Deetee
Illuminator
- Joined
- Jul 8, 2003
- Messages
- 3,789
I need guidance/help regarding some comparisons. Any advice much appreciated.
I have a small group of 9 patients with an uncommon disease X.
In 8 of them it seemed to be associated/triggered by a problem (Y) but in one case it seemed to be linked with a different problem (Z).
Now Y happens quite commonly in the general "at risk" population of 600,000 people (its incidence is 500,000), but Z is rare (100).
However, my sample is incomplete, and I don't know how many other cases of disease X are out there.
Can I determine whether having Y or Z is a greater risk factor for developing disease X?
What is the best way to compare, and what confidence limits would there be?
I have a small group of 9 patients with an uncommon disease X.
In 8 of them it seemed to be associated/triggered by a problem (Y) but in one case it seemed to be linked with a different problem (Z).
Now Y happens quite commonly in the general "at risk" population of 600,000 people (its incidence is 500,000), but Z is rare (100).
However, my sample is incomplete, and I don't know how many other cases of disease X are out there.
Can I determine whether having Y or Z is a greater risk factor for developing disease X?
What is the best way to compare, and what confidence limits would there be?
Last edited: