One week treatment for Helicobacter pylori infection

被引:39
作者
Walsh, D
Goggin, N
Rowland, M
Durnin, M
Moriarty, S
Drumm, B
机构
[1] OUR LADYS HOSP SICK CHILDREN,CHILDRENS RES CTR,PROFESSORIAL UNIT,DUBLIN 12,IRELAND
[2] UNIV DUBLIN TRINITY COLL,DEPT PAEDIAT,DUBLIN 2,IRELAND
关键词
Helicobacter pylori; treatment;
D O I
10.1136/adc.76.4.352
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Helicobacter pylori is associated with primary antral gastritis, duodenal ulceration, and gastric cancer. Current regimens for treating infection in children using bismuth and antibiotics for two to six weeks are cumbersome. The aim of this study was to evaluate a one week course of treatment. All children undergoing endoscopy were assessed for the presence of H pylori by culture, histology, rapid urease test, and C-13 urea breath test. infected children received a one week course of colloidal. bismuth subcitrate 380 mg/1.73 m(2)/day (maximum 120 mg four times a day), combined with metronidazole 20 mg/kg/day (maximum 200 mg three times a day), and clarithromycin 15 mg/kg/day (maximum 250 mg twice a day). To optimise compliance, drugs were dispensed in a 'Redidose' box containing a compartment for each day, and subcompartments marked 'breakfast', 'lunch', 'dinner', and 'bedtime'. Compliance and side effects were assessed immediately after treatment. A urea breath test was performed at least one month after treatment. Twenty two children infected with H pylori were entered into the study; 20 of these took all doses; two children suffered significant side effects (diarrhoea and vomiting). H pylori was eradicated in 21 of the 22 children (95.45%; 95% confidence interval 77% to 100%). This study shows that H pylori infection in children can be cleared by a one week course of treatment.
引用
收藏
页码:352 / 355
页数:4
相关论文
共 33 条
[1]  
[Anonymous], IARC MON EV CARC RIS
[2]   HIGH PREVALENCE OF HELICOBACTER-PYLORI METRONIDAZOLE RESISTANCE IN MIGRANTS TO EAST LONDON - RELATION WITH PREVIOUS NITROIMIDAZOLE EXPOSURE AND GASTRODUODENAL DISEASE [J].
BANATVALA, N ;
DAVIES, GR ;
ABDI, Y ;
CLEMENTS, L ;
RAMPTON, DS ;
HARDIE, JM ;
FELDMAN, RA .
GUT, 1994, 35 (11) :1562-1566
[3]   SHORT-TERM LOW-DOSE TRIPLE THERAPY FOR THE ERADICATION OF HELICOBACTER-PYLORI [J].
BAZZOLI, F ;
ZAGARI, RM ;
FOSSI, S ;
POZZATO, P ;
ALAMPI, G ;
SIMONI, P ;
SOTTILI, S ;
RODA, A ;
RODA, E .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1994, 6 (09) :773-777
[4]  
BELL GD, 1995, ALIMENT PHARM THERAP, V9, P41
[5]  
BERGERON MG, 1993, INFECTIONS MED S DEC, P12
[6]  
BLASER MJ, 1995, CANCER RES, V55, P562
[7]  
BLASER MJ, 1990, REV INFECTIOUS DI S1, V12, P99
[8]   TRIPLE THERAPY FOR THE ERADICATION OF HELICOBACTER-PYLORI AND REDUCTION OF DUODENAL-ULCER RELAPSE - COMPARISON OF 1-WEEK AND 2-WEEK REGIMENS AND RECRUDESCENCE RATES OVER 12 MONTHS [J].
CHEN, TS ;
TSAY, SH ;
CHANG, FY ;
LEE, SD .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1995, 10 (03) :300-305
[9]   ADHERENCE OF HELICOBACTER-PYLORI TO PRIMARY HUMAN GASTROINTESTINAL CELLS [J].
CLYNE, M ;
DRUMM, B .
INFECTION AND IMMUNITY, 1993, 61 (10) :4051-4057
[10]  
COUGHLAN JG, 1987, LANCET, V2, P1109