TESTING HIGHLIGHTS

INTRODUCTION

Augustus Laboratories Background

Full Chemistry Blood Testing

  • Comprehensive Metabolic Panel (CMP): Liver, kidney function, and electrolyte balance.
  • Complete Blood Count (CBC): Red/white blood cells, hemoglobin, and platelets.
  • Lipid Profile: HDL, LDL, total cholesterol, and triglycerides.
  • Liver Function Tests: Enzymes and proteins for liver health.
  • Kidney Function Tests: BUN and creatinine levels.
  • Thyroid Function Tests: TSH, T3, and T4 levels.
  • Electrolyte Panel: Sodium, potassium, chloride, and bicarbonate.
  • Glucose Testing: Blood sugar levels.
  • Calcium Testing: Calcium levels for bone health.
  • Iron Studies: Ferritin and transferrin levels.
  • Protein Testing: Total protein and albumin.

Medication Management (Toxicology) Services

  • Drug Monitoring: Ensuring therapeutic drug levels
  • Medication Adherence: Assessing compliance with regimens
  • Drug-Drug Interaction Screening: Identifying potential interactions
  • Overdose and Toxicity Detection: Managing drug overdose or toxicity
  • Substance Abuse Testing: Screening for illicit drugs
  • Pharmacokinetic Analysis: Studying drug absorption and metabolism
  • Customizable Panels: Tailored testing panels
  • Rapid Turnaround: Quick and accurate results
  • Comprehensive Reporting: Detailed reports for providers
  • Consultation Services: Expert interpretation and treatment recommendations

Medication Management (Toxicology) Services

  • Drug Monitoring: Ensuring therapeutic drug levels
  • Medication Adherence: Assessing compliance with regimens
  • Drug-Drug Interaction Screening: Identifying potential interactions
  • Overdose and Toxicity Detection: Managing drug overdose or toxicity
  • Substance Abuse Testing: Screening for illicit drugs
  • Pharmacokinetic Analysis: Studying drug absorption and metabolism
  • Customizable Panels: Tailored testing panels
  • Rapid Turnaround: Quick and accurate results
  • Comprehensive Reporting: Detailed reports for providers
  • Consultation Services: Expert interpretation and treatment recommendations

Pharmacogenomics (PGx):

  • Genetic Testing: Analyzing individual genetic profiles to understand drug metabolism.
  • Personalized Medicine: Tailoring drug therapy to maximize efficacy and minimize adverse effects.
  • Drug-Gene Interactions: Identifying potential interactions between medications and genetic markers.
  • Treatment Optimization: Adjusting dosages and selecting appropriate medications based on genetic insights.
  • Risk Management: Reducing the likelihood of adverse drug reactions through genetic screening.
  • Precision Prescribing: Enhancing the accuracy of prescriptions for conditions such as cardiovascular disease, mental health disorders, and cancer.
  • Clinical Decision Support: Providing healthcare providers with actionable genetic information for informed decision-making.

Infectious disease testing (RT-PCR):

  • Respiratory Infections: PCR and Rapid Antigen tests for pathogens causing respiratory illnesses such as influenza, RSV, and SARS-CoV-2 (COVID-19).
  • ENT Infections: Diagnostic testing for infections affecting the ear, nose, and throat, including strep throat and sinusitis.
  • Urinary Tract Infections (UTI): Tests for detecting and identifying bacteria responsible for urinary tract infections.
  • Gastrointestinal Infections: PCR and Rapid Antigen tests for pathogens causing gastrointestinal issues, such as norovirus and C. difficile.
  • Sexually Transmitted Infections (STI): Comprehensive testing for common STIs including chlamydia, gonorrhea, and herpes.
  • Women’s Health: Testing for infections affecting women’s health, including bacterial vaginosis and yeast infections.
  • Ophthalmology Infections: Diagnostic testing for infections of the eye, such as conjunctivitis and keratitis.
  • Wound Infections: Analysis of wound samples to identify infectious agents and guide appropriate treatment.
  • Nail Infections: Testing for fungal and bacterial infections affecting the nails.

Hereditary Genetic Disease Testing:

  1. Cancer Genetic Testing: Identifies genetic mutations associated with an increased risk of various cancers, enabling early detection and preventive measures.
  2. Carrier Testing: Screens for genetic mutations that could be passed on to offspring, helping prospective parents understand their risk of passing on hereditary conditions.
  3. Non-Invasive Prenatal Testing (NIPT): Analyzes fetal DNA from maternal blood to assess the risk of certain genetic disorders, such as Down syndrome, with high accuracy and minimal risk.