RESUMEN
"OBJECTIVE: To update the 2002 version of ""Clinical practice guidelines for sustained neuromuscular blockade in the adult critically ill patient."" DESIGN: A Task Force comprising 17 members of the Society of Critical Medicine with particular expertise in the use of neuromuscular-blocking agents; a Grading of Recommendations Assessment, Development, and Evaluation expert; and a medical writer met via teleconference and three face-to-face meetings and communicated via e-mail to examine the evidence and develop these practice guidelines. Annually, all members completed conflict of interest statements; no conflicts were identified. This activity was funded by the Society for Critical Care Medicine, and no industry support was provided. METHODS: Using the Grading of Recommendations Assessment, Development, and Evaluation system, the Grading of Recommendations Assessment, Development, and Evaluation expert on the Task Force created profiles for the evidence related to six of the 21 questions and assigned quality-of-evidence scores to these and the additional 15 questions for which insufficient evidence was available to create a profile. Task Force members reviewed this material and all available evidence and provided recommendations, suggestions, or good practice statements for these 21 questions. RESULTS: The Task Force developed a single strong recommendation: we recommend scheduled eye care that includes lubricating drops or gel and eyelid closure for patients receiving continuous infusions of neuromuscular-blocking agents. The Task Force developed 10 weak recommendations. 1) We suggest that a neuromuscular-blocking agent be administered by continuous intravenous infusion early in the course of acute respiratory distress syndrome for patients with a PaO2/FIO2 less than 150. 2) We suggest against the routine administration of an neuromuscular-blocking agents to mechanically ventilated patients with status asthmaticus. 3) We suggest a trial of a neuromuscular-blocking agents in life-threatening situations associated with profound hypoxemia, respiratory acidosis, or hemodynamic compromise. 4) We suggest that neuromuscular-blocking agents may be used to manage overt shivering in therapeutic hypothermia. 5) We suggest that peripheral nerve stimulation with train-of-four monitoring may be a useful tool for monitoring the depth of neuromuscular blockade but only if it is incorporated into a more inclusive assessment of the patient that includes clinical assessment. 6) We suggest against the use of peripheral nerve stimulation with train of four alone for monitoring the depth of neuromuscular blockade in patients receiving continuous infusion of neuromuscular-blocking agents. 7) We suggest that patients receiving a continuous infusion of neuromuscular-blocking agent receive a structured physiotherapy regimen. 8) We suggest that clinicians target a blood glucose level of less than 180 mg/dL in patients receiving neuromuscular-blocking agents. 9) We suggest that clinicians not use actual body weight and instead use a consistent weight (ideal body weight or adjusted body weight) when calculating neuromuscular-blocking agents doses for obese patients. 10) We suggest that neuromuscular-blocking agents be discontinued at the end of life or when life support is withdrawn. In situations in which evidence was lacking or insufficient and the study results were equivocal or optimal clinical practice varies, the Task Force made no recommendations for nine of the topics. 1) We make no recommendation as to whether neuromuscular blockade is beneficial or harmful when used in patients with acute brain injury and raised intracranial pressure. 2) We make no recommendation on the routine use of neuromuscular-blocking agents for patients undergoing therapeutic hypothermia following cardiac arrest. 3) We make no recommendation on the use of peripheral nerve stimulation to monitor degree of block in patients undergoing therapeutic hypothermia. 4) We make no recommendation on the use of neuromuscular blockade to improve the accuracy of intravascular-volume assessment in mechanically ventilated patients. 5) We make no recommendation concerning the use of electroencephalogram-derived parameters as a measure of sedation during continuous administration of neuromuscular-blocking agents. 6) We make no recommendation regarding nutritional requirements specific to patients receiving infusions of neuromuscular-blocking agents. 7) We make no recommendation concerning the use of one measure of consistent weight over another when calculating neuromuscular-blocking agent doses in obese patients. 8) We make no recommendation on the use of neuromuscular-blocking agents in pregnant patients. 9) We make no recommendation on which muscle group should be monitored in patients with myasthenia gravis receiving neuromuscular-blocking agents. Finally, in situations in which evidence was lacking or insufficient but expert consensus was unanimous, the Task Force developed six good practice statements. 1) If peripheral nerve stimulation is used, optimal clinical practice suggests that it should be done in conjunction with assessment of other clinical findings (e.g., triggering of the ventilator and degree of shivering) to assess the degree of neuromuscular blockade in patients undergoing therapeutic hypothermia. 2) Optimal clinical practice suggests that a protocol should include guidance on neuromuscular-blocking agent administration in patients undergoing therapeutic hypothermia. 3) Optimal clinical practice suggests that analgesic and sedative drugs should be used prior to and during neuromuscular blockade, with the goal of achieving deep sedation. 4) Optimal clinical practice suggests that clinicians at the bedside implement measure to attenuate the risk of unintended extubation in patients receiving neuromuscular-blocking agents. 5) Optimal clinical practice suggests that a reduced dose of an neuromuscular-blocking agent be used for patients with myasthenia gravis and that the dose should be based on peripheral nerve stimulation with train-of-four monitoring. 6) Optimal clinical practice suggests that neuromuscular-blocking agents be discontinued prior to the clinical determination of brain death."
