The Clinical Usefulness of Intravenous Cimetropium Bromide As a Premedication for Upper Gastrointestinal Endoscopy Under Conscious Sedation: A Randomized Double-Blind Controlled Trial

2008 ◽  
Vol 67 (5) ◽  
pp. AB288
Author(s):  
Young Mook Kim ◽  
Sung Jung Kim ◽  
Mi Kyeong Heo ◽  
in Suk Park ◽  
Hui Suk Jung ◽  
...  
2014 ◽  
Vol 05 (02) ◽  
pp. 051-057 ◽  
Author(s):  
Sumanth Samson ◽  
Sagiev Koshy George ◽  
B. Vinoth ◽  
Mohd Saif Khan ◽  
Bridgitte Akila

Abstract Context: Midazolam and propofol are effective sedatives for use in upper gastrointestinal endoscopy (UGIE); however, their utility is limited when used alone. In this regard, dexmedetomidine seems to be a promising sedative. Aims: The aim was to compare the hemodynamic effects and sedation efficacy of these drugs in patients undergoing elective diagnostic UGIE. Settings and Design: Randomized control double-blind study was conducted at a teaching hospital. Subjects and Methods: Patients belonging to ASA Grade I or II, undergoing diagnostic elective UGIE were enrolled in the study and randomized into three groups; Group I received midazolam infusion, Group II received propofol infusion and Group III received dexmedetomidine infusion. Hemodynamic parameters and adverse events were recorded during the procedure (intra-operative period [IOP]). Both patient and endoscopist satisfaction were rated on visual analog scale (0 = no pain/least difficulty to 10 = worst pain/maximum difficulty). Recovery was recorded as time to achieve modified Aldrete score of 10/10. Statistical Analysis: Parametric test analysis of variance was applied to compare the means of three groups of continuous data. Results: Ninety patients were analyzed. Mean arterial pressure was significantly lower in the propofol group at IOP2, IOP4, IOP8, and IOP10 compared with dexmedetomidine and midazolam group. The endoscopist satisfaction level was significantly higher in dexmedetomidine group as compared to propofol and midazolam (60%, 56.7%, 13.3%; P < 0.001). Significantly faster recovery was observed in dexmedetomidine group compared to midazolam and propofol group (7.7 ± 3.9, 18.3 ± 3.8, 12.7 ± 2.9 min; P = 0.001). Conclusions: Use of dexmedetomidine was associated with greater hemodynamic stability and faster recovery when compared to propofol and midazolam.


1989 ◽  
Vol 35 (6) ◽  
pp. 519-522 ◽  
Author(s):  
S. Birkenfeld ◽  
C. Federico ◽  
Y. Dermansky-Avni ◽  
R. Bruck ◽  
E. Melzer ◽  
...  

2015 ◽  
Vol 120 (4) ◽  
pp. 771-780 ◽  
Author(s):  
Keith M. Borkett ◽  
Dennis S. Riff ◽  
Howard I. Schwartz ◽  
Peter J. Winkle ◽  
Daniel J. Pambianco ◽  
...  

2014 ◽  
Vol 05 (02) ◽  
pp. 058-063 ◽  
Author(s):  
Avinash Supe ◽  
Sanjiv P. Haribhakti ◽  
Mohammad Ali ◽  
A. Rathnaswami ◽  
T. Zameer Ulla ◽  
...  

Abstract Background and Objectives: A novel lozenge formulation with advantages of ease of drug administration, palatable taste and improved patient compliance could be the preferred mode of topical pharyngeal anesthesia during upper gastrointestinal endoscopy (UGE). This randomized, open-label, active-controlled study was conducted to evaluate the efficacy and safety of lidocaine lozenges versus lidocaine spray in the diagnostic gastroduodenal endoscopy in Indian patients. Subjects and Methods: Two hundred and forty-seven patients of either sex (18-80 years) undergoing diagnostic gastroduodenal endoscopy were randomized either to; lidocaine lozenge 200 mg or lidocaine spray 200 mg to be applied as a single dose before gastroduodenal endoscopy. Ease of procedure, level of gag reflex, ease of application of the local anesthetic, and investigators global assessment were the primary efficacy endpoints. Need for rescue medication and patient’s global assessment were secondary efficacy endpoints. The incidence of any adverse event was the safety endpoint. Between groups, comparison was done by using appropriate statistical test. Results: Investigator reported significantly lesser procedural difficulty (P = 0.0007) and suppressed gag reflex (P < 0.0001) during UGE with lidocaine lozenge compared to spray. Ease of application of local anesthetic was reported easy in significantly more patients as compared with lidocaine spray (P = 0.001). Global assessment by patient and physician was favorable toward lozenge. Incidences of adverse events were similar in both the groups. Conclusions: The study suggests that lidocaine lozenges are an easier way of applying local oropharyngeal anesthesia, produces better suppression of gag reflex and makes the procedure easier when compared with lidocaine spray.


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