Does transcutaneous electrical nerve stimulation affect pain, neuropathic pain, and sympathetic skin responses in the treatment of chronic low back pain? A randomized, placebo- controlled study

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dc.authorid0000-0003-1534-8205en_US
dc.authorid0000-0003-1551-0559en_US
dc.authorid0000-0002-2110-4832en_US
dc.contributor.authorYakşi, Elif
dc.contributor.authorKetenci, Ayşegül
dc.contributor.authorBaslo, Mehmet Barış
dc.contributor.authorOrhan, Elif Kocasoy
dc.date.accessioned2023-07-17T09:56:38Z
dc.date.available2023-07-17T09:56:38Z
dc.date.issued2021en_US
dc.departmentBAİBÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.descriptionScientific Research Projects Coordination Unit of Istanbul University(Istanbul University)en_US
dc.description.abstractBackground: The purpose of this study was to assess the effectiveness of trans cutaneous electrical nerve stimulation (TENS) in chronic low back pain and neuropathic pain. Methods: Seventy-four patients aged 18-65 with chronic low back pain were included in the study. Baseline measurements were performed, and patients were randomized into three groups. The first group received burst TENS (bTENS), the second group conventional TENS (cTENS), and the third group placebo TENS (pTENS), all over 15 sessions. Patients' visual analogue scale (VAS) scores were evaluated before treatment (preT), immediately after treatment (postT), and in the third month after treatment (postT3). Douleur Neuropathique 4 Questions (DN4), the Modified Oswestry Low Back Pain Disability Questionnaire (MOS), the Beck Depression Inventory (BDI), and sympathetic skin response (SSR) values were also evaluated preT and postT3. Results: A statistically significant improvement was observed in mean VAS scores postT compared to preT in all three groups. Intergroup comparison revealed a significant difference between preT and postT values, that difference being assessed in favor of bTENS at multiple comparison analysis. Although significant improvement was determined in neuropathic pain DN4 scores measured at postT3 compared to preT in all groups, there was no significant difference between the groups. No statistically significant difference was also observed between the groups in terms of MOS, BDI, or SSR values at postT3 (P > 0.05). Conclusions: bTENS therapy in patients with low back pain is an effective and safe method that can be employed in short-term pain controlen_US
dc.description.sponsorshipScientific Research Projects Coordination Unit of Istanbul University [28997]en_US
dc.identifier.citationYakşi, E., Ketenci, A., Baslo, M. B., & Orhan, E. K. (2021). Does transcutaneous electrical nerve stimulation affect pain, neuropathic pain, and sympathetic skin responses in the treatment of chronic low back pain? A randomized, placebo-controlled study. The Korean journal of pain, 34(2), 217-228.en_US
dc.identifier.doi10.3344/kjp.2021.34.2.217
dc.identifier.endpage228en_US
dc.identifier.issn2005-9159
dc.identifier.issn2093-0569
dc.identifier.issue2en_US
dc.identifier.pmid33785674en_US
dc.identifier.scopus2-s2.0-85104982703en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage217en_US
dc.identifier.urihttp://dx.doi.org/10.3344/kjp.2021.34.2.217
dc.identifier.urihttps://hdl.handle.net/20.500.12491/11296
dc.identifier.volume34en_US
dc.identifier.wosWOS:000639393000010en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorYakşi, Elif
dc.language.isoenen_US
dc.publisherKorean Pain Socen_US
dc.relation.ispartofKorean Journal of Painen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectChronic Painen_US
dc.subjectDepressionen_US
dc.subjectElectromyographyen_US
dc.subjectTensen_US
dc.subjectEfficacyen_US
dc.subjectMechanismsen_US
dc.titleDoes transcutaneous electrical nerve stimulation affect pain, neuropathic pain, and sympathetic skin responses in the treatment of chronic low back pain? A randomized, placebo- controlled studyen_US
dc.typeArticleen_US

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