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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

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

The product page for the Men's Fertility Panel for Clinical Diagnostic Laboratories. Men's Fertility Panel This test includes a semen analysis to evaluate key fertility markers such as sperm count, motility (movement), and morphology (shape). It’s a simple, lab-collected test designed to help individuals and couples better understand their reproductive health—whether you're actively trying to conceive or just planning ahead. No insurance, doctor’s order, or copay required. Results are delivered securely within 2–5 business days. Ideal for : Individuals planning for pregnancy Couples facing conception delays Anyone wanting to proactively assess reproductive health $85.00 Taxes will be calculated at checkout Buy Now

Ordering information regarding a Tryptase test for Clinical Diagnostic Laboratories. Tryptase Ordering Recommendation Measure total tryptase to confirm mast cell activation in diseases such as mastocytosis, anaphylaxis, urticaria, and asthma. Not generally used acutely except where the diagnosis is unclear. Useful in the prognosis of systemic mastocytosis. Mnemonic EGGWHOLE Methodology Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay Performed Mon-Sat Reported 1-2 days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube (SST). Specimen Preparation: Allow serum to clot completely at room temperature. 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: Frozen. Unacceptable Conditions: Hemolyzed, icteric, or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 72 hours; Frozen: 1 month Reference Interval Less than 11.0 µg/L Interpretive Data Compliance Category: FDA Note This test measures total tryptase and does not distinguish between the alpha and beta protein types. Samples should preferably be collected between 15 minutes and three hours after the event suspected to have caused mast cell activation. CPT Code 83520 Components Component Chart Name Tryptase Component Test Code 0099173 LOINC 21582-2 Aliases Total Tryptase Tryptase, Autopsy (Tryptase)

Ordering information regarding an Ammonia for Clinical Diagnostic Laboratories. Ammonia, Plasma Ordering Recommendation Evaluate status of existing liver disease. Monitor treatment in patients with inborn errors of metabolism. Methodology 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: Collect: Green (sodium or lithium heparin). Collect on ice. Specimen Preparation: Separate plasma from cells and freeze within 15 minutes of draw time. Specimens need to be spun in a refrigerated centrifuge. Transfer 2 mL plasma to a standard Transport Tube. (Min: 0.25 mL) Storage/Transport Temperature: CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered. Unacceptable Conditions: Serum or blood. Non-frozen specimens. Specimens containing oxalate or citrate Remarks: Stability: After separation from cells: Ambient: Unacceptable; Refrigerated: 2 hours; Frozen: 3 weeks (do not thaw) Reference Interval 0-14 days 95 µmol/L or less 15 days-6 years 68 µmol/L or less Greater than 6 years 72 µmol/L or less Interpretive Data Note CPT Code 82140 Components Component Test Code Component Chart Name LOINC 0020043 Ammonia, Plasma 16362-6 Aliases NH3 Plasma ammonia level

Ordering information regarding a Allergen, Food, Egg Whole test for Clinical Diagnostic Laboratories. Allergen, Food, Egg Whole 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 1-3 days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Multiple patient encounters should be avoided. Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Grossly hemolyzed or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year Reference Interval Probability of IgE Mediated Clinical Reaction Reporting Range (reported in kU/L) Class Scoring No significant level detected Less than 0.10 0 0.10 - 0.34 0.35 - 0.70 Clinical relevance undetermined Low 0/1 1 0.71 - 3.50 3.51 - 17.50 Moderate High 2 3 17.51 - 50.00 50.01 - 100.00 Very high Very high 4 5 Greater than 100.00 Very high 6 Interpretive Data Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis. Compliance Category: FDA Note Components CPT Code 86003 Component Chart Name Allergen, Food, Egg Whole IgE Component Test Code 0055381 LOINC 7291-8 Aliases ImmunoCAP f245

The product page for the Cholesterol Test Panel for Clinical Diagnostic Laboratories. Cholesterol Test Get a complete picture of your heart health with this detailed cholesterol panel: Total Cholesterol – Measures the overall level of cholesterol in your blood. HDL ("Good") Cholesterol – Helps remove bad cholesterol and supports heart health. LDL ("Bad") Cholesterol – High levels may increase your risk for heart disease. Triglycerides – A type of fat in your blood linked to heart risk when elevated. HDL % of Total Cholesterol – Shows the balance between good and total cholesterol. This test helps you understand your cardiovascular risk and supports proactive decisions about your lifestyle and health. $95.00 Taxes will be calculated at checkout Buy Now

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

Ordering information regarding Clozapine for Clinical Diagnostic Laboratories. Clozapine and Metabolites, Serum or Plasma, Quantitative Ordering Recommendation Optimize drug therapy and monitor patient adherence. Methodology Quantitative Liquid Chromatography-Tandem Mass Spectrometry Performed Mon-Sat Reported 1-5 Days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Timing of specimen collection: Predose(trough) draw - at steady -state concentration. Collect: Plain red. Also acceptable: Lavender (K2 or K3EDTA) or pink (K2EDTA). Specimen Preparation: 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: Whole blood. Gel separator tubes, light blue (citrate), or yellow (SPS or ACD solution). Remarks: Stability: After separation from cells: Ambient: 24 hours; Refrigerated: 1 week; Frozen: 3 months Reference Interval Therapeutic Range Not well established Toxic Level Total Clozapine and Metabolites: Greater than or equal to 1500 ng/mL Interpretive Data Therapeutic ranges are not well established. Clozapine is metabolized to norclozapine and clozapine-N-oxide. Clozapine concentrations between 100 and 700 ng/mL may correlate more with clinical response; however, nonresponsiveness may also occur within this range. For refractory schizophrenia, clozapine concentrations greater than 350 ng/mL are suggested to achieve a therapeutic response. Toxicity: Adverse effects to clozapine therapy may include tachycardia, drowsiness, hypotension, and seizures. Therapeutic and toxic ranges are not well established in children. Note CPT Code 80159 Components Component Test Code Component Chart Name LOINC 2013458 Clozapine, S/P, Quant 6896-5 2013459 Norclozapine, S/P, Quant 10992-6 2013460 Clozapine-N-Oxide, S/P, Quant 85497-6 2013461 Total Clozapine and Metabolites 12375-2 Aliases Clopine Clozaril Denzapine FazaClo Versacloz Zaponex

This is the home page to access the Patient Portal. The patient portal allows previous and returning patients the ability to access their lab results. Your Health, One Click Away View Your Lab Results anytime, anywhere—fast, secure, and easy to use I don't have a portal set up yet and need access I have a portal setup and I'm logging in Your Lab Results, All in One Place Our new Patient Portal gives you instant access to your laboratory test results. Whether you're tracking progress, reviewing past reports, or preparing for your next visit, everything you need is now at your fingertips. Safe, secure, and always available. Sign Up for Portal Access Why Use the Patient Portal? Simple Access, Meaningful Insights 📊 Track your results over time for better health insight 🔐 Secure, private access to your lab data 📥 View current and past lab reports 🧾 Compare individual test results from different visits ✅ Set up in just a few minutes with your email How to Get Access Getting Started is Easy —Just Follow These Steps We’ll confirm your email and send you a secure sign-up link. You’ll create a password and verify your account. Log in anytime from the Patient Portal page to view your test results and trends. Contact Us to Get Started