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dc.contributor.authorSezgin Özcan, Didem
dc.contributor.authorTatlı, Hilmi Umut
dc.contributor.authorPolat, Cemile Sevgi
dc.contributor.authorAyhan Öken, Öznur
dc.contributor.authorKöseoğlu, Belma Füsun
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:49:32Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:49:32Z
dc.date.issued2019en_US
dc.identifier.citationSezgin Özcan, D., Tatlı, H. U., Polat, C. S., Ayhan Öken, Ö. ve Köseoğlu, B. F. (2019). The effectiveness of fluidotherapy in poststroke complex regional pain syndrome: A randomized controlled study. Journal of Stroke and Cerebrovascular Diseases, 28(6), 1578-1585. https://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2019.03.002en_US
dc.identifier.issn1052-3057
dc.identifier.issn1532-8511
dc.identifier.urihttps://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2019.03.002
dc.identifier.urihttps://hdl.handle.net/20.500.12511/1629
dc.descriptionWOS: 000469036700030en_US
dc.descriptionPubMed ID: 30940426en_US
dc.description.abstractObjective: To evaluate whether combining fluidotherapy to conventional rehabilitation program provides additional improvements on pain severity, upper extremity functions, and edema volume in patients with poststroke complex regional pain syndrome (CRPS). Design: Randomized controlled trial. Setting: Training and research hospital. Participants: Thirty hemiplegic patients with subacute stage CRPS type-1 of the upper extremity. Interventions: The patients randomly divided into 2 groups. Both groups received a 3 week conventional rehabilitation program (5 days/week, 2-4 hours/day). Experimental group received 15 sessions additional fluidotherapy application to the affected upper extremity (40 degrees C, 20 minutes in continuous mode, 5 sessions/week). Main Outcome Measures: We evaluated the distal upper arm edema with a volumeter. Other used clinical assessment scales were Brunnstrom recovery stages of the arm and hand for motor recovery, motor items of the functional independence measure for functional status, visual analog scale for pain severity, and the painDETECT questionnaire for presence and the severity of neuropathic pain. Results: The mean age of the participants was 64.3 +/- 11.66 (28-84). At the post-treatment evaluation, significant improvements were revealed regarding to the edema volume, pain visual analog scale, painDETECT and functional independence measure scores, and the Brunnstrom stages of upper extremity and hand in both groups (P <.05). But among the parameters mentioned above, only the decrease in edema volume and the painDETECT scores were greater in fluidotherapy group than the control group (P <.05). Conclusions: Addition of the fluidotherapy to the conventional rehabilitation program provides better improvements on neuropathic pain and edema volume in subacute stage poststroke CRPS.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectComplex Regional Pain Syndromeen_US
dc.subjectFluidotherapyen_US
dc.subjectHand Volumeen_US
dc.subjectHemiplegiaen_US
dc.subjectNeuropathic Painen_US
dc.subjectPhysical Agentsen_US
dc.subjectRehabilitationen_US
dc.titleThe effectiveness of fluidotherapy in poststroke complex regional pain syndrome: A randomized controlled studyen_US
dc.typearticleen_US
dc.relation.ispartofJournal of Stroke and Cerebrovascular Diseasesen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Fizik Tedavi ve Rehabilitasyon Ana Bilim Dalıen_US
dc.authorid0000-0003-0246-3001en_US
dc.identifier.volume28en_US
dc.identifier.issue6en_US
dc.identifier.startpage1578en_US
dc.identifier.endpage1585en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1016/j.jstrokecerebrovasdis.2019.03.002en_US
dc.identifier.wosqualityQ4en_US
dc.identifier.scopusqualityQ2en_US


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