Rocuronium-induced neuromuscular blockade is affected by chronic phenytoin therapy

被引:13
作者
Hernández-Palazón, J
Tortosa, JA
Martínez-Lage, JF
Pérez-Ayala, M
机构
[1] Hosp Univ Virgen Arrixaca, Dept Anesthesia, Murcia, Spain
[2] Hosp Univ Virgen Arrixaca, Dept Neurosurg, Murcia, Spain
[3] Hosp Univ Virgen Arrixaca, Dept Clin Chem, Murcia, Spain
关键词
muscle relaxants : rocuronium anticonvulsant : phenytoin;
D O I
10.1097/00008506-200104000-00003
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Patients receiving chronic anticonvulsant therapy have been reported to show resistance to certain nondepolarizing neuromuscular blockers. In this study, the effects of chronic phenytoin therapy on the onset, duration, and recovery of rocuronium action was assessed. Thirty-six patients scheduled for various neurosurgical procedures were studied: 18 receiving chronic phenytoin therapy (Group I) and 18 controls (Group II). Rocuronium 0.6 mg/kg (2 x DE95) was administered after induction of general anesthesia with 4-6 mg/kg thiopental sodium and 3-5 mug/kg intravenous (IV) fentanyl. Maintenance anesthesia consisted of N2O in O-2, 0.5% end-tidal isoflurane, and a fentanyl infusion. Neuromuscular block was monitored with acceleromyography of the adductor pollicis-brevis muscle by using a TOF-GUARD Biometer monitor (Biometer International A/S. Odense, Denmark). According to the amplitude of the first response of train-of-four, neither the lag time nor the onset time differed between the two groups. However, the recovery index was significantly shorter in patients chronically treated with phenytoin (mean recovery index: control group. 8.3 +/- 1.7 minutes: phenytoin group. 6.7 +/- 2.3 minutes: P <.05). In addition, the times of recovery to 10%, 25%. 75%, and 90% of the baseline response were also significantly shorter in the phenytoin group than in the control group. We conclude that the duration of action of rocuronium and the recovery index were affected by chronic phenytoin therapy.
引用
收藏
页码:79 / 82
页数:4
相关论文
共 31 条
[1]   Pharmacokinetic origin of carbamazepine-induced resistance to vecuronium neuromuscular blockade in anesthetized patients [J].
Alloul, K ;
Whalley, DG ;
Shutway, F ;
Ebrahim, Z ;
Varin, F .
ANESTHESIOLOGY, 1996, 84 (02) :330-339
[2]   A mechanistic approach to antiepileptic drug interactions [J].
Anderson, GD .
ANNALS OF PHARMACOTHERAPY, 1998, 32 (05) :554-563
[3]   Assessment of accelerography with the TOF-GUARD™:: a comparison with electromyography [J].
Dahaba, AA ;
Rehak, PH ;
List, WF .
EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 1997, 14 (06) :623-629
[4]   PRESYNAPTIC AND POSTSYNAPTIC DEPRESSANT EFFECTS OF PHENYTOIN SODIUM AT THE NEUROMUSCULAR-JUNCTION [J].
GAGE, PW ;
LONERGAN, M ;
TORDA, TA .
BRITISH JOURNAL OF PHARMACOLOGY, 1980, 69 (01) :119-121
[5]   THE EFFECT OF ACUTELY ADMINISTERED PHENYTOIN ON VECURONIUM-INDUCED NEUROMUSCULAR BLOCKADE [J].
GRAY, HSJ ;
SLATER, RM ;
POLLARD, BJ .
ANAESTHESIA, 1989, 44 (05) :379-381
[6]   PHENYTOIN-INDUCED RESISTANCE TO PANCURONIUM - USE OF ATRACURIUM INFUSION IN MANAGEMENT OF A NEUROSURGICAL PATIENT [J].
HICKEY, DR ;
SANGWAN, S ;
BEVAN, JC .
ANAESTHESIA, 1988, 43 (09) :757-759
[7]   ACCELERATED RECOVERY FROM PIPECURONIUM IN PATIENTS TREATED WITH CHRONIC ANTICONVULSANT THERAPY [J].
JELLISH, WS ;
MODICA, PA ;
TEMPELHOFF, R .
JOURNAL OF CLINICAL ANESTHESIA, 1993, 5 (02) :105-108
[8]   Recovery from mivacurium-induced neuromuscular blockade is not affected by anticonvulsant therapy [J].
Jellish, WS ;
Thalji, Z ;
Brundidge, PK ;
Tempelhoff, R .
JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY, 1996, 8 (01) :4-8
[9]   DECREASED SENSITIVITY TO METOCURINE DURING LONG-TERM PHENYTOIN THERAPY MAY BE ATTRIBUTABLE TO PROTEIN-BINDING AND ACETYLCHOLINE-RECEPTOR CHANGES [J].
KIM, CS ;
ARNOLD, FJ ;
ITANI, MS ;
MARTYN, JAJ .
ANESTHESIOLOGY, 1992, 77 (03) :500-506
[10]  
Koenig A, 1999, C++ REP, V11, P8