Skip to main content
. Author manuscript; available in PMC: 2013 Aug 21.
Published in final edited form as: Gastroenterology. 2011 May;140(6):1817–1826.e2. doi: 10.1053/j.gastro.2010.11.058

Table 6. Proposed algorithms in response to measured drug levels in the setting of symptoms of active disease.

6TGN concentration 6MMP concentration Interpretation Strategy
In therapeutic window* Normal or high^ Refractory to thiopurines Change therapy – can discontinue thiopurine or continue at same dose in conjunction with the new therapy
Low Low or normal Too low of dose or noncompliant Increase dose or educate regarding compliance
High Normal or high Refractory to thiopurines Change therapy and discontinue thiopurine or continue at same dose or lower dose
Low High Preferential shunting to 6MMP Change therapy or reduce dose and add allopurinol
Anti-Infliximab antibody Infliximab concentration Additional testing Strategy
Positive Change to another anti-TNF therapy. If persistent disease activity after changing agents, change to agent with different mechanism
In therapeutic window Active disease on endoscopy / radiology Change to agent with different mechanism
In therapeutic window Inactive disease on endoscopy / radiology Investigate for alternative etiology of symptoms
Sub-therapeutic# Increase dose or frequency. If persistent disease activity, switch to a different anti-TNF agent.
Sub-therapeutic# Alternative strategy - Switch to a different anti-TNF agent. If persistent disease activity, change to agent with different mechanism.
*

Therapeutic window for 6TGN defined as 235–450 pmol/8 _ 108 red blood cells

^

Therapeutic level of 6MMP is less than 5700 pmol/8 _ 108 RBC

A ratio of 6MMP:6TGN greater than 11

#

Sub-therapeutic infliximab concentration defined as <12 mcg/ml at 4 weeks or undetectable trough level