High cardiac output secondary to hepatic arteriovenous malformations may be isolated or associated with left heart failure with post-capillary pulmonary hypertension. More rarely, precapillary pulmonary hypertension develops, linked to obstructive pulmonary arterial remodeling, referred to as pulmonary arterial hypertension (PAH), which affects younger patients and is not necessarily associated with hepatic arteriovenous malformation. BEVACIZUMAB is an anti-VEGF treatment indicated under compassionate use guidelines for hereditary hemorrhagic telangiectasia in cases of symptomatic hepatic arteriovenous malformations, when complicated by isolated high cardiac output or post-capillary pulmonary hypertension, and in cases of refractory chronic bleeding. However, the efficacy of this treatment on pulmonary hypertension related to high cardiac output, isolated or associated with left heart failure, is poorly understood. In addition, this treatment is classified as a "possible association" for the development of PAH, according to the 7th World Congress Symposium on Pulmonary Hypertension. Indeed, Hlavaty et al. found, based on pharmacovigilance data and by searching for disproportionate effects using the Bayesian network method, a possible link between the use of BEVACIZUMAB and the development of PAH. This treatment is therefore not recommended in cases of PAH associated with hereditary hemorrhagic telangiectasia. The objective of this study is to investigate the efficacy and tolerability of Bevacizumab treatment in hereditary hemorrhagic telangiectasia with cardiac involvement (isolated symptomatic high cardiac output or associated with post-capillary PAH) secondary to severe liver damage, based on the experience of the French hereditary hemorrhagic telangiectasia network since the CIROCO registry was opened in 2009.
Study Type
OBSERVATIONAL
Enrollment
111
This is a retrospective observational study of patients who received Bevacizumab as part of their routine clinical care. The study will describe efficacy and tolerance outcomes based on existing data (including echocardiographic, right heart catheterization, respiratory function, biologic and clinical data before and after treatment)
Centre hospitalier universitaire de Poitiers
Poitiers, France
Cardiac impairement before and after bevacizumab
mean pulmonary arterial pressure (right heart catheterization) or systolic pulmonary arterial pressure (cardiac ultrasound) in mmHg before (M0) and after (M6) treatment (bevacizumab)
Time frame: 6 months
Outcome
Death or hospitalization for heart failure or liver transplantation
Time frame: 1 year
Adverse effects of bevacizumab
Adverse effects from bevacizumab such as hypertension, proteinuria, fatigue, nausea, diarrhea, joint pain, headache, dysphonia etc.
Time frame: 6 months
Right ventricular function
Peak S wave (in cm/s) measure in ultrasound
Time frame: 6 months
peak tricuspid regurgitant velocity
peak tricuspid regurgitant velocity (in m/s) mesured in cardiac ultrasound
Time frame: 6 months
Liver ultrasound before and after bevacizumab
Hepatic artery diameter (in cm)
Time frame: 6 months
Clinical evolution before and after bevacizumab
Dyspnea in NYHA
Time frame: 6 months
Cardiac output
Cardiac output in L/min before (M0) and after (M6) treatment (bevacizumab)
Time frame: 6 months
right ventricular function
TAPSE (in mm) measured in cardiac ultra sound
Time frame: 6 months
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