Medium-Term Effect of Inhaled Nitric Oxide in Mechanically Ventilated COVID-19 Patients.

Publication date: Jan 26, 2025

Background: Nitric oxide (NO) plays a key role in various physiological processes. Inhaled NO (iNO) has been studied for treating acute respiratory distress syndrome (ARDS). During the COVID-19 pandemic, interest grew in its potential role for patients with COVID-19 ARDS, with studies showing improved oxygenation over 48 h. Methods: This is a retrospective study of adult patients with severe COVID-19 ARDS and refractory hypoxemia admitted to the medical ICU requiring mechanical ventilation and treated with iNO. The effect on oxygenation, respiratory, and ventilation parameters is measured. Significant improvement is defined as an increase in PaO/FiO ≥ 20% from a baseline. Results: This study includes 87 patients (55 men, mean age 58. 7 +/- 15. 2) with 164 iNO connections (mean 1. 9 per patient). iNO is independently associated with a significant PaO/FiO ratio improvement, with an OR of 1. 26 (95% CI 1. 09-1. 46), even after accounting for these potential confounders. The time to maximal PaO/FiO improvement is 14. 5 +/- 5. 0 h for men and 78. 5 +/- 5. 5 h for women, with respective ratio increases of 42. 5 +/- 8. 1 and 52. 5 +/- 13. 6 mmHg. Conclusions: Our study demonstrates that severe ARDS COVID-19 patients may benefit from inhaled nitric oxide, with delayed oxygenation improvements lasting up to 96 h and slower responses observed in women, raising the possibility that current guidelines against its use could be reconsidered.

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Concepts Keywords
Accounting ARDS
Increases COVID-19
Nitric inhaled nitric oxide
Pandemic
Women

Semantics

Type Source Name
drug DRUGBANK Nitric Oxide
disease MESH COVID-19
disease IDO role
drug DRUGBANK Inosine
disease MESH acute respiratory distress syndrome
disease MESH hypoxemia
drug DRUGBANK Coenzyme M
drug DRUGBANK Cyclic Guanosine Monophosphate
disease IDO cell
disease IDO blood
disease MESH Sepsis
disease MESH critically ill
disease MESH infection
pathway KEGG Viral replication
disease IDO host
disease IDO history
disease MESH end of life
drug DRUGBANK Sodium lauryl sulfate
disease MESH Comorbidity
disease MESH dyslipidemia
disease MESH diabetes mellitus
disease MESH AIDS
disease MESH Atrial fibrillation
disease MESH liver disease
disease MESH Chronic kidney disease
disease MESH Cerebrovascular disease
disease MESH Obstructive lung disease
disease MESH Pulmonary hypertension
disease MESH Peripheral vascular disease
drug DRUGBANK Penciclovir
drug DRUGBANK Oxygen
drug DRUGBANK Isoxaflutole
disease MESH metabolic acidosis
disease MESH alkalosis
disease MESH respiratory acidosis
disease MESH chronic conditions
drug DRUGBANK Flunarizine
drug DRUGBANK Carbon dioxide
disease MESH tic
disease MESH clinical significance
disease MESH treatment failure
drug DRUGBANK Trestolone
disease MESH hepato pulmonary syndrome
pathway REACTOME Metabolism
disease MESH causality
disease MESH acute kidney injury
disease MESH Viral Infections
disease MESH Respiratory Failure
disease MESH Lung Injury
drug DRUGBANK Almitrine
disease MESH Pneumonia
disease MESH Coronavirus Infection

Original Article

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