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1.
Scand J Gastroenterol ; 37(12): 1395-402, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12523588

ABSTRACT

BACKGROUND: Functional dyspepsia (FD) is defined as persistent or recurrent pain/discomfort centred in the upper abdomen, where no structural explanation for the symptoms is found. The role of drug treatment remains controversial. The aim in this study was to evaluate the effect of omeprazole 20 mg twice daily (b.i.d) and to test methods for symptom assessment. METHODS: 197 patients fulfilling the criteria for FD were randomly allocated to double-blind treatment with omeprazole 20 mg b.i.d (n = 100) or placebo (n = 97) for 14 days. Patients with a known gastrointestinal disorder or with main symptoms indicating gastro-oesophageal reflux disease or irritable bowel syndrome were excluded. Helicobacter pylori testing and 24-h intra-oesophageal 24-h pH-metry were performed before randomization. The patients recorded dyspeptic symptoms on diary cards. RESULTS: A stringent endpoint, 'complete symptom relief on the last day of treatment', was the primary efficacy variable. For the APT cohort, this was achieved in 29.0% and 17.7% on omeprazole and placebo, respectively (95% CI of difference (11.3%): -0.4%-23.0%, P = 0.057). Similar figures in the PP cohort were 31.0% and 15.5%, respectively (95% Cl of difference (15.5%): 3.2%-27.7%, P = 0.018). The benefit of omeprazole in the PP cohort was confirmed by secondary endpoints such as, no dyspeptic symptoms on the last 2 days of treatment and overall treatment response. H. pylori status and the level of oesophageal acid exposure did not significantly influence the response to therapy. CONCLUSION: A subset of patients with FD will respond to therapy with omeprazole.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Dyspepsia/drug therapy , Omeprazole/therapeutic use , Adult , Aged , Anti-Ulcer Agents/administration & dosage , Double-Blind Method , Female , Humans , Hydrogen-Ion Concentration , Male , Middle Aged , Monitoring, Physiologic , Omeprazole/administration & dosage
3.
Helicobacter ; 5(1): 22-3, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10672047

ABSTRACT

BACKGROUND: The aim of our study was to test the feasibility of culturing Helicobacter pylori directly from biopsies aimed for rapid urease test in routine clinical practice. MATERIALS AND METHODS: In 260 consecutive patients referred for gastroscopy because of dyspepsia one antral biopsy was routinely used for our "in house" rapid urease test (RUT). Positive biopsies were placed in a transport medium and sent to the laboratory. The biopsies were cultured and incubated at 37 degrees C for 5-7 days. H. pylori was identified and routinely tested for antimicrobial resistance by using the E-test. RESULTS: In 118 out of 260 patients (45%) the urease test turned positive and the growth of H. pylori was sufficient to allow testing of antimicrobial resistance. CONCLUSION: H. pylori could be cultured from almost all positive RUT specimens. A liquid RUT is thus more suitable for culture, saving additional biopsies.


Subject(s)
Clinical Enzyme Tests , Helicobacter Infections/diagnosis , Helicobacter pylori/isolation & purification , Urease/analysis , Adult , Aged , Aged, 80 and over , Bacteriological Techniques , Clinical Enzyme Tests/economics , Cost-Benefit Analysis , Helicobacter pylori/enzymology , Helicobacter pylori/growth & development , Humans , Microbial Sensitivity Tests , Middle Aged
4.
J Clin Microbiol ; 36(12): 3689-90, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9817898

ABSTRACT

We have developed a PCR-based method to detect macrolide resistance and the virulence gene cagA in Helicobacter pylori within 24 h, thereby improving the lengthy process of culture-based approaches. Total DNA was prepared directly from stomach biopsy specimens. The procedure proved to be rapid and reliable and could be utilized for diagnostic purposes.


Subject(s)
Antigens, Bacterial , Bacterial Proteins/genetics , Genes, Bacterial , Helicobacter pylori/genetics , Polymerase Chain Reaction , Stomach/microbiology , Clarithromycin/pharmacology , Drug Resistance, Microbial/genetics , Helicobacter pylori/drug effects , Helicobacter pylori/pathogenicity , Humans , Virulence
6.
Lakartidningen ; 95(4): 279-81, 1998 Jan 21.
Article in Swedish | MEDLINE | ID: mdl-9469961

