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  • Pharmacy  (3)
  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1991
    In:  European Journal of Drug Metabolism and Pharmacokinetics Vol. 16, No. 3 ( 1991-7), p. 189-196
    In: European Journal of Drug Metabolism and Pharmacokinetics, Springer Science and Business Media LLC, Vol. 16, No. 3 ( 1991-7), p. 189-196
    Type of Medium: Online Resource
    ISSN: 0378-7966 , 2107-0180
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1991
    detail.hit.zdb_id: 2558337-2
    SSG: 15,3
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  • 2
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 48, No. 3 ( 2018-08), p. 370-377
    Abstract: Although autoimmune gastritis ( AIG ) is generally considered relatively rare, we frequently encounter AIG among patients at to our hospital who have experienced at least two episodes of Helicobacter pylori eradication failure. Aims We investigated the incidence of AIG in consecutive patients who consulted our department for H. pylori eradication with reference to eradication history. Methods A total of 404 consecutive patients who visited the H. pylori ‐specific out‐patient unit of our hospital from June 2015 to June 2017 were enrolled. Of these, 137 were treatment‐naive, 47 had failed treatment once (single failure), and 220 had failed treatment twice or more (multiple failures) by 13 C‐ UBT . Gastroscopy was performed in all patients. Culture tests of gastric mucosal samples were performed for H. pylori and other bacteria positive for urease activity. Anti‐parietal cell antibody ( APCA ) was measured. Patients with severe atrophy in the gastric corpus and positivity for APCA were diagnosed as having AIG . Results A total of 43 patients were diagnosed as having AIG , of whom two were treatment‐naive (1.5%, 2/137), 1 failed eradication once (2.1% 1/47), and 40 failed treatment at least twice (18.2%, 40/220). The incidence of AIG was significantly higher in the multiple failure group than in the single failure or treatment‐naive groups. Urease‐positive bacteria, such as Klebsiella pneumoniae and alpha‐streptococcus, were identified in 33 of the 35 AIG patients who underwent culture testing. Conclusion AIG patients were often misdiagnosed as refractory to eradication therapy, probably because achlorhydria in AIG might allow urease‐positive bacteria other than H. pylori to colonise the stomach, causing positive 13 C‐ UBT results.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2003094-0
    SSG: 15,3
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  • 3
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 43, No. 10 ( 2016-05), p. 1048-1059
    Abstract: Acid inhibitory effects of proton pump inhibitors ( PPI s) are influenced by CYP 2C19 genotype. In contrast, the potent acid inhibition of vonoprazan is not influenced by CYP 2C19 genotype. Aim To compare the acid inhibitory effects of vonoprazan and esomeprazole in relation to CYP 2C19 genotype. Methods Twenty‐eight healthy Japanese volunteers [7 CYP 2C19 poor metabolisers ( PM s), 11 intermediate metabolisers ( IM s) and 10 rapid metabolisers ( RM s)] received four different regimens in a randomised crossover manner: (i) vonoprazan 20 mg twice daily (b.d.), (ii) vonoprazan 20 mg daily, (iii) esomeprazole 20 mg b.d. and (iv) esomeprazole 20 mg daily. The timing of each dosing was 1 h before a meal. Twenty‐four‐hour intragastric pH monitoring was performed on day 7 on each regimen. Results In the overall genotype group, pH ≥4 holding time ratios ( pH 4 HTR s) with vonoprazan b.d., vonoprazan daily, esomeprazole b.d. and esomeprazole daily were 100%, 95%, 91%, and 68% respectively. pH 5 HTR s were 99%, 91%, 84% and 54% respectively. Vonoprazan b.d. potently suppressed acid for 24 h, and was significantly superior to other regimens irrespective of CYP 2C19 genotype. Vonoprazan daily was equivalent to esomeprazole b.d. in IM s and PM s, but superior in RM s. CYP 2C19 genotype‐dependent differences were observed in esomeprazole daily but not in vonoprazan b.d. or daily. Conclusion Vonoprazan 20 mg b.d. inhibits acid irrespective of CYP 2C19 genotype, more potently than esomeprazole 20 mg b.d., pH 4 and 5 holding time ratios reached 100% and 99%, respectively.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2016
    detail.hit.zdb_id: 2003094-0
    SSG: 15,3
    Location Call Number Limitation Availability
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