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Purpose of investigation: Difference between revisions
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* Evaluation of prognosis | * Evaluation of prognosis | ||
** Information regarding the likely outcome of the disease | ** Information regarding the likely outcome of the disease | ||
== Features of investigations == | |||
Any single test or investigation has a certain features which are important to know about, like sensitivity. | |||
=== True and false positive and negative === | |||
When researching a certain test's characteristics and usefulness in diagnosing a certain disorder, one would perform the test on both healthy people and people with the disorder. A good test will be positive in most people with the disorder and negative in most people without the disorder. However, because no test is perfect, the test will be negative in some people with the disorder, and it will be positive in some people without the disorder. | |||
After performing the test on a number of subjects, each subject will be put into one category: | |||
* True positives (TP) - those who have the disorder and tested positive with the test | |||
* False positives (FP) - those without the disorder but who tested positive anyway | |||
* True negatives (TN) - those without the disorder and who tested negative | |||
* False negatives (FN) - those with the disorder but who tested negative anyway | |||
The best tests have as few false positives and false negatives as possible. | |||
=== Sensitivity === | |||
For a given test and illness, sensitivity refers to the proportion of sick people who are tested that produce a positive test result. In terms of the above, in a certain population, sensitivity refers to the ratio of how many people are True Positives of those who have the disorder (True Positives + False Negatives). | |||
A perfectly sensitive test is 100% sensitive, meaning that 100% of tested sick people will test positive, meaning that no sick people will test negative. Few tests are 100% sensitive, and in real-life, most test which are regarded as highly sensitive have sensitivities around 95%. | |||
An example of a highly sensitive test is measuring [[D-dimer]] in suspected [[venous thromboembolism]], which has a sensitivity of 95%. | |||
An example of a test which is not sensitive is [[chest radiography]] in suspected [[lung cancer]], which has a sensitivity of approximately 90%. | |||
The sensitivity of a test is not affected by the prevalence of the disease in the tested population. | |||
=== Specificity === | |||
For a given test and illness, specificity refers to the proportion of healthy people who are tested that produce a negative test result. In terms of the above, in a certain population, specificity refers to the ratio of how many people are True Negatives of those who do not have the disorder (True Negatives + False Positives). | |||
A perfectly specific test is 100% specific, meaning that 100% of tested healthy people will test negative, meaning that no healthy people will test positive. Few tests are 100% specific, and in real-life, most test which are regarded as highly specific have specificities around 95%. | |||
An example of a highly specific test is measuring [[Anti-tissue glutaminase antibody|anti-tissue glutaminase antibodies]] in suspected [[coeliac disease]], which has a specificity of 95%. | |||
An example of a test with low specificity is measuring [[PSA]] in suspected [[prostate cancer]], which has a specificity of 20%. | |||
The specificity of a test is not affected by the prevalence of the disease in the tested population. | |||
=== Pre-test and post-test probability === | |||
The pre-test probability refers to the probability that a patient with a certain symptom or clinical finding has a certain condition ''before'' performing a test or investigation. The pre-test probability is equal to the prevalence of people in a population who have the condition and the previously mentioned symptom or clinical finding. In asymptomatic people, the pre-test probability is the same as the prevalence of the disorder in the general population. However, if the patient has symptoms or clinical findings, they have a higher probability of having the disease than the general population. | |||
As an example, the prevalence of [[urinary tract infection]] in the general population is 11%, meaning that, if you pick a random person in the world, there is an 11% chance that they have an UTI. However, among all people with typical urinary tract infection symptoms, approximately 80% of them have urinary tract infection. As such, if a person has typical urinary tract infection symptoms, the pre-test probability of them having UTI is 80%. | |||
Likewise, the post-test probability refers to the probability that a patient with a certain symptom or clinical finding has a certain condition ''after'' performing the test or investigation. | |||
=== Positive predictive value === | |||
For a given test and illness, the positive predictive value (PPV) of a test refers to the probability that a patient has the illness if they have tested positive. Intuitively, it can be difficult to understand the difference between specificity and PPV, and I've given up trying to understand why. However, it's only important to know that the positive predictive value of a test is what's ''actually'' important for us, as it tells us more about the usefulness of a test than the test's sensitivity. | |||
In a certain population, positive predictive value refers to the ratio of how many people are True Positives of those who tested positive (True Positives + False Positives). | |||
In many cases, test with high specificity have high positive predictive value as well. I can't think of any specific examples. | |||
