- Patient/Guest
- Phlebotomist
- Updates
| Glucose F and PP | - |
|---|
|
Measure fasting and postprandial glucose |
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| Synonym | See updates | |
| Test Code | CDBIOPR0005 | |
| Test Type | Biochemistry | |
| Pre-Test Condition | See updates | |
| Report Availability | 1 D(s) | |
| # Test(s) | Multiple | |
| Test details | Sample Report |
|---|---|
| Glucose F and PP |
|
| Synonym | See updates | ||
| Test Code | CDBIOPR0005 | ||
| Test Category | Diabetes | ||
| Pre-Test Condition | See updates | ||
| |
Medical History | See updates | |
| Report Availability | 1 D(s) | ||
| Specimen/Sample | Serum; 2 mL; SST | ||
| Stability @21-26 deg. C | 6 Hr(s) | ||
| Stability @ 2-8 deg. C | 7 D(s) | ||
| Stability @ Frozen | 1 M(s) | ||
| # Test(s) | Multiple | ||
| Processing Method | Spectrophotometry | ||
| **Blood Glucose Fasting and Post Prandial 2hrs****FDA Status**: Standard laboratory procedure under CLIA; no specific FDA approval required.**Other Names**: Fasting and PP Glucose Test, Diabetes Profile.**Historical Breakthrough**: Developed in the 1900s to diagnose diabetes, advancing endocrinology.**Key Purpose and Impact**: Measures fasting and 2-hour postprandial glucose to diagnose diabetes or monitor glycemic control.**Preparation and Patient History**: Blood after fasting and 2 hours post-meal; report polyuria, thirst, or diabetes history.**Consent Requirement**: Standard consent for diagnostic testing.**Clinical Value**: Sensitivity ~95%; specificity ~95%; detects diabetes in ~90% of cases; guides therapy.**References Cited**: Testing.com Diabetes Tests 2023; Labcorp Glucose Test 2025; UpToDate Diabetes 2025 |
