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Faecal calprotectin testing for identifying patients with organic gastrointestinal disease: systematic review and meta-analysis

dc.contributor.authorAn, Yoong-Kyo
dc.contributor.authorPrince, David
dc.contributor.authorGardiner OAM, Fergus
dc.contributor.authorNeeman, Teresa
dc.contributor.authorLinedale, Ecushla C.
dc.contributor.authorAndrews, Jane M.
dc.contributor.authorConnor, Susan
dc.contributor.authorBegun, Jakob
dc.date.accessioned2024-06-04T04:30:19Z
dc.date.available2024-06-04T04:30:19Z
dc.date.issued2019
dc.date.updated2024-05-19T08:18:14Z
dc.description.abstractObjectives To assess the clinical effectiveness of faecal calprotectin (FC) testing for distinguishing between organic gastrointestinal diseases (organic GID), such as inflammatory bowel disease (IBD), and functional gastrointestinal disorders (functional GIDs). Study design Studies that assessed the accuracy of FC testing for differentiating between IBD or organic GID and functional GIDs were reviewed. Articles published in English during January 1998 � June 2018 that compared diagnostic FC testing in primary care and outpatient hospital settings with a reference test and employed the standard enzyme‐linked immunosorbent FC assay method with a cut‐off of 50 or 100 μg/g faeces were included. Study quality was assessed with QUADAS‐2, an evidence‐based quality assessment tool for diagnostic accuracy studies. Data sources MEDLINE and EMBASE; reference lists of screened articles. Data synthesis Eighteen relevant studies were identified. For distinguishing patients with organic GID (including IBD) from those with functional GIDs (16 studies), the estimated sensitivity of FC testing was 81% (95% CI, 74�86%), the specificity 81% (95% CI, 71�88%); area under the curve (AUC) was 0.87. For distinguishing IBD from functional GIDs (ten studies), sensitivity was 88% (95% CI, 80�93%), specificity 72% (95% CI, 59�82%), and AUC 0.89. Assuming a population prevalence of organic GID of 1%, the positive predictive value was 4.2%, the negative predictive value 100%. The difference in sensitivity and specificity between FC testing cut‐offs of 50 μg/g and 100 μg/g faeces was not statistically significant (P = 0.77). Conclusions FC testing is clinically useful for distinguishing organic GID (including IBD) from functional GIDs, and its incorporation into clinical practice for evaluating patients with lower gastrointestinal symptoms could lead to fewer patients with functional GIDs undergoing colonoscopy, reducing costs for both patients and the health system.
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0025-729X
dc.identifier.urihttps://hdl.handle.net/1885/733713068
dc.language.isoen_AUen_AU
dc.publisherAustralasian Medical Association
dc.rights© 2019 The authors
dc.sourceMedical Journal of Australia
dc.titleFaecal calprotectin testing for identifying patients with organic gastrointestinal disease: systematic review and meta-analysis
dc.typeJournal article
local.bibliographicCitation.issue10
local.bibliographicCitation.lastpage467
local.bibliographicCitation.startpage461
local.contributor.affiliationAn, Yoong-Kyo, University of Queensland
local.contributor.affiliationPrince, David, University of New South Wales
local.contributor.affiliationGardiner OAM, Fergus, College of Health and Medicine, ANU
local.contributor.affiliationNeeman, Teresa, Services Portfolio, ANU
local.contributor.affiliationLinedale, Ecushla C., University of Adelaide
local.contributor.affiliationAndrews, Jane M., Royal Adelaide Hospital
local.contributor.affiliationConnor, Susan, University of New South Wales
local.contributor.affiliationBegun, Jakob, University of Queensland
local.contributor.authoruidGardiner OAM, Fergus, u5383043
local.contributor.authoruidNeeman, Teresa, u4321232
local.description.embargo2099-12-31
local.description.notesImported from ARIES
local.identifier.absfor320209 - Gastroenterology and hepatology
local.identifier.absseo200105 - Treatment of human diseases and conditions
local.identifier.ariespublicationu3102795xPUB5466
local.identifier.citationvolume211
local.identifier.doi10.5694/mja2.50384
local.identifier.scopusID2-s2.0-85074832742
local.identifier.thomsonIDWOS:000494012100001
local.publisher.urlhttps://onlinelibrary.wiley.com/
local.type.statusPublished Version

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