Description:

Aspirin (which inhibits platelet cyclooxygenase) reduces the risk of thrombosis in cardiovascular disease by impairing platelet function. Patients who do not respond to the platelet inhibitory effects of aspirin are designated as "aspirin resistant". The measurement of 11-dhTXB2 in urine (the principal metabolite of platelet cyclooxygenase derived thromboxane B2) may be used in individuals with cardiovascular disease prior to initiation of aspirin therapy, or in individuals non-responsive to aspirin therapy.

Alternative names: 11dhTxB2

Categories: Allergy blood testing, Heart & cholesterol,

Price: $293

Description:

ADMA and SDMA may be measured in individuals with multiple risk factors for the development of cardiovascular disease.

Patient Instructions:

Fasting is recommended but not required.

Categories: Heart & cholesterol,

Price: $211

• Check your atenolol medication levels
• Monitor heart rate and blood pressure control
• Track dosage effectiveness over time

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Price: $588

Description: This test uses equilibrium dialysis methodology.

The Testosterone test in this panel will provide levels of Total Testosterone results ranging from 0 to 9,999. However, any value greater than 9,999 will be displayed as ">10,000" (over 10,000) instead of a specific number.

Significant deviations from the normal range may require further evaluation by your physician.

Includes:

C-Reactive Protein (CRP), High Sensitivity (Cardiac Risk Assessment)

Comprehensive Metabolic Profile (includes eGFR): Albumin, Albumin/Globulin Ratio (calculated), Alkaline Phosphatase, ALT, AST, BUN/Creatinine Ratio (calculated), Calcium, Carbon Dioxide, Chloride, Creatinine with GFR Estimated, Globulin (calculated), Glucose, Potassium, Sodium, Total Bilirubin, Total Protein, Urea Nitrogen

Estradiol, Ultrasensitive, LC/MS/MS

Sex Hormone binding Globulin, Serum

Tri-iodothyronine Free (FT3)

Thyroxine Free, Direct Dialysis (FT4)

Total Testosterone, Free (Dialysis) Testosterone (calculated)

Dehydroepiandrosterone (DHEA-s) Sulfate

Ferritin, serum

Follicle-Stimulating Hormone (FSH), Serum

Gamma Glutamyl Transpeptidase (GGT)

Hemoglobin (Hgb) A1c

Urinalysis

Insulin

Luteinizing Hormone (LH), Serum

Magnesium, serum

Complete Blood Count / CBC (includes Differential and Platelets): WBC, RBC, Hemoglobin, Hematocrit, MCV, MCH, MCHC, RDW, Platelet Count, MPV and Differential (Absolute and Percent - Neutrophils, Lymphocytes, Monocytes, Eosinophils, and Basophils)

Progesterone, serum

Prolactin, serum

Total Iron, Iron Binding Capacity, % Saturation (calculated)

Lipid Panel: Cholesterol, total; high-density lipoprotein (HDL) cholesterol; low-density lipoprotein (LDL) cholesterol (calculated); triglycerides; Non-HDL Cholesterol (calculated).

Thyroid-Stimulating Hormone (TSH)

Reverse Tri-iodothyronine (RT3)

Insulin-Like Growth Factor I (IGF-I)

Patient Instructions:

You should fast for 12-14 hours before collection of the specimen. Fasting is defined as no consumption of food or beverage other than water for at least 12-14 hours before testing. Some tests in this panel may exhibit interference when sample is collected from a person who is consuming a supplement with a high dose of biotin (also termed as vitamin B7 or B8, vitamin H or coenzyme R). Samples should not be collected during or soon after the administration of heparin. If using a testosterone cream please be sure you have not rubbed any into the antecubital area of your arm for the last 24 hours as it can give elevated results. In patients receiving therapy with high biotin doses (ie, > 5 mg/day), no sample should be taken until at least eight hours after the last biotin administration. Patient should be cautioned to stop biotin consumption at least 72 hours prior to the collection of a sample.

Estimated turnaround for results is 10 business days. If confirmation testing is required, the estimated time may be extended.

Categories: Fitness, nutrition, anti-aging, Hormones & metabolism, Specific blood tests for women, Specific blood tests for men,

Price: $571

Description: This test includes sequencing and deletion/duplication analysis of the ATM gene. Individuals assigned female at birth with an ATM pathogenic variant have an elevated risk of breast cancer. Individuals with an ATM pathogenic variant have an elevated risk of pancreatic cancer.

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Price: $1348

• Detect hidden causes of persistent cough
• Screen for walking pneumonia infection
• Identify lingering respiratory infection symptoms

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Price: $797

Description: This test detects the presence of specific IgE against Aureobasidium pullulans. A positive test only indicates that a person is sensitized and potentially allergic to this allergen. A diagnosis of allergy requires clinical signs and symptoms that appear to be associated with exposure to the allergen in addition to the detection of markers of IgE sensitization [1].More specific information about this allergen can be found on the following website: https://www.thermofisher.com/phadia/us/en/resources/allergen-encyclopedia.htmlReference1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(3 Suppl 3):S1-S148.

