NSAIDs in COVID-19, friend or foe?


Reham Mahrous, Amr Abdelnasser, Raghda Fouda, Mohamed Abd Al Moniem Morsy,     Omnia Mandour
 

Author affiliation:
  1. Reham Mahrous, Cairo University, Cairo, Egypt; E-mail: reham.mahrous.aly@gmail.com; {ORCID:0000-0001-8884-5689}
  2. Amr Abdelnasser, Cairo University, Cairo, Egypt; E-mail: amrabdelnassar85@yahoo.com
  3. Raghda Fouda, Cairo University, Cairo, Egypt; E-mail: raghdafouda@gmail.com
  4. Mohamed Abd Al Moniem Morsy, Cairo University, Cairo, Egypt; E-mail: dr.mmorsy@yahoo.com
  5. Omnia Mandour, Egypt; E-mail: freeomnia@gmail.com
Correspondence: Reham Mahrous; E-mail: reham.mahrous.aly@gmail.com; Phone: 01006211832; Mobile: 20 1006211832

 

Abstract

 

At the beginning of COVID-19 pandemic the use of NSAIDS was avoided. This was because the previous studies suggesting that NSAIDs may be associated with increased risk of complications of lower respiratory tract infections. Later on studies involved the patients who used NSAIDs for some chronic conditions and showed no additional harm among these patients. Then many studied assessed the benefit of using NSAIDs in COVID-19 patients for management of pain and fever and showed no additional risk among these patients.

Key words: COVID-19; pandemic; NSAIDs

Citation: Mahrous R, Abdelnasser A, Fouda R, Morsy MAAM, Mandour O. NSAIDs in COVID-19, friend or foe? Anaesth. pain intensive care 2022;27(1):119−122; DOI: 10.35975/apic.v27i1.2123
Received: May 29, 2022; Reviewed: June 28, 2022; Accepted: July 03, 2022

 

1. Introduction

 

Coronavirus disease 2019 (COVID-19) still remains to be one of the most important challenges to the healthcare systems all around the world.1 The mode of transmission of coronavirus 2 (SARS CoV2) is direct, person-to-person via respiratory droplets.2 The most common symptoms of this disease are respiratory symptoms such as cough and dyspnea with fever.3 Digestive symptoms are also very common such as diarrhea, anorexia, and vomiting.4
It is believed that the port of entry of COVID-19 is through binding of SARS-CoV-2 to target cells through angiotensin-converting enzyme 2 (ACE2). Since  NSAID use may be associated with upregulation of ACE2 leading, an increased risk of infection was hypothesized, it was recommended to avoid its usage.5 Although ibuprofen was proved to cause upregulation of ACE 2, as found in an experimental study in rats,6 this effect has not been confirmed in humans.7
It is well known  that cytokine storm, an excessive immune reaction, is usually associated with marked patient deterioration. During the event of cytokine storm, there is elevated levels of proinflammatory cytokines, such as, interleukin-1b (IL-1b), IL-6, interferon gamma (IFN-g), and tumor necrosis factor alpha (TNF-a), in addition to chemokines such as CCL2, CCL4, CXCL9, and CXCL10.8,9  Therefore, immune suppression or reduction may be beneficial,10 which justified the use of corticosteroids in COVID-19 infection.11 NSAIDs could decrease the hyperinflammatory process of COVID-19.12 Furthermore, Ibuprofen, a commonly prescribed NSAID, was found several years ago to reduce IL-6 in human tissues,13and in the sputum.14
 

2. Pharmacology

 

Mechanism of action of NSAIDs is to inhibit the cyclooxygenase (COX) isoforms COX-1 and COX-2. COX-1 is expressed in most cells, while COX-2 expression is induced with stimulation of inflammatory process. COX-1 and COX-2 metabolize arachidonic acid into prostaglandin H2, which may be converted to several different types of prostaglandins (PGs), including PGD2, PGE2, PGF2a, and PGI2. PGs act on specific receptors to perform different roles, such as regulating immune responses and gastrointestinal barrier integrity.15
 

3. NSAIDS as an enemy?

 

