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Hygiène du matériel de nébulisation : enjeux, difficultés et propositions d'amélioration - 05/05/08

Doi : rmr-12-2007-24-10-0761-8425-101019-200720176 

G. Reychler [1],

C. Dupont [2],

J.C. Dubus [3]

pour le GAT (Groupe Aérosolthérapie de la SPLF) et le GRAM (Groupe Aérosols et Mucoviscidose de la Société Française de la Mucoviscidose)Ver las filiaciones

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Disinfection of devices for nebulization: stakes, difficulties, and improvement proposals

Introduction

Nebulization may transport with the drug some small particles containing microbes.

State of the art

These microbes may be present in all parts of the nebulizer, including the drug solution itself. Depending on the studies, contamination of the nebulizers may reach up to 55% of the devices in patients with cystic fibrosis. That's why using one nebulizer for one patient, using drug sterile ampoules, and having a good hygiene during and after the nebulization are so important. The national disinfection recommendations, usually depending on the type of the nebulizer, are variable from one to another country and are not very well validated. Moreover, the repetitive use of these disinfection techniques on the performances of the nebulizer are neither studied. In daily life, the patients respect these disinfection recommendations in 3 to 98% of the cases.

Perspectives

We propose a standardized methodology for evaluating the microbial and functional effects of all disinfectants on the nebulizers.

Conclusion

A simple, quick, efficacious, cheep, and without effect on nebulizer performances disinfectant is still waiting.

Keywords: Cystic fibrosis , Disinfection , Hygiene , Nebulization , Recommendations


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© 2007 Elsevier Masson SAS. Tous droits réservés.
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Vol 24 - N° 10

P. 1351-1361 - décembre 2007 Regresar al número
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