Search Results

Ordering information regarding a HPV Assay Test for Clinical Diagnostic Laboratories. Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by Liquid-Based Pap Test and Hologic Thin Prep Ordering Recommendation This FDA-approved test and platform is designed for primary HPV screening in individuals aged 25 and older with a cervix. It is also FDA-approved for routine cervical cancer screening in combination with cervical cytology (Pap smear) for those aged 30 and older. Additionally, it serves as a follow-up test for abnormal cytology results in individuals aged 21 and older. Mnemonic Methodology Qualitative Polymerase Chain Reaction Performed Mon-Sat Reported Within 1-5 days Specimen Required Patient Preparation: Collect: Cervical, anal, or vaginal specimen with brush or spatula from ThinPrep kit and place in PreservCyt Media Specimen Preparation: Mix well. Transfer 3 mL to a Standard Transport Tube. (Min 1.5 mL). For primary screening purposes, please submit a specimen aliquot and keep the original specimen at the client site. Storage/Transport Temperature: Refrigerated Unacceptable Conditions: Bloody or dark brown specimens. Specimens in any media other than indicated above. Remarks: Specimen source required. Stability: Ambient: 6 months; Refrigerated: 6 months; Frozen: Unacceptable Reference Interval Negative Interpretive Data This test detects the DNA of HPV16, HPV18, and 12 other high-risk HPV types (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68) that are linked to cervical cancer and its precursor lesions. The accuracy of the results may be influenced by specimen collection methods, the infection stage, and the presence of interfering substances. It's crucial to interpret these results alongside other laboratory and clinical data. A negative high-risk HPV result does not rule out the presence of other high-risk HPV types, potential future cytologic abnormalities, underlying CIN2-3, or cancer. HPV testing is not recommended for the screening or management of atypical squamous cells of undetermined significance (ASCUS) in women under 21 years of age. Note CPT Code 87624 Components Component Chart Name Component Test Code LOINC HPV Source 0060752 31208-2 2011935 HPV Genotype 16 by PCR 77399-4 2011936 2011941 HPV, Other High Risk by PCR 82675-0 HPV Genotype 18 by PCR 77400-0 Aliases HPV High Risk HPV HR ThinPrep HPV Primary screening Human papilloma virus

Ordering information regarding a Cardiolipin Antibody, IgG test for Clinical Diagnostic Laboratories. Cardiolipin Antibody, IgG Ordering Recommendation Acceptable initial test when antiphospholipid syndrome (APS) is strongly suspected. Order with Lupus Anticoagulant Reflexive Panel (0030181 ) and Beta-2 Glycoprotein 1 Antibodies, IgG and IgM (0050321 ). Cardiolipin Antibodies, IgG and IgM (0099344 ) is preferred. Mnemonic AC-IGG Performed Mon-Sat Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay Reported 1-2 days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to a Standard Transport Tube. (Min: 0.3 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma or other body fluids. Contaminated, heat-inactivated, hemolyzed, or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year Reference Interval <=14 GPL Negative 15-19 GPL Indeterminate 20-80 GPL Low to Moderately Positive 81 GPL or above High Positive Interpretive Data Anti-mitochondrial antibodies (AMA) are thought to be present in 90-95% of patients with primary biliary cholangitis (PBC). However, the frequency of detected antibodies may be cohort or assay dependent, as lower sensitivities have been reported. Not all PBC patients are positive for AMA; some patients may be positive for SP100 and/or GP210 antibodies. A negative result does not rule out PBC. Compliance Category: FDA Note CPT Code 86381 Components Component Chart Name Cardiolipin Antibody IgG Component Test Code 0050901 LOINC 3181-5 Aliases ACA aCL aCL Antibody aCL IgG Anti-Cardiolipin Anticardiolipin Anticardiolipin Antibodies Cardiolip

