2010
DOI: 10.1093/bja/aeq255
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Plasma ropivacaine concentrations after ultrasound-guided transversus abdominis plane block

Abstract: Transversus abdominus plane block using 3 mg kg(-1) of ropivacaine produces venous plasma concentrations that are potentially neurotoxic, although broadly consistent with plasma levels found after injection at other comparable sites.

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Cited by 176 publications
(112 citation statements)
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“…In an intravenous titration study involving healthy volunteers, the onset of minor neurological symptoms was observed at a mean total plasma ropivacaine concentration of 2.2 μg/mL, i.e., at a level comparable to the mean C max in plasma of 1.88± 0.37 μg/mL observed in our subjects [21]. Griffiths et al previously described similar C max values in plasma of 2.54± 0.75 μg/mL following the administration of 3 mg/kg body weight ropivacaine [22]. However, while their study investigated only female subjects with a median age of 43 years, only male, young volunteers were included in our study.…”
Section: Discussionsupporting
confidence: 87%
“…In an intravenous titration study involving healthy volunteers, the onset of minor neurological symptoms was observed at a mean total plasma ropivacaine concentration of 2.2 μg/mL, i.e., at a level comparable to the mean C max in plasma of 1.88± 0.37 μg/mL observed in our subjects [21]. Griffiths et al previously described similar C max values in plasma of 2.54± 0.75 μg/mL following the administration of 3 mg/kg body weight ropivacaine [22]. However, while their study investigated only female subjects with a median age of 43 years, only male, young volunteers were included in our study.…”
Section: Discussionsupporting
confidence: 87%
“…In one study, it was shown that 3 mg kg -1 of ropivacaine in the TAP block in adult women resulted in potentially toxic plasma concentrations. A relatively high dose of ropivacaine was used in that study and the volume of local anesthetics injected at each site was 20 mL [19]. In our study, we used a low volume and low concentration of bupivacaine successfully; the total dose of the injected bupivacaine was 75 mg.…”
Section: Discussionmentioning
confidence: 95%
“…A falta de ECR que comparem o desempenho pré-operatório ou pós-operatório do TAP para o mesmo procedimento cirúrgico torna impossí-vel a recomendação do tempo adequado para o bloqueio. Em comparação com o TAP concentrações diferentes 30,36 não demonstraram qualquer benefício no uso de uma dose mais elevada e, por causa dos potenciais efeitos tóxicos da AL no TAP e a possível superação de doses tóxicas, como Griffiths et al 60 demonstraram com doses de ropivacaína usadas habitualmente, se faz necessário o estudo das doses mínimas eficazes para reduzir os possíveis efeitos deletérios da AL.…”
Section: Conclusõesunclassified