Final Sensitivity and Specificity of Different Test Combinations in Screening

Screening is a way of looking for patients who do not seem to have major medical problems. Screening tests usually include several phases. In double phase screening, one test is to find the potential patient, and then another test is to prove the disease in those patients. The combination of these two tests is important and can be either "in series", where running or not running the second test depends on the results of the first one, or "in parallel" where the second test is independently performed regardless of what the first test result is. In this article we compared the combined tests based on their final sensitivity and specificity using mathematical analysis to determine how the order of different tests with different sensitivity, and specificity can impact the final specificity and sensitivity of the combined tests. We could prove that in none of the combined tests the final sensitivity and specificity is affected by the sequence of the tests, but the amount of intermediate false positive is affected, so that if the first test is more sensitive, we will have more false positives after the first test. The type of screening we choose relies on what our aim is for doing that screening, and a combination of tests should be selected, so that the selected tests are acceptable in terms of false positive but whether, to do the more sensitive test first or the more specific one, there is no difference in the final sensitivity or specificity.


Introduction
In health technology the final goal is divided into diagnosis, treatment and prevention.One of the most important objectives is the early diagnosis of the disease in the society which is collect screening.Screening is, in fact, the active way of looking for patients who do not seem to have major medical problems.It is performed via rapid laboratory tests, physical examinations or other methods (1).
Screening was defined in 1988 by the international committee of screening in England (2).Cost-benefit assessment is of a great importance in screening, and since it is usually implanted in large scale, it can have both benefits and also considerable costs to the society.This is true especially for the important diseases in the health care system.
Screening is performed for all or for those at high risk.Screening is done for diseases which are serious, curable and have a preclinical period during which early diagnosis is possible.Also, the window's period before the triggering agent can lead to the illness should be long enough, early treatment has to give the way to better prognosis, and the prevalence of the disease must be high.
On the other hand, a good screening test should have good sensitivity and specificity, it must be rather safe, tolerable for the patient, and also impose low cost on the individual and the society.(3) If a patient has the characteristics mentioned above, and a screening test has the required sensitivity and specificity, we still face a question: Whether to perform the screening or not to implant, it needs quite a lot of investigations and researches to prove the effectiveness of the screening in the populations.These researches should be in the form of a large clinical trials; however, the studies done are very limited and with a lots of ambiguities in the forms of cohort or case-control studies.
There are many problems in screening; one of which is the false positive.False positive can lead to significant economic and psychological damage to the individual and society even if its rate is very low; because screening is usually done in large scale.(4) Screening tests can include only one test, where a test with high sensitivity and specificity is performed, but they usually include several phases where one test is run to find the presumed patient, and then another test is done to prove the illness in that patient.In double-phase screening, it is very important how to combine the diagnostic tests.
In most text books and articles in epidemiology, it has been recommended to use the easier test for the first phase in the beginning, and then move on to a more accurate one with higher sensitivity, and specificity for those diagnosed positive in the first test (5).In this article, we aim for comparing the mixed tests by mathematical analysis based on final sensitivity and specificity, and to verify the order of the tests with different sensitivities and specificities, and their impact on the final specificity and sensitivity of the mixed test.
Mixed tests are performed either "in series" where the result of the first test determines whether to run the second test or not; or "in parallel" where, despite in series where the sequence of the tests is important, the second test is independent of the first one, and independently performed regardless of what the first test result is, and both tests are done at the same time.
The second aspect of mixed tests is "AND "or "OR".In "AND" form, we consider the screening result positive if the result of both of the tests is positive.In "OR" form, only the positive result of one test is enough to consider the screening test positive.

A SAND B
In this test, test A is performed first and test B in only run if test A is positive, and the final positive patients are those who have both test A and test B are positive.

Now we calculate sensitivity and specificity of A SAND B in an accumulative way:
If we have a population of N people where the prevalence of the disease for screening is P, n= N×P, N is the number of patients in this society.For screening, we use the combination of test A "AND" B in series.In this way, snA is test A sensitivity, and spA is test A specificity, and test B has also snB (sensitivity), and spB (specificity).

