Development of a pharmaceutical science systematic review process using a semi‐automated machine learning tool: Intravenous drug compatibility in the neonatal intensive care setting

Author:

De Silva D. Thisuri N.1ORCID,Moore Brioni R.1234ORCID,Strunk Tobias345ORCID,Petrovski Michael6ORCID,Varis Vanessa7ORCID,Chai Kevin8ORCID,Ng Leo910ORCID,Batty Kevin T.12ORCID

Affiliation:

1. Curtin Medical School Curtin University Perth Western Australia Australia

2. Curtin Health Innovation Research Institute Curtin University Perth Western Australia Australia

3. Medical School The University of Western Australia Crawley Western Australia Australia

4. Wesfarmers Centre for Vaccines and Infectious Diseases Telethon Kids Institute Nedlands Western Australia Australia

5. Neonatal Directorate King Edward Memorial Hospital, Child and Adolescent Health Service Subiaco Western Australia Australia

6. Pharmacy Department, King Edward Memorial Hospital Women and Newborn Health Service Subiaco Western Australia Australia

7. University Library, Curtin University Perth Western Australia Australia

8. School of Population Health Curtin University Perth Western Australia Australia

9. Curtin School of Allied Health Curtin University Perth Western Australia Australia

10. School of Health Sciences Swinburne University of Technology Hawthorn Victoria Australia

Abstract

AbstractOur objective was to establish and test a machine learning‐based screening process that would be applicable to systematic reviews in pharmaceutical sciences. We used the SPIDER (Sample, Phenomenon of Interest, Design, Evaluation, Research type) model, a broad search strategy, and a machine learning tool (Research Screener) to identify relevant references related to y‐site compatibility of 95 intravenous drugs used in neonatal intensive care settings. Two independent reviewers conducted pilot studies, including manual screening and evaluation of Research Screener, and used the kappa‐coefficient for inter‐reviewer reliability. After initial deduplication of the search strategy results, 27 597 references were available for screening. Research Screener excluded 1735 references, including 451 duplicate titles and 1269 reports with no abstract/title, which were manually screened. The remainder (25 862) were subject to the machine learning screening process. All eligible articles for the systematic review were extracted from <10% of the references available for screening. Moderate inter‐reviewer reliability was achieved, with kappa‐coefficient ≥0.75. Overall, 324 references were subject to full‐text reading and 118 were deemed relevant for the systematic review. Our study showed that a broad search strategy to optimize the literature captured for systematic reviews can be efficiently screened by the semi‐automated machine learning tool, Research Screener.

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,Neurology

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