Author/Authors :
Mokhtare, Marjan Colorectal Research Center - Iran university of Medical Sciences - Rasool-e-Akram Hospital, Tehran, Iran , Hosseini, Vahid Gut and Liver Research Center - Mazandaran University of Medical Sciences - Imam Khomeini Hospital, Sari, Iran , Tirgar Fakheri, Hafez Gut and Liver Research Center - Mazandaran University of Medical Sciences - Imam Khomeini Hospital, Sari, Iran , Maleki, Iradj Gut and Liver Research Center - Mazandaran University of Medical Sciences - Imam Khomeini Hospital, Sari, Iran , Taghvaei, Tarang Gut and Liver Research Center - Mazandaran University of Medical Sciences - Imam Khomeini Hospital, Sari, Iran , Valizadeh, Mohammad Gut and Liver Research Center - Mazandaran University of Medical Sciences - Imam Khomeini Hospital, Sari, Iran , Sardarian, Hossein Guilan University of Medical Sciences - International Branch - Bandar Anzali,Guilan, Iran , Agah, Shahram Colorectal Research Center - Iran university of Medical Sciences - Rasool-e-Akram Hospital, Tehran, Iran , Khalilian, Alireza Department of Biostatistics and Community Medicine - Imam Khomeini Hospital, Sari, Iran
Abstract :
Background: The effectiveness of classic standard triple therapy regimen of helicobacter pylori (H. pylori)
eradication has decreased to unacceptably low levels, largely related to development of resistance to metronidazole
and clarithromycin. Thus successful eradication of H. pylori infections remains challenging. Therefore
alternative treatments with superior effectiveness and safety should be designed and appropriately tested in all
areas depending on the native resistance patterns. Furazolidone has been used successfully in eradication regimens
previously and regimens containing furazolidone may be an ideal regimen.
Methods: H. pylori infected patients with proven gastric or duodenal ulcers and /or gastric or duodenal erosions
at Imam Khomeini Hospital in Sari/Northern Iran, were randomly allocated into three groups: group A (OABF)
with furazolidone (F) (200 mg bid.), group B (OABM-F) metronidazole (M) (500 mg bid.) for the first five days,
followed by furazolidone (F) (200 mg bid.) for the second five days and group C (OAF) with furazolidone (F)
(200 mg tid.). Omeprazole (O) (20 mg bid.) and amoxicillin (A) (1000 mg bid.) were given in all groups; bismuth
(B) (240 mg bid.) was prescribed in groups A & B. Duration of all eradication regimens were ten days. Eight
weeks after treatment, a 14C-urea breath test was performed for evaluation of H. pylori eradication.
Results: A total of 372 patients were enrolled in three groups randomly (124 patients in each group); 120 (97%)
patients in group A (OABF), 120 (97%) in group B (OABM-F) and 116 (93%) in group C (OAF) completed the
study. The intention-to-treat eradication rates were 83.7% (95% CI= 77.3–90.4), 79.8% (95% CI= 72.6–87), and
84.6% (95% CI= 78.2–91.1) and per-protocol eradication rates were 86.6% (95% CI= 80.5–92.8), 82.5% (95%
CI= 75.6–89.4), and 90.5% (95% CI= 85.1–95.9) for groups OABF, OABM-F, and OAF, respectively. No statistical
significant differences were found in case of severe drug adverse effects between the above mentioned three
groups (p> 0.05). The most common side effects, namely nausea and fever, occurred in all groups, but more
frequently in group C (OAF) (p< 0.05).
Conclusion: In developing countries such as Iran, furazolidone-based regimens can substitute clarithromycinbased
regimens for H. pylori eradication because of a very low level of resistance, low cost and high effectiveness.
Considering per-protocol eradication rate of ten days OAF regimen, and the acceptable limit of ninety
percent, we recommend this regimen in developing countries such as Iran to be substituted of classic standard
triple therapy. In order to minimize rare serious adverse effects, one week high dose OAF regimen should be
taken into consideration in other studies.
Keywords :
Treatment effectiveness , Bismuth , Furazolidone , Helicobacter pylori