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Price: $49

• Pinpoint mold allergies causing your symptoms
• Reveal hidden triggers for respiratory issues
• Clarify unexplained skin reactions effortlessly

Categories: Allergy blood testing,

Price: $243

• Screen for autoimmune disease symptoms
• Check unexplained joint pain causes
• Monitor immune system activity levels

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Price: $378

Description: Anti-GAD65 antibodies, anti-voltage gated potassium channels (VGKC), anti-CASPR2, anti-LGI1, and anti-NMDA receptor (NR1 subunit) antibodies are found in patients with epilepsy with an acute/subacute presentation without evidence of CNS infection, toxic, metabolic, or other known cause of epilepsy, and possibly with evidence of CNS inflammation.

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Price: $3462

Description: This panel may be helpful in the diagnostic evaluation of individuals with suspected autoimmune hepatitis (AIH). This panel includes an antinuclear antibody (ANA) immunofluorescence assay (IFA) screen, performed on human epithelial type 2 (HEp-2) cells, with reflex to titer and pattern; actin (smooth muscle) antibody (SMA); liver kidney microsome type 1 (LKM-1) antibody (IgG); and anti-mitochondrial antibody (AMA) with reflex to titer.The diagnosis of AIH is based on clinical features, serologic profile, and exclusion of resembling diseases such as viral hepatitis [1]. The detection of antibodies associated with AIH helps establish the diagnosis and differentiate AIH types. ANA and SMA are characteristic of type 1 AIH, while LKM-1 antibody is characteristic of type 2 AIH [2]. ANAs are detected in 75% of patients with type 1 AIH but are also common in many other autoimmune diseases [1]. SMAs are present in approximately 85% of patients with type 1 AIH but can be detected in a range of other conditions, such as viral hepatitis, malignancies, rheumatic diseases, and nonalcoholic fatty liver disease [1]. LKM-1 antibody is specific for type 2 AIH and usually is not concurrent with ANA and SMA.Up to 20% of patients with AIH are negative for ANA, SMA, and LKM-1 antibody. In these patients, testing antibodies associated with AIH, such as AMA, may help support the diagnosis [2]. AMA is the serologic hallmark of primary biliary cholangitis (PBC) but can also be detected in PBC-AIH overlap syndrome and type 1 AIH [1].The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.References1. Neuberger J, et al, eds. Autoimmune Liver Disease: Management and Clinical Practice. 1st ed. John Wiley & Sons Ltd, 2020.2. Mack CL, et al. Hepatology. 2020;72(2):671-722.

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Price: $357

Description: This panel may help diagnose or exclude autoimmune hepatitis (AIH) in patients with hepatitis C for the purpose of informing treatment options. This panel includes an antinuclear antibody (ANA) immunofluorescence assay (IFA) screen, performed on human epithelial type 2 (HEp-2) cells, with reflex to titer and pattern; smooth muscle antibody (SMA); liver kidney microsome type 1 (LKM-1) antibody; soluble liver antigen (SLA) antibody; and anti-mitochondrial antibody (AMA) with reflex to titer.Certain hepatitis C therapies, such as peginterferon and ribavirin, are contraindicated for patients with AIH or other autoimmune conditions. The detection of certain antibodies associated with AIH may help establish or exclude the diagnosis. ANA and SMA are characteristic of type 1 AIH, while LKM-1 antibody is characteristic of type 2 AIH [1]. ANAs are detected in 75% of patients with type 1 AIH but are also common in many other autoimmune diseases [2]. SMAs are present in approximately 85% of patients with type 1 AIH but can be detected in a range of other conditions, such as viral hepatitis, malignancies, rheumatic diseases, and nonalcoholic fatty liver disease [2]. LKM-1 antibody is specific for type 2 AIH and usually is not concurrent with ANA and SMA.Up to 20% of patients with AIH are negative for ANA, SMA, and LKM-1 antibody. In these patients, testing other antibodies associated with AIH, such as AMA and SLA, may help assess the diagnosis [1]. AMA is the serologic hallmark of primary biliary cholangitis (PBC) but can also be detected in PBC-AIH overlap syndrome or type 1 AIH [2]. SLA antibody is highly specific (99%) for AIH and can be detected as a sole marker in 14% to 20% of patients [1]. The presence of SLA antibody is associated with the likelihood of severe disease and relapse after drug withdrawal [1]. Unlike ANA, SMA, and LKM-1, SLA is very rarely present in patients with hepatitis C [2].The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.References1. Mack CL, et al. Hepatology. 2020;72(2):671-722.2. Neuberger J, et al, eds. Autoimmune Liver Disease: Management and Clinical Practice. 1st ed. John Wiley & Sons Ltd, 2020.

