James Rossiter

Multi-centre reproducibility of diffusion MRI parameters for clinical sequences in the brain.

The purpose of this work was to assess the reproducibility of diffusion imaging, and in particular the apparent diffusion coefficient (ADC), intra‐voxel incoherent motion (IVIM) parameters and diffusion tensor imaging (DTI) parameters, across multiple centres using clinically available protocols with limited harmonization between sequences.

A loosely coupled framework for terminology controlled distributed EHR search for patient cohort identification in clinical research

Heterogeneous data models and coding schemes for electronic health records present challenges for automated search across distributed data sources. This paper describes a loosely coupled software framework based on the terminology controlled approach to enable the interoperation between the search interface and heterogeneous data sources. Software components interoperate via common terminology service and abstract criteria model so as to promote component reuse and incremental system evolution.

Model-based auditability of clinical trial recruitment

Detailed insight into the recruitment parameters of a clinical trial is crucial to interpretation of its results, and reasons for its success or failure. Such recruitment is increasingly done through specialized software tools, sometimes linked to Electronic Health Record (EHR) systems, enabling automated capture of audit logs. However, in the absence of shared semantic models underpinning these logs, gathered data remains insular and opaque. We propose a standardized syntactical representation to capture the provenance of the recruitment task, and ground it in CRIM, a variant of the established PCROM information model for research in primary care. The method has been successfully prototyped in the EU FP7 TRANSFoRm project, where the recruitment eligibility query module has been integrated with a provenance capture infrastructure, resulting in the full reproducibility of the study design process.

Reuse of routinely collected health data for clinical research: considerations in a central England case study.

An increasing amount of electronic health data is being collected for patient care, and with it the opportunity to explore reusing this data, for example to support clinical research. We explore how researchers can be supported in identifying potential study participants using a semi-automated approach to query anonymised datasets remotely. This paper describes the socio-technical considerations when answering this question in a central England case study.

Standardised representation of healthcare information in secondary care research: a Central England case study.

Interoperability and reuse of healthcare information, for patient care and clinical research, rely on standardised approaches in its representation. The medical domain is rich with terminologies and dictionaries to support the representation of clinical data, but these are not necessarily interoperable. Secondary care research has long been conducted with study-specific requirements, and the valuable information collected was, however, difficult to reuse and share due to incomplete data collection and its non-standard representation. As a way to resolve some of these issues, we are designing and building sustainable database applications that clinicians and researchers alike can use as research registries, with the main aim to have research-quality healthcare information for future research studies and trials. This paper looks at a case study of how these applications are being developed in Central England through the use of controlled vocabularies. Specialty teams are keen to improve the interoperability, sharing and reuse of health information within and across specialties.