medicalised transport,medical assistance, plastic surgery
UTILISATION EN RÉANIMATION
La pharmacocinétique du propofol est très altérée chez les patients de réanimation. Elle est caractérisée par une augmentation majeure de la demi-vie d'élimination terminale (qui est de l'ordre de 30 heures) et du VdSS [3].
Cependant, étant donné que les concentrations sanguines adéquates (de l'ordre de 1 μg·mL-1) et les posologies nécessaires (2 à 3 mg·kg-1·h-1) sont modérées, les délais de réveil sont rapides et plus courts que ceux observés avec le midazolam.
La tolérance hémodynamique est satisfaisante mais doit faire éviter toute administration en bolus et corriger préalablement une hypovolémie. Le propofol est un des adjuvants du traitement des poussées d'hypertension intracrânienne chez le neurotraumatisé. Ses effets cérébraux ne sont favorable qu'à la condition d'un maintien strict de la pression artérielle systémique moyenne.
Le volume d'Intralipide® perfusé et le coût sont les principales limites à son emploi comme agent de sédation. Pour des durées supérieures à 3 jours et à une dose moyenne de 2,5 mg·kg-1·h-1, une augmentation des triglycérides sanguins, source potentielle d'un retard de réveil, est constatée. Pour des sédations de moins de 3 jours et à des doses inférieures à 2 mg·kg-1·h-1, il ne semble pas exister d'effet délétère sur le bilan lipidique. L'utilisation chez l'enfant de moins de 15 ans est contre-indiquée car des effets indésirables graves et des décès ont été rapportés sans que l'imputabilité soit indiscutable [139]. Cependant, associé à un morphinique à des posologies inférieures à 5 mg·kg-1 et pour des sédations de courte durée (durée moyenne de 35 heures) dans un contexte postopératoire et non septique, Martin et al n'ont pas mis en évidence d'effet indésirable chez neuf enfants dont l'âge moyen était de 19 mois [83]. Des études complémentaires sont nécessaires pour confirmer son utilisation plus large [60].
CONCLUSION
Le propofol est à la base du renouveau clinique des techniques d'anesthésie totale intraveineuse. II a permis également le développement de nouveaux concepts pharmacocinétiques et pharmacodynamiques. II est le successeur tout désigné du thiopental en tant qu'agent d'induction IV de référence. La rapidité et la qualité du réveil obtenu associées à un effet antiémétique en font un agent particulièrement adapté à la pratique ambulatoire et à l'anesthésie des patients âgés. La reproductibilité de la relation dose-effet et la possibilité de maintenir une ventilation spontanée adéquate sont particulièrement intéressantes pour les gestes pratiqués " en dehors du bloc opératoire " et la sédation de complément facilement prévenus ou corrigés s'il n'est pas administré à des patients hypovolémiques ou ayant une fonction cardiovasculaire précaire. Son coût est le principal frein à une utilisation plus large, en particulier dans le cadre de la sédation en réanimation.
Dix ans après sa commercialisation, le propofol demeure innovant puisqu'il est le premier agent anesthésique à disposer officiellement d'une nouvelle technique d'administration d'avenir : I'AIVOC.
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