Blood-test Sentence Examples
To find out if you've got HIV you need to have a blood test.
We had to have a repeat blood test following this appt as my blood tests showed I had hugh FSH levels.
Your blood test results were unusual.
If you are tired and draggy feeling, go in and get a blood test to find out.
It was all a bit hectic at the end... would they pass their second blood test?Advertisement
The helpline will invite them to attend a hospital clinic or their GP for a blood test.
You need a blood test before starting a statin, and about six weeks later.
A simple blood test can tell you if you have H. pylori.
The serology test is accurate but an animal cannot be declared free until a negative blood test 6 months after arrival.
They are usually diagnosed through a physical exam, although some pediatricians prefer to use a blood test to make any further diagnoses.Advertisement
The vet will be able to determine if it is hormonal with a simple blood test.
Since this disease mimics so many other ailments, the best way to quickly and correctly diagnose it is through a blood test.
A blood test can be administered to test for this disease.
It's important not to storm into the teen's room and start going through his or her clothes (at least while your teen is in the room) or dragging the teen off to the doctor for a blood test on suspicion drug use.
So now every year, I give them a "titers" blood test.Advertisement
Once the dogs have all of their antibodies, they then do the "titers" blood test to check the dogs' antibodies levels.
A blood test is available to determine if a dog has JDC.
Testing can involve anything from a simple blood test or skin punch to x-rays for joint problems.
A blood test may also be performed to check for toxic levels of the drug in the bloodstream.
A blood test is available, but it is not very reliable.Advertisement
A simple blood test at the doctor's office can alert you to possible deficiencies you have.
The low platelet count may be discovered in the course of a routine blood test.
A blood test for autoantibodies may be performed early in the diagnostic process as well as a test for antiplatelet antibodies.
An abnormal blood test might suggest leukemia; however, the diagnosis has to be confirmed by more specific tests.
In addition, there is a blood test for fifth disease, but it is generally used only for pregnant women and for people who have weakened immune systems or who suffer from blood disorders, such as sickle cell anemia.Advertisement
An inexpensive blood test can also determine the presence of antibodies to the mononucleosis virus.
Many allergists, or doctors who specialize in allergies, will do a skin-prick test followed by a blood test.
This blood test measures the level of immunoreactive trypsinogen, which is generally higher in babies with CF than those without it.
In the early 2000s, a blood test has been developed that can identify carriers of the gene for some types of albinism; a similar test during amniocentesis can diagnose some types of albinism in an unborn child.
A special type of blood test called a karyotype may be done to analyze the girl's chromosomes if the doctor suspects Turner's syndrome or another genetic disorder.
Women who are carriers of the defective gene can also be identified by a blood test.
Gaucher disease may be suspected, based on symptoms, and is confirmed with a blood test for levels of the deficient enzyme.
Carriers of the Tay-Sachs related gene can be identified with a blood test.
A simple blood test can help determine if the infant has allergies to certain foods and other substances.
As children often outgrow allergies, they should have a second blood test to see if the allergies persist.
Laboratory blood test looks for the virus or to confirm the presence of antibodies that fight the virus.
The majority of children diagnosed in childhood are type 1, but if blood test results indicate prediabetes and a child is significantly overweight and has a history of type 2 diabetes in her family, type 2 is a possibility.
Children born into families with a history of Wilson's disease should have a blood test for the disease at some point in their second year of life, before symptoms of the disease develop.
A blood test that measures levels of the enzyme lactate dehydrogenase (LDH) can help predict the likelihood of a specific patient's survival.
The only sure way to confirm a case of rubella is by isolating the virus with a blood test or in a laboratory culture.
A blood test is done to check for rubella antibodies.
A blood test can be used either to confirm a recent infection (IgG and IgM) or determine whether a person has immunity to rubella (IgG only).
A blood test will be performed prior to surgery in order to determine the child's blood type, clotting time, and complete blood count.
If mononucleosis is suspected, a physician will typically conduct a physical examination, including a "Monospot" antibody blood test that can indicate the presence of proteins or antibodies produced in response to infection with the EBV.
A blood test for Bartonella henselae may be ordered to confirm the doctor's diagnosis.
