4.4 Article

Developing a dynamic simulation model to support the nationwide implementation of whole genome sequencing in lung cancer

Journal

BMC MEDICAL RESEARCH METHODOLOGY
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12874-022-01571-3

Keywords

Implementation; Whole genome sequencing; Dynamic simulation modeling; Diagnostics; Oncology

Funding

  1. ZonMW [80-84600-98-1002]

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This study demonstrates the application of dynamic simulation modeling in analyzing the nationwide implementation of Whole Genome Sequencing (WGS) for non-small cell lung cancer (NSCLC). The results show that the organization of the diagnostic pathway and referral patterns significantly impact the duration of the diagnostic process when implementing WGS.
Background This study shows how dynamic simulation modeling can be applied in the context of the nationwide implementation of Whole Genome Sequencing (WGS) for non-small cell lung cancer (NSCLC) to inform organizational decisions regarding the use of complex and disruptive health technologies and how these decisions affect their potential value. Methods Using the case of the nationwide implementation of WGS into clinical practice in lung cancer in the Dutch healthcare system, we developed a simulation model to show that including service delivery features across the diagnostic pathway can provide essential insight into the affordability and accessibility of care at the systems level. The model was implemented as a hybrid Agent-Based Model and Discrete-Event Simulation model in AnyLogic and included 78 hospital agents, 7 molecular tumor board agents, 1 WGS facility agent, and 5313 patient agents each year in simulation time. Results The model included patient and provider heterogeneity, including referral patterns, capacity constraints, and diagnostic workflows. Patient preference and adoption by healthcare professionals were also modeled. The model was used to analyze a scenario in which only academic hospitals have implemented WGS. To prevent delays in the diagnostic pathway, the capacity to sequence at least 1600 biopsies yearly should be present. There is a two-fold increase in mean diagnostic pathway duration between no patients referred or all patients referred for further diagnostics. Conclusions The systems model can complement conventional health economic evaluations to investigate how the organization of the workflow can influence the actual use and impact of WGS. Insufficient capacity to provide WGS and referral patterns can substantially impact the duration of the diagnostic pathway and thus should be considered in the implementation of WGS.

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