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Price: $499

Description: A comprehensive approach to detection of known antineuronal autoantibodies aids the diagnosis of paraneoplastic syndromes and autoimmune encephalopathies and related conditions. Identification of specific antineuronal autoantibodies may direct evaluation for idiopathic autoimmune disease or underlying often occult malignancy. Characterization of autoantibody specificity may allow syndromic classification and assist in diagnosis and management. Antineuronal antibodies are detected and characterized based on indirect immunofluorescence staining pattern on multiple neuronal, non-neuronal tissues, and transformed substrate cells, and radioimmunoassays, and line blot analysis.

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Price: $20519

Description: Uncovering autoimmune disease through specific autoimmune blood tests can lead to treatments designed to prevent or slow your immune system from attacking itself. Autoimmune blood tests and other screening tests of the immune system can help limit illnesses and offer more favorable outcomes.

Significant deviations from the normal range may require further evaluation by your physician.

Includes:
ANA Screen IFA w/ Ref to Titer and Pattern
If ANA Screen, IFA is positive, ANA Titer and Pattern will be performed.
Anti-dsDNA (Double-Stranded) Antibiodies, EIA
Complement Component C3c 

Estimated turnaround for results is 5 business days.

Categories: Autoimmune diseases,

Price: $127

Description: This test detects the presence of specific IgE against avocados. A positive test only indicates that a person is sensitized and potentially allergic to this allergen. A diagnosis of allergy requires clinical signs and symptoms that appear to be associated with exposure to the allergen in addition to the detection of markers of IgE sensitization [1].More specific information about this allergen can be found on the following website: https://www.thermofisher.com/phadia/us/en/resources/allergen-encyclopedia.htmlReference1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(3 Suppl 3):S1-S148.

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Price: $49

• Pinpoint avocado sensitivity causing discomfort
• Reveal hidden food intolerances affecting you
• Clarify digestive issues linked to avocado

Categories: Allergy blood testing,

Price: $120

Description: ⁠⁠⁠⁠⁠⁠⁠Babesia duncani, also known as WA1, causes symptoms similar to those seen in cases of babesiosis caused by Babesia microti. Most of the documented cases have occurred in the Pacific Northwest.

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Price: $340

Description: This test is for the detection of IgG and IgM antibodies against Babesia microti to aid in the diagnosis of Babesiosis. Babesiosis is a tickborne disease caused by transmission of the protozoa via the bite of an infected tick. B. microti is most common in the northern and upper Midwestern United States.Testing for B. microti is based on a clinical evaluation and risk of tick exposure with consideration to the geographic region. Symptoms may be nonspecific, including headache, fever/chills, malaise, myalgia, and gastrointestinal symptoms. Infection can have similarities with other tickborne illnesses with overlapping vectors, geographic endemicity, and similar clinical signs and symptoms, including Anaplasma spp, Ehrlichia spp, and Borrelia burgdorferi (Lyme disease).Negative results can occur early in infection. Nucleic acid amplification tests are the preferred method for diagnosis during acute infection. Seroconversion or a four-fold increase between acute and convalescent sera can be used to support a diagnosis. The presence of IgG alone may indicate past infection, and IgM may persist for many months after infection has resolved. Antibody levels may remain elevated for several years after acute illness. Other less common Babesia species in different geographic regions have been identified to infect humans, such as B. duncani and B. divergens. The extent of cross-reactivity between Babesia species is variable and may not be detected by this assay. Therefore, interpretation of serologic results is done in the context of pertinent clinical picture, including timing from symptom onset.References:1. Tickborne Diseases of the United States. A Reference Manual for Healthcare Providers, Sixth Edition, 2022. Centers for Disease Control and Prevention.2. Clinical Testing and Diagnosis for Ehrlichiosis. Centers for Disease Control and Prevention. Last updated May 15, 2024. https://www.cdc.gov/ehrlichiosis/hcp/diagnosis-testing/index.html⁠⁠⁠⁠⁠⁠⁠3. Krause, PJ. et al. Clinical Practice Guidelines by the Infectious Diseases Society of America (IDSA): 2020 Guideline on Diagnosis and Management of Babesiosis. Clin Infect Dis. 2021 Jan 27;72(2):e49-e64. doi: 10.1093/cid/ ciaa1216.