Many doctors, however, skip this test if the child has the typical heliotrope rash, shows signs of muscle weakness during the physical examination, and has high muscle enzyme levels in the blood test.
If nephrotic syndrome is present, the urine test may indicate an abnormally large quantity of protein, and the blood test may show abnormally high levels of cholesterol.
If the diagnosis is still questionable, a genetic blood test can reveal the existence of certain substances in people who have a tendency to develop narcolepsy.
In some cases, however, the doctor may order a blood test to rule out Wilson's disease or other metabolic disorders, or order a throat culture if the child has recently had strep throat.
If the doctor suspects that the child has a PANDAS disorder, he or she may order a blood test to measure the level of antibodies against group A streptococci.
If the blood test is positive, the baby should receive vaccine along with hepatitis B immune globulin (HBIG) at birth.
Episodes of hypoglycemia in children and adolescents with diabetes can be confirmed with a blood test on a home blood glucose monitor.
A blood test may also be done to rule out a more serious infection or condition and to check the white blood cell count to see if the body is responding to the infection.
Diagnosis of a pervasive developmental disorder is difficult because there is no specific medical test, like a blood test or imaging test that can confirm the diagnosis.
Without a blood test for serum iron, there is no way to differentiate these causes.
If celiac disease is suspected, based on symptoms, physical appearance, or delayed growth, a blood test should be ordered.
The doctor will order a blood test to screen the child for an immunodeficiency disorder.
The diagnosis of a vitamin deficiency usually involves a blood test.
An overnight fast is usually recommended as preparation prior to withdrawal of the blood test so that vitamin-fortified foods do not affect the test results.
In the event that rheumatic fever is suspected, the doctor does a blood test.
This blood test measures the amount of CO that is bound to hemoglobin in the body.
If the levels are low, the physician will likely repeat the blood test to confirm the diagnosis.
The blood test is extremely accurate, but some doctors doubt its ability to detect mild hypothyroidism.
Hepatitis A symptoms often go unrecognized because they are not specific to hepatitis A, thus a blood test (IgM anti-HAV) is required to diagnose HAV infection.
The alpha-fetoprotein (AFP) test is a blood test that is performed during pregnancy to screen the fetus for certain conditions; it is also used to screen for certain diseases in infants and children.
Other than making sure the bleeding stops from the needle puncture site and watching for any signs of infection at the needle site, there is no specific aftercare involved with this blood test.
A blood test for anemia may be performed at this visit if it was not done at the nine-month exam.
A simple blood test can be performed to determine the amount of thyroid hormone in the patient's blood.
Hepatitis B can be identified through a blood test for the hepatitis B surface antigen (HBsAg) in pregnant women.
Human immunodeficiency virus (HIV) can be detected using a blood test and is part of most prenatal screening programs.
Pregnant women are usually tested for syphilis as part of the prenatal screening, generally with a blood test.
Chromosome analysis provides the definitive diagnosis of cri du chat syndrome and can be performed from a blood test.
A stair-stepping test may be used to evaluate stamina, but a blood test is required to diagnose iron deficiency.
In February 1999 the Food and Drug Administration (FDA) approved a new blood test for Lyme disease called PreVue.
A positive result from the PreVue test is confirmed by a second blood test known as the Western blot, which must be done in a laboratory.
The amount of antibody can be measured by a blood test that will show how sensitive the patient is to a particular allergen.
Mothers with acute or chronic infectious hepatitis B can be identified by a blood test for HBsAg.
A child's immune response to either hepatitis B infection or to HBV can be measured by a blood test for antibodies to HBsAg (anti-HBs).
If parents receive a call from a healthcare provider saying the screening test indicates possible galactosemia, they should promptly stop milk products and have a blood test done for galactosemia through their doctor.
If a blood test reveals low hemoglobin, supplementation with iron may be recommended.
Alpha fetoprotein test-A screening blood test that can be done after the sixteenth week of pregnancy to evaluate the possibility of spina bifida and other neural tube defects in the fetus.
However, a doctor may do a throat culture or blood test to rule out a secondary infection.
In addition to a general physical examination, the doctor may order a blood test to look for the presence of elevated IgE levels in the blood serum.
