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. 2023 Jul 31;13(8):1670. doi: 10.3390/life13081670

Table 4.

Advantages, limitations, and cost–benefit analysis of current diagnostic measures of UGS in the field setting.

Diagnosis Advantages Limitations Cost–Benefit Analysis
Urine microscopy Standard method
Familiar in most endemic areas
High specificity (96.6–100%)
Low sensitivity (25.9–46.4%)
Very low sensitivity in ultra-light infections (<10%)
Good
Cheap cost
Feasible
CCA/CAA High sensitivity (89%) and moderate specificity (55%)
for intestinal schistosomiasis
Good for field surveys in areas with ultra-light infection
Reliable for S. mansoni infections
Not acceptable for diagnosis of UGS
Cross reactions with other types of schistosomiasis
Limited supply of the kit
Moderate
Moderate cost
Most feasible in the field setting for IS
Urine reagent strips for microhematuria High sensitivity (71–79%)
High specificity (84–90%)
Easy to implement
Not standard, supplementary to UM Good
Cheap cost
Most feasible in the field setting for UGS
Gross screening of macrohematuria Cheap
Easy
High specificity
Reflects acute infections
Low sensitivity (<10%) with numerous false-negative cases Most cheap
Serology (ELISA) High sensitivity (87–96%)
Optimal in non-endemic areas
Low specificity (31–32%)
Not practical in the endemic field setting in SSA
Moderate
Moderate cost
Lab facilities required
Molecular diagnosis (PCR, qPCR, and LAMP) High sensitivity (>90%)
High specificity (>95%)
Optimal for setting gold standard
Expensive reagents and high technique
Well-established lab support, not practical in the field setting
Feasible for small-scale surveys
Poor
Expensive method and feasible only in lab
Ultrasound High sensitivity (>80%)
High specificity (>80%)
Morbidity information of UGS on site
Detection of other co-morbidities
Experienced sonographer
Expensive sonograph
Feasible for small-scale surveys
Poor
Expensive method
Feasible with a portable sonograph

UGS = urogenital schistosomiasis, CCA = circulating cathodic antigen, CAA = circulating anodic antigen, UM = urine microscopy, ELISA = enzyme-linked immunosorbent assay, PCR = polymerase chain reaction, qPCR = quantitative polymerase chain reaction, LAMP = loop-mediated isothermal amplification.