Diagnostic accuracy and utility of three dengue diagnostic tests for the diagnosis of acute dengue infection in Malaysia

• Published in: BMC infectious diseases Vol. 20; no. 1; pp. 210 - 11
• Main Authors: Chong, Zhuo Lin, Sekaran, Shamala Devi, Soe, Hui Jen, Peramalah, Devi, Rampal, Sanjay, Ng, Chiu-Wan
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 12.03.2020; BioMed Central; BMC
• Subjects: Accuracy; Adolescent; Adult; Aged; Ambulatory care facilities; Antibodies; Antigens; Biosensors; Child; Child, Preschool; Communicable diseases; Communicable Diseases, Emerging - diagnosis; Communicable Diseases, Emerging - virology; Comparative analysis; Cross-Sectional Studies; Dengue; Dengue - diagnosis; Dengue - virology; Dengue fever; Dengue Virus - classification; Detection equipment; Diagnosis; Diagnostic systems; Diagnostic tests; Diagnostic Tests, Routine; Disease; Diseases; Enzyme-Linked Immunosorbent Assay; Enzymes; Evaluation; Female; Future predictions; Health; Humans; Immunoglobulin G; Immunoglobulin G - blood; Immunoglobulin M - blood; Infant; Infections; Infectious diseases; Laboratories; Malaysia; Male; Medical equipment; Medical research; Medical tests; Middle Aged; Patients; Point-of-Care Systems; Polymerase chain reaction; Probability; Prospective Studies; Rapid diagnostic test; Sample size; Sensitivity and Specificity; Serotyping; Setting (Literature); Vector-borne diseases; Viral diseases; Young Adult; Malaysia; Denmark; Evaluation; Rapid diagnostic test; Biosensors; Dengue diagnosis; Dengue
• ISSN: 1471-2334; 1471-2334
• DOI: 10.1186/s12879-020-4911-5

Dengue is an emerging infectious disease that infects up to 390 million people yearly. The growing demand of dengue diagnostics especially in low-resource settings gave rise to many rapid diagnostic tests (RDT). This study evaluated the accuracy and utility of ViroTrack Dengue Acute - a new biosensors-based dengue NS1 RDT, SD Bioline Dengue Duo NS1/IgM/IgG combo - a commercially available RDT, and SD Dengue NS1 Ag enzyme-linked immunosorbent assay (ELISA), for the diagnosis of acute dengue infection. This prospective cross-sectional study consecutively recruited 494 patients with suspected dengue from a health clinic in Malaysia. Both RDTs were performed onsite. The evaluated ELISA and reference tests were performed in a virology laboratory. The reference tests comprised of a reverse transcription-polymerase chain reaction and three ELISAs for the detection of dengue NS1 antigen, IgM and IgG antibodies, respectively. The diagnostic performance of evaluated tests was computed using STATA version 12. The sensitivity and specificity of ViroTrack were 62.3% (95%CI 55.6-68.7) and 95.0% (95%CI 91.7-97.3), versus 66.5% (95%CI 60.0-72.6) and 95.4% (95%CI 92.1-97.6) for SD NS1 ELISA, and 52.4% (95%CI 45.7-59.1) and 97.7% (95%CI 95.1-99.2) for NS1 component of SD Bioline, respectively. The combination of the latter with its IgM and IgG components were able to increase test sensitivity to 82.4% (95%CI 76.8-87.1) with corresponding decrease in specificity to 87.4% (95%CI 82.8-91.2). Although a positive test on any of the NS1 assays would increase the probability of dengue to above 90% in a patient, a negative result would only reduce this probability to 23.0-29.3%. In contrast, this probability of false negative diagnosis would be further reduced to 14.7% (95%CI 11.4-18.6) if SD Bioline NS1/IgM/IgG combo was negative. The performance of ViroTrack Dengue Acute was comparable to SD Dengue NS1 Ag ELISA. Addition of serology components to SD Bioline Dengue Duo significantly improved its sensitivity and reduced its false negative rate such that it missed the fewest dengue patients, making it a better point-of-care diagnostic tool. New RDT like ViroTrack Dengue Acute may be a potential alternative to existing RDT if its combination with serology components is proven better in future studies.