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Laboratory Report Template

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Laboratory Report Template

Patient Information

Patient Name: [Last, First]
Medical Record Number: [MRN]
Date of Birth: [MM/DD/YYYY]
Age/Sex: [Age years, M/F]

Ordering Physician: [Name]
Location: [Inpatient unit / Outpatient clinic]


Specimen Information

Specimen Type: [Blood / Serum / Plasma / Urine / CSF / Other]
Collection Date/Time: [MM/DD/YYYY at HH:MM]
Received Date/Time: [MM/DD/YYYY at HH:MM]
Reported Date/Time: [MM/DD/YYYY at HH:MM]

Accession Number: [Lab accession number]
Specimen Condition: [Acceptable / See comments]
Fasting Status: [Fasting / Non-fasting / Unknown] (if relevant)


Laboratory Results

Test NameResultUnitsReference RangeFlag
[Test][Value][Unit][Normal range][L/H/Critical]

Example: Complete Blood Count (CBC)

TestResultUnitsReference RangeFlag
White Blood Cell Count12.5× 10³/μL4.5-11.0H
Hemoglobin10.2g/dL12.0-16.0 (F), 14.0-18.0 (M)L
Hematocrit31.5%36.0-48.0 (F), 42.0-52.0 (M)L
Platelet Count245× 10³/μL150-400-
MCV88.5fL80.0-100.0-
MCH29.5pg27.0-33.0-
MCHC33.2g/dL32.0-36.0-
RDW14.5%11.5-14.5-

Differential:

Cell TypeResultUnitsReference RangeFlag
Neutrophils75%40-70H
Lymphocytes15%20-40L
Monocytes7%2-10-
Eosinophils2%1-4-
Basophils1%0-2-

Example: Basic Metabolic Panel (BMP)

TestResultUnitsReference RangeFlag
Sodium138mEq/L136-145-
Potassium3.2mEq/L3.5-5.0L
Chloride102mEq/L98-107-
CO224mEq/L22-30-
Blood Urea Nitrogen28mg/dL7-20H
Creatinine1.8mg/dL0.6-1.2 (F), 0.7-1.3 (M)H
Glucose145mg/dL70-100 (fasting)H
eGFR42mL/min/1.73m²>60L

Interpretation / Comments

[Clinical interpretation when applicable]

Example for Anemia:

Normocytic anemia with elevated WBC. Differential diagnosis includes anemia of chronic 
disease, recent blood loss, or hemolysis. Consider reticulocyte count, iron studies, 
and peripheral smear for further evaluation. Clinical correlation recommended.

Example for Electrolyte Abnormality:

Hypokalemia detected (K+ 3.2 mEq/L). Common causes include diuretic use, GI losses, or 
inadequate intake. Recommend potassium repletion and follow-up testing. Moderate 
azotemia present, consistent with acute kidney injury or chronic kidney disease. 
Clinical correlation with patient history and prior results recommended.

Critical Values

[If any results meet criteria for critical values]

Critical Result: [Test name] = [Value] [Units]
Reference Range: [Normal range]
Significance: [Life-threatening, requires immediate action]

Notification:

  • Called to: [Name and title of person notified]
  • Date/Time: [MM/DD/YYYY at HH:MM]
  • Read-back verified: [Yes]
  • Notified by: [Lab personnel name]

Example Critical Values:

  • Glucose <40 mg/dL or >500 mg/dL
  • Potassium <2.5 mEq/L or >6.5 mEq/L
  • Sodium <120 mEq/L or >160 mEq/L
  • Hemoglobin <5.0 g/dL
  • Platelets <20 × 10³/μL
  • WBC <1.0 × 10³/μL or >50 × 10³/μL
  • INR >5.0 (on warfarin)
  • Positive blood culture
  • Positive CSF Gram stain

Quality Control

Specimen Quality: [Acceptable / See note]

QC Notes:

  • Specimen collected in appropriate tube
  • Specimen adequately labeled
  • Specimen volume sufficient
  • No hemolysis, lipemia, or icterus
  • Specimen processed within acceptable time

Issues (if any):

  • Hemolyzed - may affect [specific tests]
  • Clotted - unable to perform coagulation studies
  • Insufficient volume - limited testing performed
  • Delayed processing - stability concerns for [specific analytes]

