HOMEPAGEMEDNEMOABSTRACTSANESTESIARIANIMAZIONET.DOLORE
TERAPIA IPERBARICAFARMACOLOGIAEMERGENZECERCALINKSCONTATTI

ANESTESIA

RIANIMAZIONE

TERAPIA DEL DOLORE

AVVELENAMENTI

 
ABSTRACTS DI ANESTESIA - APRILE 2002

Ultimo Aggiornamento: 31 Dicembre 2002

46 citations found

Anaesthesia 2002 Mar;57(3):312-3

e-Surveys.

Ball DR, Jefferson P

Publication Types:

  • Letter

PMID: 11892671, UI: 21889407


Anaesthesia 2002 Mar;57(3):308-9

A new angle on a Tuohy needle.

Wright DA, Rucklidge MW

Publication Types:

  • Letter

PMID: 11892663, UI: 21889398


Anaesthesia 2002 Mar;57(3):304-5

Aspirin and central neural blockade.

Harding SA, Severn AM, Calvert J

Publication Types:

  • Letter

PMID: 11892656, UI: 21889378


Anaesthesia 2002 Mar;57(3):302-4

Hypotension prophylaxis for Ceasarean section.

Loughrey YR, Datta S, Tsen LC

Publication Types:

  • Letter

PMID: 11892654, UI: 21889373


Anaesthesia 2002 Mar;57(3):299-300

Report of vaporiser malfunction.

MacLeod DM, McEvoy L, Walker D

Publication Types:

  • Letter

PMID: 11892650, UI: 21889369


Anaesthesia 2002 Mar;57(3):289-90

Call for an alternative coupling system for regional equipment.

Cyna A, Simmons S

Publication Types:

  • Letter

PMID: 11892644, UI: 21889359


Anaesthesia 2002 Mar;57(3):288-9

The Pro-Seal laryngeal mask airway.

Cook TM, Nolan JP

Publication Types:

  • Letter

PMID: 11892642, UI: 21889354


Anaesthesia 2002 Mar;57(3):288

Overfilling of vaporisers.

Daniels D

Publication Types:

  • Letter

PMID: 11892641, UI: 21889353


Anaesthesia 2002 Mar;57(3):281-3

The effect of swabs soaked in bupivacaine and epinephrine for pain relief following simple dental extractions in children.

Andrzejowski J, Lamb L

Department of Anaesthesia, Charles Clifford Dental Hospital, Sheffield, UK.

We studied 133, ASA I or II children, aged 5-12 years undergoing general anaesthesia for simple dental extractions. Induction and maintenance of anaesthesia were achieved using sevoflurane in nitrous oxide and oxygen. At the end of surgery, patients had swabs soaked in a trial solution placed over the exposed teeth sockets. The bupivacaine group had swabs soaked in bupivacaine 0.25% with epinephrine 1:200 000, the saline group had swabs soaked in saline. Pain scores were recorded on a 4-point scale as follows: 0 = I don't hurt at all; 1 = I hurt a bit; 2 = I hurt a lot; 3 = I hurt the most. Nurse pain assessments and the patient's own scores were recorded at 15 and 30 min following recovery from anaesthesia. The median pain scores (2 at 15 min and 1 at 30 min postoperatively) were the same in both groups.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11892639, UI: 21889348


Anaesthesia 2002 Mar;57(3):277-80

An evaluation of ultrasound imaging for identification of lumbar intervertebral level.

Furness G, Reilly MP, Kuchi S

Altnagelvin Area Hospital, Londonderry, UK.

The accuracy of ultrasound imaging to identify lumbar intervertebral level was assessed in 50 patients undergoing X-ray of the lumbar spine. Using an ultraviolet marker, an anaesthetist attempted to mark the L2/3, L3/4 and L4/5 intervertebral spaces. A radiologist unaware of these marks attempted to mark the same spaces with the aid of ultrasound imaging. X-ray-visible pellets were taped to the back at the various marks prior to lateral lumbar X-ray. Ultrasound imaging identified the correct level in up to 71% of cases, but palpation was successful in only 30% (p < 0.001). Up to 27% of marks using the palpation method were more than one spinal level above or below the assumed level using palpation, but none were more than one level high or low using ultrasound guidance.

Publication Types:

  • Evaluation studies

PMID: 11892638, UI: 21889346


Anaesthesia 2002 Mar;57(3):270-5

The management of pain following day-case surgery.

McHugh GA, Thoms GM

University Department of Anaesthesia, Manchester Royal Infirmary, UK.

The object of this study was to assess patients' experience of pain management following day surgery. One hundred and two patients agreed to take part in a telephone survey, 2 and 4 days following day surgery. The majority of patients (73%) were broadly satisfied with the quality of pain management they received, however, there was room for improvement. Despite modern anaesthesia and surgery, 17% of patients surveyed reported having severe pain immediately following day-case surgery. The majority (82%) of patients left the day-case ward in pain and an even higher proportion (88%) had pain at some time between 2 and 4 days postoperatively. Severe levels of pain following discharge from hospital were a concern for 21% of patients. It was reported that day-case staff did not always ask patients whether they were in pain. Communication with patients is vital in the delivery of optimal care. More support and more information are needed to manage patients' pain effectively, whilst in the day-case wards and also following discharge, at home.

PMID: 11892636, UI: 21889341


Anaesthesia 2002 Mar;57(3):266-70

Patient-controlled epidural fentanyl following spinal fentanyl at Caesarean section.

