The effect of venlafaxine HCl on painful peripheral diabetic neuropathy in patients with type 2 diabetes mellitus
dc.contributor.author | Kadiroglu, Ali Kemal | |
dc.contributor.author | Sit, Dede | |
dc.contributor.author | Kayabasi, Hasan | |
dc.contributor.author | Tuzcu, Alpaslan Kemal | |
dc.contributor.author | Tasdemir, Nebahat | |
dc.contributor.author | Yilmaz, M. Emin | |
dc.date.accessioned | 2024-04-24T16:15:03Z | |
dc.date.available | 2024-04-24T16:15:03Z | |
dc.date.issued | 2008 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Objective: The objective of this study was to evaluate the efficacy of venlafaxine HCl in the symptomatic treatment of painful peripheral diabetic neuropathy (PPDN) among patients with type 2 diabetes mellitus (DM). Design: This study was designed as a prospective, randomized, and controlled trial. Setting: This study was conducted at the Dicle University Medical Faculty (Diyarbakir, Turkey). Patients: Sixty type 2 DM outpatients (47 females and 13 males) with PPDN who had a minimum visual analog scale (VAS) score of 40 mm were enrolled in this study. Interventions: Patients randomized to the treatment group (n=30) received venlafaxine HCl, whereas those randomized to the control group (n=30) received a combination of vitamins B-1 and B-6 tablets. Measures: Severity of pain was measured by VAS, Short-Form McGill Pain Questionnaire, and numerical analog scale scores at admission and at the second, fourth, and eighth weeks of the study. Polyneuropathy was supported by electromyelography. Outcome: In the treatment group, severity of pain was measured as 70.0+/-13.0 in the VAS, as 24.9+/-6.2 in the Short-Form McGill Pain Questionnaire, and as 7.2+/-1.1 in the numerical analog scale. In the control group, it was measured as 73.0+/-8.0 in the VAS, as 26.8+/-6.2 in the Short-Form McGill Pain Questionnaire, and as 7.4+/-0.8 in the numerical analog scale (P>.05). Results: The most common form of PPDN was distal symmetrical sensorimotor polyneuropathy in both groups (46.8% vs. 50.0%). At the end of the study, there was a significant difference in severity of pain between the groups. In the treatment group, scores were 8.5+/-5.2 and 3.1+/-1.6 in the Short-Form McGill Pain Questionnaire and numerical analog scale, respectively; in the control group, these were 20.5+/-7.0 and 5.5+/-1.6, respectively (P<.001). Conclusions: Venlafaxine HCl is a safe and well-tolerable analgesic drug in the symptomatic treatment of PPDN; however, it has minimal adverse effects. It showed its efficacy markedly in the second week of therapy. (C) 2008 Elsevier Inc. All rights reserved. | en_US |
dc.identifier.doi | 10.1016/j.jdiacomp.2007.03.010 | |
dc.identifier.endpage | 245 | en_US |
dc.identifier.issn | 1056-8727 | |
dc.identifier.issn | 1873-460X | |
dc.identifier.issue | 4 | en_US |
dc.identifier.pmid | 18413214 | |
dc.identifier.scopus | 2-s2.0-45849106140 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 241 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.jdiacomp.2007.03.010 | |
dc.identifier.uri | https://hdl.handle.net/11468/15618 | |
dc.identifier.volume | 22 | en_US |
dc.identifier.wos | WOS:000257868200003 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Inc | en_US |
dc.relation.ispartof | Journal of Diabetes and Its Complications | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Diabetic Neuropathy | en_US |
dc.subject | Pain | en_US |
dc.subject | Venlafaxine Hcl | en_US |
dc.title | The effect of venlafaxine HCl on painful peripheral diabetic neuropathy in patients with type 2 diabetes mellitus | en_US |
dc.title | The effect of venlafaxine HCl on painful peripheral diabetic neuropathy in patients with type 2 diabetes mellitus | |
dc.type | Article | en_US |