General Model: OnlyEs andEEs
Logit PðXÞ¼aþ~
q
i¼ 1
biEiþ~
q
i¼ 1
~
i^0 ¼ 1
i 6 ¼i^0
q
d*ii 0 EiEi 0
Modeling Strategy: All Es, no Cs
Step 1: Define initial model (above formula)
Step 2: Assess interaction involving Es
Option A*: Overall chunk test for EEs,
followed by backward elimination of EEs
Step 4: Test for nonsignif Es if not components
of significant EEs
EXAMPLE
MRSA example Initial Model, Special
case (b)
Logit PðXÞ¼aþb 1 E 1 þb 2 E 2 þd*E 1 E 2
Final model: AllEs, noCs:
Logit PðXÞ¼aþb 1 E 1 þb 2 E 2 ;
whereE 1 ¼PREVHOSP and
E 2 ¼PAMU
One other issue: specifying the
initial model
(MRSA example)
EXAMPLE
Possible Causal Diagrams for MRSA
Study
Diagram 1
Diagram 2
V 1
V 1 V 2
V 2
E 2
E 2
D
D
E 1
E 1
D = MRSA (0,1)
V 1 = AGE
V 2 = GENDER
E 1 = PREVHOSP
E 2 = PAMU
Diagram 1)PAMU intervening
variable;
AGE and GENDER
confounders
In this case (b), our general model takes the
simplified form shown at the left.
For this model, we recommend a correspond-
ingly simplified strategy as shown at the left
that involves statistical testing only, first for
EEterms, and then forEs that are not compo-
nents of significant EEs. In terms of the
options we previously described, we only need
to consider a modified version of Option A, and
that Step 3, once again, can be omitted.
Applying this situation to our MRSA data, the
initial model (w/o theCs) is shown at the left.
TestingH 0 :d*¼0 in this model yields a nonsig-
nificant result (data not shown), and the final
model (since individualEs cannot be dropped)
is the no-interaction model shown here.
We now address one other issue, which con-
cerns how to specify the initial model. We
describe this issue in the context of the MRSA
example.
At the left, we consider two possiblecausal
diagramsfor the MRSA data.
Diagram 1 indicates that PAMU (i.e.,E 2 )isan
intervening variable in the causal pathway
between PREVHOSP (i.e.,E 1 ) and MRSA out-
come, and that AGE and GENDER (i.e.,V 1
and V 2 ) are confounders of the relationship
between PREVHOSP and MRSA.
Presentation: II. Modeling Strategy for Several Exposure Variables 261