Comparison of rapid tests and multiplex PCR for dengue, malaria and chikungunya in acute febrile illness
BMC Infectious Diseases · 2017
Curated peer-reviewed / authoritative reference. Open the source link for the full text.
Simultaneous detection of viruses, parasites and bacteria causing acute febrile illness and pyrexia of unknown origin from one sample.
Pyrexia of unknown origin remains a clinical challenge despite better understanding of causative diseases and wider access to tests — about 51% of PUO cases remain undiagnosed in the literature cited by ID Labs. Fever accounts for a large share of consultations and is one of the most common reasons for hospital admission, with real mortality and loss of life expectancy when diagnosis is delayed.
In tropical practice, malaria, dengue (all four serotypes), chikungunya, enteric (typhoid) fever, leptospirosis, scrub typhus and influenza-like illness present with overlapping, non-specific features. Multiplex PCR differentiates the causes of febrile illness — including malaria, radiologically confirmed pneumonia and typhoid fever — from a single sample.
Culture is significant only for bacterial infections and takes ~72 hours; serology takes 5–7 days and contributes little to acute management. Symptom-based empirical diagnosis alone cannot separate treatable causes that demand completely different therapies.
Malaria smear and antigen tests, dengue NS1/antibody serology, blood culture for enteric fever, and single-plex PCRs each answer one question at a time, consume separate samples and extend the diagnostic odyssey.
ID-Fever Multiplex assays simultaneously detect viruses, parasites and bacteria in one sample, enabling faster and more appropriate treatment decisions when they matter most — including serotype-level dengue differentiation and species-level Plasmodium identification by distinct amplification signatures.
Evacuated blood tube · Cap: Lavender / Purple
Additive: K2/K3 EDTA (anticoagulant)
Volume: 3 mL
Invert gently 8–10 times after collection. Do not freeze.
Swab transport tube · Cap: Varies
Additive: Viral transport medium
Volume: 2–3 mL VTM
Break swab shaft into medium; cap tightly.
| Characteristic | Value | Source |
|---|---|---|
| Scope | Viruses, parasites and bacteria in one sample, providing a comprehensive patient profile | ID Labs Specification |
| Turnaround time | Approximately 5 hours | ID Labs Specification |
| Analytical / clinical performance | Performance characteristics: please contact ID Labs — data to be updated. | ID Labs Validated Performance |
Use early in the workup of undifferentiated fever, particularly in endemic seasons and returning travellers. Early aetiological diagnosis supports treatment, surveillance, outbreak control and rational antimicrobial use.
| Conventional fever workup vs ID-Fever Multiplex | |||
|---|---|---|---|
| Feature | Culture | Serology | ID-Fever Multiplex |
| Pathogens per test | Bacteria only | Single pathogen | Viruses + parasites + bacteria |
| Time | ≈ 72 hours | 5–7 days | ≈ 5 hours |
| Value in acute management | Confirmatory | Low | Directly guides therapy |
BMC Infectious Diseases · 2017
Curated peer-reviewed / authoritative reference. Open the source link for the full text.
Published Scientific Evidence (various authors)
Peer-reviewed literature
The published literature supports syndromic multiplex PCR as a tool for the differential diagnosis of undifferentiated febrile illness, particularly where multiple treatable pathogens (dengue, malaria, enteric fever, rickettsioses, leptospirosis) present with overlapping clinical features. Specific assay performance is target- and platform-dependent. Full citations for this collection are being curated.
Medical Research Archives (ESMED) · 2024
Curated peer-reviewed / authoritative reference. Open the source link for the full text.
Multiplex molecular testing for bacterial, viral and fungal ocular pathogens from minute ocular specimens.
Rapid molecular investigation of multiple pathogens associated with meningitis and encephalitis from a single CSF sample.
Rapid detection of more than 30 sepsis-causing pathogens and their drug-resistance markers directly from whole blood.
Comprehensive viral and bacterial respiratory pathogen detection from swabs, sputum or BAL in a single multiplex assay.
Broad molecular screening for opportunistic viral, bacterial and fungal pathogens in transplant and immunocompromised patients.
Rapid syndromic testing tailored to febrile and seriously ill children, designed around small sample volumes.
Panel configuration, specimen logistics and turnaround details on request.
Information on this page is educational and does not replace professional clinical judgment. Performance values are labelled by source (ID Labs Specification / ID Labs Validated Performance / Manufacturer Specification / Published Scientific Evidence). Molecular results must be correlated clinically and, where appropriate, confirmed by culture and phenotypic susceptibility testing.