Literature DB >> 27323425

Safe Cytotoxic Drug Preparation Using Closed-system Transfer Device: Technical and Practical Evaluation of a New Device (Vialshield/Texium) Comparatively to a Reference One (Phaseal).

Philippe Garrigue, Marc Montana, Christophe Ventre, Amandine Savry, Laurence Gauthier-Villano, Pascale Pisano, Bertrand Pourroy.   

Abstract

Closed-system transfer devices enhance the drug handlers' protection against hazardous drugs exposure by prohibiting the escape of liquid or vapor from the system. PhaSeal (Becton Dickinson), a reference closed-system transfer device, includes a vial protector with an expansion chamber, and an injector with an enclosed needle. VialShield (CareFusion) is another more recent closed-system transfer device including an expansion-chamber and a non-return valve, designed to be used in association with Texium (CareFusion), a closed, needle-free male luer with its preassembled syringe. Evaluation of VialShield/Texium was done comparatively to a classic spike device (Spike Swan, Codan) and PhaSeal. Evaluation methods consisted in practical evaluation by pharmacy technicians (evaluation of ease to use by nine operators in practical conditions during a complete week of production), microbiological safety performance (by Media Fill Test), and leakage assessment (fluorescein, titanium tetrachloride smoke, and radioactive tracer). Results showed that 100% of those operators evaluated would be ready to use VialShield/Texium for daily use, whereas only 75% of them would be ready to use PhaSeal. The use of PhaSeal and VialShield/Texium increased the duration of preparations compared to Spike Swan. No microbiological growth was observed with any of the three devices. A leakage of smoke was observed only with Spike Swan. Fluorescein leakage assessment confirmed that PhaSeal is a performing closed system with a dry connection. Spike Swan showed fluorescein leaks. Fluorescein drops were visible on the connection sites of the VialShield/Texium. Nevertheless, no fluorescein was found on compress after connections swapping. Transfer performance, assessed using technetium-99m, was 98.1 ± 1.4%, 97.9 ± 1.1% and 97.0 ± 1.3% and dead volume of the devices, were 1.0 ± 0.8%, 1.7 ± 0.6%, and 3.0 ± 1.1% for Spike Swan, PhaSeal, and VialShield/Texium, respectively. VialShield/Texium appeared as a very interesting device with performances close to PhaSeal (except dry connection), with a higher satisfaction assessment from the operators.

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Year:  2016        PMID: 27323425

Source DB:  PubMed          Journal:  Int J Pharm Compd        ISSN: 1092-4221


  4 in total

1. 

Authors:  Annaelle Soubieux; Caroline Plante; Johann-François Ouellette-Frève; Audrey Chouinard; Jean-François Bussières
Journal:  Can J Hosp Pharm       Date:  2020-02-01

Review 2.  Review of studies examining microbial contamination of vials used for preparations done with closed-system drug transfer devices.

Authors:  Annaelle Soubieux; Cynthia Tanguay; Jean-François Bussières
Journal:  Eur J Hosp Pharm       Date:  2019-05-15

3.  Implementation and validation of an in-house combined fluorescein/media-fill test to qualify radiopharmacy operators.

Authors:  Cyril Fersing; Emmanuel Deshayes; Sarah Langlet; Laurence Calas; Vincent Lisowski; Pierre Olivier Kotzki
Journal:  EJNMMI Radiopharm Chem       Date:  2021-01-07

Review 4.  Closed-system drug-transfer devices plus safe handling of hazardous drugs versus safe handling alone for reducing exposure to infusional hazardous drugs in healthcare staff.

Authors:  Kurinchi Selvan Gurusamy; Lawrence Mj Best; Cynthia Tanguay; Elaine Lennan; Mika Korva; Jean-François Bussières
Journal:  Cochrane Database Syst Rev       Date:  2018-03-27
  4 in total

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