However, and this is important to know, the positive predictive value of a test depends not only on the test's characteristics but also the pre-test probability of the disorder, which in turn is equal to the prevalence of the disorder (if there are no symptoms). When the pre-test probability increases, the PPV increases as well. As such, even if the test is really accurate and has a high specificity and sensitivity, the test may have a low positive predictive value regardless if the prevalence is low (the disease is rare). | |||
=== Negative predictive value === | |||
For a given test and illness, the negative predictive value (NPV) of a test refers to the probability that a patient does not have the illness if they have tested negative. Like positive predictive value, the negative predictive value is important as it tells us the probability that the patient does not have the disease if they test negative. | |||
In a certain population, negative predictive value refers to the ratio of how many people are True Negatives of those who tested negative (True Negatives + False Negatives). | |||
In many cases, tests with high sensitivity have high negative predictive value as well. For example, unless the pre-test probability is high, a negative D-dimer has a close to 100% negative predictive value for venous thromboembolism. As such, patients with a low or medium pre-test probability for VTE who test negative for D-dimer have VTE ruled out. | |||
As with PPV, the negative predictive value of a test depends not only on the test's characteristics but also the pre-test probability of the disorder. However, in contrast to PPV, NPV ''decreases'' as the prevalence increases. As such, even if the test is really accurate and has a high specificity and sensitivity, the test may have a low negative predictive value regardless if the prevalence is high (the disease is common). | |||
== Value to the patient == | == Value to the patient == | ||
An investigation should have some form of value for the patient (except if done in a research setting or for epidemiological purpose, in which case the investigation has value for other patients). Common examples to consider: | An investigation should have some form of value for the patient (except if done in a research setting or for epidemiological purpose, in which case the investigation has value for other patients). The value to the patient should also weigh up for any negative consequences of the investigation. | ||
Common examples to consider: | |||
* A frail elderly patient living in an institution (like a nursing home) has a positive faecal occult blood test. The physician considers to refer them to colonoscopy, but stops to consider: how will a colonoscopy be of value to the patient? In their current state, even if the colonoscopy would show colorectal cancer, the patient would not be a candidate for any anticancer surgery or chemotherapy, so even if a diagnosis is made, nothing will change for the patient (except the stress of knowing they have cancer). In addition, colonoscopy is an invasive investigation which requires strict patient preparation, which can be difficult for a frail elderly to perform or even survive. | * A frail elderly patient living in an institution (like a nursing home) has a positive faecal occult blood test. The physician considers to refer them to colonoscopy, but stops to consider: how will a colonoscopy be of value to the patient? In their current state, even if the colonoscopy would show colorectal cancer, the patient would not be a candidate for any anticancer surgery or chemotherapy, so even if a diagnosis is made, nothing will change for the patient (except the stress of knowing they have cancer). In addition, colonoscopy is an invasive investigation which requires strict patient preparation, which can be difficult for a frail elderly to perform or even survive. | ||
** If they have colorectal cancer and it grows and eventually causes intestinal obstruction, colonoscopy may be indicated for stenting the bowel, in which case the colonoscopy would have value for the patient as palliative therapy | ** If they have colorectal cancer and it grows and eventually causes intestinal obstruction, colonoscopy may be indicated for stenting the bowel, in which case the colonoscopy would have value for the patient as palliative therapy | ||
* A young male has had back pain for a few days. The pain is not severe, and there are no red flags for cauda equina syndrome. He wants an MRI to know what's going on, but the physician stops to consider: how will an MRI be of value to the patient? The patient may or may not have a herniated disc, but even if they do, | ** One can also argue that even performing a faecal occult blood test in this case has no value for the patient, because the next step after a positive test would be a colonoscopy, a procedure which would not be of value to the patient anyway | ||
* A young male has had back pain for a few days. The pain is not severe, and there are no red flags for cauda equina syndrome. He wants an MRI to know what's going on, but the physician stops to consider: how will an MRI be of value to the patient? The patient may or may not have a herniated disc, but even if they do, a herniated disk without red flags isn't an indication for surgery anyway. As such, whether the MRI shows a herniated disc or not, the management will be the same (no surgery, only physical therapy and pain relief), and the MRI is therefore of no value to the patient (and it is resource-intensive) | |||
