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.