ABSTRACT

AIM: Primary resistance of H pylori strains to antimicrobials has direct therapeutical implications. For this reason we studied the prevalence of primary resistance of H pylori of Sweden, in a regional setting. MATERIAL AND METHODS: A total of 244 patients referred to our endoscopy unit have been evaluated prospectively for the occurrence of H pylori. Helicobacter pylori infection was established by a positive rapid urease test on an antral biopsy. If positive the biopsy specimen was transferred to a transportmedium for culture on a Skirrow medium. Antimicrobial resistance was evaluated by the E-test. RESULTS: In 109 patients H pylori infection was seen and in all of them the culture was positive. No resistance was seen for amoxycillin and tetracycline. The resistance against metronidazole was 40.3% and and against clarithromycin it was 2.8%. For metronidazole there was a significantly higher resistance seen in women compared to men (53.3% vs 31.2%; p < 0.001). CONCLUSIONS: Primary resistance to metronidazole was higher than expected and over average in Europe. The resistance for clarithromycin is still rare. Further monitoring is mandatory to detect changes in the community.


Subject(s)
Antitrichomonal Agents/therapeutic use , Drug Resistance, Multiple , Helicobacter Infections/drug therapy , Helicobacter pylori/drug effects , Metronidazole/therapeutic use , Antitrichomonal Agents/adverse effects , Female , Helicobacter Infections/immunology , Helicobacter pylori/immunology , Humans , Male , Metronidazole/adverse effects , Sweden
10.
Helicobacter ; 2(4): 188-93, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9421122

ABSTRACT

BACKGROUND: This double-blind, randomized study evaluated the efficacy of dual and triple therapies including ranitidine for treatment of Helicobacter pylori infection. MATERIALS AND METHODS: Dyspeptic patients (n = 105) with a positive rapid urease test formed the intention-to-treat population (ITT). All patients were assigned to 14 days treatment with ranitidine 300 mg b.i.d and clarithromycin 750 mg b.i.d. Group A (n = 53) also received a placebo twice daily, while group B (n = 52) received lymecycline 300 mg b.i.d. Treatment with ranitidine, 150 mg b.i.d, was continued for an additional 30 days. H. pylori infection was verified by culture. Twelve weeks after antibiotic treatment, H. pylori status was investigated by culture and 14C-urea breath test (UBT). The per-protocol (PP) group consisted of 73 patients (A, n = 38; B, n = 35). RESULTS: Cure rates were 87% (95% C.I. = 72% to 94%) vs. 72% (95% C.I. = 58% to 83%) in the ITT-group and 89% (95% C.I. = 73% to 97%) vs. 87% (95% C.I. = 72% to 96%) in the PP-population (culture and UBT) when triple and dual therapies were compared. In all patients who were not cured, clarithromycin resistance of H. pylori was acquired. Side effects were experienced by 54% of patients. CONCLUSIONS: The difference in efficacy between the two treatment regimens was not significant. However, the cure rates in this study are comparable to combination treatments with omeprazole. Treatment failures were due to acquired clarithromycin resistance.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Anti-Ulcer Agents/therapeutic use , Clarithromycin/therapeutic use , Helicobacter Infections/drug therapy , Helicobacter pylori/drug effects , Ranitidine/therapeutic use , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/adverse effects , Anti-Ulcer Agents/adverse effects , Clarithromycin/adverse effects , Diarrhea/chemically induced , Double-Blind Method , Drug Resistance, Microbial , Drug Therapy, Combination , Female , Helicobacter Infections/diagnosis , Humans , Lymecycline/therapeutic use , Male , Middle Aged , Mouth Diseases/chemically induced , Nausea/chemically induced , Ranitidine/adverse effects , Sensitivity and Specificity , Taste Disorders/chemically induced , Tongue/drug effects
12.
Aliment Pharmacol Ther ; 10(3): 275-7, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8791950

