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Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19
BACKGROUND: Despite millions of COVID‐19 cases in the United States, it remains unknown whether a history of COVID‐19 infection impacts the safety of pharmacologic myocardial perfusion imaging stress testing (pharmacologic MPI). HYPOTHESIS: The aim of this study was to assess if a prior COVID‐19 inf...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189073/ https://www.ncbi.nlm.nih.gov/pubmed/36951276 http://dx.doi.org/10.1002/clc.24008 |
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author | Skali, Hicham Walker, David Jiang, Jeanette Gurumoorthy, Giridharan Davies, Kalatu Kimura, Tomomi |
author_facet | Skali, Hicham Walker, David Jiang, Jeanette Gurumoorthy, Giridharan Davies, Kalatu Kimura, Tomomi |
author_sort | Skali, Hicham |
collection | PubMed |
description | BACKGROUND: Despite millions of COVID‐19 cases in the United States, it remains unknown whether a history of COVID‐19 infection impacts the safety of pharmacologic myocardial perfusion imaging stress testing (pharmacologic MPI). HYPOTHESIS: The aim of this study was to assess if a prior COVID‐19 infection was associated with a higher risk of complications during and following pharmacologic MPI testing. METHODS: This retrospective cohort analysis included 179 803 adults (≥18 years) from the PharMetrics® Plus claims database who underwent pharmacologic MPI between March 1, 2020 and February 28, 2021. Patients with a history of COVID‐19 infection (COVID‐19 group) were compared with propensity‐score matched no‐COVID‐19 history group for reversal agent use, 30‐day resource use, and post‐MPI cardiac events/procedures. RESULTS: The most commonly used stress agent was regadenoson (91.7%). The COVID‐19 group (n = 6372; 3.5%) had slightly higher: reversal agent use (difference 1.13% [95% confidence interval [CI]: 0.33, 1.92]), all‐cause costs (difference USD $128 [95% CI: $73–$181]), and office visits (81.5% vs. 77.0%) than the no‐COVID‐19 group. Prior COVID‐19 infection did not appear to impact subsequent cardiac events/procedures. CONCLUSIONS: COVID‐19 history was associated with slightly higher reversal agent use, all‐cause costs, and office visits after pharmacologic MPI; however, the differences were not clinically meaningful. Concerns for use of stress agents in patients with prior COVID‐19 do not appear to be warranted. |
format | Online Article Text |
id | pubmed-10189073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101890732023-05-18 Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 Skali, Hicham Walker, David Jiang, Jeanette Gurumoorthy, Giridharan Davies, Kalatu Kimura, Tomomi Clin Cardiol Clinical Trial Result BACKGROUND: Despite millions of COVID‐19 cases in the United States, it remains unknown whether a history of COVID‐19 infection impacts the safety of pharmacologic myocardial perfusion imaging stress testing (pharmacologic MPI). HYPOTHESIS: The aim of this study was to assess if a prior COVID‐19 infection was associated with a higher risk of complications during and following pharmacologic MPI testing. METHODS: This retrospective cohort analysis included 179 803 adults (≥18 years) from the PharMetrics® Plus claims database who underwent pharmacologic MPI between March 1, 2020 and February 28, 2021. Patients with a history of COVID‐19 infection (COVID‐19 group) were compared with propensity‐score matched no‐COVID‐19 history group for reversal agent use, 30‐day resource use, and post‐MPI cardiac events/procedures. RESULTS: The most commonly used stress agent was regadenoson (91.7%). The COVID‐19 group (n = 6372; 3.5%) had slightly higher: reversal agent use (difference 1.13% [95% confidence interval [CI]: 0.33, 1.92]), all‐cause costs (difference USD $128 [95% CI: $73–$181]), and office visits (81.5% vs. 77.0%) than the no‐COVID‐19 group. Prior COVID‐19 infection did not appear to impact subsequent cardiac events/procedures. CONCLUSIONS: COVID‐19 history was associated with slightly higher reversal agent use, all‐cause costs, and office visits after pharmacologic MPI; however, the differences were not clinically meaningful. Concerns for use of stress agents in patients with prior COVID‐19 do not appear to be warranted. John Wiley and Sons Inc. 2023-03-23 /pmc/articles/PMC10189073/ /pubmed/36951276 http://dx.doi.org/10.1002/clc.24008 Text en © 2023 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Trial Result Skali, Hicham Walker, David Jiang, Jeanette Gurumoorthy, Giridharan Davies, Kalatu Kimura, Tomomi Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 |
title | Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 |
title_full | Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 |
title_fullStr | Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 |
title_full_unstemmed | Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 |
title_short | Clinical and economic outcomes of pharmacological stress tests in patients with a history of COVID‐19 |
title_sort | clinical and economic outcomes of pharmacological stress tests in patients with a history of covid‐19 |
topic | Clinical Trial Result |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189073/ https://www.ncbi.nlm.nih.gov/pubmed/36951276 http://dx.doi.org/10.1002/clc.24008 |
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