Study Results
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Basic Information
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COMPLETED
500 participants
OBSERVATIONAL
2017-09-01
2018-09-30
Brief Summary
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The beginning of the disease at pediatric age is considered to be a poor prognostic factor and is considered to be more aggressive than that of adults: more extensive, more active and requiring more immunosuppressive treatments, with a more frequent dependence on corticosteroids and a shorter delay between the beginning of symptoms and the first surgery. After 5 years of evolution, 13 to 50% of patients with early pediatric MC have undergone intestinal resection.
The Paris' classification defined 3 phenotypes or behaviors in pediatric Crohn's disease. Penetrating phenotype (B3) is a heterogeneous group defined by the presence of intra-abdominal perforation, fistulas or abscesses. The B3 phenotype is a risk factor for pejorative evolution in CD with a risk increased of surgical resection.
In the pediatric population, the natural history of patients with penetrating CD is unknown. Most studies focus on CD beginning at pediatric age but with penetrating complications occurring in adulthood or pediatric penetrating CD but with relatively short follow-up. The risk of recurrence of the penetrating disease after a first complication in childhood is unknown, the factors influencing this risk also. And, there is no consensus either concerning optimal B3 management in children, and the practices are variable from specialist to specialist.
After describing the pediatric population with penetrating CD, the aim of this study was to know the incidence of bowel resection for B3 episode. The secondary aims were to describe the immediate management and long-term evolution of these patients and to identify risk factors for adverse evolution.
Detailed Description
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All patients diagnosed with CD who had underwent a B3 complication (intra-abdominal abscess, fistula, perforation, peritonitis, or phlegmon) before the age of 18. Patient having isolated perineal disease, indeterminate colitis or with too much missing data were excluded.
The main endpoint: incidence of intestinal resection performed for B3 complication.
The secondary endpoints:
* description of the pediatric population with B3 complication with:
* demographic data: sex, family history, phenotype of the disease according to the Paris classification, age at diagnosis of B3, period of diagnosis of B3 (before or after 2001), time between the diagnosis of CD and the diagnosis of B3, a history of medical and surgical treatment for CD received before B3.
* clinical data: type of B3 complication, presence of stenosis and its location, clinical symptoms (fever, obstructive symptoms), nutritional status.
* description of the immediate management of these patients, specifying: the place of care, the type of immediate management performed, the drug treatments received in the acute phase, the medical treatments for CD introduced for the B3 episode, the intestinal resections performed for the B3 episode, the realization of a stoma, the radiological drainage of abscesses, the immediate complications of B3.
* description of the long-term evolution of these patients, specifying: the given drug treatments, the clinical recurrence of the CD, the recurrence of B3, the need for intestinal resection during follow-up, the occurrence of other events
* identification of risk factors for pejorative evolution defined by "recurrence of B3" or "intestinal resection" in these patients.
Conditions
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Keywords
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* patients refuse the use of medical data will be excluded.
18 Years
ALL
No
Sponsors
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Pediatric gastroenterology service, Toulouse University Hospital: Dr Breton
UNKNOWN
Adult gastroenterology service, Montpellier University Hospital: Dr Pineton de Chambrun
UNKNOWN
Pediatric gastroenterology service, Montpellier University Hospital: Dr Kollen
UNKNOWN
EPIMAD Registry: Dr Gower-Rousseau
UNKNOWN
University Hospital, Montpellier
OTHER
Responsible Party
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Principal Investigators
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Laura Kollen, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospitals of Montpellier
Locations
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Uh Montpellier
Montpellier, , France
Countries
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Other Identifiers
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RECHMPL19_0366
Identifier Type: -
Identifier Source: org_study_id