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Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study

BACKGROUND: Cost-containment strategies are required to face the challenge of rising drug expenditures in Oncology. Drug wastage leads to economic loss, but little is known about the size of the problem in this field. METHODS: Starting January 2005 we introduced a day-to-day monitoring of drug wasta...

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Autores principales: Fasola, Gianpiero, Aita, Marianna, Marini, Luisa, Follador, Alessandro, Tosolini, Marina, Mattioni, Laura, Mansutti, Mauro, Piga, Andrea, Brusaferro, Silvio, Aprile, Giuseppe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374784/
https://www.ncbi.nlm.nih.gov/pubmed/18380901
http://dx.doi.org/10.1186/1472-6963-8-70
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author Fasola, Gianpiero
Aita, Marianna
Marini, Luisa
Follador, Alessandro
Tosolini, Marina
Mattioni, Laura
Mansutti, Mauro
Piga, Andrea
Brusaferro, Silvio
Aprile, Giuseppe
author_facet Fasola, Gianpiero
Aita, Marianna
Marini, Luisa
Follador, Alessandro
Tosolini, Marina
Mattioni, Laura
Mansutti, Mauro
Piga, Andrea
Brusaferro, Silvio
Aprile, Giuseppe
author_sort Fasola, Gianpiero
collection PubMed
description BACKGROUND: Cost-containment strategies are required to face the challenge of rising drug expenditures in Oncology. Drug wastage leads to economic loss, but little is known about the size of the problem in this field. METHODS: Starting January 2005 we introduced a day-to-day monitoring of drug wastage and an accurate assessment of its costs. An internal protocol for waste minimisation was developed, consisting of four corrective measures: 1. A rational, per pathology distribution of chemotherapy sessions over the week. 2. The use of multi-dose vials. 3. A reasonable rounding of drug dosages. 4. The selection of the most convenient vial size, depending on drug unit pricing. RESULTS: Baseline analysis focused on 29 drugs over one year. Considering their unit price and waste amount, a major impact on expense was found to be attributable to six drugs: cetuximab, docetaxel, gemcitabine, oxaliplatin, pemetrexed and trastuzumab. The economic loss due to their waste equaled 4.8% of the annual drug expenditure. After the study protocol was started, the expense due to unused drugs showed a meaningful 45% reduction throughout 2006. CONCLUSION: Our experience confirms the economic relevance of waste minimisation and may represent a feasible model in addressing this issue. A centralised unit of drug processing, the availability of a computerised physician order entry system and an active involvement of the staff play a key role in allowing waste reduction and a consequent, substantial cost-saving.
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spelling pubmed-23747842008-05-09 Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study Fasola, Gianpiero Aita, Marianna Marini, Luisa Follador, Alessandro Tosolini, Marina Mattioni, Laura Mansutti, Mauro Piga, Andrea Brusaferro, Silvio Aprile, Giuseppe BMC Health Serv Res Research Article BACKGROUND: Cost-containment strategies are required to face the challenge of rising drug expenditures in Oncology. Drug wastage leads to economic loss, but little is known about the size of the problem in this field. METHODS: Starting January 2005 we introduced a day-to-day monitoring of drug wastage and an accurate assessment of its costs. An internal protocol for waste minimisation was developed, consisting of four corrective measures: 1. A rational, per pathology distribution of chemotherapy sessions over the week. 2. The use of multi-dose vials. 3. A reasonable rounding of drug dosages. 4. The selection of the most convenient vial size, depending on drug unit pricing. RESULTS: Baseline analysis focused on 29 drugs over one year. Considering their unit price and waste amount, a major impact on expense was found to be attributable to six drugs: cetuximab, docetaxel, gemcitabine, oxaliplatin, pemetrexed and trastuzumab. The economic loss due to their waste equaled 4.8% of the annual drug expenditure. After the study protocol was started, the expense due to unused drugs showed a meaningful 45% reduction throughout 2006. CONCLUSION: Our experience confirms the economic relevance of waste minimisation and may represent a feasible model in addressing this issue. A centralised unit of drug processing, the availability of a computerised physician order entry system and an active involvement of the staff play a key role in allowing waste reduction and a consequent, substantial cost-saving. BioMed Central 2008-04-01 /pmc/articles/PMC2374784/ /pubmed/18380901 http://dx.doi.org/10.1186/1472-6963-8-70 Text en Copyright © 2008 Fasola et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Fasola, Gianpiero
Aita, Marianna
Marini, Luisa
Follador, Alessandro
Tosolini, Marina
Mattioni, Laura
Mansutti, Mauro
Piga, Andrea
Brusaferro, Silvio
Aprile, Giuseppe
Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study
title Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study
title_full Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study
title_fullStr Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study
title_full_unstemmed Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study
title_short Drug waste minimisation and cost-containment in Medical Oncology: Two-year results of a feasibility study
title_sort drug waste minimisation and cost-containment in medical oncology: two-year results of a feasibility study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374784/
https://www.ncbi.nlm.nih.gov/pubmed/18380901
http://dx.doi.org/10.1186/1472-6963-8-70
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