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Heart doi:10.1136/heartjnl-2012-303549
  • Pulmonary hypertension
  • Original article

Balloon pulmonary angioplasty in patients with inoperable chronic thromboembolic pulmonary hypertension

  1. Rune Andersen3
  1. 1Department of Cardiology, Oslo University Hospital Rikshospitalet, Oslo, Norway
  2. 2Department of Cardiovascular and Thoracic Surgery, Oslo University Hospital Rikshospitalet, Oslo, Norway
  3. 3Department of Radiology, Oslo University Hospital Rikshospitalet, Oslo, Norway
  1. Correspondence to Arne K Andreassen, Department of Cardiology, Oslo University Hospital Rikshospitalet, Oslo N-0027, Norway; aandreas{at}ous-hf.no
  • Received 21 December 2012
  • Revised 30 May 2013
  • Accepted 31 May 2013
  • Published Online First 11 July 2013

Abstract

Objective To examine the effect of balloon pulmonary angioplasty (BPA) on chronic thromboembolic pulmonary hypertension (CTEPH) in patients with inoperable disease or persistent pulmonary hypertension after pulmonary endarterectomy.

Design Observational cohort study.

Setting Referred patients with inoperable or persistent CTEPH.

Patients Twenty consecutive CTEPH patients (10 females), aged 60±10 years.

Interventions BPA.

Main outcome measures Right heart catheterisation, functional capacity (cardiopulmonary exercise testing (CPET) and NYHA class) and blood sampled biomarkers N-terminal pro-brain natriuretic peptide (NT-proBNP) and troponin T examined at the time of diagnosis and repeated in all patients 3 months after the last BPA.

Results Seventy-three catheterisations were performed with 18.6±6.1 BPAs per patient on segmental and subsegmental arteries. Two deaths occurred following the first BPA, with an overall 10% periprocedural death rate. Reperfusion oedema complicated seven procedures. Comparisons before and after BPA showed significant haemodynamic improvements, including decreased mean pulmonary artery pressure (mPAP) (45±11 mm Hg vs 33±10 mm Hg; p<0.001) and increased cardiac output (4.9±1.6 L/min vs 5.4±1.9 L/min; p=0.011). Reduced right ventricular strain was indicated by significantly lower plasma levels of NT-proBNP and troponin T. Significant improvement in functional capacity was evident as assessed by NYHA class (3.0±0.5 vs 2.0±0.5; p<0.001) and CPET (13.6±5.6 mL/kg/min vs 17.0±6.5 mL/kg/min; p<0.001). Seventeen patients (85%) were alive after 51±30 months of follow-up.

Conclusions BPA may offer an alternative form of treatment in selected CTEPH patients. While prognostic markers such as haemodynamics, functional capacity and biomarkers improve, significant periprocedural complications must be recognised. Randomised trials are warranted.

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