Positive predictive value
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The positive predictive value, or precision rate, is the proportion of patients with positive test results who are correctly diagnosed. It is considered the physician's gold standard, as it reflects the probability that a positive test reflects the underlying condition being tested for.
Contents |
Worked example
- Relationships among terms
| Condition (as determined by "Gold standard") | ||||
| True | False | |||
| Test outcome | Positive | True Positive | False Positive (Type I error, P-value) | → Positive predictive value |
| Negative | False Negative (Type II error) | True Negative | → Negative predictive value | |
| ↓ Sensitivity | ↓ Specificity | |||
- A worked example
- the Fecal occult blood (FOB) screen test is used in 203 people to look for bowel cancer:
| Patients with bowel cancer (as confirmed on endoscopy) | ||||
| True | False | ? | ||
| FOB test | Positive | TP = 2 | FP = 18 | = TP / (TP + FP) = 2 / (2 + 18) = 2 / 20 ≡ 10% |
| Negative | FN = 1 | TN = 182 | = TN / (TN + FN) 182 / (1 + 182) = 182 / 183 ≡ 99.5% | |
| ↓ = TP / (TP + FN) = 2 / (2 + 1) = 2 / 3 ≡ 66.67% | ↓ = TN / (FP + TN) = 182 / (18 + 182) = 182 / 200 ≡ 91% | |||
Related calculations
- False positive rate (α) = FP / (FP + TN) = 18 / (18 + 182) = 9% = 1 - specificity
- False negative rate (β) = FN / (TP + FN) = 1 / (2 + 1) = 33% = 1 - sensitivity
- Power = 1 − β
Hence with large numbers of false positives and few false negatives, a positive FOB screen test is in itself poor at confirming cancer (PPV=10%) and further investigations must be undertaken, it will though pickup 66.7% of all cancers (the sensitivity). However as a screening test, a negative result is very good at reassuring that a patient does not have cancer (NPV=99.5%) and at this initial screen correctly identifies 91% of those who do not have cancer (the specificity).
Definition
The Positive Predictive Value can be defined as
or, alternatively,
Problems with positive predictive value
Predictive values are often used in medical research to evaluate the usefulness of a diagnostic test. Hence the PPV is used to indicate the probability that in case of a positive test, that the patient really has the specified disease. However there may be more than one cause for a disease and any single potential cause may not always result in the overt disease seen in a patient.
An example is the microbiological throat swab used in patients with a sore throat. Usually publications stating PPV of a throat swab are reporting on the probability that this bacteria is present in the throat, rather than that the patient is ill from the bacteria found. If presence of this bacteria always resulted in a sore throat, then the PPV would be very useful. However the bacteria may colonise individuals in a harmless way and never result in infection or disease. Sore throats occurring in these individuals is caused by other agents such as a virus. In this situation the gold standard used in the evaluation study represents only the presence of a bacteria (that might be harmless) but not a causal bacterial sore throat illness. It can be proven that this problem will affect positive predictive value far more than negative predictive value. To evaluate diagnostic tests where the gold standard looks only at potential causes of disease, one may use an extension of the predictive value termed the Etiologic Predictive Value.
See also
References
- Altman DG, Bland JM (9 Jul 1994). "Diagnostic Tests 2 - Predictive Values". British Medical Journal 309 (6947): 102.
- Gunnarsson RK, Lanke J. The predictive value of microbiologic diagnostic tests if asymptomatic carriers are present. Statist. Med. 2002; 21:1773-1785de:Positiver Vorhersagewert
he:ערך ניבוי חיובי nl:Predictieve waarde
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

