Design of shared unit-dose drug distribution network using multi-level particle swarm optimization

Unit-dose drug distribution systems provide optimal choices in terms of medication security and efficiency for organizing the drug-use process in large hospitals. As small hospitals have to share such automatic systems for economic reasons, the structure of their logistic organization becomes a very...

Full description

Saved in:
Bibliographic Details
Published inHealth care management science Vol. 22; no. 2; pp. 304 - 317
Main Authors Chen, Linjie, Monteiro, Thibaud, Wang, Tao, Marcon, Eric
Format Journal Article
LanguageEnglish
Published New York Springer US 01.06.2019
Springer Nature B.V
Springer Verlag
Subjects
Online AccessGet full text
ISSN1386-9620
1572-9389
1572-9389
DOI10.1007/s10729-018-9438-6

Cover

More Information
Summary:Unit-dose drug distribution systems provide optimal choices in terms of medication security and efficiency for organizing the drug-use process in large hospitals. As small hospitals have to share such automatic systems for economic reasons, the structure of their logistic organization becomes a very sensitive issue. In the research reported here, we develop a generalized multi-level optimization method – multi-level particle swarm optimization (MLPSO) – to design a shared unit-dose drug distribution network. Structurally, the problem studied can be considered as a type of capacitated location-routing problem (CLRP) with new constraints related to specific production planning. This kind of problem implies that a multi-level optimization should be performed in order to minimize logistic operating costs. Our results show that with the proposed algorithm, a more suitable modeling framework, as well as computational time savings and better optimization performance are obtained than that reported in the literature on this subject.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1386-9620
1572-9389
1572-9389
DOI:10.1007/s10729-018-9438-6