Search Results

Ordering information regarding a Cyclic Citrullinated Peptide (CCP) Antibody, IgG test for Clinical Diagnostic Laboratories. Cyclic Citrullinated Peptide (CCP) Antibody, IgG Ordering Recommendation Highly specific serologic test that aids in the workup of suspected rheumatoid arthritis or undifferentiated inflammatory arthritides. Rheumatoid Arthritis Panel (3004055 ) is the preferred test. Mnemonic Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay Performed Mon-Sat Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube (SST). Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to a Standard Transport Tube. (Min: 0.3 mL) Storage/Transport Temperature: Refrigerated Unacceptable Conditions: Urine or plasma. Contaminated, hemolyzed, grossly icteric, heat-inactivated, or severely lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval 19 Units or less 20-39 Units Negative Weak Positive 40-59 Units Moderate Positive 60 Units or Greater Strong Positive Interpretive Data Anti-cyclic citrullinated peptide (anti-CCP), IgG antibodies are present in about 69-83 percent of patients with rheumatoid arthritis (RA) and have specificities of 93-95 percent. These autoantibodies may be present in the preclinical phase of disease, are associated with future RA development, and may predict radiographic joint destruction. Patients with weak positive results should be monitored and testing repeated. Note CPT Code 86200 Components Component Chart Name Cyclic Citrullinated Peptide Ab, IgG Component Test Code 0055256 LOINC 33935-8 Aliases ACPA Antibody Anti Citrullinated Antibody Anti Citrulline Anti-CCP Anti-CCP Antibody Anti-Citrullinated Ab Anti-Citrullinated Antibody Anti-Citrullinated Protein/Peptide Antibody (ACPA) Anti-Citrulline Antibody Anti-Cyclic Citrullinated Peptide AntiCCP Antibody Anticitrullinated Antibody Anticitrullinated Protein/Peptide Antibody (ACPA) Anticitrulline Antibody Anticyclic Citrullinated Peptide (CCP) Antibody CCP CCP3 Antibody Citrullinated Ab Citrullinated Antibody Citrullinated Protein/Peptide Antibody (ACPA) Citrulline An tibody Soft-CCP

Ordering information regarding a Lipid Panel test for Clinical Diagnostic Laboratories. Lipid Panel Ordering Recommendation Use to assess cardiovascular disease risk and guide therapy. Mnemonic Methodology Quantitative Enzymatic Assay Performed Mon-Sat Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Refer to individual components. Collect: Plasma separator tube or serum separator tube. Specimen Preparation: Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells within 2 hours of collection. Transfer 1 mL serum or plasma to a standard transport tube. (Min: 0.5 mL) Storage/Transport Temperature: Refrigerated Unacceptable Conditions: Body fluid (refer to Cholesterol, Fluid; Triglycerides, Fluid; and Chylomicron Screen, Body Fluid). Remarks: Stability: After separation from cells: Ambient: 24 hours; Refrigerated: 7 days; Frozen: 3 months Reference Interval Interpretive Data An HDL cholesterol less than 40 mg/dL is low and constitutes a coronary heart disease risk factor. An HDL cholesterol greater than 60 mg/dL is a negative risk factor for coronary heart disease. Non-HDL cholesterol is a secondary target of therapy in persons with high serum triglycerides (greater than 199 mg/dL). The goal for non-HDL cholesterol in persons with high triglycerides is 30 mg/dL higher than their LDL cholesterol goal. CHD Risk Factors +1 Men, 45 years and older +1 Women, 55 years and older or premature menopause without estrogen therapy +1 Family history of premature CHD +1 Current smoking +1 Hypertension +1 Diabetes mellitus +1 Low HDL cholesterol: 39 mg/dL or less -1 High HDL cholesterol: 60 mg/dL or greater Desirable Adult Values Higher Risk Borderline Total Cholestorol Triglycerides 199 mg/dL or less 149 mg/dL or less 200-239 mg/dL 150-199 mg/dL 240 mg/dL or greater 200-499 mg/dL HDL Cholestorol LDL Cholesterol (calculated) 40 mg/dL or greater 129 mg/dL or less (99 mg/dL or less if patient has CHD) 39 mg/dL or less 130-159 mg/dL 160 mg/dL or greater VLDL Cholesterol (calculated) 30 mg/dL or less Desirable Children & Adolescents Higher Risk Borderline Total Cholestorol 169 mg/dL or less 170-199 mg/dL Triglycerides 149 mg/dL or less 150-199 mg/dL HDL Cholestorol LDL Cholesterol (calculated) 40 mg/dL or greater 109 mg/dL or less 110-129 mg/dL VLDL Cholesterol (calculated) 30 mg/dL or less 200 mg/dL or greater 200-499 mg/dL 39 mg/dL or less 130 mg/dL or greater Note CPT Code 80061 Components Component Test Code 0020031 0020040 0020051 0020053 0020551 0020705 0020008 0020023 0020024 0020025 0020027 0020029 0020030 0020032 0020396 3004293 Component Chart Name Sodium, Serum or Plasma Potassium, Serum or Plasma Chloride, Serum or Plasma Carbon Dioxide, Serum or Plasma Alkaline Phosphatase Aspartate Aminotransferase Alanine Aminotransferase Urea Nitrogen, Serum or Plasma Glucose, Serum or Plasma Creatinine, Serum or Plasma Calcium, Serum or Plasma Protein Total, Serum/Plasma Albumin, Serum or Plasma Bilirubin, Total, Serum or Plasma Anion Gap UH EGFR LOINC 2951-2 2823-3 2075-0 2028-9 6768-6 1920-8 1742-6 3094-0 2345-7 2160-0 17861-6 2885-2 1751-7 1975-2 33037-3 Aliases ACPA Antibody Anti Citrulline Anti-CCP C12 Chem 12 Chemistry Panel Chemistry Screen CMP SMA 12 SMA 20 SMAC

