Find test for Insight Diagnostics

Pre-Test Information: N/A

Test Type: Blood

Test Description:

• What is 1,25-Di Hydroxy Cholecalciferol?
• This test measures the level of 1,25-Di Hydroxy Cholecalciferol (the biologically active form of Vitamin D) in the blood.

TAT: 1 week

Pre-Test Information: N/A

Test Type: Blood

Test Description:

• Why Get Tested?
• To screen for liver damage and/or to help diagnose liver disease
• When To Get Tested?
• When a healthcare practitioner thinks that you have symptoms of a liver disorder, such as abdominal pain, nausea and vomiting, jaundice (yellowish discoloration of the skin or white of the sclerae), or potential exposure to hepatitis viruses; it can also be ordered as part of a comprehensive metabolic panel (CMP) when you have a routine health exam.
• What is being tested?
• Alanine aminotransferase (ALT) is an enzyme found mostly in the cells of the liver and kidney. Much smaller amounts of it are also found in the heart and muscles. Normally, ALT levels in blood are low, but when the liver is damaged, ALT is released into the blood and the level increases. This test measures the level of ALT in the blood and is useful for early detection of liver disease.
• The function of ALT is to convert alanine, an amino acid found in proteins, into pyruvate, an important intermediate in cellular energy production. In healthy individuals, ALT levels in the blood are low. When the liver is damaged, ALT is released into the blood, usually before more obvious signs of liver damage occur, such as jaundice.
• The liver is a vital organ located in the upper right side of the abdomen, just beneath the rib cage. It is involved in many important functions in the body. The liver helps to process the body's nutrients, manufactures bile to help digest fats, produces many important proteins such as blood clotting factors and albumin, and breaks down potentially toxic substances into harmless ones that the body can use or eliminate.
• A number of conditions can cause damage to liver cells, resulting in an increase in ALT. The test is most useful in detecting damage due to hepatitis (inflammation of the liver) or as a result of drugs or other substances that are toxic to the liver.
• ALT is commonly tested in conjunction with aspartate aminotransferase (AST), another liver enzyme, as part of a liver panel. Both ALT and AST levels usually rise whenever the liver is being damaged, although ALT is more specific for the liver and, in some cases, may be the only one of the two to be increased. An AST/ALT ratio may be calculated to aid in distinguishing between different causes and severity of liver injury and to help distinguish liver injury from damage to heart or muscles.

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To screen for and help diagnose a liver disorder or kidney disease; sometimes to evaluate nutritional status, especially in hospitalized patients
• When To Get Tested?
• Routinely as part of the blood tests done for a health exam or prior to a planned surgery; when a healthcare practitioner thinks that you have symptoms of a liver disorder or kidney disease; sometimes when you have unintended weight loss or have symptoms associated with malnutrition
• What is being tested?
• Albumin is a protein made by the liver. It makes up about 60% of the total protein in the blood and plays many roles. This test measures the level of albumin in the blood.
• Albumin keeps fluid from leaking out of blood vessels, nourishes tissues, and transports hormones, vitamins, drugs, and substances like calcium throughout the body. Levels of albumin may decrease, to a greater or lesser degree, when conditions interfere with its production by the liver, increase protein breakdown, increase protein loss via the kidneys, and/or expand the volume of plasma, the liquid portion of blood (diluting the blood).
• Two important causes of low blood albumin include:
• Severe liver disease—since albumin is produced by the liver, its level can decrease with loss of liver function; however, this typically occurs only when the liver has been severely affected.
• Kidney disease—one of the many functions of the kidneys is to conserve plasma proteins such as albumin so that they are not released along with waste products when urine is produced. Albumin is present in high concentrations in the blood, and when the kidneys are functioning properly, virtually no albumin is lost in the urine. However, if a person's kidneys become damaged or diseased, they begin to lose their ability to conserve albumin and other proteins. This is frequently seen in chronic diseases, such as diabetes and hypertension. In nephrotic syndrome, very high amounts of albumin are lost through the kidneys.

TAT: Same day

Pre-Test Information: N/A

Test Type: Blood

Test Description:

