No abstract available.
Anesthetics, Intravenous*

No abstract available
Anesthetics, Intravenous* ; Pharmacogenetics*

No abstract available.
Infusions, Intravenous* ; Urography*

Drip infusion pyelography by Schencker technique was carried out on total of 20 cases, 7 normal and 13 abnormal. Of 13 abnormal cases, definite diagnosis could be obtained in 1 cases in which conventional urography had not been helpful in establishment of diagnosis, and significant information could be obtained in 6 cases. This is the first report on drip infusion pyelography in this country and no complication was observed during the examination. Drip infusion pyelography was found valuable in cases with the following problems; 1) When valuable information can not be obtained through the conventional urography. 2) When renal function is poor. 3) When delineation of anatomical details is desirable. 4) When retrograde pyelography is contraindicated. Drip infusion pyelography is a safe, new and widely accepted diagnostic procedure in urographic study.
Diagnosis ; Infusions, Intravenous* ; Urography*

Awake craniotomy is a neurosurgical technique that involves an awake neurological testing during the resection of an intracranial lesion in eloquent cerebral cortical areas representing motor, language, and speech. This technique is highlighted by an intra-operative cortical mapping that requires active participation by the patient and poses unique challenges to the anesthesiologist. The surgical and anesthetic techniques have evolved significantly over time, as the neurosurgeon and the anesthesiologist learn new steps in making this technique safe to achieve reasonable patient satisfaction. A thorough understanding of this surgical technique's rationale will guide the anesthesiologist in planning the anesthetic management depending on the surgery and neurologic testing. Constant communication between the neurosurgeon, anesthesiologist, and the patient will define this surgical technique's success. It is already a well-established procedure; however, factors that contribute to failures in awake craniotomy procedures have not been well characterized in the literature. Failure is defined as the inability to conduct awake neurologic testing during the awake craniotomy procedure because of various factors which will be described. This paper aims to review the challenges in the performance of three (3) cases of awake craniotomies performed in the Philippine General Hospital. The challenges described in these three (3) cases reveal that this can be experienced by the neurosurgeon, neuroanesthesiologist, and most especially the patient in an acute critical condition. Identification of the procedures' failure and the steps taken to manage such situations with the patient's safety in mind are discussed.
Anesthesia, Intravenous ; Anesthesia, General

BACKGROUND: The induction and maintenance of intravenous anesthesia by propofol-TCI has been popular. When infusing propofol with other drugs at the same intravenous access line, incompatibility may result. We attempted to evaluate the incompatibilities between propofol and rocuronium by subtherapeutic dosing of rocuronium. METHODS: Eighty patients were randomized into two groups. Induction of anesthesia was done by propofol-TCI. The patients in group 1 received rocuronium 0.6 mg/kg at the same intravenous access line with propofol infusion and in group 2 received rocuronium at the different intravenous access line with propofol infusion. One Hz single twitch responses were measured by acceleromyography after rocuronium administration. Intubation was done when the twitch height depressed more than 95% of the baseline. The intubating conditions were assessed and graded as excellent, good, poor and bad. Onset time, recovery index and duration were compared between the two groups. RESULTS: The onset was significantly delayed in group 1 (124.9 +/- 35.5 vs. 101.8 +/- 22.1), but there were no significant differences in the intubating condition, recovery index, duration and the incidence of withdrawal response to rocuronium injection. CONCLUSIONS: Onset time was delayed when administrating rocuronium at the same intravenous access line with propofol-TCI. So giving rocuronium at the different intravenous access line with propofol infusion would be helpful to achieve adequate intubating condition rapidly.
Anesthesia ; Anesthesia, Intravenous ; Humans ; Incidence ; Injections, Intravenous* ; Intubation ; Propofol*

BACKGROUND: The start-up behavior of syringe and syringe pump is known to be one of the causes of inaccurate intravenous infusion. This study evaluated the method of priming the infusion system (PRIMING), and its impact on the target-controlled infusion (TCI) of two remifentanil diluents. METHODS: PRIMING was performed using an evacuation of 2.0 ml to the atmosphere prior to TCI. Forty-eight TCI, using 50 microg/ml (Remi50) or 20 microg/ml (Remi20) of diluents, were performed targeting 4.0 ng/ml of effect-site concentration (Ceff), with PRIMING or not. The gravimetrical measurements of the delivered infusates reproduced actual Ceff. The bolus amount and time to reach 95% target were compared. RESULTS: Without PRIMING, Remi50 infused less bolus (43 +/- 23 %) than Remi20 (19 +/- 9 %) (P = 0.003), and showed more delayed increase of Ceff (11.2 +/- 4.0 min) than Remi20 (7.4 +/- 0.4 min) (P = 0.028). However, PRIMING significantly decreased the deficit of the bolus (2 +/- 1%), as well as the delay of the increase of Ceff in Remi50 (1.2 +/- 0.2 min) (both P < 0.001). In addition, with PRIMING, the start-up bolus showed minimal difference to the nominal bolus (1 and 2%), and Ceff were increased to 4.0 +/- 0.1 ng/ml at the expected time of peak effect, irrespective of the diluents. CONCLUSIONS: Proper operation of the syringe pump used in the priming of the syringe may be helpful in reduction of the inaccuracy of TCI, particularly during the early phase of infusion, or the infusion of a more concentrated diluent.
Atmosphere ; Infusions, Intravenous ; Piperidines ; Syringes

No abstract available.
Anesthesia, Intravenous* ; Brugada Syndrome* ; Humans

No abstract available.
Anesthesia, Intravenous* ; Humans ; Propofol* ; Respiration*

Objective: To determine the effect of a single intravenous dose of tranexamic acid on intraoperative bleeding, duration of surgery and surgical field visualization during endoscopic sinus surgery. Methods: Study Design: Double-blind, randomized, placebo-controlled trial. Setting: Tertiary Government Hospital in Quezon City Participants: 10 patients aged 18-75 years old diagnosed with chronic rhinosinusitis with or without nasal polyposis and unresponsive to medical treatment, who underwent endoscopic sinus surgery from September 2016 to August 2017, were randomly allocated to treatment group and control group respectively. The “odd” numbers were assigned to the treatment group (intravenous Tranexamic acid) given 1 dose of 100mg/ml (500mg tranexamic acid per 5 ml) tranexamic acid slow intravenous drip 1 hour prior to the procedure, while the “even” numbers assigned to the control group received the same amount of normal saline solution. Results: The mean duration of surgery of the tranexamic group was 185 minutes (standard deviation, SD 55.23) and the control group was 122.6 minutes (SD 42.03) showing no significant difference (p=.08). The mean blood loss of the tranexamic group was less at 240ml (SD 108.39) compared with the control group at 290ml (SD 74.16), although there was no statistically significant difference (p=.42). Intraoperative surgical field assessed by the surgeon based on the Boezart grading scale showed that 2 (40%) of the tranexamic group had higher bleeding score compared with the placebo group. However, this was not found to be statistically significant (p=.460). Due to the small sample size, a type II error occurred with alpha level of 0.05 and estimated power of 0.0885, with not enough basis to refute that a single dose of intravenous tranexamic acid has no effect in improving surgical field visualization during endoscopic sinus surgery. No drug side effects were noted after administration until after surgery. Conclusion Single dose intravenous tranexamic acid in functional endoscopic sinus surgery decreased mean intraoperative blood loss (but this was statistically insignificant), but its effect on surgical field visualization cannot totally be assessed due to small sample size. There was also no change in the observed duration of surgery. No untoward side effects associated were noted from administration of the drug until after the surgery finished.
Administration, Intravenous ; Tranexamic Acid ; Sinusitis