2016
DOI: 10.17265/2328-2150/2016.03.004
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Safety and Efficacy of Digoxin Therapy—Where Are We Now?

Abstract: Abstract:The aim of our study was to determine the criteria and key factors for the effectiveness of digoxin therapy. A prospective opened-type study was carried out in conditions of everyday clinical practice. The concentrations of digoxin were quantified from blood samples taken following the achievement of drug steady-state (using AxSYM microparticle enzyme immunoassay-MEIA). The risk/benefit ratio was evaluated based upon the correlation between measured blood concentrations of the drug and clinical respon… Show more

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Cited by 3 publications
(2 citation statements)
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“…Considering the narrow therapeutic range and limited availability of serum digoxin measurements, a digoxin 'holiday' is given where the patient is given the dose 5-6 days a week to minimise digoxin toxicity due to the lack of therapeutic drug monitoring. [19] It is not clear whether this 'holiday' is justified in all cases since digoxin plasma levels might decrease to below therapeutic levels. [20,21] Despite this fact, 'digoxin holiday' is frequently used in many countries.…”
Section: Rationale Behind Digoxin Holidaymentioning
confidence: 99%
“…Considering the narrow therapeutic range and limited availability of serum digoxin measurements, a digoxin 'holiday' is given where the patient is given the dose 5-6 days a week to minimise digoxin toxicity due to the lack of therapeutic drug monitoring. [19] It is not clear whether this 'holiday' is justified in all cases since digoxin plasma levels might decrease to below therapeutic levels. [20,21] Despite this fact, 'digoxin holiday' is frequently used in many countries.…”
Section: Rationale Behind Digoxin Holidaymentioning
confidence: 99%
“…42 Kadar digoksin di dalam darah sebesar >2 ng/mL tidak menunjukkan adanya tanda toksisitas. 30 Namun, perlu adanya kewaspadaan apabila kadar digoksin di dalam darah mencapai >2 ng/mL, hal ini disebabkan kadar digoksin di dalam darah yang mencapai >3 ng/mL dapat menyebabkan toksisitas pada pasien. 16 Kadar fenitoin di dalam darah yang memiliki rentang kadar terapi (10-20 mg/L) dapat menimbulkan ADR seperti mual yang dapat terjadi selama menggunakan fenitoin.…”
Section: Pembahasanunclassified