• Why Get Tested?
• To detect an elevated level of ammonia in the blood that may be caused by severe liver disease, kidney failure, or certain rare genetic disorders; to help investigate the cause of changes in behavior and consciousness; to help diagnose hepatic encephalopathy or Reye syndrome
• When To Get Tested?
• When someone with or without liver disease or kidney failure experiences mental changes or lapses into a coma; when a newborn experiences frequent vomiting and increased lethargy or when a child has continuous vomiting and unusual sleepiness during recovery from a viral illness, such as the flu or chickenpox
• What is being tested?
• Ammonia is a waste product formed primarily by bacteria in the intestines during the digestion of protein. If not processed and cleared from the body appropriately, excess ammonia can accumulate in the blood. This test measures the amount of ammonia in the blood.
• Ammonia is normally transported in the blood to the liver, where it is converted into two substances called urea and glutamine. The urea is then carried to the kidneys, where it is eliminated in the urine. If this "urea cycle" does not complete the breakdown of ammonia, ammonia builds up in the blood and can pass from the blood into the brain.
• Ammonia is toxic to the brain. For example, when liver function is significantly reduced due to disorders such as cirrhosis or hepatitis, ammonia and other compounds processed by the liver can accumulate in the brain and cause a condition called hepatic encephalopathy.
• Hepatic encephalopathy causes mental and neurological changes that can lead to confusion, disorientation, sleepiness, and eventually to coma and even death.
• Infants and children with increased ammonia levels may vomit frequently, be irritable, and be increasingly lethargic. Left untreated, they may experience seizures, have difficulty breathing, and may lapse into a coma.
• Problems with ammonia processing can arise from conditions such as:
• Severe liver disease – damage limits the ability of the liver to process ammonia; spikes in ammonia blood levels may be seen in people with stable liver disease, especially following a triggering event such as gastrointestinal bleeding or an electrolyte imbalance.
• Decreased blood flow to the liver – ammonia is less able to get to the liver to be processed.
• Reye syndrome – a rare condition that affects the blood, brain, and liver; it typically causes a rise in ammonia levels and a fall in glucose. It affects primarily children and young adults. In most cases, it follows and appears to be triggered by a viral infection, such as the flu or chickenpox. Children who are given aspirin are at an increased risk.
• Kidney (renal) failure – the kidneys are unable to effectively rid the body of urea, leading to a build-up of ammonia in the blood.
• Rare genetic disorder such as a defect in the urea cycle – a deficiency in one of the enzymes necessary to complete the conversion of ammonia to urea.

TAT: 3 days

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• What is aldolase?
• Aldolase is an enzyme that helps convert glucose (sugar) into energy. It is found throughout the body but is primarily found in high levels in muscle tissue.
• Aldolase levels in the blood rise when a person has muscle damage. The aldolase blood test may be ordered to diagnose and monitor certain conditions related to skeletal muscle. It largely has been replaced by other muscle enzyme tests, especially CK (creatine kinase). However, a minority of people with muscle pain may have an elevated aldolase level even though their creatine kinase is normal. Therefore, the test may sometimes be requested by rheumatologists in addition to creatine kinase.

TAT: 3 days

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To help diagnose the cause of early onset emphysema and/or liver dysfunction; to establish the risk of emphysema and/or liver disease due to alpha-1 antitrypsin deficiency and determine the likelihood that children might inherit the risk
• When To Get Tested?
• When your infant or young child show signs of liver disease; when you develop emphysema before age 40; when you have chronic obstructive pulmonary disease (COPD) or unexplained liver disease at any age; when you have a close relative with alpha-1 antitrypsin deficiency
• What is being tested?
• Alpha-1 antitrypsin (AAT) is a protein in the blood that protects the lungs from damage caused by activated enzymes. Laboratory tests measure the level of AAT in blood or identify abnormal forms of AAT that a person has inherited to help diagnose alpha-1 antitrypsin deficiency.
• AAT helps to inactivate several enzymes, the most important of which is elastase. Elastase is an enzyme produced by white blood cells called neutrophils and is part of the body's normal response to injury and inflammation. Elastase breaks down proteins so that they can be removed and recycled by the body. If its action is not regulated by AAT, elastase will also begin to break down and damage lung tissue.
• Each individual inherits two copies of the gene that codes for AAT. It is called the protease inhibitor (SERPINA1) gene. This gene is co-dominant, which means that each SERPINA1 gene copy is responsible for producing half of the body's AAT. If there is a change or mutation in one or both of the gene copies, then less AAT and/or AAT with reduced function is produced.
• When AAT production drops below 30% of normal, the affected person will experience a disorder called alpha-1 antitrypsin deficiency. People with this disorder are at a considerable risk of developing emphysema, a progressive lung disease, in early adulthood. If they smoke or are exposed to occupational dust or fumes, the lung damage tends to occur sooner and be more severe.
• Certain types of dysfunctional AAT accumulate in the liver cells, where it is produced. As AAT builds up in these cells, it forms abnormal protein chains and begins to destroy the cells and damage the liver. About 10% of newborns with AAT deficiency have liver damage and are jaundiced. In severe cases, these infants may require a liver transplant to survive. AAT deficiency is currently the most common genetic cause of liver disease in the pediatric population.
• In adults with AAT deficiency, the risk of developing chronic liver disease, cirrhosis, and liver cancer (hepatocellular carcinoma) is increased. Few adults with AAT deficiency actually have signs or symptoms of liver disease, however. The amount and function of the AAT depends on the gene mutation that is inherited. While there are more than 120 different alleles in the SERPINA1 gene, only a few are common. Most people in the U.S., about 90%, have two copies of the normal "wild type" M gene (MM). The most common abnormal genes are labeled S and Z.