On 14 March 2020 in France, it was recommended that NSAIDs use should be avoided as it might worsen the outcome in COVID-19 patients based on unpublished reports.16 This was based on previous studies suggesting that NSAIDs may be associated with increased risk of complications of lower respiratory tract infections.17-21 NSAIDs can mask initial signs of infection such as fever leading to delayed diagnosis and treatment.22
Furthermore, NSAIDs may cause selective inhibition of interferon gamma production by natural killer and T-cells leading to worse clinical outcome during viral infections.23 Also, NSAIDs have been found to inhibit antibody production in response to viral infection, but it is unclear if this affects disease severity or not.24,25
NSAIDs may cause nephrotoxicity,26,27 which is more likely to worsen the condition in patients seriously affected by COVID-19 and may be exacerbated by fever and dehydration. It was recommended that NSAIDs should not be used as the first-line treatment for fever and pain in patients with COVID-19 according to an editorial done by Little P.28
A review article, done by Sodhi M, found that studies performed to find association between use of NSAIDs and COVID-19 illness severity are often at risk of several types of biases. Biases include that correlation between ibuprofen administration and increased severity of COVID-19 disease is more likely to be inaccurate as deterioration may be caused by disease’s natural course of severity rather than NSAIDs administration. Furthermore, NSAIDs may not be used unless in the setting of more severe symptoms. Also, many patients receiving NSAIDs for long periods of time likely suffer from other chronic medical conditions that can increase their risk profile resulting in poor COVID-19 outcomes.29
 

4. NSAIDS as a friend?

 

Several studies concluded that patients recieving drugs that upregulate  ACE-2 such as NSAIDs, ACEIs, or ARBs, have no increased risk of severe pneumonia. Furthermore, they found that upregulating ACE-2 might have beneficial effects.30-32
Naproxen was believed to have both antiviral and anti-inflammatory properties so it may be added to the standard COVID-19 treatment.33
In a study published early in the COVID-19 pandemic, significantly higher angiotensin II levels were found in samples of plasma of infected patients compared to healthy individuals. The levels were directly proportional to viral load and lung injury. The authors suggested that angiotensin receptor blocker (ARB) drugs may be used in treatment of COVID- 19. This study is against the theory that upregulation of ACE2 is associated with poorer outcomes, as ACE2 acts as a negative regulator and lowers angiotensin II levels.34
Additionally, it was reported that among COVID-19 patients requiring hospitalization, individuals treated with ibuprofen or naproxen were less likely to require ventilation.10
No harmful effect of NSAID use among patients with COVID-19 was reported by several studies done in 2020.35-37
A cohort study done in England last year recommended that patients who receive NSAIDs for their long-term conditions should continue their medications because there is  no association between NSAIDs and COVID-19 related death when comparing current NSAIDS users to non-users.16
An observational study done in Saudi Arabia, included 503 COVID-19 patients and found no association between the acute and chronic use of NSAIDs and increased risk of mortality, severe COVID-19 disease, or the  need for oxygen support, with no difference in time to clinical improvement and length of hospital stay compared to non-NSAID users in admitted patients. 38
A retrospective cohort study of 403 patients, was conducted to evaluate whether ibuprofen administration to individuals with COVID-19 was associated with worse clinical outcomes, compared with paracetamol or no antipyretic. Authors did not observe an increased risk for mortality or the need for respiratory support in patients who received ibuprofen. Although the need for respiratory support was higher in patients treated with paracetamol with borderline significance, this might be due to that elderly patients with more severe chronic illnesses were more likely to be treated with paracetamol to avoid ibuprofen induced renal injury.39
Additionally, a systematic review and meta‑analysis done by Moore N. et al. reported that use of NSAIDS does not cause an increased risk in COVID-19 patients, and the previous irrelevant experimental data might have deprived patients of an effective drug for pain and fever management.40
Finally, a recently published systematic review and meta‑analysis, in April 2022, concluded that NSAIDs use was not found to be associated with higher mortality, ICU admission rate, need for respiratory support or mechanical ventilation. Furthermore, there is no clear evidence to support that NSAID might worsen the prognosis of COVID-19.41
 

5. Conclusion

 

The use of NSAIDs in patients with COVID-19 is not associated with higher risk regarding mortality or mechanical ventilation. Patients receiving NSAIDS benefit from the upregulation of ACE-2, and management of pain and fever.

