Literature DB >> 16968914

Cost considerations of malaria chemoprophylaxis including use of primaquine for primary or terminal chemoprophylaxis.

Joe P Bryan1.   

Abstract

The costs of mefloquine, chloroquine, doxycycline, primaquine, and atovaquone/proguanil are calculated for various durations of exposure to malaria. The cost is included for detecting glucose 6-phosphate dehydrogenase (G6PD) deficiency before administering primaquine for primary or terminal prophylaxis. For durations of exposure ranging from 3 to 730 days, if no terminal prophylaxis is given, doxycycline (generic) is the least expensive regimen. Compared with doxycycline hyclate, chloroquine costs three to four times more, and primaquine, after screening for G6PD, costs about eight times more. Atovaquone/proguanil is less expensive than mefloquine for a 3-day exposure, but more expensive for 7 or more days. When terminal chemoprophylaxis with primaquine for 14 days is used in addition to doxycycline, mefloquine, chloroquine, or atovaquone/proguanil, primaquine alone is the least expensive regimen for exposures of < 10 days. Thereafter, doxycycline plus 14 days of primaquine is most economical. For subsequent exposures when G6PD status is already known, primaquine alone is the least expensive regimen for up to 9 days of exposure, but doxycycline is less expensive thereafter. In general, generic doxycycline hyclate is the least expensive regimen. Primaquine alone is economically attractive. Mefloquine, doxycyline monohydrate, and atovaquone/proguanil, the most expensive regimens, are similar in cost for a 7-day exposure, but thereafter, atovaquone/proguanil is much more expensive.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16968914

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  8 in total

Review 1.  Review: Malaria chemoprophylaxis for travelers to Latin America.

Authors:  Laura C Steinhardt; Alan J Magill; Paul M Arguin
Journal:  Am J Trop Med Hyg       Date:  2011-12       Impact factor: 2.345

2.  Primaquine administration after falciparum malaria treatment in malaria hypoendemic areas with high incidence of falciparum and vivax mixed infection: pros and cons.

Authors:  Polrat Wilairatana; Noppadon Tangpukdee; Shigeyuki Kano; Srivicha Krudsood
Journal:  Korean J Parasitol       Date:  2010-06-17       Impact factor: 1.341

3.  Safety, Tolerability, and Compliance with Long-Term Antimalarial Chemoprophylaxis in American Soldiers in Afghanistan.

Authors:  David L Saunders; Eric Garges; Jessica E Manning; Kent Bennett; Sarah Schaffer; Andrew J Kosmowski; Alan J Magill
Journal:  Am J Trop Med Hyg       Date:  2015-06-29       Impact factor: 2.345

4.  A Deadly Wait for U.S. Health Insurance Coverage-Sitting on the Couch with Malaria.

Authors:  Jonathan S Schultz; Adam J Atherly; Andrés F Henao-Martínez
Journal:  Am J Trop Med Hyg       Date:  2018-05-10       Impact factor: 2.345

5.  Doxycycline for malaria chemoprophylaxis and treatment: report from the CDC expert meeting on malaria chemoprophylaxis.

Authors:  Kathrine R Tan; Alan J Magill; Monica E Parise; Paul M Arguin
Journal:  Am J Trop Med Hyg       Date:  2011-04       Impact factor: 2.345

6.  Cost risk benefit analysis to support chemoprophylaxis policy for travellers to malaria endemic countries.

Authors:  Eduardo Massad; Ben C Behrens; Francisco A B Coutinho; Ronald H Behrens
Journal:  Malar J       Date:  2011-05-17       Impact factor: 3.469

7.  Clinical development of new prophylactic antimalarial drugs after the 5th Amendment to the Declaration of Helsinki.

Authors:  Geoffrey S Dow; Alan J Magill; Colin Ohrt
Journal:  Ther Clin Risk Manag       Date:  2008-08       Impact factor: 2.423

Review 8.  Rational Risk-Benefit Decision-Making in the Setting of Military Mefloquine Policy.

Authors:  Remington L Nevin
Journal:  J Parasitol Res       Date:  2015-10-22
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.