Objective: There exist various diagnostic tests to detect
visceral leishmaniasis, but the most efficient ones have not been demonstrated
yet. Herein, we evaluated the accuracy of these diagnostic tests in Iran.
Methodology: English and Persian database searching was done from
1993 to 2016. According to heterogeneity of the studies, estimations of the
study were pooled by random-effects model. Totally, twenty investigations were
eligible for current review with 2115 patients as pooled sample size.
Results:
The
overall pooled estimate of sensitivity and specificity for all diagnostic tests
were 0.92 ([95% CI = 0.90–0.95]) and 0.92 ([95% CI = 0.89–0.94]), respectively.
Also, the separate sensitivity and specificity of each test were as follow:
PCR: 1.00 ([95% CI = 0.99–1.01]) and 0.37 ([95% CI = 0.25–0.49]); DAT: 0.93
([95% CI = 0.89–0.96]) and 0.92 ([95% CI = 0.89–0.94]); ELISA: 0.78 ([95% CI =
0.47–1.09]) and 1.00 ([95% CI = 0.99–1.01]) as well as IFA: 0.50 ([95% CI =
0.29–0.72]) and 0.96 ([95% CI = 0.95–0.97]).
Visceral Leishmaniasis sensitivity specificity diagnostic tests L. infantum Iran
Birincil Dil | İngilizce |
---|---|
Bölüm | Research Article |
Yazarlar | |
Yayımlanma Tarihi | 15 Mart 2019 |
Yayımlandığı Sayı | Yıl 2019 Cilt: 09 Sayı: 01 |