Proton Pump Inhibitors

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Robert Maclaren - One of the best experts on this subject based on the ideXlab platform.

  • Proton Pump Inhibitors for stress ulcer prophylaxis in critically ill patients
    Annals of Pharmacotherapy, 2002
    Co-Authors: Rose Jung, Robert Maclaren
    Abstract:

    OBJECTIVE:To evaluate the use of Proton-Pump Inhibitors (PPIs) for stress ulcer prophylaxis in critically ill adults.DATA SOURCES:Computerized biomedical literature search of MEDLINE (1966–June 2002) was conducted using the MeSH headings Proton-Pump inhibitor, ulcer, critical care, and acid. References of selected articles were reviewed. A manual search of critical care, surgery, trauma, gastrointestinal, and pharmacy journals was conducted to identify relevant abstracts.DATA SYNTHESIS:Traditional medications used for stress ulcer prophylaxis include antacids, histamine2 receptor antagonists (H2RAs), and sucralfate. Few studies have evaluated PPIs for stress ulcer prophylaxis. The majority of studies have demonstrated that enteral or intravenous administration of PPIs to critically ill patients elevates intragastric pH and consistently maintains pH ≥4.0. PPIs are safe and seem to be as efficacious as H2RAs or sucralfate for prevention of bleeding from stress-related mucosal damage (SRMD) and they may prov...

  • Proton Pump Inhibitors for stress ulcer prophylaxis in critically ill patients
    Annals of Pharmacotherapy, 2002
    Co-Authors: Rose Jung, Robert Maclaren
    Abstract:

    OBJECTIVE:To evaluate the use of Proton-Pump Inhibitors (PPIs) for stress ulcer prophylaxis in critically ill adults.DATA SOURCES:Computerized biomedical literature search of MEDLINE (1966–June 2002) was conducted using the MeSH headings Proton-Pump inhibitor, ulcer, critical care, and acid. References of selected articles were reviewed. A manual search of critical care, surgery, trauma, gastrointestinal, and pharmacy journals was conducted to identify relevant abstracts.DATA SYNTHESIS:Traditional medications used for stress ulcer prophylaxis include antacids, histamine2 receptor antagonists (H2RAs), and sucralfate. Few studies have evaluated PPIs for stress ulcer prophylaxis. The majority of studies have demonstrated that enteral or intravenous administration of PPIs to critically ill patients elevates intragastric pH and consistently maintains pH ≥4.0. PPIs are safe and seem to be as efficacious as H2RAs or sucralfate for prevention of bleeding from stress-related mucosal damage (SRMD) and they may prov...

Ulrich Klotz - One of the best experts on this subject based on the ideXlab platform.

  • relative potency of Proton Pump Inhibitors comparison of effects on intragastric ph
    European Journal of Clinical Pharmacology, 2009
    Co-Authors: Julia Kirchheiner, Ulrich Klotz, Silke Glatt, Uwe Fuhr, Ingolf Meineke, T Seufferlein, J Brockmoller
    Abstract:

    Aim Comparative potency of Proton-Pump Inhibitors (PPIs) is an important clinical issue. Most available trials have compared the different PPIs at one or a few selected specific dosages, making it difficult to derive quantitative equivalence dosages. Here we derived PPI dose equivalents based on a comprehensive assessment of dose-dependent effects on intragastric pH.

  • Proton Pump Inhibitors an update of their clinical use and pharmacokinetics
    European Journal of Clinical Pharmacology, 2008
    Co-Authors: Shaojun Shi, Ulrich Klotz
    Abstract:

    Background Proton Pump Inhibitors (PPIs) represent drugs of first choice for treating peptic ulcer, Helicobacter pylori infection, gastrooesophageal reflux disease, nonsteroidal anti-inflammatory drug (NSAID)-induced gastrointestinal lesions (complications), and Zollinger-Ellison syndrome.

  • CYP2C19 Polymorphism and Proton Pump Inhibitors
    Basic & clinical pharmacology & toxicology, 2004
    Co-Authors: Ulrich Klotz, Matthias Schwab, Gerhard Treiber
    Abstract:

    Proton Pump Inhibitors such as omeprazole (esomeprazole), lansoprazole, pantoprazole and rabeprazole are eliminated by the hepatic route and the polymorphic CYP2C19 is mainly involved in their metabolism. In different populations three phenotypes have been identified: extensive metabolizers, poor metabolizers and individuals carrying one wild type and one mutant allele (het extensive metabolizers). Systemic exposure to the Proton Pump Inhibitors as expressed by the AUC (area under the plasma level time profiles) is 5-12-times higher in poor metabolizers than in extensive metabolizers. As the pharmacodynamic response (elevation of intragastric pH) to the Proton Pump Inhibitors is related directly to their AUC, a much higher pH can be monitored over 24 hr in poor metabolizers than in extensive metabolizers. Furthermore, clinical efficacy of all Proton Pump Inhibitors depend on maintaining intragastric pH above certain threshold levels and significantly higher eradication rates of Helicobacter pylori have been observed in patients of the poor metabolizers and het extensive metabolizers phenotype if compared to extensive metabolizers. Likewise, limited data suggest that Proton Pump Inhibitors-induced healing rates in gastro-oesophageal reflux disease are apparently higher in poor metabolizers/het extensive metabolizers than in extensive metabolizers of CYP2C19. Therefore initial genotyping for this enzyme and higher dosage in extensive metabolizers is likely to improve the clinical efficacy of Proton Pump Inhibitors.

Deborah J Cook - One of the best experts on this subject based on the ideXlab platform.

Joseph R. Pisegna - One of the best experts on this subject based on the ideXlab platform.

Paul Moayyedi - One of the best experts on this subject based on the ideXlab platform.