Abstract
This study was conducted to evaluate two routinely microscopic diagnostic methods in comparison with single-round PCR assay as the reference technique to detect Entamoeba histolytica/dispar/moshkovskii. Examination was performed on 500 stool samples obtained from Orang Asli communities in different states of Malaysia using formalin-ether sedimentation, trichrome staining and single-round PCR techniques. Ninety-three stool samples were detected E. histolytica/dispar/moshkovskii positive by routine microscopy, while single-round PCR detected 106 positive samples. Additional positives detected by PCR assay were eventually confirmed to be negative by both microscopic techniques. Detection rate of E. histolytica/dispar/moshkovskii was highest in combination techniques (18.6%), followed by trichrome staining (13.4%) and formalin-ether sedimentation (11.2%) techniques. Single-round PCR detected 21.2% of the stool samples. The sensitivity and specificity of formalin-ether sedimentation and trichrome staining techniques compared to the reference technique were 31.1% (95% CI: 29.0–36.0) and 94.2% (95% CI: 89.8–98.9), and 53.8% (95% CI: 46.0–76.2) and 97.5% (95% CI: 92.8–99.1), respectively. However, the sensitivity [59.4% (95% CI: 48.9–78.5)] of the method increased when both techniques were performed together, but the specificity decreased to 92.4% (95% CI: 81.0–98.0). The agreement between the reference technique, trichrome staining and combination techniques were statistically significant by Kappa statistics (trichrome staining: K=0.592, p<0.05; combination techniques: K=0.543, p<0.05). Hence, the combination technique is recommended to be used as a screening method in the diagnosis of E. histolytica/dispar/moshkovskii infections either for clinical or epidemiological study.
► Sensitivity and specificity of trichrome staining is higher than formalin-ether sedimentation technique. ► The sensitivity of the method increased when both techniques were performed together. ► Combination technique is recommended to be used as a screening method for E. histolytica/dispar/moshkovskii infection.