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1.
Br J Anaesth ; 88(6): 809-13, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12173198

RESUMO

BACKGROUND: Ropivacaine has been claimed to produce less motor block than bupivacaine during epidural analgesia. However, this advantage has not been clearly confirmed in obstetric studies using low analgesic concentrations in a ratio close to that suggested to be equianalgesic. METHODS: This double-blind, randomized, prospective study was performed in 140 parturients who requested epidural analgesia. After a lumbar epidural catheter had been placed, patients received either 0.10% bupivacaine plus sufentanil 0.5 microgram ml-1 or 0.15% ropivacaine plus sufentanil 0.5 microgram ml-1 followed by a continuous infusion. Additional boluses were used for inadequate levels of analgesia. Visual analogue pain scores, motor block, level of sensory block, supplementary boluses and main characteristics of labour were recorded. RESULTS: No differences were observed between the two groups for pain scores, total volume of anaesthetic solution used [59 (23) and 57 (24) ml in the bupivacaine and ropivacaine groups respectively], duration of labour, mode of delivery, side-effects or satisfaction score. The incidence of motor block was not statistically different between the groups (54 and 69% in the bupivacaine and ropivacaine groups respectively, P = 0.07). However, when motor block occurred, survival analysis showed that it occurred sooner in the course of labour with ropivacaine compared with bupivacaine (log rank test, P = 0.012). CONCLUSION: Combined with sufentanil 0.5 microgram ml-1, 0.10% bupivacaine and 0.15% ropivacaine produce effective and equivalent analgesia during labour, with similar incidences of motor block.


Assuntos
Amidas , Analgesia Epidural/métodos , Analgesia Obstétrica/métodos , Analgésicos Opioides , Adulto , Bupivacaína , Método Duplo-Cego , Combinação de Medicamentos , Feminino , Humanos , Movimento/efeitos dos fármacos , Medição da Dor , Gravidez , Estudos Prospectivos , Ropivacaina , Sufentanil
2.
J Fr Ophtalmol ; 23(4): 375-9, 2000 Apr.
Artigo em Francês | MEDLINE | ID: mdl-10794988

RESUMO

We present one case of acquired Toxoplasma gondii retinochoroiditis after livrer transplantation. Three weeks after receiving liver transplant from a seropositive donor for Toxoplasma gondii, the fundus examination showed a vitreal haze and an edematous retinal lesion with retinal hemorrhages. Routine screening tests for uveitis were performed. The serum toxoplasmosis titers revealed a seroconversion for toxoplasmosis (pre-transplantation tests were negative). The PCR assay on aqueous humor resulted in an amplified product identical to toxoplasmosis. This immunocompromised patient likely received an infected hepatic transplant. The patient's ocular inflammation cleared on 1-month pyrimethamine-sulfadiazine medication. Four months later, the patient developed a retinal detachment with massive proliferative vitreoretinopathy.


Assuntos
Transplante de Fígado , Complicações Pós-Operatórias , Toxoplasmose Ocular/transmissão , Uveíte/etiologia , Adulto , Antiprotozoários/uso terapêutico , Feminino , Angiofluoresceinografia , Humanos , Pirimetamina/uso terapêutico , Sulfadiazina/uso terapêutico , Toxoplasmose Ocular/diagnóstico , Toxoplasmose Ocular/tratamento farmacológico , Uveíte/diagnóstico
3.
Ann Fr Anesth Reanim ; 18(8): 843-7, 1999 Oct.
Artigo em Francês | MEDLINE | ID: mdl-10575499

RESUMO

OBJECTIVE: In France, a preanaesthetic assessment (PAA) several days prior to hospital admission for a scheduled surgical or diagnostic procedure under anaesthesia, associated with a preanaesthetic visit (PAV) the day before, are compulsory. This study aimed at comparing the benefits of PAA with those of a PAV not preceded by a PAA. STUDY DESIGN: Prospective, controlled, randomized study. PATIENTS: The study included 296 patients undergoing either a urologic, or ophthalmologic, or ENT procedure, randomly allocated either to a PAA (followed by a PAV) group or a PAV (without previous PAA) group. METHODS: The main criterion of comparison was the duration of preanaesthetic hospital stay and the secondary criteria were the incidence of procedure postponements and patients' satisfaction respectively. RESULTS: In the PAA group, the preanaesthetic hospital stay was shorter by 0.4 days (P = 0.001). Out of the 19 postponed procedures (7%), the cause of postponement was a medical one in 15 patients: 13 in the PAV group and 2 in the PAA group respectively (P = 0.009). The PAA was not considered as a constraint by most patients. CONCLUSION: The PAA shortens the duration of preanaesthetic hospital stay and decreases the incidence of procedures postponed for a medical cause.


Assuntos
Anestesiologia , Encaminhamento e Consulta , Análise de Variância , Anestesia Geral , Feminino , França , Hospitalização , Humanos , Incidência , Tempo de Internação , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Procedimentos Cirúrgicos Oftalmológicos , Procedimentos Cirúrgicos Otorrinolaringológicos , Admissão do Paciente , Satisfação do Paciente , Estudos Prospectivos , Fatores de Tempo , Procedimentos Cirúrgicos Urológicos
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