Cooper DW, Garcia E, Mowbray P, Millar MA

Department of Anaesthesia, Cheriton House, James Cook University Hospital, Middlesbrough, Cleveland, UK. Drdavidcooper@aol.com

Spinal fentanyl can improve analgesia during Caesarean section. However, there is evidence that, following its relatively short-lived analgesic effect, there is a more prolonged spinal opioid tolerance effect. The effectiveness of postoperative epidural fentanyl analgesia may therefore be reduced following the use of spinal fentanyl at operation. This randomised, double-blind study was designed to assess whether patient-controlled epidural fentanyl could produce effective analgesia following 25 microg of spinal fentanyl at operation. Patients undergoing elective Caesarean section received spinal bupivacaine combined with either fentanyl 25 microg (fentanyl group; n = 18) or normal saline (saline group; n = 18). Patient-controlled epidural fentanyl was used for postoperative analgesia. The fentanyl group used a mean of 23.4 (SD 14.5) microg x h(-1) of fentanyl, compared with 27.0 (10.8) microg x h(-1) for the saline group (p =0.41). Using a 0-100 mm visual analogue score for pain, the maximum pain score recorded at rest for the fentanyl group was median 24 [IQR 15-35] mm, compared with 15 [13-45] mm for the saline group (p = 0.41). The maximum pain score recorded on coughing for the fentanyl group was 29 [24-46] mm, compared with 27 [19-47] mm for the saline group (p = 0.44). Nine of the fentanyl group rated postoperative analgesia as excellent and nine as good, compared with 10 of the saline group who rated it as excellent and eight as good (p = 0.74). Epidural fentanyl can produce effective analgesia following the use of 25 microg spinal fentanyl at Caesarean section.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11892635, UI: 21889337


Anaesthesia 2002 Mar;57(3):294-5

Airway management of a child with temporomandibular joint ankylosis following otitis media.

Kawasaki T, Sata T, Kawasaki C, Ogata M, Shigematsu A

Publication Types:

  • Letter

PMID: 11879227, UI: 21868425


Anaesthesia 2002 Mar;57(3):293

A new cause of airway obstruction.

Boumphrey S

Publication Types:

  • Letter

PMID: 11879225, UI: 21868423


Anaesthesia 2002 Mar;57(3):233-41

The effects of subanaesthetic concentrations of xenon in volunteers.

Bedi A, McCarroll C, Murray JM, Stevenson MA, Fee JP

The Department of Anaesthetics and Intensive Care Medicine, The Queen's University of Belfast, Northern Ireland. a.bedi@ntlworld.com

This study reports the subjective, psychomotor and physiological properties of subanaesthetic concentrations of xenon. Ten healthy male volunteers received either xenon or nitrous oxide in a randomised crossover study design. The subjects breathed either xenon (Xe) or nitrous oxide (N2O) from a closed circuit breathing system, according to a randomised, double-blind protocol. The concentration of xenon required to produce sedation, ranged between 27 and 45% (median 35%). All subjects completed the xenon protocol. Subjects were tested using the Critical Flicker Fusion test and derived electroencephalogram parameters, however, neither test was found to reliably predict sedation. The respiratory rate decreased markedly during sedation with xenon. The subjects did not experience any airway irritability (coughing, breath-holding or laryngospasm) during administration of either gas. One subject required anti-emetic treatment in the N2O group compared to none in the Xe group. Eight subjects reported that they found sedation with xenon pleasant and preferable to nitrous oxide. Xenon sedation was well tolerated and was not associated with any adverse physiological effects, however, it was reported to be subjectively dissimilar to nitrous oxide.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11879212, UI: 21868410


Anesth Analg 2002 Jan;94(1 Suppl):S44-6

Pulse oximetry in the management of children in the PICU.

Miyasaka K

Department of Anesthesia and ICU, National Children's Hospital, Tokyo, Japan. kmiyasaka@nch.go.jp

The noninvasive and continuous nature of pulse oximetry is a considerable asset inpatient monitoring in the PICU. Its use in the PICU is constantly challenged by the combined presence of vigorous body motion and poor peripheral circulation, conditions which demand special consideration in developing a better pulse oximeter. This is a point of fierce competition among manufacturers.

PMID: 11900038, UI: 21896704


Anesthesiology 2002 Feb;96(2):517

The safety of rapid sequence induction.

Adnet F, Borron SW, Lapostolle F

Publication Types:

  • Letter

PMID: 11818796, UI: 21676129


Anesthesiology 2002 Feb;96(2):516; discussion 517

The intubating dose of succinylcholine.

Kopman AF

Publication Types:

  • Letter

PMID: 11818795, UI: 21676128


Anesthesiology 2002 Feb;96(2):515-6

Extrapolating beyond the data.

Fisher DM

Publication Types:

  • Letter

PMID: 11818794, UI: 21676127


Anesthesiology 2002 Feb;96(2):467-84

Perioperative shivering: physiology and pharmacology.

De Witte J, Sessler DI

Department of Anesthesia and Intensive Care, OLV Hospital, Aalst, Belgium. jan.de.witte@olvz-aalst.be

Publication Types:

  • Review
  • Review, academic

PMID: 11818783, UI: 21676116


Anesthesiology 2002 Feb;96(2):346-51

Sympathetic neural activation evoked by mu-receptor blockade in patients addicted to opioids is abolished by intravenous clonidine.

Kienbaum P, Heuter T, Michel MC, Scherbaum N, Gastpar M, Peters J

Abteilung fur Anasthesiologie und Intensivmedizin, Universitatsklinikum, Essen, Germany. peter.kienbaum@uni-essen.de

BACKGROUND: Mu-opioid receptor blockade by naloxone administered for acute detoxification in patients addicted to opioids markedly increases catecholamine plasma concentrations, muscle sympathetic activity (MSA), and is associated with cardiovascular stimulation despite general anesthesia. The current authors tested the hypothesis that the alpha2-adrenoceptor agonist clonidine (1) attenuates increased MSA during mu-opioid receptor blockade for detoxification, and (2) prevents cardiovascular activation when given before detoxification. METHODS: Fourteen mono-opioid addicted patients received naloxone during propofol anesthesia. Clonidine (10 microg x kg(-1) administered over 5 min + 5 microg x kg(-1) x h(-1) intravenous) was infused either before (n = 6) or after (n = 6) naloxone administration. Two patients without immediate clonidine administration occurring after naloxone administration served as time controls. Muscle sympathetic activity (n = 8) in the peroneal nerve, catecholamine plasma concentrations (n = 14), arterial blood pressure, and heart rate were assessed in awake patients, during propofol anesthesia before and after mu-opioid receptor blockade, and after clonidine administration. RESULTS: Mu-receptor blockade markedly increased MSA from a low activity (burst frequency: from 2 burst/min +/- 1 to 24 +/- 8, means +/- SD). Similarly, norepinephrine (41 pg/ml +/- 37 to 321 +/- 134) and epinephrine plasma concentration (13 pg/ml +/- 6 to 627 +/- 146) significantly increased, and were associated with, increased arterial blood pressure and heart rate. Clonidine immediately abolished both increased MSA (P < 0.001) and catecholamine plasma concentrations (P < 0.001). When clonidine was given before mu-opioid receptor blockade, catecholamine plasma concentrations and hemodynamic variables did not change. CONCLUSIONS: Administration of the alpha2-adrenoceptor agonist clonidine decreases both increased MSA and catecholamine plasma concentrations observed after mu-opioid receptor blockade for detoxification. Furthermore, clonidine pretreatment prevents the increase in catecholamine plasma concentration that otherwise occurs during mu-opioid receptor blockade.

