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SUXAMETHONIUM
ROCURONIUM FOR INTUBATION
Indian J.BHATIA,
Anaesth.TULSIANI
2004; 48 :(2)
: 129-133
129
Methods
After obtaining institutional ethical committee
clearence the study was carried out on 40 patients in the
department of anaesthesiology, Dr. S.N. Medical College,
Jodhpur. The patients were randomly selected from either
sex and between 16 to 60 years. Patients, excluded from
the study were pregnant females, patients suffering from
neuromuscular disorders, obese patients and patients with
ASA grade III and IV.
130
Jaw relaxation
(Laryngoscopy)
Vocal
cords
Response to
intubation
Poor (impossible)
Closed
Severe coughing
or bucking
Minimal (difficult)
Closed
Mild coughing
Moderate (fair)
Moving
Slight diaphragmatic
movement
Good (easy)
Open
None
Group - B (n=20)
Age (yrs.)
Range
18-58
19-60
Mean
35.79
35.26
S.D.
12.81
14.84
p>0.1
Sex
M:F
11:9
11:9
Range
42-68
38-76
Mean
58.95
64.74
S.D.
8.172
12.33
0.05<p<0.1
Group - B
Range
58-68
71-90
Mean
65.89
87.94
S.D.
4.63
5.90
Range
198-474
1482-1920
Mean
318.0
1705.8
S.D.
60.0
132.0
P<0.001
Duration of action (sec)
P<0.001
Group - B
Range
1-9
4-9
Mean
7.368
7.789
S.D.
2.068
1.274
p>0.1
Complications
131
Group - B
No.
No.
Bradycardia
10
Tachycardia
10
50
12
60
Laryngospasm
V.P.B.S.
Others
Nil
30
30
Discussion
Traditionally suxamethonium has been the
neuromuscular blocking drug of choice for rapid sequence
induction and minimizing the chances of regurgitation and
aspiration. The use of suxamethonium can however be
associated with many side effects. Hence, a non depolarising
neuromuscular blocker with a rapid onset of action,
preferably of a shorter duration is desirable.
Initial studies in animals showed that rocuronium,
being a low potency compound, was associated with a
rapid onset of effect when compared with other compounds
such as pancuronium and vecuronium.2,3 This has since
been demonstrated in many clinical studies that the onset
of action of rocuronium is significantly faster when
compared to equipotent doses of atracurium and vecuronium,
although slightly slower than that of suxamethonium.4 Thats
why rocuronium was selected for the purpose of rapid
sequence induction, in the present study.
Initial studies in animals demonstrated rocuronium
to be 10-20% as potent as vecuronium and ED90 doses were
found to be from 0.26 mgkg-1 to 0.30 mgkg-1.5 Intubating
dose of rocuronium used in this study is 600 gmkg-1
(i.e. 2xED90).
Previous studies have shown that intubating
conditions at 60 secs are generally excellent or good with
a dose of 0.6 mgkg-1 and are 95% clinically acceptable at
45 seconds.6,7,8 Although Prien and Zann9 have used
rocuronium 0.3 mgkg -1 (1xED 90) under alfentanil/
propofol and fentanly/thiopentone/enflurane anaesthesia
but they required a deeper plane of anaesthesia as a
prerequisite for this low dose relaxant technique to facilitate
tracheal intubation. Onset time was found to be 657 secs
and 6912 secs in propofol/alfentanil and fentanyl/
thiopentone/enflurane groups respectively. The intubating
conditions were good or excellent in majority of cases but
slight muscular reactions to tube placement occurred
frequently. The extra anaesthetic depth needed, coupled
Clinical judgement
2.
3.
132
Clinically
non acceptable
Authors
Year
Puhringer et al7
1992
Roc.
Suxa
100
100
0
0
Cooper et al14
1993
Roc.
Suxa
95
100
5
0
Pollart et al16
1995
Roc.
80
20
Wierda et al17
1995
Roc.
100
Dubois et al18
1995
Roc.
Sux.
100
92.5
0
7.5
Our Series
Roc = Rocuronium
Roc.
95
(0.6 mgkg-1)
Sux.
85
5
15
Sux = Suxamethonium
133
References