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Record W2579934954 · doi:10.1093/ofid/ofw172.85

Norovirus Stool Loads in Cancer Patients With Norovirus Gastroenteritis

2016· article· en· W2579934954 on OpenAlexaff
Taojun He, Tracy McMillen, Liang Hua Chen, Yuanyuan Qiu, Xue-dong Lu, Mini Kamboj, Yi‐Wei Tang

Bibliographic record

VenueOpen Forum Infectious Diseases · 2016
Typearticle
Languageen
FieldMedicine
TopicViral gastroenteritis research and epidemiology
Canadian institutionsUniversity of Alberta
Fundersnot available
KeywordsNorovirusMedicineAcute gastroenteritisFecesDiarrheaVirologyMicrobiologyGastroenterologyVirusBiology

Abstract

fetched live from OpenAlex

Background. Norovirus (NoV) infections are associated with substantial morbidity in immunocompromised patients. The relationship between stool norovirus viral loads (VLs) on immediate and long-term complications of NoV gastroenteritis in cancer patients has not been previously examined. We developed a real-time quantitative polymerase chain reaction (NoV-qPCR) assay to determine NoV genogroup GI and GII VL in stool. The VL at the time of diagnosis was determined and correlated with clinical characteristics as well as outcomes associated with NoV gastroenteritis patients with cancer. Methods. From March 2014 until January 2016, NoV PCR-positive stool specimens as determined by the Luminex xTAG Gastrointestinal Pathogen Panel (GPP) were included and subsequently tested by the NoV-qPCR assay. Each specimen was tested in duplicate, and geometric mean copies per gram of stool (GMC) were calculated. Electronic medical records were reviewed to extract relevant information on clinical severity of NoV infections based on modified Vesikari scores (MVS). Results. During the 23-month study period, 6918 stool specimens were submitted for testing by GPP. A total of 234 specimens (3.4%) from 154 patients were positive for NoV (GI, 33; GII, 201). The NoV-GII GMC ± standard deviation was 5.35 ± 1.59, which was significantly higher than that of NV-GI (3.94 ± 1.57, odds ratio [OR] = 7.87, p = 0.001). Based on the MVS criteria, 210 episodes were divided into mild (n = 122, GMC = 4.28 ± 1.49), moderate (n = 33, GMC = 5.55 ± 1.32), and severe (n = 55, GMC = 6.66 ± 0.86) clinical severity groups, respectively. In univariate analysis, higher stool NoVs were associated with GII infections, longer diarrhea duration, and more diarrhea frequency, longer vomiting duration, and more vomiting frequency, higher fever, as well as more total parenteral nutrition and deeper dehydration. In multivariate analysis, higher stool NoV VL at the time of diagnosis correlated with GII infections (OR = 3.25, 95% confidence interval [CI] = 1.18–8.97, P = 0.023) and predicted clinical severity (OR = 6.56, 95% CI = 2.35–18.36, P = 0.001). Conclusion. Norovirus GII infections are associated with a higher VL compared with GI. Regardless of infecting NoV genogroup, higher VL at diagnosis is associated with severe clinical disease and poor outcome. This quantification method may have utility for clinical monitoring. Disclosures. All authors: No reported disclosures.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.012
GPT teacher head0.305
Teacher spread0.293 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2016
Admission routes1
Has abstractyes

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