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THE ANTICOAGULATION OF CALF THROMBOSIS (ACT) PROJECT: RESULTS FROM THE RANDOMISED CONTROLLED EXTERNAL PILOT TRIAL

2013· article· en· W2055796033 on OpenAlexaff
Daniel Horner, Kerstin Hogg, Richard Body, Michael J. Nash, Kevin Mackway‐Jones

Bibliographic record

VenueEmergency Medicine Journal · 2013
Typearticle
Languageen
FieldMedicine
TopicVenous Thromboembolism Diagnosis and Management
Canadian institutionsOttawa Hospital
Fundersnot available
KeywordsMedicineRandomized controlled trialPulmonary embolismDeep veinConfidence intervalVenous thrombosisThrombosisHazard ratioClinical trialAmbulatoryEmergency departmentNumber needed to treatSurgeryRelative riskEmergency medicineInternal medicine

Abstract

fetched live from OpenAlex

Objectives & Background There is currently little evidence defining the clinical importance of detecting and treating isolated distal deep vein thrombosis (IDDVT). Contemporary international guidelines vary regarding diagnostic and therapeutic advice. The potential benefits of anticoagulation remain poorly defined. We sought to evaluate the feasibility of a randomised controlled trial within a modern emergency department cohort. Methods A pragmatic, open label, external pilot randomised controlled trial conducted from January 2011 to April 2012. Consecutive ambulatory symptomatic IDDVT patients were approached for inclusion. Participants were randomised to receive either conservative management (control) or phased therapeutic anticoagulation (intervention). All patients underwent assessor blinded color duplex imaging after 7 and 21 days, and clinical follow up at three months. Principal feasibility outcomes were recruitment rate and attrition. The primary clinical outcome was a composite of proximal propagation, pulmonary embolism, death attributable to venous thromboembolic disease or major bleeding. Analysis was by intention to treat. Results Acute IDDVT was detected in 93 cases. 79 were subsequently deemed eligible and 70 (88.6% of those eligible) recruited. 59/70 (84.3%, 95% CI 74.0–91.0%) patients completed the full protocol. All patients but 1 were followed up by direct contact after 90 days. Allocation crossover occurred in 15 (21.4%) cases. All predefined feasibility outcomes were achieved. The primary clinical outcome occurred in 4/35 (11.4%) controls and 0/35 in the intervention group (Absolute Risk Reduction [ARR] 11.4%, 95% Confidence Interval [CI] −1.5 to 26.7, p=0.11, number needed to treat [NNT] of 9). There were no cases of major bleeding in either group. Propagation to any site occurred in 11/35 (31.4%) of conservatively treated patients compared with 2/35 (5.7%) of those randomized to anticoagulation (ARR 25.7%, 95% CI 5.9 to 44.3%, P=0.001, NNT 4). Minor bleeding occurred in 3/35 (8.6%) controls and 7/35 (20.0%) anticoagulated patients (p=0.31). Conclusion We have established feasibility for a definitive trial on the value of therapeutic anticoagulation for IDDVT. Our pilot study currently provides the largest prospective randomised clinical dataset on this topic and demonstrates a non-significant trend towards reduction in complications with anticoagulation.

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)0.019
metaresearch head score (Gemma)0.036
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.019
Threshold uncertainty score0.099

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0190.036
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0030.003
Bibliometrics0.0010.001
Science and technology studies0.0000.002
Scholarly communication0.0020.002
Open science0.0010.001
Research integrity0.0030.002
Insufficient payload (model declined to judge)0.0070.001

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 head0.062
GPT teacher head0.342
Teacher spread0.279 · 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 designRandomized trial
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
Published2013
Admission routes1
Has abstractyes

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