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1.
Rev Esp Anestesiol Reanim ; 57(2): 109-14, 2010 Feb.
Artículo en Español | MEDLINE | ID: mdl-20337003

RESUMEN

Acquired long QT syndrome is a rare condition whose diagnosis is of vital importance given the risk of torsade de pointes and sudden death. This syndrome may be triggered by various events in patients with a genetic predisposition. Patients usually have a normal baseline QT interval. Some of the factors that may prolong the interval are exposure to common drugs such as antibiotics or agents used for general anesthesia. Diagnosis of the condition is essential, as is knowledge of how to manage anesthesia and prevent ventricular fibrillation, which is the most feared complication. We report the case of a man with no relevant medical history who underwent emergency surgery for a peritonsillar abscess. The patient developed long QT syndrome, with several episodes of torsade de pointes and cardiorespiratory arrest.


Asunto(s)
Paro Cardíaco/etiología , Síndrome de QT Prolongado/etiología , Absceso Peritonsilar/cirugía , Complicaciones Posoperatorias/etiología , Torsades de Pointes/etiología , Fibrilación Ventricular/etiología , Adyuvantes Anestésicos/efectos adversos , Antagonistas Adrenérgicos beta/uso terapéutico , Combinación Amoxicilina-Clavulanato de Potasio/uso terapéutico , Anestésicos por Inhalación/efectos adversos , Antibacterianos/uso terapéutico , Antiinfecciosos/efectos adversos , Antiinfecciosos/farmacología , Antiinfecciosos/uso terapéutico , Terapia Combinada , Drenaje , Cardioversión Eléctrica , Paro Cardíaco/terapia , Humanos , Síndrome de QT Prolongado/tratamiento farmacológico , Masculino , Éteres Metílicos/efectos adversos , Metronidazol/efectos adversos , Metronidazol/farmacología , Metronidazol/uso terapéutico , Persona de Mediana Edad , Absceso Peritonsilar/complicaciones , Absceso Peritonsilar/tratamiento farmacológico , Complicaciones Posoperatorias/tratamiento farmacológico , Compuestos de Amonio Cuaternario/efectos adversos , Sevoflurano , Torsades de Pointes/tratamiento farmacológico , Fibrilación Ventricular/terapia
2.
Rev Esp Anestesiol Reanim ; 55(4): 217-26, 2008 Apr.
Artículo en Español | MEDLINE | ID: mdl-18543504

RESUMEN

OBJECTIVE: To analyze the frequency and methods of sedation used in the context of regional anesthesia in adults by means of a national survey. MATERIAL AND METHODS: We carried out a survey of participants at the courses of an anesthesiology training organization (Fundación Europea de Enseñanza en Anestesiología), held in Spain in 2006. The survey questionnaires asked about indications for sedation used during surgery under regional anesthesia as well as the form of administration, follow-up, and complications. RESULTS: A total of 375 questionnaires were sent out and 185 responses were received (49.3%). Sedation is always used to accompany regional anesthesia by 69.2% of the respondents; 13.5% of them discuss the technique to be used with the patient and come to an agreement. The same type of sedation, regardless of the regional block performed, is used by 49.2% of respondents, and 64.3% use a scale to evaluate the level of sedation. The most favored sedation technique is continuous infusion, followed by target controlled infusion and boluses on demand. The most commonly used technique is sedation with bolus injections. Sixty percent use a single agent and 38.9% use combinations. The most commonly reported adverse effects are variability of patient response (53.5%) and respiratory complications (27%). In cases of ineffective regional blockade, 49.2% of those surveyed switch to general anesthesia. CONCLUSIONS: Sedation is very often used to complement regional anesthesia in adult patients. Even though continuous infusion is considered to be the most appropriate form of administration, the most commonly used form is injection of boluses. Sedation with a single drug is used more frequently than drug combinations. Variability of individual response is the complication most commonly reported by the respondents.


Asunto(s)
Anestesia de Conducción , Sedación Consciente/estadística & datos numéricos , Adyuvantes Anestésicos/administración & dosificación , Adulto , Sedación Consciente/efectos adversos , Sedación Consciente/métodos , Recolección de Datos , Femenino , Humanos , Hipnóticos y Sedantes/administración & dosificación , Hipnóticos y Sedantes/efectos adversos , Infusiones Intravenosas , Inyecciones Intravenosas , Complicaciones Intraoperatorias/epidemiología , Complicaciones Intraoperatorias/etiología , Masculino , Midazolam/administración & dosificación , Persona de Mediana Edad , Complicaciones Posoperatorias/epidemiología , Complicaciones Posoperatorias/etiología , Pautas de la Práctica en Medicina/estadística & datos numéricos , España , Encuestas y Cuestionarios
3.
Rev Esp Anestesiol Reanim ; 53(7): 426-36, 2006.
Artículo en Español | MEDLINE | ID: mdl-17066862

RESUMEN

Few pharmacologically new anesthetics have appeared in recent years, but great progress has been made toward improving some existing ones. Such is the case with propofol. New formulations have been developed to reduce or avoid adverse side effects associated with the original drug produced by Astra-Zeneca. The unwanted effects for which solutions have been sought are pain upon intravenous injection of the drug, elevated serum concentrations of triglycerides, and the risk of bacterial contamination. Some new formulations contain excipients with bactericidal action, such as propofol with ethylenediaminetetraacetic acid or metabisulfite, and others use lipuro rather than intralipid. Other more advanced products are propofol in cyclodextrin or IDD-D propofol, which makes use of nanoparticle technology. A grasp of the pharmacokinetics and pharmacodynamics of the original formulation must be the basis for understanding the differences between these new products.


