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1.
Br J Anaesth ; 106(1): 124-30, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21059701

ABSTRACT

BACKGROUND: Previous studies have demonstrated that lower local anaesthetic (LA) volumes can be used for ultrasound (US)-guided interscalene brachial plexus block (ISB). However, no study has examined whether US can reduce the volume required when compared with nerve stimulation (NS) for ISB. Our aim was to do this by comparing the minimum effective analgesic volumes (MEAVs). METHODS: After ethics approval and informed consent, patients undergoing shoulder surgery were recruited to this randomized, double-blind, up-down sequential allocation study. The volume used for both US and NS was dependent upon the success or failure of the previous block. Success was defined as a verbal rating score of 0/10, 30 min after surgery. Ten needle passes were allowed before defaulting to the opposite group. Patients received general anaesthesia. Pain scores and analgesic consumption were assessed by a blinded observer. Statistical comparisons of continuous variables were performed using Student's t-test and Mann-Whitney U-test as appropriate. Categorical variables were analysed using χ² test. MEAV values were estimated using log-transformed up-down independent pairs analysis and probit regression. Significance was assumed at P<0.05 (two-sided). RESULTS: The MEAV required to provide effective analgesia was significantly (P=0.034) reduced to 0.9 ml [95% confidence interval (CI) 0.3-2.8] in the US group from 5.4 ml (95% CI 3.4-8.6) in the NS group. Fewer needle passes were needed to identify the brachial plexus with US (1 vs 3; P<0.0001) and patients had less pain at 30 min after surgery (P=0.03). CONCLUSIONS: US reduces the number of attempts, LA volume, and postoperative pain when compared with NS for ISB.


Subject(s)
Anesthetics, Local/administration & dosage , Nerve Block/methods , Adult , Aged , Arthroscopy , Brachial Plexus/anatomy & histology , Brachial Plexus/diagnostic imaging , Brachial Plexus/physiology , Double-Blind Method , Drug Administration Schedule , Electric Stimulation/methods , Female , Fentanyl/administration & dosage , Humans , Male , Middle Aged , Pain Measurement/methods , Shoulder Joint/surgery , Ultrasonography, Interventional/methods
2.
Br J Anaesth ; 101(4): 549-56, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18682410

ABSTRACT

BACKGROUND: Interscalene brachial plexus block (ISBPB) is an effective nerve block for shoulder surgery. However, a 100% incidence of phrenic nerve palsy limits the application of ISBPB for patients with limited pulmonary reserve. We examined the incidence of phrenic nerve palsy with a low-volume ISBPB compared with a standard-volume technique both guided by ultrasound. METHODS: Forty patients undergoing shoulder surgery were randomized to receive an ultrasound-guided ISBPB of either 5 or 20 ml ropivacaine 0.5%. General anaesthesia was standardized. Both groups were assessed for respiratory function by sonographic diaphragmatic assessment and spirometry before and after receiving ISBPB, and after surgery. Motor and sensory block, pain, sleep quality, and analgesic consumption were additional outcomes. Statistical comparison of continuous variables was analysed using one-way analysis of variance and Student's t-test. Non-continuous variables were analysed using chi(2) tests. Statistical significance was assumed at P<0.05. RESULTS: The incidence of diaphragmatic paralysis was significantly lower in the low-volume group compared with the standard-volume group (45% vs 100%). Reduction in forced expiratory volume in 1 s, forced vital capacity, and peak expiratory flow at 30 min after the block was also significantly less in the low-volume group. In addition, there was a significantly greater decrease in postoperative oxygen saturation in the standard-volume group (-5.85 vs -1.50, P=0.004) after surgery. There were no significant differences in pain scores, sleep quality, and total morphine consumption up to 24 h after surgery. CONCLUSIONS: The use of low-volume ultrasound-guided ISBPB is associated with fewer respiratory and other complications with no change in postoperative analgesia compared with the standard-volume technique.


Subject(s)
Anesthetics, Local/administration & dosage , Brachial Plexus/diagnostic imaging , Nerve Block/methods , Respiratory Paralysis/etiology , Ultrasonography, Interventional/methods , Adolescent , Adult , Aged , Aged, 80 and over , Analgesics, Opioid/administration & dosage , Anesthetics, Local/adverse effects , Dose-Response Relationship, Drug , Double-Blind Method , Drug Administration Schedule , Female , Humans , Male , Middle Aged , Morphine/administration & dosage , Nerve Block/adverse effects , Pain Measurement/methods , Pain, Postoperative/prevention & control , Phrenic Nerve/injuries , Respiratory Insufficiency/etiology , Respiratory Insufficiency/prevention & control , Respiratory Paralysis/prevention & control , Shoulder Joint/surgery
3.
Clin Ther ; 20(1): 110-24, 1998.
Article in English | MEDLINE | ID: mdl-9522109

ABSTRACT

The known effects of commonly used nonsteroidal anti-inflammatory drugs (NSAIDs) on hemostatic parameters have led to concern over their use in the perioperative period. Nabumetone, unlike other NSAIDs, has little effect on collagen-induced platelet aggregation. To evaluate the effect of nabumetone 2000 mg daily on other hemostatic parameters (e.g., bleeding time, prothrombin time, and partial thromboplastin time) in the clinical setting, this double-masked study was conducted in patients with osteoarthritis undergoing arthroscopic knee surgery. After a 1-week placebo washout period, 58 patients were randomized to receive nabumetone and 53 were randomized to receive placebo. They were assessed before surgery (after 1 to 2 weeks of treatment) and again after surgery (after an additional 3 weeks of treatment). The study was designed to have 90% power to show equivalence in bleeding time to within 1.5 minutes, a difference assumed to be of no clinical importance. No meaningful differences were observed between the groups in any of the measured hemostatic parameters. Before surgery, the bleeding time increased by only 0.3 minutes with nabumetone and decreased by 0.2 minutes with placebo. The mean (+/- SD) difference between the groups in change from baseline was 0.5 +/- 0.3 minutes. After surgery, the changes were 0.1 minutes and 0.0 minutes, respectively, and the difference between groups was 0.2 +/- 0.3 minutes. These differences were neither statistically nor clinically significant, and maximum individual increases were similar in each group. Furthermore, there were no reports of abnormal bleeding in the operative knees. The results of this study show that nabumetone had little or no effect on hemostasis and suggest that this drug can be used safely in the perioperative period.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Arthroscopy , Butanones/adverse effects , Hemostasis/drug effects , Knee/surgery , Adult , Aged , Bleeding Time , Double-Blind Method , Female , Humans , Male , Middle Aged , Nabumetone , Platelet Aggregation/drug effects
4.
Clin Orthop Relat Res ; (328): 155-8, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8653949

ABSTRACT

A 54-year-old woman with a history of right total knee replacement had right knee pain and swelling for 6 months. Radiographs of the knee showed significant fragmentation and resorption of the patella consistent with osteonecrosis. Evidence of increased anteroposterior laxity was noted on physical examination. Revision surgery to a posterior stabilized prosthesis with excision of the patellar fragments resulted in a marked improvement in her symptoms and functional capabilities 2 years after surgery. The authors review the blood supply to the patella and how it may be disturbed by knee surgery and speculate that this patient's symptoms may have been worsened by the anteroposterior instability of her prosthesis.


Subject(s)
Bone Resorption , Knee Prosthesis/adverse effects , Osteonecrosis/etiology , Patella , Female , Humans , Middle Aged , Reoperation
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