Literature DB >> 36262537

Clinical utility of thiopurine metabolite monitoring in inflammatory bowel disease and its impact on healthcare utilization in Singapore.

Jia Qi Yeo1, Hua Heng McVin Cheen2, Amanda Wong2, Teong Guan Lim2, Balram Chowbay3,4,5, Wai Fook Leong5, Chunyan Wang6, Ennaliza Salazar7, Webber Pak Wo Chan7, San Choon Kong8, Wan Chee Ong2.   

Abstract

Background and Aim: Thiopurines are recommended for maintenance of steroid-free remission (SFR) in inflammatory bowel disease (IBD). Thiopurine metabolite monitoring (MM) is increasingly used in the West but remains novel in Singapore, with limited information on its therapeutic and economic benefits. Hence, this study aims to investigate MM's clinical utility and its impact on healthcare resource utilization in Singaporean IBD patients.
Methods: A retrospective observational study was conducted at Singapore General Hospital outpatient IBD Centre. Patients with IBD, baseline MM during 2014-2017, and weight-based thiopurine doses for ≥4 weeks were followed up for 1 year. Actions were taken to optimize therapy, and metabolite levels before and after the first action were documented. Outcomes assessed included SFR, no therapy escalation or surgery, healthcare resource utilization, and direct healthcare costs.
Results: Ninety IBD patients (50 Crohn's disease, 40 ulcerative colitis) were included. Among them, 40% had baseline metabolite levels within therapeutic range, 31.1% sub-therapeutic, 21.1% supra-therapeutic, and 7.8% shunters. Repeated MM with subsequent dose optimization helped 67.2% of patients achieve therapeutic levels after 1 year. Overall, 87.8% of patients achieved SFR and 90% had no therapy escalation or surgery. Despite greater outpatient visits and laboratory investigations with MM, the median total healthcare costs at 1 year only increased marginally (S$6407.66 [shunters] vs S$5215.20 [supra-therapeutic] vs S$4970.80 [sub-therapeutic] vs S$4370.48 [control (within therapeutic range)], P = 0.592).
Conclusion: MM guided timely therapy escalation for non-responders, identification of non-adherence, and reversal of shunting. Therefore, it is a useful clinical tool to optimize thiopurines without significantly increasing healthcare costs.
© 2022 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  Crohn's disease; inflammatory bowel disease; metabolite monitoring; thiopurine; ulcerative colitis

Year:  2022        PMID: 36262537      PMCID: PMC9575318          DOI: 10.1002/jgh3.12798

Source DB:  PubMed          Journal:  JGH Open        ISSN: 2397-9070


  30 in total

Review 1.  The role of thiopurine metabolite monitoring in inflammatory bowel disease.

Authors:  Lauren Beswick; Antony B Friedman; Miles P Sparrow
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2014-03-31       Impact factor: 3.869

2.  Thiopurine metabolite testing in inflammatory bowel disease.

Authors:  Rimma Goldberg; Gregory Moore; Georgina Cunningham; Julien Schulberg; Philip Marsh; Steven Brown; William Connell; Mark Lust; Michael A Kamm; Sally Bell
Journal:  J Gastroenterol Hepatol       Date:  2016-03       Impact factor: 4.029

3.  New Zealand Society of Gastroenterology Guidelines on Therapeutic Drug Monitoring in Inflammatory Bowel Disease.

Authors:  Afrasyab Khan; Arvenia B Berahmana; Andrew S Day; Murray L Barclay; Michael Schultz
Journal:  N Z Med J       Date:  2019-03-08

4.  Clinical usefulness of therapeutic drug monitoring of thiopurines in patients with inadequately controlled inflammatory bowel disease.

Authors:  Melissa L Haines; Yousef Ajlouni; Peter M Irving; Miles P Sparrow; Rosemary Rose; Richard B Gearry; Peter R Gibson
Journal:  Inflamm Bowel Dis       Date:  2010-09-01       Impact factor: 5.325

5.  Higher Thioguanine Nucleotide Metabolite Levels are Associated With Better Long-term Outcomes in Patients With Inflammatory Bowel Diseases.

Authors:  Andres J Yarur; Bilal Gondal; Ayal Hirsch; Britt Christensen; Russell D Cohen; David T Rubin
Journal:  J Clin Gastroenterol       Date:  2018-07       Impact factor: 3.062

6.  The impact of introducing thioguanine nucleotide monitoring into an inflammatory bowel disease clinic.

Authors:  M Smith; P Blaker; C Patel; A Marinaki; M Arenas; E Escuredo; S Anderson; P Irving; J Sanderson
Journal:  Int J Clin Pract       Date:  2012-12-17       Impact factor: 2.503

7.  Clinical significance of azathioprine active metabolite concentrations in inflammatory bowel disease.

Authors:  S Wright; D S Sanders; A J Lobo; L Lennard
Journal:  Gut       Date:  2004-08       Impact factor: 23.059

8.  Cost-effectiveness of thiopurine methyltransferase genotype screening in patients about to commence azathioprine therapy for treatment of inflammatory bowel disease.

Authors:  J Winter; A Walker; D Shapiro; D Gaffney; R J Spooner; P R Mills
Journal:  Aliment Pharmacol Ther       Date:  2004-09-15       Impact factor: 8.171

Review 9.  Safety of thiopurines in the treatment of inflammatory bowel disease.

Authors:  D J de Jong; L J J Derijks; A H J Naber; P M Hooymans; C J J Mulder
Journal:  Scand J Gastroenterol Suppl       Date:  2003

10.  Prospective Evaluation of Pharmacogenomics and Metabolite Measurements upon Azathioprine Therapy in Inflammatory Bowel Disease: An Observational Study.

Authors:  Zhang Fangbin; Gao Xiang; Ding Liang; Liu Hui; Wang Xueding; Chen Baili; Bi Huichang; Xiao Yinglian; Cheng Peng; Zhao Lizi; Chu Yanjun; Xu Feng; Chen Minhu; Huang Min; Hu Pinjin
Journal:  Medicine (Baltimore)       Date:  2016-04       Impact factor: 1.889

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