Patient-Based Health Status Measurement in Clinical Practice: A Study of Its Impact on Epilepsy Patients' Care
The objective was to assess the potential benefits of the routine use of the MOS SF-36 Health Survey (SF-36) in the care of ambulatory patients. The design was a longitudinal, prospective, randomized, controlled study set in the outpatient neurology clinic at the New England Medical Center. There we...
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Veröffentlicht in: | Quality of life research 1997-05, Vol.6 (4), p.329-341 |
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description | The objective was to assess the potential benefits of the routine use of the MOS SF-36 Health Survey (SF-36) in the care of ambulatory patients. The design was a longitudinal, prospective, randomized, controlled study set in the outpatient neurology clinic at the New England Medical Center. There were 163 consecutive patients with epilepsy who had 210 follow-up visits with one of two epileptologists. The patients completed the SF-36 before the patient-physician encounter and the forms were optically scanned. The SF-36 results of the intervention group patients were given to the physicians before the encounter and withheld for control group patients. For intervention group patients, the physicians completed a questionnaire assessing the impact of the SF-36 on the process of care. After the visit, all patients completed a satisfaction questionnaire. The main outcome measures were the physicians' responses to standardized questions about the usefulness of the SF-36 for communication with and management of epilepsy patients and the patients' responses to standardized questions about their satisfaction with care. The physicians indicated that the SF-36 provided new information in 63% of the intervention group encounters. A change in therapy was prompted in 13%. The physicians rated the SF-36 as at least moderately useful for communication in 14% of the encounters and to management in 8%. The lower (indicating worse health status) the patients' SF-36 scale scores, the more useful the SF-36 results were rated by the physicians for communication and management. It was concluded that the routine use of health status measures may enhance patients' care. |
doi_str_mv | 10.1023/a:1018479209369 |
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Wagner ; Bruce L. Ehrenberg ; Teresa A. Tran ; Bungay, Kathleen M. ; Diane J. Cynn ; Rogers, William H.</creator><creatorcontrib>Anita K. Wagner ; Bruce L. Ehrenberg ; Teresa A. Tran ; Bungay, Kathleen M. ; Diane J. Cynn ; Rogers, William H.</creatorcontrib><description>The objective was to assess the potential benefits of the routine use of the MOS SF-36 Health Survey (SF-36) in the care of ambulatory patients. The design was a longitudinal, prospective, randomized, controlled study set in the outpatient neurology clinic at the New England Medical Center. There were 163 consecutive patients with epilepsy who had 210 follow-up visits with one of two epileptologists. The patients completed the SF-36 before the patient-physician encounter and the forms were optically scanned. The SF-36 results of the intervention group patients were given to the physicians before the encounter and withheld for control group patients. For intervention group patients, the physicians completed a questionnaire assessing the impact of the SF-36 on the process of care. After the visit, all patients completed a satisfaction questionnaire. The main outcome measures were the physicians' responses to standardized questions about the usefulness of the SF-36 for communication with and management of epilepsy patients and the patients' responses to standardized questions about their satisfaction with care. The physicians indicated that the SF-36 provided new information in 63% of the intervention group encounters. A change in therapy was prompted in 13%. The physicians rated the SF-36 as at least moderately useful for communication in 14% of the encounters and to management in 8%. The lower (indicating worse health status) the patients' SF-36 scale scores, the more useful the SF-36 results were rated by the physicians for communication and management. It was concluded that the routine use of health status measures may enhance patients' care.</description><identifier>ISSN: 0962-9343</identifier><identifier>EISSN: 1573-2649</identifier><identifier>DOI: 10.1023/a:1018479209369</identifier><identifier>PMID: 9248315</identifier><language>eng</language><publisher>Netherlands: Rapid Communications of Oxford Ltd</publisher><subject>Activities of Daily Living ; Adult ; Communication ; Control groups ; Epilepsy ; Epilepsy - psychology ; Female ; Health Status ; Health Surveys ; Humans ; Longitudinal Studies ; Male ; Medical practice ; Middle Aged ; Neurology ; Outcome Assessment (Health Care) ; Patient Satisfaction ; Patients ; Physician-Patient Relations ; Physicians ; Prospective Studies ; Quality of Health Care ; Quality of life ; Questionnaires ; Surveys and Questionnaires ; Wellbeing</subject><ispartof>Quality of life research, 1997-05, Vol.6 (4), p.329-341</ispartof><rights>Copyright 1997 Rapid Science Publishers</rights><rights>Chapman and Hall 1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-a67899616365ecf2b81a120f3581e93d16679969123587fbedc7a0891ce06df03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4034736$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4034736$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27923,27924,58016,58249</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9248315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anita K. Wagner</creatorcontrib><creatorcontrib>Bruce L. Ehrenberg</creatorcontrib><creatorcontrib>Teresa A. Tran</creatorcontrib><creatorcontrib>Bungay, Kathleen M.</creatorcontrib><creatorcontrib>Diane J. Cynn</creatorcontrib><creatorcontrib>Rogers, William H.