医学
强的松
溃疡性结肠炎
脉搏(音乐)
内科学
胃肠病学
皮质类固醇
外科
心脏病学
随机对照试验
作者
Jordina Llaó,Míriam Mañosa,Eduardo Martín-Arranz,Yamile Zabana,Mercè Navarro‐Llavat,Marta Téller,Esther García-Planella,David Busquets,David Monfort,Juan-Ramón Pineda,Ana Gutiérrez,Albert Villòria,Luís Menchén,Guillermo Bastida,Francisco Javier García‐Alonso,Montserrat Rivero,María Chaparro,Ruth de Francisco,Olga Merino,Iago Rodríguez–Lago
标识
DOI:10.1093/ecco-jcc/jjaf182
摘要
BACKGROUND: Oral corticosteroids remain the treatment of choice for moderately active ulcerative colitis (UC), achieving clinical remission in 30%-60% of patients. OBJECTIVE: To compare the rates of steroid-free clinical-endoscopic remission at weeks 8 and 54 in patients treated with 3 methyl-prednisolone pulses before oral corticosteroids in moderately active UC versus those only receiving oral corticosteroids. DESIGN: Prospective, open, multicentre, randomized, controlled trial. Patients with left/extensive, moderately active UC, naive to immunosuppressants and biological agents, were randomized to receive conventional treatment (CT) with oral prednisone 60 mg/day or the same regimen preceded by an additional daily pulse (AP) of 500 mg of methyl-prednisolone for 3 days. All patients who responded started oral mesalazine and were followed up until month 12 or clinical relapse. RESULTS: Seventy-five patients were randomized: 39 were allocated to the CT arm and 36 to the AP arm. Overall, 21 patients achieved clinical-endoscopic remission (28%; 95% confidence interval [CI]: 23%-33%) at both weeks 8 and 54 without needing rescue treatments, being not significantly different between both study groups (23% [95%CI: 14%-32%] CT vs. 33% [95%CI: 21%-45%] AP; P = 0.323). Patients in the AP group had higher rates of clinical response at day 3 and remission at day 7. No significant differences in adverse events were observed. Due to early termination, the study was underpowered, and findings should be interpreted as exploratory. CONCLUSIONS: The addition of 3 pulses of high-dose corticosteroids to a conventional regimen of oral prednisone does not improve medium and long-term clinical outcomes in moderately active UC. TRIAL REGISTRATION CODES: EudraCT number 2016-001170-15; ClinicalTrials.gov identifier NCT02921555.
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