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Early intervention with biologic therapy in Crohn´s disease: how early is early?
Revés, Joana; Mascarenhas, André; José Temido, Maria; Morão, Bárbara; Neto Nascimento, Catarina; Rita Franco, Ana; Mendes, Raquel R; Palmela, Carolina; Chagas, Cristina; Figueiredo, Pedro Narra; Glória, Luísa; Portela, Francisco; Torres, Joana.
Afiliação
  • Revés J; Gastroenterology Division, Hospital Beatriz Ângelo, Loures, Portugal.
  • Mascarenhas A; Gastroenterology Division, Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal.
  • José Temido M; Gastroenterology Division, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
  • Morão B; Gastroenterology Division, Hospital Beatriz Ângelo, Loures, Portugal.
  • Neto Nascimento C; Gastroenterology Division, Hospital Beatriz Ângelo, Loures, Portugal.
  • Rita Franco A; Gastroenterology Division, Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal.
  • Mendes RR; Gastroenterology Division, Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal.
  • Palmela C; Gastroenterology Division, Hospital Beatriz Ângelo, Loures, Portugal.
  • Chagas C; Gastroenterology Division, Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal.
  • Figueiredo PN; Gastroenterology Division, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
  • Glória L; Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
  • Portela F; Gastroenterology Division, Hospital Beatriz Ângelo, Loures, Portugal.
  • Torres J; Gastroenterology Division, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
J Crohns Colitis ; 17(11): 1752-1760, 2023 Nov 24.
Article em En | MEDLINE | ID: mdl-37220397
BACKGROUND: Early biologic therapy within the first 18-24 months after diagnosis is associated with improved clinical outcomes in Crohn's disease [CD]. However, the definition of the best time to initiate biologic therapy remains unclear. We aimed to assess if there is an optimal timing for early biologic therapy initiation. METHODS: This was a multicentre retrospective cohort study including newly diagnosed CD patients who started anti-tumour necrosis factor [TNF] therapy within 24 months from diagnosis. The timing of initiation of biologic therapy was categorised as ≤6, 7-12, 13-18, and 19-24 months. The primary outcome was CD-related complications defined as a composite of progression of Montreal disease behaviour, CD-related hospitalisations, or CD-related intestinal surgeries. Secondary outcomes included clinical, laboratory, endoscopic, and transmural remission. RESULTS: We included 141 patients where 54%, 26%, 11%, and 9% started biologic therapy at ≤6, 7-12, 13-18, and 19-24 months after diagnosis, respectively. A total of 34 patients [24%] reached the primary outcome: 8% had progression of disease behaviour, 15% were hospitalised, and 9% required surgery. There was no difference in the time to a CD-related complication according to the time of initiation of biologic therapy within the first 24 months. Clinical, endoscopic, and transmural remission was achieved in 85%, 50%, and 29%, respectively, but no differences were found according to the time of initiation of biologic therapy. CONCLUSION: Starting anti-TNF therapy within the first 24 months after diagnosis was associated with a low rate of CD-related complications and high rates of clinical and endoscopic remission, although we found no differences with earlier initiation within this window of opportunity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Crohn Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Crohns Colitis Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Crohn Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Crohns Colitis Ano de publicação: 2023 Tipo de documento: Article