IMD Panel Quantitative Blood Test
Short Name: IMD Panel Test
Also known as: Newborn Screening Test for IEM, Metabolic Disorder Panel
IMD Panel Quantitative Blood Test test available at DNA Labs India for ₹7,000. Uses Tandem Mass Spectrometry on Heel prick blood on filter paper samples. Results in Reports are typically available the next day after sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
The purpose of the IMD Panel Quantitative Blood Test is to detect and quantify biomarkers associated with Inborn Errors of Metabolism, including amino acids, acylcarnitines, adenosine, 2'-deoxyadenosine, and molar ratios. This aids in diagnosing metabolic disorders early, enabling timely treatment and management.
- Test Code
- 858
- Price
- ₹7,000
- Sample Type
- Heel prick blood on filter paper
- Result Time
- Reports are typically available the next day after sample receipt.
- Fasting Required
- No
- Method
- Tandem Mass Spectrometry
Sample Collection
Clinical details and drug history must accompany the sample. Ensure the infant is well-hydrated and comfortable.
Method: Heel prick
Laboratory Analysis
Heel prick blood collection is performed on filter paper, with 1 drop per spot on 3 spots.
Report Delivery
Sample should be shipped refrigerated or frozen as per stability guidelines.
Timeline: Reports are typically available the next day after sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the IMD Panel Quantitative Blood Test is to detect and quantify biomarkers associated with Inborn Errors of Metabolism, including amino acids, acylcarnitines, adenosine, 2'-deoxyadenosine, and molar ratios. This aids in diagnosing metabolic disorders early, enabling timely treatment and management.
How to Prepare
- Use filter paper provided by LPL
- Collect 1 drop of blood per spot on 3 spots
- Avoid contaminating the sample
- Label the sample correctly with patient details
- Ship refrigerated or frozen immediately after collection
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"This test is essential for early detection and management of metabolic disorders in newborns, preventing long-term health issues."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Contaminated or hemolyzed sample
- Improper storage or delayed shipment
- Missing clinical details or drug history
Understanding Your Results
Normal levels
No indication of common metabolic disorders; clinical correlation recommended.
Elevated amino acids
May indicate amino acid disorders like phenylketonuria; further testing needed.
Abnormal acylcarnitines
Suggests fatty acid oxidation defects or organic acidemias; requires specialist evaluation.
Low adenosine levels
Could be associated with immunodeficiency disorders; clinical assessment advised.
Abnormal molar ratios
May indicate metabolic imbalances; follow-up with genetic counseling recommended.
Consult a doctor if symptoms such as fever, fatigue, or developmental delays persist, or if test results indicate abnormal biomarker levels.
Limitations
- ⚠May not detect all variants of metabolic disorders
- ⚠Results require interpretation by a qualified healthcare professional
- ⚠False positives or negatives possible due to technical factors
- ⚠Not a standalone diagnostic tool; clinical correlation needed
Risks & Considerations
- ●Minor discomfort or bruising at the collection site
- ●Infection risk is very low with proper technique
- ●Rare allergic reaction to antiseptic
Interfering Factors
- ●Recent meals or fasting status may affect some biomarkers
- ●Certain medications or supplements
- ●Improper sample collection or storage
- ●Contamination during sample handling
Frequently Asked Questions
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