Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/33067
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dc.contributor.authorHayes, Peteren_UK
dc.contributor.authorKielty, Hannahen_UK
dc.contributor.authorCasey, Monicaen_UK
dc.contributor.authorGlynn, Liam Gen_UK
dc.contributor.authorMolloy, Gerard Jen_UK
dc.contributor.authorDurand, Hannahen_UK
dc.contributor.authorNewell, Johnen_UK
dc.contributor.authorMurphy, Andrew Wen_UK
dc.date.accessioned2021-08-11T00:06:37Z-
dc.date.available2021-08-11T00:06:37Z-
dc.date.issued2018en_UK
dc.identifier.other43en_UK
dc.identifier.urihttp://hdl.handle.net/1893/33067-
dc.description.abstractBackground Most cases of hypertension can be effectively treated with lifestyle changes together with medications, but within this population lies a group with more difficult to treat hypertension—those with apparent treatment-resistant hypertension (aTRH). The American Heart Association and the UK National Institute for Health and Care Excellence have both highlighted the need for further research into the prognosis of patients with resistant hypertension, both apparent and true. Methods In 16 practices affiliated to a university research network, 646 patients had been identified with apparent treatment-resistant hypertension. To inform a planned full cohort study of these patients, we conducted a feasibility study within three practices to determine participation of practices and patients, availability of outcome measures and data collection times. Results All three practices fully participated and 205/210 (98%) patients were followed up for a median of 23 months. Thirty-five outcome events of interest occurred—the most common was the new onset of retinopathy (9 cases). Eight percent (17/210) had the main composite outcome of death or serious incident cardiovascular event. Of the six patients who died, identification of cause of death was possible from practice records in five; the national General Register Office was successfully used for the final patient. There were 123 admissions, both day and overnight, recorded in 94 individual patients. Average manual systolic blood pressure measurements improved from baseline by 5 mmHg to 138 (SD 19) mmHg; diastolic remained the same at 75 (SD 12) mmHg. Average eGFR increased from 58.8 (SD17.4) to 66 (SD19.7) mls/min/1.73m2. The average time for data collection per patient was 12 mins. Conclusions This study demonstrates that the proposed methodology for a full cohort study within general practice of patients with apparent treatment hypertension is both acceptable to practices and feasible. An adequately powered subsequent follow-up study of the entire cohort appears possible.en_UK
dc.language.isoenen_UK
dc.publisherSpringer Science and Business Media LLCen_UK
dc.relationHayes P, Kielty H, Casey M, Glynn LG, Molloy GJ, Durand H, Newell J & Murphy AW (2018) Prognosis of patients with apparent treatment-resistant hypertension—a feasibility study. Pilot and Feasibility Studies, 4 (1), Art. No.: 43. https://doi.org/10.1186/s40814-018-0232-5en_UK
dc.rightsThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectHypertensionen_UK
dc.subjectPrimary careen_UK
dc.subjectTreatment resistant hypertensionen_UK
dc.subjectPrognosisen_UK
dc.subjectFeasibilityen_UK
dc.titlePrognosis of patients with apparent treatment-resistant hypertension—a feasibility studyen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/s40814-018-0232-5en_UK
dc.identifier.pmid29423261en_UK
dc.citation.jtitlePilot and Feasibility Studiesen_UK
dc.citation.issn2055-5784en_UK
dc.citation.volume4en_UK
dc.citation.issue1en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderHealth Research Boarden_UK
dc.author.emailhannah.durand@stir.ac.uken_UK
dc.citation.date30/01/2018en_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.contributor.affiliationUniversity of Limerick, Irelanden_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.contributor.affiliationNational University of Ireland - Galwayen_UK
dc.identifier.scopusid2-s2.0-85046784391en_UK
dc.identifier.wtid1745992en_UK
dc.contributor.orcid0000-0002-8761-0519en_UK
dc.date.accepted2018-01-10en_UK
dcterms.dateAccepted2018-01-10en_UK
dc.date.filedepositdate2021-08-10en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorHayes, Peter|en_UK
local.rioxx.authorKielty, Hannah|en_UK
local.rioxx.authorCasey, Monica|en_UK
local.rioxx.authorGlynn, Liam G|en_UK
local.rioxx.authorMolloy, Gerard J|en_UK
local.rioxx.authorDurand, Hannah|0000-0002-8761-0519en_UK
local.rioxx.authorNewell, John|en_UK
local.rioxx.authorMurphy, Andrew W|en_UK
local.rioxx.projectHRA-POR-2014-615|Health Research Board|http://dx.doi.org/10.13039/100010414en_UK
local.rioxx.freetoreaddate2021-08-10en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2021-08-10|en_UK
local.rioxx.filenames40814-018-0232-5.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source2055-5784en_UK
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