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Price: $327

Description: This test is intended for the qualitative detection of Babesia microti DNA in whole blood or ticks. Babesia microti is a protozoan parasite that infects red blood cells and causes Babesiosis. Transmission to humans occurs primarily through the bite of an infected Ixodes scapularis or Ixodes pacificus tick, occasionally through transfusion of contaminated blood products, and rarely through organ transplantation or from an infected mother to her baby during pregnancy or delivery. Clinical diagnosis of human babesiosis can be difficult, especially in the early stages. Symptoms are nonspecific and typically include fever, chills, headache, myalgia, and anorexia. Hepatomegaly and splenomegaly may also be present. Severe disease most commonly occurs in elderly and/or immunocompromised patients and is associated with higher levels of parasitemia (≥4 percent), nausea, vomiting, and diarrhea. Symptoms typically appear one to four weeks after infection via tick bite but may appear after a longer incubation period for infections from a contaminated blood product. Babesia parasitemia may persist in asymptomatic hosts for months or years, leading to concerns about the safety of blood products since there are currently no licensed tests for donor screening. Laboratory evaluation for Babesia microti infection includes examination of thin blood smears for the presence of parasites within red blood cells, serological assays for antibody detection in serum, and molecular identification of Babesia microti DNA in whole blood or ticks. The Babesia microti DNA, Real-Time PCR assay is rapid, sensitive and does not detect DNA sequences from the closely related canine pathogen Babesia gibsoni. A Babesia microti PCR result should be considered in the context of clinical observations, patient history, and epidemiological data when making a final diagnosis and patient management decisions. A negative result means that Babesia microti DNA was not present in the specimen above the limit of detection but does not exclude the possibility of infection.

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Price: $763

Description: Therapeutic drug monitoring.

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Price: $455

Description: Bacterial 16S rDNA sequencing is a genotypic test used as an adjunct to the phenotypic characteristics of an unknown bacterial isolate in order to determine the genus and/or the genus and species of the isolate. Genotypic tests are useful in the identification of unusual and new emerging pathogens.

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Price: $740

Description: The clinical significance of an isolate varies with the body site of origin and clinical symptoms manifested.

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Price: $68

Description: G. vaginalis is associated (in concert with other organisms) with bacterial vaginosis. Trichomonas and candida species are known agents of vaginitis.

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Price: $361

Description: This test quantifies an individual’s IgE response to Bahia grass. It is an in vitro quantitative assay, which is intended to be used in conjunction with other clinical information to aid in the diagnosis of allergic diseases [1]. While allergen-specific serum IgE testing is considered comparable to skin testing in many instances, both the American Academy of Allergy, Asthma, and Immunology and the American College of Allergy, Asthma, and Immunology recognize that allergen-specific serum IgE testing may be preferred in some clinical situations. These include 1) the presence of widespread skin disease, 2) the recent use of antihistamines or other medications that can affect the results of allergy skin tests, 3) uncooperative patients, and 4) medical history suggesting that allergen skin testing would pose a significant risk for a serious allergic reaction [1]. A definitive clinical diagnosis of allergy should not be based on the results of any single diagnostic method, but should be made by a trained healthcare professional after all clinical and laboratory findings have been evaluated. More specific information about this allergen can be found at http://www.phadia.com/en/products/allergy-testing-products/immunocap-allergen-information/grass-pollens/allergens/bahia-grass-/ Reference 1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(suppl 3):S1-S148.

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Price: $49

Description: This test detects the presence of specific IgE against bananas. A positive test only indicates that a person is sensitized and potentially allergic to this allergen. A diagnosis of allergy requires clinical signs and symptoms that appear to be associated with exposure to the allergen in addition to the detection of markers of IgE sensitization [1].More specific information about this allergen can be found on the following website: https://www.thermofisher.com/phadia/us/en/resources/allergen-encyclopedia.htmlReference1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(3 Suppl 3):S1-S148.

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Price: $49

• Detect banana-related digestive discomfort
• Check food sensitivity symptom triggers
• Monitor skin reactions after eating

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Price: $118

Description: Loss of BAP1 expression can be useful in distinguishing benign from malignant mesothelial proliferations, and in identifying atypical Spitz tumor and uveal melanoma.

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Price: $442

Description: Loss of BAP1 expression can be useful in distinguishing benign from malignant mesothelial proliferations, and in identifying atypical Spitz tumor and uveal melanoma.

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Price: $370

Description: This test includes sequencing and deletion/duplication analysis of the BAP1 gene. Individuals with a BAP1 pathogenic variant have an elevated risk of uveal and cutaneous melanoma, and malignant mesothelioma Individuals also have an elevated risk for renal cell carcinoma, atypical Spitz tumors, and basal cell carcinoma.

