From: Utilization of EHRs for clinical trials: a systematic review
Author, year | Country | Aim of study |
---|---|---|
Mohammad B Ateya 2016 [16] | USA | To quantify the proportion of eligibility criteria that can be addressed with data in electronic health records and to compare the content of eligibility criteria in primary care with previous |
Ariel Beresniak 2016 [17] | Switzerland | To evaluate the efficacy of EHR4CR (Electronic Health Records for Clinical Research) solutions in comparison to current practices, from the viewpoint of clinical trial sponsors. |
Philipp Bruland 2016 [18] | Germany | To determine the most commonly used data elements in clinical trials and their availability in hospital EHR systems. |
Jake Carrion 2018 [19] | USA | To examine the observed benefits and drawbacks of using Electronic Health Record (EHRs) to enhance various patient-centered aspects of the clinical trial process, specifically its potential to improve patient recruitment, patient retention, and data collection |
GeorgesDe Moor 2015 [20] | Belgium | To describe the EHR4CR project which aims to demonstrate a scalable, widely acceptable and efficient approach to interoperability between Electronic Health Record (EHR) systems and clinical research systems. |
Peter J. Embi 2005 [21] | Ohio | To determine if the use of EHR-based Clinical Trial Alert (CTAs) could enhance physicians’ participation in subject recruitment and increase physician-generated recruitment rates for an ongoing clinical trial. |
Natalie C. Ernecof 2018 [22] | USA | To develop an EHR phenotype for identifying patients with late-stage dementia for a clinical trial of palliative care consultation. |
Jae Hyun Kim 2021 [23] | USA | To evaluate the impact of eligibility criteria on recruitment and observable clinical outcomes of COVID-19 clinical trials using EHR data |
Jeffrey Kirshner 2021 [24] | USA | To facilitate identification of clinical trial participation candidates, the researchers developed a machine learning tool that automates the determination of a patient's metastatic status, on the basis of unstructured EHR data. |
Niina Laaksonen 2021 [25] | Finland | To evaluate the accuracy of a commercially available EHR Research Platform, “InSite”, in identifying potential trial participants from the EHR system of a large tertiary care hospital. |
Mengyang Li 2021 [26] | China | To develop a patient-screening tool for clinical research using openEHR to address concept mismatch and enhance query performance. |
Stéphane M. Meystre 2019 [27] | USA | To assess the feasibility of determining a patient's eligibility for a sample of breast cancer clinical trials by automatically mapping coded clinical trial eligibility criteria to the corresponding clinical information extracted from text in the EHR. |
Riccardo Miotto 2015 [28] | USA | To develop a cost-effective, case-based reasoning framework for clinical research eligibility screening by reusing only the EHRs of a minimal number of enrolled participants to represent the target patient for each trial under consideration. |
Sarah J Nelson 2021 [29] | USA | To develop a service line for extracting study population estimates from EHR systems to aid in selecting enrollment sites for multicenter clinical trials. |
Yizhao Ni 2019 [30] | USA | To evaluate the impact of Automated Clinical Trial Eligibility Screener (ACTES) on the institutional workflow, both prospectively and comprehensively. |
Emily C. O’Brien 2021 [31] | USA | To describe the current site-level processes for utilizing the EHR to identify and screen potential participants for an ongoing clinical trial. |
James R. Rogers 2021 [32] | USA | To identify the extent of main clinical differences between clinical trial participants and nonparticipants using a combination of electronic health record and trial enrollment data. |
Yingcheng Sun 2021 [33] | USA | To systematically estimate the representativeness of the population in clinical trials using EHR data during the early design stage. |
Lindsay P. Zimmerman 2018 [34] | USA | To present a novel strategy for recruiting underrepresented, community-based participants for pragmatic research studies that leverage routinely collected EHR data. |