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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Online Access: | https://doi.org/10.1515/pthp-2015-0009 |
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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 |
work_keys_str_mv |
AT vazquezraphael impactofhandlingerrorsforchemicalcrosscontaminationriskforthepreparationofparenteralcytotoxicdrugs AT boubetkevin impactofhandlingerrorsforchemicalcrosscontaminationriskforthepreparationofparenteralcytotoxicdrugs AT guerraultmoromarienoelle impactofhandlingerrorsforchemicalcrosscontaminationriskforthepreparationofparenteralcytotoxicdrugs AT craustemancietsylvie impactofhandlingerrorsforchemicalcrosscontaminationriskforthepreparationofparenteralcytotoxicdrugs |
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1716846805889581056 |