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Price: $628

• Screen for sedative drug use
• Detect barbiturate presence quickly
• Check unexplained drowsiness causes

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Price: $303

Description: This definitive drug assay is used to confirm presumptive positive results and identify the specific barbiturates in serum. Urine and oral fluid are the specimens of choice for routine monitoring of patients taking prescription drugs. Use of serum/plasma should be limited to anuretic patients, or where a patient's clinical appearance does not coincide with their prescribed medications.Barbiturates are a group of central nervous system (CNS) depressants that are used as sedatives, hypnotics, anesthetics, and anticonvulsants. Because barbiturates have a low therapeutic index and high abuse potential, they have been largely replaced by benzodiazepines for sedative and hypnotic purposes. Measurement of barbiturates in serum is helpful in the diagnosis and management of barbiturate intoxication as well as monitoring therapy [1]. Immunoassays are usually used to screen for barbiturate intoxication; positive screening results can then be confirmed with quantitative chromatography/mass spectrometry testing [1,2].The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.References1. Porter WH. Clinical toxiology. In: Burtis CA, et al, eds. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. 4th ed. Elsevier Inc; 2006:1325-1328.2.Drug fact sheet: Barbiturates. Untied State Drug Enforcement Administration. Accessed November 5, 2021. https://www.dea.gov/sites/default/files/2020-06/Barbiturates-2020_0.pdf

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Price: $326

• Check barium exposure from work environments
• Screen for heavy metal related symptoms
• Monitor muscle and heart health risks

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Price: $352

• Screen for barium exposure risks
• Check kidney clearance of metals
• Monitor workplace toxin exposure levels

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Price: $352

Description: This test detects the presence of specific IgE against barley. A positive test only indicates that a person is sensitized and potentially allergic to this allergen. A diagnosis of allergy requires clinical signs and symptoms that appear to be associated with exposure to the allergen in addition to the detection of markers of IgE sensitization [1].More specific information about this allergen can be found on the following website: https://www.thermofisher.com/phadia/us/en/resources/allergen-encyclopedia.htmlReference1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(3 Suppl 3):S1-S148.

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Price: $49

Description: This test quantifies an individual's IgE response to barley pollen. Allergen-specific serum IgE testing is considered comparable to skin testing and may be preferred in some clinical situations. However, a positive test result only indicates that a patient is sensitized to the allergen of concern. Many IgE-sensitized individuals do not develop any symptoms when exposed to the allergen. A diagnosis of allergy should only be made by a trained medical provider after conducting a thorough clinical evaluation [1].More specific information about this allergen can be found on the following website: https://www.thermofisher.com/phadia/us/en/resources/allergen-encyclopedia.htmlReference 1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(3 Suppl 3):S1-S148.

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Price: $49

Description: Bartonella DNA PCR is a highly specific and sensitive method to detect the presence of Bartonella species DNA in clinical specimens. This assay can differentiate between Bartonella henselae and Bartonella quintana. The diagnosis of Bartonella infection should not rely solely on the result of a PCR assay. A negative PCR result indicates only the absence of Bartonella species DNA in the sample tested and does not exclude the diagnosis of the disease. Patients with a positive PCR result should be evaluated with other tests to further establish the diagnosis of the disease. A positive result should be considered in conjunction with clinical presentation and additional established clinical tests.

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Price: $724

Description: Bartonella henselae infections have been associated with many clinical presentation, including cat scratch disease, bacillary angiomatosis, peliosis hepatitis, and bacteremia.

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Price: $287

Description: Bartonella henselae IgG results may aid in the diagnosis of recent or current B. henselae infection. Recent infection is indicated by seroconversion or increasing IgG titers when comparing results for acute and convalescent specimens tested on the same assay run.

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Price: $198

Description: Bartonella quintana infections have been associated with many clinical presentations, including urban trench fever, endocarditis, bacillary angiomatosis, bacilary peliosis, and bacteremia.

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Price: $287

Description: Bartonella quintana IgG results may aid in the diagnosis of recent or current B. quintana infection. Recent infection is indicated by seroconversion or increasing IgG titers when comparing results for acute or convalescent specimens tested on the same assay run.

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Price: $198

Description: This antibody panel helps diagnose infections with Bartonella henselae and Bartonella quintana. This panel includes IgM and IgG antibodies with reflexes to titers for positive results.B henselae causes cat scratch disease, a self-limiting bacterial infection transmitted via exposure to cats or cat fleas. B quintana causes trench fever, a febrile bacteremic illness transmitted via body lice. B henselae and B quintana are the 2 Bartonella species that most frequently cause blood culture-negative endocarditis. In immunocompromised individuals, infections with B henselae and B quintana may present as bacillary angiomatosis, a vasculoproliferative disease of the skin [1-4].Because of the fastidious nature of B henselae and B quintana, recovery of these bacteria is rarely successful, especially from blood. Serology is commonly used for diagnosing Bartonella infections [1,3]. Confirmation of recent or current infection with either B henselae or B quintana may require testing of serial specimens to demonstrate a 4-fold increase of IgG titers or the presence of IgM. A B henselae or B quintana IgG titer of 1:800 has been proposed as a major criterion for diagnosing Bartonella endocarditis [4].IgG cross-reactivity between B henselae and B quintana often occurs [1,3]. Qualitative real-time polymerase chain reaction is a highly specific and sensitive method to detect the presence of Bartonella species DNA in clinical specimens and can differentiate between B henselae and B quintana.The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.References1. Dumler JS, et al. Bartonella. In: Carroll KC, et al, eds. Manual of Clinical Microbiology. 12th ed. ASM Press; 2019. https://www.clinmicronow.org/doi/book/10.1128/9781683670438.MCM.ch502. Centers for Disease Control and Prevention. Bartonella infection (cat scratch disease, trench fever, and Carrion's disease). Last reviewed December 18, 2019. Accessed January 28, 2022. https://www.cdc.gov/bartonella/clinicians/index.html3. Miller JM, et al. Clin Infect Dis. 2018;67(6):813-816.4. Okaro U, et al. Clin Microbiol Rev. 2017;30(3):709-746.

