Mc. Dubinsky et al., Clinical utility of serodiagnostic testing in suspected pediatric inflammatory bowel disease, AM J GASTRO, 96(3), 2001, pp. 758-765
OBJECTIVES: Confronted with nonspecific symptoms, accurate screening tests
would be useful to clinicians to distinguish between functional childhood d
isorders and inflammatory bowel disease (IBD), thus avoiding invasive diagn
ostic testing. Traditional ulcerative colitis-specific perinuclear antineut
rophil cytoplasmic antibody (pANCA) and Crohn's disease-specific anti-Sacch
aromyces cerevisiae antibody (ASCA) serodiagnostic assays have recently bee
n modified, with ELISA cut-off values recalculated to maximize sensitivity.
The aim of this study was to determine whether the combination of these se
rodiagnostic tests could maximize diagnostic accuracy and minimize invasive
investigations in pediatric patients presenting with nonspecific symptoms
suggestive nf IBD.
METHODS: With investigators blinded to clinical diagnoses, ASCA, ANCA, and
pANCA profiles were obtained prospectively from 128 patients undergoing com
plete diagnostic evaluation for IBD. In phase I, diagnostic accuracy and pr
edictive values of the modified and traditional assays were compared for th
e IBD (n = 54) and non-IBD groups (n = 74). In phase II, the overall accura
cy of a novel sequential diagnostic testing strategy was determined. Additi
onally, the potential number of invasive investigations avoided with the hy
pothetical application of this strategy to the cohort was determined.
RESULTS: For phase I, the modified serodiagnostic assay was more sensitive
(81 vs 69%), whereas the traditional assay had a higher specificity (96 vs
72%) for IBD (p < 0.05) For phase II, false-positive diagnoses would have b
een reduced by 81%, yielding an overall sequential testing strategy accurac
y of 84%.
CONCLUSIONS: The incorporation of sequential noninvasive testing into a dia
gnostic strategy may avoid unnecessary and costly evaluations and facilitat
e clinical decision making when the diagnosis of IBD in children is initial
ly uncertain. <(c)> 2001 by Am. Cell. of Gastroenterology.