BACKGROUND: Lidocaine is a useful intravenous and topical adjunct to facilitate tracheal intubation. We evaluated the effect of tracheal lidocaine on tracheal intubating conditions without neuromuscular blocking agent and hemodynamics during anesthesia induction with propofol and remifentanil target-controlled infusion (TCI). METHODS: Fifty patients, aged 18-60 years, scheduled for closed reduction of fractured nasal bone were randomly assigned to the control group (n = 25) or lidocaine group (n = 25). Anesthesia was induced with propofol-remifentanil TCI with the effect-site concentration of 5 microg/ml and 5 ng/ml. Four minutes after the start of propofol-remifentanil TCI, 4% lidocaine or saline 3 ml was instilled to larynx and trachea, and intubation was performed 1 min later. Acceptable intubation was defined as excellent or good intubating conditions. Hemodynamic data, induction and recovery profiles were recorded. RESULTS: Intubating condition was clinically acceptable in 13 out of 25 (52%) patients in the control group and in 22 out of 25 (88%) in the lidocaine group, and there was a significant difference between the two groups in regard to acceptable intubating conditions (P = 0.005). Mean arterial pressure change over time was significantly different between the two groups. There were no significant differences in the heart rate between the two groups. CONCLUSIONS: This study demonstrated that laryngotracheal administration of 4% lidocaine could increase the percentage of acceptable conditions for tracheal intubation during propofol and remifentanil anesthesia without neuromuscular blockade.
Anesthesia* ; Anesthesia, Intravenous ; Arterial Pressure ; Heart Rate ; Hemodynamics ; Humans ; Intubation ; Larynx ; Lidocaine* ; Nasal Bone ; Neuromuscular Blockade* ; Piperidines ; Propofol ; Trachea

BACKGROUND: We investigated the correction methods following wrong-settings of emulsion concentrations of propofol as a countermeasure against erroneous target-controlled infusions (TCI). METHODS: TCIs were started with targeting 4.0 microg/ml of effect-site concentration (C(eff)) of propofol, and the emulsion concentrations were selected for 2.0% instead of 1.0% (FALSE(1-2), n = 24), or 1.0% instead of 2.0% (FALSE(2-1), n = 24). These wrong TCIs were corrected at 3 min after infusion start. During FALSE(1-2), the deficit was filled up while injecting after equilibrium (n = 12), or while overriding (n = 12). During FALSE(2-1), the overdose was evacuated while targeting C(eff) (n = 12) or targeting plasma concentration (C(p)) (n = 12). The gravimetrical measurements of TCI reproduced the C(p) and C(eff) using simulations. The reproduced C(eff) at 3 min (C(eff-3min)) and the time to be normalized within +/- 5% of target C(eff) (T(+/-5%)), were compared between the correction methods. RESULTS: During the wrong TCI, C(eff-3min) was 1.98 +/- 0.01 microg/ml in FALSE(1-2), and 7.99 +/- 0.05 microg/ml in FALSE(2-1). In FALSE(1-2), T(+/-5%) was significantly shorter when corrected while overriding (3.9 +/- 0.25 min), than corrected after equilibrium (6.9 +/- 0.05 min) (P < 0.001). In FALSE(2-1), T(+/-5%) was significantly shorter during targeting C(p) (3.6 +/- 0.04 min) than targeting C(eff) (6.7 +/- 0.15 min) (P < 0.001). CONCLUSIONS: The correction methods, based on the pharmacokinetic and pharmacodynamic characteristics, could effectively and rapidly normalize the wrong TCI following erroneously selections of the emulsion concentration of propofol.
Drug Delivery Systems ; Infusion Pumps ; Infusions, Intravenous ; Plasma ; Propofol*

BACKGROUND: The methods of arrangement of combined intravenous parallel infusions using anti-reflux valve (ARV), with and without anti-syphon valve (ASV) that could decrease occlusion alarm delay were investigated. METHODS: Occlusion challenge tests were mainly performed as bench experiments of four kinds of multiple parallel infusions (10 ml/h and 50 ml/h infusions), which were connected at the proximal or distal portion of ARV, with or without ASV. Alarm threshold was set to 1000 mmHg. Occlusion alarm delays and the compliances of the infusion systems were compared among groups. RESULTS: Without ASV, compared to 10 ml/h infusion alone distal to anti-reflux valve, 50 ml/h infusion distal to anti-reflux valve reduced the mean alarm delay from 416 +/- 7 s to 81 +/- 3 s (P < 0.001). Compared to 50 ml/h infusion alone, combined 10 ml/h and 50 ml/h infusion distal to ARV prolonged the alarm delay from 81 +/- 3 s to 133 +/- 6 s (P < 0.001). However, combined infusions distal to ARV with ASV significantly reduced the alarm delay from 133 +/- 6 s to 74 +/- 5 s (P < 0.001), and also reduced the compliance of the infusion system from 2.31 +/- 0.12 to 1.20 +/- 0.08 microl/mmHg (P < 0.001). CONCLUSIONS: The infusion setup of faster infusion rate, lower compliant system using ASV could effectively decrease occlusion alarm delay during multiple intravenous parallel infusions using ARV.
Anesthetics ; Compliance ; Equipment Safety ; Infusions, Intravenous

