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1 ns with cisatracurium vs. 35 to 85 mins with atracurium).
2  long-term, relatively high-dose infusion of atracurium.
3 tized patients displayed a negative BAT with atracurium.
4 .2 microg/kg/min, and for patients receiving atracurium 10.4 +/- 0.9 microg/kg/min.
5  Train-of-Four ratio (cisatracurium 60 mins, atracurium 57 mins), although there was considerable int
6 f the infusion, and plasma concentrations of atracurium and laudanosine were measured at, and after,
7 t patients with perioperative anaphylaxis to atracurium and seven individuals experiencing perioperat
8                                              Atracurium and vecuronium were the most commonly used ag
9                  Cisatracurium, an isomer of atracurium, appears to be a suitable agent for providing
10  or best clinical assessment while receiving atracurium by continuous infusion.
11                      However, metocurine and atracurium could potentiate the responses of fetal-type
12                                       Of the atracurium-exposed individuals with a negative atracuriu
13                         The patient received atracurium for 38 days, at rates ranging from 0.3 to 0.9
14 ndepolarizing neuromuscular blocking agents (atracurium, gallamine, metocurine, and pancuronium) to a
15                                       Use of atracurium in high doses or for a long period of time ha
16 The BAT proves to be a useful diagnostic for atracurium-induced anaphylaxis and may be complementary
17       Despite long-term use of high doses of atracurium infusion and the increased elimination half-l
18 asured at, and after, the termination of the atracurium infusion.
19                                   Allergy to atracurium is a rare condition with serious consequences
20                                              Atracurium is sometimes used for muscle relaxation in pa
21 +/- 4.2 [SEM] hrs), and 21 patients received atracurium (mean duration 46.1 +/- 5.8 hrs).
22 ity of the basophil activation test (BAT) in atracurium sensitization and to investigate its role in
23                   ROC analyses between eight atracurium-sensitized patients and seven nonexposed cont
24 racurium-exposed individuals with a negative atracurium skin test (ST), two individuals had a clear p
25          Although most patients demonstrated atracurium tolerance over time, there was no difference
26                     Basophil activation with atracurium was analysed flow cytometrically.
27                                          BAT atracurium was positive in one cisatracurium-sensitized
28  by continuous infusions of cisatracurium or atracurium were administered.
29            The interaction of metocurine and atracurium with acetylcholine at fetal-type receptors co

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