Associations between interarm differences in blood pressure and cardiovascular disease outcomes: protocol for an individual patient data meta-analysis and development of a prognostic algorithm.

2.50
Hdl Handle:
http://hdl.handle.net/11287/620403
Title:
Associations between interarm differences in blood pressure and cardiovascular disease outcomes: protocol for an individual patient data meta-analysis and development of a prognostic algorithm.
Authors:
Clark, C.E.; Boddy, K.; Warren, F. C.; Taylor, R. S.; Aboyans, V.; Cloutier, L.; McManus, R. J.; Shore, Angela ( 0000-0003-3039-308x ) ; Campbell, J. L.
Abstract:
Individual cohort studies in various populations and study-level meta-analyses have shown interarm differences (IAD) in blood pressure to be associated with increased cardiovascular and all-cause mortality. However, key questions remain, such as follows: (1) What is the additional contribution of IAD to prognostic risk estimation for cardiovascular and all-cause mortality? (2) What is the minimum cut-off value for IAD that defines elevated risk? (3) Is there a prognostic value of IAD and do different methods of IAD measurement impact on the prognostic value of IAD? We aim to address these questions by conducting an individual patient data (IPD) meta-analysis.
Citation:
Associations between interarm differences in blood pressure and cardiovascular disease outcomes: protocol for an individual patient data meta-analysis and development of a prognostic algorithm. 2017, 7 (6):e016844 BMJ Open
Publisher:
BMJ
Journal:
BMJ open
Issue Date:
2-Jul-2017
URI:
http://hdl.handle.net/11287/620403
DOI:
10.1136/bmjopen-2017-016844
PubMed ID:
28674148
Additional Links:
http://bmjopen.bmj.com/cgi/pmidlookup?view=long&pmid=28674148
Note:
This article is freely available via Open Access. Click on the Additional Link above to access the full-text via the publisher's site.
Type:
Journal Article
Language:
en
ISSN:
2044-6055
Appears in Collections:
Cardiology; 2017 RD&E publications

Full metadata record

DC FieldValue Language
dc.contributor.authorClark, C.E.en
dc.contributor.authorBoddy, K.en
dc.contributor.authorWarren, F. C.en
dc.contributor.authorTaylor, R. S.en
dc.contributor.authorAboyans, V.en
dc.contributor.authorCloutier, L.en
dc.contributor.authorMcManus, R. J.en
dc.contributor.authorShore, Angelaen
dc.contributor.authorCampbell, J. L.en
dc.date.accessioned2017-09-18T13:03:32Z-
dc.date.available2017-09-18T13:03:32Z-
dc.date.issued2017-07-02-
dc.identifier.citationAssociations between interarm differences in blood pressure and cardiovascular disease outcomes: protocol for an individual patient data meta-analysis and development of a prognostic algorithm. 2017, 7 (6):e016844 BMJ Openen
dc.identifier.issn2044-6055-
dc.identifier.pmid28674148-
dc.identifier.doi10.1136/bmjopen-2017-016844-
dc.identifier.urihttp://hdl.handle.net/11287/620403-
dc.description.abstractIndividual cohort studies in various populations and study-level meta-analyses have shown interarm differences (IAD) in blood pressure to be associated with increased cardiovascular and all-cause mortality. However, key questions remain, such as follows: (1) What is the additional contribution of IAD to prognostic risk estimation for cardiovascular and all-cause mortality? (2) What is the minimum cut-off value for IAD that defines elevated risk? (3) Is there a prognostic value of IAD and do different methods of IAD measurement impact on the prognostic value of IAD? We aim to address these questions by conducting an individual patient data (IPD) meta-analysis.en
dc.language.isoenen
dc.publisherBMJen
dc.relation.urlhttp://bmjopen.bmj.com/cgi/pmidlookup?view=long&pmid=28674148en
dc.rightsArchived with thanks to BMJ openen
dc.subjectWessex Classification Subject Headings::Cardiologyen
dc.titleAssociations between interarm differences in blood pressure and cardiovascular disease outcomes: protocol for an individual patient data meta-analysis and development of a prognostic algorithm.en
dc.typeJournal Articleen
dc.identifier.journalBMJ openen
dc.description.noteThis article is freely available via Open Access. Click on the Additional Link above to access the full-text via the publisher's site.en
dc.type.versionPublisheden

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