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  • Pharmacy  (5)
  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2014
    In:  BMC Pharmacology and Toxicology Vol. 15, No. 1 ( 2014-12)
    In: BMC Pharmacology and Toxicology, Springer Science and Business Media LLC, Vol. 15, No. 1 ( 2014-12)
    Abstract: It is unclear whether concomitant use of clopidogrel and proton-pump inhibitors (PPIs) increases the risk of recurrence of cardiovascular disease or death in patients at high risk of upper gastrointestinal (GI) bleeding. Methods Based on the Swedish Patient Register, a cohort of cardiovascular disease (including acute myocardial infarction, stroke and angina, from 2006 to 2008) was selected from a population with any diagnosis of upper GI bleeding. Data on drug prescription was retrieved from the Prescribed Drug Register. Patients entered into the cohort after their first discharge for cardiovascular disease and were followed up to death, recurrence of cardiovascular disease, or 90 days. A Cox regression model was conducted and hazard ratios (HRs) with 95% confidence intervals (CIs) were estimated to evaluate the risks among users of different drug prescriptions. Results Patients who were current users of only PPIs (HR 2.02, 95% CI 1.19-3.44), only clopidogrel (HR 1.14, 95% CI 0.53-2.45) and nonusers of both (HR 2.36, 95% CI 1.39-4.00) were at a higher risk of death compared with patients with a concomitant use. Results were similar among 1779 patients who had any history of upper GI bleeding (HR 2.05, 95% CI 1.18-3.54; HR 1.25, 95% CI 0.57-2.72; HR 2.30, 95% CI 1.33-3.98, respectively). Conclusion Among patients at high risk of upper GI bleeding, those with a concomitant use of PPIs and clopidogrel were at a decreased risk of mortality, and possibly also a decreased risk of recurrence of cardiovascular disease.
    Type of Medium: Online Resource
    ISSN: 2050-6511
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2014
    detail.hit.zdb_id: 2680259-4
    SSG: 15,3
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  • 2
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2022
    In:  Cardiovascular Drugs and Therapy Vol. 36, No. 6 ( 2022-12), p. 1121-1128
    In: Cardiovascular Drugs and Therapy, Springer Science and Business Media LLC, Vol. 36, No. 6 ( 2022-12), p. 1121-1128
    Abstract: Due to shared hepatic metabolism, concomitant medication with a proton pump inhibitor (PPI) and clopidogrel might reduce the effectiveness of clopidogrel in the prevention of cardiovascular events after percutaneous coronary intervention (PCI). We aimed to examine the risk of major cardiovascular events after PCI comparing patients who used clopidogrel together with PPI with those who used clopidogrel alone. Methods This Swedish nationwide cohort study included patients who received clopidogrel after primary PCI in 2005–2019. Patients were followed for up to 12 months after PCI. Data were retrieved from the Swedish Prescribed Drug Registry, Patient Registry, Cancer Registry, and Cause of Death Registry. Multivariable Cox regression provided hazard ratios (HRs) with 95% confidence intervals (CIs) for cardiovascular events comparing PPI users (exposed) with non-users of PPI (non-exposed). The HRs were adjusted for sex, age, comorbidity, calendar period, obesity, diabetes, anti-diabetic medication, tobacco-related diseases, hypertension, and congestive heart failure. Results The cohort included 99,836 patients who received clopidogrel after primary PCI. Among these, 35,772 (35.8%) received concomitant PPI. Compared to non-users, PPI users had increased adjusted HRs of all study outcomes, i.e., the main outcome myocardial infarction (HR = 1.23, 95% CI 1.15–1.32) and the secondary outcomes coronary heart disease (HR = 1.28, 95% CI 1.24–1.33), stroke (HR = 1.21, 95% CI 1.05–1.40), and death due to coronary heart disease (HR = 1.52, 95% CI 1.37–1.69). The results were similar in analyses including both primary and secondary PCIs. Conclusions In patients who receive clopidogrel after PCI, concomitant use of PPI seems to increase the risk of major cardiovascular events.
    Type of Medium: Online Resource
    ISSN: 0920-3206 , 1573-7241
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2022
    detail.hit.zdb_id: 2003553-6
    SSG: 15,3
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 1987
    In:  Biochemical Pharmacology Vol. 36, No. 18 ( 1987-09), p. 2985-2991
    In: Biochemical Pharmacology, Elsevier BV, Vol. 36, No. 18 ( 1987-09), p. 2985-2991
    Type of Medium: Online Resource
    ISSN: 0006-2952
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1987
    detail.hit.zdb_id: 1496199-4
    SSG: 15,3
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  • 4
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2011
    In:  Drugs & Aging Vol. 28, No. 6 ( 2011-06), p. 469-476
    In: Drugs & Aging, Springer Science and Business Media LLC, Vol. 28, No. 6 ( 2011-06), p. 469-476
    Type of Medium: Online Resource
    ISSN: 1170-229X
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2011
    detail.hit.zdb_id: 2043689-0
    SSG: 15,3
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  • 5
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Alimentary Pharmacology & Therapeutics Vol. 50, No. 2 ( 2019-07), p. 159-166
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 50, No. 2 ( 2019-07), p. 159-166
    Abstract: Gastric bypass is considered an effective treatment of co‐existing gastro‐oesophageal reflux (GERD) and obesity. Previous studies have had small sample sizes, short follow‐up or substantial loss to follow‐up. Aim To assess the long‐term risk of remaining/recurring reflux symptoms after gastric bypass. Methods This was a nationwide cohort study of all adults with preoperative reflux who underwent gastric bypass in Sweden between 2006 and 2015, with complete follow‐up through 2016. The outcome was remaining/recurring reflux symptoms, defined as use of proton pump inhibitors or histamine‐2 receptor antagonists for 〉 6 months after surgery. Cumulative incidence and risk factors of reflux were assessed with multivariable Poisson regression. Results Among 2454 participants (81.7% female; mean age: 46.1 years, SD: 9.8 years), who were followed for median 4.6 years (interquartile range: 3.1‐6.3 years), reflux recurred in 48.8% (95% confidence interval [95% CI], 46.8‐51.0) of participants within 2 years of gastric bypass and remained stable up to 10 years after surgery (yearly change in incidence rate ratio [IRR] of 1.00; 95% CI, 0.99‐1.02). Risk factors for recurring reflux were high preoperative dose of anti‐reflux medication (IRR 1.77; 95% CI, 1.60‐1.96 compared with low dose), older age (IRR 1.12; 95% CI 1.02‐1.24 comparing age 〉 50 with 〈 40 years), female sex (IRR 1.28; 95% CI, 1.16‐1.42) and comorbidity (IRR 1.26; 95% CI, 1.14‐1.39 comparing Charlson Comorbidity Index ≥2 with 0). Conclusions Reflux symptoms decrease rapidly after gastric bypass, but around half of operated patients require continuous anti‐reflux medication. The treatment efficacy of gastric bypass on reflux symptoms might have been overestimated.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2003094-0
    SSG: 15,3
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