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Real-life Anti-tumor Necrosis Factor Experience in More Than 500 Patients: High Co-immunosuppression Rates But Low Rates of Quantifying Treatment Response.
Merrick, Victoria M; Mortier, Kajal; Williams, Linda J; Muhammed, Rafeeq; Auth, Marcus K H; Elawad, Mamoun; Fell, John M E; Beattie, R Mark; Loganathan, Sabarinathan; Torrente, Franco; Morris, Mary-Anne; Charlton, Charles; Croft, Nick M; Rodrigues, Astor; Furman, Mark; Vadamalayan, Babu; Jenkins, Huw; Zamvar, Veena; Mitton, Sally G; Chong, Sonny; Cosgrove, Mike; Akobeng, Anthony; Wilson, David C; Russell, Richard K.
Afiliação
  • Merrick VM; Child Life and Health, University of Edinburgh, Edinburgh.
  • Mortier K; UK IBD Audit, Royal College of Physicians, Regent's Park, London.
  • Williams LJ; Usher Institute of Population Health Sciences & Informatics, University of Edinburgh, Edinburgh.
  • Muhammed R; Department of PGHAN, Birmingham Children's Hospital, Birmingham.
  • Auth MKH; Department of PGHAN, Alder Hey Children's NHS Foundation Trust, Liverpool.
  • Elawad M; Department of PGHAN, Great Ormond Street Hospital, London.
  • Fell JME; Department of PGHAN, Chelsea and Westminster Hospital, London.
  • Beattie RM; Department of PGHAN, Southampton Children's Hospital, Southampton.
  • Loganathan S; Department of PGHAN, Royal Aberdeen Children's Hospital, Forresterhill, Aberdeen.
  • Torrente F; Department of PGHAN, Addenbrooke's Hospital, Cambridge.
  • Morris MA; Jenny Lind Children's Hospital, Norfolk and Norwich University Hospital, Norwich.
  • Charlton C; Department of PGHAN, Nottingham Children's Hospital, Nottingham.
  • Croft NM; Department of PGHAN, The Royal London Children's Hospital, Barts Health NHS Trust, London.
  • Rodrigues A; Department of PGHAN, Children's Hospital, John Radcliffe Hospital, Oxford.
  • Furman M; Department of PGHAN, Royal Free Hospital.
  • Vadamalayan B; Department of PGHAN, King's College Hospital, London.
  • Jenkins H; Department of PGHAN, Children's Hospital for Wales, Cardiff.
  • Zamvar V; Department of PGHAN, Clarendon Wing, Leeds General Infirmary, Leeds, West Yorkshire.
  • Mitton SG; Department of PGHAN, St George's Hospital, Tooting, London.
  • Chong S; Queen Mary's Hospital for Children, Carshalton.
  • Cosgrove M; Department of paediatrics, Singleton Hospital, Sketty, Swansea.
  • Akobeng A; Department of PGHAN, Royal Manchester Children's Hospital, Manchester.
  • Wilson DC; Department of PGHAN, Royal Hospital for Sick Children, Edinburgh.
  • Russell RK; Department of PGHAN, Royal Hospital for Children, Glasgow, UK.
J Pediatr Gastroenterol Nutr ; 66(2): 274-280, 2018 02.
Article em En | MEDLINE | ID: mdl-29356768
ABSTRACT

OBJECTIVE:

The aim of this study was to measure the effectiveness, safety, and use of anti-tumor necrosis Factor (TNF) therapy in pediatric inflammatory bowel disease in the United Kingdom (UK).

METHODS:

Prospective UK audit of patients newly starting anti-TNF therapy. Disease severity was assessed using Physician Global Assessment +/or the Paediatric Crohn Disease Activity Index.

RESULTS:

A total of 37 centers participated (23/25 specialist pediatric inflammatory bowel disease sites). A total of 524 patients were included 429 with Crohn disease (CD), 76 with ulcerative colitis (UC), and 19 with IBD unclassified (IBDU). Eighty-seven percent (488/562) of anti-TNF was infliximab; commonest indication was active luminal CD 77% (330/429) or chronic refractory UC/IBDU 56% (53/95); 79% (445/562) had concomitant co-immunosuppression. In CD (267/429 male), median time from diagnosis to treatment was 1.42 years (interquartile range 0.63-2.97). Disease (at initiation) was moderate or severe in 91% (156/171) by Physician Global Assessment compared to 41% (88/217) by Paediatric Crohn Disease Activity Index (Kappa (κ) 0.28 = only "fair agreement"; P < 0.001.Where documented, 77% (53/69) of patients with CD responded to induction; and 65% (46/71) entered remission. A total of 2287 infusions and 301.96 years of patient' follow-up (n = 385) are represented; adverse events affected 3% (49/1587) infliximab and 2% (2/98) adalimumab infusions (no deaths or malignancies). Peri-anal abscess drainage was less common after anti-TNF initiation (CD), that is 26% (27/102) before, 7% (3/42) after (P = 0.01); however, pre and post anti-TNF data collection was not over equal time periods.

CONCLUSIONS:

Anti-TNFs are effective treatments, usually given with thiopurine co-immunosuppression. This study highlights deficiencies in formal documentation of effect and disparity between disease severity scoring tools, which need to be addressed to improve ongoing patient care.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Doenças Inflamatórias Intestinais / Terapia de Imunossupressão / Fator de Necrose Tumoral alfa / Anticorpos Monoclonais Humanizados Tipo de estudo: Clinical_trials / Observational_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Doenças Inflamatórias Intestinais / Terapia de Imunossupressão / Fator de Necrose Tumoral alfa / Anticorpos Monoclonais Humanizados Tipo de estudo: Clinical_trials / Observational_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article