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Smear for Microfilaria (MF)
Parameters : 1
Also known as : Smear for Microfilaria (MF)
EXCLUSIVE PRICE
250
Report Delivery
1 Day
Free Sample Collection
Bookings above 500
Pre - Instruction
No preparation required.
Covid Safety
Assured
Test Details
Test Code BOBT00485
Test Category Individual Test
Sample Type Blood
Details of Smear for Microfilaria (MF)
What is Smear for Microfilaria (MF)?
Diagnostic tools for lymphatic filariasis (LF) elimination programs are useful in mapping the distribution of the disease, delineating areas where mass drug administrations (MDA) are required, and determining when to stop MDA. The prevalence and burden of LF have been drastically reduced following mass treatments, and the evaluation of the performance of circulating filarial antigen (CFA)-based assays was acknowledged to be of high interest in areas with low residual LF endemicity rates after multiple rounds of MDA. The objective of this study was therefore to evaluate the immunochromatographic test (ICT) sensitivity in low endemicity settings and, specifically, in individuals with low intensity of lymphatic filariasis infection.
Methods
To perform this study, calibrated thick blood smears, ICT, and Og4C3 enzyme-linked immunosorbent assay (ELISA) were carried out by night to identify Wuchereria bancrofti microfilarial and circulating filarial antigen carriers. A threshold determination assay regarding ICT and ELISA was performed using serial plasma dilutions from individuals with positive microfilarial counts.
Results
All individuals harboring microfilariae (positive blood films) were detected by ICT and ELISA, but among individuals positive for ELISA, only 35.7 % of them were detected using ICT (Chi-square: 4.57; p-value?=?0.03), indicating a moderate agreement between both tests (kappa statistics?=?0.49). Threshold determination analyses showed that ELISA was still positive at the last plasma dilution with a negative ICT result.
Conclusions
These findings suggest a loss of sensitivity for ICT in low endemicity settings, especially in people exhibiting low levels of circulating filarial antigen, raising serious concern regarding the monitoring and evaluation procedures in the framework of the LF elimination program.
Routine Tests
Smear for Microfilaria (MF)
Parameters : 1
Also known as : Smear for Microfilaria (MF)
EXCLUSIVE PRICE
250
Report Delivery
1 Day
Free Sample Collection
Bookings above 500
Pre - Instruction
No preparation required.
Covid Safety
Assured
Test Details
Test Code BOBT00485
Test Category Individual Test
Sample Type Blood
Details of Smear for Microfilaria (MF)
What is Smear for Microfilaria (MF)?
Diagnostic tools for lymphatic filariasis (LF) elimination programs are useful in mapping the distribution of the disease, delineating areas where mass drug administrations (MDA) are required, and determining when to stop MDA. The prevalence and burden of LF have been drastically reduced following mass treatments, and the evaluation of the performance of circulating filarial antigen (CFA)-based assays was acknowledged to be of high interest in areas with low residual LF endemicity rates after multiple rounds of MDA. The objective of this study was therefore to evaluate the immunochromatographic test (ICT) sensitivity in low endemicity settings and, specifically, in individuals with low intensity of lymphatic filariasis infection.
Methods
To perform this study, calibrated thick blood smears, ICT, and Og4C3 enzyme-linked immunosorbent assay (ELISA) were carried out by night to identify Wuchereria bancrofti microfilarial and circulating filarial antigen carriers. A threshold determination assay regarding ICT and ELISA was performed using serial plasma dilutions from individuals with positive microfilarial counts.
Results
All individuals harboring microfilariae (positive blood films) were detected by ICT and ELISA, but among individuals positive for ELISA, only 35.7 % of them were detected using ICT (Chi-square: 4.57; p-value?=?0.03), indicating a moderate agreement between both tests (kappa statistics?=?0.49). Threshold determination analyses showed that ELISA was still positive at the last plasma dilution with a negative ICT result.
Conclusions
These findings suggest a loss of sensitivity for ICT in low endemicity settings, especially in people exhibiting low levels of circulating filarial antigen, raising serious concern regarding the monitoring and evaluation procedures in the framework of the LF elimination program.
 

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