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Health Technology Assessment | 2014

The opportunities and challenges of pragmatic point-of-care randomised trials using routinely collected electronic records: Evaluations of two exemplar trials

Tjeerd-Pieter van Staa; Lisa Dyson; Gerard McCann; Shivani Padmanabhan; Rabah Belatri; Ben Goldacre; Jackie Cassell; Munir Pirmohamed; David Torgerson; Sarah Ronaldson; Joy Adamson; Adel Taweel; Brendan Delaney; Samhar Mahmood; Simona Baracaia; Thomas Round; Robin Fox; Tommy Hunter; Martin Gulliford; Liam Smeeth

BACKGROUND Pragmatic trials compare the effects of different decisions in usual clinical practice. OBJECTIVES To develop and evaluate methods to implement simple pragmatic trials using routinely collected electronic health records (EHRs) and recruiting patients at the point of care; to identify the barriers and facilitators for general practitioners (GPs) and patients and the experiences of trial participants. DESIGN Two exemplar randomised trials (Retropro and eLung) with qualitative evaluations. SETTING Four hundred and fifty-nine English and Scottish general practices contributing EHRs to a research database, of which 17 participated in the trials. PARTICIPANTS Retropro aimed to recruit 300 patients with hypercholesterolaemia and high cardiovascular risk and eLung aimed to recruit 150 patients with a chronic obstructive pulmonary disease exacerbation. INTERVENTIONS Retropro randomised between simvastatin and atorvastatin and eLung between immediate antibiotics and deferred or non-use. eLung recruited during an unscheduled consultation using EHR flagging. MAIN OUTCOME MEASURE Successful trial completion with implementation of information technology (IT) system for flagging and data processing and documentation of operational and scientific experiences. DATA SOURCES EHR research database. RESULTS The governance approval process took over 3 years. A total of 58.8% of the practices (n = 270) expressed interest in participating. The number of interested practices dropped substantially with each stage of the governance process. In Retropro, 6.5% of the practices (n = 30) were eventually approved and 3.7% (n = 17) recruited patients; in eLung, these numbers were 6.8% (n = 31) and 1.3% (n = 6) respectively. Retropro successfully completed recruitment (301 patients) whereas eLung recruited 31 patients. Retropro recruited 20.6% of all statin starters in recruiting practices and 1.1% in the EHR database; the comparable numbers for eLung were 32.3% and 0.9% respectively. The IT system allowed for complex eligibility criteria with central on and off control of recruitment and flagging at a practice. Good Clinical Practice guidelines, governance and consent procedures were found to have substantially affected the intended simple nature of the trials. One qualitative study of 13 clinicians found that clinicians were generally positive about the principle of computerised trial recruitment (flagging during consultation). However, trials which did not include patients with acute illness were favoured. The second qualitative process evaluation interviewed 27 GPs about their actual experiences, including declining, recruiting and non-recruiting GPs. Opportunistic patient recruitment during a routine GP consultation was found to be the most controversial element. The actual experiences of recruiting patients during unscheduled consultation were generally more positive than the hypothetical views of GPs. Several of the recruiting GPs reported the process took 5 minutes and was straightforward and feasible on most occasions. Almost all GPs expressed their strong support for the use of EHRs for trials. Ten eLung participants were interviewed, all of whom considered it acceptable to be recruited during a consultation and to use EHRs for trials. CONCLUSIONS EHR point-of-care trials are feasible, although the recruitment of clinicians is a major challenge owing to the complexity of trial approvals. These trials will provide substantial evidence on clinical effectiveness only if trial interventions and participating clinicians and patients are typical of usual clinical care and trials are simple to initiate and conduct. Recommendations for research include the development of evidence and implementation of risk proportionality in trial governance and conduct. TRIAL REGISTRATION Current Controlled Trials ISRCTN33113202 and ISRCTN72035428. FUNDING This project was funded by the NIHR Health Technology Assessment programme and the Wellcome Trust and will be published in full in Health Technology Assessment; Vol. 18, No. 43. See the NIHR Journals Library website for further project information.


Archive | 2015

Ethics and consent

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

List of Read codes used to identify potential influenza cases in Hospital Episode Statistics data

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

Covariate code lists

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

Semistructured interview guide used to evaluate general practitioner user experience of study technological interface

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

FLU-CATs Data Handbook

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

FLU-CATs protocol

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

Influenza-related Read codes used by general practitioners for patient assessment prior to an admission to hospital with a discharge diagnosis of influenza and chosen to trigger Local Eligibility Patient Identification Software

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Archive | 2015

Stata algorithms for data management and analysis ‘do files’

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple


Health Technology Assessment | 2015

Development of processes allowing near real-time refinement and validation of triage tools during the early stage of an outbreak in readiness for surge: the FLU-CATs Study

Sudhir Venkatesan; Puja R. Myles; Gerard McCann; Antonis A Kousoulis; Maimoona Hashmi; Rabah Belatri; Emma Boyle; Alan Barcroft; Tjeerd van Staa; Jamie Kirkham; Jonathan S Nguyen Van Tam; Tim Williams; Malcolm G. Semple

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Gerard McCann

Medicines and Healthcare Products Regulatory Agency

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Adel Taweel

Guy's and St Thomas' NHS Foundation Trust

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Ben Goldacre

University of Cambridge

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Jackie Cassell

Brighton and Sussex Medical School

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