Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/37726
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dc.contributor.authorAbaraogu, Ukachukwu Okoroaforen_UK
dc.contributor.authorEzenwankwo, Elochukwu Fortuneen_UK
dc.contributor.authorDall, Philippa Margareten_UK
dc.contributor.authorSeenan, Chris Andrewen_UK
dc.contributor.editorAndras, Alinaen_UK
dc.date.accessioned2025-12-19T01:06:57Z-
dc.date.available2025-12-19T01:06:57Z-
dc.date.issued2018-11-15en_UK
dc.identifier.othere0207456en_UK
dc.identifier.urihttp://hdl.handle.net/1893/37726-
dc.description.abstractBackground Peripheral arterial disease (PAD) has a significant negative impact on the quality of life of individuals. Understanding the experiences of people living with PAD will be useful in developing comprehensive patient-centred secondary prevention therapies for this population. Aim The aim of this study is to identify first-hand accounts of patients’ experiences of living with PAD. Methods Six databases (CINALH, PsyclNFO, MEDLINE, AMED, EMBASE, Social citation index/Science citation index via Web of Science (WOS)) and reference lists of identified studies were searched until September 2017 (updated February 2018). Qualitative studies reporting patients’ account of living with PAD were eligible for inclusion. A framework thematic synthesis was implemented. Results Fourteen studies with 360 participants were included. Pain and walking limitation were recurrent among the varied symptom descriptions. Patients’ ignorance and trivialisation of symptoms contributed to delays in diagnosis. Inadequate engagement in disease understanding and treatment decisions meant patients had poor attitudes towards walking treatments and unrealistic expectations about surgery. Depending on symptom progression, patients battle with walking impairment, powerlessness, and loss of independence which were a source of burden to them. Lack of disease understanding is central through patients’ journey with PAD and, although they subsequently began adaptation to long term living with PAD, many worried about their future. Conclusions Disease understanding is vital across the illness trajectory in patients with PAD. Although certain experiences are common throughout patient journey, some might be unique to a particular stage (e.g. unrealistic expectation about surgery, or rationale of walking in spite of pain in a supervised exercise program). Given that PAD is an overarching construct ranging from the mildest form of intermittent claudication to severe critical limb ischemia with ulceration and gangrene, consideration of important patient constructs specific to each stage of the disease may enhance treatment success. Systematic review registration CRD42017070417.en_UK
dc.language.isoenen_UK
dc.publisherPublic Library of Science (PLoS)en_UK
dc.relationAbaraogu UO, Ezenwankwo EF, Dall PM & Seenan CA (2018) Living a burdensome and demanding life: A qualitative systematic review of the patients experiences of peripheral arterial disease. Andras A (Editor) <i>PLOS ONE</i>, 13 (11), Art. No.: e0207456. https://doi.org/10.1371/journal.pone.0207456en_UK
dc.rightsCopyright: © 2018 Abaraogu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.titleLiving a burdensome and demanding life: A qualitative systematic review of the patients experiences of peripheral arterial diseaseen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1371/journal.pone.0207456en_UK
dc.identifier.pmid30440040en_UK
dc.citation.jtitlePLoS ONEen_UK
dc.citation.issn1932-6203en_UK
dc.citation.issn1932-6203en_UK
dc.citation.volume13en_UK
dc.citation.issue11en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderGlasgow Caledonian Universityen_UK
dc.author.emailchristopher.seenan@stir.ac.uken_UK
dc.citation.date15/11/2018en_UK
dc.contributor.affiliationUniversity of Nigeriaen_UK
dc.contributor.affiliationUniversity of Nigeriaen_UK
dc.contributor.affiliationGlasgow Caledonian Universityen_UK
dc.contributor.affiliationGlasgow Caledonian Universityen_UK
dc.identifier.isiWOS:000450254000082en_UK
dc.identifier.scopusid85056534352en_UK
dc.identifier.wtid2212045en_UK
dc.contributor.orcid0000-0002-1967-1459en_UK
dc.contributor.orcid0000-0001-8483-9302en_UK
dc.contributor.orcid0000-0003-4379-7913en_UK
dc.date.accepted2018-10-31en_UK
dcterms.dateAccepted2018-10-31en_UK
dc.date.filedepositdate2025-12-16en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorAbaraogu, Ukachukwu Okoroafor|0000-0002-1967-1459en_UK
local.rioxx.authorEzenwankwo, Elochukwu Fortune|0000-0001-8483-9302en_UK
local.rioxx.authorDall, Philippa Margaret|en_UK
local.rioxx.authorSeenan, Chris Andrew|0000-0003-4379-7913en_UK
local.rioxx.projectProject ID unknown|Glasgow Caledonian University|http://dx.doi.org/10.13039/100010010en_UK
local.rioxx.contributorAndras, Alina|en_UK
local.rioxx.freetoreaddate2025-12-16en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2025-12-16|en_UK
local.rioxx.filenamefile (1).pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1932-6203en_UK
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