eHealth: Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis

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Standard

eHealth : Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis. / Pedersen, Natalia; Thielsen, Peter; Martinsen, Lars; Bennedsen, Mette; Haaber, Anne; Langholz, Ebbe; Végh, Zsuzsanna; Duricova, Dana; Jess, Tine; Bell, Sally; Burisch, Johan; Munkholm, Pia.

I: Inflammatory Bowel Diseases, Bind 20, Nr. 12, 12.2014, s. 2276-2285.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Pedersen, N, Thielsen, P, Martinsen, L, Bennedsen, M, Haaber, A, Langholz, E, Végh, Z, Duricova, D, Jess, T, Bell, S, Burisch, J & Munkholm, P 2014, 'eHealth: Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis', Inflammatory Bowel Diseases, bind 20, nr. 12, s. 2276-2285. https://doi.org/10.1097/MIB.0000000000000199

APA

Pedersen, N., Thielsen, P., Martinsen, L., Bennedsen, M., Haaber, A., Langholz, E., Végh, Z., Duricova, D., Jess, T., Bell, S., Burisch, J., & Munkholm, P. (2014). eHealth: Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis. Inflammatory Bowel Diseases, 20(12), 2276-2285. https://doi.org/10.1097/MIB.0000000000000199

Vancouver

Pedersen N, Thielsen P, Martinsen L, Bennedsen M, Haaber A, Langholz E o.a. eHealth: Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis. Inflammatory Bowel Diseases. 2014 dec.;20(12):2276-2285. https://doi.org/10.1097/MIB.0000000000000199

Author

Pedersen, Natalia ; Thielsen, Peter ; Martinsen, Lars ; Bennedsen, Mette ; Haaber, Anne ; Langholz, Ebbe ; Végh, Zsuzsanna ; Duricova, Dana ; Jess, Tine ; Bell, Sally ; Burisch, Johan ; Munkholm, Pia. / eHealth : Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis. I: Inflammatory Bowel Diseases. 2014 ; Bind 20, Nr. 12. s. 2276-2285.

Bibtex

@article{7b9701255936459abf421ff6ba1e9b6e,
title = "eHealth: Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis",
abstract = "BACKGROUND: To individualize treatment with mesalazine for ulcerative colitis relapses through a self-managed, web-based solution to optimize the short-term disease course.METHODS: Prospective, open-label, web-guided study with 3 months mesalazine therapy among patients with mild-to-moderate ulcerative colitis. Once a week, patients completed the simple clinical colitis activity index (SCCAI) and registered fecal calprotectin (FC) on the web application: www.meza.constant-care.dk. SCCAI and FC were summed and resulted in a total inflammatory burden score (TIBS). Deep remission was defined as SCCAI ≤1; FC = 0, and TIBS ≤1.RESULTS: A total of 95 patients (62% females; median age 45 yr) were included in the study and allocated 4.8 g mesalazine per day. Of these, 82 (86%) patients were adherent to web therapy, completing 3 months of web-guided mesalazine therapy. Of the 82 adherent patients, 72 (88%) continued mesalazine and 10 (12%) needed rescue therapy. From weeks 0 to 12, patients had experienced a significant reduction in mean SCCAI (4.6 versus 1.6, P < 0.001), mean FC (437 versus 195, P < 0.001), and mean TIBS (6.7 versus 2.4, P < 0.001). Based on TIBS values (≤1), the dose of mesalazine was reduced to 2.4 g in 25% of patients at week 3 in 50% of subjects at week 5 and in 88% of patients at week 12.CONCLUSIONS: Web-guided therapy with mesalazine in mild-to-moderate ulcerative colitis helps to individualize the dose and improve adherence to therapy. The study confirms mesalazine efficacy in mild-to-moderate UC, significantly improving TIBS values in majority of the patients.",
author = "Natalia Pedersen and Peter Thielsen and Lars Martinsen and Mette Bennedsen and Anne Haaber and Ebbe Langholz and Zsuzsanna V{\'e}gh and Dana Duricova and Tine Jess and Sally Bell and Johan Burisch and Pia Munkholm",
year = "2014",
month = dec,
doi = "10.1097/MIB.0000000000000199",
language = "English",
volume = "20",
pages = "2276--2285",
journal = "Inflammatory Bowel Diseases",
issn = "1078-0998",
publisher = "Lippincott Williams & Wilkins",
number = "12",