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Price: $427

• Pinpoint the cause of chronic inflammation
• Reveal hidden factors affecting your energy levels
• Clarify the source of persistent aches

Includes:

Sedimentation Rate, Modified Westergren

C-Reactive Protein (CRP)

Patient Instructions:

There are no special instructions/requirements for the tests you ordered. Fasting is not required.

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Price: $64

• Detect early signs of cancer effortlessly
• Reveal hidden health risks quickly
• Confirm your peace of mind with certainty

Includes:

Comprehensive Metabolic Profile ( includes eGFR ): Albumin, Albumin/Globulin Ratio (calculated), Alkaline Phosphatase, ALT, AST, BUN/Creatinine Ratio (calculated), Calcium, Carbon Dioxide, Chloride, Creatinine with GFR Estimated, Globulin (calculated), Glucose, Potassium, Sodium, Total Bilirubin, Total Protein, Urea Nitrogen

Complete Blood Count / CBC (includes Differential and Platelets): WBC, RBC, Hemoglobin, Hematocrit, MCV, MCH, MCHC, RDW, Platelet Count, MPV and Differential (Absolute and Percent - Neutrophils, Lymphocytes, Monocytes, Eosinophils, and Basophils)

Sedimentation Rate, Modified Westergren

C-Reactive Protein (CRP)

CA 19-9

Carcinoembryonic Antigen (CEA)

Patient Instructions:

You should fast for 12 hours before collection of the specimen. Fasting is defined as no consumption of food or beverage other than water for at least 12 hours before testing.

Estimated turnaround for results is 3 business days. If confirmation testing is required, the estimated time may be extended.

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Price: $143

Description: Detection of in utero exposure to drugs of abuse consistent with maternal use during the second and third trimesters of pregnancy; Newborn (neonatal) toxicology.

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Price: $682

Description: This panel comprises a group of 8 specific tests that provide information on the status of an individual?s blood electrolytes, glucose levels, kidney status, and acid-base balance. The panel is usually ordered as part of a routine health examination or physical [1].The Basic Metabolic Panel is also commonly ordered during hospital and emergency-room admission, and to monitor the metabolism and vital signs of hospitalized individuals with conditions, such as hypertension, who are being treated with diuretics or other appropriate interventions. [1].Significant changes in electrolytes, acid-base balance, renal function, and blood glucose may be associated with kidney failure, respiratory distress, and impaired cognitive status. Changes in sodium, potassium, and calcium alter the excitability of neurons, cardiac, and skeletal muscles that can produce arrhythmias, weakness, and spasms/tremors [1].Basic metabolic panel test results are usually evaluated in conjunction with one another for patterns of results. A single abnormal test result could be indicative of something different than if more than 1 of the test results are abnormal. Many conditions can cause abnormal results, including kidney failure, respiratory distress, and diabetes-related complications [1].The section below outlines the roles of the analytes assessed with this panel [1].Sodium: Plays a central role in maintaining the normal distribution of water and osmotic pressure.Potassium: Essential for proper muscle and nerve function.Chloride: Helps keep the balance of fluids, maintain blood volume, stabilize blood pressure, and balance the pH of body fluids.CO2 (carbon dioxide, bicarbonate): Used to evaluate the total carbonate buffering system and acid-base balance.Glucose: A critical energy source for cells and organs. Used to diagnose diabetes and hypoglycemia.Calcium: Essential for nerve, muscle, and heart functions and bone formation.BUN (blood urea nitrogen): Evaluation of kidney function.Creatinine: Useful for diagnosis of renal insufficiency and estimation of glomerular filtration rate.References1. Rao LV, et al. Laboratory tests. In Rao LV, eds. Wallach's Interpretation of Diagnostic Tests. Pathways to Arriving at a Clinical Diagnosis. 11th ed. New York, NY: Wolters Kluwer; 2020, 6-463.

