Clinical and operational impact of rapid point-of-care SARS-CoV-2 detection in an emergency department.

ABSTRACT:

Study objective

Rapid point-of-care (POC) SARS-CoV-2 detection with Abbott ID NOW™ COVID-19 test has been implemented in our Emergency Department (ED) for several months. We aimed to evaluate the operational impact and potential benefits of this innovative clinical pathway.

Methods

We conducted a prospective, descriptive, interventional, non-randomized study, before-after trial with the comparison of patient cohorts from two consecutive periods of seven weeks (observational pre-POC period vs interventional POC period).

Results

In 2020, throughout weeks 37 to 50, 3333 patients were assessed for eligibility and among them 331 (9.9%) were positive for SARS-CoV-2 infections. Among the included patients, 136 (9.2%) were positive for SARS-CoV-2 infection in the pre-POC peri

SUBMITTER: Gerlier C 

PROVIDER: S-EPMC8479552 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature