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Stomach
Dig Dis 2007;25:203–205
DOI: 10.1159/000103885
How to Proceed in Helicobacter pylori -Positive
Chronic Gastritis Refractory to First- and
Second-Line Eradication Therapy
Dino Vaira
a
Chiara Ricci
b
Alberto Lanzini
b
Federico Perna
a
Antonio Romano
a
Roberto Corinaldesi
a
a
Department of Internal Medicine and Gastroenterology, University of Bologna, Bologna, and
b
Gastroenterology Unit, University of Brescia, Brescia, Italy
Helicobacter pylori infection is a cause of peptic ulcer
disease, gastric mucosa-associated lymphoreticular tis-
sue (MALT) lymphoma and gastric cancer [1]. Standard
treatments for H. pylori that have been endorsed by US
and European authorities rely on clarithromycin or met-
ronidazole in conjunction with other antibiotics and acid
inhibitors [2, 3]. The prevalence of clarithromycin and
metronidazole resistance has increased significantly in
recent years and there has been a corresponding decline
in the eradication rate for H. pylori [4]. Eradication rates
in most Western countries have declined to unacceptable
values with approximately 1/5 patients failing eradication
therapy [5]. A simple, short treatment regimen that would
return eradication levels to the high values seen at the
advent of H. pylori treatment is urgently needed [5]. Such
a treatment regimen should have high efficacy against
clarithromycin- and metronidazole-resistant strains of
H. pylori as these strains are increasingly encountered in
routine clinical practice.
Triple therapy with a proton pump inhibitor (PPI),
clarithromycin, and either amoxicillin or metronidazole
is the most popular treatment regimen to cure H. pylori
infection among primary care physicians and gastroen-
terologists in the USA and Europe [6–8] . However, two
double-blind, US multicenter studies recently found dis-
appointingly low eradication rates with this regimen. In
one study, 75.6% of 402 patients and in the other, 77.2%
Key Words
Helicobacter pylori infection Chronic gastritis Eradication
therapy Peptic ulcer disease
Abstract
Helicobacter pylori is a widespread disease causing most of
the peptic ulcer diseases and low-grade mucosa-associated
lymphoreticular tissue (MALT) lymphoma. Moreover, H. py-
lori is a proven environmental risk factor for gastric carcino-
ma and it has been recognized as a type 1 carcinogen factor.
A combination of drugs has been proposed, using a proton
pump inhibitor (PPI), amoxicillin, clarithromycin, metronida-
zole and tetracycline to treat the infection. Since 1996, ac-
cording to the European guidelines, the first-line approach
using PPI, amoxicillin and clarithromycin or metronidazole
has been suggested. Seven days of quadruple therapy with
PPI (or ranitidine), tetracycline, bismuth salts and metronida-
zole has been reserved as second-line treatment. To improve
the eradication rate of the triple therapy, a different combi-
nation of the available antibiotics has been proposed, con-
sisting of a 10-day sequential regimen. A second-line levo-
floxacin-amoxicillin-based triple therapy given for 10 days
has been proposed, obtaining a high eradication rate, sug-
gesting this regimen to be a suitable retreatment option in
eradication failure. A third-line treatment with rifabutin-
based regimen has been proposed.
Copyright © 2007 S. Karger AG, Basel
Prof. Dino Vaira
Department of Internal Medicine and Gastroenterology, S. Orsola Hospital
Via Massarenti 9, IT–40138 Bologna (Italy)
Tel. +39 051 636 4140
E-Mail vairadin@med.unibo.it
© 2007 S. Karger AG, Basel
0257–2753/07/0253–0203$23.50/0
Accessible online at:
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