Literature DB >> 32436029

Nitric oxide inhalation as an interventional rescue therapy for COVID-19-induced acute respiratory distress syndrome.

Jun Kobayashi1, Isamu Murata2.   

Abstract

COVID-19 is an emerging disease of public health concern. While there is no specific recommended treatment for COVID-19, nitric oxide has the potential to be of therapeutic value for managing acute respiratory distress syndrome in patients with COVID-19. However, inhaled nitric oxide has not yet been formally evaluated. Given the extent of the COVID-19 pandemic, and the large numbers of hospitalized patients requiring respiratory support, clinical use of inhaled nitric oxide may become an alternate rescue therapy before extracorporeal membrane oxygenation for the management of acute respiratory distress syndrome in patients with COVID-19.

Entities:  

Year:  2020        PMID: 32436029      PMCID: PMC7238394          DOI: 10.1186/s13613-020-00681-9

Source DB:  PubMed          Journal:  Ann Intensive Care        ISSN: 2110-5820            Impact factor:   6.925


Novel coronavirus disease 2019 (COVID-19) is an emerging disease of public health concern, and the current pandemic is having a major global impact. Increasing attention is being focused on the development of therapeutic strategies against this disease. We read, with great interest, the article by Li et al. “Therapeutic strategies for critically ill patients with COVID-19” published in this journal [1]. While there is no specific recommended antiviral treatment, and vaccines have yet to be developed, the authors provided a powerful pharmacological strategy for the treatment of critically ill patients with COVID-19 acute respiratory distress syndrome (ARDS). In this review article, the drug applications for COVID-19 are well described according to disease severity; however, nitric oxide (NO) inhalation therapy, which is not described in this review, may be included in the strategy as a promising therapeutic candidate. In 2004, during the severe acute respiratory syndrome coronavirus (SARS-CoV) outbreak, a pilot study showed that low-dose inhaled NO (max 30 ppm) could shorten the time of ventilatory support for patients infected with SARS-CoV [2]. Although epidemiological evidence supporting the use of inhaled NO in treating COVID-19 has not yet been identified, similar therapeutic effects of NO can be expected for patients with COVID-19 due to the genetic similarities between the two viruses [3]. Based on this experience, clinical trials have begun in several medical institutes in the United States, and now a phase 2 clinical trial of inhaled NO is being conducted for mechanically ventilated patients with COVID‑19 ARDS to confirm whether NO inhalation will become an interventional therapy to rescue patients with this disease [4]. The inflammatory cytokine storm induced by virus infection is closely related to the development and progression of ARDS. Given the common pathological process leading to virus-induced ARDS [3], previous experience suggests that inhaled NO may be useful for managing COVID-19 ARDS. Previously published in vitro studies indicated that NO possessed inhibitory effects on SARS-CoV replication. Moreover, growing evidence has shown that inhaled NO can reduce inflammatory cell-mediated lung injury by inhibiting neutrophil activation and subsequent pro-inflammatory cytokine release. Due to its potent and selective pulmonary vasodilation, inhaled NO can lower pulmonary vascular resistance and decrease edema in the alveolar spaces, which enhances ventilation/perfusion matching. In addition, recent evidence also suggests that inhaled NO could have a wide range of systemic effects via cGMP-dependent and -independent mechanisms leading to a decrease in vascular tone, and a reduced risk of thrombosis and leukocyte adhesion to pulmonary and systemic vascular endothelium [5]. Because NO acts as a pro-inflammatory and an anti-inflammatory agent, depending on the amount of NO generation and its source, early and timely initiation of inhaled NO therapy may prevent cytokine storms following abnormal vascular endothelium/leukocyte interactions. In severe COVID-19 ARDS with hypoxemia despite optimizing ventilation and other rescue strategies, extracorporeal membrane oxygenation (ECMO) is the final therapeutic option [1]. However, given the high running cost, limited number of devices, and the skilled medical staff required to perform ECMO, inhaled NO, which is relatively of low cost and readily available, may be a promising interventional therapy for patients with severe COVID-19 ARDS. Because inhaled NO has been extensively applied to treat pulmonary hypertension, ARDS, and other respiratory diseases with a relatively good safety profile, we advocate for a clinical trial exploring the use of inhaled NO for the management of COVID-19 ARDS to be conducted as a matter of urgency.
  4 in total

Review 1.  Extrapulmonary effects of inhaled nitric oxide: role of reversible S-nitrosylation of erythrocytic hemoglobin.

Authors:  Timothy J McMahon; Allan Doctor
Journal:  Proc Am Thorac Soc       Date:  2006-04

Review 2.  Therapeutic strategies for critically ill patients with COVID-19.