ABSTRACT

BACKGROUND: One-week triple therapy consisting of omeprazole 20 mg b.d., clarithromycin 250 mg b.d. and tinidazole 500 mg b.d. is an effective therapy for H. pylori infection with a cure rate of 93%. We therefore compared two similar 1-week regimens consisting of a lansoprazole, clarithromycin and either metronidazole or tetracycline in a prospective study. METHODS: Two cohorts, each of 60 patients suffering from H. pylori infection associated with peptic ulcer disease or ulcer-like dyspepsia, were treated for 1 week with either lansoprazole 30 mg b.d., clarithromycin 250 mg b.d. and either metronidazole 400 mg b.d. (cohort A, n = 60) or tetracycline 300 mg b.d. (cohort B, n = 60). Four weeks after treatment, cure of H. pylori infection was evaluated by endoscopy using rapid urease testing together with histology. RESULTS: In cohort A, 55 patients out of 60 showed cure of H. pylori infection (92%); the treatment was well tolerated, but three patients suffered from side-effects. In cohort B, which was free of metronidazole, 50 out of 60 patients showed cure of H. pylori infection (83%); two patients reported side-effects. The differences between the two cohorts were not statistically significant. CONCLUSION: Triple therapy for 1 week with lansoprazole as the antisecretory agent seems to be as effective as is reported for omeprazole-based regimens.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Drug Therapy, Combination/therapeutic use , Helicobacter Infections/drug therapy , Helicobacter pylori , Metronidazole/therapeutic use , 2-Pyridinylmethylsulfinylbenzimidazoles , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/administration & dosage , Anti-Ulcer Agents/administration & dosage , Anti-Ulcer Agents/therapeutic use , Clarithromycin/administration & dosage , Clarithromycin/therapeutic use , Drug Therapy, Combination/administration & dosage , Female , Helicobacter Infections/microbiology , Humans , Lansoprazole , Male , Metronidazole/administration & dosage , Middle Aged , Omeprazole/administration & dosage , Omeprazole/analogs & derivatives , Omeprazole/therapeutic use , Tetracycline/administration & dosage , Tetracycline/therapeutic use
14.
Am J Gastroenterol ; 90(6): 943-5, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7771426

ABSTRACT

OBJECTIVES: The aim of this study was to confirm the efficacy and tolerability of a new, low dose, short-term triple therapy for cure of Helicobacter pylori infection, as suggested by Bazzoli, in a larger population. METHODS: On an "intention-to-treat" basis, 116 patients with active (n = 41) or healed (n = 47) peptic ulcer disease or ulcer-like dyspepsia (n = 28) and H. pylori infection received a 1-wk course of omeprazole 20 mg b.i.d., clarythromycin 250 mg b.i.d., and tinidazole 500 mg b.i.d.. Four weeks after treatment withdrawal, cure of H. pylori infection was evaluated by rapid urease test and histology. RESULTS: One hundred and sixteen patients returned for follow-up. In 108 patients, H. pylori could not be identified 4 wk after cessation of therapy. The eradication rate was calculated to 93%. In addition, all patients with active peptic ulcers showed complete healing at follow-up despite no further treatment. Drug acceptance and compliance was excellent. CONCLUSION: Triple therapy as suggested by Bazzoli with omeprazole (in this study given b.i.d. for better compliance), clarythromycin, and tinidazole is indeed highly effective for both cure of H. pylori infection and for healing of peptic ulcers, is easy to perform, is cheap, and is without clinically significant side effects, even in a larger population.


Subject(s)
Clarithromycin/administration & dosage , Helicobacter Infections/drug therapy , Helicobacter pylori , Omeprazole/administration & dosage , Peptic Ulcer/drug therapy , Tinidazole/administration & dosage , Adult , Aged , Aged, 80 and over , Drug Administration Schedule , Drug Therapy, Combination , Female , Helicobacter Infections/complications , Humans , Male , Middle Aged , Peptic Ulcer/microbiology
20.
Hepatogastroenterology ; 35(6): 289-94, 1988 Dec.
Article in English | MEDLINE | ID: mdl-3215625

ABSTRACT

The clinical features of primary sclerosing cholangitis were studied in 46 consecutive patients. Jaundice was the most common symptom (57%), followed by pruritus (28%), pain (24%), and fever (15%). Thirty-three per cent of the patients had no symptoms, merely laboratory changes. No significant relationship was observed between a numerical score of radiological bile duct changes at diagnosis and the clinical picture, or the clinical course during follow-up. If clinical deterioration occurred, this seemed to happen within the first eight years after the clinical presentation. Patients with only intra-hepatic bile duct changes (n = 10) did not differ clinically from those with extrahepatic changes as well. Forty-three out of 44 patients examined had inflammatory bowel disease, usually ulcerative colitis, with total colitis in 84%. Radiological bile duct changes had a significantly higher score in patients who had to be treated with a combination of sulfasalazine and steroids, suggesting a weak relationship between severity of bowel disease and bile duct disease.


Subject(s)
Bile Ducts, Intrahepatic/diagnostic imaging , Cholangitis, Sclerosing/diagnostic imaging , Inflammatory Bowel Diseases/diagnostic imaging , Adult , Cholangiography , Cholangiopancreatography, Endoscopic Retrograde , Cholangitis, Sclerosing/complications , Female , Humans , Inflammatory Bowel Diseases/complications , Liver/pathology , Male , Middle Aged
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