Original site: www.cdc.gov/mmwr/preview/mmwrhtml/00046529.htm RestoredCDC.org is an independent project and is not affiliated with, endorsed by, or associated with the Centers for Disease Control and Prevention (CDC) or any government entity. The CDC provides information free of change at CDC.gov. Note the following: 1) Due to archival on January 6, 2025, no information on recent outbreaks is available. 2) Videos have not been restored. 3) Use of this site implies acceptance of this disclaimer.
Appendix -- Microscopic Procedures for Diagnosing Malaria
To establish the diagnosis of malaria, a blood smear must be
prepared
from fresh finger-prick blood ((Figure_A1) and
(Figure_A2)). * The
thin smear is fixed in methanol before staining; the thick smear is
stained
unfixed. Many hospitals have a Wright-Giemsa stain available, which
is
acceptable; however, Wright stain alone will not reliably stain
Plasmodium
parasites. For best results, the smear should be stained with a 3%
Giemsa
solution (pH of 7.2) for 30-45 minutes. In P. falciparum
infections, the
parasite density should be estimated by counting the percentage of
red
blood cells infected -- not the number of parasites -- under an oil
immersion on a thin film.
Thick blood smears are more sensitive in detecting malaria
parasites
because the blood is concentrated, allowing a greater volume of
blood to be
examined. However, thick smears are more difficult to read, and
thin smears
may be preferred by laboratories that have limited experience.
Plasmodium
parasites are always intracellular, and they demonstrate, if
stained
correctly, blue cytoplasm with a red chromatin dot. Common errors
in
reading malaria smears are caused by platelets overlying a red
blood cell,
concerin about missing a positive slide, and misreading artifacts
as
parasites. Persons suspected of having malaria but whose blood
smears do
not demonstrate the presence of parasites should have blood smears
repeated approximately every 12-24 hours for 3 consecutive days. If
smears
remain negative, then the diagnosis of malaria is unlikely.
For rapid diagnosis, make the thick and thin films on separate
slides.
Air dry the thin film, fix it with methyl alcohol, and immediately
stain it.
If no parasites are found on the thin film, wait until the thick
film is
dry and examine it for organisms that may not have been detected on
the
thin preparation.
In Figures A1 and A2, the hands are shown ungloved to better
illustrate
their placement during the procedures. However, wearing gloves
while
processing blood specimens is recommended to prevent transmission
of Figure_A1
Disclaimer
All MMWR HTML versions of articles are electronic conversions from ASCII text into HTML. This conversion may have resulted in character translation or format errors in the HTML version. Users should not rely on this HTML document, but are referred to the electronic PDF version and/or the original MMWR paper copy for the official text, figures, and tables. An original paper copy of this issue can be obtained from the Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact GPO for current prices.
**Questions or messages regarding errors in formatting should be addressed to mmwrq@cdc.gov.
