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6

t h

A n n u a l E u r o p e a n C o n f e r e n c e o n

Gastroenterology

Euro Gastro 2018

J u n e 1 9 - 2 0 , 2 0 1 8

P a r i s , F r a n c e

Page 33

Journal of Clinical Gastroenterology and Hepatology

ISSN 2575-7733

T

he most widely prescribed regimen for first-line

H. pylori

eradication has

been a triple therapy with proton pump inhibitor (PPI) and 2 antibiotics.

However, the eradication rate of PPI-based regimen has been declining over

the years, mainly due to resistance to antibiotics. To exert sufficient

H. pylori

killing effect of antibiotics, maintenance of intragastric pH around 6 to 7 is

mandatory. Development of potent gastric acid secretion-lowering agents

should improve the eradication rate. Potassium-competitive acid blocker

(PCAB) possess approximately 350 times more potent inhibitory effects

than typical PPIs, works immediately, and the effect lasts for a long time.

Additionally, metabolic elimination is independent of cytochrome P450 (CYP)

2C19 polymorphism, which is distinct from PPI. This new agent is expected to

offer clinical advantages over conventional PPI-based eradication therapies.

Biography

John Ignatius G Ledesma is the head of the GI Endoscopy

unit of Riverside Medical Center, Bacolod City, Philippines. He

completed his Postgraduate training at the Makati Medical

Center where he was awarded the most outstanding intern and

most outstanding chief resident. He was the Chief of fellows

and by far the only Research Fellow in Gastroenterology. He

has been a speaker in over 250 local, national and international

scientific meetings. He is the recipient of over a dozen awards

of distinction, recognition, achievement, services and most

recently, The Canlaon Medical Society most outstanding

Physician of 2017.

drjohnignatiusledesma@yahoo.com

Management of

Helicobacter pylori

in the era of potassium-

competitive acid blocker

John Ignatius G Ledesma

Riverside Medical Center, Philippines

John Ignatius, J Clin Gastroenterol Hepatol 2018, Volume: 2

DOI: 10.21767/2575-7733-C1-002