# Clinical Application of Inhaled Nitric Oxide in Conditions of Excessive Right Heart Load: A Review from Neonatal Pulmonary Hypertension to Perioperative Cardiac Surgery Management

**Authors:** Chengming Hu, Zhe Chen, Lizhi Lv, Yan Zhu, Yan Chen, Qiang Wang

PMC · DOI: 10.3390/jcdd13020081 · Journal of Cardiovascular Development and Disease · 2026-02-08

## TL;DR

This review examines the use of inhaled nitric oxide to manage right heart strain in neonates and cardiac surgery patients, highlighting its benefits and limitations in various clinical settings.

## Contribution

The paper provides a comprehensive synthesis of iNO's clinical applications and outcomes in conditions of excessive right heart load across different patient populations.

## Key findings

- iNO improves oxygenation in neonates with PPHN but does not significantly affect survival or neurodevelopment.
- In adults with ARDS, iNO offers temporary benefits without mortality reduction and may increase acute kidney injury risk.
- Perioperative iNO use in cardiac surgery can reduce pulmonary hypertension crises and ICU stays, though survival benefits remain unproven.

## Abstract

Excessive right heart load imposes an acute or chronic injury on the right ventricle (RV), predisposing critically ill neonates and cardiac surgical patients to RV failure, low cardiac output syndrome, and death. Inhaled nitric oxide (iNO) is a selective pulmonary vasodilator that improves ventilation–perfusion matching and unloads the RV without systemic hypotension; nonetheless, its application beyond established neonatal indications remains contentious. Our review synthesizes current mechanistic, translational, and clinical evidence regarding iNO use in three major settings characterized by excessive RV load: (1) neonatal pulmonary hypertension, particularly PPHN; (2) acute and chronic RV overload in older children and adults, including secondary pulmonary hypertension, acute respiratory distress syndrome (ARDS), and acute pulmonary embolism; and (3) perioperative and post-cardiopulmonary bypass (CPB) management in congenital and adult cardiac surgery. In term and near-term infants with hypoxic respiratory failure, pivotal randomized trials show that iNO consistently improves oxygenation and reduces extracorporeal membrane oxygenation (ECMO) use, but this has little effect on survival and long-term neurodevelopment. In ARDS and other adult critical-care indications, iNO provides transient improvements in gas exchange and RV performance without reducing mortality or ventilator duration, and meta-analyses signal an increased risk of acute kidney injury, particularly with prolonged use. In contrast, perioperative studies around CPB demonstrate that prophylactic postoperative iNO and intra-CPB nitric oxide administration can attenuate pulmonary hypertensive crises, facilitate separation from CPB, shorten ventilation and intensive care stay, and, in selected high-risk cohorts, may reduce cardiac surgery-associated acute kidney injury, although survival benefits remain unproven. Across these scenarios, iNO should be used judiciously and in a pathophysiology-driven manner as a time-limited, targeted adjunct to stabilize patients with documented or anticipated RV strain rather than a disease-modifying therapy. Future work should refine patient selection, timing, dosing, and weaning strategies, and define the long-term safety and cost-effectiveness of iNO within contemporary multimodal RV support pathways.

## Linked entities

- **Chemicals:** nitric oxide (PubChem CID 145068)
- **Diseases:** pulmonary hypertension (MONDO:0005149), PPHN (MONDO:0022430), acute respiratory distress syndrome (MONDO:0006502), acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, F12 (coagulation factor XII) [NCBI Gene 2161] {aka HAE3, HAEX, HAF}, NOS3 (nitric oxide synthase 3) [NCBI Gene 4846] {aka EC-NOS, ECNOS, MYMY8, NOSIII, cNOS, eNOS}, Gucy1a1 (guanylate cyclase 1 soluble subunit alpha 1) [NCBI Gene 497757] {aka Gucy1a3, SGC}, KLK4 (kallikrein related peptidase 4) [NCBI Gene 9622] {aka AI2A1, ARM1, EMSP, EMSP1, KLK-L1, PRSS17}, PDE5A (phosphodiesterase 5A) [NCBI Gene 8654] {aka CGB-PDE, CN5A, PDE5}
- **Diseases:** PE (MESH:D011655), ARDS (MESH:D012128), hypotension (MESH:D007022), ischaemia (MESH:D007511), ECMO (MESH:D000860), Group 2 (OMIM:214110), hemolysis (MESH:D006461), Neonatal Pulmonary Hypertension (OMIM:615371), damage to (MESH:D020263), hypoxic (MESH:D002534), iNO (MESH:D015208), impaired left ventricular filling (MESH:D018487), Hypoxic Respiratory Failure (MESH:D012131), pneumonia (MESH:D011014), acute kidney injury (MESH:D058186), stroke (MESH:D020521), chronic lung disease (MESH:D029424), myocardial injury (MESH:D009202), lung disease (MESH:D008171), endothelial dysfunction (MESH:D014652), cardiogenic shock (MESH:D012770), RV Failure (MESH:D051437), lung injury (MESH:D055370), edema (MESH:D004487), PPHN (MESH:D010547), CPB (MESH:D006323), pulmonary edema (MESH:D011654), critical illness (MESH:D016638), AVSD (MESH:C562831), inflammation (MESH:D007249), circulatory collapse (MESH:D012769), injury (MESH:D014947), surfactant deficiency (MESH:C580477), acute pulmonary hypertension (MESH:D006976), chronic (MESH:D002908), tissue injury (MESH:D017695), perfusion (MESH:D001480), neurologic sequelae (MESH:D009422), kidneys (MESH:D007674), PAH (MESH:D010661), heart failure (MESH:D006333), Group 5 PH (MESH:D008232), heart disease (MESH:D006331), RV hypertrophy (MESH:D017380), pulmonary vein obstruction (MESH:D000071078), neurodevelopmental, auditory, and respiratory sequelae (MESH:D015619), ventricular remodeling (MESH:D020257), VSD (MESH:D004310), d-TGA (MESH:C538319), LCOS (MESH:D002303), PDA (MESH:D004374), COVID-19 (MESH:D000086382), dilation (MESH:D002311), right ventricular dysfunction (MESH:D018497), CHD (MESH:D006330), pulmonary arterial obstruction (MESH:D000071079), anomalous pulmonary venous drainage (MESH:D012587), acute or chronic right ventricular failure (MESH:D065290), reperfusion injury (MESH:D015427), RV dilation (MESH:C535682)
- **Chemicals:** prostacyclin (MESH:D011464), S-nitrosothiols (MESH:D026403), NO (MESH:D009569), monocrotaline (MESH:D016686), NO2 (MESH:D009585), cGMP (MESH:D006152), oxygen (MESH:D010100), nitrate (MESH:D009566), Milrinone (MESH:D020105), tadalafil (MESH:D000068581), calcium (MESH:D002118), peroxynitrite (MESH:D030421), LPS (MESH:D008070), tetrahydrobiopterin (MESH:C003402), nitrite (MESH:D009573), thiol (MESH:D013438), L-arginine (MESH:D001120), Inhaled nitric oxide (-), superoxide (MESH:D013481), sildenafil (MESH:D000068677), dobutamine (MESH:D004280)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

114 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940944/full.md

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Source: https://tomesphere.com/paper/PMC12940944