Ordering information regarding a T- Uptake test for Clinical Diagnostic Laboratories. T Uptake Ordering Recommendation The preferred alternative to this test is Thyroxine, Free (Free T4) Methodology Quantitative Electrochemiluminescent Immunoassay (ECLIA) Performed Mon-Sat Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube or green (lithium heparin). Also acceptable: lavender Specimen Preparation: Allow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection. Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Grossly hemolyzed specimens. Remarks: Stability: After separation of cells: Ambient: 8 days; Refrigerated: 2 weeks; Frozen: 2 years Reference Interval Components Available Separately Reference Interval Thyroxine, Total T4 0.8-1.3 TBI Interpretive Data Thyroxine, Free (Free T4) is the preferred test alternative for T Uptake and Free Thyroxine Index tests. Note CPT Code 84479 Components Component Test Code Component Chart Name LOINC 3005979 T Uptake 74795-6 Aliases T3 Uptake T4 uptake, S T4U, Serum TBC THBR Thyroid Binding Ratio Thyroxine-binding capacity Throxine Binding Index Triiodothyronine uptake, serum

Conveniently pay your Clinical Diagnostic Laboratories invoice online. Secure, easy, and quick payment options for all patients. Access your billing information and settle your account with just a few clicks. Pay Your Bill ONLINE With our convenient system. Your information is protected with top-notch security measures, ensuring your transactions are safe and secure. Experience hassle-free bill payments with our user-friendly portal. Pay Now Mail Contact Us if you have any questions

