Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/6157
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dc.contributor.authorReid, C.-
dc.contributor.authorNelson, M.-
dc.contributor.authorBeckinsale, P.-
dc.contributor.authorRyan, P.-
dc.contributor.authorMarley, J.-
dc.contributor.authorWing, L.-
dc.contributor.authorBeilin, L.-
dc.contributor.authorBrown, M.-
dc.contributor.authorJennings, G.-
dc.contributor.authorJohnston, C.-
dc.contributor.authorMcNeil, J.-
dc.contributor.authorMorgan, T.-
dc.contributor.authorShaw, J.-
dc.contributor.authorSteven, I.-
dc.contributor.authorWest, M.-
dc.date.issued1997-
dc.identifier.citationClinical and Experimental Pharmacology and Physiology, 1997; 24(5):370-373-
dc.identifier.issn0305-1870-
dc.identifier.issn1440-1681-
dc.identifier.urihttp://hdl.handle.net/2440/6157-
dc.descriptionArticle first published online: 28 JUN 2007-
dc.description.abstract1. The present study aimed to determine the feasibility of conducting a 5 year cardiovascular outcome trial of the treatment of 6000 elderly hypertensive patients in Australian general practices. 2. General practitioners (GPs) were invited to participate by mail and personal follow-up. Patient records were reviewed to identify subjects for a blood pressure (BP) screening programme. Blood pressure was measured on three occasions and eligible subjects were included if the average BP was geqslant R: gt-or-equal, slanted 160 mmHg systolic or geqslant R: gt-or-equal, slanted 90 mmHg diastolic if systolic BP was geqslant R: gt-or-equal, slanted 140 mmHg. 3. Seven hundred and forty-one GPs were approached and 89 were enrolled in the study (12% of mail invites and 75% of those receiving a personal contact). In 16 practices where screening was completed, 82 000 records were reviewed to identify 4% patients eligible for screening. Twenty-two per cent of eligible subjects attended screening. Of 1938 subjects screened, 180 (9%) had BP 5=160/90 mmHg. Forty-seven percent of subjects (n = 916) were receiving antihypertensive therapy and 184 (20%) were withdrawn from therapy. One hundred and sixteen (63%) of these subjects had BP return to study entry levels within 6 weeks. Fifty-seven newly diagnosed and 81 previously treated subjects were randomized (7% of the screened population). 4. Based on the high participation rate of GPs, the response rate of patients to attend a BP screening programme and the 7% randomization to screening ratio for entry into the study, the ANBP2 pilot study has demonstrated that it is feasible to recruit subjects from Australian general practices to a cardiovascular outcome trial.-
dc.language.isoen-
dc.publisherBlackwell Science-
dc.source.urihttp://dx.doi.org/10.1111/j.1440-1681.1997.tb01204.x-
dc.subjectcardiovascular outcome-
dc.subjectelderly-
dc.subjectgeneral practice-
dc.subjecthypertension-
dc.subjectpilot study-
dc.titleFeasibility of conducting cardiovascular outcome research in Australian General Practice - results from the ANBP2 Pilot Study-
dc.typeJournal article-
dc.identifier.doi10.1111/j.1440-1681.1997.tb01204.x-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest
General Practice publications

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