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1.
Anesth Analg ; 115(1): 160-9, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22467898

RESUMO

BACKGROUND: Intrathecal morphine (ITM) provides effective analgesia after posterior spinal fusion (PSF). Although most anesthetic drugs have well-characterized effects on evoked potentials, there is little data on the effects of ITM on transcranial electric motor-evoked potentials (tceMEPs). We performed this study to assess the effects of ITM on tceMEPs in the first 30 minutes after administration. We hypothesized that administration of ITM in doses currently used at our institution would not significantly affect mean tceMEP amplitudes and latencies of an ITM study group relative to control patients who did not receive the drug. METHODS: tceMEPs were recorded before ITM injection and 5, 10, 20, and 30 minutes after injection in 14 subjects ages 11 through 18 years undergoing PSF. These recordings were compared to an age-matched control group undergoing PSF in which ITM was not injected. The effects of ITM on tceMEP amplitude and latency were compared between the 2 groups. RESULTS: Fourteen subjects were enrolled in the ITM group and 16 served as controls. There were no significant differences in the baseline mean response amplitudes of the 2 groups for any of the 8 muscles studied. Mean response amplitudes over the 30-minute posttreatment period in the ITM group did not differ significantly from those of the control subjects. Average response amplitudes collapsed across all muscles for each subject were not significantly different during the baseline period (95% CI = -38% to 45%; P = 0.783), nor were they significantly different between the 2 groups during the posttreatment period (95% CI = -30% to 78%; P = 0.640). There also were no significant differences in the mean response latencies of the 2 groups in either the baseline or posttreatment periods. Average response latencies collapsed across all muscles for each subject were 4% larger for the ITM group than for controls during the baseline period (95% CI = -5% to 13%; P = 0.377), and 3% larger for the ITM group than for controls during the posttreatment period (95% CI = -4% to 12%; P = 0.359). CONCLUSIONS: Administration of ITM in doses currently used at our institution did not cause more than a 70% attenuation of mean tceMEP amplitudes or latency changes of an ITM study group relative to control subjects during the 30-minute period after injection. Further studies are required to determine if there are delayed effects after this initial time period.


Assuntos
Analgésicos Opioides/administração & dosagem , Estimulação Elétrica , Potencial Evocado Motor/efeitos dos fármacos , Monitorização Intraoperatória/métodos , Morfina/administração & dosagem , Fusão Vertebral , Adolescente , Fatores Etários , Análise de Variância , Estudos de Casos e Controles , Criança , Eletroencefalografia , Feminino , Humanos , Injeções Espinhais , Masculino , Philadelphia , Estudos Prospectivos , Tempo de Reação/efeitos dos fármacos , Fatores de Tempo
2.
Paediatr Anaesth ; 21(1): 54-61, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21155927

RESUMO

OBJECTIVE/AIMS: To assess the effect of prophylactic administration of fresh-frozen plasma (FFP) in the form of reconstituted blood in children undergoing craniofacial reconstruction. The outcomes of interest included immediate postoperative coagulation laboratory test results, postoperative surgical drain output, and the number of unique blood donor exposures incurred. BACKGROUND: We recently changed our intraoperative transfusion strategy in children undergoing craniofacial reconstruction surgery to one in which blood loss is replaced with donor-matched reconstituted blood rather than traditional blood component therapy. METHODS: We performed a query of our prospective craniofacial surgery perioperative registry for children who underwent fronto-orbital advancement or posterior cranial vault reconstruction. Registry data from this query were compared to data from a historical cohort. RESULTS: Data for 46 registry cases were compared to 150 historical cohort cases. The median number of unique donor exposures for the reconstituted blood group was 2 vs 3 in the historical cohort (P=0.004). The reconstituted blood group had a decreased incidence of postoperative derangements in soluble clotting factor tests (fibrinogen, PT, or aPTT; 2% vs 24%, P=0.001), while there was no evidence for a difference in the incidence of thrombocytopenia. There was no evidence for differences in postoperative surgical drain output in the reconstituted blood group and historical cohort over the first 12, 24, and 48 h. CONCLUSIONS: Prophylactic administration of FFP in the form of donor-matched reconstituted blood in children undergoing craniofacial reconstruction was associated with improved postoperative coagulation parameters, reduced blood donor exposures, and unchanged postoperative surgical drain output.


Assuntos
Doadores de Sangue , Transfusão de Sangue/métodos , Anormalidades Craniofaciais/cirurgia , Plasma , Procedimentos de Cirurgia Plástica , Coagulação Sanguínea , Testes de Coagulação Sanguínea , Transfusão de Componentes Sanguíneos , Perda Sanguínea Cirúrgica , Pré-Escolar , Estudos de Coortes , Craniossinostoses/cirurgia , Feminino , Humanos , Lactente , Masculino , Cuidados Pós-Operatórios , Sistema de Registros , Estudos Retrospectivos , Trombocitopenia/prevenção & controle , Resultado do Tratamento
3.
Anesth Analg ; 111(5): 1259-63, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20736433

RESUMO

BACKGROUND: Bradycardia is a complication associated with inhaled induction of anesthesia with halothane in children with Down syndrome. Although bradycardia has been reported after anesthetic induction with sevoflurane in these children, the incidence is unknown. OBJECTIVES: In this study we compared the incidence and characteristics of bradycardia after induction of anesthesia with sevoflurane in children with Down syndrome to healthy controls. METHODS: We reviewed electronic anesthetic records of 209 children with Down syndrome and 268 healthy control patients who had inhaled induction of anesthesia with sevoflurane over an 8-year period. Data extracted from the medical record included demographics, history of congenital heart disease, heart rate, oxyhemoglobin saturation, expired sevoflurane concentrations, arterial blood pressure, and any treatment of bradycardia during the first 360 seconds after the start of induction of anesthesia. Bradycardia and hypotension were defined as heart rate and arterial blood pressure below the critical limits recommended for activating a pediatric rapid response team to the bedside of a hospitalized child for quick intervention. Factors associated with bradycardia were identified in a univariate analysis. A step-wise backward multiple logistic regression model was used to identify independent factors. Differences between the 2 groups were computed using Fisher's exact test or χ(2) tests for categorical data and t tests for continuous data. RESULTS: Univariate analysis demonstrated that Down syndrome, low ASA physical status, congenital heart disease, and mean sevoflurane concentrations were factors associated with bradycardia. However, multivariate analysis showed that only Down syndrome and low ASA physical status remained as independent factors associated with bradycardia. CONCLUSION: Bradycardia during anesthetic induction with sevoflurane was common in children with Down syndrome, with and without a history of congenital heart disease.


Assuntos
Anestésicos Inalatórios/efeitos adversos , Bradicardia/induzido quimicamente , Síndrome de Down/complicações , Éteres Metílicos/efeitos adversos , Adolescente , Anestésicos Inalatórios/administração & dosagem , Pressão Sanguínea/efeitos dos fármacos , Bradicardia/epidemiologia , Bradicardia/fisiopatologia , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , Criança , Pré-Escolar , Feminino , Frequência Cardíaca/efeitos dos fármacos , Hospitais Pediátricos , Humanos , Hipotensão/induzido quimicamente , Incidência , Lactente , Modelos Logísticos , Masculino , Éteres Metílicos/administração & dosagem , Philadelphia , Estudos Retrospectivos , Medição de Risco , Fatores de Risco , Sevoflurano
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