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  • Online-Ressource  (6)
  • S. Karger AG  (6)
  • 1
    Online-Ressource
    Online-Ressource
    S. Karger AG ; 2004
    In:  Cellular Physiology and Biochemistry Vol. 14, No. 4-6 ( 2004), p. 343-350
    In: Cellular Physiology and Biochemistry, S. Karger AG, Vol. 14, No. 4-6 ( 2004), p. 343-350
    Materialart: Online-Ressource
    ISSN: 1015-8987 , 1421-9778
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 2004
    ZDB Id: 1482056-0
    SSG: 12
    SSG: 15,3
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    S. Karger AG ; 1999
    In:  Chemotherapy Vol. 45, No. 6 ( 1999), p. 491-495
    In: Chemotherapy, S. Karger AG, Vol. 45, No. 6 ( 1999), p. 491-495
    Kurzfassung: Gemifloxacin is a novel fluoroquinolone with a broad spectrum of activity. This double-blind, randomized, parallel-group study was designed to demonstrate the lack of effect of steady-state concentrations of gemifloxacin on the pharmacodynamic effects of warfarin. Healthy male subjects received loading doses of warfarin on days 1 and 2. The warfarin dose was freely titrated until day 10, with the aim of achieving a stable international normalized ratio (INR) for prothrombin time within the range 1.3–1.8 by day 14. On days 14–24 the dose of warfarin was fixed. On days 18–24, subjects also received 320 mg of gemifloxacin or matched placebo, once daily. Thirty-five subjects entered into and completed the co-administration phase of the study. The mean (standard deviation) baseline INR (mean of days 16–18) and INR for day 24 for gemifloxacin plus warfarin were 1.52 (0.12) and 1.46 (0.15), respectively. Corresponding values for placebo plus warfarin were 1.46 (0.11) and 1.42 (0.17). The point estimate (90% confidence interval) for the difference in day 24 INR, adjusted for baseline, between gemifloxacin and placebo was 0.02 (–0.08, 0.12), which translates to an INR (relative to placebo least squares mean of 1.43) of 1.02 (0.95, 1.09). The 90% confidence interval for the difference in INR between the gemifloxacin and placebo groups was completely contained within the 25% equivalence range. There were no changes of clinical significance in vital signs, 12-lead electrocardiogram readings or laboratory parameters for any subject during the co-administration phase of the study, and no adverse experiences relating to coagulation were reported during this period. It is concluded that the pharmacodynamic effects of warfarin are not affected by gemifloxacin, and therefore both drugs can be co-administered without dosage adjustment.
    Materialart: Online-Ressource
    ISSN: 0009-3157 , 1421-9794
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 1999
    ZDB Id: 1482111-4
    SSG: 15,3
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    In: Digestion, S. Karger AG, Vol. 67, No. 3 ( 2003), p. 138-145
    Kurzfassung: 〈 i 〉 Background and Aims: 〈 /i 〉 To assess the risk of bleeding after percutaneous liver biopsy, we retrospectively analyzed 629 procedures with particular respect to patients with an increased a priori bleeding risk. 〈 i 〉 Methods: 〈 /i 〉 Factors possibly related to the risk of bleeding were analyzed by univariate analysis. Those variables which were significant in the univariate analysis were then entered into a forward conditional logistic regression model. 〈 i 〉 Results: 〈 /i 〉 Biopsy-related bleeding events defined as clinically overt complication (n = 10; 1.6%), an otherwise unexplained drop in serum hemogloblin concentration of greater than 2 g/dl (n = 45; 7.1%) or intra- or extrahepatic hematoma assessed by ultrasound (n = 17; 2.7%) were identified in 72 patients. 58% of the bleeding events occurred in patients with particular risk factors for bleeding. Biopsy-related mortality in the study cohort was 0.48%. Logistic regression analysis indicated mycobacterial infection [odds ratio (OR) 24.0], pre-biopsy prophylactic platelet substitution (OR 9.9), acute liver failure (OR 9.1), heparin administration on the day of biopsy (OR 8.7), advanced liver cirrhosis (OR 5.1), therapy with corticosteroids (OR 3.5) or metamizole (OR 2.8) and leukemia or lymphoma (OR 2.8) as significant (p ≤ 0.05) independent risk factors. Delayed bleeding ( 〉 24 h after biopsy) was identified in 70% of the bleeding events. 〈 i 〉 Conclusions: 〈 /i 〉 In our study cohort which comprised a high proportion of patients with particular risk factors for bleeding, biopsy-related bleeding occurred more frequently and later than commonly observed and was associated with only a few prognostic factors. Considering these predictors before liver biopsy will aid to reduce the rate of bleeding complications.
