Diagnostic performance of the STANDARD™ Q Dengue DUO rapid diagnostic test in a resource-limited setting: a laboratory-based evaluation in the Republic of Niger

Dengue fever is an expanding public health threat in sub-Saharan Africa, yet access to laboratory-confirmed diagnosis remains severely constrained in resource-limited settings. Rapid diagnostic tests (RDTs) offer a practical alternative to molecular and serological diagnostic methods, but their performance must be validated in local epidemiological contexts before integration into national testing algorithms. We conducted a retrospective laboratory-based diagnostic accuracy study using 221 archived serum samples from suspected dengue patients admitted to public and private hospitals in Niamey between October and December 2023. The STANDARD™ Q Dengue DUO (SD Biosensor) was compared against qRT-PCR (NS1 reference) and ELISA IgM (IgM reference). Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated with 95% Wilson score confidence intervals. Performance was stratified by viral load (Ct value) and time since symptom onset. Dengue infection was confirmed in 68/221 (30.8%) samples by qRT-PCR and 69/221 (31.2%) by IgM ELISA. For NS1 detection, the STANDARD™ Q demonstrated sensitivity of 79.4% (95% CI: 68.4–87.3%) and specificity of 85.5% (95% CI: 78.0–90.7%), with sensitivity increasing to 83.8% when combined with IgM. NS1 sensitivity was highest in samples with low and moderate viral load (Ct 20–30: 100%). NS1 sensitivity was 84.4% in the acute phase (≤ 7 days) versus 57.1% in the recovery phase (> 7 days). For IgM detection, sensitivity was 49.3% (95% CI: 38.2–60.4%) but specificity was 98.6% (95% CI: 95.0–99.6%), with IgM sensitivity rising to 100% in the recovery phase. The STANDARD™ Q Dengue DUO demonstrated adequate NS1 accuracy and high IgM specificity. Combined NS1 and IgM testing improves case detection across infection phases. Thus, we recommend this RDT as a first-line diagnostic tool in decentralized healthcare settings in Niger, although molecular testing remains essential for surveillance and serotyping purposes.

Authors

Institutions

Publication Details

Journal
BMC Infectious Diseases
Published
2026-08-03
DOI
https://doi.org/10.1186/s12879-026-14158-w
Primary Topic
Mosquito-borne diseases and control
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Diagnostic performance of the STANDARD™ Q Dengue DUO rapid diagnostic test in a resource-limited setting: a laboratory-based evaluation in the Republic of Niger

Abdullahi Balarabe Sallau, Balki Aoula, Adamou Lagaré, Hadiza Ousmane et al.
BMC Infectious Diseases
Mosquito-borne diseases and control
article

Diagnostic performance of the STANDARD™ Q Dengue DUO rapid diagnostic test in a resource-limited setting: a laboratory-based evaluation in the Republic of Niger

Abdullahi Balarabe Sallau, Balki Aoula, Adamou Lagaré, Hadiza Ousmane, Fatimata Hassane, Moussa Issa, Aliyu Muhammad, Absatou Daouda Ousseini, Hassane Ousmane, Nassirou Seyni Hamani
article en

Abstract

Dengue fever is an expanding public health threat in sub-Saharan Africa, yet access to laboratory-confirmed diagnosis remains severely constrained in resource-limited settings. Rapid diagnostic tests (RDTs) offer a practical alternative to molecular and serological diagnostic methods, but their performance must be validated in local epidemiological contexts before integration into national testing algorithms. We conducted a retrospective laboratory-based diagnostic accuracy study using 221 archived serum samples from suspected dengue patients admitted to public and private hospitals in Niamey between October and December 2023. The STANDARD™ Q Dengue DUO (SD Biosensor) was compared against qRT-PCR (NS1 reference) and ELISA IgM (IgM reference). Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated with 95% Wilson score confidence intervals. Performance was stratified by viral load (Ct value) and time since symptom onset. Dengue infection was confirmed in 68/221 (30.8%) samples by qRT-PCR and 69/221 (31.2%) by IgM ELISA. For NS1 detection, the STANDARD™ Q demonstrated sensitivity of 79.4% (95% CI: 68.4–87.3%) and specificity of 85.5% (95% CI: 78.0–90.7%), with sensitivity increasing to 83.8% when combined with IgM. NS1 sensitivity was highest in samples with low and moderate viral load (Ct 20–30: 100%). NS1 sensitivity was 84.4% in the acute phase (≤ 7 days) versus 57.1% in the recovery phase (> 7 days). For IgM detection, sensitivity was 49.3% (95% CI: 38.2–60.4%) but specificity was 98.6% (95% CI: 95.0–99.6%), with IgM sensitivity rising to 100% in the recovery phase. The STANDARD™ Q Dengue DUO demonstrated adequate NS1 accuracy and high IgM specificity. Combined NS1 and IgM testing improves case detection across infection phases. Thus, we recommend this RDT as a first-line diagnostic tool in decentralized healthcare settings in Niger, although molecular testing remains essential for surveillance and serotyping purposes.

BMC Infectious Diseases
Ahmadu Bello University (NG), Centre de Recherche Médicale et Sanitaire (NE)
Openalex Percentile: Top 7%
Mosquito-borne diseases and control
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.