Publication Types:

  • Clinical trial

PMID: 11818767, UI: 21676100


Anesthesiology 2002 Feb;96(2):300-5

Electroacupuncture prophylaxis of postoperative nausea and vomiting following pediatric tonsillectomy with or without adenoidectomy.

Rusy LM, Hoffman GM, Weisman SJ

Department of Pediatric Anesthesiology, Medical College of Wisconsin-Children's Hospital of Wisconsin, Milwaukee, Wisconsin 53226, USA. lrusy@mcw.edu

BACKGROUND: Electrical stimulation of acupuncture point P6 reduces the incidence of postoperative nausea or vomiting (PONV) in adult patients. However, acupressure, laser stimulation of P6, and acupuncture during anesthesia have not been effective for reducing PONV in the pediatric population. The authors studied the effect of electrical P6 acupuncture in awake pediatric patients who had undergone surgery associated with a high incidence of PONV. METHODS: Patients aged 4-18 yr undergoing tonsillectomy with or without adenoidectomy were randomly assigned to acupuncture, sham acupuncture, or control groups. Acupuncture needles at P6 and a neutral point were placed while patients were anesthetized, and low-frequency electrical stimulation was applied to these points for 20 min in the recovery room while the patients were awake (P6 Acu group). This treatment was compared with sham needles along the arm at acupuncture points not associated with antiemesis (sham group) and a no-needle control group. The arms were wrapped to prevent identification of treatment group, and anesthetic, analgesic, and surgical technique were standardized. Assessed outcomes were occurrence of nausea, occurrence and number of episodes of vomiting, time to vomiting, and use of antiemetic rescue medication. RESULTS: One hundred twenty patients were enrolled in the study, 40 per group. There were no differences in age, weight, sex, or opioid administration between groups. The PONV incidence was significantly lower with P6 acupuncture (25 of 40 or 63%; odds ratio, 0.135; number needed to treat, 3.3; P < 0.001) compared with controls (37 of 40 or 93%). Sham puncture had no effect on PONV (35 of 40 or 88%; P = not significant). Occurrence of nausea was significantly less in P6 Acu (24 of 40 or 60%; odds ratio, 0.121; P < 0.01), but not in the sham group (34 of 40 or 85%) compared with the control group (37 of 40 or 93%). Vomiting occurred in 25 of 40 or 63% in P6 Acu; 35 of 40 or 88% in the sham group, and 31 in 40 or 78% in the control group (P = not significant). Patients receiving sham puncture vomited significantly earlier (P < 0.02) and needed more rescue treatment (33 of 40 or 83%; odds ratio, 3.48; P < 0.02) compared with P6 Acu (23 of 40 or 58%) and the control group (24 of 40 or 60%). CONCLUSIONS: Perioperative P6 electroacupuncture in awake patients significantly reduced the occurrence of nausea compared with the sham and control groups, but it did not significantly reduce the incidence or number of episodes of emesis or the use of rescue antiemetics. Sham acupuncture may exacerbate the severity but not the incidence of emesis. The efficacy of P6 acupuncture for PONV prevention is similar to commonly used pharmacotherapies. Its appropriate role in prevention and treatment of PONV requires further study.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11818760, UI: 21676093


Anesthesiology 2002 Feb;96(2):276-82

Absence of beneficial effect of acute normovolemic hemodilution combined with aprotinin on allogeneic blood transfusion requirements in cardiac surgery.

Hohn L, Schweizer A, Licker M, Morel DR

Department of Anesthesiology, Pharmacology and Surgical Intensive Care, University Hospital of Geneva, Geneva, Switzerland.

BACKGROUND: The efficacy of acute normovolemic hemodilution (ANH) in decreasing allogeneic blood requirements remains controversial during cardiac surgery. METHODS: In a prospective, randomized study, 80 adult cardiac surgical patients with normal cardiac function and no high risk of ischemic complications were subjected either to ANH, from a mean hematocrit of 43% to 28%, or to a control group. Aprotinin and intraoperative blood cell salvage were used in both groups. Blood (autologous or allogeneic) was transfused when the hematocrit was less than 17% during cardiopulmonary bypass, less than 25% after cardiopulmonary bypass, or whenever clinically indicated. RESULTS: The amount of whole blood collected during ANH ranged from 10 to 40% of the patients' estimated blood volume. Intraoperative and postoperative blood losses were not different between control and ANH patients (total blood loss, control: 1,411 +/- 570 ml, n = 41; ANH: 1,326 +/- 509 ml, n = 36). Allogeneic blood was given in 29% of control patients (median, 2; range, 1-3 units of packed erythrocytes) and in 33% of ANH patients (median, 2; range, 1-5 units of packed erythrocytes; P = 0.219). Preoperative and postoperative platelet count, prothrombin time, and partial thromboplastin time were similar between groups. Perioperative morbidity and mortality were not different in both groups, and similar hematocrit values were observed at hospital discharge (33.7 +/- 3.9% in the control group and 32.6 +/- 3.7% in the ANH group; nonsignificant) CONCLUSIONS: Hemodilution is not an effective means to lower the risk of allogeneic blood transfusion in elective cardiac surgical patients with normal cardiac function and in the absence of high risk for coronary ischemia, provided standard intraoperative cell saving and high-dose aprotinin are used.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11818756, UI: 21676089


Anesthesiology 2002 Feb;96(2):271-5

Involvement of renin-angiotensin system in pressure-flow relationship: role of angiotensin-converting enzyme gene polymorphism.