Brain death results in adverse pathophysiologic effects in many brain-dead donors with cardiovascular instability. We experienced a brain-dead donor with continuous renal replacement therapy (CRRT) who was in a severe metabolic, electrolyte derangement and poor pulmonary function. The thirty-nine-year-old male patient with subarachnoid hemorrhage and intraventricular hemorrhage was admitted into the intensive care unit (ICU). After sudden cardiac arrest, he went into a coma state and was referred to as a potential organ donor. When he was transferred, his vital sign was unstable even under the high dose of inotropics and vasopressors. Even with aggressive treatment, the level of blood sugar was 454 mg/dl, serum K+ 7.1 mEq/L, lactate 5.33 mmol/L and PaO2/FiO2 60.3. We decided to start CRRT with the mode of continuous venovenous hemodiafiltration (CVVHDF). After 12 hours of CRRT, vital sign was maintained well without vasopressors, and blood sugar, serum potassium and lactate levels returned to 195 of PaO2/FiO2. Therefore, he was able to donate his two kidneys and his liver.
Blood Glucose ; Brain ; Brain Death ; Coma ; Death, Sudden, Cardiac ; Hemodiafiltration ; Hemorrhage ; Humans ; Intensive Care Units ; Kidney ; Lactic Acid ; Liver ; Male ; Potassium ; Renal Replacement Therapy ; Subarachnoid Hemorrhage ; Tissue Donors ; Vital Signs

Uterine artery embolization for the treatment of uterine leiomyomas is gaining acceptance as an effective alternative to surgical treatment in preserving uterus and reducing symptoms. Vaginal expulsion of leiomyomas after UAE is uncommon, and has been regarded as a side effect of the procedure, as well as a natural phenomenon of treatment response. A-28-year-old unmarried woman who has been suffered from menorrhagia underwent UAE. MRI revealed the remnant leiomyomas were reduced in size and volume and also symptoms of leiomyomas were much improved. After 6 month, We've made sure about non-visualization of leiomyoma on follow-up pelvic dynamic MRI. We report this rare case of vaginal expusion of intramural leoimyoma with a brief literature.
Female ; Follow-Up Studies ; Humans ; Leiomyoma* ; Magnetic Resonance Imaging ; Menorrhagia ; Single Person ; Uterine Artery Embolization* ; Uterine Artery* ; Uterus

OBJECTIVE: The purpose of this study is to evaluate the effectiveness and safety of uterine artery embolization for the treatment of symptomatic leiomyomas in the patients who want to preserve uterus, want fertility or feel fear for operation. METHODS: From January 2003 to June 2005, among the patients with symptomatic uterine leiomyoma, fifteen women who wanted to preserve uterus or wanted fertility or had fear for operation were included in this retrospective study. Bilateral Uterine artery embolization (UAE) was performed. At the preprocedure and at 2, 6, and 12 weeks of postprocedure, transvaginal ultrasonography was performed for all patients. Clinical symptoms and follow-up information for each patient were evaluated. RESULTS: 15 leimyomas were treated with UAE. The initial mean volume of leiomyomas was 55.4 (46.3-67.4) cm3. The mean volume decrease was 58.6+/-9.7%, 77.5+/-12.3%, 86.8+/-23.5% at 2, 6, 12 weeks. The outcome of clinical symptoms were as followed; 'much improved' 20% (3/15), 'somewhat improved' 60% (6/15), 'no improvement' 20% (3/15), 'somewhat worsen's 0% (0/15), and 'much worsen' was 0% (0/15). There was no case of hysterectomy or myomectomy after UAE. And also no case of increasement of volume nor worsening of clinical symptoms were found. Lower abdominal pain was the most common symptoms after UAE, but complications were not detected. CONCLUSION: In this study, UAE to treat patients with uterine leiomyoma is proved to be effective not only in volume reduction, but also in symptom improvement. And it is a relatively less-invasive procedure which decreases the risk of side effects of operation. Above all things, it preserves fecundity in young women. Therefore, UAE is very effective and safe procedure in the treatment of symptomatic uterine leiomyoma.
Abdominal Pain ; Female ; Fertility ; Follow-Up Studies ; Humans ; Hysterectomy ; Leiomyoma* ; Retrospective Studies ; Ultrasonography ; Uterine Artery Embolization ; Uterus

