Did the study patients represent the full spectrum of those who present with this clinical
problem?
Were the criteria for each final diagnosis explicit and credible?
Was the diagnostic work-up comprehensive and consistently applied?
For initially undiagnosed patients, was follow-up sufficiently long and complete?
What were the diagnoses and their probabilities?
How precise are these estimates of disease probability?
Are the study patients similar to my own?
Is it unlikely that the disease possibilities or probabilities have changed since this
evidence gathered?
Diagnostic Hypothesis |
Description |
Implications for Testing |
|
1. Leading hypothesis, or “working diagnosis” |
Single best explanation of patient’s illness |
Choose tests to confirm: High specificity High LR+ (>>1) |
|
2. Active alternatives, or “rule outs” |
Not as good as No. 1, but likely, serious or treatable enough to be actively sought in this patient |
Choose tests to exclude: High sensitivity Low LR-(<<1) |
|
3. Other alternatives |
Not likely, serious or treatable enough to be pursued now, but not yet excluded |
Hold off on tests now (may test for these later) |
|
4. Excluded hypotheses |
Causes of the problem that have been disapproved |
No further tests necessary |