Skip Standard Navigation Links
CDC Home
Safer, Healthier People
CDC HomeCDC SearchHealth Topics A-Z
   
  WONDER Home FAQ Help Contact Us Search  
 

Warning:

This site is being maintained for historical purposes, but has had no new entries since October 1998. To find more recent articles, please visit the following:
  • MMWR at http://www.cdc.gov/mmwr/mmwrsrch.htm
  • CDC Web Search at http://www.cdc.gov/search.do


Notices to Readers Treatment of Severe Plasmodium falciparum Malaria with Quinidine Gluconate: Discontinuation of Parenteral Quinine from CDC Drug Service

MMWR 40(14);240

Publication date: 04/12/1991


Table of Contents

Article

References

POINT OF CONTACT FOR THIS DOCUMENT:


Article

CDC has recently reviewed data on the reported incidence in the United States of Plasmodium falciparum malaria and has evaluated information on the effective management of severe life-threatening infections. As a result of this review, CDC has concluded that the drug of choice in the United States for treatment of complicated P. falciparum infections is parenteral quinidine gluconate. Therefore, effective immediately, parenteral quinine dihydrochloride will no longer be available from the CDC Drug Service.

Patients with severe malaria in the United States should be treated in intensive-care facilities where central hemodynamic and electrocardiographic monitoring is available. Based on a study of patients with P. falciparum treated in the United States (1), continuous infusion of quinidine gluconate is recommended. A loading dose of 10 mg of quinidine gluconate (equivalent to 6.2 mg quinidine base) per kg of body weight is given over 1-2 hours, followed by a constant infusion of 0.02 mg quinidine gluconate per kg per minute. This regimen is highly effective and well-tolerated in monitored patients (2,3).

The Food and Drug Administration and the drug manufacturer are amending the indications for the use of quinidine gluconate to include therapy of life-threatening P. falciparum malaria. Reasons for recommending the routine use of parenteral quinidine gluconate in the United States include the demonstrated efficacy and safety of parenteral quinidine gluconate and the unavailability of parenteral quinine that has caused delays in administering an antimalarial drug to critically ill persons. An expanded report on the use of quinidine gluconate for the treatment of P. falciparum malaria will be published in an MMWR Recommendations and Reports. Information regarding treatment of P. falciparum malaria is available from the Malaria Branch, Division of Parasitic Diseases, Center for Infectious Diseases, CDC, telephone (404) 488-4046.

Reported by: Malaria Br, Div of Parasitic Diseases, Center for Infectious Diseases, CDC.


References

References

  1. Miller KD, Greenberg AE, Campbell CC. Treatment of malaria in the United States with a continuous infusion of quinidine gluconate and exchange transfusion. N Engl J Med 1989;321:65-70.
  2. White NJ, Plorde JJ. Malaria. In: Wilson JD, Braunwald E, Isselbacher KJ, et al, eds. Harrison's principles of internal medicine. 12th ed. New York: McGraw-Hill, 1990.
  3. Krogstad DJ. Malaria. In: Wyngaarden JB, Smith LH, Bennett JC, Plum F, eds. Cecil's textbook of medicine. 19th ed. Philadephia: WB Saunders, 1991.


POINT OF CONTACT FOR THIS DOCUMENT:

To request a copy of this document or for questions concerning this document, please contact the person or office listed below. If requesting a document, please specify the complete name of the document as well as the address to which you would like it mailed. Note that if a name is listed with the address below, you may wish to contact this person via CDC WONDER/PC e-mail.
For single issue purchase 800-843-6356
DIVISION OF PARASITIC DISEASES
State/Fed Gov: For free copies
write to: CDC, MMWR MS(C-08)
Atlanta, GA 30333



This page last reviewed: Wednesday, August 29, 2007
This information is provided as technical reference material. Please contact us at cwus@cdc.gov to request a simple text version of this document.