Lasocki S, Iglarz M, Seince PF, Vuillaumier-Barrot S, Vicaut E, Henrion D, Levy B, Desmonts JM, Philip I, Benessiano J

Departement d' Anesthesie-Reanimation, Hopital Bichat, Paris, France.

BACKGROUND: The renin-angiotensin system is involved in blood pressure regulation. The insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme (ACE) gene is known to be associated with variation of plasma and cellular ACE concentrations. Furthermore, changes in arterial function have been suggested to be associated to the DD genotype. The aim of the study was to investigate the arterial vascular response to a physiologic stimulus (i.e., flow) according to the I/D ACE gene polymorphism. METHODS: Sixty patients scheduled for coronary artery bypass grafting (n = 24) or valve surgery (n = 36) under normothermic cardiopulmonary bypass were genotyped in a blind manner by polymerase chain reaction. Mean arterial pressure was measured at pump flows ranging from 1 to 3 l x min(-1) x m (-2) by 0.25 l x min(-1) x m(-2) step each 15 s, to obtain a pressure-flow relation. Independent factors associated with the variation of the slope of the pressure-flow relation curve were assessed by multivariate analysis. RESULTS: We found a D allelic frequency of 0.54. Patients were separated in two groups (DD, n = 16; ID/II, n = 44). There were no significant difference with regard to preoperative and intraoperative data between the two groups. DD patients had their pressure-flow relation curves shifted upward (with higher pressures as flow increased), indicating a lesser decrease in vascular resistance. Furthermore, DD genotype was the only independent predictor of the slope of the curves (21.5 +/- 4.2 vs. 18.1 +/- 5 mmHg/[l x min(-1) x m(-2)] for DD and ID/II, respectively; P = 0.02; values are mean +/-SD). CONCLUSION: These results show that vasomotor properties are influenced by the I/D polymorphism of the ACE gene.

PMID: 11818755, UI: 21676088


Anesthesiology 2002 Feb;96(2):264-70

Perioperative myocardial ischemia and infarction: identification by continuous 12-lead electrocardiogram with online ST-segment monitoring.

Landesberg G, Mosseri M, Wolf Y, Vesselov Y, Weissman C

Department of Anesthesiology and Critical Care Medicine, Hadassah University Hospital, Ein-Kerem, Jerusalem, Israel. gio@cc.huji.ac.il

BACKGROUND: Perioperative myocardial ischemia is conventionally monitored using five electrocardiographic leads, with only one precordial lead placed at V5. This is based on studies from more than a decade ago. The authors reassessed this convention by analyzing data obtained from continuous on-line 12-lead electrocardiographic monitoring. METHODS: One hundred eighty-five consecutive patients undergoing vascular surgery were monitored by continuous 12-lead ST-trend analysis during and for 48-72 h after surgery. Cardiac troponin I was measured in the first 3 postoperative days, and cardiac outcome was prospectively recorded. Ischemia was defined as ST deviation, relative to the reference preanesthesia electrocardiogram, of 0.2 mV or more in one lead or 0.1 mV or more in two contiguous leads, lasting more than 10 min. RESULTS: During 11,132 patient-hours of monitoring, 38 patients (20.5%) had 66 transient ischemic events, with all but one denoted by ST-segment depression. Twelve patients (6.5%) sustained postoperative infarction (cardiac troponin I > 3.1 ng/ml). Among the 38 patients with ischemia, lead V3 most frequently (86.8%) demonstrated ischemia, followed by V4 (78.9%) and V5 (65.8%). Among the 12 patients with infarction, V4 was most sensitive to ischemia (83.3%), followed by V3 and V5 (75% each). Combining two precordial leads increased the sensitivity for detecting ischemia (97.4% for V3 + V5 and 92.1% for either V4 + V5 or V3 + V4) and infarction (100% for V4 + V5 or V3 + V5 and 83.3% for V3 + V4). On average, baseline preanesthesia ST was above isoelectric in V1 through V3 and below isoelectric in V5 through V6. Lead V4 was closest to the isoelectric level on the baseline electrocardiogram, rendering it most suitable for ischemia monitoring. CONCLUSIONS: As a single lead, V4 is more sensitive and appropriate than V5 for detecting prolonged postoperative ischemia and infarction. Two precordial leads or more are necessary so as to approach a sensitivity of greater than 95% for detection of perioperative ischemia and infarction.

Publication Types:

  • Clinical trial
  • Evaluation studies

PMID: 11818754, UI: 21676087


Anesthesiology 2002 Feb;96(2):259-61

Multilead precordial ST-segment monitoring: "the next generation?".

London MJ

Publication Types:

  • Comment
  • Editorial

PMID: 11818752, UI: 21676085



Links:

BMJ 2002 Apr 6;324(7341):806A

Indian group seeks ban on use of electroconvulsive therapy without anaesthesia.

Mudur G

New Delhi.

[Medline record in process]

PMID: 11934766, UI: 21932118


Br J Anaesth 2002 Jan;88(1):94-100

Concurrent ketamine and alfentanil administration: pharmacokinetic considerations.

Edwards SR, Minto CF, Mather LE

Centre for Anaesthesia and Pain Management Research, University of Sydney at Royal North Shore Hospital, St Leonards, NSW, Australia.