</creatorcontrib><title>Patient-Based Health Status Measurement in Clinical Practice: A Study of Its Impact on Epilepsy Patients' Care</title><title>Quality of life research</title><addtitle>Qual Life Res</addtitle><description>The objective was to assess the potential benefits of the routine use of the MOS SF-36 Health Survey (SF-36) in the care of ambulatory patients. The design was a longitudinal, prospective, randomized, controlled study set in the outpatient neurology clinic at the New England Medical Center. There were 163 consecutive patients with epilepsy who had 210 follow-up visits with one of two epileptologists. The patients completed the SF-36 before the patient-physician encounter and the forms were optically scanned. The SF-36 results of the intervention group patients were given to the physicians before the encounter and withheld for control group patients. For intervention group patients, the physicians completed a questionnaire assessing the impact of the SF-36 on the process of care. After the visit, all patients completed a satisfaction questionnaire. The main outcome measures were the physicians' responses to standardized questions about the usefulness of the SF-36 for communication with and management of epilepsy patients and the patients' responses to standardized questions about their satisfaction with care. The physicians indicated that the SF-36 provided new information in 63% of the intervention group encounters. A change in therapy was prompted in 13%. The physicians rated the SF-36 as at least moderately useful for communication in 14% of the encounters and to management in 8%. The lower (indicating worse health status) the patients' SF-36 scale scores, the more useful the SF-36 results were rated by the physicians for communication and management. It was concluded that the routine use of health status measures may enhance patients' care.</description><subject>Activities of Daily Living</subject><subject>Adult</subject><subject>Communication</subject><subject>Control groups</subject><subject>Epilepsy</subject><subject>Epilepsy - psychology</subject><subject>Female</subject><subject>Health Status</subject><subject>Health Surveys</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical practice</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Outcome Assessment (Health Care)</subject><subject>Patient Satisfaction</subject><subject>Patients</subject><subject>Physician-Patient Relations</subject><subject>Physicians</subject><subject>Prospective Studies</subject><subject>Quality of Health Care</subject><subject>Quality of life</subject><subject>Questionnaires</subject><subject>Surveys and Questionnaires</subject><subject>Wellbeing</subject><issn>0962-9343</issn><issn>1573-2649</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkEtLw0AURgdRaq2u3SgMCLqKziOZR3c1VFuoWFDXYTq5wZS8zEwW_fcONLhwdeGew8e9H0LXlDxSwviTmVNCVSw1I5oLfYKmNJE8YiLWp2hKtGCR5jE_RxfO7QkhShM2QRPNYsVpMkXN1vgSGh89Gwc5XoGp_Df-8MYPDr-BcUMPdeC4bHBalU1pTYW3vbG-tDDHi6AO-QG3BV57h9d1FwhuG7zsygo6d8BjvnvAqenhEp0VpnJwNc4Z-npZfqaraPP-uk4Xm8hyLXxkhFRaCyq4SMAWbKeooYwUPFEUNM-pEDJwTVnYyGIHuZUm_EYtEJEXhM_Q_TG369ufAZzP6tJZqCrTQDu4TGoqBVMsiHf_xH079E24LaNEMaYkUTRYt6M17GrIs64va9MfsrHGwG-OfO982__hmPBYcsF_AbJge30</recordid><startdate>19970501</startdate><enddate>19970501</enddate><creator>Anita K. 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Wagner</au><au>Bruce L. Ehrenberg</au><au>Teresa A. Tran</au><au>Bungay, Kathleen M.</au><au>Diane J. Cynn</au><au>Rogers, William H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patient-Based Health Status Measurement in Clinical Practice: A Study of Its Impact on Epilepsy Patients' Care</atitle><jtitle>Quality of life research</jtitle><addtitle>Qual Life Res</addtitle><date>1997-05-01</date><risdate>1997</risdate><volume>6</volume><issue>4</issue><spage>329</spage><epage>341</epage><pages>329-341</pages><issn>0962-9343</issn><eissn>1573-2649</eissn><abstract>The objective was to assess the potential benefits of the routine use of the MOS SF-36 Health Survey (SF-36) in the care of ambulatory patients. The design was a longitudinal, prospective, randomized, controlled study set in the outpatient neurology clinic at the New England Medical Center. There were 163 consecutive patients with epilepsy who had 210 follow-up visits with one of two epileptologists. The patients completed the SF-36 before the patient-physician encounter and the forms were optically scanned. The SF-36 results of the intervention group patients were given to the physicians before the encounter and withheld for control group patients. For intervention group patients, the physicians completed a questionnaire assessing the impact of the SF-36 on the process of care. After the visit, all patients completed a satisfaction questionnaire. The main outcome measures were the physicians' responses to standardized questions about the usefulness of the SF-36 for communication with and management of epilepsy patients and the patients' responses to standardized questions about their satisfaction with care. The physicians indicated that the SF-36 provided new information in 63% of the intervention group encounters. A change in therapy was prompted in 13%. The physicians rated the SF-36 as at least moderately useful for communication in 14% of the encounters and to management in 8%. The lower (indicating worse health status) the patients' SF-36 scale scores, the more useful the SF-36 results were rated by the physicians for communication and management. It was concluded that the routine use of health status measures may enhance patients' care.</abstract><cop>Netherlands</cop><pub>Rapid Communications of Oxford Ltd</pub><pmid>9248315</pmid><doi>10.1023/a:1018479209369</doi><tpages>13</tpages></addata></record> |
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subjects | Activities of Daily Living Adult Communication Control groups Epilepsy Epilepsy - psychology Female Health Status Health Surveys Humans Longitudinal Studies Male Medical practice Middle Aged Neurology Outcome Assessment (Health Care) Patient Satisfaction Patients Physician-Patient Relations Physicians Prospective Studies Quality of Health Care Quality of life Questionnaires Surveys and Questionnaires Wellbeing |
title | Patient-Based Health Status Measurement in Clinical Practice: A Study of Its Impact on Epilepsy Patients' Care |
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