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Pan Fungal Detection ID PCR Test -
Detects fungal DNA to diagnose fungal infections, causing fever or respiratory issues
Synonym Pan Fungal ID Test
Test Code MOLT26040157
Test Type Molecular Pathology
Pre-Test Condition No special
Report Availability 3–5 D(s)
# Test(s) 1
Test details Sample Report
Pan Fungal Detection ID PCR Test Sample Report Cowin-PathLab
Synonym Pan Fungal ID Test
Test Code MOLT26040157
Test Category Fungal Infections
Pre-Test Condition No special
Medical History Share & see Updates
Report Availability 3–5 D(s)
Specimen/Sample Refer Updates
Stability @21-26 deg. C 24 H(s)
Stability @ 2-8 deg. C 48 H(s)
Stability @ Frozen Not frozen
# Test(s) 1
Processing Method PCR
Overview: Pan Fungal Detection ID PCR Test
Introduction: The Pan Fungal Detection ID PCR Test detects fungal DNA to diagnose fungal infections, causing fever or respiratory issues. Aligned with 2023 IDSA guidelines, it uses PCR for high specificity, supporting infection screening. This test is critical for guiding diagnosis, treatment planning, and improving outcomes in molecular pathology for patients with suspected fungal infections, such as aspergillosis or candidiasis.
Other Names: Pan Fungal ID Assay, Fungal DNA Identification Test.
FDA Status: Laboratory-developed test (LDT), meeting molecular pathology standards for diagnostic accuracy.
Historical Milestone: Fungal PCR testing began in the 1990s with Candida research. NGS and PCR methods improved in the 2010s, enhancing diagnostic precision.
Purpose: Detects fungal DNA to diagnose fungal infections, guides treatment, and evaluates patients with fever or respiratory issues.
Test Parameters: 1. Fungal DNA Identification
Pretest Condition: No fasting required. Collect whole blood, tissue, BAL, sputum, CSF, or saliva. Report history of fever, respiratory issues, or fungal infection symptoms.
Specimen: Whole Blood (EDTA, 2-5 mL), Tissue (sterile container, 0.5-2 cma³), Bronchoalveolar Lavage (sterile container, 5-10 mL), Sputum (sterile container, 5-10 mL), CSF (sterile container, 1-2 mL), Saliva (sterile container, 1-2 mL). Transport in a biohazard container.
Sample Stability at Room Temperature: 24 hours
Sample Stability at Refrigeration: 48 hours
Sample Stability at Frozen: Not frozen
Medical History: Document fever, respiratory issues, or history of immunosuppression. Include current medications, especially antifungals.
Consent: Written consent required, detailing the tests purpose, fungal infection implications, and risks of sample collection.
Procedural Considerations: Uses PCR to identify fungal DNA (e.g., Aspergillus, Candida). Results are available in 3-5 days, supporting clinical decisions. Performed in laboratories, often for fungal infection diagnosis.
Factors Affecting Result Accuracy: Low DNA yield or improper sample storage can affect results. Contamination may reduce specificity.
Clinical Significance: Identified fungal DNA confirms infection, guiding antifungal therapy. Negative results may require culture confirmation.
Specialist Consultation: Consult an infectious disease specialist for result interpretation and treatment planning.
Additional Supporting Tests: Fungal culture, galactomannan assay, or imaging (CT/chest X-ray) to confirm fungal infection diagnosis.
Test Limitations: Not all fungi are detectable by PCR; clinical correlation is needed. Sample quality affects sensitivity.
References: IDSA Fungal Guidelines, 2023; Clinical Infectious Diseases, Patterson TF, 2022.

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