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Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)

BACKGROUND: Statins and aspirin have been proposed for treatment of COVID-19 because of their anti-inflammatory and anti-thrombotic properties. Several observational studies have shown favourable results. There is a need for a randomised controlled trial. METHODS: In this single-center, open-label,...

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Autores principales: Ghati, Nirmal, Bhatnagar, Sushma, Mahendran, Manjit, Thakur, Abhishek, Prasad, Kshitij, Kumar, Devesh, Dwivedi, Tanima, Mani, Kalaivani, Tiwari, Pawan, Gupta, Ritu, Mohan, Anant, Saxena, Anita, Guleria, Randeep, Deepti, Siddharthan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270743/
https://www.ncbi.nlm.nih.gov/pubmed/35810307
http://dx.doi.org/10.1186/s12879-022-07570-5
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author Ghati, Nirmal
Bhatnagar, Sushma
Mahendran, Manjit
Thakur, Abhishek
Prasad, Kshitij
Kumar, Devesh
Dwivedi, Tanima
Mani, Kalaivani
Tiwari, Pawan
Gupta, Ritu
Mohan, Anant
Saxena, Anita
Guleria, Randeep
Deepti, Siddharthan
author_facet Ghati, Nirmal
Bhatnagar, Sushma
Mahendran, Manjit
Thakur, Abhishek
Prasad, Kshitij
Kumar, Devesh
Dwivedi, Tanima
Mani, Kalaivani
Tiwari, Pawan
Gupta, Ritu
Mohan, Anant
Saxena, Anita
Guleria, Randeep
Deepti, Siddharthan
author_sort Ghati, Nirmal
collection PubMed
description BACKGROUND: Statins and aspirin have been proposed for treatment of COVID-19 because of their anti-inflammatory and anti-thrombotic properties. Several observational studies have shown favourable results. There is a need for a randomised controlled trial. METHODS: In this single-center, open-label, randomised controlled trial, 900 RT-PCR positive COVID-19 patients requiring hospitalisation, were randomly assigned to receive either atorvastatin 40 mg (Group A, n = 224), aspirin 75 mg (Group B, n = 225), or both (Group C, n = 225) in addition to standard of care for 10 days or until discharge whichever was earlier or only standard of care (Group D, n = 226). The primary outcome variable was clinical deterioration to WHO Ordinal Scale for Clinical Improvement ≥ 6. The secondary outcome was change in serum C-reactive protein, interleukin-6, and troponin I. RESULTS: The primary outcome occurred in 25 (2.8%) patients: 7 (3.2%) in Group A, 3 (1.4%) in Group B, 8 (3.6%) in Group C, and 7 (3.2%) in Group D. There was no difference in primary outcome across the study groups (P = 0.463). Comparison of all patients who received atorvastatin or aspirin with the control group (Group D) also did not show any benefit [Atorvastatin: HR 1.0 (95% CI 0.41–2.46) P = 0.99; Aspirin: HR 0.7 (95% CI 0.27–1.81) P = 0.46]. The secondary outcomes revealed lower serum interleukin-6 levels among patients in Groups B and C. There was no excess of adverse events. CONCLUSIONS: Among patients admitted with mild to moderate COVID-19 infection, additional treatment with aspirin, atorvastatin, or a combination of the two does not prevent clinical deterioration. Trial Registry Number CTRI/2020/07/026791 (http://ctri.nic.in; registered on 25/07/2020) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07570-5.
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spelling pubmed-92707432022-07-10 Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial) Ghati, Nirmal Bhatnagar, Sushma Mahendran, Manjit Thakur, Abhishek Prasad, Kshitij Kumar, Devesh Dwivedi, Tanima Mani, Kalaivani Tiwari, Pawan Gupta, Ritu Mohan, Anant Saxena, Anita Guleria, Randeep Deepti, Siddharthan BMC Infect Dis Research BACKGROUND: Statins and aspirin have been proposed for treatment of COVID-19 because of their anti-inflammatory and anti-thrombotic properties. Several observational studies have shown favourable results. There is a need for a randomised controlled trial. METHODS: In this single-center, open-label, randomised controlled trial, 900 RT-PCR positive COVID-19 patients requiring hospitalisation, were randomly assigned to receive either atorvastatin 40 mg (Group A, n = 224), aspirin 75 mg (Group B, n = 225), or both (Group C, n = 225) in addition to standard of care for 10 days or until discharge whichever was earlier or only standard of care (Group D, n = 226). The primary outcome variable was clinical deterioration to WHO Ordinal Scale for Clinical Improvement ≥ 6. The secondary outcome was change in serum C-reactive protein, interleukin-6, and troponin I. RESULTS: The primary outcome occurred in 25 (2.8%) patients: 7 (3.2%) in Group A, 3 (1.4%) in Group B, 8 (3.6%) in Group C, and 7 (3.2%) in Group D. There was no difference in primary outcome across the study groups (P = 0.463). Comparison of all patients who received atorvastatin or aspirin with the control group (Group D) also did not show any benefit [Atorvastatin: HR 1.0 (95% CI 0.41–2.46) P = 0.99; Aspirin: HR 0.7 (95% CI 0.27–1.81) P = 0.46]. The secondary outcomes revealed lower serum interleukin-6 levels among patients in Groups B and C. There was no excess of adverse events. CONCLUSIONS: Among patients admitted with mild to moderate COVID-19 infection, additional treatment with aspirin, atorvastatin, or a combination of the two does not prevent clinical deterioration. Trial Registry Number CTRI/2020/07/026791 (http://ctri.nic.in; registered on 25/07/2020) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07570-5. BioMed Central 2022-07-09 /pmc/articles/PMC9270743/ /pubmed/35810307 http://dx.doi.org/10.1186/s12879-022-07570-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ghati, Nirmal
Bhatnagar, Sushma
Mahendran, Manjit
Thakur, Abhishek
Prasad, Kshitij
Kumar, Devesh
Dwivedi, Tanima
Mani, Kalaivani
Tiwari, Pawan
Gupta, Ritu
Mohan, Anant
Saxena, Anita
Guleria, Randeep
Deepti, Siddharthan
Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)
title Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)
title_full Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)
title_fullStr Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)
title_full_unstemmed Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)
title_short Statin and aspirin as adjuvant therapy in hospitalised patients with SARS-CoV-2 infection: a randomised clinical trial (RESIST trial)
title_sort statin and aspirin as adjuvant therapy in hospitalised patients with sars-cov-2 infection: a randomised clinical trial (resist trial)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270743/
https://www.ncbi.nlm.nih.gov/pubmed/35810307
http://dx.doi.org/10.1186/s12879-022-07570-5
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