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Price: $49

Description: This panel comprises a group of 8 specific tests that provide information on the status of an individual's blood electrolytes, glucose levels, kidney status, and acid-base balance. The panel is usually ordered as part of a routine health examination or physical [1]. The Basic Metabolic Panel is also commonly ordered during hospital and emergency room admission, and to monitor the metabolism and vital signs of hospitalized individuals with conditions, such as hypertension, who are being treated with diuretics or other appropriate interventions [1]. Significant changes in electrolytes, acid-base balance, renal function, and blood glucose may be associated with kidney failure, respiratory distress, and impaired cognitive status. Changes in sodium, potassium, and calcium alter the excitability of neurons, cardiac, and skeletal muscles that can produce arrhythmias, weakness, and spasms/tremors [1]. The results of the panel components are usually evaluated jointly for patterns. The section below outlines the roles of the analytes assessed with this panel [1]. Sodium: An electrolyte that plays a central role in maintaining the normal distribution of water and appropriate pressure to assure that substances do not leak from cells and organs. Sodium measurements are useful in the diagnosis and treatment of diseases involving electrolyte imbalance. Potassium: An electrolyte that is essential for proper muscle and nerve function and helps keep the balance of fluids. Potassium measurements are useful in assessing electrolyte balance in the diagnosis and treatment of conditions characterized by low or high blood potassium levels. Chloride: An electrolyte that helps maintain volume, acidity, and electrical neutrality of the body fluids. Chloride measurements are useful in the diagnosis and treatment of electrolyte and metabolic disorders, such as cystic fibrosis and diabetic acidosis. Carbon dioxide (bicarbonate): A type of blood gas used to evaluate the total carbonate buffering system and acid-base balance. Carbon dioxide is generally evaluated with other common electrolytes; the measurements are useful in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance. Glucose: A type of sugar that serves as the body's main energy source. Glucose measurements are useful in the diagnosis of diabetes and low blood sugar. Calcium: A mineral in the body that is essential for nerve, muscle, and heart functions and bone formation. Calcium measurements are useful in the diagnosis of parathyroid disease, some bone disorders, and chronic kidney disease. Blood urea nitrogen (BUN): The principal waste product of protein catabolism. BUN measurements are useful in the diagnosis and treatment of certain kidney and metabolic diseases. Creatinine: A waste product of the muscles. Creatinine measurements are useful in the evaluation of kidney function and in monitoring renal dialysis. Creatinine-based estimated glomerular filtration rate (eGFR): A value calculated using serum creatinine measurements and the patient's age and sex to reflect kidney function. eGFR is useful in detecting and monitoring chronic kidney disease in adults. References 1. Rao LV, et al. Laboratory tests. In: Rao LV, eds. Wallach's Interpretation of Diagnostic Tests. Pathways to Arriving at a Clinical Diagnosis. 11th ed. Wolters Kluwer; 2020.

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Price: $49

Description: This panel comprises a group of 7 specific tests that provide information on the status of an individual's blood electrolytes, glucose levels, kidney status, and acid-base balance. The panel is usually ordered as part of a routine health examination or physical [1].The Basic Metabolic Panel is also commonly ordered during hospital and emergency room admission, and to monitor the metabolism and vital signs of hospitalized individuals with conditions, such as hypertension, who are being treated with diuretics or other appropriate interventions. [1].Significant changes in electrolytes, acid-base balance, renal function, and blood glucose may be associated with kidney failure, respiratory distress, and impaired cognitive status. Changes in sodium, potassium, and calcium alter the excitability of neurons, cardiac, and skeletal muscles that can produce arrhythmias, weakness, and spasms/tremors [1].The results of the panel components are usually evaluated jointly for patterns. The section below outlines the roles of the analytes assessed with this panel [1].Sodium: An electrolyte that plays a central role in maintaining the normal distribution of water and appropriate pressure to assure that substances do not leak from cells and organs. Sodium measurements are useful in the diagnosis and treatment of diseases involving electrolyte imbalance.Potassium: An electrolyte that is essential for proper muscle and nerve function and helps keep the balance of fluids. Potassium measurements are useful in assessing electrolyte balance in the diagnosis and treatment of conditions characterized by low or high blood potassium levels.Chloride: An electrolyte that helps maintain volume, acidity, and electrical neutrality of the body fluids. Chloride measurements are useful in the diagnosis and treatment of electrolyte and metabolic disorders, such as cystic fibrosis and diabetic acidosis.Carbon dioxide (bicarbonate): A type of blood gas used to evaluate the total carbonate buffering system and acid-base balance. Carbon dioxide is generally evaluated with other common electrolytes; the measurements are useful in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance.Glucose: A type of sugar that serves as the body's main energy source. Glucose measurements are useful in the diagnosis of diabetes and low blood sugar.Blood urea nitrogen (BUN): The principal waste product of protein catabolism. BUN measurements are useful in the diagnosis and treatment of certain kidney and metabolic diseases.Creatinine: A waste product of the muscles. Creatinine measurements are useful in the evaluation of kidney function and in monitoring renal dialysis.Creatinine-based estimated glomerular filtration rate (eGFR): A value calculated using serum creatinine measurements and the patient's age and sex to reflect kidney function. eGFR is useful in detecting and monitoring chronic kidney disease in adults.References1. Rao LV, et al. Laboratory tests. In: Rao LV, eds. Wallach's Interpretation of Diagnostic Tests. Pathways to Arriving at a Clinical Diagnosis. 11th ed. Wolters Kluwer; 2020.

