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Proposition of reengineering methodology for the product driven of manufacturing systems : application to the medication-use process

Identifieur interne : 000122 ( Hal/Corpus ); précédent : 000121; suivant : 000123

Proposition of reengineering methodology for the product driven of manufacturing systems : application to the medication-use process

Auteurs : Jean-Charles Huet

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RBID : Hal:tel-00636342

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Abstract

The reengineering of the medication-use process is an important challenge in order to reduce medication errors and costs for the pharmacy (increase of the efficience ; reduce the amount of work time spent by nurses in the medication administration process. . .). The use of the nominative dispensing, automatic systems (robots, pneumatic circuit, cart dispensing. . .),control system of administration to the patient are solutions which can avoid the human errors. We propose in this study to use the concept used in industrial systems in order to improve the safety and the traceability on the medication-use process. We use the paradigm of Product Driven System which proposes to place the product in the centre of the system using identification technology as RFID. We made an analogy between the medication-use process and an assembly system : the product is considered as a preparation of the prescription for a patient and an operation of assembly is considered as an addition of medication. The goal of this thesis is to propose a reengineering methodology based on MDA (Model Driven Architecture) and ASDI (Analysis-Specification-Design-Implementation) in order to implement a system based on product driven synchronizing the physical and informational flow. In particular,this methodology is applied to the medicament-use process. Finally, we present an example of application of this modelling to the hospital of Clermont-Ferrand through simulation software which allows testing different scenarios to help the pharmacists and managers of the hospital to make up their decisions.

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<abstract xml:lang="fr">Le circuit du médicament est un élément primordial dans l’organisation des établissements de santé. Sa sécurisation et sa modernisation permettent de baisser sensiblement le nombre de personnes victimes d’erreurs médicamenteuses et de réduire les coûts (augmentation du rendement, libération de poste préparateur et gain de temps infirmière. . .). L’utilisation de la DJIN (Dispensation Journalière Individuelle Nominative), de systèmes de préparation et de transport sécurisés (robots, circuit pneumatique, chariots de dispensation. . .), de systèmes de contrôle de l’administration au lit du patient sont les solutions permettant d’éviter les erreurs humaines. Nous proposons dans cette étude d’utiliser des concepts du milieu industriel pour améliorer la sécurité et la traçabilité du circuit du médicament. Nous utilisons le paradigme de Système Contrôlé par le Produit (SCP) qui propose de mettre le produit au coeur du système en utilisant des nouvelles technologies tel que la RFID. Nous comparons le circuit du médicament avec un système d’assemblage : l’opération d’assemblage est vue comme un ajout de médicaments et le produit comme la préparation de la prescription pour un patient. Le but de cette thèse est de proposer une méthodologie de réingénierie, basée surl e MDA et ASCI, pour le contrôle par le produit en synchronisant les flux physiques et informationnels, puis de l’appliquer au circuit du médicament. Enfin, nous l’instancions au CHU de Clermont-Ferrand en testant différents scénarios à travers un logiciel de simulation afin de proposer une aide à la décision pour les pharmaciens et les responsables du CHU.</abstract>
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