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Published on: May 11, 2015
Invasive haemodynamics predict outcomes in paediatric pulmonary artery hypertension
Rupesh Kumar Natarajan1, Nathan Rodgers1, Shanti Narasimhan1
1Division of Pediatric Cardiology, University of Minnesota, Minneapolis, MN, USA.
Insights
Invasive hemodynamics in children with pulmonary artery hypertension can predict long-term outcomes. Key indicators like mean pulmonary artery pressure and diastolic pressure gradient are crucial for assessing patient prognosis.
Area of Science:
- Pediatric Cardiology
- Pulmonary Hypertension Research
- Hemodynamic Monitoring
Background:
- Invasive hemodynamics guide pulmonary artery hypertension (PAH) therapy.
- Predictive value of hemodynamic indices for long-term outcomes in pediatric PAH is largely unknown.
Purpose of the Study:
- To evaluate invasive hemodynamic data for predicting outcomes in pediatric pulmonary artery hypertension.
Main Methods:
- Retrospective review of cardiac catheterization data (2006-2019) from 46 pediatric PAH patients.
- Defined combined adverse outcome: pericardial effusion, shunt creation, lung transplant, or death.
- Analyzed hemodynamic indices and clinical outcomes.
Main Results:
- 76% of patients had congenital heart disease (CHD).
- Adverse outcomes (9 patients) associated with higher mean pulmonary artery pressure, indexed pulmonary vascular resistance, and right ventricular stroke work index (p < 0.05).
Conclusions:
- Invasive hemodynamics at initial catheterization predict outcomes in pediatric PAH.
- Mean pulmonary artery pressure and diastolic pressure gradient are key predictive factors.
Background:
Invasive haemodynamics are often performed for initiating and guiding pulmonary artery hypertension therapy. Little is known about the predictive value of invasive haemodynamic indices for long-term outcomes in children with pulmonary artery hypertension. We aimed to evaluate invasive haemodynamic data to help predict outcomes in paediatric pulmonary artery hypertension.
Methods:
Patients with pulmonary artery hypertension who underwent cardiac catheterisation (2006-2019) at a single centre were included. Invasive haemodynamic data from the first cardiac catheterisation and clinical outcomes were reviewed. The combined adverse outcome was defined as pericardial effusion (due to right ventricle failure), creation of a shunt for pulmonary artery hypertension (atrial septal defect or reverse Pott's shunt), lung transplant, or death.
Results:
Among 46 patients with a median [interquartile range (IQR)] age of 13.2 [4.1-44.7] months, 76% had CHD. Median mean pulmonary artery pressure was 37 [28-52] mmHg and indexed pulmonary vascular resistance was 6.2 [3.6-10] Woods units × m2. Median pulmonary artery pulsatility index was 4.0 [3.0-4.7] and right ventricular stroke work index was 915 [715-1734] mmHg mL/m2. After a median follow-up of 2.4 years, nine patients had a combined adverse outcome (two had a pericardial effusion, one underwent atrial level shunt, one underwent reverse Pott's shunt, and six died). Patients with an adverse outcome had higher systolic and mean pulmonary artery pressures, higher diastolic and transpulmonary pressure gradients, higher indexed pulmonary vascular resistance, higher pulmonary artery elastance, and higher right ventricular stroke work index (p < 0.05 each).
Conclusion:
Invasive haemodynamics (especially mean pulmonary artery pressure and diastolic pressure gradient) obtained at first cardiac catheterisation in children with pulmonary artery hypertension predicts outcomes.
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