Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12926
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dc.contributor.authorHowes, L Gen
dc.contributor.authorLouis, William Jen
dc.date.accessioned2015-05-16T02:41:19Z
dc.date.available2015-05-16T02:41:19Z
dc.date.issued1988-03-01en
dc.identifier.citationClinical and Experimental Pharmacology & Physiology; 15(3): 199-202en
dc.identifier.govdoc3078275en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12926en
dc.description.abstract1. Large scale studies have failed to show a substantial benefit of antihypertensive therapy on the incidence of ischaemic heart disease. 2. This may be due to adverse effects of antihypertensive drugs on plasma lipoproteins or because of failure to adequately manage other risk factors for atherogenesis. 3. Hypercholesterolaemia is very common in patients receiving antihypertensive therapy, and is difficult to manage successfully using existing treatment strategies. 4. The achievement of a reduction in mortality and morbidity from ischaemic heart disease amongst hypertensive patients represents a major challenge. Success will probably depend upon the development of adequate methods of lowering plasma cholesterol levels.en
dc.language.isoenen
dc.subject.otherAntihypertensive Agents.therapeutic useen
dc.subject.otherCardiovascular Diseases.drug therapy.physiopathologyen
dc.subject.otherHumansen
dc.subject.otherRisk Factorsen
dc.titleEffects of antihypertensive drugs on cardiovascular risk factors.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical and Experimental Pharmacology & Physiologyen
dc.identifier.affiliationUniversity of Melbourne, Department of Medicine, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages199-202en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/3078275en
dc.type.austinJournal Articleen
local.name.researcherLouis, William J
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
crisitem.author.deptClinical Pharmacology and Therapeutics-
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