technical
performance and side effects of remifentanil as patient-maintained tci in
comparison with morphin bolus pca after major abdominal surgery
U Mohl, C Zimmermann, M Zammert, J Flaschar, S Schraag
Department of Anaesthesiology, University of
Ulm, D-89075 Ulm, Germany
Background and
Goal of study:
Remifentanil (REMI) is increasingly used as the analgesic component during
general anaesthesia. However, the appropriate transition to post-operative
analgesia remains a challenge. The use of a manual controlled REMI infusion has
been associated with a high incidence of respiratory side effects and periods
of inadequate analgesia (1)(2). We tested the technical performance and safety
of a patient-maintained Remifentanil target-controlled infusion (TCI) against
standard Morphine PCA.
Materials and
Methods
After obtained institutional ethic`s committee approval and written informed
consent, 62 male premedicated patients undergoing elective radical
prostatectomy in Propofol-Remifentanil anaesthesia were studied. They were
allocated randomly in three groups to receive postoperative Remifentanil
TCI-PCA (Group 1), Morphine PCA, with additional priming of either a low-dose bolus (0.1 mg kg-1,
Group 2), or a high-dose bolus (0.25 mg kg-1, Group 3) 15min prior
to end of surgery. Study design was double-blind and double-dummy. During the
24 hour observation period any episode of patient- or technology-related side
effects and problems were noted. Statistical analysis was provided by the
nonparametric Kruskal-Wallis test with a significance level of a=0.05.
Results and Discussion: Incidence of
side effects across 24 hours treatment related to either drug effect in
patients or technology are listed in the table below (values given in %,
CP=cardiopulmonary):
|
GROUP |
REMI PCA-TCI (n=23) |
MO PCA low (n=20) |
MO PCA high (n=19) |
p-value |
|
Patient: |
|
|
|
|
|
Nausea |
30.4 |
10.0 |
26.3 |
0.025 |
|
Vomiting |
8.7 |
5.0 |
5.2 |
0.42 |
|
Shivering |
26.0 |
25.0 |
5.2 |
0.17 |
|
CP Side effects |
13.1 |
5.0 |
0 |
0.22 |
|
Rescue analgesia |
8.7 |
0 |
0 |
n.d. |
|
Technology: |
|
|
|
|
|
No consequence |
4.3 |
5.0 |
5.2 |
0.98 |
|
With consequence |
21.7 |
0 |
0 |
n.d. |
Only one patient both in the REMI and MO low group
had a respiration rate < 10 min–1 over 5 minutes and two patients
in the REMI group developed bradycardia with a HR < 45 bpm.
Conclusion: Patient-maintained REMI TCI
appears to be a safe alternative when compared to standard MO PCA. Besides a
higher incidence in shivering, the drug related side effects are comparable
between both techniques. However, a significant amount of technical problems
which interfered with the delivery of analgesia requires further refinement of
the REMI prototype system and the observation of the patients in a high
dependency environment.
References:
[1] Schüttler J et al. Anaesthesia
1997; 52:307-17.
[2} Bowdle TA et al Anesth Analg 1996;
83:1292-7.