Literature DB >> 31776555

Drug interactions with antimalarial medications in older travelers: a clinical guide.

Jelena Lewis1, Tania Gregorian1, Ivan Portillo2, Jeff Goad1.   

Abstract

Increasingly older adults are traveling to international destinations with malaria as a present risk. Surveillance systems indicate that older adults are more likely to suffer severe complications from malaria. The role of health care providers in selecting an appropriate medication for chemoprophylaxis or treatment of malaria in adults becomes more difficult as older adults undergo physiologic changes that alter the pharmacokinetic and pharmacodynamic nature of medications potentially causing increased drug interactions, adverse events and altered drug action. A comprehensive literature search from 1970 to present, with a focus on the past 10 years, was conducted on drug interactions, pharmacokinetic and pharmacodynamic effects on antimalarials in adults. It was determined that due to pharmacodynamic and pharmacokinetic changes in older adults, especially renal and cardiovascular, special attention should be given to this population of travelers in order to minimize the likelihood of adverse events or altered drug efficacy. Antimalarial drug-disease interactions in older adults can occur more often due to QT prolongation, exacerbation of hypoglycemia, decreased renal elimination and decreased hepatic metabolism. Older antimalarials have well-documented drug-drug interactions. Tafenoquine, a new antimalarial, requires glucose-6-phosphate dehydrogenase screening like primaquine and monitoring of new potential drug interaction with MATE1 and OCT2 substrates. While drug-drug interactions in older travelers may occur more often as a result of polypharmacy, data did not indicate adverse reactions or decreased drug efficacy is greater compared with younger adults. Overall, with the exception of recently approved tafenoquine, much is known about antimalarial drug and disease interactions, but new drugs are always being approved, requiring travel health providers to understand the pharmacokinetics and pharmacodynamics of antimalarial drugs to predict the impact on safety and efficacy in travelers. This guide provides travel health providers with valuable insights on potential outcomes associated with drug interactions in adults and recommended monitoring or drug regimen modification. © International Society of Travel Medicine 2019. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Older traveler; QT prolongation; artemether; artemisinins; artesunate; atovaquone-proguanil; chloroquine; doxycycline; hepatic enzyme induction; mefloquine; primaquine; tafenoquine

Year:  2020        PMID: 31776555     DOI: 10.1093/jtm/taz089

Source DB:  PubMed          Journal:  J Travel Med        ISSN: 1195-1982            Impact factor:   8.490


  4 in total

1.  Cost-Benefit Analysis of Tafenoquine for Radical Cure of Plasmodium vivax Malaria in Korea.

Authors:  Jiyeon Suh; Jung Ho Kim; Jong-Dae Kim; Changsoo Kim; Jun Yong Choi; Jeehyun Lee; Joon-Sup Yeom
Journal:  J Korean Med Sci       Date:  2022-07-11       Impact factor: 5.354

2.  Caring for Individuals With Intellectual and Developmental Disabilities in the COVID-19 Crisis.

Authors:  Jessica Solomon Sanders; Seth Keller; Bhooma R Aravamuthan
Journal:  Neurol Clin Pract       Date:  2021-04

Review 3.  Drug-drug interactions with candidate medications used for COVID-19 treatment: An overview.

Authors:  Haleh Rezaee; Fariba Pourkarim; Samira Pourtaghi-Anvarian; Taher Entezari-Maleki; Touraj Asvadi-Kermani; Masoud Nouri-Vaskeh
Journal:  Pharmacol Res Perspect       Date:  2021-02

4.  Top 20 drug - drug interactions, polypharmacy and analysis of the nature of risk factors due to QT interval prolonging drug use in elderly psychiatry outpatients.

Authors:  Biswadeep Das; Saravana Kumar Ramasubbu; Barun Kumar; Vikram Singh Rawat
Journal:  J Family Med Prim Care       Date:  2020-12-31
  4 in total

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