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Increasing Pulmonary Artery Pulsatile Flow Improves Hypoxic Pulmonary Hypertension in Piglets
Published on: May 11, 2015
Phenylephrine increases pulmonary blood flow in children with tetralogy of Fallot
Katsuya Tanaka1, Hiroshi Kitahata, Shinji Kawahito
1Department of Anaesthesiology, Tokushima University School of Medicine, Tokushima, Japan. ktanaka@mcw.edu
Insights
Increasing blood pressure with phenylephrine improved oxygen levels in children with tetralogy of Fallot. This suggests that higher blood pressure boosts pulmonary blood flow, enhancing arterial oxygen saturation in these patients.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Physiology
- Congenital Heart Disease
Background:
- Tetralogy of Fallot (TOF) is a complex congenital heart defect.
- Improved blood pressure has been anecdotally linked to better oxygenation in TOF patients.
- Prospective studies are needed to confirm the relationship between blood pressure and pulmonary blood flow in TOF.
Purpose of the Study:
- To investigate if phenylephrine-induced hypertension increases pulmonary blood flow in children with TOF.
- To determine if this increase in pulmonary blood flow leads to improved arterial oxygenation.
Main Methods:
- 14 children with TOF (2-32 months) received intravenous phenylephrine.
- Transesophageal pulsed Doppler recorded pulmonary venous flow (PVF) velocity.
- Arterial blood gases and hemodynamics were measured; minute distance (MD) was calculated.
Main Results:
- Phenylephrine increased mean arterial blood pressure (54 to 73 mmHg).
- Significant increases in SaO(2) (92.0% to 95.0%) and PVF minute distance (1318 to 1533 cm x min(-1)) were observed.
- A strong correlation (r=0.72) existed between changes in MD and SaO(2).
Conclusions:
- Phenylephrine-induced hypertension increases pulmonary blood flow in tetralogy of Fallot.
- This enhanced pulmonary blood flow is a likely mechanism for improved arterial oxygenation in TOF.
- The findings support a potential therapeutic role for blood pressure management in TOF.
Purpose:
Although it has been reported that the increase in blood pressure improves arterial oxygen saturation (SaO(2)) in children with tetralogy of Fallot, no prospective study has demonstrated that an increase in blood pressure induces an increase in pulmonary blood flow in these patients. The purpose of this study was to see whether a phenylephrine-induced increase in systemic blood pressure increased pulmonary blood flow, resulting in improved arterial oxygenation in tetralogy of Fallot.
Methods:
In 14 consecutive children with tetralogy of Fallot (2-32 months old), transesophageal pulsed Doppler signals of left upper pulmonary venous flow (PVF) velocity were recorded before and four minutes after 10 micro g x kg(-1) of phenylephrine i.v. Simultaneously, arterial blood gas analysis and hemodynamic measurements were performed. The minute distance (MD) was calculated as the product of the heart rate and the sum of time-velocity integrals of PVF.
Results:
Phenylephrine iv increased mean arterial blood pressure from 54 +/- 8 mmHg to 73 +/- 10 mmHg. This phenylephrine-induced hypertension significantly increased SaO(2) and MD (92.0 +/- 7.5 vs 95.0 +/- 5.0% and 1318 +/- 344 vs 1533 +/- 425 cm x min(-1), respectively). There was a significant correlation (r = 0.72) between the change in MD and the change in SaO(2).
Conclusion:
Our results suggest that the phenylephrine-induced increase in systemic blood pressure produces an increase in pulmonary blood flow in tetralogy of Fallot. Our results further suggest that this increase in pulmonary blood flow is involved in the mechanism of phenylephrine-induced improvement of arterial oxygenation in tetralogy of Fallot.
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