BACKGROUND: A ketamine-alfentanil combination has been suggested for total i.v. anaesthesia. We determined the pharmacokinetics of ketamine and alfentanil, alone and together, in three groups of adult male rats, to assess any pharmacokinetic interaction. METHODS: Group 1 animals were infused with i.v. ketamine for 5 min; in group 2, constant low plasma concentrations of alfentanil were maintained by computer-controlled infusion; in group 3, the treatments were combined. Serial plasma and terminal tissue concentrations were measured by high performance liquid chromatography or gas chromatography-mass spectrometry. RESULTS: In the presence of alfentanil, the mean plasma ketamine concentration-time area under the curve (AUC) value was significantly lower (by 13%, P<0.05), while clearance (CIT) and volume of distribution (Vss) were significantly higher (by 16 and 28%, respectively, both P<0.05). Tissue:plasma distribution coefficients for ketamine in the presence of alfentanil were significantly higher in forebrain (by 128%, P<0.005), hindbrain (by 207%, P<0.01), gut (by 254%, P<0.005), and fat (by 344%, P<0.0001). Mean AUC values for alfentanil did not differ significantly in the presence of ketamine, but alfentanil tissue concentrations were significantly lower in forebrain (by 77%, P<0.0001), hindbrain (by 28%, P<0.01), heart (by 33%, P<0.01), lung (30%, P<0.05), and gut (by 21%, P<0.05). Corresponding tissue:plasma distribution coefficients were significantly lower for forebrain (by 69%, P<0.0001) alone. CONCLUSIONS: The finding that the distribution of ketamine into the brain was increased by low plasma concentrations of alfentanil could have important clinical applications for pain management.

PMID: 11881891, UI: 21873324


Br J Anaesth 2002 Jan;88(1):65-71

Randomized controlled trial to investigate influence of the fluid challenge on duration of hospital stay and perioperative morbidity in patients with hip fractures.

Venn R, Steele A, Richardson P, Poloniecki J, Grounds M, Newman P

Department of Anaesthesia and Intensive Care, Worthing Hospital, W. Sussex UK.

BACKGROUND: A prospective, randomized controlled trial comparing conventional intraoperative fluid management with two differing methods of invasive haemodynamic monitoring to optimize intraoperative fluid therapy, in patients undergoing proximal femoral fracture repair under general anaesthesia. METHODS: Ninety patients randomized to three groups; conventional intraoperative fluid management (Gp CON, n=29), and two groups receiving additional repeated colloid fluid challenges guided by central venous pressure (Gp CVP, n=31) or oesophageal Doppler ultrasonography (Gp DOP, n=30). Primary outcome measures were time to medical fitness to discharge, hospital stay and postoperative morbidity. RESULTS: The fluid challenge resulted in significantly greater perioperative changes in central venous pressure between Gp CVP and Gp CON (mean 5 (95% confidence interval 3-7) mm Hg) (P<0.0001). Important perioperative changes were also shown in Gp DOP with increases of 49.4 ms (19.7-79.1 ms) in the corrected flow time, 13.5 ml (7.4-19.6 ml) in stroke volume, and 0.9 (0.49-1.39) litre min(-1) in cardiac output. As a result, fewer patients in Gp CVP and Gp DOP experienced severe intraoperative hypotension (Gp CON 28% (8/29), Gp CVP 9% (3/31), Gp DOP 7% (2/30), P=0.048 (chi-squared, 2 degrees of freedom (df). No differences were seen between the three groups when major morbidity and mortality were combined, P=0.24 (chi-squared, 2 df). Postoperative recovery for survivors, as defined by time to be deemed medically fit for discharge, was significantly faster, in comparison with Gp CON, in both the Gp CVP (10 vs 14 (95% confidence interval 8-12 vs 12-17) days, P=0.008 (t-test)), and Gp DOP (8 vs 14 (95% confidence interval 6-12 vs 12-17) days, P=0.023 (t-test). There were no significant differences between groups, for survivors, with respect to acute orthopaedic hospital and total hospital stay. CONCLUSIONS: Invasive intraoperative haemodynamic monitoring with fluid challenges during repair of femoral fracture under general anaesthetic shortens time to being medically fit for discharge.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11881887, UI: 21873320


Br J Anaesth 2002 Jan;88(1):4-5

Oxygen and elective caesarean section.

Backe SK, Lyons G

Publication Types:

  • Comment
  • Editorial

PMID: 11881882, UI: 21873310


Br J Anaesth 2002 Jan;88(1):129-32

Deep topical fornix nerve block versus peribulbar block in one-step adjustable-suture horizontal strabismus surgery.

Aziz ES, Rageh M

Department of Anaesthesia, Faculty of Medicine, Cairo University, Zamalek, Egypt.

BACKGROUND: We compared the efficacy of deep topical fornix nerve block anaesthesia (DTFNBA), which does not paralyse the extraocular muscles, with peribulbar block in patients undergoing one-step adjustable-suture horizontal strabismus surgery. Patients with a vertical, oblique squint were excluded from the study. METHODS: We studied 100 patients, allocated randomly to two groups. Group 1 (n=50) received peribulbar block with 5 ml of 1:1 mixture of 0.5% plain bupivacaine and 2% lignocaine supplemented with hyaluronidase 300 i.u. ml(-1). Group 2 (n=50) received DTFNBA with placement of a sponge soaked in 0.5% bupivacaine deep into the conjunctival fornices for 15 min. No sedation was given to either group. Analgesia was assessed by direct questioning of patients during the procedure. A three-point scoring system was used (no pain = 0, discomfort = 1, pain =2). If the pain score was 1, the patient was asked to look in the opposite direction to decrease the tension on the periosteal attachment of the muscle to relieve discomfort. If the pain score was 2 at any stage of the operation, general anaesthesia was given. RESULTS: In Group 2, significantly more patients (15) experienced discomfort than in Group 1 (no patients) (P<0.05), but general anaesthesia was not needed. CONCLUSIONS: DTFNBA is a useful technique for intraoperative adjustable-suture strabismus surgery. It does not alter muscle tone, thus allowing the surgeon to adjust the muscle sutures intraoperatively, and reducing the incidence of under- or over-correction of the squint in the immediate postoperative period.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11881868, UI: 21873328



Links:

Br J Pharmacol 2001 Dec;134(8):1724-30

Antianginal effects of hydroxyfasudil, a Rho-kinase inhibitor, in a canine model of effort angina.

Utsunomiya T, Satoh S, Ikegaki I, Toshima Y, Asano T, Shimokawa H

Institute of Life Science Research, Asahi Kasei Corporation, 632-1, Mifuku, Ohito-Cho, Tagata-Gun, 410-2321, Japan.

