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Laboratory Interventions to Eliminate Unnecessary Rapid COVID-19 Testing During a Reagent Shortage.
Wulff, Regina T; Qiu, Yuqing; Wu, Caroline; Calfee, David P; Singh, Harjot K; Hatch, Ian; Steel, Peter A D; Scofi, Jean E; Westblade, Lars F; Cushing, Melissa M.
  • Wulff RT; Department of Pathology and Laboratory Medicine, New York, NY, USA.
  • Qiu Y; Department of Population Health Sciences, New York, NY, USA.
  • Wu C; Department of Information Technology Business Solutions, NewYork-Presbyterian Hospital, New York, NY, USA.
  • Calfee DP; Department of Medicine, New York, NY, USA.
  • Singh HK; Department of Medicine, New York, NY, USA.
  • Hatch I; Department of Pathology and Laboratory Medicine, New York, NY, USA.
  • Steel PAD; Department of Emergency Medicine, New York, NY, USA.
  • Scofi JE; Department of Emergency Medicine, New York, NY, USA.
  • Westblade LF; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Cushing MM; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Am J Clin Pathol ; 158(3): 401-408, 2022 09 02.
Article in English | MEDLINE | ID: covidwho-2287109
ABSTRACT

OBJECTIVES:

In the fall of 2020, US medical centers were running out of rapid coronavirus disease 2019 (COVID-19) tests. The aim of this study is to evaluate the impact of an intervention to eliminate rapid test misutilization and to quantify the effect of the countermeasures to control rapid test ordering using a test utilization dashboard.

METHODS:

Interventions were made to preserve a severely limited supply of rapid diagnostic tests based on real-time analysis of a COVID-19 test utilization dashboard. This study is a retrospective observational study evaluating pre- and postintervention rates of appropriate rapid test use, reporting times, and cost/savings of resources used.

RESULTS:

This study included 14,462 severe acute respiratory syndrome coronavirus 2 reverse transcriptase polymerase chain reaction tests ordered during the study period. After the intervention, there was a 27.3% decrease in nonconforming rapid tests. Rapid test reporting time from laboratory receipt decreased by 1.47 hours. The number of days of rapid test inventory on hand increased by 39 days.

CONCLUSIONS:

Performing diagnostic test stewardship, informed by real-time review of a test utilization dashboard, was associated with significantly improved appropriate utilization of rapid diagnostic COVID-19 tests, improved reporting times, implied cost savings, and improved reagent inventory on hand, which facilitated the management of scarce resources during a pandemic.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Humans Language: English Journal: Am J Clin Pathol Year: 2022 Document Type: Article Affiliation country: Ajcp

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Humans Language: English Journal: Am J Clin Pathol Year: 2022 Document Type: Article Affiliation country: Ajcp