Evidence map›Paper›PMID 32816898›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2022

Determination of the cross-contamination and validation of the cleaning process for an automated personalised dosing system.

Alexander Ferro Uriguen, Idoia Beobide Telleria, Silvia Martínez Arrechea, Blanca Miró Isasi, Carmen Sampedro Yangüela, Mikel Urretavizcaya Anton

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Article in European journal of hospital pharmacy : science and practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Alexander Ferro UriguenPharmacy Service, Hospital Ricardo Bermingham, San Sebastian, País Vasco, Spain alex.ferro@matiafundazioa.eus.ORCID 0000-0002-5484-9646
Idoia Beobide TelleriaPharmacy Service, Hospital Ricardo Bermingham, San Sebastian, País Vasco, Spain.ORCID 0000-0003-0699-7035
Silvia Martínez ArrecheaPharmacy Service, Hospital Ricardo Bermingham, San Sebastian, País Vasco, Spain.ORCID 0000-0002-1670-1720
Blanca Miró IsasiPharmacy Service, Hospital Ricardo Bermingham, San Sebastian, País Vasco, Spain.
Carmen Sampedro YangüelaAlava Central Analysis Service, Lascaray Ikergunea Building, University of the Basque Country - Alava Campus, Vitoria Gasteiz, País Vasco, Spain.
Mikel Urretavizcaya AntonPharmacy Service, Fundacion Onkologikoa, San Sebastian, Pais Vasco, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the degree of cross-contamination and to validate a cleaning process for an Automated Personalised Dosing System (APDS), respecting the permitted residue transfer limits.

methodAn analytical determination by high pressure liquid chromatography with mass spectrometry was performed for 11 drugs considered critical for their potential for contamination, toxicity (National Institute for Occupational Safety and Health (NIOSH) List 2016) and/or narrow therapeutic index. The test was carried out for three consecutive weeks, seven repetitions per week, in a state of maximum contamination and maximum cleanliness. The main validation criterion of the cleaning protocol was to quantify that the active ingredients measured were below the Permitted Daily Exposure index or fraction 1/1000 of the minimum daily dose, both in a state of maximum contamination and when the APDS is in a clean condition, for an average number of tablets consumed per person per day.

resultsIn all the samples analysed, some compound could always be quantified below 2% of the permitted transfer limits, highlighting the presence of paracetamol and carbamazepine. In the state of maximum contamination, the mean±SD values of paracetamol and carbamazepine were 5.83±1.56 µg and 0.22±0.07 µg, respectively, without significant differences in mean values over the 3 weeks of the study. After the cleaning protocol was executed, only paracetamol and carbamazepine were detected, with the average values being 4.67 µg (95% CI 3.92 to 5.43, p<0.05) and 0.07 µg (95% CI 0.03 to 0.10, p<0.05) lower than the state of maximum contamination, respectively.

conclusionsIn all cases the level of cross-contamination for an APDS was below the pre-established limits. The cleaning protocol has been validated, confirming APDS decontamination of the most critical medicines.

Indexed as

AcetaminophenDrug ContaminationCarbamazepineHumansUnited StatesAcetaminophenCarbamazepineaudit, self-inspectiondispensing robotsdrug packaginghospital pharmacy automationquality in health carerisk management

Identifiers

PMID32816898
PMCPMC9047934

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