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To help evaluate adrenal gland function; to detect adrenal tumors or cancers; to help determine the cause of male physical characteristics (virilization) in females or early puberty in boys; to evaluate androgen production and function of ovaries in women or testicular function in men; when congenital adrenal hyperplasia (CAH) is suspected; to monitor treatment for CAH
• When To Get Tested?
• When a woman has excess facial and body hair (hirsutism), acne, no monthly menstrual periods (amenorrhea), fewer than 6-8 menstrual cycle per year (oligomenorrhea), or infertility; when a boy is undergoing very early (precocious) puberty or a girl is showing signs of virilization; when puberty is delayed; when diagnosing CAH; periodically when being treated for CAH
• Test Preparation Needed?
• In menstruating women, there may be specific instructions as to timing of the sample collection.
• What is being tested?
• Androstenedione is an androgen, one of several "male" sex hormones that are responsible for the onset of sexual differentiation in males and females and the development of secondary male physical characteristics such as a deep voice and facial hair. Though it is considered to be a "male" sex hormone, it is present in the blood of both men and women and is a precursor that can be converted by the body into more potent androgens, such as testosterone, or converted into the female hormone estrogen. This test measures the amount of androstenedione in the blood.
• Androstenedione is produced by the ovaries in women, the testicles in men, and by the adrenal glands in both.
• The pituitary hormone LH stimulates the release of androstenedione by the ovaries and testicles.
• The pituitary hormone adrenocorticotropic hormone (ACTH) stimulates the release of androstenedione by the adrenal glands.
• The level of androstenedione in the blood will vary during the day in a "diurnal pattern," and it will vary during a woman's menstrual cycle. Because of its origins, androstenedione can be useful as a marker of adrenal gland function, of androgen production, and of the function of the ovaries or testicles. An androstenedione test is often performed after results of other tests, such as testosterone or 17-hydroxyprogesterone, are found to be abnormal.
• An excess level of androstenedione and other androgens can cause children to have sex organs that are not clearly male or female (ambiguous external genitalia), excess body hair (hirsutism), and abnormal menstrual periods in girls and precocious (early) puberty in girls and boys.
• Adrenal tumors, ACTH-producing tumors, and adrenal hyperplasia can lead to the overproduction of androstenedione. Women with polycystic ovary syndrome (PCOS) may have higher levels of androstenedione as well. While elevated levels may not be noticed in adult men, they can lead to noticeable male physical characteristics (virilization) and a lack of monthly menstrual periods (amenorrhea) in females.

TAT: 4 days

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To help diagnose and monitor sarcoidosis; to help differentiate this systemic condition from other disorders causing similar symptoms
• When To Get Tested?
• When you have granulomas that produce small bumps under the skin, a lingering cough, red watery eyes, and/or other symptoms suggestive of sarcoidosis; regularly when you have active sarcoidosis to monitor its course
• What is being tested?
• Angiotensin-converting enzyme (ACE) is an enzyme that helps regulate blood pressure. An increased blood level of ACE is sometimes found in sarcoidosis, a systemic disorder of unknown cause that often affects the lungs but may also affect many other body organs, including the eyes, skin, nerves, liver, and heart., This test measures the amount of ACE in the blood.
• A classic feature of sarcoidosis is the development of granulomas, small tumor-like masses of immune and inflammatory cells and fibrous tissue that form nodules under the skin and in organs throughout the body. Granulomas change the structure of the tissues around them and, in sufficient numbers, they can cause damage and inflammation and may interfere with normal functions. The cells found at the outside borders of granulomas can produce increased amounts of ACE. The level of ACE in the blood may increase when sarcoidosis-related granulomas develop.

TAT: 4 days

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To detect liver damage and/or to help diagnose liver disease
• When To Get Tested?
• When a healthcare practitioner thinks that you have symptoms of a liver disorder, such as abdominal pain, nausea and vomiting, jaundice (yellow skin), or potential exposure to a hepatitis virus; as part of a comprehensive metabolic panel when you have a routine health exam
• What is being tested?
• Aspartate aminotransferase (AST) is an enzyme found in cells throughout the body but mostly in the heart and liver and, to a lesser extent, in the kidneys and muscles. In healthy individuals, levels of AST in the blood are low. When liver or muscle cells are injured, they release AST into the blood. This makes AST a useful test for detecting or monitoring liver damage.
• The liver is a vital organ located in the upper right-hand side of the abdominal area just beneath the rib cage. It is involved in many important functions in the body. The liver helps to process the body's nutrients, manufactures bile to help digest fats, produces many important proteins such as blood clotting factors, and breaks down potentially toxic substances into harmless ones that the body can use or excrete.
• A number of conditions can cause injury to liver cells and may cause increases in AST. The test is most useful in detecting liver damage due to hepatitis, drugs toxic to the liver, cirrhosis, or alcoholism. AST, however, is not specific for the liver and may be increased in conditions affecting other parts of the body.
• An AST test is often performed along with an alanine aminotransferase (ALT) test. Both are enzymes found in the liver that become elevated in the blood when the liver is damaged. A calculated AST/ALT ratio is useful for differentiating between different causes of liver injury and in recognizing when the increased levels may be coming from another source, such as heart or muscle injury.

