TY - JOUR
T1 - Low-dose thiopurine with allopurinol co-therapy overcomes thiopurine intolerance and allows thiopurine continuation in inflammatory bowel disease
AU - Vasudevan, Abhinav
AU - Beswick, Lauren
AU - Friedman, Antony B.
AU - Moltzen, Alicia
AU - Haridy, James
AU - Raghunath, Ajay
AU - Sparrow, Miles
AU - van Langenberg, Daniel
PY - 2018/7
Y1 - 2018/7
N2 - Aims: To assess the utility and tolerability of thiopurine-allopurinol co-therapy in inflammatory bowel disease (IBD) patients with intolerance to thiopurine monotherapy. Methods: A retrospective observational study assessed cases of thiopurine intolerance then switched to thiopurine allopurinol co-therapy between 2011 and 2015 at two centres. Indications for switch, dosing and subsequent clinical outcomes (including thiopurine persistence) were recorded. Results: Of 767 patients on thiopurines for IBD, 89 (12%) were switched to co-therapy for intolerance. 64/89 (72%) had Crohn's disease, 38 (43%) were males, median age at switch was 40y (range 17–78), median IBD duration 6y (0–29). Median follow-up was 1.9y (0–5). Reasons for switching to co-therapy included fatigue (37%), hepatotoxicity (23%), nausea (23%), arthralgia (10%), headache (12%) and hypersensitivity reaction (4%). Overall, 66 (74%) patients remained on co-therapy until most recent review and achieved a clinical response. High rates of overcoming intolerance (62–100%) occurred with co-therapy for all reasons above, although fatigue was less amenable to switching than non-fatigue indications (62% vs 91%, p = <0.001). Of 34 patients not escalated to biologics with endoscopic data, 15 were in remission (44%) at most recent review. Conclusion: Low-dose thiopurine combined with allopurinol appears safe and effective in overcoming intolerances to thiopurine monotherapy in many cases.
AB - Aims: To assess the utility and tolerability of thiopurine-allopurinol co-therapy in inflammatory bowel disease (IBD) patients with intolerance to thiopurine monotherapy. Methods: A retrospective observational study assessed cases of thiopurine intolerance then switched to thiopurine allopurinol co-therapy between 2011 and 2015 at two centres. Indications for switch, dosing and subsequent clinical outcomes (including thiopurine persistence) were recorded. Results: Of 767 patients on thiopurines for IBD, 89 (12%) were switched to co-therapy for intolerance. 64/89 (72%) had Crohn's disease, 38 (43%) were males, median age at switch was 40y (range 17–78), median IBD duration 6y (0–29). Median follow-up was 1.9y (0–5). Reasons for switching to co-therapy included fatigue (37%), hepatotoxicity (23%), nausea (23%), arthralgia (10%), headache (12%) and hypersensitivity reaction (4%). Overall, 66 (74%) patients remained on co-therapy until most recent review and achieved a clinical response. High rates of overcoming intolerance (62–100%) occurred with co-therapy for all reasons above, although fatigue was less amenable to switching than non-fatigue indications (62% vs 91%, p = <0.001). Of 34 patients not escalated to biologics with endoscopic data, 15 were in remission (44%) at most recent review. Conclusion: Low-dose thiopurine combined with allopurinol appears safe and effective in overcoming intolerances to thiopurine monotherapy in many cases.
KW - Azathioprine
KW - Colitis
KW - Crohn's
KW - Mercaptopurine
KW - Tolerability
UR - http://www.scopus.com/inward/record.url?scp=85042932706&partnerID=8YFLogxK
U2 - 10.1016/j.dld.2018.02.001
DO - 10.1016/j.dld.2018.02.001
M3 - Article
C2 - 29525182
AN - SCOPUS:85042932706
SN - 1590-8658
VL - 50
SP - 682
EP - 688
JO - Digestive and Liver Disease
JF - Digestive and Liver Disease
IS - 7
ER -