1. The effects of Rho-kinase inhibitor, fasudil, and of a more specific Rho-kinase inhibitor, hydroxyfasudil, on pacing-induced myocardial ischaemia were determined in anaesthetized open-chest dogs. 2. The dogs were subjected to left anterior descending coronary artery (LAD) stenosis producing a sufficient ischaemia as measured by ST-segment depression on electrocardiograms only when the hearts were paced 60 beats min(-1) above the baseline. After a recovery (nonpacing) period, drugs or saline were infused intravenously over 30 min. The animals were again subjected to 5 min of pacing 25 min after the initiation of the treatment. 3. Hydroxyfasudil (0.1 and 0.3 mg kg(-1)) and fasudil (0.3 mg kg(-1)) suppressed the ST-segment depression. Hydroxyfasudil and fasudil also increased the regional blood flow of the LAD perfused endomyocardium region in the canine model of effort angina. 4. To determine the flow profile for hydroxyfasudil in dogs, blood flow in three vascular beds was measured. Hydroxyfasudil (0.3 mg kg(-1) for 30 min) significantly increased coronary blood flow and vertebral blood flow, without significantly changing the femoral blood flow. 5. Hydroxyfasudil had no inotropic or chronotropic effect on the isolated hearts of guinea-pigs. Hydroxyfasudil (2 mg kg(-1) for 20 min) did not affect the PR or QTc interval in anaesthetized dogs. 6. Inhibition of Rho-kinase appears to protect myocardium subjected to pacing-induced ischaemia through the increase in the regional myocardial blood flow. Hydroxyfasudil may be categorized as a novel type of anti-anginal drug, without any inotropic or chronotropic effects.

PMID: 11739249, UI: 21600022



Links:

Br J Pharmacol 2001 Dec;134(8):1705-10

Activation of central melanocortin receptors by MT-II increases cavernosal pressure in rabbits by the neuronal release of NO.

Vemulapalli R, Kurowski S, Salisbury B, Parker E, Davis H

CNS/CV Biological Research, Schering-Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, New Jersey, NJ 07033, USA. subbarao.Vemulapalli@spcorp.com

1. Melanotan-II had been reported to cause penile erections in men with erectile dysfunction. In the present study, we investigated the mechanisms by which systemic administration of MT-II increases intracavernosal pressure in anaesthetized rabbits. 2. MT-II (10 microM) had no effect on electrical field stimulation-evoked relaxations of rabbit corpus cavernosal strips in vitro. 3. Intravenous injection of MT-II (66 and 133 microg kg(-1) elicited dose-related increases in cavernosal pressure. SHU 9119 (3 microg kg(-1), i.v.), a non-selective antagonist of MC(3) and MC(4) receptors did not significantly affect either cavernosal pressure or systemic blood pressure but abolished the MT-II-induced increases in cavernosal pressure. SHU 9119 also inhibited the depressor response produced by MT-II. 4. Intracavernosal injection 100 microl of the cocktail containing phentolamine mesylate (1 mg ml(-1)), papaverine (20 mg ml(-1)) and PGE1 (20 microg ml(-1)) increased the cavernosal pressure by about 4 fold. 5. The role of NO-cyclic GMP dependent pathway to MT-II-induced increases in cavernosal pressure was investigated by bilateral transection of the pudendal nerves and by inhibition of NO synthase with L-NAME (20 mg kg(-1), i.v. over 30 min). Ablation of the pudendal nerves or pretreatment with L-NAME abolished the MT-II-induced increases in intracavernosal pressure in anaesthetized rabbits. 6. The data suggest that activation of central melanocortin receptors by MT-II increases cavernosal pressure by the neuronal release of NO.

PMID: 11739247, UI: 21600020



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Can J Anaesth 2002 Apr;49(4):438-9

Problem with Ohmeda Excel 210 SE anesthetic machine.

Sharma ML

Liverpool, Uk.

[Medline record in process]

PMID: 11927488, UI: 21924584



Links:

Can J Anaesth 2002 Apr;49(4):417-9

Best evidence in anesthetic practice: Prevention: dopamine does not prevent death, acute renal failure, or need for dialysis.

Bracco D, Parlow JL

Lausanne, Switzerland Kingston, Ontario.

[Medline record in process]

PMID: 11927484, UI: 21924580



Links:

Can J Anaesth 2002 Apr;49(4):361-368

Midlatency auditory evoked potentials do not allow the prediction of recovery from general anesthesia with isoflurane: [Les potentiels evoques auditifs de milatence ne permettent pas de predire la recuperation apres une anesthesie generale a l'isoflurane].

Rundshagen I, Schnabel K, Schulte Am Esch J

Department of Anesthesiology, University Hospital Charite, Humboldt University of Berlin, Campus Charite Mitte, Berlin, Germany. the Department of Psychology, University of Michigan, Ann Arbor, USA. the Department of Anesthesiology, University-Hospital Eppendorf, Hamburg, Germany.

[Record supplied by publisher]

PURPOSE: To investigate midlatency auditory evoked potentials (MLAEP) waveforms during recovery from anesthesia. The hypothesis was that MLAEP are sensitive variables to discriminate between states of consciousness and unconsciousness during emergence from anesthesia. METHODS: MLAEP were recorded in the awake state and during the wake-up phase from isoflurane anesthesia in 22 female patients undergoing ophthalmologic surgery. During emergence from anesthesia the changes in latency and amplitude of MLAEP components Na, Pa and Nb were compared with the awake level. The next day the patients were asked for explicit memory for the recovery period. RESULTS: In 72% of the patients the MLAEP waveforms were completely suppressed during isoflurane anesthesia. When the patients responded and opened their eyes spontaneously 38 +/- 12 min after anesthesia, the latencies of Na (18.3 +/- 1.2 vs 17.6 +/- 1.3; P = 0.013) and Nb (47.4 vs 7.1 vs 44.7 +/- 7.8; P = 0.048) remained prolonged compared with awake values. In contrast, the amplitudes NaPa and PaNb had regained baseline level. Nine patients had explicit memory for the immediate recovery period. However, there was no difference for any MLAEP component between patients with and without memory at any time. CONCLUSIONS: The persistent changes of MLAEP latency components Na and Nb indicated impaired auditory signal processing 38 min after isoflurane anesthesia. There was a marked intra- and inter-individual variability during reversal of the anesthetic induced MLAEP changes. This limits the prediction of recovery of consciousness in the individual patient during emergence from anesthesia.