 

6. Conflict of interest
Nil declared by the authors.

 

7. Author contribution
AA: Bibliography

RF: Data collection and revision

MAM: Searching and sorting of references

OM: Scientific writing and revision

 

8. References

 
  1. Yousefifard M, Zali A, Zarghi A, Madani Neishaboori A, Hosseini M, Safari S. Non-steroidal anti-inflammatory drugs in management of COVID-19; A systematic review on current evidence. Int J Clin Pract. 2020 Sep 1;74(9). [PubMed] DOI: 1111/ijcp.13557
  2. Meyerowitz EA, Richterman A, Gandhi RT, Sax PE. Transmission of SARS-CoV-2: A Review of Viral, Host, and Environmental Factors. Ann Intern Med. 2021 Jan 1;174(1):69–79. [PubMed] DOI: 7326/M20-5008
  3. Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507–13. [PubMed] DOI: 1016/S0140-6736(20)30211-7
  4. Gao QY, Chen YX, Fang JY. 2019 Novel coronavirus infection and gastrointestinal tract. J Dig Dis. 2020 Mar;21(3):125-126. [PubMed] DOI: 1111/1751-2980.12851
  5. Zhou P, Yang X Lou, Wang XG, Hu B, Zhang L, Zhang W, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. 2020 Mar;579(7798):270-273. [PubMed] DOI: 10.1038/s41586-020-2012-7
  6. Qiao W, Wang C, Chen B, Zhang F, Liu Y, Lu Q, et al. Ibuprofen attenuates cardiac fibrosis in streptozotocin-induced diabetic rats. Cardiology. 2015 Jun 1;131(2):97–106. [PubMed] DOI: 1159/000375362
  7. Fang L, Karakiulakis G, Roth M. Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection? Lancet Respir Med. 2020 Apr 1;8(4):e21. [PubMed] DOI: 1016/S2213-2600(20)30116-8
  8. Lucas C, Wong P, Klein J, Castro TBR, Silva J, Sundaram M, et al. Longitudinal analyses reveal immunological misfiring in severe COVID-19. 2020 Aug;584(7821):463-469. [PubMed] DOI: 10.1038/s41586-020-2588-y
  9. Mann ER, Menon M, Knight SB, Konkel JE, Jagger C, Shaw TN, et al. Longitudinal immune profiling reveals key myeloid signatures associated with COVID-19. Sci Immunol. 2020 Sep 1;5(51). [PubMed] DOI: 1126/sciimmunol.abd6197
  10. Castro VM, Ross RA, McBride SM, Perlis RH. Identifying common pharmacotherapies associated with reduced COVID-19 morbidity using electronic health records. medRxiv. 2020 Aug 28;2020.04.11.20061994. DOI: 1101/2020.04.11.20061994
  11. Russell B, Moss C, George G, Santaolalla A, Cope A, Papa S, et al. Associations between immune-suppressive and stimulating drugs and novel COVID-19-a systematic review of current evidence. Ecancermedicalscience. 2020 Mar 27;14. [PubMed] DOI: 3332/ecancer.2020.1022
  12. Russell B, Moss C, Rigg A, Van Hemelrijck M. COVID-19 and treatment with NSAIDs and corticosteroids: should we be limiting their use in the clinical setting? Ecancermedicalscience. 2020 Mar 30;14. [PubMed] DOI: 3332/ecancer.2020.1023
  13. Gallelli L, Galasso O, Falcone D, Southworth S, Greco M, Ventura V, et al. The effects of nonsteroidal anti-inflammatory drugs on clinical outcomes, synovial fluid cytokine concentration and signal transduction pathways in knee osteoarthritis. A randomized open label trial. Osteoarthr Cartilage. 2013 Sep;21(9):1400–8. [PubMed] DOI: 1016/j.joca.2013.06.026
  14. Chmiel JF, Konstan MW, Accurso FJ, Lymp J, Mayer-Hamblett N, VanDevanter DR, et al. Use of ibuprofen to assess inflammatory biomarkers in induced sputum: Implications for clinical trials in cystic fibrosis. J Cyst Fibros. 2015 Nov 1;14(6):720–6. [PubMed] DOI: 1016/j.jcf.2015.03.007