The product page for the Diabetes Panel for Clinical Diagnostic Laboratories. Diabetes and Heart Health Panel A powerful combo panel to evaluate your blood sugar control and cardiovascular risk: Hemoglobin A1c – Measures your average blood sugar levels over the past 2–3 months. Total Cholesterol – Gives an overall picture of your blood cholesterol. HDL ("Good") Cholesterol – Helps protect your heart by removing bad cholesterol. LDL ("Bad") Cholesterol – High levels are linked to increased heart disease risk. Triglycerides – Elevated levels can signal a higher risk of diabetes and heart disease. HDL % of Total Cholesterol – Indicates the balance between good and total cholesterol. Lipoprotein(a) – A genetic marker that may elevate your risk of cardiovascular issues. $99.00 Taxes will be calculated at checkout Buy Now

Ordering information regarding a Anti-Mitochondrial Antibody (AMA) test for Clinical Diagnostic Laboratories. Mitochondrial M2 Antibody, IgG (ELISA) Ordering Recommendation May be useful in confirming a diagnosis of primary biliary cholangitis. Mnemonic AMA Performed Mon-Sat Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL to a Standard Transport Tube. (Min: 0.3 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma. Contaminated, hemolyzed, grossly icteric, 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 20.0 Units or less Negative 20.1-24.9 Units 25.0 Units or greater Equivocal Positive Interpretive Data Anti-mitochondrial antibodies (AMA) are thought to be present in 90-95% of patients with primary biliary cholangitis (PBC). However, the frequency of detected antibodies may be cohort or assay dependent, as lower sensitivities have been reported. Not all PBC patients are positive for AMA; some patients may be positive for SP100 and/or GP210 antibodies. A negative result does not rule out PBC. Compliance Category: FDA Note CPT Code 86381 Components Component Chart Name Mitochondrial (M2) Antibody, IgG Component Test Code 0050065 LOINC 14251-3 Aliases AMA ANTI-MITOCHONDIRAL ANTIBODY ANTIBODIES TO MICROTUBULE ASSOCIATED PROTEIN 2 ANTIMITOCHONDRIAL ANTIBODIES IMMUNOLOGY PROFILE (AMA) MITOCHONDRIAL ANTIBODIES, SERUM

Ordering information regarding a Cardiolipin Antibody, IgA test for Clinical Diagnostic Laboratories. Cardiolipin Antibody, IgA Ordering Recommendation Preferred second-line test when seronegative antiphospholipid syndrome (APS) is strongly suspected. Order incrementally or concurrently with other noncriteria antiphospholipid antibody tests. Mnemonic CARDIO IGA Performed Mon-Sat Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay Reported 1-2 days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to a Standard Transport Tube. (Min: 0.3 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma or other body fluids. Contaminated, heat-inactivated, hemolyzed, or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval <=12 MPL Negative 13-19 MPL Indeterminate 20-80 MPL Low to Moderately Positive 81 MPL or above High Positive Interpretive Data The persistent presence of IgG and/or IgM cardiolipin (CL) antibodies in moderate or high levels (greater than 40 GPL and/or greater than 40 MPL units) is a laboratory criterion for the diagnosis of antiphospholipid syndrome (APS). Persistence is defined as moderate or high levels of IgG and/or IgM CL antibodies detected in two or more specimens drawn at least 12 weeks apart (J Throm Haemost. 2006;4:295-306). Lower positive levels of IgG and/or IgM CL antibodies (above cutoff but less than 40 GPL and/or less than 40 MPL units) may occur in patients with the clinical symptoms of APS; therefore, the actual significance of these levels is undefined. Results should not be used alone for diagnosis and must be interpreted in light of APS-specific clinical manifestations and/or other criteria phospholipid antibody tests. Compliance Category: FDA Note MPL = IgM phospholipid units CPT Code 86147 Components Component Chart Name Cardiolipin Antibody IgM Component Test Code 0050902 LOINC 3182-3 Aliases ACA aCL aCL Antibody aCL IgG Anti-Cardiolipin Anticardiolipin Anticardiolipin Antibodies Cardiolip

