Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs

The aim of the study was to evaluate the risk of chemical cross-contamination between preparations of cytotoxic drugs performed in hospital pharmacy. Simulation of handling process errors was performed with two selected tracers, thiamine and retinol to mimic hydrophilic and lipophilic cytotoxic drug...

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Main Authors: Vazquez Raphael, Boubet Kevin, Guerrault-Moro Marie-Noelle, Crauste-Manciet Sylvie
Format: Article
Language:English
Published: De Gruyter 2016-09-01
Series:Pharmaceutical Technology in Hospital Pharmacy
Subjects:
Online Access:https://doi.org/10.1515/pthp-2015-0009
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spelling doaj-23033920cb4946d6b282b57627c9dfe22021-10-02T19:25:15ZengDe GruyterPharmaceutical Technology in Hospital Pharmacy2365-24112365-242X2016-09-011311512210.1515/pthp-2015-0009Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic DrugsVazquez Raphael0Boubet Kevin1Guerrault-Moro Marie-Noelle2Crauste-Manciet Sylvie3Centre Hospitalier Intercommunal de Poissy-Saint-Germain-en-Laye, Saint-Germain-en-Laye, Île-de-France, FranceCentre Hospitalier Intercommunal de Poissy-Saint-Germain-en-Laye, Saint-Germain-en-Laye, Île-de-France, FranceCentre Hospitalier Intercommunal de Poissy-Saint-Germain-en-Laye, Saint-Germain-en-Laye, Île-de-France, FranceARNA Laboratory, ChemBioPharm, U1212 INSERM - UMR 5320 CNRS, Bordeaux University, 146, rue Léo Saignat, Bordeaux 33076, FranceThe aim of the study was to evaluate the risk of chemical cross-contamination between preparations of cytotoxic drugs performed in hospital pharmacy. Simulation of handling process errors was performed with two selected tracers, thiamine and retinol to mimic hydrophilic and lipophilic cytotoxic drugs. Four types of handling errors were simulated: errors associated with the re-use of a disposable transfer device: syringe, spike and needle and errors associated with surface contamination such as the use of a contaminated pad. The results show rates of contamination above the limit of quantification with the re-use of a syringe, a needle or a spike. For example, with the thiamine solution at 50 mg/ml final concentration, the re-use of a spike led to a contamination of approximately 100 µl equivalent to 5 mg. By contrast, the use of a surface contaminated pad failed to detect a cross-contamination. Cross-contamination related to a contamination of surface by a cytotoxic drug represents a low risk. However, the re-use of a single medical device due to handling human error led to quantifiable risk of cross-contamination. Furthermore, this type of error is very difficult to detect and may be frequent enough to have potential impact on patient.https://doi.org/10.1515/pthp-2015-0009cytotoxic drugscross-contaminationhuman errorshandling errors
collection DOAJ
language English
format Article
sources DOAJ
author Vazquez Raphael
Boubet Kevin
Guerrault-Moro Marie-Noelle
Crauste-Manciet Sylvie
spellingShingle Vazquez Raphael
Boubet Kevin
Guerrault-Moro Marie-Noelle
Crauste-Manciet Sylvie
Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs
Pharmaceutical Technology in Hospital Pharmacy
cytotoxic drugs
cross-contamination
human errors
handling errors
author_facet Vazquez Raphael
Boubet Kevin
Guerrault-Moro Marie-Noelle
Crauste-Manciet Sylvie
author_sort Vazquez Raphael
title Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs
title_short Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs
title_full Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs
title_fullStr Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs
title_full_unstemmed Impact of Handling Errors for Chemical Cross-contamination Risk for the Preparation of Parenteral Cytotoxic Drugs
title_sort impact of handling errors for chemical cross-contamination risk for the preparation of parenteral cytotoxic drugs
publisher De Gruyter
series Pharmaceutical Technology in Hospital Pharmacy
issn 2365-2411
2365-242X
publishDate 2016-09-01
description The aim of the study was to evaluate the risk of chemical cross-contamination between preparations of cytotoxic drugs performed in hospital pharmacy. Simulation of handling process errors was performed with two selected tracers, thiamine and retinol to mimic hydrophilic and lipophilic cytotoxic drugs. Four types of handling errors were simulated: errors associated with the re-use of a disposable transfer device: syringe, spike and needle and errors associated with surface contamination such as the use of a contaminated pad. The results show rates of contamination above the limit of quantification with the re-use of a syringe, a needle or a spike. For example, with the thiamine solution at 50 mg/ml final concentration, the re-use of a spike led to a contamination of approximately 100 µl equivalent to 5 mg. By contrast, the use of a surface contaminated pad failed to detect a cross-contamination. Cross-contamination related to a contamination of surface by a cytotoxic drug represents a low risk. However, the re-use of a single medical device due to handling human error led to quantifiable risk of cross-contamination. Furthermore, this type of error is very difficult to detect and may be frequent enough to have potential impact on patient.
topic cytotoxic drugs
cross-contamination
human errors
handling errors
url https://doi.org/10.1515/pthp-2015-0009
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