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• As part of an electrolyte panel or metabolic panel to identify or monitor an electrolyte imbalance or acid-base (pH) imbalance
• When To Get Tested?
• During a routine health exam or as recommended by your healthcare practitioner if you are experiencing symptoms such as weakness, confusion, prolonged vomiting, or breathing problems that could indicate an electrolyte imbalance or an acid-base imbalance (acidosis or alkalosis)
• What is being tested?
• Bicarbonate is an electrolyte, a negatively charged ion that is used by the body to help maintain the body's acid-base (pH) balance. It also works with the other electrolytes (sodium, potassium, and chloride) to maintain electrical neutrality at the cellular level. This test measures the total amount of carbon dioxide (CO2) in the blood, which occurs mostly in the form of bicarbonate (HCO3-). The CO2 is mainly a by-product of various metabolic processes.
• Measuring bicarbonate as part of an electrolyte or metabolic panel may help diagnose an electrolyte imbalance or acidosis or alkalosis. Acidosis and alkalosis describe the abnormal conditions that result from an imbalance in the pH of the blood caused by an excess of acid or alkali (base). This imbalance is typically caused by some underlying condition or disease.
• The lungs and kidneys are the major organs involved in regulating blood pH through the removal of excess bicarbonate.
• The lungs flush acid out of the body by exhaling CO2. Raising and lowering the respiratory rate alters the amount of CO2 that is breathed out, and this can affect blood pH within minutes.
• The kidneys eliminate acids in the urine and they regulate the concentration of bicarbonate (HCO3-, a base) in blood. Acid-base changes due to increases or decreases in HCO3- concentration occur more slowly than changes in CO2, taking hours or days.
• Any disease or condition that affects the lungs, kidneys, metabolism, or breathing has the potential to cause acidosis or alkalosis.
• The bicarbonate test gives a healthcare practitioner a rough estimate of your acid-base balance. This is usually sufficient, but measurements of gases dissolved in the blood (blood gases) may be done if more information is needed. Bicarbonate is typically measured along with sodium, potassium, and possibly chloride in an electrolyte panel as it is the balance of these molecules that gives the healthcare practitioner the most information.

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To evaluate the health of your kidneys; to help diagnose kidney disease; to monitor the effectiveness of dialysis and other treatments related to kidney disease or damage
• When To Get Tested?
• As part of a routine comprehensive or basic metabolic panel (CMP or BMP) during a health exam; when you have signs and symptoms that may be due to kidney disease or you have a condition that may cause or be worsened by kidney dysfunction; at regular intervals when you are being treated for kidney disease or damage
• What is being tested?
• Urea is a waste product formed in the liver when protein is metabolized into its component parts (amino acids). This process produces ammonia, which is then converted into the less toxic waste product urea. This test measures the blood urea nitrogen (BUN) level in the blood. Sometimes, a BUN to creatinine ratio is calculated to help determine the cause of elevated levels.
• Nitrogen is a component of both ammonia and urea. Urea and urea nitrogen are referred to somewhat interchangeably because urea contains nitrogen and because urea/urea nitrogen is the "transport method" used by the body to rid itself of excess nitrogen. Urea is formed in and released by the liver into the blood and is carried to the kidneys, where it is filtered out of the blood and released into the urine. Since this is an ongoing process, there is usually a small but stable amount of urea nitrogen in the blood. However, when the kidneys cannot filter wastes out of the blood due to disease or damage, then the level of urea in the blood will rise.
• The kidneys are a pair of bean-shaped organs that are located at the bottom of the ribcage in the right and left sides of the back. Within them are about a million tiny blood filtering units called nephrons. In each nephron, blood is continually filtered through a microscopic cluster of looping blood vessels, called glomerulus. The glomerulus allows the passage of water and small molecules but retains blood cells and larger molecules. Attached to each glomerulus is a tiny tube (tubule) that collects the fluid and molecules that pass through the glomerulus and then reabsorbs what still can be used by the body. The remaining waste forms urine.
• Most diseases or conditions that affect the kidneys or liver have the potential to affect the amount of urea present in the blood. If increased amounts of urea are produced by the liver or if the kidneys are not working properly and have difficulty filtering wastes out of the blood, then urea levels will rise in the blood. If significant liver damage or disease inhibits the production of urea, then BUN levels may fall.