}

RIS

TY - JOUR

T1 - eHealth

T2 - Individualization of Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis

AU - Pedersen, Natalia

AU - Thielsen, Peter

AU - Martinsen, Lars

AU - Bennedsen, Mette

AU - Haaber, Anne

AU - Langholz, Ebbe

AU - Végh, Zsuzsanna

AU - Duricova, Dana

AU - Jess, Tine

AU - Bell, Sally

AU - Burisch, Johan

AU - Munkholm, Pia

PY - 2014/12

Y1 - 2014/12

N2 - BACKGROUND: To individualize treatment with mesalazine for ulcerative colitis relapses through a self-managed, web-based solution to optimize the short-term disease course.METHODS: Prospective, open-label, web-guided study with 3 months mesalazine therapy among patients with mild-to-moderate ulcerative colitis. Once a week, patients completed the simple clinical colitis activity index (SCCAI) and registered fecal calprotectin (FC) on the web application: www.meza.constant-care.dk. SCCAI and FC were summed and resulted in a total inflammatory burden score (TIBS). Deep remission was defined as SCCAI ≤1; FC = 0, and TIBS ≤1.RESULTS: A total of 95 patients (62% females; median age 45 yr) were included in the study and allocated 4.8 g mesalazine per day. Of these, 82 (86%) patients were adherent to web therapy, completing 3 months of web-guided mesalazine therapy. Of the 82 adherent patients, 72 (88%) continued mesalazine and 10 (12%) needed rescue therapy. From weeks 0 to 12, patients had experienced a significant reduction in mean SCCAI (4.6 versus 1.6, P < 0.001), mean FC (437 versus 195, P < 0.001), and mean TIBS (6.7 versus 2.4, P < 0.001). Based on TIBS values (≤1), the dose of mesalazine was reduced to 2.4 g in 25% of patients at week 3 in 50% of subjects at week 5 and in 88% of patients at week 12.CONCLUSIONS: Web-guided therapy with mesalazine in mild-to-moderate ulcerative colitis helps to individualize the dose and improve adherence to therapy. The study confirms mesalazine efficacy in mild-to-moderate UC, significantly improving TIBS values in majority of the patients.

AB - BACKGROUND: To individualize treatment with mesalazine for ulcerative colitis relapses through a self-managed, web-based solution to optimize the short-term disease course.METHODS: Prospective, open-label, web-guided study with 3 months mesalazine therapy among patients with mild-to-moderate ulcerative colitis. Once a week, patients completed the simple clinical colitis activity index (SCCAI) and registered fecal calprotectin (FC) on the web application: www.meza.constant-care.dk. SCCAI and FC were summed and resulted in a total inflammatory burden score (TIBS). Deep remission was defined as SCCAI ≤1; FC = 0, and TIBS ≤1.RESULTS: A total of 95 patients (62% females; median age 45 yr) were included in the study and allocated 4.8 g mesalazine per day. Of these, 82 (86%) patients were adherent to web therapy, completing 3 months of web-guided mesalazine therapy. Of the 82 adherent patients, 72 (88%) continued mesalazine and 10 (12%) needed rescue therapy. From weeks 0 to 12, patients had experienced a significant reduction in mean SCCAI (4.6 versus 1.6, P < 0.001), mean FC (437 versus 195, P < 0.001), and mean TIBS (6.7 versus 2.4, P < 0.001). Based on TIBS values (≤1), the dose of mesalazine was reduced to 2.4 g in 25% of patients at week 3 in 50% of subjects at week 5 and in 88% of patients at week 12.CONCLUSIONS: Web-guided therapy with mesalazine in mild-to-moderate ulcerative colitis helps to individualize the dose and improve adherence to therapy. The study confirms mesalazine efficacy in mild-to-moderate UC, significantly improving TIBS values in majority of the patients.

U2 - 10.1097/MIB.0000000000000199

DO - 10.1097/MIB.0000000000000199

M3 - Journal article

C2 - 25248002

VL - 20

SP - 2276

EP - 2285

JO - Inflammatory Bowel Diseases

JF - Inflammatory Bowel Diseases

SN - 1078-0998

IS - 12

ER -

ID: 135548737