN surname: HAWKER fullname: HAWKER, GILLIAN organization: TORONTO (HAWKER, WRIGHT, COYTE); RESEARCH TRIANGLE PARK, NORTH CAROLINA (PAUL); INDIANAPOLIS (DITTUS); TORONTO (CROXFORD); INDIANAPOLIS (KATZ); TORONTO, ONTARIO, CANADA (BOMBARDIER); INDIANAPOLIS, INDIANA (HECK, FREUND). Investigation performed at the Departments of Medicine, Surgery, Statistics, and Health Administration, University of Toronto, Toronto; Institute for Policy Analysis, Toronto; the Departments of Medicine, Regenstrief Institute for Health Care, Bowen Research Centre, and School of Public and Environmental Affairs, Indiana University, Indianapolis; and Research Triangle Institute and Glaxo Wellcome, Research Triangle Park. No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. Funds were received in total or partial support of the research or clinical study presented in this article. The funding sources were Grant 06432 of the Agency for Health Care Policy and Research to Indiana University and subgrantees (University of Toronto, Research Triangle Institute, Pittsburgh Research Institute, and University of Indiana) and Medical Research Council Scholarships (G. H. and J. W.). (HAWKER) Women's College Hospital, Burton Hall, Room 416, 60 Grosvenor Street, Toronto, Ontario M5S 1B6, Canada. (WRIGHT) Division of Orthopaedic Surgery, The Hospital for Sick Children, 555 University Avenue, Room S107, Toronto, Ontario M5G 1X8, Canada. (COYTE) Department of Health Administration, University of Toronto, McMurrich Building, Second Floor, 12 Queen's Park West, Toronto, Ontario M5S 1A8, Canada. (PAUL) Care Management Division, Clinical Economics Outcomes Assessment, Glaxo Wellcome, 5 Moore Drive, Research Triangle Park, North Carolina 27709. (DITTUS) Vanderbilt Medical Center, Seventh Floor, Medical Center East, Nashville, Tennessee 37232. (CROXFORD) Sunnybrook Health Science Centre, Institute for Clinical Evaluative Science, G Wing, 2075 Bayview Avenue, North York, Ontario M4N 3M5, Canada. (KATZ) Division of Biostatistics, Indiana University School of Medicine, 699 West Drive, Riley Research Wing, Room 135, Indianapolis, Indiana 46202-5200. (BOMBARDIER) Institute for Work and Health, 250 Bloor Street East, Suite 702, Toronto, Ontario M4W 1E6, Canada. (HECK) 541 Clinical Drive, Room 600, Indianapolis, Indiana 46202-5111. (FREUND) Office of Academic Affairs, Bryan Hall, Room 109, Indiana University, Bloomington, Indiana 47405 – sequence: 2 givenname: JAMES surname: WRIGHT fullname: WRIGHT, JAMES – sequence: 3 givenname: PETER surname: COYTE fullname: COYTE, PETER – sequence: 4 givenname: JOHN surname: PAUL fullname: PAUL, JOHN – sequence: 5 givenname: ROBERT surname: DITTUS fullname: DITTUS, ROBERT – sequence: 6 givenname: RUTH surname: CROXFORD fullname: CROXFORD, RUTH – sequence: 7 givenname: BARRY surname: KATZ fullname: KATZ, BARRY – sequence: 8 givenname: CLAIRE surname: BOMBARDIER fullname: BOMBARDIER, CLAIRE – sequence: 9 givenname: DAVID surname: HECK fullname: HECK, DAVID – sequence: 10 givenname: DEBORAH surname: FREUND fullname: FREUND, DEBORAH |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2180707$$DView record in Pascal Francis |
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Title | Health-Related Quality of Life after Knee Replacement: Results of the Knee Replacement Patient Outcomes Research Team Study |
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