Abstract
Purpose
Propofol is a potential vector of infection, because it contains no preservative. Thus, the manufacturer’s specific recommendations for preparing injections or infusions go beyond the guidelines commonly used in our operating rooms for preparing other iv drugs. The purpose of the present study was to determine whether in the daily routine of an operating theatre a modified propofol handling technique can prevent contamination as effectively as do the manufacturer’s handling recommendations.
Methods
A total of 160 consecutive neurosurgical patients were allocated to either Group I (manufacturer’s handling recommendations: i.e., 1) disinfecting propofol vials and ampoules before filling syringes; 2) replacing empty syringes; 3) discarding all material at the end of surgery); or Group II (modified propofol handling protocol: i.e., I) refilling empty syringes; 2) renewing only the infusion line to the patient).
Results
Total contamination rates were comparable in both groups (Group I: 14/160 (8.75%), Group II: 13/160 (8.13%) (χ2 = 0.074; P = 0.96). Frequency of contamination was not different between groups; either in sample I taken at the beginning of the procedure, (Group I: 5/80 (6.25%) vs Group II: 6/80 (7.5%); χ2 = 0.098; P = 0.76) or in sample 2, taken at the end, (Group I: 9/80 (11.25%) vs Group II: 7/80 (8.75%); χ2 = 0.278; P = 0.598).
Conclusion
We conclude that in the daily routine of the operating theatre following a modified propofol handling protocol prevents contamination of propofol syringes as effectively as does adhering to the manufacturer’s specific handling recommendations. However, neither of the tested guidelines completely prevented contamination.
Résumé
Objectif
Le propofol, ne contenant aucun agent de conservation, est un vecteur potentiel d’infection. C’est pourquoi les recommandations spécifiques du fabricant au sujet de la préparation d’injections ou de perfusions vont au delà des directives habituellement suivies dans nos salles d’opération pour la préparation d’autres médicaments intraveineux. Nous avons voulu déterminer si, en modifiant le maniement du propofol en salle d’opération, nous pouvions prévenir la contamination aussi efficacement qu’en suivant à la lettre les recommandations du fabricant.
Méthode
Un total de 160 patients successifs de neurochirurgie ont été répartis en deux groupes. Pour le Groupe I on a suivi les recommandations du fabricant en 1) désinfectant les flacons et les ampoules de propofol avant de remplir les seringues; 2) remplaçant les seringues vides; 3) jetant tout le matériel à la fin de l’intervention chirurgicale. Pour le Groupe II, on a modifié le maniement du propofol en 1) remplissant les seringues vides et 2) en renouvelant seulement les tubulures à perfusion des patients.
Résultats
Les taux de contamination totale sont comparables : 14/160 (8,75 %) dans le Groupe I et 13/160 (8,13 %) dans le Groupe II (χ2 = 0,074; P = 0,96). La fréquence de contamination ne diffère pas d’un groupe à l’autre, pour l’échantillon I prélevé au début de l’opération (Groupe I : 5/80 (6,25 %) vs Groupe II : 6/80 (7,5 %); χ2 = 0,098; P = 0,76) ou l’échantillon 2 à la fin (Groupe I : 9/80 (11,25 %)vs Groupe II : 7/80 (8,75 %); χ2 = 0,278; P = 0,598).
Conclusion
Lusage quotidien d’un protocole modifié de maniement du propofol en salle d’opération prévient aussi efficacement la contamination des seringues que l’adhésion aux recommandations spécifiques du fabricant. Aucune des directives testées n’a permis d’éliminer complètement la contamination.
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Lorenz, I.H., Kolbitsch, C., Lass-Flörl, C. et al. Routine handling of propofol prevents contamination as effectively as does strict adherence to the manufacturer’s recommendations. Can J Anesth 49, 347–352 (2002). https://doi.org/10.1007/BF03017321
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DOI: https://doi.org/10.1007/BF03017321