Asunto(s)
Humanos , Femenino , Adulto , Bloqueo Neuromuscular , Bloqueantes Neuromusculares , Cuidado Terminal , Enfermedad Crítica , Monitoreo Neuromuscular , Bloqueantes Neuromusculares/uso terapéutico , Unión NeuromuscularAsunto(s)
Nivel de Alerta/efectos de los fármacos , Sedación Consciente , Monitoreo de Drogas/métodos , Electroencefalografía/métodos , Hipnóticos y Sedantes/uso terapéutico , Lorazepam/uso terapéutico , Examen Neurológico/métodos , Bloqueantes Neuromusculares/uso terapéutico , Evaluación en Enfermería/métodos , Procesamiento de Señales Asistido por Computador , Sedación Consciente/efectos adversos , Sedación Consciente/métodos , Sedación Consciente/enfermería , Cuidados Críticos/métodos , Monitoreo de Drogas/enfermería , Electroencefalografía/enfermería , Humanos , Masculino , Persona de Mediana Edad , Examen Neurológico/enfermería , Neumonía/terapia , Guías de Práctica Clínica como Asunto , Respiración ArtificialAsunto(s)
Acidosis Láctica/inducido químicamente , Hipnóticos y Sedantes/efectos adversos , Hipoxia/terapia , Lorazepam/efectos adversos , Propilenglicol/envenenamiento , Insuficiencia Respiratoria/terapia , Solventes/envenenamiento , Acidosis Láctica/sangre , Combinación de Medicamentos , Humanos , Hipnóticos y Sedantes/administración & dosificación , Hipoxia/sangre , Hipoxia/complicaciones , Infusiones Intravenosas , Ácido Láctico/sangre , Lorazepam/administración & dosificación , Masculino , Persona de Mediana Edad , Concentración Osmolar , Terapia por Inhalación de Oxígeno , Respiración con Presión Positiva , Propilenglicol/administración & dosificación , Ácido Pirúvico/sangre , Insuficiencia Respiratoria/sangre , Insuficiencia Respiratoria/etiología , Solventes/administración & dosificaciónRESUMEN
Learn how neuromuscular blocking agents work and how to assess and manage a patient receiving these drugs.
Asunto(s)
Bloqueo Neuromuscular/enfermería , Bloqueantes Neuromusculares/farmacología , Unión Neuromuscular/fisiología , Analgésicos Opioides/farmacología , Interacciones Farmacológicas , Monitoreo de Drogas/enfermería , Humanos , Hipnóticos y Sedantes/farmacología , Unión Neuromuscular/efectos de los fármacos , Evaluación en EnfermeríaAsunto(s)
Ansiedad/prevención & control , Sedación Consciente/métodos , Sedación Consciente/enfermería , Cuidados Críticos/métodos , Enfermedad Crítica/terapia , Delirio/prevención & control , Dolor/prevención & control , Agitación Psicomotora/prevención & control , Adulto , Analgésicos/farmacología , Analgésicos/uso terapéutico , Antipsicóticos/farmacología , Antipsicóticos/uso terapéutico , Ansiedad/etiología , Sedación Consciente/efectos adversos , Delirio/etiología , Monitoreo de Drogas/métodos , Monitoreo de Drogas/enfermería , Humanos , Hipnóticos y Sedantes/farmacología , Hipnóticos y Sedantes/uso terapéutico , Evaluación en Enfermería/métodos , Dolor/etiología , Guías de Práctica Clínica como Asunto , Agitación Psicomotora/etiologíaAsunto(s)
Hipnóticos y Sedantes/administración & dosificación , Infusiones Intravenosas/efectos adversos , Lorazepam/administración & dosificación , Vehículos Farmacéuticos/efectos adversos , Propilenglicol/efectos adversos , Acidosis/etiología , Humanos , Masculino , Tasa de Depuración Metabólica , Persona de Mediana Edad , Vehículos Farmacéuticos/farmacocinética , Propilenglicol/farmacocinética , Desconexión del VentiladorAsunto(s)
Lesiones Encefálicas/complicaciones , Circulación Cerebrovascular/fisiología , Hipertensión Intracraneal/prevención & control , Hipertensión Intracraneal/fisiopatología , Presión Intracraneal/fisiología , Cuidados Críticos/métodos , Humanos , Hipertensión Intracraneal/etiología , Hipertensión Intracraneal/enfermería , Monitoreo FisiológicoRESUMEN
Tumors within the brain and spinal cord can have far-reaching effects on the health and long-term survival of the patient. In addition, implications of the diagnosis place stress upon the family unit. Until recently, aggressive management of these lesions carried the risk of additional neurological injury. With the rapidly expanding use of lasers, ultrasonic aspiration and real-time intraoperative ultrasonography, it is possible to aggressively resect tumors from within critical areas of the central nervous system, including the spinal cord. Additionally, it is possible to provide real-time evaluation of the operative field to assess tumor volume definition and completeness of tumor resection. This minimizes the risk of surgical injury and leads to improved patient outcomes.
Asunto(s)
Neoplasias del Sistema Nervioso Central/diagnóstico por imagen , Neoplasias del Sistema Nervioso Central/terapia , Terapia por Láser/métodos , Monitoreo Intraoperatorio/métodos , Succión/métodos , Terapia por Ultrasonido/métodos , Adulto , Terapia Combinada , Femenino , Humanos , Control de Infecciones , Terapia por Láser/instrumentación , Seguridad , Resultado del Tratamiento , Terapia por Ultrasonido/instrumentación , UltrasonografíaRESUMEN
Stereotaxis has existed since the early 1900s, originating in Western Europe. Its practice was originally limited to isolation of nerve tracts, drainage of superficial abscesses and early attempts at psychosurgery. Today, with stereotactic-compatible imaging techniques and equipment, many types of intracranial lesions can be precisely localized and resected. Stereotactic approaches to therapy, including aggressive surgical resection, have become the treatments of choice for many types of potentially devastating lesions. A case study illustrates a stereotactic resection procedure, as well as the nursing plan of care and implications for the neuroscience nurse.