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1.
J Ultrasound Med ; 32(1): 143-8, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23269719

ABSTRACT

OBJECTIVES: Needle visualization is important for sonographically guided regional anesthesia procedures. Needle characteristics that improve needle visualization are therefore important to anesthesiologists. This study compared several echogenic needle designs by defining characteristics of needle echogenicity and assessing regional anesthesiologist preferences for these characteristics across various needle angles. METHODS: Twelve blinded regional anesthesiologists graded 5 randomized block needles (1 nonechogenic control and 4 echogenic) on 4 predefined characteristics (overall brightness of the needle, overall clarity of the needle, brightness of the needle tip, and clarity of the needle tip). In-plane needle images in a gel phantom were obtained at 4 needle angles (15°, 30°, 45°, and 60°). Participants rated specific needle characteristics for each needle at each angle and then ranked their overall needle preferences. RESULTS: Significant differences in all 4 needle characteristics were found across needle types (P< .01). Clarity of the needle tip was significantly associated with overall needle rank (P = .009). Other needle visualization characteristics were not significantly correlated with needle rank. The SonoPlex Stim needle (Pajunk Medical Systems, Tucker, GA) was rated highest in all 4 predefined needle characteristics as well as overall needle rank. CONCLUSIONS: This study shows that anesthesiologists prefer certain visual characteristics of needles used in sonographically guided regional anesthesia procedures. Specifically, needle tip clarity most closely predicted clinician needle preferences. These results support the idea that all echogenic needle designs do not uniformly enhance needle visualization. Further studies are needed to determine whether needles with superior tip clarity predict not only clinician preferences but also improved sonographically guided regional anesthetic outcomes.


Subject(s)
Anesthesia, Conduction/instrumentation , Needles , Ultrasonography, Interventional/methods , Humans , Logistic Models , Phantoms, Imaging
3.
Anesthesiol Clin ; 28(2): 251-66, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20488393

ABSTRACT

The use of local anesthetics in ambulatory surgery offers multiple benefits in line with the goals of modern-day outpatient surgery. A variety of regional techniques can be used for a wide spectrum of procedures; all are shown to reduce postprocedural pain; reduce the short-term need for opiate medications; reduce adverse effects, such as nausea and vomiting; and reduce the time to dismissal compared with patients who do not receive regional techniques. Growth in ambulatory procedures will likely continue to rise with future advances in surgical techniques, changes in reimbursement, and the evolution of clinical pathways that include superior, sustained postoperative analgesia. Anticipating these changes in practice, the role of, and demand for, regional anesthesia in outpatient surgery will continue to grow.


Subject(s)
Ambulatory Surgical Procedures , Anesthesia, Conduction/methods , Humans , Nerve Block/methods , Orthopedic Procedures
4.
Anesth Analg ; 107(4): 1438-40, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18806066

ABSTRACT

The green light potassium-titanyl-phosphate laser photoselective vaporization of the prostate is the latest modality for treatment of benign prostatic obstruction. Because of effective superficial tissue coagulation, intravascular absorption of fluid is minimal; therefore, development of transurethral resection syndrome is unlikely. To our knowledge, this is the first report of a patient undergoing photoselective vaporization of the prostate who developed full-blown transurethral resection syndrome because of intravascular absorption of sterile water. Absorption of hypotonic irrigant presumably occurred through the injury induced during insertion of the laser cystoscope.


Subject(s)
Acute Kidney Injury/etiology , Anemia, Hemolytic/etiology , Intraoperative Complications , Lasers, Solid-State/adverse effects , Transurethral Resection of Prostate/adverse effects , Urethra/injuries , Water Intoxication/etiology , Aged , Humans , Male , Prostatic Hyperplasia/surgery , Syndrome , Therapeutic Irrigation/adverse effects
5.
Anesth Analg ; 107(1): 229-31, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18635493

ABSTRACT

Fluorescein is a fluorochrome dye occasionally administered by intrathecal injection to identify and localize cerebrospinal fluid leaks. Although generally considered to be a benign intervention, intrathecal administration of fluorescein has resulted in adverse events. We report a case of status epilepticus after intrathecal administration of fluorescein. Anesthesia providers should be aware of complications associated with intrathecal fluorescein use and be prepared to manage neurologic complications during the perioperative period.


