Factors associated with the persistence of oral 5-aminosalicylic acid monotherapy in ulcerative colitis: a nationwide Norwegian cohort study

被引:3
作者
Fossmark, Reidar [1 ,2 ]
Olaisen, Maya [1 ,2 ]
Martinsen, Tom Christian [1 ,2 ]
Melberg, Hans Olav [3 ]
机构
[1] NTNU Norwegian Univ Sci & Technol, Fac Med & Hlth Sci, Dept Clin & Mol Med, Prinsesse Kristinas Gate 1, N-7491 Trondheim, Norway
[2] Trondheim Reg & Univ Hosp, St Olavs Hosp, Dept Gastroenterol & Hepatol, Trondheim, Norway
[3] Univ Oslo, Inst Hlth & Soc, Oslo, Norway
关键词
5-aminosalicylic acid; drug persistence; ulcerative colitis; COLONIC MUCOSAL CONCENTRATIONS; VS; 2.4; G/DAY; ASCEND-I; MESALAZINE; MESALAMINE; RELEASE; NONADHERENCE; THERAPY; FORMULATIONS; MODERATE;
D O I
10.1177/17562848211021760
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Oral 5-aminosalicylic acid (5-ASA) is the mainstay treatment of ulcerative colitis (UC) and therapy with oral 5-ASA is associated with beneficial outcomes. We have examined factors associated with the persistence of oral 5-ASA treatment in a national cohort of UC patients. Methods: Patients with newly diagnosed UC from 2010 to 2014 using oral 5-ASA monotherapy were identified by combining data from the Norwegian Patient Registry and the Norwegian Prescription Database. The median follow-up time was 1029 days. Drug persistence was defined as duration of oral 5-ASA preparation as monotherapy. Non-persistence of a oral 5-ASA preparation as monotherapy was defined as stopping oral 5-ASA, initiation of any further anti-inflammatory treatment including a course of glucocorticoids and a change to another oral 5-ASA preparation. Drug persistence was analyzed using the Kaplan-Meier method and influence of covariates on drug persistence was analyzed with the Cox proportional hazard model. Results: A total of 3421 patients were identified. The overall median 5-ASA drug persistence was 179 days. In univariate analyses, persistence was associated with preparation type and high-dose treatment, while oral glucocorticoid use or hospitalization around the start of oral 5-ASA were associated with shorter 5-ASA persistence. In multivariate analyses, oral glucocorticoids [HR 1.67 (1.54-1.80), p < 0.005] and hospitalization around start of 5-ASA [HR 1.23 (1.14-1.34), p < 0.005] were associated with non-persistence, whereas high dose (> 3 g/day) 5-ASA was associated with longer persistence [HR 0.68 (0.65-0.71), p < 0.005]. Conclusion: High-dose treatment with oral 5-ASA was associated with longer persistence of oral 5-ASA monotherapy, whereas the presence of factors indicating more severe disease around initiation of 5-ASA monotherapy was associated with a shorter persistence.
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页数:10
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共 35 条
[1]   The Role of Early Biologic Therapy in Inflammatory Bowel Disease [J].
Berg, Dana Rachel ;
Colombel, Jean-Frederic ;
Ungaro, Ryan .
INFLAMMATORY BOWEL DISEASES, 2019, 25 (12) :1896-1905
[2]   Once daily MMX mesalazine for the treatment of mild-to-moderate ulcerative colitis: a phase II, dose-ranging study [J].
D'Haens, G. ;
Hommes, D. ;
Engels, L. ;
Baert, F. ;
Van der Waaij, L. ;
Connor, P. ;
Ramage, J. ;
Dewit, O. ;
Palmen, M. ;
Stephenson, D. ;
Joseph, R. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2006, 24 (07) :1087-1097
[3]   5-ASA colonic mucosal concentrations resulting from different pharmaceutical formulations in ulcerative colitis [J].
D'Inca, Renata ;
Paccagnella, Martina ;
Cardin, Romilda ;
Pathak, Surajit ;
Baldo, Vincenzo ;
Giron, Maria Cecilia ;
Sturniolo, Giacomo Carlo .
WORLD JOURNAL OF GASTROENTEROLOGY, 2013, 19 (34) :5665-5670
[4]   CONCENTRATIONS OF 5-ASA AND AC-5-ASA IN HUMAN ILEOCOLONIC BIOPSY HOMOGENATES AFTER ORAL 5-ASA PREPARATIONS [J].
DEVOS, M ;
VERDIEVEL, H ;
SCHOONJANS, R ;
PRAET, M ;
BOGAERT, M ;
BARBIER, F .
GUT, 1992, 33 (10) :1338-1342
[5]   Mucosal 5-aminosalicylic acid concentration inversely correlates with severity of colonic inflammation in patients with ulcerative colitis [J].
Frieri, G ;
Giacomelli, R ;
Pimpo, M ;
Palumbo, G ;
Passacantando, A ;
Pantaleoni, G ;
Caprilli, R .
GUT, 2000, 47 (03) :410-414
[6]   Mucosal concentrations of N-acetyl-5-aminosalicylic acid related to endoscopic activity in ulcerative colitis patients with mesalamine [J].
Fukuda, Tomohiro ;
Naganuma, Makoto ;
Takabayashi, Kaoru ;
Hagihara, Yuya ;
Tanemoto, Shun ;
Nomura, Ena ;
Yoshimatsu, Yusuke ;
Sugimoto, Shinya ;
Nanki, Kosaku ;
Mizuno, Shinta ;
Mikami, Yohei ;
Fukuhara, Kayoko ;
Sujino, Tomohisa ;
Mutaguchi, Makoto ;
Inoue, Nagamu ;
Ogata, Haruhiko ;
Iwao, Yasushi ;
Abe, Takayuki ;
Kanai, Takanori .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2020, 35 (11) :1878-1885
[7]   Delayed-release oral mesalamine 4.8 g/day (800 mg tablets) compared with 2.4 g/day (400 mg tablets) for the treatment of mildly to moderately active ulcerative colitis: The ASCEND I trial [J].
Hanauer, Stephen B. ;
Sandborn, William J. ;
Dallaire, Christian ;
Archambault, Andre ;
Yacyshyn, Bruce ;
Yeh, Chyon ;
Smith-Hall, Nancy .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2007, 21 (12) :827-834
[8]   Third European Evidence-based Consensus on Diagnosis and Management of Ulcerative Colitis. Part 2: Current Management (Publication with Expression of Concern) [J].
Harbord, Marcus ;
Eliakim, Rami ;
Bettenworth, Dominik ;
Karmiris, Konstantinos ;
Katsanos, Konstantinos ;
Kopylov, Uri ;
Kucharzik, Torsten ;
Molnar, Tamas ;
Raine, Tim ;
Sebastian, Shaji ;
de Sousa, Helena Tavares ;
Dignass, Axel ;
Carbonnel, Franck .
JOURNAL OF CROHNS & COLITIS, 2017, 11 (07) :769-784
[9]   Review article: delivery and efficacy of topical 5-aminosalicylic acid (mesalazine) therapy in the treatment of ulcerative colitis [J].
Harris, M. S. ;
Lichtenstein, G. R. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2011, 33 (09) :996-1009
[10]   Systematic review: impact of non-adherence to 5-aminosalicylic acid products on the frequency and cost of ulcerative colitis flares [J].
Higgins, P. D. R. ;
Rubin, D. T. ;
Kaulback, K. ;
Schoenfield, P. S. ;
Kane, S. V. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2009, 29 (03) :247-257