In this test, running test B relies on test A result, and we consider an individual with both test A & test B positive results as a patient.
If test A is performed first, the number of people diagnosed as patients by this test is n×snA.On the other hand, healthy individuals diagnosed mistakenly as patients by this test is: (N-n)×(1-spA).These people enter the second phase of screening having been positive for test A, on the other hand (N-n) ×spA are the healthy people correctly diagnosed as healthy, and n-(n × snA) are the patients having the illness but incorrectly diagnosed as healthy.These patients are the ones with final negative screening results.Sensitivity is the proportion of real patients who have been correctly diagnosed as patients: Specificity is the proportion of healthy individuals who have been correctly considered healthy.Sensitivity is the proportion of the real patients who have been correctly diagnosed as patients: Specificity is the proportion of the healthy individuals who have been correctly considered healthy.
So far, we conclude that if only sensitivity and specificity are to be considered, when there are two tests with different sensitivities and specificities, it does not make any difference if we do any of the two tests first if the two tests are "in series" and "AND" form.

A SOR B
This method is a series mixture of two tests A "OR" B, and we only need one of the tests positive to consider the whole screening test as positive.
If test A is performed, the people diagnosed as patients by this test are n × snA.On the other hand, the healthy individuals diagnosed incorrectly as patients by the test is (N-n) × (1-spA), and because of "OR" of A and B tests in this method, they will be categorized as final positives in the screening.On the other hand, (N-n) × spAare of the healthy people correctly diagnosed and n(1-snA) of the patients will be incorrectly diagnosed as healthy, and enter the second phase of screening.
Of those false negative ones in test A, n(1-spA) × snB will be correctly diagnosed as  N-n) spA] × (1-spB) will be incorrectly diagnosed as false positive, and these will be considered on the final positives in the screening.Thus, n(1-snB) × snA of those false negatives have been identified; and of those real negative ones [(N-n) spB] × spA will have a test B negative result and will be in the final negatives in the screening.
Hence, [n ×snA + n (1-snA)] ×snB is the real positive number, and is the false positives of this screening.
Finally, sensitivity is the real patients which are the proportion of real positives to all patients: Specificity is the proportion of healthy individuals correctly diagnosed as healthy: Of those false negative ones in test B, n× (1-spB) × snA will be correctly diagnosed as positive in test A, and of those true negative ones [(N-n) ×spB] × (1-spA) will be incorrectly diagnosed as false positive, and these will be considered as final positives in the screening.
Therefore, n (1-snA) × snB of those false negatives have been identified; and of those true negative ones [ (N-n) spA ] × spB will have a test B negative result, and will be in the final negatives in the screening.Therefore, true positive of the screening is [n× snB + n(1-snB)] ×snA, and the false positives of this screening is The real negative ones are (N-n) × spB×spA and false negative ones is n× (1-snB)(1-snA).Finally, sensitivity is the real patient which is the proportion of real positives to all patients: Specificity is the proportion of healthy; individuals correctly diagnosed as healthy: The results are similar to the previous method.It means in the "OR" method there is no difference in the final sensitivity and specificity of the screening test if we do either test first.
] and the sensitivity of this mixed screening is the proportion of real positives diagnosed by this screening to all patients in society: Specificity is the proportion of real negatives of the screening to the healthy individuals of the population: positives after the first test.Therefore, the type of the screening we choose relies on what our aim is for doing that screening.