Subject(s)
Cerebrospinal Fluid Rhinorrhea/diagnosis , Fluorescein/adverse effects , Status Epilepticus/chemically induced , Female , Fluorescein/administration & dosage , Humans , Injections, Spinal , Middle Aged
6.
Anesth Analg ; 106(5): 1581-4, table of contents, 2008 May.
Article in English | MEDLINE | ID: mdl-18420882

ABSTRACT

Simulation training is rapidly becoming an integral element of the education curriculum of anesthesia residency programs. We report a case of successful resuscitation of bupivacaine-induced cardiac arrest treated with i.v. lipid emulsion by providers who had recently participated in simulation training involving a scenario nearly identical to this case. Upon debriefing, it was determined that the previous training influenced execution of the following steps: rapid problem recognition, prompt initiation of specific therapy in the setting of supportive advanced cardiac life support measures, and coordinated team efforts. Although the true cause of efficient resuscitation and ultimate recovery cannot be proven, the efficiency of the resuscitation process, including timely administration of lipid emulsion, is evidence that simulation may be useful for training providers to manage rare emergencies.


Subject(s)
Advanced Cardiac Life Support , Anesthesiology/education , Anesthetics, Local/administration & dosage , Bupivacaine/adverse effects , Education, Medical, Continuing/methods , Fat Emulsions, Intravenous/therapeutic use , Heart Arrest/therapy , Patient Simulation , Aged, 80 and over , Clinical Competence , Curriculum , Electrocardiography , Heart Arrest/chemically induced , Heart Arrest/diagnosis , Humans , Internship and Residency , Male , Patient Care Team , Treatment Outcome
7.
Reg Anesth Pain Med ; 33(6): 510-7, 2008.
Article in English | MEDLINE | ID: mdl-19258965

ABSTRACT

BACKGROUND AND OBJECTIVES: Patients undergoing major orthopedic surgery experience significant postoperative pain. Failure to provide adequate analgesia may impede early physical therapy and rehabilitation, which are important factors for maintaining joint range of motion and facilitating hospital dismissal. We examined the effect of a pre-emptive, multimodal, perioperative analgesic regimen emphasizing peripheral nerve block in patients undergoing total hip (THA) and total knee (TKA) arthroplasty. Perioperative outcomes and major postoperative complications were evaluated. METHODS: One hundred consecutive patients undergoing primary or revision THA or TKA using the Mayo Clinic Total Joint Regional Anesthesia (TJRA) protocol were retrospectively reviewed. The TJRA protocol is a pre-emptive, multimodal, perioperative analgesic regimen emphasizing peripheral nerve block that was jointly developed by the Departments of Anesthesiology and Orthopedic Surgery. Identified patients were matched 1:1 with historical controls undergoing identical surgical procedures with traditional anesthetic techniques. Matching criteria included patient age, gender, surgeon, date of surgery, and American Society of Anesthesiologists physical status. Patient demographics, preoperative joint range of motion, and anesthetic management were recorded for each patient. The primary study outcome was hospital length of stay. Secondary outcome variables included time to ambulation, joint range of motion, and discharge eligibility. Postoperative verbal analog pain scores (VAS), opioid requirements, side effects, and perioperative complications were also documented. RESULTS: One hundred patients underwent THA or TKA using the newly implemented Mayo Clinic TJRA protocol. Matched controls (n = 100) received intravenous patient-controlled analgesia with subsequent conversion to oral analgesics for postoperative pain management. TJRA patients had significantly shorter hospital lengths of stay (3.8 days v 5.0 days; P < .001), achieved discharge eligibility significantly sooner (1.7 +/- 1.9 days earlier; P < .0001), and had improved joint range of motion (90 degrees v 85 degrees ; P = .008) when compared with matched controls. TJRA patients had significantly improved postoperative analgesia, including lower VAS pain scores (postoperative day 0 through postoperative day 3; P < .001), and lower opioid requirements (postoperative day 0 to postoperative day 2; P = .04). Adverse outcomes such as postoperative urinary retention (50% v 31%; P < .001), and ileus formation (7% v 1%; P = .01) occurred more frequently among control patients. CONCLUSIONS: Patients undergoing THA or TKA using a comprehensive, pre-emptive, multimodal analgesic regimen emphasizing peripheral nerve block may have significantly improved perioperative outcomes, and fewer adverse events, when compared with patients receiving traditional intravenous opioids during the initial postoperative period. Improved perioperative outcomes include a shortened hospital length of stay, and a significant reduction in postoperative urinary retention and ileus formation.


