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P0812 ELEVATED SERUM TRYSPSINOGEN AMONG CHILDHOOD ALLOGENEIC HEMATOPOETIC STEM CELL TRANSPLANT RECIPIENTS: AN INDICATOR OF POOR OUTCOME?

2004· article· en· W2095455119 on OpenAlexaff
M Dirks, Staci Martin, L. Hagen, Mary Barron, Winnie Ip, S. Beharri, John Doyle, Peter R. Durie

Bibliographic record

VenueJournal of Pediatric Gastroenterology and Nutrition · 2004
Typearticle
Languageen
FieldMedicine
TopicHematopoietic Stem Cell Transplantation
Canadian institutionsSickKids FoundationHospital for Sick Children
Fundersnot available
KeywordsMedicineInternal medicineGastroenterologySubclinical infectionTrypsinogenProspective cohort studyAcute pancreatitisPancreatitisMalabsorptionTransplantationSurgeryTrypsin

Abstract

fetched live from OpenAlex

Introduction: Diarrhea, malabsorption and malnutrition are commonly encountered follow hematopoetic stem cell transplantation (HSCT). We had previously reported 4 cases of pancreatic insufficiency following allogeneic HSCT in children. Prospective data of the frequency of pancreatitis and pancreatic dysfunction in children undergoing HSCT have not been reported. Methods: A prospective, single centre study of all children undergoing a HSCT over a one year period (2001–2). Serial serum trypsinogen values were followed at 0, 1, 6 and 12 months (normal range 16.6–46.5 ng/mL) following HSCT. A high trypsinogen is suggestive of pancreatic inflammation, while a value of <7 ng/ml suggests exocrine pancreatic insufficiency. Aim: To determine the frequency of subclinical pancreatitis, its natural history, and its relationship to outcome in HSCT. Results: 52 of 62 eligible HSCT recipients (mean age 7.2 years) were recruited. Among these, 34/52 (65%) patients enrolled received an allogeneic HSCT (23 from matched unrelated donor). Prospective clinical data regarding diagnosis, treatment, and complications before and up to one year following HSCT were collected. 19/34 (56%) of allogeneic recipients had an elevated serum trypsinogen >50ng/ml at 1 and /or 6 months compared to only 2/18 (11%) of autologous HSCT recipients. Overall mortality at 1 year was 23.1% (allogeneic 26.4%, autologous 11.1%). Among allogeneic recipients with an elevated trypsinogen level, 47.4% died prior to 1 year of follow-up, as compared to 17.6% of those allogeneic HSCT recipients with normal trypsinogen levels (OR=5.1, 95% CI 1.1–23.3). 6/25 1 year survivors of allogeneic HSCT had persistently elevated trypsinogen levels. No case of pancreatic insufficiency was observed up to 1 year’s follow-up. Conclusion: Elevated serum trypsinogen, which probably reflects subclinical pancreatic inflammation, occurs more commonly in allogeneic transplant recipients. These results suggest that elevated serum trypsinogen is associated with a significant increase in mortality following allogeneic HSCT. Further analysis of the data will determine whether an association with acute graft-versus host disease (GVHD) exists. Follow up of this cohort will ascertain whether persistently elevated trypsinogen levels in transplant survivors, is a risk factor for the development of exocrine pancreatic failure subsequently.

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)0.001
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 score0.002
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
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 head0.011
GPT teacher head0.239
Teacher spread0.228 · 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".

Quick stats

Citations1
Published2004
Admission routes1
Has abstractyes

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