    Materialart: Online-Ressource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 2003
    ZDB Id: 1482218-0
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    S. Karger AG ; 1999
    In:  Chemotherapy Vol. 45, No. 6 ( 1999), p. 478-484
    In: Chemotherapy, S. Karger AG, Vol. 45, No. 6 ( 1999), p. 478-484
    Kurzfassung: Gemifloxacin is a novel fluoroquinolone, currently in development for the treatment of respiratory tract infections. This double-blind (with respect to gemifloxacin), randomized, crossover study investigated the possibility of pharmacokinetic interaction between gemifloxacin and theophylline. After a 4–8-day run-in phase to establish the dose of theophylline required to achieve a trough plasma concentration range of 8–15 mg/l, 15 healthy volunteers entered a randomized treatment phase. Volunteers then received oral theophylline, 300–400 mg twice daily, for 22 days. On days 5–11 and 16–22, they also received either placebo or gemifloxacin, 320 mg p.o. once daily, in a crossover fashion. Blood samples were collected up to 12 h after the morning dose of theophylline on days 11 and 22. Theophylline pharmacokinetics were not affected by the co-administration of gemifloxacin. The maximum plasma concentration (C 〈 sub 〉 max 〈 /sub 〉 ) for theophylline ranged from 8.12 to 17.71 mg/l and from 8.79 to 16.35 mg/l during concomitant administration with gemifloxacin and placebo, respectively. The corresponding ranges of the area under the plasma concentration-time curve from time zero to the last quantifiable plasma concentration (AUC 〈 sub 〉 (0–12) 〈 /sub 〉 ) were 84.6–177.5 mg·h/l and 94.8–165.1 mg·h/l during gemifloxacin and placebo administration, respectively. The point estimates (90% confidence intervals) for dose-normalized AUC 〈 sub 〉 (0–12) 〈 /sub 〉 and C 〈 sub 〉 max 〈 /sub 〉 (theophylline + gemifloxacin):(theophylline + placebo) were 0.99 (0.93, 1.05) and 1.02 (0.93, 1.11), respectively, which were entirely within the equivalence range (0.80, 1.25). The co-administration of gemifloxacin and theophylline was well tolerated, with no clinically significant changes seen in vital signs, 12-lead electrocardiogram readings or laboratory parameters. Adverse events were generally transient, mild to moderate in nature and similar during the gemifloxacin and placebo treatment periods. In conclusion, theophylline and gemifloxacin may be co-administered without any adjustment in theophylline dose.
    Materialart: Online-Ressource
    ISSN: 0009-3157 , 1421-9794
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 1999
    ZDB Id: 1482111-4
    SSG: 15,3
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    In: Kompass Onkologie, S. Karger AG, Vol. 9, No. 1 ( 2022), p. 3-12
    Kurzfassung: Bei der Impfung handelt es sich um eine der erfolgreichsten medizinischen Maßnahmen, die bereits Millionen von Menschen das Leben gerettet hat. Die Impfung ist besonders wichtig bei Patienten mit einem Multiplen Myelom, deren Infektionsrisiko aufgrund der krankheitsinhärenten Immunsuppression sowie der immunsuppressiven Wirkung der Therapie erhöht ist. Daher sollten alle geeigneten Maßnahmen ergriffen werden, um eine wirksame Immunantwort gegen weitverbreitete Krankheitserreger wie Influenza, Pneumokokken, das Varicella-Zoster-Virus sowie gegen Bakterien und Viren (Haemophilus influenzae, Meningokokken und Hepatitis), die häufig ein erhebliches Risiko für Patienten mit einem Multiplen Myelom darstellen, anzuregen. Patienten nach autologer und insbesondere nach allogener Transplantation haben stark reduzierte Antikörpertiter und benötigen daher ein breiteres Impfspektrum. Die Impfreaktion ist bei Myelom-Patienten oft weniger stark ausgeprägt als in der Allgemeinbevölkerung, sodass entweder die Messung der Antikörpertiter nach der Impfung und/oder eine Wiederholungsimpfung erforderlich ist. In dieser Arbeit stellen wir die Daten zusammen, die zur Impfung von Patienten mit Multiplem Myelom existieren, und geben Empfehlungen für die klinische Praxis.
    Materialart: Online-Ressource
    ISSN: 2296-5416 , 2296-5386
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 2022
    ZDB Id: 3050162-3
    ZDB Id: 2754730-9
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    In: Cellular Physiology and Biochemistry, S. Karger AG, Vol. 17, No. 1-2 ( 2006), p. 29-36
    Materialart: Online-Ressource
    ISSN: 1421-9778 , 1015-8987
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 2006
    ZDB Id: 1482056-0
    SSG: 12
    SSG: 15,3
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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