Subject(s)
Analgesia, Patient-Controlled/methods , Arthroplasty, Replacement, Hip , Arthroplasty, Replacement, Knee , Nerve Block/methods , Postoperative Complications/prevention & control , Aged , Analgesics, Opioid/therapeutic use , Case-Control Studies , Clinical Protocols , Combined Modality Therapy , Female , Humans , Ileus/prevention & control , Length of Stay , Male , Pain Measurement , Peripheral Nerves , Range of Motion, Articular/drug effects , Retrospective Studies , Treatment Outcome , Urinary Retention/prevention & control
9.
J Clin Anesth ; 17(8): 621-3, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16427534

ABSTRACT

This case report illustrates that median, radial, and ulnar nerve blocks at the elbow provides anesthesia for ambulatory carpal tunnel release surgery. This report discusses 3 patients with medical conditions, including vascular access problems and morbid obesity, which made nerve blocks at the elbow advantageous compared with other anesthetic techniques. Peripheral nerve blocks at the elbow were done before surgery in a block room, so the patients spent less time in the operating room. Nerve blocks at the elbow are effective anesthesia for hand procedures with no patient requiring further local anesthetic injection and opioids for pain or expressing any discomfort during surgery. The blocks are easy to perform and set up quickly, and using long-acting local anesthetics, elbow blocks provide postoperative pain control for approximately 10 hours. The nerve blocks at the elbow facilitate the perioperative process by being done out of the operating room and providing prolonged pain control without the need for opioids, so nausea may be avoided.


Subject(s)
Carpal Tunnel Syndrome/surgery , Elbow/innervation , Nerve Block/methods , Peripheral Nerves/drug effects , Aged , Aged, 80 and over , Anesthetics, Intravenous/administration & dosage , Anesthetics, Local/administration & dosage , Bronchodilator Agents/administration & dosage , Epinephrine/administration & dosage , Humans , Mepivacaine/administration & dosage , Midazolam/administration & dosage , Tetracaine/administration & dosage , Treatment Outcome
10.
Can J Anaesth ; 51(1): 20-4, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14709455

ABSTRACT

PURPOSE: To compare the analgesic effects of remifentanil and alfentanil during breast biopsy under monitored anesthesia care (MAC). METHODS: Sixty patients received sedation with propofol (50 microg.kg(-1).min(-1)). After receiving a loading dose of opioid (either remifentanil 0.5 microg.kg(-1), or alfentanil 2.5 microg.kg(-1)), an infusion was initiated (remifentanil 0.05 microg.kg(-1).min(-1) or alfentanil 0.25 microg.kg(-1).min(-1)), and this was supplemented with local anesthetic infiltration. The pain was evaluated with a ten-point visual analogue scale (VAS) during local anesthetic infiltration and deep tissue dissection. Inadequate analgesia, defined as VAS scores > or = 5, was treated first with boluses of opioid (remifentanil group 10 microg or alfentanil group 50 microg) and if inadequate after two treatments with additional local anesthetic. Postoperative times were recorded including the times until discharge criteria were achieved and patient's actual discharge. RESULTS: The pain scores were similar between the two groups during the initial injections of local anesthetic in the breast, however, patients in the remifentanil group had lower mean pain scores during deep tissue dissection (2.3 vs 4.3, P < 0.01). Patients in the remifentanil group required fewer rescue doses of opioid (1.9 vs 3.6, P < 0.03) and local anesthetic (5 vs 15, P < 0.006). The two study groups had comparable speed of recovery. CONCLUSION: Remifentanil was a better opioid choice than alfentanil for breast biopsy under MAC at the doses studied, but it did not increase the rapidity in which patients recovered postoperatively.


Subject(s)
Alfentanil/therapeutic use , Analgesics, Opioid/therapeutic use , Anesthesia , Biopsy/adverse effects , Breast/pathology , Piperidines/therapeutic use , Adult , Double-Blind Method , Female , Humans , Middle Aged , Monitoring, Intraoperative , Pain Measurement/drug effects , Patient Satisfaction , Remifentanil
11.
Anesth Analg ; 98(2): 318-320, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14742361

ABSTRACT

UNLABELLED: Octreotide may be a life-saving treatment in the case of an acute carcinoid crisis, but when given as an i.v. bolus in larger doses, it may cause significant effects on the cardiac conduction system. We describe cardiac conduction impairment observed during octreotide administration in a patient undergoing carcinoid tumor surgery. In this patient, i.v. boluses of 100 microg of octreotide resulted in symptomatic bradycardia, Mobitz type II atrioventricular block, and complete heart block. Perioperative physicians especially need to be aware of these potential effects because they may be more likely to occur during surgery because of the larger doses and boluses that are used to treat acute symptoms secondary to tumor manipulation. IMPLICATIONS: In some susceptible patients, i.v. bolus administration of octreotide may cause significant bradycardia and cardiac conduction defects. Therefore, when octreotide is administered as a bolus, it may be advisable to give it slowly while monitoring the electrocardiogram.


Subject(s)
Bradycardia/chemically induced , Carcinoid Tumor/surgery , Heart Block/chemically induced , Hormones/adverse effects , Liver Neoplasms/surgery , Octreotide/adverse effects , Aged , Anesthesia , Electrocardiography , Hormones/administration & dosage , Humans , Laparoscopy , Laparotomy , Male , Octreotide/administration & dosage
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