Ordering information regarding a Urine Culture test for Clinical Diagnostic Laboratories. Urine Culture Ordering Recommendation Quantitative culture to identify bacterial causes of urinary tract infections. Methodology Culture/Methods may include biochemical, mass spectrometry, or sequencing. Performed Mon-Sat Reported 1-3 Days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Midstream urine or foley catheter urine. Specimen Preparation: Transfer urine to a sterile container. (Min: 1 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Urine from catheter bag. Multiple (more than one in 24 hours), 24-hour, or pooled specimens. Foley catheter tips (syringe with needle attached). Delayed transport of unpreserved urine (greater than two hours at room temperature or greater than 24 hours refrigerated). Remarks: Specimen source required. Stability: Ambient: 2 hours; Refrigerated: 24 hours; Frozen: Unacceptable. Reference Interval No growth. Identification and susceptibility tests are performed on significant isolates Interpretive Data Note Identification and susceptibility tests are billed separately from culture. Gram stain is performed by request only. Results indicate colony count plus identification of significant isolates. CPT Code 87086 Components Component Test Code Component Chart Name LOINC 0060131 Culture, Urine 630-4 Aliases Aerobic Bacteria Culture, Urine Bacterial Culture, Aerobic, Urine Culture, Aerobic Bacteria, Urine Culture, Urine

Are you interested in scheduling an appointment for blood testing, COVID, FLU, Allergy testing, or some other medical test? Schedule an appointment with us here. SCHEDULE AN APPOINTMENT Clinical Diagnostic Laboratories is a leading medical laboratory providing a wide variety of tests and services, such as routine blood work, H. Pylori tests, STD testing, drug screening, allergy testing, COVID-19, Flu, and much more. Use our easy scheduling tool below to make an appointment. Also, be sure to check out our FAQs page to address any problems you might have. You may also email us or give us a phone call at (703) 430-1111 .

Clinical Diagnostic Laboratories is an affordable and efficient medical laboratory located in Northern Virginia in Sterling, VA and in Ashburn, VA just minutes from One Loudoun. At our facility, we strive to provide the highest possible quality testing for doctors, companies and organizations, and for individual patients. OUR CURRENT HOURS ARE: Monday 9am - 3pm Tuesday 9am - 3pm Wednesday 9am - 3pm Thursday 9am - 3pm Friday 9am - 3pm Saturday 9am - 3pm* Sunday: Closed* *Appointments are highly recommended on Monday-Saturdays and major Holidays are by appointment only Please contact us ahead of time to verify if walk-ins are available. Schedule An Appointment ABOUT CLINICAL DIAGNOSTIC LABORATORIES Preferred Diagnostic Center in Loudoun County Our main goal is to provide an alternative testing facility for individuals: doctors, as well as hospitals that is affordable and convenient. What makes Clinical Diagnostics Laboratories different from the others? We provide excellent service with a personal and friendly touch. We have an on-call Director at the Lab who has a Ph.D. in Pathology. Our Full-time Technologist has over ten years of experience in the Medical Lab field. Clinical Diagnostic Laboratories has grown quickly throughout the area with respect to returning individuals, referrals and walk-ins because we treat our patients with dignity and respect. About Us “Clinical Diagnostic Laboratories is recognized as the TOP Diagnostic Lab for the Northern Virginia, Washington, DC and Maryland regions and is featured on the TOP Doctors Interviews which are seen on CNN Headline News, MSNBC, Oprah Winfrey Network, BRAVO and other networks” Services We Provide Our laboratory provides services for a variety of organizations and companies across a wide array of industries. Whether you're a private organization, government contractor, medical facility, small to large company, or something else entirely, we have the resources to help you achieve your desired goals. Please inquire for more information. View All Services We Accept Most Insurances At our Medical Laboratory, we accept most forms of insurance. We strive to make our services as accessible as possible, so nearly all forms of insurance are accepted. However due to the ever-changing nature of policies and individual insurance plans, we highly recommend that you check with your insurance provider prior to any appointment in order to make sure your coverage is up-to-date and covered at our facility. Let Us Come to You Our on-site services extend to Northern Virginia, Maryland, and Washington DC We care about our patients and understand that being home-bound or taking time out of your busy schedule can make diagnostic testing inconvenient, that is why Clinical Diagnostics Laboratories will come to you. Schedule An Appointment