Asunto(s)
Anestésicos Intravenosos , Propofol , Anestésicos Intravenosos/farmacocinética , Anestésicos Intravenosos/farmacología , Humanos , Propofol/farmacocinética , Propofol/farmacología
4.
Rev Esp Anestesiol Reanim ; 63(4): 197-206, 2016 Apr.
Artículo en Inglés, Español | MEDLINE | ID: mdl-26675536

RESUMEN

OBJECTIVES: For major laparoscopic surgery, as with open surgery, a multimodal analgesia plan can help to control postoperative pain. Placing a wound catheter intraoperatively following colon surgery could optimize the control of acute pain with less consumption of opioids and few adverse effects. METHODS: We conducted a prospective, randomized, study of patients scheduled to undergo laparoscopic colon surgery for cancer in Galdakao-Usansolo Hospital from January 2012 to January 2013. Patients were recruited and randomly allocated to wound catheter placement plus standard postoperative analgesia or standard postoperative analgesia alone. A physician from the acute pain management unit monitored all patients for pain at multiple points over the first 48 hours after surgery. The primary outcome variables were verbal numeric pain scale scores and amount of intravenous morphine used via patient controlled infusion. RESULTS: 92 patients were included in the study, 43 had a wound catheter implanted and 49 did not. Statistically significant differences in morphine consumption were observed between groups throughout the course of the treatment period. The mean total morphine consumption at the end of the study was 5.63±5.02mg among wound catheter patients and 21. 86±17.88mg among control patients (P=.0001). Wound catheter patients had lower pain scale scores than control patients throughout the observation period. No adverse effects associated with the wound catheter technique were observed. The wound catheter group showed lower hospital stays with statistically significant difference (P=.02). CONCLUSIONS: In patients undergoing laparoscopic colon surgery, continuous infusion of local anaesthetics through interfascial wound catheters during the first 48h aftersurgery reduced the level of perceived pain and also reduced parenteral morphine consumption with no associated adverse effects and lower hospital stays.


Asunto(s)
Enfermedades del Colon , Dolor Postoperatorio/tratamiento farmacológico , Analgesia Controlada por el Paciente , Analgésicos Opioides , Anestésicos Locales , Humanos , Morfina , Manejo del Dolor , Dimensión del Dolor , Estudios Prospectivos
11.
Clin Exp Dermatol ; 27(2): 115-7, 2002 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11952701

RESUMEN

We report a 38-year-old man who presented with a generalized papular eruption that was clinically and histologically consistent with lichen nitidus. This patient's condition had been persistent for approximately 1 year; however, soon after assuming employment that entailed significant, regular sun exposure, the patient noted marked clearing of his lesions in sun-exposed areas. This case corroborates previous reports that suggest that generalized lichen nitidus can be successfully managed with ultraviolet light therapy.


Asunto(s)
Liquen Nítido/terapia , Terapia Ultravioleta/métodos , Adulto , Humanos , Masculino , Remisión Espontánea , Luz Solar
12.
Anaesthesia ; 43(11): 955-7, 1988 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-2975150

RESUMEN

A 38-year-old woman developed symptoms of anaphylactic shock after intravenous atropine and required adrenaline to maintain perfusion pressure. A strongly positive response was obtained on intradermal testing. The Prausnitz-Kuestner test was also positive, which indicated the presence of drug specific IgE antibodies. No response was obtained after hyoscine.


Asunto(s)
Anafilaxia/inducido químicamente , Atropina/efectos adversos , Adulto , Erupciones por Medicamentos/etiología , Femenino , Humanos , Pruebas Intradérmicas
13.
Anesthesiology ; 88(3): 624-8, 1998 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-9523804

RESUMEN

BACKGROUND: Hyperbaric 5% lidocaine has been associated with transient neurologic symptoms (TNSs) after spinal anesthesia. A prospective, masked, randomized study was conducted to compare the incidence of TNSs after spinal anesthesia with hyperbaric 5% lidocaine or 5% prilocaine to assess the utility of prilocaine as an alternative to lidocaine in patients having short surgical procedures. METHODS: The number of patients to be enrolled (100 per group) was determined by power analysis (80%, P = 0.05) considering an incidence of TNSs after spinal anesthesia with lidocaine of at least 11% according to data reported in other studies. Two hundred patients scheduled for elective surgery expected to last <60 min were allocated at random to receive spinal anesthesia with hyperbaric 5% lidocaine or hyperbaric 5% prilocaine. Three to 5 days after spinal anesthesia, all patients were interviewed by an anesthesiologist who was blinded to the group assignment and details of the anesthetic and surgical technique using a standardized symptom checklist. Patients with symptoms underwent neurologic examination. RESULTS: Both groups were comparable with regard to demographic data and details of the surgical and anesthetic procedures. The incidence of TNSs in both groups was low and differences were not found (4% in the lidocaine group and 1% in the prilocaine group). The mean age of patients with TNSs (58 yr) was higher than that of patients without TNSs (48 yr; P < 0.05). No relation with any of the other variables was found. CONCLUSIONS: The low incidence of TNSs among lidocaine-anesthetized patients (4%) may account for the lack of significant differences between hyperbaric 5% lidocaine and 5% prilocaine and to the insufficient power of the study to exclude the possibility of a type II error.


Asunto(s)
Anestesia Raquidea/efectos adversos , Lidocaína/efectos adversos , Enfermedades del Sistema Nervioso/inducido químicamente , Prilocaína/efectos adversos , Adulto , Anciano , Presión Atmosférica , Dolor de Espalda/inducido químicamente , Femenino , Humanos , Masculino , Persona de Mediana Edad , Factores de Tiempo
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