Methodology

Test Method: [Instrumentation and methodology]

Examples:

  • CBC: Automated cell counter (Sysmex XN-1000)
  • Chemistry: Spectrophotometry (Beckman AU5800)
  • Glucose: Enzymatic assay, hexokinase method
  • HbA1c: HPLC (high-performance liquid chromatography)
  • Troponin: High-sensitivity immunoassay
  • Drug levels: Liquid chromatography-mass spectrometry (LC-MS/MS)

Special Tests Examples

Hemoglobin A1c

TestResultUnitsInterpretation
HbA1c8.5%Consistent with poorly controlled diabetes
HbA1c8.5% (69 mmol/mol)Target <7% for most patients

Reference Ranges:

  • Non-diabetic: 4.0-5.6%
  • Prediabetes: 5.7-6.4%
  • Diabetes diagnosis: ≥6.5%
  • Treatment target: <7% (individualized)

Lipid Panel

TestResultUnitsReference RangeDesirable
Total Cholesterol245mg/dL-<200
LDL Cholesterol160mg/dL-<100
HDL Cholesterol38mg/dL->40 (M), >50 (F)
Triglycerides235mg/dL-<150
VLDL Cholesterol (calc)47mg/dL-<30

Coagulation Studies

TestResultUnitsReference RangeFlag
PT18.5seconds11.0-13.5H
INR2.8ratio0.8-1.2H
PTT42seconds25-35H

Therapeutic Ranges (INR):

  • Atrial fibrillation: 2.0-3.0
  • Mechanical heart valve: 2.5-3.5
  • DVT/PE treatment: 2.0-3.0

Thyroid Function Tests

TestResultUnitsReference RangeFlag
TSH8.5μIU/mL0.4-4.0H
Free T40.7ng/dL0.8-1.8L
Free T32.1pg/mL2.3-4.2L

Interpretation: Findings consistent with primary hypothyroidism

Urinalysis

Physical Examination:

  • Color: [Yellow / Amber / Other]
  • Clarity: [Clear / Cloudy / Turbid]
  • Specific Gravity: [1.005-1.030]

Chemical Examination:

TestResultReference
pH6.05.0-8.0
ProteinTraceNegative
GlucoseNegativeNegative
KetonesNegativeNegative
Blood2+Negative
BilirubinNegativeNegative
UrobilinogenNormalNormal
NitriteNegativeNegative
Leukocyte EsterasePositiveNegative

Microscopic Examination (if indicated):

  • WBCs: [number] /hpf (normal <5)
  • RBCs: [number] /hpf (normal <3)
  • Epithelial cells: [Few/Moderate/Many]
  • Bacteria: [None/Few/Moderate/Many]
  • Casts: [Type and number]
  • Crystals: [Type if present]

Microbiology Report Format

Culture Results

Specimen Source: [Blood / Urine / Sputum / Wound / Other]
Collection: [Date and time]

Gram Stain: [Results of Gram stain if performed] Example: "Many Gram-positive cocci in clusters, many WBCs"

Culture Results:

Organism: [Identified organism]
Quantity: [Light / Moderate / Heavy growth] or [CFU count]

Antimicrobial Susceptibility Testing:

AntibioticResultMIC (μg/mL)
[Drug name]S/I/R[Value]

Example:

AntibioticResultMIC
AmpicillinR>16
CeftriaxoneS≤1
LevofloxacinS0.5
VancomycinS1

Interpretation: S = Susceptible, I = Intermediate, R = Resistant


Molecular/Genetic Testing

Test: [Specific test name]
Method: [PCR / Sequencing / Array / Other]
Result: [Detected / Not detected / Variant identified]

Interpretation: [Clinical significance of result]


Reference Laboratory Results

[For send-out tests]

Test: [Name]
Performed by: [Reference lab name and location]
Result: [Value]
Reference Range: [Range]
Method: [Methodology]
Reported: [Date]


Laboratory Director Signature

Medical Director:
[Name, MD]
[Board Certifications]
[CLIA License Number]

Electronically signed: [Date]


LOINC Codes (for interoperability)

[LOINC codes for each test when applicable for electronic reporting]

Example:

  • Hemoglobin: 718-7
  • Glucose: 2345-7
  • Creatinine: 2160-0
  • TSH: 3016-3