TAT: Same Day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To screen for, diagnose, and monitor a range of medical conditions
• When To Get Tested?
• As part of a routine metabolic panel; when you have symptoms of a disorder, or known presence of one, affecting your kidneys, bones, thyroid, parathyroid, or nerves or when symptoms of significantly increased or decreased calcium concentrations are present; when someone is critically ill, to monitor ionized calcium levels; when someone has certain types of cancer; when someone is being treated for abnormal calcium levels, to evaluate the effectiveness of treatment
• What is being tested?
• Calcium is the most abundant and one of the most important minerals in the body. It is essential for cell signaling and the proper functioning of muscles, nerves, and the heart. Calcium is needed for blood clotting and is crucial for the formation, density, and maintenance of bones and teeth. This test measures the amount of calcium in the blood or urine, which reflects the amount of total and ionized calcium in the body.
• About 99% of calcium is found complexed in the bones, while the remaining 1% circulates in the blood. Calcium levels are tightly controlled; if there is too little absorbed or ingested, or if there is excess loss through the kidney or gut, calcium is taken from bone to maintain blood concentrations. Roughly half of the calcium in the blood is "free" and is metabolically active. The remaining half is "bound" to proteins, primarily albumin and to a lesser extend globulins, with a smaller amount complexed to anions, such as phosphate, and these bound and complexed forms are metabolically inactive.
• There are two tests to measure blood calcium. The total calcium test measures both the free and bound forms. The ionized calcium test measures only the free, metabolically active form.
• Some calcium is lost from the body every day, filtered from the blood by the kidneys and excreted into the urine and sweat. Measurement of the amount of calcium in the urine is used to determine how much calcium the kidneys are eliminating.

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To help diagnose and monitor C-cell hyperplasia and medullary thyroid cancer; to screen those at risk for multiple endocrine neoplasia type 2 (MEN 2)
• When To Get Tested?
• When a healthcare practitioner suspects that you have or when you are being treated for medullary thyroid cancer, or when a family member has medullary thyroid cancer or MEN 2
• Test Preparation Needed?
• Overnight fasting may be required; follow instructions provided by your healthcare practitioner or the laboratory.
• What is being tested?
• Calcitonin is a hormone produced by special cells in the thyroid called C-cells. The thyroid is a small butterfly-shaped gland that lies over and flat against the windpipe in the throat. It produces calcitonin and several hormones that help control the rate of metabolism, primarily thyroxine (T4) and triiodothyronine (T3). This test measures the amount of calcitonin in the blood.
• Calcitonin is involved in the regulation of calcium levels in the blood through inhibiting bone breakdown (resorption) and decreasing kidney reabsorption of calcium. However, its role in calcium regulation is minor compared with parathyroid hormone (PTH) and 1,25-dihydroxyvitamin D. Thus, the measurement of calcitonin in blood is not useful for diagnosis of disorders of calcium regulation.
• In two rare conditions, C-cell hyperplasia and medullary thyroid cancer, excessive amounts of calcitonin are produced. C-cell hyperplasia is a benign condition that may or may not progress to become medullary thyroid cancer. Medullary thyroid cancer is malignant – it can spread beyond the thyroid and can be difficult to treat if it is not discovered early.
• Medullary cancer is a rare form of thyroid cancer that accounts for 1-2% of all thyroid cancers in the United States. About 75-80% of medullary thyroid cancer cases are sporadic, occurring in those who do not have a family history of the disease. About 20-25% of cases are related to an inherited mutation in the RET gene that leads to multiple endocrine neoplasia type 2 (MEN 2). MEN 2 is a syndrome associated with several related diseases, including medullary thyroid cancer and pheochromocytomas. The altered RET gene is inherited in an autosomal dominant fashion. Only one copy of the mutated gene – from either a father or mother – is required to have a greatly increased risk of developing medullary thyroid cancer. Most cases of sporadic medullary thyroid cancer develop when people are in their 40s or 50s, and the prevalence is higher in women. The inherited form affects both sexes equally and can occur at an earlier age.