  15. Ricciotti E, Fitzgerald GA. Prostaglandins and inflammation. Arterioscler Thromb Vasc Biol. 2011 May;31(5):986–1000. [PubMed] DOI: 1161/ATVBAHA.110.207449
  16. Wong AYS, MacKenna B, Morton CE, Schultze A, Walker AJ, Bhaskaran K, et al. Use of non-steroidal anti-inflammatory drugs and risk of death from COVID-19: an OpenSAFELY cohort analysis based on two cohorts. Ann Rheum Dis. 2021 Jul 1;80(7):943–51. [PubMed] DOI: 1136/annrheumdis-2020-219517
  17. Basille D, Plouvier N, Trouve C, Duhaut P, Andrejak C, Jounieaux V. Non-steroidal Anti-inflammatory Drugs may Worsen the Course of Community-Acquired Pneumonia: A Cohort Study. Lung. 2017 Apr 1;195(2):201–8. [PubMed]
  18. Basille D, Thomsen RW, Madsen M, Duhaut P, Andrejak C, Jounieaux V, et al. Nonsteroidal Antiinflammatory Drug Use and Clinical Outcomes of Community-acquired Pneumonia. Am J Respir Crit Care Med. 2018 Jul 1;198(1):128–31. [PubMed] DOI: 1164/rccm.201802-0229LE
  19. Kotsiou OS, Zarogiannis SG, Gourgoulianis KI. Prehospital NSAIDs use prolong hospitalization in patients with pleuro-pulmonary infection. Respir Med. 2017 Feb 1;123:28–33. [PubMed] DOI: 1016/j.rmed.2016.12.005
  20. Le Bourgeois M, Ferroni A, Leruez-Ville M, Varon E, Thumerelle C, Brémont F, et al. Nonsteroidal Anti-Inflammatory Drug without Antibiotics for Acute Viral Infection Increases the Empyema Risk in Children: A Matched Case-Control Study. J Pediatr. 2016 Aug 1;175:47-53.e3. [PubMed] DOI: 1016/j.jpeds.2016.05.025
  21. Messika J, Sztrymf B, Bertrand F, Billard-Pomares T, Barnaud G, Branger C, et al. Risks of nonsteroidal antiinflammatory drugs in undiagnosed intensive care unit pneumococcal pneumonia: younger and more severely affected patients. J Crit Care. 2014;29(5):733–8. [PubMed] DOI: 1016/j.jcrc.2014.05.021
  22. Voiriot G, Philippot Q, Elabbadi A, Elbim C, Chalumeau M, Fartoukh M. Risks Related to the Use of Non-Steroidal Anti-Inflammatory Drugs in Community-Acquired Pneumonia in Adult and Pediatric Patients. J Clin Med. 2019 Jun 1;8(6). [PubMed] DOI: 3390/jcm8060786
  23. Giollo A, Adami G, Gatti D, Idolazzi L, Rossini M. Coronavirus disease 19 (Covid-19) and non-steroidal anti-inflammatory drugs (NSAID). Ann Rheum Dis. 2021 Feb 1;80(2). [PubMed] DOI: 1136/annrheumdis-2020-217598
  24. Bernard MP, Bancos S, Chapman TJ, Ryan EP, Treanor JJ, Rose RC, et al. Chronic inhibition of cyclooxygenase-2 attenuates antibody responses against vaccinia infection. Vaccine. 2010 Feb 3;28(5):1363–72. [PubMed] DOI: 1016/j.vaccine.2009.11.005
  25. Arvin AM, Fink K, Schmid MA, Cathcart A, Spreafico R, Havenar-Daughton C, et al. A perspective on potential antibody-dependent enhancement of SARS-CoV-2. 2020 Aug;584(7821):353-363. [PubMed] DOI: 10.1038/s41586-020-2538-8
  26. Clavé S, Rousset-Rouvière C, Daniel L, Tsimaratos M. The Invisible Threat of Non-steroidal Anti-inflammatory Drugs for Kidneys. Front Pediatr. 2019 Dec 17;7. [PubMed] DOI: 3389/fped.2019.00520
  27. Zhang X, Donnan PT, Bell S, Guthrie B. Non-steroidal anti-inflammatory drug induced acute kidney injury in the community dwelling general population and people with chronic kidney disease: systematic review and meta-analysis. BMC Nephrol. 2017 Aug 1;18(1). [PubMed] DOI: 1186/s12882-017-0673-8
  28. Little P. Non-steroidal anti-inflammatory drugs and covid-19. BMJ. 2020 Mar 27;368. [PubMed] DOI: 1136/bmj.m1185