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Price: $49

Description: This panel comprises a group of 7 specific tests that provide information on the status of an individual's blood electrolytes, glucose levels, kidney status, and acid-base balance. The panel is usually ordered as part of a routine health examination or physical [1].The Basic Metabolic Panel is also commonly ordered during hospital and emergency room admission, and to monitor the metabolism and vital signs of hospitalized individuals with conditions, such as hypertension, who are being treated with diuretics or other appropriate interventions. [1].Significant changes in electrolytes, acid-base balance, renal function, and blood glucose may be associated with kidney failure, respiratory distress, and impaired cognitive status. Changes in sodium, potassium, and calcium alter the excitability of neurons, cardiac, and skeletal muscles that can produce arrhythmias, weakness, and spasms/tremors [1].The results of the panel components are usually evaluated jointly for patterns. The section below outlines the roles of the analytes assessed with this panel [1].Sodium: An electrolyte that plays a central role in maintaining the normal distribution of water and appropriate pressure to assure that substances do not leak from cells and organs. Sodium measurements are useful in the diagnosis and treatment of diseases involving electrolyte imbalance.Potassium: An electrolyte that is essential for proper muscle and nerve function and helps keep the balance of fluids. Potassium measurements are useful in assessing electrolyte balance in the diagnosis and treatment of conditions characterized by low or high blood potassium levels.Chloride: An electrolyte that helps maintain volume, acidity, and electrical neutrality of the body fluids. Chloride measurements are useful in the diagnosis and treatment of electrolyte and metabolic disorders, such as cystic fibrosis and diabetic acidosis.Carbon dioxide (bicarbonate): A type of blood gas used to evaluate the total carbonate buffering system and acid-base balance. Carbon dioxide is generally evaluated with other common electrolytes; the measurements are useful in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance.Glucose: A type of sugar that serves as the body's main energy source. Glucose measurements are useful in the diagnosis of diabetes and low blood sugar.Blood urea nitrogen (BUN): The principal waste product of protein catabolism. BUN measurements are useful in the diagnosis and treatment of certain kidney and metabolic diseases.Creatinine: A waste product of the muscles. Creatinine measurements are useful in the evaluation of kidney function and in monitoring renal dialysis.References1. Rao LV, et al. Laboratory tests. In: Rao LV, eds. Wallach's Interpretation of Diagnostic Tests. Pathways to Arriving at a Clinical Diagnosis. 11th ed. Wolters Kluwer; 2020

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Price: $49

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Description: This test is an allergen-specific IgE antibody test that quantifies an individual’s IgE response to basil. It is an in vitro quantitative assay, which is intended to be used in conjunction with other clinical information to aid in the diagnosis of food allergy [1]. While allergen-specific serum IgE testing is considered comparable to skin testing in many instances, both the American Academy of Allergy, Asthma, and Immunology and the American College of Allergy, Asthma, and Immunology recognize that allergen-specific serum IgE testing may be preferred in some clinical situations. These include 1) the presence of widespread skin disease, 2) the recent use of antihistamines or other medications that can affect the results of allergy skin tests, 3) uncooperative patients, and 4) medical history suggesting that allergen skin testing would pose a significant risk for a serious allergic reaction [1]. Food-specific IgE tests are extremely sensitive. However, a positive test result only indicates that a patient is IgE sensitized to the food of concern. Many IgE-sensitized patients do not develop any symptoms when this food is ingested. A diagnosis of food allergy should only be made by a trained medical provider, after conducting a thorough clinical evaluation [2,3]. While food-specific IgE test results may contribute to that evaluation, they cannot replace it. In this regard, detection of food-specific IgE in serum provides evidence of IgE sensitization, but a history of clinical reactivity to the food of concern, is required to make a diagnosis of IgE-mediated food allergy. Moreover, several forms of food hypersensitivity are not associated with the presence of food-specific IgE in serum. More specific information about this allergen can be found at http://www.phadia.com/en/products/allergy-testing-products/immunocap-allergen-information/food-of-plant-origin/spices/basil/ References 1. Bernstein IL, et al. Ann Allergy Asthma Immunol. 2008;100(suppl 3):S1-S148. 2. Sampson HA, et al. J Allergy Clin Immunol. 2014;134:1016-1025. 3. Boyce JA, et al. J Allergy Clin Immunol. 2010;126(6 suppl):S1-S58.

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Price: $49