Recycled incomplete identification procedures for blood screening

Autor(en): Bar-Lev, Shaul K.
Boxma, Onno
Kleiner, Igor
Perry, David
Stadje, Wolfgang 
Stichwörter: ACCURACY; Blood screening; Business & Economics; Combinatorial urn problems; DISEASE; Group testing; GROUP-TESTING MODELS; HCV; HIV; Management; Markov chain; Operations Research & Management Science; POOLED SERA; POPULATION; PREVALENCE; QUEUES; Recycled group testing; VIRUS
Erscheinungsdatum: 2017
Herausgeber: ELSEVIER SCIENCE BV
Enthalten in: EUROPEAN JOURNAL OF OPERATIONAL RESEARCH
Band: 259
Ausgabe: 1
Startseite: 330
Seitenende: 343
Zusammenfassung: 
The operation of blood banks aims at the cost-efficient supply of uncontaminated human blood. Each unit of donated blood goes through multiple testing for the presence of various pathogens which are able to cause transfusion-transmitted diseases. The blood screening process is comprised of two phases. At the first phase, blood units are screened together in pooled groups of a certain size by the ELISA (Enzyme Linked Immuno-Sorbent Assay) test to detect various virus-specific antibodies. The second phase of the screening process is conducted by PCR (Polymerase Chain Reaction) testing of the individual blood units of the groups found clean by the initial ELISA phase. Thousands of units of donated blood arrive daily at the central blood bank for screening. Each screening scheme has associated testing costs and testing times. In addition, each blood unit arrives with an expiration date. As a result, the shorter the testing time, the longer the residual lifetime that is left for the blood unit for future use. The controller faces a natural and well-motivated operations management problem. He will attempt to shorten the testing period and reduce the testing costs without compromising too much on the reliability. To achieve these goals, we propose a new testing procedure that we term Recycled Incomplete Identification Procedure (RIIP). In RIIP, groups of pooled blood units which are found contaminated in the ELISA test are divided into smaller subgroups and again group-tested by ELISA, and so forth, until eventually the PCR test is conducted for those subgroups which are found clean. We analyze and optimize the performance of RIIP by deriving explicit formulas for the cost components of interest and maximize the profit associated with the procedure. Our numerical results suggest that it can indeed be profitable to do several cycles at ELISA. (C) 2016 Elsevier B.V. All rights reserved.
ISSN: 03772217
DOI: 10.1016/j.ejor.2016.10.005

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