Conventional microscopy is the gold standard for malaria diagnosis. The CellaVision DM96 is a digital hematology analyzer that utilizes neural networks to locate, digitize, and preclassify leukocytes and characterize red blood cell morphology. This study compared the detection rates of Plasmodium and Babesia species on peripheral blood smears utilizing the CellaVision DM96 with the rates for a routine red blood cell morphology scan. A total of 281 slides were analyzed, consisting of 130 slides positive for Plasmodium or Babesia species and 151 negative controls. Slides were blinded, randomized, and analyzed by CellaVision and microscopy for red cell morphology scans. The technologists were blinded to prior identification results. The parasite detection rate was 73% (95/130) for CellaVision and 81% (105/130) for microscopy for positive samples. The interobserver agreement between CellaVision and microscopy was fair, as Cohen's kappa coefficient equaled 0.36. Pathologist review of CellaVision images identified an additional 15 slides with parasites, bringing the total number of detectable positive slides to 110 of 130 (85%). Plasmodium ovale had the lowest rate of detection at 56% (5 of 9); Plasmodium malariae and Babesia spp. had the highest rate of detection at 100% (3/3 and 6/6, respectively). The detection rate by CellaVision was 100% (23/23) when the parasitemia was >2.5%. The detection rate for <0.1% parasitemia was 63% (15/24). Technologists appropriately classified all negative specimens. The percentage of positive specimens detectable by CellaVision (73%) approaches results for microscopy on routine scan of peripheral blood smears for red blood cell morphology.
Malaria is a global disease with an estimated 219 million cases and 660,000 deaths reported in 2010 (1). In the United States, 1,691 cases were reported in 2010, up from 767 cases in 2003, mostly from travelers to areas of endemicity (2). The recognition and diagnosis of malaria often depend on clinical signs and symptoms, including fever, headache, fatigue, myalgia, abdominal pain, nausea, vomiting, and splenomegaly. These symptoms are often nonspecific and can be easily missed by physicians unfamiliar with the presentation of malaria (3). In addition, a large proportion of infected individuals in countries in which malaria is endemic are asymptomatic or subclinical. Some studies have reported microscopy-detected malaria carriage in up to 39.2% of asymptomatic individuals (4). The prevalence of asymptomatic carriers has been reported to be highest in children and adolescents due to the fact that children in regions where malaria is endemic often acquire clinical immunity to malaria from repetitive infections, resulting in the ability to tolerate malaria parasites without developing fever (4, 5). These asymptomatic carriers typically do not seek medical treatment and can serve as a reservoir of parasites not only in high-prevalence areas but also potentially in developed countries due to increased international travel (3, 4). Effective routine scre...