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1.
The Korean Journal of Pain ; : 260-265, 2014.
Article in English | WPRIM | ID: wpr-221022

ABSTRACT

BACKGROUND: To evaluate the results of conventional radiofrequency thermorhizotomy (CRT) for trigeminal neuralgia (TN) in patients with failed medical management. METHODS: Patients with Trigeminal neuralgia who were referred to us for 'limited intervention' during the time frame July-2011 to Jan-2013 were enrolled for this study. CRT was administered by the Sweet technique. Pain relief was evaluated by the principle investigator. RESULTS: Eighteen patients were enrolled and completed a mean follow-up of 18.0 months. Pain relief was observed in 14 of 18 (77.8%) patients on the post-operative day, 14 of 18 (77.8%) at 1-month follow-up, 14 of 17 (82.4%) at 3-months follow-up, 12 of 15 (80%) at 6-months follow-up, 7 of 11 (63.6%) at 1-year follow-up and 2 of 6 (33.3%) 1.5 years of follow-up. Four patients required a repeat cycle of CRT; two at six months of follow-up and two at one year of follow-up. One patient was transferred for surgical intervention at six months of follow-up. Side-effects included facial hypoesthesia (n = 6); nausea/vomiting (n = 2), diminished corneal reflex (n = 13) and difficulty in chewing (n = 11). Severity of adverse effects gradually diminished and none of the patients who are beyond 6 months of follow-up have any functional limitation. CONCLUSIONS: CRT is an effective method of pain relief for patients with Trigeminal neuralgia. Successful outcome (excellent or good) can be expected in 66.7% of patients after first cycle of CRF. The incidence and severity of adverse effects is less and the procedure is better tolerated by the patients.


Subject(s)
Humans , Follow-Up Studies , Hypesthesia , Incidence , Mastication , Reflex , Research Personnel , Trigeminal Ganglion , Trigeminal Neuralgia
2.
SJA-Saudi Journal of Anaesthesia. 2012; 6 (2): 140-144
in English | IMEMR | ID: emr-131523

ABSTRACT

The aim of this double-blind, prospective, randomized, controlled study was to compare the effect of addition of ketamine; fentanyl and saline with propofol anesthesia on hemodynamic profile and laryngeal mask airway [LMA] insertion conditions in oral clonidine premedicated children. 180 children [age 2 - 10 years] were at first given oral clonidine [4 microg/kg] 90 minutes before operation, and then were randomly allocated to receive either ketamine 0.5 mg/kg [n=60], fentanyl 1 micro g/kg [n=60] or 0.9% normal saline [n=60] before induction with propofol 3.0 mg/kg. Insertion of LMA was performed within 1 minute of injection of propofol. Heart rate and mean blood pressure were noted 1 min before induction [baseline], immediately after induction, before and after insertion of LMA for up to 3 min. Following LMA insertion, 6 subjective end points were noted-mouth opening, coughing, swallowing, patient's movement, laryngospasm, and ease of an insertion. LMA insertion summed score was prepared depending upon these variables. LMA insertion summed score was nearly similar in ketamine and fentanyl group, which were significantly better than saline group [P<0.004]. Mean blood pressure and heart rate were maintained in ketamine than with fentanyl or saline group. Incidence of prolonged apnea [>120 secs.] was higher in fentanyl group compared to ketamine and saline group. Even in oral clonidine premedicated children, addition of ketamine with propofol provides hemodynamic stability and comparable conditions for LMA insertion like fentanyl propofol with significantly less prolonged apnea


Subject(s)
Humans , Male , Female , Ketamine , Fentanyl , Sodium Chloride , Propofol , Clonidine , Hemodynamics , Laryngeal Masks , Premedication , Child , Prospective Studies , Double-Blind Method
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