Frautest candida - test for determination of thrush (yeast Candida)
Approximately 75% of women at least once in their lifetime were diagnosed vulvovaginal candidiasis (thrush), 40-50% of them suffer from repeated infections, and 5% develop chronic candidiasis. Symptoms of candidiasis: severe itching, soreness of the vagina, irritation, burning sensation, which may increase urination, copious white cheesy discharge. But we must remember that the number of infectious and noninfectious diseases can cause similar symptoms, so an accurate diagnosis more research is needed.
Now, thrush can be defined in the home, using a test Frautest candida. This test is a rapid test intended for the qualitative detection of Candida (yeast) in cervical secretions vagina. The accuracy of the method is 90%.
HOW IT WORKS
The test is based on the immune method, in which antigens of Candida in the current fluid interact with specific antibodies to Candida, coupled with the blue latex particles, forming a blue stripe.
The presence of the blue band in the test region indicates a positive result. Latex particles interact with lower test area with other specific antibodies, forming the control strip. Blue band in the control zone indicates the correctness of the test.
This test is a rapid test intended for the qualitative detection of Candida (yeast) in cervical secretions vagina at home.
Testing
1. Open the foil package, remove the test and put it on a horizontal surface.
Approximately 75% of women at least once in their lifetime were diagnosed vulvovaginal candidiasis (thrush), 40-50% of them suffer from repeated infections, and 5% develop chronic candidiasis. Symptoms of candidiasis: severe itching, soreness of the vagina, irritation, burning sensation, which may increase urination, copious white cheesy discharge. But we must remember that the number of infectious and noninfectious diseases can cause similar symptoms, so an accurate diagnosis more research is needed.
Now, thrush can be defined in the home, using a test Frautest candida. This test is a rapid test intended for the qualitative detection of Candida (yeast) in cervical secretions vagina. The accuracy of the method is 90%.
HOW IT WORKS
The test is based on the immune method, in which antigens of Candida in the current fluid interact with specific antibodies to Candida, coupled with the blue latex particles, forming a blue stripe.
The presence of the blue band in the test region indicates a positive result. Latex particles interact with lower test area with other specific antibodies, forming the control strip. Blue band in the control zone indicates the correctness of the test.
This test is a rapid test intended for the qualitative detection of Candida (yeast) in cervical secretions vagina at home.
Testing
1. Open the foil package, remove the test and put it on a horizontal surface.
2. Hold the test with one hand, the second, carefully remove foil cap covering the colored cap. WARNING! Color cap contains a liquid.
3. Open the individual package with a sterile swab applicator.
4. Enter a tampon applicator into the vagina to a depth of 2 cm Gently rotate the swab for 20 seconds. Carefully remove it from the vagina.
5. Place the swab into the opening colored cap, and rotate it for 20 seconds (Fig. 1).
6. Carefully remove the tampon applicator by pushing it on the inner wall of the colored cap. Discard the swab. WARNING! Do not leave the tampon applicator in the cap during further testing.
7. Hold the test with one hand, turn the other colored cap (Fig. 2) in the direction of the arrow (counterclockwise) rotation by a quarter to go. Deepening of the upper and lower parts of the cap must be met (Fig. 3). Then return the cap to its original position (Fig. 1).
3. Open the individual package with a sterile swab applicator.
4. Enter a tampon applicator into the vagina to a depth of 2 cm Gently rotate the swab for 20 seconds. Carefully remove it from the vagina.
5. Place the swab into the opening colored cap, and rotate it for 20 seconds (Fig. 1).
6. Carefully remove the tampon applicator by pushing it on the inner wall of the colored cap. Discard the swab. WARNING! Do not leave the tampon applicator in the cap during further testing.
7. Hold the test with one hand, turn the other colored cap (Fig. 2) in the direction of the arrow (counterclockwise) rotation by a quarter to go. Deepening of the upper and lower parts of the cap must be met (Fig. 3). Then return the cap to its original position (Fig. 1).
