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Comparison of patient-controlled epidural bolus administration of 0.1% ropivacaine and 0.1% levobupivacaine, both with 0.0002% fentanyl, for analgesia during labour.
Purdie, N L; McGrady, E M.
Afiliação
  • Purdie NL; University Department of Anaesthesia, Glasgow Royal Infirmary, Alexandra Parade, Glasgow, G31 2ER, UK. niall.purdie@utoronto.ca
Anaesthesia ; 59(2): 133-7, 2004 Feb.
Article em En | MEDLINE | ID: mdl-14725515
ABSTRACT
The aim of the study was to compare the relative potencies and clinical characteristics of epidural ropivacaine and levobupivacaine in labour using patient-controlled epidural analgesia (PCEA). In a randomised double-blinded study, 60 ASA I or II primigravidae requesting epidural analgesia in early labour were allocated to receive either 0.1% ropivacaine with fentanyl 0.0002% or 0.1% levobupivacaine with 0.0002% fentanyl via a patient-controlled analgesia pump. Analgesia was established with 15 ml of study solution and maintained using 5-ml boluses of study solution with a 5-min lockout interval. There were no significant differences in onset time, duration and quality of analgesia, motor and sensory blockade, local anaesthetic consumption, mode of delivery, neonatal outcome or maternal satisfaction between the groups. We conclude that 0.1% ropivacaine with 0.0002% fentanyl and 0.1% levobupivacaine with 0.0002% fentanyl are clinically indistinguishable for labour analgesia and appear pharmacologically equipotent when using PCEA.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bupivacaína / Analgesia Epidural / Analgesia Obstétrica / Analgesia Controlada pelo Paciente / Amidas Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Anaesthesia Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Reino Unido
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bupivacaína / Analgesia Epidural / Analgesia Obstétrica / Analgesia Controlada pelo Paciente / Amidas Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Anaesthesia Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Reino Unido