TAT: 1 week

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To determine the concentration of carbamazepine in the blood to establish an appropriate dose and maintain a therapeutic level
• When To Get Tested?
• At regular intervals to monitor the drug's level; when indicated to detect low or excessive (potentially toxic) concentrations
• Test Preparation Needed?
• None, but you should talk to your healthcare provider about the timing of the sample collection. Often, the recommended time is when the level in the blood is expected to be at its lowest, just before the next dose is taken.
• What is being tested?
• Carbamazepine is a drug that is primarily used to treat certain seizure disorders (also called epilepsy) but is also prescribed to stabilize the moods of people with bipolar disease, to ease alcohol withdrawal, and to help alleviate some types of nerve pain. It may be prescribed by itself or in combination with other antiepileptic drugs. This test measures the level of carbamazepine in the blood.
• Carbamazepine levels are monitored because the drug must be maintained within a narrow therapeutic range. If the level is too low, the drug may not be effective and the person may experience a recurrence of symptoms (i.e., seizures, mania, or pain); if the level is too high, the person may experience toxic side effects. Maintaining a therapeutic level of this drug can be a challenge to achieve for several different reasons:
• Oral doses of carbamazepine are absorbed in the gastrointestinal tract at widely variable rates.
• Since carbamazepine is metabolized by the liver, anything that affects liver function can affect blood levels of the drug.
• Upon a long-term administration, carbamazepine induces its own metabolism.
• Much of the drug is bound to plasma protein, but it is the free portion of the drug that is active. Conditions that affect protein binding of the drug may affect therapeutic effectiveness. This may occur when someone has low blood albumin, kidney failure, or when they are very young (newborn) or elderly.
• The metabolite of carbamazepine, carbamazepine-10,11-epoxide, is also therapeutically active and contributes to the overall effect of the medication.
• Several drugs, if taken in conjunction with carbamazepine, may interact or affect its metabolism and blood levels.
• Dosages of carbamazepine must be adjusted carefully in order to reach a steady concentration in the blood. The actual amount of drug required to reach this steady state will vary from person to person and may change over time.
• Carbamazepine is usually monitored long-term because it is prescribed to treat the chronic conditions epilepsy, bipolar disorder, trigeminal neuralgia, and nerve pain from diabetes.
• Epilepsy affects the brain's ability to transmit electrical impulses and to regulate nerve activity. During a seizure, a person may experience changes in consciousness, alterations in sight, smell, and taste, and may experience convulsions. The frequency of seizures varies from a single episode, to occasional seizures, to recurrent seizures. Carbamazepine is prescribed to help prevent specific types of recurrent seizures.
• Bipolar disorder is a mental condition that is characterized by cycles of depression and mania that may last for days, weeks, months, or years. During a depressive episode, those affected may feel sad, hopeless, worthless, and have thoughts of suicide. During a manic episode, those affected may be euphoric, irritable, use poor judgment, and participate in risky behaviors. Carbamazepine is prescribed to help even out the moods of the person with bipolar disorder, especially mania.
• Trigeminal neuralgia, a condition associated with facial nerve pain and muscle spasms, and paroxysmal choreoathetosis, a movement disorder that causes involuntary movements of the limbs, trunk, and facial muscles, are also sometimes treated with carbamazepine. So is diabetic peripheral neuropathic pain, which affects the functionality, mood, and sleep patterns of approximately 10-20% of people with diabetes mellitus.

TAT: 3 days

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• Primarily to monitor cancer treatment, including response to therapy and recurrence; as an indicator of the amount of cancer or size of tumor present (tumor burden) and to assist in cancer staging; occasionally as follow up to a positive screening test for cancer, to compare whether the level falls to normal (indicating that the cancer was all likely removed) after treatment for the cancer
• When To Get Tested?
• When you have been diagnosed with colon, pancreas, breast, lung, ovarian, medullary thyroid or other cancer prior to starting cancer treatment and then, if elevated, at intervals during and after therapy; occasionally when cancer is suspected but not confirmed – to aid in its detection
• What is being tested?
• Carcinoembryonic antigen (CEA) is a protein that is present in certain tissues of a developing baby (fetus). By the time a baby is born, it drops to a very low level. In adults, CEA is normally present at very low levels in the blood but may be elevated with certain types of cancer. This test measures the amount of CEA in the blood to help evaluate individuals diagnosed with cancer.
• CEA is a tumor marker. Originally, it was thought that CEA was a specific marker for colon cancer, but further study has shown that an increase in CEA may be seen in a wide variety of other cancers. CEA can also be increased in some non-cancer-related conditions, such as inflammation, cirrhosis, peptic ulcer, ulcerative colitis, rectal polyps, emphysema, and benign breast disease, and in smokers. For this reason, it is not useful as a general cancer screening tool, but it does have a role in evaluating response to cancer treatment. When an individual has been diagnosed with cancer, an initial baseline test for CEA may be performed. If this level is elevated, then subsequent serial testing of CEA may be performed to monitor the cancer as the individual undergoes treatment.

TAT: 2 Days

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To measure the amount of ceruloplasmin in the blood; to help diagnose Wilson disease; sometimes to help identify conditions associated with copper deficiencies
• When To Get Tested?
• When you have jaundice, fatigue, abdominal pain, behavioral changes, tremors, or other symptoms that a health practitioner thinks may be due to Wilson disease or, rarely, to copper deficiency; at intervals when monitoring is recommended
• What is being tested?
• Ceruloplasmin is a copper-containing enzyme that plays a role in the body's iron metabolism. This test measures the amount of ceruloplasmin in the blood.
• Copper is an essential mineral that plays a role in the regulation of iron metabolism, formation of connective tissue, energy production at the cellular level, and the function of the nervous system. It is absorbed from food and liquids by the intestines and then transported to the liver, where it is stored or used to produce a variety of enzymes.
• The liver binds copper to a protein to produce ceruloplasmin and then releases it into the bloodstream. About 95% of the copper in the blood is bound to ceruloplasmin. Because of this, the ceruloplasmin test can be used along with one or more copper tests to help diagnose Wilson disease, an inherited disorder that can lead to excess storage of copper in the liver, brain, and other organs.

