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1.
Anesth Analg ; 131(2): 510-517, 2020 08.
Artículo en Inglés | MEDLINE | ID: mdl-31490817

RESUMEN

BACKGROUND: Pupillometry monitoring under general anesthesia is based on the assumption that pupillary diameter variations reflect the adequacy of the provided analgesia to the intensity of the nociceptive surgical stimulus. The accurate interpretation of pupillometric data requires establishing clearly what the expected baseline unstimulated pupillary diameter at each specific level of hypnosis is. Opioids decrease pupillary diameter in a dose-dependent fashion. In contrast, the effects of hypnotic drugs on pupillary diameter are not well known. Our aim was to describe the potential relationship between propofol predicted effect-site concentrations (Cets) ranging from 1 to 3 µg/mL and pupillary diameter. METHODS: Patients were randomized to receive propofol by target-controlled infusion at a predicted Cet of 1, 2, or 3 µg/mL (groups P1, P2, and P3, respectively). Pupillary diameter measurements were performed after 10 minutes of steady-state propofol infusion at the randomized Cet. No stimulation was performed during the study. Heart rate and bispectral index (BIS) were continuously recorded. RESULTS: Forty patients were included: (13, 14, and 13 in groups P1, P2, and P3, respectively). Mean pupillary diameter was 5.7 mm (1 mm) in group P1, 4.8 mm (1.3 mm) in group P2, and 3.3 mm (0.8 mm) in group P3. Propofol had a dose-dependent effect on pupillary diameter (linear regression R = 0.45, P < .001). Pupillary diameter was positively correlated with the BIS (Spearman r = 0.75 [95% confidence interval (CI), 0.54 to -0.87] P < .001). CONCLUSIONS: From 1 to 3 µg/mL of predicted Cet, propofol has a dose-dependent effect on pupillary diameter. Within this concentrations range, there is a positive correlation between BIS and pupillary diameter. The subcortical effect of propofol on pupillary diameter is correlated to its effect on the cortex. Studies assessing pupillary diameter as a marker of the nociception-antinociception balance should be performed in patients with a standardized depth of hypnosis.


Asunto(s)
Anestésicos Intravenosos/administración & dosificación , Hipnóticos y Sedantes/administración & dosificación , Monitoreo Intraoperatorio/métodos , Propofol/administración & dosificación , Pupila/efectos de los fármacos , Adolescente , Adulto , Relación Dosis-Respuesta a Droga , Método Doble Ciego , Femenino , Humanos , Masculino , Estudios Prospectivos , Pupila/fisiología , Adulto Joven
2.
Eur Spine J ; 25(10): 3316-3323, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27155826

RESUMEN

PURPOSE: Acute pancreatitis is a possible complication after scoliosis surgery. Although some risk factors have been documented in the literature, clinical description of pancreatitis diagnosis and ensuing course still remain very poor. The aim of this study was to describe characteristics of acute pancreatitis after scoliosis surgery. METHODS: A descriptive, retrospective and single-center study of fourteen adolescents with postoperative acute pancreatitis after spine fusion surgery in scoliosis management between April 2003 and August 2012 was performed. RESULTS: Acute pancreatitis occurred within 9.5 days (4-51) after surgery. Abdominal pain was atypical and was expressed in only half of the children. Ileus, nausea and vomiting were the most frequent signs. None of the acute pancreatitis cases was severe. CONCLUSION: Acute pancreatitis is an early complication of scoliosis surgery. Clinical signs are atypical and non-severe and can induce misleading forms. Presence of delayed digestive problems should alert the clinician to the risk of pancreatitis in the aftermath of scoliosis surgery.


Asunto(s)
Pancreatitis/diagnóstico , Complicaciones Posoperatorias/diagnóstico , Escoliosis/cirugía , Enfermedad Aguda , Adolescente , Niño , Femenino , Estudios de Seguimiento , Humanos , Masculino , Pancreatitis/etiología , Estudios Retrospectivos , Resultado del Tratamiento , Adulto Joven
3.
Eur J Pediatr ; 172(7): 991-3, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-23224344

RESUMEN

UNLABELLED: Button battery ingestion in children is not a rare occurrence and may be unwitnessed and can be soon life-threatening or responsible for severe sequelae. We report herein an original history of previously healthy 16-month-old boy with an unwitnessed and misdiagnosis of lithium cell coin battery ingestion which leads to bilateral vocal palsy. The patient underwent a unilateral posterior cordotomy and was successfully extubated. CONCLUSION: Early recognition of a lithium cell coin battery for rapid removal, even if insufficient at first, is the main condition to limit complications. Unusual upper respiratory distress in a young child should alert practitioners in performing a chest and neck X-ray without undue delay.


Asunto(s)
Esófago/diagnóstico por imagen , Cuerpos Extraños/complicaciones , Parálisis de los Pliegues Vocales/etiología , Pliegues Vocales/cirugía , Crup/diagnóstico , Errores Diagnósticos , Suministros de Energía Eléctrica , Cuerpos Extraños/cirugía , Humanos , Lactante , Intubación Intratraqueal , Masculino , Radiografía , Parálisis de los Pliegues Vocales/diagnóstico , Parálisis de los Pliegues Vocales/cirugía
6.
Crit Care Med ; 32(2): 565-8, 2004 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-14758180

RESUMEN

OBJECTIVE: In children, like in adults, tracheal intubation is a painful procedure that may induce hypertension, tachycardia, and other undesirable hemodynamic disorders. Although premature neonates are very sensitive to pain and vulnerable to its long-term effects, the need for sedation before tracheal intubation is still discussed in neonatal units. Our objective was to investigate the practice of premedication before tracheal intubation in neonatal and pediatric units and determine the influence of premedication on intubating conditions. DESIGN: We performed a 10-day prospective survey in 75 neonatal and pediatric intensive care units among the 98 licensed in France. A questionnaire was completed for each intubation performed in each surveyed unit. SUBJECTS: A total of 204 patients were studied: 140 neonates, 52 infants, and 12 children. MAIN RESULTS: Data on 204 tracheal intubations were collected from 223 that were performed during the study period (participation rate, 91.4%). Premedication was used before intubation for 37.1%, 67.3%, and 91.7% of neonates, infants, and children, respectively (p <.0001). In the subgroup of neonates, premedication was particularly rare for the youngest and the smallest infants. Midazolam was the principle hypnotic used in neonates, whereas propofol was mainly used in children. Opioids or muscle relaxants were used in 16.2% and 4.4% of the patients, respectively. A low success rate and a high incidence of hypoxemia and bradycardia were correlated with the inexperience of the operator. Premedication did not significantly influence either the success rate or the undesirable events associated with tracheal intubation. CONCLUSION: Use of premedication before tracheal intubation is limited in neonates and increases according to the age of the patient. Midazolam does not seem to be an accurate choice to improve intubating conditions in neonates and infants. Because tracheal intubation is a technique that requires a skill only developed by regular practice, operators who have limited experience with intubating children should be supported by senior operators.


Asunto(s)
Anestesia , Sedación Consciente , Intubación Intratraqueal , Niño , Preescolar , Humanos , Lactante , Recién Nacido , Unidades de Cuidados Intensivos , Intubación Intratraqueal/métodos , Estudios Prospectivos , Encuestas y Cuestionarios
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