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      UK guideline on transition of adolescent and young persons with chronic digestive diseases from paediatric to adult care

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          Abstract

          The risks of poor transition include delayed and inappropriate transfer that can result in disengagement with healthcare. Structured transition care can improve control of chronic digestive diseases and long-term health-related outcomes. These are the first nationally developed guidelines on the transition of adolescent and young persons (AYP) with chronic digestive diseases from paediatric to adult care. They were commissioned by the Clinical Services and Standards Committee of the British Society of Gastroenterology under the auspices of the Adolescent and Young Persons (A&YP) Section. Electronic searches for English-language articles were performed with keywords relating to digestive system diseases and transition to adult care in the Medline (via Ovid), PsycInfo (via Ovid), Web of Science and CINAHL databases for studies published from 1980 to September 2014. The quality of evidence and grading of recommendations was appraised using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system. The limited number of studies in gastroenterology and hepatology required the addition of relevant studies from other chronic diseases to be included.

          These guidelines deal specifically with the transition of AYP living with a diagnosis of chronic digestive disease and/or liver disease from paediatric to adult healthcare under the following headings;

          1. Patient populations involved in AYP transition

          2. Risks of failing transition or poor transition

          3. Models of AYP transition

          4. Patient and carer/parent perspective in AYP transition

          5. Surgical perspective

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          Most cited references86

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          Transition from child-centered to adult health-care systems for adolescents with chronic conditions. A position paper of the Society for Adolescent Medicine.

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            Management of pediatric ulcerative colitis: joint ECCO and ESPGHAN evidence-based consensus guidelines.

            Pediatric ulcerative colitis (UC) shares many features with adult-onset disease but there are some unique considerations; therefore, therapeutic approaches have to be adapted to these particular needs. We aimed to formulate guidelines for managing UC in children based on a systematic review (SR) of the literature and a robust consensus process. The present article is a product of a joint effort of the European Crohn's and Colitis Organization (ECCO) and the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). A group of 27 experts in pediatric IBD participated in an iterative consensus process including 2 face-to-face meetings, following an open call to ESPGHAN and ECCO members. A list of 23 predefined questions were addressed by working subgroups based on a SR of the literature. A total of 40 formal recommendations and 68 practice points were endorsed with a consensus rate of at least 89% regarding initial evaluation, how to monitor disease activity, the role of endoscopic evaluation, medical and surgical therapy, timing and choice of each medication, the role of combined therapy, and when to stop medications. A management flowchart, based on the Pediatric Ulcerative Colitis Activity Index (PUCAI), is presented. These guidelines provide clinically useful points to guide the management of UC in children. Taken together, the recommendations offer a standardized protocol that allows effective, timely management and monitoring of the disease course, while acknowledging that each patient is unique.
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              Poor prognosis of young adults with type 1 diabetes: a longitudinal study.

              To determine the role of early behavioral and psychological factors on later outcomes in young adults with childhood- or adolescent-onset type 1 diabetes. We conducted a longitudinal cohort study of patients recruited from the register of the young adult outpatient diabetes clinic, Oxford, U.K. A total of 113 individuals (51 male subjects) aged 17-25 years completed assessments, and 87 (77%) were reinterviewed as older adults (aged 28-37 years). Longitudinal assessments were made of glycemic control (HbA(1c)) and complications. Psychological state at baseline was assessed using the Present State Examination and self-report Symptom Checklist, with corresponding interview schedules administered at follow-up. There was no significant improvement between baseline and follow-up in mean HbA(1c) levels (8.5 vs. 8.6% in men, 9.3 vs. 8.7% in women). The proportion of individuals with serious complications (preproliferative or laser-treated retinopathy, proteinuria or more severe renal disease, peripheral neuropathy, and autonomic neuropathy) increased from 3-37% during the 11-year period. Women were more likely than men to have multiple complications (23 vs. 6%, difference 17%, 95% CI 4-29%, P = 0.02). Psychiatric disorders increased from 16 to 28% (20% in men, 36% in women at follow-up, difference NS), and 8% had psychiatric disorders at both assessments. Baseline psychiatric symptom scores predicted follow-up scores (beta = 0.32, SE [beta] 0.12, P = 0.008, 95% CI 0.09-0.56) and recurrent admissions with diabetic ketoacidosis (odds ratio 9.1, 95% CI 2.9-28.6, P < 0.0001). The clinical and psychiatric outcome in this cohort was poor. Psychiatric symptoms in later adolescence and young adulthood appeared to predict later psychiatric problems.
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                Author and article information

                Journal
                Gut
                Gut
                gutjnl
                gut
                Gut
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0017-5749
                1468-3288
                June 2017
                21 February 2017
                : 66
                : 6
                : 988-1000
                Affiliations
                [1 ]Academic Department of Gastroenterology, Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital , Sheffield, UK
                [2 ]Centre for Gastroenterology and Hepatology, Royal Free Hospital , London, UK
                [3 ]Department of Surgery, UCLH, London, UK
                [4 ]Royal Liverpool University Hospital , Liverpool, UK
                [5 ]Queen Elizabeth Hospital NHS Foundation Trust, University of East Anglia, King's Lynn, Norfolk, UK
                [6 ]Sheffield Children's Hospital NHS Foundation Trust , Sheffield, UK
                [7 ]Glasgow Royal Infirmary , Glasgow, UK
                [8 ]Deparment of Gastroenterology, Royal Victoria Hospital , Belfast, UK
                [9 ]Liver Unit, Birmingham Children's Hospital , Birmingham, UK
                [10 ]NIHR LCRN (Y&H) Gastroenterology Speciality Co-Lead, Hull & East Yorkshire NHS Trust , Hull, UK
                [11 ]Queen Elizabeth Hospital Birmingham NHS Foundation Trust , Birmingham, UK
                [12 ]GI Services Division, University College London Hospital , London, UK
                [13 ]London, UK
                [14 ]Department of Paediatric Gastroenterology, The Royal Hospital for Children Glasgow , Glasgow, UK
                [15 ]Department of Gastroenterology, UCLH , London, UK
                [16 ]Bart's Health NHS Trust, The Royal London Hospital , London, UK
                [17 ]Centre for Immunology and Infectious Disease, Blizard Institute, Barts and the London School of Medicine, Queen Mary University of London , London, UK
                Author notes
                [Correspondence to ] Dr James O Lindsay, Bart's Health NHS Trust, The Royal London Hospital, London E1 1BB, UK; James.Lindsay@ 123456bartshealth.nhs.uk

                *Brooks and Smith are joint first authors.

                Article
                gutjnl-2016-313000
                10.1136/gutjnl-2016-313000
                5532456
                28228488
                8a7c4815-b09a-4403-8527-fc6afa391e33
                Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

                History
                : 5 September 2016
                : 10 January 2017
                : 24 January 2017
                Categories
                Guidelines

                Gastroenterology & Hepatology
                liver,paediatric gastroenterology,gastrointestinal tract,inflammatory bowel disease

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