SCREEN TEST HORMONE HCG PREGNANCY IN URINE SCREEN TEST HCG 2 PIECES
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912359231
8059015832832
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SCREEN TEST HORMONE HCG PREGNANCY IN URINE SCREEN TEST HCG 2 PIECES
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8059015832832
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Descriptive sheet
9 SCREEN
PREGNANCY TEST
ultra-sensitive
9
SCREEN
MOM TEST
PREGNANCY TESTultra-sensitive
Description
The hCG Rapid Pregnancy Test is a rapid, lateral flow, midstream immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine to aid in the diagnosis of pregnancy.
The test uses a combination of antibodies including monoclonal hCG to selectively detect elevated levels of hCG.
The test is performed by pouring urine onto the hydrophilic stick and obtaining the result based on the colored lines.
Precautions
Please read all information before taking the test.
1. Do not use beyond the expiration date printed on the sealed package.
2. Store in a dry place at 2-30°C or 35.6-86°F. Do not freeze.
3. Do not use if package is opened or damaged.
4. Keep out of reach of children.
5. For in vitro diagnostic use only. Not for internal use.
6. Do not open the sealed test package until you are ready to perform the test.
7. The used test should be disposed of according to local regulations.
How to use
1. Remove the test from the sealed pouch and perform it immediately within one hour.
2. Remove the test cap, then urinate directly on it or immerse it in a urine specimen collected in a clean container for at least 15 seconds.
3. Place the cap back on the test, then place everything on a clean, flat surface and start the timer immediately.
4. Wait 3 minutes to read the result; do not wait more than 10 minutes.
Reading the results
POSITIVE: Two distinct colored lines appear. One should be in the control region (C) and the other in the test region (T). One line may be fainter than the other; they should not match. This means you are probably pregnant.
NEGATIVE: A line appears in the control region (C). No line appears in the test region (T). This means you are probably not pregnant.
NULL: The result is null if no line appears in the control region (C), even if a faint line appears in the test region (T). The test must be repeated with a new device.
Limits
There is a possibility that this midstream test may produce false results. Consult your healthcare provider before making any medical decisions.
1. Drugs that contain hCG (such as Pregnyl, Profasi, Pergonal, APL) may produce a false positive result. Alcohol, oral contraceptives, pain relievers, antibiotics, or hormone therapies that do not contain hCG should not affect the test.
2. Very dilute urine samples, as indicated by a low specific gravity, may not contain representative levels of hCG. If pregnancy is still suspected, a new early morning urine sample should be collected 48 hours later and tested.
3. Very low levels of hCG (less than 50mIU/ml) are present in urine samples immediately after fertilization. However, since a large number of pregnancies end in the first trimester due to natural causes, a weak positive test result should be reconfirmed by testing a new early morning urine sample 48 hours later.
4. This test may give false positive results. A number of conditions other than pregnancy, including gestational trophoblastic disease and some non-trophoblastic neoplasms, including testicular, prostate, breast and lung cancers, cause elevated hCG levels2,3. Therefore, the presence of hCG in urine should not be used to diagnose pregnancy unless these conditions are excluded.
5. This test may produce false negative results. False negative results may occur when hCG levels are below the sensitivity level of the test. If pregnancy is still suspected, a new early morning urine sample should be collected 48 hours later and tested. If pregnancy is suspected but the test continues to produce negative results, consult a doctor for further diagnosis.
6. This test provides a presumptive diagnosis of pregnancy. A confirmatory diagnosis should be made only by a physician, after evaluating all clinical and laboratory tests.
Format
Case containing 2 pieces.
BIBLIOGRAPHY
1. Steier JA, P Bergsjo, OL Myking Human chorionic gonadotropin in maternal plasma after induced abortion, spontaneous abortion and removed ectopic pregnancy, Obstet. Gynecol.1984; 64(3): 391-394
2. Dawood MY, BB Saxena, R Landesman Human chorionic gonadotropin and its subunits inhydatidiform mole and choriocarcinoma, Obstet. Gynecol. 1977; 50(2): 172-181
3. Braunstein GD, JL Vaitukaitis, PP Carbone, GT Ross “Ectopic production of human chorionic gonadotropin by neoplasms”, Ann. Intern Med. 1973; 78(1): 39-45
The hCG Rapid Pregnancy Test is a rapid, lateral flow, midstream immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine to aid in the diagnosis of pregnancy.