TAT: 4 days

Pre-Test Information:

• 8 hours fasting is mandatory
• Minimum 12 hours fasting is mandatory

Test Type: Serum

Test Description:

• Why Get Tested?
• To determine your risk of developing heart disease
• When To Get Tested?
• Screening: as part of a regular health exam with a lipid profile when no risk factors for heart disease are present; once every four to six years in adults; children should have a lipid profile screening at least once between the ages of 9 and 11 and then again between the ages of 17 and 21.
• Monitoring: may be done more frequently and at regular intervals as part of a lipid profile when risk factors for heart disease are present, when prior results showed high risk levels, and/or when undergoing treatment for unhealthy lipid levels
• Test Preparation Needed?
• If this test is to be performed as part of a complete lipid profile, fasting for 9 to 12 hours typically will be required; only water is permitted. Your healthcare practitioner may decide that you may be tested without fasting. Follow any instructions you are given and tell the person drawing your blood whether or not you have fasted. For youths without risk factors, testing may be done without fasting.
• What is being tested?
• High-density lipoprotein (HDL cholesterol, HDL-C) is one of the classes of lipoproteins that carry cholesterol in the blood. HDL-C consists primarily of protein with a small amount of cholesterol. It is considered to be beneficial because it removes excess cholesterol from tissues and carries it to the liver for disposal. Hence, HDL cholesterol is often termed "good" cholesterol. The test for HDL cholesterol measures the amount of HDL-C in blood.
• High levels of cholesterol have been shown to be associated with the development of hardening of the arteries (atherosclerosis) and heart disease. When cholesterol levels in the blood increase (not enough is removed by HDL), it may be deposited on the walls of blood vessels. These deposits, termed plaques, can build up, causing vessel walls to become more rigid, and may eventually narrow the openings of blood vessels, constricting the flow of blood.
• A higher level of blood HDL-C is usually associated with a lower risk of developing plaques, lowering the risk of heart attack or stroke.

TAT: Same day

Pre-Test Information:

• Minimum 12 hours fasting is mandatory

Test Type: Serum

Test Description:

• Why Get Tested?
• To determine your risk of developing heart disease; to monitor effectiveness of lipid-lowering therapy
• When To Get Tested?
• Screening: as part of a health exam with a lipid profile; every four to six years in adults with no risk factors for heart disease; youth should be tested at least once between the ages of 9 and 11 and once again between the ages of 17 and 21
• Monitoring: may be done more frequently and at regular intervals when risk factors for heart disease are present, when prior results showed high risk levels, and/or when undergoing treatment for unhealthy lipid levels
• Test Preparation Needed?
• Laboratory tests for LDL-C typically require a 9 to 12-hour fast; only water is permitted. Your healthcare practitioner may decide that you may be tested without fasting. Follow any instructions you are given and tell the person drawing your blood whether or not you have fasted. For youths without risk factors, testing may be done without fasting.
• What is being tested?
• Low-density lipoprotein (LDL cholesterol, LDL-C) is one type of lipoprotein that carries cholesterol in the blood. LDL-C consists mostly of cholesterol and similar substances with a small amount of protein. Most often, this test involves using a formula to calculate the amount of LDL-C in blood based on results of a lipid profile. Occasionally, LDL-C is measured directly.
• Monitoring and maintaining healthy levels of lipids is important for staying healthy. Eating too much of foods that are high in saturated fats and trans unsaturated fats (trans fats) or having an inherited predisposition can result in a high level of cholesterol in the blood. The extra cholesterol may be deposited in plaques on the walls of blood vessels. Plaques can narrow or eventually block the opening of blood vessels, leading to hardening of the arteries (atherosclerosis) and increased risk of numerous health problems, including heart disease and stroke.
• LDL-C is considered to be undesirable and is often called "bad" cholesterol because it deposits excess cholesterol in blood vessel walls and contributes to hardening of the arteries and heart disease. This is in contrast to high-density lipoproteins (HDL) that tend to transport cholesterol from the arteries to the liver. HDL is thought to protect against heart disease and so it is often called "good" cholesterol.
• The LDL-C test can help determine an individual's risk of heart disease and help guide decisions about what treatment may be best if the person is at borderline or high risk. The results are considered along with other known risk factors of heart disease to develop a plan of treatment and follow up. Treatment options may involve lifestyle changes such as diet and exercise or lipid-lowering medications such as statins.
• The results of a standard lipid profile, which consists of total cholesterol, HDL-C, and triglycerides, are usually used to calculate the amount of LDL-C in the blood. The results are entered into a formula that calculates the amount of cholesterol present in LDL (see below). In most cases, the formula provides a good estimate of the LDL-C, but it becomes less accurate with increased triglyceride levels when, for example, a person has not fasted before having blood drawn. In this situation, the only way to accurately determine LDL-C is to measure it directly. Direct measurement of LDL-C is less affected by triglycerides and can be used when an individual is not fasting or has significantly elevated triglycerides (above 400 mg/dL).

