Carvedilol for reducing portal pressure in primary prophylaxis of variceal bleeding: a dose-response study
Carvedilol for reducing portal pressure in primary prophylaxis of variceal bleeding: a dose-response study
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DOI:
10.1111/apt.14576
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发表时间:
2018-04-01
影响因子:
7.6
通讯作者:
Ferlitsch, A.
中科院分区:
文献类型:
--
作者:
Schwarzer, R.;Kivaranovic, D.;Ferlitsch, A.
Background: Sequential measurements of hepatic venous pressure gradient (HVPG) are used to assess the haemodynamic response to nonselective betablockers (NSBBs) in patients with portal hypertension.Aims: To assess the rates of HVPG response to different doses of carvedilol.Methods: Consecutive patients with cirrhosis undergoing HVPG-guided carvedilol therapy for primary prophylaxis of variceal bleeding between 08/2010 and 05/2015 were retrospectively included. After baseline HVPG measurement, carvedilol 6.25 mg/d was administered and HVPG response (HVPG-decrease >= 20% or to = 10% or to = 20% with carvedilol 6.25 mg/d and another 10 (14%) with carvedilol 12.5 mg/d. Forty (56%) patients had a HVPG decrease >= 10% with carvedilol 6.25 mg/d and 24 (33%) with carvedilol 12.5 mg/d. Thus, in total, a HVPG-response of >= 20% and >= 10% and was achieved in 38 (53%) and 55 (76%) and of patients respectively. Notably, 6 patients (n = 4 with ascites) did not tolerate an increase to 12.5 mg/d due to hypotension/bradycardia. However, none of the other patients had a SAP < 90 mm Hg at the final HVPG measurement.Conclusion: Carvedilol 12.5 mg/d was more effective than 6.25 mg/d in decreasing HVPG in primary prophylaxis. A total of 76% of patients achieved a HVPG-response of >= 10% to carvedilol 12.5 mg/d, however, arterial hypotension might occur, especially in patients with ascites.