PMID: 11927474



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Can J Anaesth 2002 Apr;49(4):353-360

Rocuronium pharmacokinetic-pharmacodynamic relationship under stable propofol or isoflurane anesthesia : [La relation pharmacocinetique-pharmacodynamique du rocuronium pendant une anesthesie avec propofol ou isoflurane].

Dragne A, Varin F, Plaud B, Donati F

De la Faculte de pharmacie, Universite de Montreal, et du Departement d'anesthesiologie, Universite de Montreal et Centre Hospitalier de l'Universite de Montreal (Hotel-Dieu), Montreal, Quebec, Canada.

[Record supplied by publisher]

PURPOSE: To compare the pharmacokinetics, pharmacodynamics and the concentration-effect relationship of rocuronium in patients under stable propofol or isoflurane anesthesia. METHODS: Ten patients were randomized to receive fentanyl, propofol and nitrous oxide (60%) or fentanyl, thiopental, isoflurane (1.2% end-tidal concentration) and nitrous oxide (60%). To obtain good intubation conditions and maintain adequate muscle relaxation during surgery, patients received two bolus doses of rocuronium: 0.5 mg*kg(-1) (1.7 x ED(95)) at induction followed one hour later by 0.3 mg*kg(-1) (1 x ED(95)). Arterial blood samples were obtained over six hours after the second bolus dose. Plasma concentrations of rocuronium were measured using high pressure liquid chromatography. Muscle twitch tension was monitored by mechanomyography for the two doses. Pharmacokinetic and pharmacodynamic parameters were determined. RESULTS: No differences in rocuronium pharmacokinetic parameters were observed between both groups. After the second bolus, clinical duration was 20 +/- 6 min in the propofol group vs 39 +/- 8 min in the isoflurane group (P <0.05). The effect compartment concentration corresponding to 50% block, EC(50,) was higher under propofol anesthesia: 1008 vs 592 &mgr;g*L(-1) (P <0.05). CONCLUSION: Rocuronium body disposition is similar under stable propofol or isoflurane anesthesia. In contrast to isoflurane, propofol does not prolong the neuromuscular block. Therefore, the potentiating effect of isoflurane is of pharmacodynamic origin only, as explained by an increased sensitivity at the neuromuscular junction. In contrast with isoflurane anesthesia where the dose of rocuronium has to be decreased under stable conditions, no dose adjustment is required under propofol anesthesia.

PMID: 11927473



Links:

Can J Anaesth 2002 Apr;49(4):335-8

Is there a future for xenon anesthesia?/Le xenon a-t-il un avenir en anesthesie ?

Goto T

Department of Anesthesia, Teikyo University Ichihara Hospital, Ichihara-shi, Japan.

[Medline record in process]

PMID: 11927470, UI: 21924566



Links:

Can J Anaesth 2002 Apr;49(4):329-34

Observational studies and "real world" anesthesia pharmacoeconomics/Les etudes par observation et la realite pharmacoeconomique de l'anesthesie.

Miller DR, Tierney M

Departments of Anesthesia and Pharmacy, The Ottawa Hospital, and the University of Ottawa, Ottawa, Ontario, Canada.

[Medline record in process]

PMID: 11927469, UI: 21924565


Neurosci Lett 2002 Feb 15;319(2):95-8

Sympathetic blockade significantly improves cardiovascular alterations immediately after spinal cord injury in rats.

Bravo G, Hong E, Rojas G, Guizar-Sahagun G

Departamento Farmacobiologia, CINVESTAV, IPN, Calzada de los Tenorios 235, Col. Granjas Coapa, 14330 Mexico D.F., Mexico. gbravof@prodigy.net.mx

Immediately after an experimental spinal cord injury (SCI) in rats, there is a large fall in mean arterial pressure (MAP) and heart rate (HR), followed by an abrupt increase in MAP. To better understand the mechanism involved in these early cardiovascular alterations, we tested the effect of treatment with ganglionic and sympathetic blockers in anesthetized rats subjected to T-5 SCI. Fall in MAP was partially diminished by propranolol and pentolinium, while increase in MAP was abolished by propranolol and pentolinium. Adrenalectomy did not diminish the fall in MAP and HR, however, the increase in MAP was significantly reduced. Likewise, propranolol and pentolinium completely abolished the effects in HR. These data suggest that the early cardiovascular alterations secondary to SCI results from an increased parasympathetic activity and a sympathetic withdrawal.

PMID: 11825679, UI: 21683941


Paediatr Anaesth 2002 Feb;12(2):187-91

Perioperative management of a child with very-long-chain acyl-coenzyme A dehydrogenase deficiency.

Steiner LA, Studer W, Baumgartner ER, Frei FJ

Department of Anaesthesia, Universitatskinderspital beider Basel (UKBB), Basel, Switzerland. las30@cam.ac.uk

Very-long-chain acyl-coenzyme A dehydrogenase deficiency is an inborn error of fatty acid metabolism. The clinical presentation of this disease in children is either a severe form with onset of symptoms in the first months of life, cardiomyopathy, metabolic acidosis, myopathy and a high mortality, or a less severe form manifesting mainly with hypoglycaemia. Perioperative fasting and (even emotional) stress can trigger metabolic decompensation through the altered metabolism of endogenous fatty acids resulting in hypoglycaemia, acute cardiac and hepatic dysfunction and rhabdomyolysis. We report the perioperative management of a 9-year-old boy suffering from the severe form of this disease who underwent circumcision. Metabolism was kept stable in this child by using a glucose--electrolyte infusion throughout the perioperative period to avoid the biochemical consequences of fasting and a benzodiazepine--opioid technique combined with regional anaesthesia to minimize the stress response. Considering reports about a possible interference of propofol with fatty acid oxidation and to avoid the unnecessary administration of fatty acids, propofol should not be used in these patients.

PMID: 11882234, UI: 21877529


Paediatr Anaesth 2002 Feb;12(2):140-5

Comparison of rocuronium and suxamethonium for rapid tracheal intubation in children.

