The report did not detail the patients’ diuretic therapy or renal function, leaving uncertainty as to whether they had been maximally treated with conservative therapy. Although the median hemoglobin at study entry was 120 g/L, the range was wide and one patient had a baseline hemoglobin of 51 g/L. It would appear that a subgroup of patients had significant baseline anemia that might have contributed to their symptoms and might have improved with

specific therapies (e.g., blood transfusions, iron infusions, or nasal surgery). Highly symptomatic patients with HHT are very difficult to treat and an innovative successful strategy would be quite www.selleckchem.com/products/pirfenidone.html important. As mentioned previously, this particular cohort was somewhat healthier than patients referred to some HHT centers with heart Crizotinib cell line failure from LVMs.4 They had a median age of 59 years (maximum 68 years) and most lacked echocardiographic evidence of severe pulmonary hypertension (estimated RV systolic pressure median 33 mmHg, maximum 79 mmHg). Also, the study excluded patients with atrial fibrillation, which generally represents an advanced manifestation of the high output heart

failure syndrome. Whether bevacizumab would be effective in more advanced patients remains to be investigated. In moderately symptomatic patients who fail intensive medical therapy, liver transplantation remains the only established approach to prevent progressive heart failure. Bevacizumab might be considered as a bridge to transplantation, except that it inhibits wound healing and the general recommendations are that treatment be discontinued for at least 1 month prior to surgery. This consideration would preclude cadaveric liver transplant, although elective transplantation would still be feasible with

a living donor. The effects 上海皓元 of bevacizumab on the liver were carefully evaluated in this study with hepatic computed tomography (CT) scans, Doppler ultrasound, and liver function tests (LFTs). A prior case report had suggested that bevacizumab was associated with a dramatic reduction in liver volume,12 raising hope that antiangiogenic therapy would lead to substantial remodeling of the liver AVMs. However, the French study did not show any changes in liver volume, hepatic artery diameter, or peak hepatic arterial flow velocity. There was significant prolongation of the transit time between the hepatic artery and the hepatic veins, perhaps demonstrating some effect on vascular remodeling. LFTs in this cohort at baseline showed only expected minor abnormalities, mostly in the alkaline phosphatase. There was no improvement in LFTs and there was some concern that five patients demonstrated an increase in aminotransferase levels to 1.5 times their initial values. Thus, the French study is a pioneering contribution, supporting the concept that antiangiogenic therapy might be a novel strategy to treat patients with LVMs and symptomatic heart failure.