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To help assess the risk of developing heart disease
• When To Get Tested?
• As part of a lipid profile during a regular medical exam (at least once every 4-6 years for adults; for children, at least once between the ages of 9 and 11 and again between the ages of 17 and 21); more frequently if you have risk factors for heart disease
• Test Preparation Needed?
• Current standards recommend that testing be done when you are fasting. For 9 to 12 hours before the test, only water is permitted. In addition, alcohol should not be consumed for 24 hours just before the test. Your healthcare practitioner may decide that you may be tested without fasting. Follow any instructions you are given and tell the person drawing your blood whether or not you have fasted.
• What is being tested?
• Very low-density lipoprotein (VLDL, VLDL-C) is one of the four major lipoprotein particles. The other three are high-density lipoprotein (HDL), low-density lipoprotein (LDL), and chylomicrons. Each particle contains a mixture of cholesterol, triglyceride, and protein, but in varying amounts unique to each type of particle. LDL contains the highest amount of cholesterol. HDL contains the highest amount of protein. VLDL and chylomicrons contain the highest amount of triglyceride.
• VLDL particles are released into the blood by the liver and circulate in the bloodstream, ultimately being converted into LDL as they lose triglyceride, having carried it to other parts of the body. According to the National Heart, Lung and Blood Institute's National Cholesterol Education Program Guidelines ATP III, there is growing evidence that VLDL plays an important role in atherogenesis, in which plaques form on the interior walls of arteries, narrowing these passageways and restricting blood flow, which can lead to heart disease and increase the risk of stroke.
• Currently, direct measurement of VLDL cholesterol requires specialized testing. However, since VLDL-C contains most of the circulating triglyceride (if a person is fasting) and since the composition of the different particles is relatively constant, it is possible to estimate the amount of VLDL-C based on the triglyceride value. To estimate VLDL-C, divide the triglyceride value by 5 if the value is in mg/dL or divide by 2.2 if the value is in mmol/L. In most cases, this formula provides a good estimate of VLDL-C.
• However, this formula becomes less accurate with increased triglyceride levels when, for example, a person has not fasted before having blood drawn. The calculation is not valid when the triglyceride level is greater than 400 mg/dl (4.5 mmol/L) because other lipoproteins are usually present. In this situation, VLDL-C may be measured directly using specialized testing.

TAT: Same day

Pre-Test Information: N/A

Test Type: Serum

Test Description:

• Why Get Tested?
• To determine if you have been exposed to and/or poisoned by certain organophosphate chemicals found in pesticides; to monitor cholinesterase levels if you work with pesticides
• Sometimes to identify individuals with inherited pseudocholinesterase deficiency before they are given anesthesia with the muscle relaxant succinylcholine or to help determine the cause of prolonged apnea after surgical anesthesia
• When To Get Tested?
• When you have symptoms of pesticide poisoning or on a regular basis when you are at risk of exposure to organophosphates, such as through work in the agriculture industry and/or frequent use of
• organophosphate insecticides
• When you or a close relative have experienced prolonged apnea and muscle paralysis after use of the drug succinylcholine for a surgical operation
• What is being tested?
• Cholinesterases are enzymes that are involved in helping the nervous system to function properly. There are two separate cholinesterase enzymes in the body: (1) acetylcholinesterase, found in red blood cells as well as in the lungs, spleen, nerve endings, and the gray matter of the brain, and (2) pseudocholinesterase (butyrylcholinesterase), found in the serum as well as the liver, muscle, pancreas, heart, and white matter of the brain. Cholinesterase tests measure the activity of these enzymes.
• Acetylcholinesterase is involved in transmission of nerve impulses by breaking down acetylcholine, a chemical that helps to transmit signals across nerve endings. A decrease in the activity of the enzyme acetylcholinesterase results in excess acetylcholine at nerve endings. This can lead to overstimulation of nerves within body tissues and organs. Pseudochlinesterase is involved in processing and metabolizing drugs.
• The two most common reasons for testing activity levels in the blood are:
• Organophosphate pesticide exposure. Insecticides containing organophosphates can inhibit cholinesterase and pseudocholinesterase activity. Symptoms can be severe with acute exposure to these pesticides or can gradually appear with chronic exposure. Absorption can occur by inhalation, ingestion, or contact with the skin. Testing red blood cell acetylcholinesterase and serum pseudocholinesterase may be done to detect acute poisoning or to monitor those with occupational exposure to these chemicals, such as farm workers or those who work with industrial chemicals.
• Inherited pseudocholinesterase deficiency. Some individuals have an inherited deficiency due to a genetic variant of the enzyme pseudocholinesterase. This enzyme is used by the body to inactivate (metabolize) succinylcholine, a muscle relaxant that is commonly used during surgery. People who have low levels or defective pseudocholinesterase may experience prolonged effects of the drug, with protracted muscle paralysis and apnea following anesthesia. In addition, those who are homozygous for genetic variants may be at greater risk of adverse effects than those who are heterozygous. Pseudocholinesterase testing can be performed prior to surgery on those with a family history of prolonged apnea after use of succinylcholine to determine if they are at risk of complications related to this drug.

TAT: Same day