Meeting Abstracts

Program and Abstracts from the Canadian Digestive Diseases Week 2016

Table 52

Contingency table for initial clinical decision made (without level knowledge), 6 month clinical outcomes (post-levels), and ITLs and FCPLs with hypothetical decision prompts%.

ITLFCPInitial clinical decision6 month clinical outcome
No actionAction – investigationAction – dose De-escalationNo change
(stable IFX and steroid free)
Dose escalation
IFX
(no steroids)
Dose De-escalationInvestigationHospitalization or surgeryDose escalation, steroids, and hospitalization or surgery

<3.0 μg/mL (Action – Dose Escalation)<250 μg/g
(No Action Required)
1/31 (3.2%)00000001/31 (3.2%)
≥250 μg/g
(Action Required)
1/31 (3.2%)001/31 (3.2%)00000

3.0–7.0 μg/mL
(No Action)
<250 μg/g
(No Action Required)
4/31 (12.9%)004/31 (12.9%)00000
≥250 μg/g
(Action Required)
5/31 (16.1%)1/31 (3.2%)05/31 (16.1%)001/31 (3.2%)00

>7.0 μg/mL
(Action – Dose De-escalation)
<250 μg/g
(No Action Required)
12/31 (38.7%)3/31 (9.7%)010/31 (32.3%)3/31 (9.7%)1/31 (3.2%)01/31 (3.2%)0
≥250 μg/g
(Action Required)
3/31 (9.7%)01/31 (3.2%)4/31 (12.9%)00000

A FCPL of <250 μg/g should prompt “no action" while a FCPL of ≥250 μg/g should prompt “action" (e.g., investigation, dose escalation etc.); ITLs <3.0 μg/mL should prompt “action - dose escalation”, ITLs 3.0–7.0 μg/mL should prompt “no action”, and ITLs >7.0 μg/mL should prompt “action – dose de-escalation.”
Investigation refers to endoscopy.
Dose de-escalation refers to the dose of IFX being decreased and/or decreasing the frequency of IFX dosing.
Dose escalation refers to the dose of IFX being increased and/or increasing the frequency of IFX dosing.