A bilirubin test is a diagnostic blood test performed to measure levels of bile pigment in an individual's blood serum and to help evaluate liver function.
A high level of lead in the blood can be detected with a simple blood test.
A blood test is more sensitive than a urine test, allowing your doctor to easily determine if you are pregnant.
Yes. Your doctor may be able to perform a blood test that can pick up hCG amounts earlier than urine tests.
In fact, if you were to take a home pregnancy test, which indicated a negative, but you still felt like you were pregnant, a blood test may actually show a positive.
A blood test for the pregnancy hormone human chorionic gonadotropin (HGC) will probably be abnormal.
The only way you can be absolutely sure is through a blood test.
A pregnancy blood test is the best test to truly confirm that you are pregnant.
A pregnancy blood test can measure not just the presence of HCG, but the amount of it in your blood.
Depending on your genetic background, you and your partner may also want to have a pregnancy blood test for genetic problems such as sickle cell disease or Tay-Sachs.
The triple screen is a pregnancy blood test that's done around the 15th to 18th week.
He/she can schedule a blood test to clear up any confusion.
A simple blood test will be able to determine the presence of this condition.
After an hour, you'll have a blood test to check your glucose level.
Research is ongoing in a hope that there will one day be a blood test that will be able to identify fetal cells to determine the presence of genetic abnormality without the need for an invasive procedure that carries undesirable risk.
During the physical examination, an obstetrician determines an approximate date of conception using your history and a blood test of hormone levels.
Two tests are done during the screening--a blood test and an ultrasound.
The blood test given during the first trimester screening is for chromosomal abnormalities in the baby, including Down's Syndrome (trisomy 21), Edwards Syndrome (trisomy 18), skeletal defects, or heart defects.
A cancer antigen 125 (CA 125) is a blood test that can detect health conditions, including endometriosis.
Your doctor will do a blood test to find out the level of hCG in your blood.
The results of this blood test are the official and most accurate sign you are pregnant.
Typically, the woman will have a blood test to determine if she has become pregnant.
A home pregnancy test is a urine test, while a pregnancy test performed in a doctor's office is often a blood test.
If you visit a doctor's office, a blood test can detect pregnancy seven to 12 days from conception.
Your healthcare provider can conduct a blood test that can pick up lower levels of hCG than what can be evaluated by a home pregnancy test.
If you get the result you've been hoping for, your doctor will confirm the pregnancy with a blood test and get you started with your prenatal care.
You may include additional supplementation with doctor's recommendation, but it's wise to have a blood test done to determine your current vitamin D status and seek guidance to develop a supplement regimen.
If you're concerned about vitamin deficiency, don't take matters into your own hands and fumble blindly -- talk to your doctor and get a blood test.
If you are exhibiting any of the above symptoms, your doctor can do a simple serum blood test to check for vitamin D deficiency.
There are many over-the-counter vitamin deficiency tests available on the market, but only a blood test run by your doctor will tell you for sure if you have a vitamin deficiency.
The only way to tell for sure whether or not you have a vitamin D deficiency is to visit your doctor and get a simple blood test.
Doctors can test vitamin D levels through a simple blood test and assess whether or not you have enough or if your levels are too low.
Additional supplementation may be done upon a doctor's recommendation but it's wise to have a blood test done to determine your current vitamin D status, and seek guidance to develop a supplement regimen.
If you fit into any of the above populations or suspect you may be deficient in vitamin D, it is possible to get your vitamin D levels tested through a simple blood test.
A simple blood test may reveal whether or not you are deficient in this essential prohormone.
The only sure way to tell if you are deficient is through a simple blood test.
A simple blood test will diagnose the disease based on the presence of certain antibodies.
This is a simple blood test that checks for the presence of gliadin antibodies in your bloodstream.
Beginning an elimination diet before testing could cause a false negative result and delay your treatment process.The test is carried out like any other blood test.
A simple blood test will reveal MECP2 mutation, but this mutation is also seen in other types of development disorders.
Doctors cannot make a diagnosis of the syndrome just from this blood test.
A blood test can identify when high levels of antibodies are present in the blood stream, which is a strong indicator of the disorder.
If you're really interested in having your testosterone levels checked, ask your doctor if you can undergo a blood test immediately before and after your exercise routine.