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. 2017 Sep;47(10-11):609–616. doi: 10.1016/j.ijpara.2017.02.005

Table 1.

Results of quantitative real time kinetoplast DNA (qRT-kDNA) PCR targeting Leishmania DNA extracted from samples collected with microbiopsy (MB) device types 1 and 2 (MB1, MB2) and finger pricks (FP) from 10 hospitalized leishmaniasis patients during the pilot study.

Noa Parasite concentrations (per ml)
Patient information
MB type MB Location
FP
Arm Back Nape of Neck Face
1 MB1 0 10 (0.1) 278 Pre-treated VL+
MB2 60 30 (34·5)
2 MB1 80 10 92,714 Pre-treated VL+
MB2 3,920 2,850
3 MB1 10 10 2,810 Pre-treated VL+
MB2 2,710 80
4 MB1 10 279 Pre-treated VL+
MB2 70
5 MB1 20 0 0 405 Pre-treated VL+
MB2 20 260 930
7 MB1 10 829 Pre-treated VL+
MB2 20 340
6 MB1 20 0 18 VL+ 6th day of treatment with Sodium stibogluconate
MB2 70 10
8 MB1b 20,130 >106 Co-infection VL+ HIV, hard skin nodules, signs of PKDL
MB2 1,080
9 MB1c 1,160 7,156 PKDL Grade 1
MB2 650
10 MB1 60 250 Diffuse CL, 3 years treatment
MB2 10

VL, visceral leishmaniasis; HIV, human immunodeficiency virus; CL, cutaneous leishmaniasis.

a

Patients 1 to 8 were diagnosed serologically using rK39 rapid tests followed by splenic punctures.

b

MB1 device was applied to a papular post-kala azar dermal leishmaniasis (PKDL) lesion (scattered lesions were observed only on the face restricted to areas around the nose and mouth).

c

MB1 device was applied directly on the surface of a hard skin nodule in the forearm.