** On the other hand, if the patient has debilitating pain or there are red flags present, he may have cauda equina syndrome, in which case surgery is indicated. In this case, MRI has value: it determines whether they need surgery or not | ** On the other hand, if the patient has debilitating pain or there are red flags present, he may have cauda equina syndrome, in which case surgery is indicated. In this case, MRI has value: it determines whether they need surgery or not | ||
* A middle aged woman has symptoms of an upper respiratory tract infection. After taking the anamnesis and physical examination, you're certain that it's a viral infection. You reflexively want to order a CRP or leukocyte count, but you stop to consider: will the laboratory investigation be of value to the patient? You know that viral URTIs only cause mildly elevated inflammatory parametres, so that's likely what you'll find anyway. And even if the CRP is higher than you expect, you're certain enough that this is not a bacterial infection, so you won't be administering antibiotics anyway. So even after making the investigation, you'll most likely not be changing your management of this patient; managing their symptoms and encouraging rest, without antibiotics | * A middle aged woman has symptoms of an upper respiratory tract infection. After taking the anamnesis and physical examination, you're certain that it's a viral infection. You reflexively want to order a CRP or leukocyte count, but you stop to consider: will the laboratory investigation be of value to the patient? You know that viral URTIs only cause mildly elevated inflammatory parametres, so that's likely what you'll find anyway. And even if the CRP is higher than you expect, you're certain enough that this is not a bacterial infection, so you won't be administering antibiotics anyway. So even after making the investigation, you'll most likely not be changing your management of this patient; managing their symptoms and encouraging rest, without antibiotics | ||
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* [[Faecal occult blood test]] in middle-aged/elderly | * [[Faecal occult blood test]] in middle-aged/elderly | ||
** Used to detect early [[colorectal cancer]] or bleeding [[Colonic polyps|colon polyps]] | ** Used to detect early [[colorectal cancer]] or bleeding [[Colonic polyps|colon polyps]] | ||
* Screening for [[inborn errors of metabolism]] in newborns | * Screening for [[inborn errors of metabolism]] and [[developmental dysplasia of the hip]] in newborns | ||
A screening test is most useful when it has high sensitivity. It would be great if a screening test also had high specificity, but there is often a trade-off between sensitivity and specificity. Therefore, most screening tests have low specificity. | A screening test is most useful when it has high [[sensitivity]]. It would be great if a screening test also had high [[specificity]], but there is often a trade-off between sensitivity and specificity. Therefore, most screening tests have low specificity. | ||
Because screening test have low specificity, a positive screening test must always be confirmed by a more specific test. | Because screening test have low specificity, a positive screening test must always be confirmed by a more specific test. | ||
=== Difficulties with screening === | |||
== Diagnosis == | == Diagnosis == | ||
When an investigation is ordered for diagnosis, one should already have a list of differential diagnoses before ordering the test, and the test should be able to narrow down the list of differential diagnoses. It's important to consider the test's specificity, sensitivity, positive predictive value, and negative predictive value in this. | When an investigation is ordered for diagnosis, one should already have a list of differential diagnoses before ordering the test, and the test should be able to narrow down the list of differential diagnoses. It's important to consider the test's specificity, sensitivity, positive predictive value, and negative predictive value in this. There is no reason to perform an investigation if it doesn't help narrow doen the number of differential diagnoses. | ||
=== Using test characteristics wisely === | |||
Because positive and negative predictive values depend on the prevalence of the disorder in the population, it's important to keep the prevalence of the disorder in mind. | |||
For example, a negative D-dimer has a high negative predictive value for VTE. However, negative predictive value decreases with increasing prevalence. If the patient has a high pre-test probability, often determined by their Wells score (a scoring system used to determine the pre-test probability for DVT/PE), the patient no longer has the same pre-test probability as the general population (which is low). The | |||
== Follow-up and monitoring == | == Follow-up and monitoring == | ||
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However, it's important to keep in mind the requirement of value for the patient. In the first scenario, there is value as a lack of normalisation of inflammatory parametres in a patient treated with antibiotic for a bacterial infection may be a sign that the antibiotic is ineffective, which may require administration of a different antibiotic. In the second scenario, there is also value, as the earlier one can catch recurrence of a meningeoma, the better the prognosis after treatment. However, if the patient is in a condition where they will not receive treatment anyway (for example, if they are terminal), monitoring is not of value to the patient. | However, it's important to keep in mind the requirement of value for the patient. In the first scenario, there is value as a lack of normalisation of inflammatory parametres in a patient treated with antibiotic for a bacterial infection may be a sign that the antibiotic is ineffective, which may require administration of a different antibiotic. In the second scenario, there is also value, as the earlier one can catch recurrence of a meningeoma, the better the prognosis after treatment. However, if the patient is in a condition where they will not receive treatment anyway (for example, if they are terminal), monitoring is not of value to the patient. | ||
== Evaluation of prognosis == | |||
In some cases, performing an investigation even though it won't change patient management can be useful if it provides information on patient prognosis. This is most common in case of patients with cancer. | |||
== External resources == | == External resources == | ||
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[[Category:Radiology]] | [[Category:Radiology]] | ||
[[Category:Laboratory Medicine]] | [[Category:Laboratory Medicine]] | ||
[[Category:Public Health]] | |||