Authors:  Lei Li; Ranran Li; Zhixiong Wu; Xianghong Yang; Mingyan Zhao; Jiao Liu; Dechang Chen
Journal:  Ann Intensive Care       Date:  2020-04-20       Impact factor: 6.925

3.  Inhalation of nitric oxide in the treatment of severe acute respiratory syndrome: a rescue trial in Beijing.

Authors:  Luni Chen; Peng Liu; He Gao; Bing Sun; Desheng Chao; Fei Wang; Yuanjue Zhu; Göran Hedenstierna; Chen G Wang
Journal:  Clin Infect Dis       Date:  2004-10-22       Impact factor: 9.079

4.  Lung pathology of fatal severe acute respiratory syndrome.

Authors:  John M Nicholls; Leo L M Poon; Kam C Lee; Wai F Ng; Sik T Lai; Chung Y Leung; Chung M Chu; Pak K Hui; Kong L Mak; Wilina Lim; Kin W Yan; Kwok H Chan; Ngai C Tsang; Yi Guan; Kwok Y Yuen; J S Malik Peiris
Journal:  Lancet       Date:  2003-05-24       Impact factor: 79.321

  4 in total
  18 in total

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2.  Gaseous Nitric Oxide and Dinitrosyl Iron Complexes with Thiol-Containing Ligands as Potential Medicines that Can Relieve COVID-19.

Authors:  A F Vanin; A V Pekshev; A B Vagapov; N A Sharapov; V L Lakomkin; A A Abramov; A A Timoshin; V I Kapelko
Journal:  Biophysics (Oxf)       Date:  2021-04-27

Review 3.  Potential Anti-SARS-CoV-2 Therapeutics That Target the Post-Entry Stages of the Viral Life Cycle: A Comprehensive Review.

Authors:  Rami A Al-Horani; Srabani Kar
Journal:  Viruses       Date:  2020-09-26       Impact factor: 5.048

4.  Real-world use of inhaled nitric oxide therapy in patients with COVID-19 and mild-to-moderate acute respiratory distress syndrome.

Authors:  Steven H Abman; Nicholas R Fox; M Ibrahim Malik; Sneha S Kelkar; Shelby L Corman; Sanika Rege; Jenna Bhaloo; Rachel Shah; Ren-Jay Shei; Dana Saporito; Nisreen Shamseddine; Erik DeBoer; George J Wan
Journal:  Drugs Context       Date:  2022-04-11

5.  Multi-omics-based identification of SARS-CoV-2 infection biology and candidate drugs against COVID-19.

Authors:  Debmalya Barh; Sandeep Tiwari; Marianna E Weener; Vasco Azevedo; Aristóteles Góes-Neto; M Michael Gromiha; Preetam Ghosh
Journal:  Comput Biol Med       Date:  2020-10-10       Impact factor: 4.589

Review 6.  Pathophysiology and potential future therapeutic targets using preclinical models of COVID-19.

Authors:  Rahul Kumar; Michael H Lee; Claudia Mickael; Biruk Kassa; Qadar Pasha; Rubin Tuder; Brian Graham
Journal:  ERJ Open Res       Date:  2020-12-07

Review 7.  Glycyrrhizic Acid: A Natural Plant Ingredient as a Drug Candidate to Treat COVID-19.

Authors:  Zhong Sun; Guozhong He; Ninghao Huang; Karuppiah Thilakavathy; Jonathan Chee Woei Lim; S Suresh Kumar; Chenglong Xiong
Journal:  Front Pharmacol       Date:  2021-07-09       Impact factor: 5.810

8.  COVID-19 and haemoglobin oxygen affinity: some clarity?

Authors:  Michael J Shattock; Yvonne Daniel; Beverley J Hunt; Andrew Retter; Katherine Henderson; Sarah Wilson; Claire C Sharpe
Journal:  Br J Haematol       Date:  2020-08-17       Impact factor: 6.998

9.  Inhaled nitric oxide in mechanically ventilated patients with COVID-19.

Authors:  Michele Ferrari; Alessandro Santini; Alessandro Protti; Davide T Andreis; Giacomo Iapichino; Gianluca Castellani; Valerio Rendiniello; Elena Costantini; Maurizio Cecconi
Journal:  J Crit Care       Date:  2020-08-11       Impact factor: 3.425

Review 10.  COVID-19 and Phosphodiesterase Enzyme Type 5 Inhibitors.

Authors:  Hayder M Al-Kuraishy; Ali I Al-Gareeb; Marwa S Al-Niemi; Ali K Al-Buhadily; Nasser A Al-Harchan; Claire Lugnier
Journal:  J Microsc Ultrastruct       Date:  2020-12-10
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