Literature DB >> 26505271

Pharmacological treatment of cardiac glycoside poisoning.

Darren M Roberts1,2, Gamini Gallapatthy3, Asunga Dunuwille3, Betty S Chan4.   

Abstract

Cardiac glycosides are an important cause of poisoning, reflecting their widespread clinical usage and presence in natural sources. Poisoning can manifest as varying degrees of toxicity. Predominant clinical features include gastrointestinal signs, bradycardia and heart block. Death occurs from ventricular fibrillation or tachycardia. A wide range of treatments have been used, the more common including activated charcoal, atropine, β-adrenoceptor agonists, temporary pacing, anti-digoxin Fab and magnesium, and more novel agents include fructose-1,6-diphosphate (clinical trial in progress) and anticalin. However, even in the case of those treatments that have been in use for decades, there is debate regarding their efficacy, the indications and dosage that optimizes outcomes. This contributes to variability in use across the world. Another factor influencing usage is access. Barriers to access include the requirement for transfer to a specialized centre (for example, to receive temporary pacing) or financial resources (for example, anti-digoxin Fab in resource poor countries). Recent data suggest that existing methods for calculating the dose of anti-digoxin Fab in digoxin poisoning overstate the dose required, and that its efficacy may be minimal in patients with chronic digoxin poisoning. Cheaper and effective medicines are required, in particular for the treatment of yellow oleander poisoning which is problematic in resource poor countries.
© 2015 The British Pharmacological Society.

Entities:  

Keywords:  Fab; antibody; digoxin; oleander; pacing; toxicity

Mesh:

Substances:

Year:  2015        PMID: 26505271      PMCID: PMC4767196          DOI: 10.1111/bcp.12814

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  41 in total

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Journal:  Vet Hum Toxicol       Date:  1999-02

9.  Multiple-dose activated charcoal for treatment of yellow oleander poisoning: a single-blind, randomised, placebo-controlled trial.

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Review 10.  Acute plant poisoning and antitoxin antibodies.

Authors:  Michael Eddleston; Hans Persson
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Review 3.  Who gets antidotes? choosing the chosen few.

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4.  Clinical Pharmacokinetics in Kidney Disease: Fundamental Principles.

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Review 5.  The Daniel K. Inouye College of Pharmacy Scripts: The Tantalizing Toxins of Tantalus, A Brief Review of Select Natural Poisons of O'ahu.

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7.  Inflammasome inhibition blocks cardiac glycoside cell toxicity.

Authors:  Doris L LaRock; Jenna S Sands; Ethan Ettouati; Marine Richard; Paul J Bushway; Eric D Adler; Victor Nizet; Christopher N LaRock
Journal:  J Biol Chem       Date:  2019-07-12       Impact factor: 5.157

8.  Oleander and Datura Poisoning: An Update.

Authors:  Vijay V Pillay; Anu Sasidharan
Journal:  Indian J Crit Care Med       Date:  2019-12

9.  3'-epi-12β-hydroxyfroside, a new cardenolide, induces cytoprotective autophagy via blocking the Hsp90/Akt/mTOR axis in lung cancer cells.

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10.  Acute myocardial infarction in yellow oleander poisoning.

Authors:  D Anandhi; K N J Prakash Raju; M H Basha; V R Pandit
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