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1.
Intern Emerg Med ; 15(1): 127-134, 2020 01.
Artículo en Inglés | MEDLINE | ID: mdl-31655972

RESUMEN

Neuromuscular blocking agents play a significant role in improving the success rate for urgent intubation, although there is limited evidence about the effect on subsequent outcomes, such as the incidence of tracheostomy. In this retrospective cohort study, we aimed to examine the association between avoidance of neuromuscular blocking agents for urgent tracheal intubation and incidence of tracheostomy among patients in the intensive care unit (ICU). The setting of this study was an eight-bed ICU at a tertiary-care hospital in Okayama, Japan. We included patients who underwent urgent tracheal intubation at the emergency department or the ICU and were admitted to the ICU between April 2013 and November 2017. We extracted data on methods and medications of intubation, predictors for difficult intubation, Cormack-Lehane grade, patient demographics, primary diagnoses, reintubation. We estimated odds ratios and their 95% confidence intervals for elective tracheostomy during the ICU stay using logistic regression models. Of 411 patients, 46 patients underwent intubation without neuromuscular blocking agents and 61 patients underwent tracheostomy. After adjusting for potential confounders, patients who avoided neuromuscular blocking agents had more than double the odds of tracheostomy (odds ratio 2.59, 95% confidence interval 1.06-6.34, p value = 0.04). When stratifying the subjects by risk status for tracheostomy, the association was more pronounced in high-risk group, while we observed less significant association in the low-risk group. Avoidance of neuromuscular blocking agents for urgent intubation increases the risk of tracheostomy among emergency patients, especially those who have a higher risk for tracheostomy.


Asunto(s)
Intubación Intratraqueal/métodos , Bloqueantes Neuromusculares/normas , Factores de Tiempo , Traqueostomía/métodos , Adulto , Femenino , Humanos , Intubación Intratraqueal/instrumentación , Japón , Tiempo de Internación/estadística & datos numéricos , Masculino , Persona de Mediana Edad , Bloqueantes Neuromusculares/uso terapéutico , Estudios Retrospectivos , Medición de Riesgo/métodos , Factores de Riesgo
2.
Anesth Analg ; 107(5): 1609-17, 2008 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-18931219

RESUMEN

BACKGROUND: Conventional incremental bolus administration of neuromuscular blocking (NMB) drugs is associated with limitations in intraoperative control, potential delays in recovery, and residual blockade in the postanesthetic period. To overcome such limitations, we developed a novel adaptive control computer program, the Neuromuscular Blockade Advisory System (NMBAS). The NMBAS advises the anesthesiologist on the timing and dose of NMB drugs based on a sixth-order Laguerre model and the history of the patient's electromyographic responses. Here, we tested the hypothesis that the use of the NMBAS improves NMB compared to standard care. METHODS: We conducted a prospective, randomized, controlled, blinded, parallel-group, clinical trial with n = 73 patients (ASA physical status I-III) undergoing abdominal surgery under general anesthesia > or =1.5 h with NMB using rocuronium. Patients were allocated to standard care or NMBAS-guided rocuronium administration. The primary outcome variable was the incidence of intraoperative events reflecting inadequate NMB. Secondary outcome variables included train-of-four (TOF) ratios at the end of surgery before reversal, the total doses of rocuronium, reversal agents, anesthetics and other drugs, the incidence of postoperative adverse events, and the incidence of anesthesiologist noncompliance with NMBAS recommendations. RESULTS: Of 73 enrolled patients, n = 30 per group were eligible for analysis. Patient demographics were comparable between the groups. The incidence in total intraoperative events associated with inadequate NMB was significantly lower in the NMBAS group compared to standard care (8/30 vs 19/30; P = 0.004). Mean TOF ratios at the end of surgery before reversal were higher in the NMBAS group (0.59 [95% CI, 0.48-0.69] vs 0.14 [95% CI, 0.04-0.24]; P < 0.0001). Total administered doses of rocuronium, reversal drugs, and other drugs, and the incidence of postoperative adverse events were not different. CONCLUSIONS: Compared to standard practice, NMBAS-guided care was associated with improved NMB quality and higher TOF ratios at the end of surgery, potentially reducing the risk of residual NMB and improving perioperative patient safety.


Asunto(s)
Comités Consultivos/organización & administración , Anestesia General/normas , Bloqueo Neuromuscular/normas , Bloqueantes Neuromusculares/uso terapéutico , Abdomen/cirugía , Adulto , Anciano , Androstanoles/administración & dosificación , Atracurio/administración & dosificación , Femenino , Estado de Salud , Humanos , Complicaciones Intraoperatorias/epidemiología , Complicaciones Intraoperatorias/prevención & control , Masculino , Persona de Mediana Edad , Bloqueantes Neuromusculares/administración & dosificación , Bloqueantes Neuromusculares/normas , Pancuronio/administración & dosificación , Rocuronio , gamma-Ciclodextrinas/administración & dosificación
3.
Anesthesiol Clin ; 25(3): 483-509, viii-ix, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17884705

RESUMEN

A variety of different pathologies result in disease phenotypes that are summarized as neuromuscular diseases because they share commonalty in their clinical consequences for the patient: a progressive weakening of the skeletal muscles. Distinct caution and appropriate changes to the anesthetic plan are advised when care is provided during the perioperative period. The choice of anesthetic technique, anesthetic drugs, and neuromuscular blockade always depends on the type of neuromuscular disease and the surgical procedure planned. A clear diagnosis of the underlying disease and sufficient knowledge and understanding of the pathophysiology are of paramount importance to the practitioner and guide optimal perioperative management of affected patients.


Asunto(s)
Anestesia General , Anestesiología/métodos , Enfermedades Neuromusculares , Anestesia General/efectos adversos , Anestesia General/métodos , Anestesiología/normas , Anestésicos/farmacología , Anestésicos/normas , Humanos , Bloqueo Neuromuscular/efectos adversos , Bloqueantes Neuromusculares/farmacología , Bloqueantes Neuromusculares/normas , Atención Perioperativa
4.
Semin Neurol ; 24(1): 83-94, 2004 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15229795

RESUMEN

Myasthenia gravis (MG) is an autoimmune disease of the neuromuscular junction. Current anesthetic practice may require the use of neuromuscular blocking (NMB) drugs that act at this junction to facilitate control of the airway and allow procedures to be performed on a motionless MG patient. This competes with the goals of rapid emergence and recapture of preoperative muscle strength following anesthesia. In particular, avoiding prolonged periods of postoperative mechanical ventilation is a paramount concern of patients, families, and physicians. Standard anesthetic agents and, if needed, judiciously titrated NMB drugs generally allow safe emergence and immediate extubation for most low-risk MG patients. If necessary, postoperative mechanical ventilation is accomplished with the use of specialized monitoring devices that help monitor awareness and depth of sedation. Currently used intravenous sedatives allow titrated depth of sedation and rapid emergence when extubation is appropriate. Communication to the patient, family, and other caregivers of the goals of the anesthetic plan and of the patient's evolving status are also very important duties of the anesthesiologist.


Asunto(s)
Anestesia/efectos adversos , Anestesia/normas , Miastenia Gravis/fisiopatología , Miastenia Gravis/cirugía , Atención Perioperativa/normas , Estimulación Eléctrica/métodos , Humanos , Hipnóticos y Sedantes/uso terapéutico , Monitoreo Fisiológico/normas , Miastenia Gravis/tratamiento farmacológico , Bloqueantes Neuromusculares/efectos adversos , Bloqueantes Neuromusculares/normas , Respiración Artificial/efectos adversos , Respiración Artificial/normas
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