Cheng CA, Aun CS, Gin T

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, The Prince of Wales Hospital, Shatin, New Territories, Hong Kong.

BACKGROUND: The purpose of our study was to determine whether a smaller dose of rocuronium than previously reported could provide similar intubating conditions to suxamethonium during rapid-sequence induction of anaesthesia in children. METHODS: One hundred and twenty ASA I, unpremedicated children, aged 1-10 years, who were undergoing elective surgery, were randomized into three groups to receive rocuronium 0.6 mg.kg-1, rocuronium 0.9 mg.kg-1 or suxamethonium 1.5 mg.kg-1. The study was double-blinded, anaesthesia and timing of injection was standardized to alfentanil 10 microg.kg-1, thiopentone 5 mg.kg-1 and the study drug. Intubation was attempted at 30 s after injection of neuromuscular relaxant and intubating conditions graded as excellent, good, poor or impossible. RESULTS: All 120 children were successfully intubated within 60 s without need for a second attempt after administration of neuromuscular relaxant. Differences between suxamethonium and rocuronium 0.6 mg.kg-1 and between the two doses of rocuronium were statistically significant (P=0.016 and 0.007, respectively). CONCLUSIONS: Rocuronium 0.9 mg.kg-1 provides similar intubating conditions to suxamethonium 1.5 mg.kg-1 during modified rapid-sequence induction using alfentanil and thiopentone in children (P=0.671). Rocuronium 0.6 mg.kg-1 was inadequate.

Publication Types:

  • Clinical trial
  • Randomized controlled trial

PMID: 11882225, UI: 21877520


Paediatr Anaesth 2002 Feb;12(2):131-9

The effects of an educational programme on the anxiety and satisfaction level of parents having parent present induction and visitation in a postanaesthesia care unit.

Chan CS, Molassiotis A

Department of Nursing, Faculty of Medicine, The Chinese University of Hong Kong, School of Nursing, University of Nottingham, Nottingham, UK. connychan@cuhk.edu.hk

BACKGROUND: In Hong Kong, some hospitals have established the practice of Parental Presence Induction (PPI) and visitation in Postanaesthesia Care Units (PACU) for children receiving surgery. The literature indicates that parents reported extreme anxiety and discomfort after being present at induction of anaesthesia and suggests that it would seem appropriate to devise a programme of education to reduce anxiety for parents. METHODS: A quasi-experimental pretest and post-test design was employed. Parents in the experimental group received an educational programme about the role and expectations of parents having PPI and visitation in PACU together with an information pamphlet. The comparison group received routine (verbal) instructions. The Chinese version of the State and Trait Anxiety Inventory and the Parental Satisfaction with Care Questionnaire were used to assess parents' anxiety and satisfaction with care. RESULTS: A total of 50 parents (mostly mothers) were recruited. Twenty-five were allocated in the intervention group and 25 in the comparison group. The children were aged 1--9 years with a mean age of 2.9 years. There were 46 male and four female children. The results demonstrate that parents who received an education programme reported a decrease in anxiety (P < 0.001) and an increase in their satisfaction with the care provided (P < 0.001). A significant negative relationship (r= -0.61, P < 0.001) between parental anxiety postoperatively and the satisfaction with care score was also obtained, suggesting that lower levels of parental anxiety are associated with higher levels of satisfaction. CONCLUSIONS: The study suggests that an educational programme preparing parents for their child's induction of anaesthesia and visitation to the PACU should be offered, as it can reduce their anxiety with the practice of PPI and visitation in the PACU and increase parents' satisfaction with care.

PMID: 11882224, UI: 21877519


Paediatr Anaesth 2002 Feb;12(2):118-23

Is haemostasis biological screening always useful before performing a neuraxial blockade in children?

Roux CL, Lejus C, Surbleb M, Renaudin M, Guillaud C, Windt A, Lasnier B, Pinaud M

Department of Anaesthesiology, Hotel Dieu, CHU Nantes, France.

BACKGROUND: Because of the lack of controlled studies, there is no consensus of opinion about the practice of routine haemostasis tests before neuraxial blockade in children. The purpose of this study was to compare the influence of two different strategies of coagulation evaluation on the incidence of diagnosed coagulopathies leading to a modification of the preoperative or anaesthetic management in children who were scheduled for caudal, epidural or intrathecal block. METHODS: For a 24-month period (period 1, retrospective study, n=751), haemostasis screening was undertaken only after family and personal history and physical examination in all patients. For the following 24 months (period 2, prospective study, n=958), a standardized questionnaire was used. In addition, routine tests (prothrombin, partial thromboplastin time, platelet count) were performed in children who where not yet walking. In older children, coagulation tests were undertaken as in period 1. RESULTS: Overall, 26 significant abnormalities were diagnosed. Coagulation tests were performed in 16.2% (period 1) and 78.2% (period 2) of the children, who were not yet walking. Routine tests did not improve the diagnosis of haemostasis abnormalities justifying a modification of the preoperative and anaesthetic management (2.2% from 406 children in period 1 vs 4.1% from 266 children in period 2). The predictive positive value of routine tests (period 2) was 19%, vs 45% for specific tests (period 1) (P < 0.001). In older children, the use of a standardized form increased the number of haemostasis screenings without improvement of diagnosis leading to modified preoperative management (0.3% from 315 children in period 1 vs 0.5% from 628 children in period 2). CONCLUSIONS: When routine testing is performed in nonwalking children, the screening number increases without leading to a higher number of anaesthetic management changes, suggesting that routine testing does not seem to provide much extra information in the absence of a positive history.

PMID: 11882222, UI: 21877517


Paediatr Anaesth 2002 Feb;12(2):110-7

Cardiac trauma in children.

Baum VC

Department of Anesthesiology, University of Virginia, Charlottesville, VA, USA.

Publication Types:

  • Review
  • Review, tutorial

PMID: 11882221, UI: 21877516


Paediatr Anaesth 2002 Feb;12(2):107-9

Preparing parents for their child's surgery: preoperative parental information and education.

Koinig H

Publication Types:

  • Comment
  • Editorial

PMID: 11882220, UI: 21877515

 
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