Conclusion
Combined tests are either "in series", where performing or not performing the second test depends on the first test result; or "in parallel" where, despite series form, the second test is independent of the first one and both tests are run concomitantly.
In the screenings, it is recommended to use "AND" methods if the aim is to enhance the final sensitivity of the test.However, "OR" methods are usually used if the target is to enhance the final specificity of the test.In none of the "series" or "parallel" mixtures, the sequence of the tests does not affect its final sensitivity and specificity.So,it does not make any difference whether to do the more sensitive test first or the more specific one.
But the rate of intermediate false positive results of these combinations is affected by the sequence of the tests, and if the first test is more sensitive, the false positive rate after the first test will be higher.
Therefore, choosing the type of screening test depends on the aim of that screening, and a combination of the tests should be selected, so that the test proves acceptable in terms of false positive rates; the harm to the patient coursed by the test, and also the cost imposed on the society.However, whether to do the more sensitive or specific test first, does not impact the final sensitivity and specificity of the screening.
_______________Shahram Yazdani, Atousa Iranpour Asli, Arash Iranpour Asli, Parvin Sarbakhsh and Saman Salemi (2014), JMED Research, DOI: 10.5171/2014.558523Taking into account the mentioned items, we face at least seven mixed forms: Series mixture of A "AND" B (A SAND B) Series mixture of B "AND" A (B SAND A) Series mixture of A "OR" B (A SOR B) Series mixture of B "OR" A (B SOR A) Parallel mixture of A "OR" B (A por B) Parallel mixture of B "OR" A (B por A) Parallel mixture of A "AND" B (A PAND B) Now we verify each of the methods individually to find out how different methods can affect the find sensitivity and specificity.
Those positive A test patients enter the second phase for test B. (n×snA)×snB are the real positive ones, and [(N-n)(1-spA)] × (1-spB) are the false positive ones of test A who will be diagnosed as patients by test B. Also, in test B, (n × snA) -[(n × snA) × snB] are those real first test positive ones who will be incorrectly diagnosed as healthy; and [(N-n) × (1-spA)] × snB] are those false positive ones of test A who will be correctly diagnosed as healthy, and will be categorized as negative in the final screening result .Finally, (n× snA) × snBare the real positive ones, and [(N-n) × (1-spA)] × (1-spB) are the final false positive ones in the screening.Also, [(N-n) × spA] + [(N-n) × (1-spA)] × spB are the real negative ones and [n-(n× snA)] + [(n× snA)(1-snB)] are those with false negative results.
diagnosed incorrectly as patients by this test are: (N-n) × (1-spB).These people entered the second phase of screening having been positive for test B. On the other hand, (N-n) × spB are the healthy people correctly diagnosed as healthy, and n-(n× snB) are the patients with the illness but incorrectly diagnosed as healthy.These patients are the ones with final negative screening results.Those positive B test people enter the second phase for test A. (n× snB) × snA are the real positive ones, and [(N-n)(1 -spB)] × (1 -spA) are the false positive ones of test B, who will be diagnosed as patients by test A. Also in test A, (n × snB)-[(n× snB) × snA] are those real first test positive ones who will be incorrectly diagnosed as healthy; and [(N-n) × (1 -spB)] × spA are those false positive ones of test B who will be correctly diagnosed as healthy, and will be categorized as negative in the final screening result.Finally, (n × snB) × snA are the real positive ones and[(N-n) (1 -spB)] × (1 -spA) are the final false positive ones in the screening._______________ Shahram Yazdani, Atousa Iranpour Asli, Arash Iranpour Asli, Parvin Sarbakhsh and Saman Salemi (2014), JMED Research, DOI: 10.5171/2014.558523Also, [(N-n) × spB] + [(N-n) × (1-spB)] × spA are the real negative ones, and [n-(n×snB)]+[(n×snB)(1-snA)] are those with false negative results.

Figure 2 :
Figure 2: ShowsExpressions in this Test, Test B is Performed First, and Test A is Only Performed if Test B Result is Positive, and Final Positive Patients are Those Who Have Both,Test B and Test A arePositive.

Figure 3 :
Figure 3: Showsthe Expressions in this Method as a Series Mixture of Two Tests A "OR" B, and We Only Need One of the Tests Positive to Consider the Whole Screening Test as Positive B SOR A This method is a mixture of two tests B "OR" A. and if only one test is positive or both tests are positive, we consider the individual as patient.If test B is performed first, true positives are n × snB.On the other hand, the healthy

Figure 4 :
Figure 4: Showsthat the Expressions inthis Method areMixture of Two Tests B "OR" A. and if Only One Test Is Positive or Both Tests are Positive, We Consider the Individual as a Patient A PAND B = B PAND A parallel mixture of two tests: In the series screening, performing the second test depends on the result of the first

Figure 5 :
Figure 5: Shows that the Expressionsin the Series Screening, Performing the Second Test Depend on the Result of the First Test, while in Parallel Mixture the Two Tests are Performedat the Same Time A POR B = B POR A The Parallel mixture of two tests, if the two tests are performed at the same time, and one or both of the tests are positive, the

Figure 1: ShowsExpressions in this Test, Test A is Performed First and Test B in Only Run if Test A is Positive, and the Final Positive Patients are Those Who Have Both the Test A and Test B are Positive.
_______________Shahram Yazdani, Atousa Iranpour Asli, Arash Iranpour Asli, Parvin Sarbakhsh and Saman Salemi (2014), JMED Research, DOI: 10.5171/2014.558523B SANB A In this method, test B is performed first, and test A is only performed if test B result is positive, and the final positive patients are those who have both test B and test A are positive.