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Inhaled nitric oxide therapy after Fontan-type operations
Naoki Yoshimura1, Masahiro Yamaguchi, Shigeteru Oka
1Department of Cardiothoracic Surgery, Kobe Children's Hospital, 1-1-1 Takakura-dai, Suma-ku, Kobe 654-0081, Japan.
Surgery Today
|December 29, 2004
Summary
Inhaled nitric oxide (NO) therapy effectively reduced pulmonary vascular resistance in children after Fontan-type operations. Appropriate indications include elevated central venous pressure or transpulmonary pressure gradient.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Surgery
- Pulmonary Hypertension
Background:
- The Fontan-type operation is a complex surgical procedure for single-ventricle congenital heart defects.
- Pulmonary vascular resistance can remain elevated post-Fontan, leading to significant morbidity.
- Inhaled nitric oxide (NO) is a vasodilator explored to manage pulmonary hypertension.
Purpose of the Study:
- To evaluate the efficacy of inhaled nitric oxide (NO) therapy in reducing pulmonary vascular resistance after Fontan-type operations.
- To determine the appropriate clinical indications for inhaled NO therapy in this patient population.
Main Methods:
- Retrospective review of 47 children undergoing inhaled NO therapy post-Fontan-type operation (1996-2002).
- Doses of inhaled NO ranged from 5 to 30 ppm (median 10 ppm).
- Therapy duration varied from 5 hours to 52 days (median 2 days).
Main Results:
- Inhaled NO significantly decreased central venous pressure (CVP) and transpulmonary pressure gradient.
- Systolic systemic arterial pressure increased significantly with inhaled NO.
- Patients with fenestration showed improved oxygen saturation (SaO2) with inhaled NO.
- No significant hemodynamic changes were observed in patients with low CVP or transpulmonary pressure gradient.
Conclusions:
- Inhaled NO therapy is effective in improving hemodynamics in select pediatric patients post-Fontan-type operation.
- Appropriate indications for inhaled NO include a CVP ≥15 mmHg or a transpulmonary pressure gradient ≥8 mmHg.
- This therapy may help manage pulmonary vascular resistance and improve outcomes in this challenging patient group.