Recurrent Autonomic Dysreflexia; A Case Report and Review of the Literature

dc.contributor.authorYigitoglu, Pembe Hare
dc.contributor.authorEker, Amber
dc.contributor.authorGuenay, Levent Mert
dc.contributor.authorHarman, Ferhat
dc.contributor.authorRasmussen, Finn
dc.date.accessioned2026-02-06T18:21:40Z
dc.date.issued2023
dc.departmentDoğu Akdeniz Üniversitesi
dc.description.abstractAutonomic dysreflexia is induced by spinal reflex mechanisms which continue to be intact in spite of the patient's injury. Any proprioceptive or noxious stimuli below the injury level generates an afferent impulse. This initiates a generalized sympathetic response. In response, it results in vasoconstriction below the neurologic lesion. We present a case of a male patient with C6 ASIA-A tetraplegia who developed recurrent dysreflexic episodes which were relieved by replacing the clean intermittent catheterization by indwelling Foley catheterization.
dc.identifier.doi10.4274/cjms.2022.2021-52
dc.identifier.endpage320
dc.identifier.issn2149-7893
dc.identifier.issn2536-507X
dc.identifier.issue4
dc.identifier.orcid0000-0001-9997-4662
dc.identifier.orcid0000-0003-4685-2201
dc.identifier.orcid0000-0002-2884-4200
dc.identifier.orcid0000-0002-7579-3098
dc.identifier.scopusqualityN/A
dc.identifier.startpage318
dc.identifier.trdizinid1261131
dc.identifier.urihttps://doi.org/10.4274/cjms.2022.2021-52
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1261131
dc.identifier.urihttps://hdl.handle.net/11129/9429
dc.identifier.volume8
dc.identifier.wosWOS:001069490200010
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.publisherGalenos Publ House
dc.relation.ispartofCyprus Journal of Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260204
dc.subjectAutonomic dysreflexia
dc.subjecttetraplegia
dc.subjectrehabilitation
dc.titleRecurrent Autonomic Dysreflexia; A Case Report and Review of the Literature
dc.typeReview Article

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