Contralateral acute subdural hematomas that occur during removal of brain tumors under general anesthesia are extremely rare, and there are no reports of this developing during awake craniotomy for brain tumors. We report a case of a 12-year-old boy who complained of sudden and severe headache and nausea around the completion of removal of a glial tumor of the frontal lobe under awake anesthesia. Postoperative computerized tomography scan revealed the presence of contralateral acute minimal subdural hematoma. We suggest that during craniotomy with awake anesthesia for brain tumors, contralateral acute subdural hematoma may occur, even in the absence of brain bulging or changes in vital signs. Sudden intra-operative headache and nausea should be investigated by immediate postoperative computerized tomography scans to ascertain diagnosis.
Anesthesia ; Anesthesia, General ; Brain ; Brain Neoplasms ; Child ; Craniotomy ; Frontal Lobe ; Headache ; Hematoma, Subdural ; Hematoma, Subdural, Acute ; Humans ; Nausea ; Vital Signs

Contralateral acute subdural hematomas that occur during removal of brain tumors under general anesthesia are extremely rare, and there are no reports of this developing during awake craniotomy for brain tumors. We report a case of a 12-year-old boy who complained of sudden and severe headache and nausea around the completion of removal of a glial tumor of the frontal lobe under awake anesthesia. Postoperative computerized tomography scan revealed the presence of contralateral acute minimal subdural hematoma. We suggest that during craniotomy with awake anesthesia for brain tumors, contralateral acute subdural hematoma may occur, even in the absence of brain bulging or changes in vital signs. Sudden intra-operative headache and nausea should be investigated by immediate postoperative computerized tomography scans to ascertain diagnosis.
Anesthesia ; Anesthesia, General ; Brain ; Brain Neoplasms ; Child ; Craniotomy ; Frontal Lobe ; Headache ; Hematoma, Subdural ; Hematoma, Subdural, Acute ; Humans ; Nausea ; Vital Signs

OBJECTIVE: The aim of the present study was to determine the treatment-seeking behaviors of Korean university women with premenstrual symptoms. METHODS: Of 1419 subjects who randomly selected in 4 women's university in Seoul, 771 who experienced at least one premenstrual symptom during past three months were included in this study. Treatment-seeking behaviors for relieving premenstrual symptoms were grouped into five categories [doctor's prescription, self-prescription with over-the-counter drug, use of oriental medicine, use of other conservative-alternative medicine (CAM), nonpharmacological treatment]. We investigated what the preferential treatment was and how many subjects were experienced the medical evaluation by doctor. The attitude and knowledge to premenstrual symptoms were evaluated. RESULTS: Subjects who experienced at least one kind of treatment for relieving premenstrual symptoms were 50.2% of women with premenstrual syndrome (PMS) and 63.6% of premenstrual dysphoric disorder (PMDD). Nonpharmacological treatment such as exercise or rest was the most preferential treatment. Only 2.3% of PMDD was examined and prescribed by doctor. Subjects with doctor's or oriental doctor's prescription had more severe premenstrual symptoms and showed functional impairment than others. Only 7% of university women reported to know well about premenstrual symptoms and their treatment. CONCLUSIONS: This study shows that Korean university women prefer self-diagnosis and self-prescription to the evaluation and prescription by doctor for relieving premenstrual symptoms even though they suffer from PMDD. It indicates that the adequate evaluation and treatment for premenstrual symptoms are not carried out because of the lack of knowledge about them. Therefore, the correct information about symptoms and management of PMS and PMDD should be serviced to general population. Also, systematic evaluation of efficacy and safety of oriental medicine and other CAM for premenstrual symptom is needed.
Female ; Humans ; Medicine, East Asian Traditional ; Premenstrual Syndrome ; Prescriptions ; Seoul

Intraoperative transesophageal echocardiography (TEE) has become an important monitoring device for patients undergoing cardiac or noncardiac surgery. Complications associated with TEE are unusual, but the potential for TEE probe compression of the posterior vascular structures has been reported in pediatric patients. We present here a case of occlusion of the right subclavian artery in an adult patient with a vascular ring after insertion of a TEE probe.
Adult ; Echocardiography, Transesophageal ; Humans ; Subclavian Artery