  29. Sodhi M, Etminan M. Safety of Ibuprofen in Patients With COVID-19: Causal or Confounded? Chest. 2020 Jul 1;158(1):55–6. [PubMed] DOI: 1016/j.chest.2020.03.040
  30. Kuster GM, Pfister O, Burkard T, Zhou Q, Twerenbold R, Haaf P, et al. SARS-CoV2: should inhibitors of the renin-angiotensin system be withdrawn in patients with COVID-19? Eur Heart J. 2020 May 14;41(19):1801–3. [PubMed] DOI: 1093/eurheartj/ehaa235
  31. Trifirò G, Crisafulli S, Andò G, Racagni G, Drago F, Berrino L, et al. Should Patients Receiving ACE Inhibitors or Angiotensin Receptor Blockers be Switched to Other Antihypertensive Drugs to Prevent or Improve Prognosis of Novel Coronavirus Disease 2019 (COVID-19)? Drug Saf. 2020 Jun 1;43(6):507. [PubMed] DOI: 1007/s40264-020-00935-2
  32. Vaduganathan M, Vardeny O, Michel T, McMurray JJV, Pfeffer MA, Solomon SD. Renin-Angiotensin-Aldosterone System Inhibitors in Patients with Covid-19. N Engl J Med. 2020 Apr 23;382(17):1653–9. [PubMed] DOI: 1056/NEJMsr2005760
  33. Terrier O, Dilly S, Pizzorno A, Chalupska D, Humpolickova J, Bouřa E, et al. Antiviral Properties of the NSAID Drug Naproxen Targeting the Nucleoprotein of SARS-CoV-2 Coronavirus. Molecules. 2021;26(9). [PubMed] DOI: 3390/molecules26092593
  34. Liu Y, Yang Y, Zhang C, Huang F, Wang F, Yuan J, et al. Clinical and biochemical indexes from 2019-nCoV infected patients linked to viral loads and lung injury. Sci China Life Sci. 2020 Mar 1;63(3):364–74. [PubMed] DOI: 1007/s11427-020-1643-8
  35. Choi MH, Ahn H, Ryu HS, Kim BJ, Jang J, Jung M, et al. Clinical Characteristics and Disease Progression in Early-Stage COVID-19 Patients in South Korea. J Clin Med. 2020 Jun 1;9(6):1–19. [PubMed] DOI: 3390/jcm9061959
  36. Gianfrancesco M, Hyrich KL, Al-Adely S, Carmona L, Danila MI, Gossec L, et al. Characteristics associated with hospitalisation for COVID-19 in people with rheumatic disease: data from the COVID-19 Global Rheumatology Alliance physician-reported registry. Ann Rheum Dis. 2020 Jul 1;79(7):859–66. [PubMed] DOI: 1136/annrheumdis-2020-217871
  37. Bruce E, Barlow-Pay F, Short R, Vilches-Moraga A, Price A, McGovern A, et al. Prior Routine Use of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) and Important Outcomes in Hospitalised Patients with COVID-19. J Clin Med. 2020 Aug 1;9(8):2586. [PubMed] DOI: 3390/jcm9082586
  38. Abu Esba LC, Alqahtani RA, Thomas A, Shamas N, Alswaidan L, Mardawi G. Ibuprofen and NSAID Use in COVID-19 Infected Patients Is Not Associated with Worse Outcomes: A Prospective Cohort Study. Infect Dis Ther. 2021 Mar 1;10(1):253–68. [PubMed] DOI: 1007/s40121-020-00363-w
  39. Rinott E, Kozer E, Shapira Y, Bar-Haim A, Youngster I. Ibuprofen use and clinical outcomes in COVID-19 patients. Clin Microbiol Infect. 2020 Sep 1;26(9):1259.e5-1259.e7. [PubMed] DOI: 1016/j.cmi.2020.06.003
  40. Moore N, Bosco-Levy P, Thurin N, Blin P, Droz-Perroteau C. NSAIDs and COVID-19: A Systematic Review and Meta-analysis. Drug Saf. 2021 Sep 1;44(9):929–38. [PubMed] DOI: 1007/s40264-021-01089-5
  41. Zhou Q, Zhao S, Gan L, Wang Z, Peng S, Li Q, et al. Use of non-steroidal anti-inflammatory drugs and adverse outcomes during the COVID-19 pandemic: A systematic review and meta-analysis. EClinicalMedicine. 2022 Apr;46:101373. [PubMed] DOI: 1016/j.eclinm.2022.101373