Ml. Dubey et al., Comparative evaluation of methods of malaria parasite density determination in blood samples from patients & experimental animals, I J MED RES, 109, 1999, pp. 20-27
Three methods for the quantitation of parasitaemia in malaria were compared
with the standard method for ascertaining the accuracy in patients, Plasmo
dium berghei infected mice and P. knowlesi infected Rhesus monkeys. Techniq
ue I, where parasitaemia was calculated from the number of PRBCs in 10,000
RBCs in thin blood film and the total RBC count of the host, was used as th
e standard. Technique II, where parasitaemia was calculated based on the nu
mber of PRBCs per WBC and average total WBC count (8000/mu l), was least ac
curate. Technique IV, where parasitaemia was calculated from the number of
PRBCs per oil immersion field (OIF) of microscope and the estimated amount
of blood in one OIF of a thick smear, was most accurate when parasitaemia w
as low as in malaria patients and experimental animals with <1 per cent par
asitaemia. In mice with moderate parasitaemia (5-10%) and in falciparum mal
aria cases (with 3-7% parasitaemia) also technique IV was most accurate. In
both animal models showing high (15-25%) and in monkeys with moderate para
sitaemia, technique III based on the number of PRBCs per WBC and actual tot
al WBC count, was the most accurate. Thus, technique IV being simpler and c
ost effective, with standardization of the amount of blood used in making a
thick smear, may be used routinely for quantitation of parasitaemia.