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Predicting the Individual Risk of Acute Severe Colitis at Diagnosis

Cesarini, Monica (author)
Oxford Univ Hosp, Translat Gastroenterol Unit, Oxford, England.;Sapienza Univ Rome, Dipartimento Med Interna & Specialita Med, Rome, Italy.
Collins, Gary S. (author)
Univ Oxford, Ctr Stat Med, Oxford, England.
Rönnblom, Anders (author)
Uppsala universitet,Gastroenterologi/hepatologi
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Santos, Antonieta (author)
Cambridge Univ Hosp, Gastroenterol Unit, Cambridge, England.;Hosp Amato Lusitano, Gastroenterol Unit, Castelo Branco, Portugal.
Wang, Lai Mun (author)
Oxford Univ Hosp, Dept Cellular Pathol, Oxford, England.
Sjöberg, Daniel, 1974- (author)
Uppsala universitet,Gastroenterologi/hepatologi
Parkes, Miles (author)
Oxford Univ Hosp, Translat Gastroenterol Unit, Oxford, England.
Keshav, Satish (author)
Oxford Univ Hosp, Translat Gastroenterol Unit, Oxford, England.
Travis, Simon P. L. (author)
Oxford Univ Hosp, Translat Gastroenterol Unit, Oxford, England.
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Oxford Univ Hosp, Translat Gastroenterol Unit, Oxford, England;Sapienza Univ Rome, Dipartimento Med Interna & Specialita Med, Rome, Italy. Univ Oxford, Ctr Stat Med, Oxford, England. (creator_code:org_t)
2016-09-19
2017
English.
In: Journal of Crohn's & Colitis. - : OXFORD UNIV PRESS. - 1873-9946 .- 1876-4479. ; 11:3, s. 335-341
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background and Aims: Acute severe colitis [ASC] is associated with major morbidity. We aimed to develop and externally validate an index that predicted ASC within 3 years of diagnosis. Methods: The development cohort included patients aged 16-89 years, diagnosed with ulcerative colitis [UC] in Oxford and followed for 3 years. Primary outcome was hospitalization for ASC, excluding patients admitted within 1 month of diagnosis. Multivariable logistic regression examined the adjusted association of seven risk factors with ASC. Backwards elimination produced a parsimonious model that was simplified to create an easy-to-use index. External validation occurred in separate cohorts from Cambridge, UK, and Uppsala, Sweden. Results: The development cohort [Oxford] included 34/111 patients who developed ASC within a median 14 months [range 1-29]. The final model applied the sum of 1 point each for extensive disease, C-reactive protein [CRP] >10 mg/l, or haemoglobin < 12 g/dl F or < 14 g/dl M at diagnosis, to give a score from 0/3 to 3/3. This predicted a 70% risk of developing ASC within 3 years [score 3/3]. Validation cohorts included different proportions with ASC [Cambridge = 25/96; Uppsala = 18/298]. Of those scoring 3/3 at diagnosis, 18/18 [Cambridge] and 12/13 [Uppsala] subsequently developed ASC. Discriminant ability [c-index, where 1.0 = perfect discrimination] was 0.81 [Oxford], 0.95 [Cambridge], 0.97 [Uppsala]. Internal validation using bootstrapping showed good calibration, with similar predicted risk across all cohorts. A nomogram predicted individual risk. Conclusions: An index applied at diagnosis reliably predicts the risk of ASC within 3 years in different populations. Patients with a score 3/3 at diagnosis may merit early immunomodulator therapy.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Gastroenterologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Gastroenterology and Hepatology (hsv//eng)

Keyword

Biomarkers
clinical trials
acute severe colitis
prediction
ulcerative colitis

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