8. Repeat step 7 2 more times. In the final position of the deepening of the upper and lower parts of the cap must be met (Fig. 3).
9. Evaluate the results after 10 minutes, but no later than 20 minutes.
ASSESSMENT OF RESULTS
C - control zone, and T - Test Zone
Positive result
Candida is present in your discharge.
In the area of control and test there were two separate clearly visible painted blue stripes. Hue test strip may vary, but should be regarded as a positive even in the case of weak staining.
A negative result
Candida is not in your discharge.
In the control area there was a painted blue band.
Its appearance indicates adequate excreta and swabs done properly tested.
Candida is not in your discharge.
In the control area there was a painted blue band.
Its appearance indicates adequate excreta and swabs done properly tested.
An erroneous result
Does not appear colored line in the control zone.
The most common reason for lack of a control strip may be insufficient swab discharge or improper performance testing. It should repeat the test using a new test.
Does not appear colored line in the control zone.
The most common reason for lack of a control strip may be insufficient swab discharge or improper performance testing. It should repeat the test using a new test.
WARNING!
1. Upon receipt of a positive test result should seek medical attention for the appointment of appropriate treatment.
2. Upon receipt of a negative test result and the presence of the above symptoms should seek medical advice and take a smear on the other reproductive tract infections.
3. The presence of other pathogens of bacterial vaginosis: Gardnerella vaginalis, Prevotella bivia, Streptococcus A and B, Mobilincuscurtissi not affect the test result.
4. The presence of bleeding in the sample can cause false positive results, so the test during the menstrual period is not carried out.
5. Do not use test within 7 days after receiving the drug for the treatment of vaginal infections.
6. Do not use this test within 24 hours after applying the cream, gel, foam and other hygiene products.
7. If you rotate colored cap prior to the test, this test may not be used.
8. The test can be performed at any time.
9. Do not use the test after the expiration date.
10. Do not use test if the packaging has been damaged.
11. The test should remain in packaging until use.
12. To obtain the stroke, use only sterile swab applicator that comes with a set of tests.
Each individual package contains:
1. Test
2. Sterile swab applicator
3. Instruction
Manufacturer: Savyon Diagnostics Ltd., 3 Habosen Street, Ashdod, 77 610, Israel. Savion Diagnostics Ltd.., 3 Habosen Street, Ashdod, 77 610, Israel.
Registration certificate № 2010/08094 SPF of 22.10.2010g.
We invite you to visit the site www.frautest.ru, which is all the additional information about the tests FRAUTEST.
1. Upon receipt of a positive test result should seek medical attention for the appointment of appropriate treatment.
2. Upon receipt of a negative test result and the presence of the above symptoms should seek medical advice and take a smear on the other reproductive tract infections.
3. The presence of other pathogens of bacterial vaginosis: Gardnerella vaginalis, Prevotella bivia, Streptococcus A and B, Mobilincuscurtissi not affect the test result.
4. The presence of bleeding in the sample can cause false positive results, so the test during the menstrual period is not carried out.
5. Do not use test within 7 days after receiving the drug for the treatment of vaginal infections.
6. Do not use this test within 24 hours after applying the cream, gel, foam and other hygiene products.
7. If you rotate colored cap prior to the test, this test may not be used.
8. The test can be performed at any time.
9. Do not use the test after the expiration date.
10. Do not use test if the packaging has been damaged.
11. The test should remain in packaging until use.
12. To obtain the stroke, use only sterile swab applicator that comes with a set of tests.
Each individual package contains:
1. Test
2. Sterile swab applicator
3. Instruction
Manufacturer: Savyon Diagnostics Ltd., 3 Habosen Street, Ashdod, 77 610, Israel. Savion Diagnostics Ltd.., 3 Habosen Street, Ashdod, 77 610, Israel.
Registration certificate № 2010/08094 SPF of 22.10.2010g.
We invite you to visit the site www.frautest.ru, which is all the additional information about the tests FRAUTEST.