2002
DOI: 10.1034/j.1399-6576.2002.460524.x
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Tachycardia and convulsions induced by accidental intravascular ropivacaine injection during sciatic block

Abstract: Ropivacaine, a recently introduced local anesthetic of the amide family (1), seems to show less toxicity than bupivacaine (2-4). Nevertheless, both neurologic and cardiovascular toxicities are possible. Six cases of ropivacaine-induced convulsions have previously been reported (5-10), of which three cases also showed cardiovascular toxicity. In three cases, total plasma concentrations were measured (Table 1).

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Cited by 47 publications
(21 citation statements)
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“…[1][2][3] However, it is a potent local anesthetic and ropivacaine-induced convulsions, cardiac dysrhythmias and even cardiac arrests have been described after unintentional intravascular injection during peripheral nerve blocks. [5][6][7][8][9][10][11][12] In a recent case report by Klein et al successful resuscitation after ropivacaine-induced ventricular fibrillation was described where resuscitation measures were successful without defibrillation. 13 Defibrillation was planned, but with the use of oxygen, propofol, intubation and chest compression, the circulation returned before the defibrillator was ready to use.…”
mentioning
confidence: 99%
“…[1][2][3] However, it is a potent local anesthetic and ropivacaine-induced convulsions, cardiac dysrhythmias and even cardiac arrests have been described after unintentional intravascular injection during peripheral nerve blocks. [5][6][7][8][9][10][11][12] In a recent case report by Klein et al successful resuscitation after ropivacaine-induced ventricular fibrillation was described where resuscitation measures were successful without defibrillation. 13 Defibrillation was planned, but with the use of oxygen, propofol, intubation and chest compression, the circulation returned before the defibrillator was ready to use.…”
mentioning
confidence: 99%
“…Em diferentes estudos, concentrações plasmáticas elevadas de ropivacaína, após anestesias regionais (de 2 a 5,6 mg.l -1 ), foram alcança-das sem toxicidade neurológica e cardíaca 16,17 . Contudo, vários acidentes após a utilização da ropivacaína têm sido relatados [18][19][20][21][22][23][24][25] . Estes acidentes foram conseqüência de injeções intravasculares diretas (início rápido) ou secundárias à absorção plasmática por excesso de dose (evento clínico tardio).…”
Section: Discussionunclassified
“…In different studies, high ropivacaine plasma concentrations after regional anesthesia (2 to 5.6 mg.L -1 ) were reached without neurological and cardiac toxicity 16,17 . However, several ropivacaine-related accidents have been reported [18][19][20][21][22][23][24][25] . These accidents were caused by direct intravascular injections (fast onset) or secondary to plasma absorption due to overdose (late clinical event).…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3][4][5] This possibility is of particular concern at the upper extremity since many of the nerve targets are located in highly vascular regions. Methods to minimize this risk include the use of slow incremental injection, the aspiration of syringes prior to injection of local anesthetic, and monitoring heart rate or T-wave amplitude changes following injection of a test dose of epinephrine.…”
Section: Résumémentioning
confidence: 99%