The test uses a combination of antibodies including monoclonal hCG to selectively detect elevated levels of hCG.
The test is performed by pouring urine onto the hydrophilic stick and obtaining the result based on the colored lines.
Precautions
Please read all information before taking the test.
1. Do not use beyond the expiration date printed on the sealed package.
2. Store in a dry place at 2-30°C or 35.6-86°F. Do not freeze.
3. Do not use if package is opened or damaged.
4. Keep out of reach of children.
5. For in vitro diagnostic use only. Not for internal use.
6. Do not open the sealed test package until you are ready to perform the test.
7. The used test should be disposed of according to local regulations.
How to use
1. Remove the test from the sealed pouch and perform it immediately within one hour.
2. Remove the test cap, then urinate directly on it or immerse it in a urine specimen collected in a clean container for at least 15 seconds.
3. Place the cap back on the test, then place everything on a clean, flat surface and start the timer immediately.
4. Wait 3 minutes to read the result; do not wait more than 10 minutes.
Reading the results
POSITIVE: Two distinct colored lines appear. One should be in the control region (C) and the other in the test region (T). One line may be fainter than the other; they should not match. This means you are probably pregnant.
NEGATIVE: A line appears in the control region (C). No line appears in the test region (T). This means you are probably not pregnant.
NULL: The result is null if no line appears in the control region (C), even if a faint line appears in the test region (T). The test must be repeated with a new device.
Limits
There is a possibility that this midstream test may produce false results. Consult your healthcare provider before making any medical decisions.
1. Drugs that contain hCG (such as Pregnyl, Profasi, Pergonal, APL) may produce a false positive result. Alcohol, oral contraceptives, pain relievers, antibiotics, or hormone therapies that do not contain hCG should not affect the test.
2. Very dilute urine samples, as indicated by a low specific gravity, may not contain representative levels of hCG. If pregnancy is still suspected, a new early morning urine sample should be collected 48 hours later and tested.
3. Very low levels of hCG (less than 50mIU/ml) are present in urine samples immediately after fertilization. However, since a large number of pregnancies end in the first trimester due to natural causes, a weak positive test result should be reconfirmed by testing a new early morning urine sample 48 hours later.
4. This test may give false positive results. A number of conditions other than pregnancy, including gestational trophoblastic disease and some non-trophoblastic neoplasms, including testicular, prostate, breast and lung cancers, cause elevated hCG levels2,3. Therefore, the presence of hCG in urine should not be used to diagnose pregnancy unless these conditions are excluded.
5. This test may produce false negative results. False negative results may occur when hCG levels are below the sensitivity level of the test. If pregnancy is still suspected, a new early morning urine sample should be collected 48 hours later and tested. If pregnancy is suspected but the test continues to produce negative results, consult a doctor for further diagnosis.
6. This test provides a presumptive diagnosis of pregnancy. A confirmatory diagnosis should be made only by a physician, after evaluating all clinical and laboratory tests.
Format
Case containing 2 pieces.
BIBLIOGRAPHY
1. Steier JA, P Bergsjo, OL Myking Human chorionic gonadotropin in maternal plasma after induced abortion, spontaneous abortion and removed ectopic pregnancy, Obstet. Gynecol.1984; 64(3): 391-394
2. Dawood MY, BB Saxena, R Landesman Human chorionic gonadotropin and its subunits inhydatidiform mole and choriocarcinoma, Obstet. Gynecol. 1977; 50(2): 172-181
3. Braunstein GD, JL Vaitukaitis, PP Carbone, GT Ross “Ectopic production of human chorionic gonadotropin by neoplasms”, Ann. Intern Med. 1973; 78(1): 39-45
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