The Terms and Conditions of Clinical Diagnostic Laboratories located in Sterling and Ashburn is located on this page. Terms & Conditions 1. Acceptance of Terms Welcome to Clinical Diagnostic Laboratories ("we," "us," or "our"). By accessing or using our services, including our website and any related applications (collectively referred to as the "Services"), you agree to comply with and be bound by these Terms and Conditions. If you do not agree to these terms, please refrain from using our Services. 2. Services Offered Clinical Diagnostic Laboratories provides comprehensive diagnostic testing services including, but not limited to, blood panels, allergy tests, COVID tests, and Influenza tests. These services are available at our two separate locations: 2 Pidgeon Hill Dr., Suite 150, Sterling, VA 20165, and 44355 Premier Plaza, Suite 240, Ashburn, VA 20147. 3. Test Accuracy and Interpretation While we strive to provide accurate and reliable test results, it is important to note that medical tests may have limitations and potential variations. Test results should be interpreted by qualified medical professionals, and we strongly recommend consulting a healthcare provider for accurate diagnosis and treatment recommendations based on the test results. 4. Privacy and Data Security We are committed to protecting your privacy and the security of your personal and medical information. Our Privacy Policy outlines the types of data we collect, how it is used, and the measures we take to safeguard your information. By using our Services, you agree to our Privacy Policy. 5. Payment and Billing We offer various payment options for our services. Payment details, including pricing and payment methods, are available on our website and will be provided during the checkout process. Any additional fees, taxes, or charges associated with the services will be clearly communicated. 6. Appointments and Cancellations Appointments for tests are subject to availability and can be scheduled through our website or by contacting our customer service. If you need to cancel or reschedule an appointment, please provide notice in advance according to our cancellation policy, which will be communicated during the appointment scheduling process. 7. Test Preparation Instructions Specific tests may require certain preparations, such as fasting or medication restrictions. Customers are responsible for following these instructions to ensure accurate test results. 8. Turnaround Time for Results We strive to provide test results within a specific timeframe. However, factors such as test complexity and demand may impact the turnaround time. 9. Refund and Return Policy If services are paid for but not utilized, our refund and return policy applies. Details can be found on our website or obtained by contacting customer service. 10. Communication Channels For inquiries, support, or appointment scheduling, contact us via email, phone, or our designated customer portal. 11. Insurance and Coverage Information about insurance coverage, billing procedures, and reimbursement for services covered by insurance can be found on our website or by contacting us directly. 12. Laboratory Accreditation and Certifications Clinical Diagnostic Laboratories maintains specific accreditations and certifications that demonstrate our commitment to q uality and accuracy. 13. Health and Safety Measures To ensure a safe testing environment, we adhere to rigorous health and safety protocols for the protection of both patients and staff. 14. Dispute Resolution Any disputes will be resolved through mediation or arbitration, with the applicable jurisdiction specified. 15. Legal Disclaimers Our services are for diagnostic purposes only. Customers should consult healthcare professionals for medical advice and treatment. 16. User Accounts (if applicable) If you create a user account on our platform, terms related to account creation, management, and security apply. 17. Governing Law These Terms and Conditions are governed by and construed in accordance with the laws of the state of Virginia, without regard to its conflict of laws principles. 18. Conta ct Us If you have any questions, concerns, or feedback regarding these Terms and Conditions or our Services, please contact us at: Clinical Diagnostic Laboratories 2 Pidgeon Hill Dr., Suite 150, Sterling, VA 20165 44355 Premier Plaza, Suite 240, Ashburn, VA 20147 Email: info@clinicaldiagnosticlab.com Phone: (703) 430-1111 Fax: (703) 722-3890

Ordering information regarding an Allergen, Food, Whole Egg, IgG test for Clinical Diagnostic Laboratories. Allergen, Food, Whole Egg, IgG Ordering Recommendation Not recommended for initial thyroid disorders testing. Distinguish thyroid autoimmune disorders from nonautoimmune disease or hypothyroidism. Mnemonic EGGWHOLE Methodology Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay Performed Mon-Sat Reported 1-8 days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube (SST). Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Hemolyzed, icteric, or lipemic specimens. Remarks: Stability: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year Reference Interval Less than 30.21 mcg/mL Interpretive Data Values less than 2.00 mcg/mL represent absent or undetectable levels of allergen-specific IgG antibody. This test has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes. Compliance Category: FDA Note CPT Code 86001 Components Component Chart Name Allergen, Food, Whole Egg IgG Component Test Code 2011820 LOINC 45201-1 Aliases

OOPS! There’s Nothing Here...yet. Clinical Diagnostic Laboratories is working hard to make the experience for our physicians and patients as seamless as possible. The page you’re looking for is still under construction. Please come back at a later date or Contact Us if you have any questions. Back to Homepage