2013
DOI: 10.2147/opth.s43553
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Efficacy and safety of 0.5% levobupivacaine versus 0.5% bupivacaine for peribulbar anesthesia

Abstract: BackgroundThis randomized double-blind study examined the use of a new anesthetic agent, levobupivacaine 0.5%, which is the S(−)-enantiomer of a racemic mixture of bupivacaine, for peribulbar anesthesia and compared it with racemic bupivacaine 0.5% alone or in combination with hyaluronidase 10 IU/mL.MethodsA total of 160 patients undergoing ophthalmic surgery were randomized into four groups (n = 40 each) to receive inferotemporal peribulbar injection of levobupivacaine 0.5% (group L), racemic bupivacaine 0.5%… Show more

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Cited by 15 publications
(19 citation statements)
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“…It is produced during the degradation of lysine and, in humans, it accumulates in the body fluids causing pipecolic acidemia in subjects suffering from Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease 2. A wide range of pharmacologically active compounds with a pipecolic acid fragment in their structure are known, for example the local anaesthetic analogue ropivacaine (Figure 2),3 the immunosuppressive agents rapamycin1c,4 and FK506,1c,5 and the antitumor antibiotic, sandramycin 6. Among its derivatives, 3‐, 4‐, and 5‐hydroxy‐substituted pipecolic acids 2 – 7 are natural compounds that play an important role in medicinal chemistry either as molecular scaffolds and α‐amino acid analogues for the preparation of conformationally restricted peptides and pharmaceutically active compounds or because they are essential structural components of naturally occurring compounds possessing noteworthy biological activity 1a,1b.…”
Section: Introductionmentioning
confidence: 99%
“…It is produced during the degradation of lysine and, in humans, it accumulates in the body fluids causing pipecolic acidemia in subjects suffering from Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease 2. A wide range of pharmacologically active compounds with a pipecolic acid fragment in their structure are known, for example the local anaesthetic analogue ropivacaine (Figure 2),3 the immunosuppressive agents rapamycin1c,4 and FK506,1c,5 and the antitumor antibiotic, sandramycin 6. Among its derivatives, 3‐, 4‐, and 5‐hydroxy‐substituted pipecolic acids 2 – 7 are natural compounds that play an important role in medicinal chemistry either as molecular scaffolds and α‐amino acid analogues for the preparation of conformationally restricted peptides and pharmaceutically active compounds or because they are essential structural components of naturally occurring compounds possessing noteworthy biological activity 1a,1b.…”
Section: Introductionmentioning
confidence: 99%
“…al, 2001;Hamada et al, 2005;Remy et al, 2008;Pacella et al, 2013) bem como a diminuição de efeitos adversos pós-anestesia (Hamada et al, 2005), sendo utilizada quase que exclusivamente com sucesso para anestesia oftalmológica. Os estudos mais recentes em oftalmologia testam anestésicos diversos, alcalinizados ou não, mas todos utilizam a HIA como padrão de comparação com novos fármacos ou técnicas (Islam et al, 2012;Gordazi et al, 2011;Pacella et al, 2010;Jaichandran et al, 2010).…”
Section: Discussionunclassified
“…Quanto à metodologia para avaliação do bloqueio da função sensitiva, optamos pela utilização dos testes com o analgesímetro (que avalia reflexo de retirada da pata) (Araujo et al, 2006) e de pinçamento da pata Popitz-Bergez et al, 1995) (Dempsey et al,1997, Mantovani et al, 2001Pacella et al, 2013) Esperava-se um resultado favorável com a utilização de diluições, com base em indícios já conhecidos na literatura de que a citotoxicidade dos anestésicos locais são tempo e dose dependentes (Perez-Castro et al, 2009;Yang et al, 2011) e acentuado pelo uso de nanotecnologia que possibilita a utilização de quantidades menores de anestésicos (Okamoto et al, 1999). Ademais, as CD apresentam, ainda, a vantagem de alterar a duração e intensidade do efeito dos fármacos devido à baixa absorção sistêmica dos complexos (Araújo et al, 2003) e por possibilitar que o fármaco permaneça por mais tempo restrito ao sítio de injeção (De Paula et al, 2010).…”
Section: Discussionunclassified
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