AJTMH Transactions of the Royal Society of Tropical Medicine and Hygiene
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 2(6), 1953, pp. 949-957
Copyright © 1953 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cooper, W. C.
Right arrow Articles by Coatney, G. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cooper, W. C.
Right arrow Articles by Coatney, G. R.

Studies in Human Malaria

XXXI. Comparison of Primaquine, Isopentaquine, SN-3883, and Pamaquine as Curative Agents Against Chesson Strain Vivax Malaria1

W. Clark Cooper2, Albert V. Myatt, Thomas Hernandez, Geoffrey M. Jeffery AND G. Robert Coatney
Laboratory of Tropical Diseases, National Microbiological Institute, National Institutes of Health, Bethesda 14, Maryland

In Part I of this study six therapeutic regimens employing four different 8-aminoquinoline derivatives were tested under strictly controlled conditions in mosquito-transmitted Chesson strain vivax malaria, experimentally induced in volunteers in a Federal penal institution. Thirty-four men were treated with each regimen. Test drugs were given every 6 hours for 14 days, in combination with quinine sulfate, 250 mg. of base every 6 hours for the same period. The relapse incidence after primary attacks was as follows:

  1. Primaquine 20 mg. (base) daily 15 per cent
  2. Primaquine 10 mg. (base) daily 65 per cent
  3. Isopentaquine 60 mg. (base) daily 35 per cent
  4. SN-3883 60 mg. (base) daily 9 per cent
  5. SN-3883 30 mg. (base) daily 21 per cent
  6. Pamaquine 60 mg. (base) daily 82 per cent

Although toxic manifestations were not alarming with any of the compounds, primaquine at the effective dosage of 20 mg. per day was exceptionally well tolerated, and under the conditions of the test was regarded as the best of the four drugs.

Part II of the study dealt with the trial of three therapeutic regimens employing two different 8-aminoquinolines under the same conditions as outlined above. Ten men were treated with each regimen. The test drugs were given in a single dose daily for 7 days; chloroquine, 1.5 gm. (base) total dose, was given concomitantly during the first 3 days for the management of the acute attack. Relapse incidence after the acute attack was as follows:

  1. Primaquine 30 mg. (base) single dose daily 90 per cent
  2. Primaquine 20 mg. (base) single dose daily 80 per cent
  3. SN-3883 60 mg. (base) single dose daily 100 per cent

There were no toxic manifestations, but the high relapse incidence indicates the limited curative efficacy of these shorter regimens against severe Chesson strain vivax infections and consequently that they are not generally applicable curative regimens.


1 This work was conducted under a contract between the Office of the Surgeon General, Department of the Army and the National Institutes of Health.


2 Address now—Occupational Health Field Headquarters, 1014 Broadway, Cincinnati 2, Ohio.




This article has been cited by other articles:


Home page
Am J Trop Med HygHome page
W. E. Collins, J. S. Sullivan, G. M. Jeffery, A. Williams, G. G. Galland, D. Nace, T. Williams, and J. W. Barnwell
The Chesson Strain of Plasmodium vivax in Humans and Different Species of Aotus Monkeys
Am J Trop Med Hyg, January 1, 2009; 80(1): 152 - 159.
[Abstract] [Full Text] [PDF]


Home page
Am J Trop Med HygHome page
D. R. HILL, J. K. BAIRD, M. E. PARISE, L. S. LEWIS, E. T. RYAN, and A. J. MAGILL
PRIMAQUINE: REPORT FROM CDC EXPERT MEETING ON MALARIA CHEMOPROPHYLAXIS I.
Am J Trop Med Hyg, September 1, 2006; 75(3): 402 - 415.
[Abstract] [Full Text] [PDF]


Home page
Arch Intern MedHome page
A. V. MYATT and G. R. COATNEY
PRESENT CONCEPTS AND TREATMENT OF PLASMODIUM VIVAX MALARIA
Arch Intern Med, February 1, 1954; 93(2): 191 - 196.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1953 by the American Society of Tropical Medicine and Hygiene.