The product page for the Respiratory Panel for Clinical Diagnostic Laboratories. Complete Respiratory Allergy Scan Breathe easier with answers. This panel is designed to identify airborne allergens that may be behind your sneezing, congestion, itchy eyes, or asthma-like symptoms. Whether it’s seasonal discomfort or year-round sensitivity, this test helps pinpoint the specific environmental triggers affecting your respiratory health. Here’s what it checks — and why it matters: IgE Total, Serum – Measures your body’s overall allergic sensitivity, giving a baseline for reactivity. Environmental & Airborne Allergens – Tests for 23 common respiratory irritants, including: Molds: Alternaria Alternata, Aspergillus Fumigatus, Cladosporium Herbarum, Penicillium Chrysogenum Grasses & Weeds: Bermuda Grass, Johnson Grass, Timothy Grass, Rough Pigweed, Common Ragweed Trees & Pollens: Mountain Cedar, Birch, Cottonwood, Elm, Maple (Box Elder), Oak White, Pecan Hickory, Sheep Sorrel Animals: Cat Dander, Dog Dander, German Cockroach, Mouse Urine Other: Dernariohagoides (Dust Mite), White Mulberry From mold spores to pet dander and pollen, this test helps you understand exactly what’s causing your symptoms — so you can take smart steps to avoid triggers, improve your indoor air quality, and feel more comfortable year-round. Fast results, no referral needed, and no guesswork. $288.00 Taxes will be calculated at checkout Buy Now

Ordering information regarding a Double-Stranded DNA (DsDNA) Antibody test for Clinical Diagnostic Laboratories. Double-Stranded DNA (DsDNA) Antibody Ordering Recommendation Secondary screening for systemic lupus erythematosus (SLE) based on ANA results. Mnemonic Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay/Semi-Quantitative Indirect Fluorescent Antibody Performed Mon-Sat Reported 1-3 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. Transfer 1 mL serum to a Standard Transport Tube. (Min: 0.5 mL) Storage/Transport Temperature: Refrigerated Unacceptable Conditions: Plasma. Contaminated, hemolyzed, or severely lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 month (avoid repeated freeze/thaw cycles) Reference Interval 24 IUs or less Double-Stranded DNA (dsDNA) Ab IgG ELISA Interpretive Data Positivity for anti-double stranded DNA (anti-dsDNA) IgG antibody is a diagnostic criterion of systemic lupus erythematosus (SLE). Specimens are initially screened by enzyme-linked immunosorbent assay (ELISA). If ordered as reflex (0050215), positive ELISA results (>24 IU) will be reflexed to a highly specific IFA titer (Crithidia luciliae indirect fluorescent test [CLIFT]) for confirmation. Some patients with early or inactive SLE may be positive for anti-dsDNA IgG by ELISA but negative by CLIFT. If the patient is negative by CLIFT but positive by ELISA and clinical suspicion remains, consider antinuclear antibody (ANA) testing by IFA. Note If dsDNA IgG antibody is detected, the result will be confirmed by Double-Stranded DNA (dsDNA) Antibody, IgG by IFA (using Crithidia luciliae). Additional charges apply. CPT Code 86225; if reflexed, add 86256 Components Component Chart Name Component Test Code LOINC Double-Stranded DNA (dsDNA) Ab IgG ELISA 0050215 58465-6 Aliases anti-DNA Anti-dsDNA Antibody Anti-Native DNA Antibody to ds-DNA Crithidia luciliae DNA ds Ab Double stranded DNA antibody ds DNA Ab ds-DNA ds-DNA IgG dsDNA reflex dsDNA reflex panel Native double-stranded DNA antibody