Fatma Ozkan Sipahioglu, Filiz Karaca Akaslan, Ozge Yamankilic Mumcu, R. Polat, F. Sandikci, A. Donmez
{"title":"Comparison of Different Strategies for Prevention of Catheter-Related Bladder Discomfort: A Randomized Controlled Trial","authors":"Fatma Ozkan Sipahioglu, Filiz Karaca Akaslan, Ozge Yamankilic Mumcu, R. Polat, F. Sandikci, A. Donmez","doi":"10.4274/haseki.galenos.2022.8421","DOIUrl":null,"url":null,"abstract":"Aim: Catheter-related bladder discomfort (CRBD) is characterized by pain and a burning sensation in the suprapubic region caused by stimulation of type 3 muscarinic (M3) receptors. The aim of this study was to compare the effects of tramadol and dexmedetomidine on CRBD, which have inhibitory effects on the M3 receptor. Methods: A total of 135 male patients with ASA I-II, aged between 18 and 70 years and scheduled to undergo elective retrograde intrarenal surgery between March and July 2020, were included in the study. Patients were randomized into three groups: tramadol (group T), dexmedetomidine (group D), and control (group C). Patients were evaluated for the incidence and severity of CRBD and postoperative pain at the postoperative 0 th (t 0 ), 1 st (t 1 ), 3 rd (t 2 ), and 6 th (t 3 ) hours. Results: The incidence and severity of CRBD were lower in group D at t 1 than in the other groups (p<0.05). The incidence and severity of CRBD were similar between groups T and D, and they were significantly lower than those in group C at t 2 and t 3 (p<0.01). Postoperative pain levels were significantly lower in groups T and D than in group C at t 0 and t 1 (p<0.01). Postoperative recovery time was significantly longer in group D (p<0.01). Conclusion: Both dexmedetomidine and tramadol are effective in preventing CRBD and in postoperative analgesia. Dexmedetomidine is more potent than tramadol in the early period; however, it may delay post-anesthesia recovery time.","PeriodicalId":42416,"journal":{"name":"Haseki TIp Bulteni-Medical Bulletin of Haseki","volume":null,"pages":null},"PeriodicalIF":0.3000,"publicationDate":"2022-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Haseki TIp Bulteni-Medical Bulletin of Haseki","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4274/haseki.galenos.2022.8421","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: Catheter-related bladder discomfort (CRBD) is characterized by pain and a burning sensation in the suprapubic region caused by stimulation of type 3 muscarinic (M3) receptors. The aim of this study was to compare the effects of tramadol and dexmedetomidine on CRBD, which have inhibitory effects on the M3 receptor. Methods: A total of 135 male patients with ASA I-II, aged between 18 and 70 years and scheduled to undergo elective retrograde intrarenal surgery between March and July 2020, were included in the study. Patients were randomized into three groups: tramadol (group T), dexmedetomidine (group D), and control (group C). Patients were evaluated for the incidence and severity of CRBD and postoperative pain at the postoperative 0 th (t 0 ), 1 st (t 1 ), 3 rd (t 2 ), and 6 th (t 3 ) hours. Results: The incidence and severity of CRBD were lower in group D at t 1 than in the other groups (p<0.05). The incidence and severity of CRBD were similar between groups T and D, and they were significantly lower than those in group C at t 2 and t 3 (p<0.01). Postoperative pain levels were significantly lower in groups T and D than in group C at t 0 and t 1 (p<0.01). Postoperative recovery time was significantly longer in group D (p<0.01). Conclusion: Both dexmedetomidine and tramadol are effective in preventing CRBD and in postoperative analgesia. Dexmedetomidine is more potent than tramadol in the early period; however, it may delay post-anesthesia recovery time.