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Enregistrement W2557379370 · doi:10.1182/blood.v126.23.1117.1117

Assessing Incidence of and Risk Predictors Ascertained at Diagnosis for Symptomatic Venous Thrombotic Events in Pediatric Cancer Patients: A 20-Year Population Based Study from the Maritimes, Canada

2015· article· en· W2557379370 sur OpenAlexaffabout
Zeina Asyyed, Tamara MacDonald, Victoria Price, Conrad V. Fernandez, Mark L. Bernstein, Ketan Kulkarni

Notice bibliographique

RevueBlood · 2015
Typearticle
Langueen
DomaineHealth Professions
ThématiqueCentral Venous Catheters and Hemodialysis
Établissements canadiensIzaak Walton Killam Health CentreDalhousie University
Organismes subventionnairesnon disponible
Mots-clésMedicineCancer registryIncidence (geometry)Pediatric cancerCancerGeneralizability theoryPopulationMedical recordCohortPediatricsEmergency medicineSurgeryInternal medicineEnvironmental health

Résumé

récupéré en direct d'OpenAlex

Abstract Background: Symptomatic venous thrombotic events (sVTE) are a well-recognized complication in pediatric cancer patients. Accurate data on true incidence of sVTE is limited due to large variability in design and methodology of previously published reports. As well, risk factors are unclear. Moreover, the limitations of several of the previously described risk factors for sVTE include (i) limited generalizability to all pediatric cancers, (ii) hemostatic protein lab values are altered by cancer itself, (iii) long turn-around times from laboratories and (iv) testing restricted to specialized labs. There is a need to identify risk factors for sVTE in pediatric cancer patients that are easily evaluated at the time of cancer diagnosis. Aims: Establish incidence of sVTE and identify risk factors associated with sVTE in pediatric cancer patients. Methods: All pediatric cancer patients in the 3 Maritime Provinces of Nova Scotia, New Brunswick and Prince Edward Island are treated at IWK Health Center (IWK) in a shared care model. This provides a population-based cohort of pediatric cancer patients from the Maritimes. After ethics approval, all pediatric cancer patients treated at the IWK from 1995 to 2014 with sVTE were identified through a conceptual framework as follows. Clinical (including sVTE) and laboratory data was extracted from the: (i) Pediatric oncology hospital database (ii) Provincial Cancer in Young People registry (iii) Electronic medical records (iv) Pharmacy database (v) IWK Central Venous Access Database and (vi) Hospital health records. After extraction, data from all sources was amalgamated and cross-verified. SPSS version 21 was used for statistical analysis. Central veins were defined as veins including and proximal to the axillary vein in the upper extremity and femoral vein in the lower extremity. sVTE was defined as radiologically documented VTE with at least one sign/symptom directly associated with VTE. Patients with VTE during relapsed disease and those with asymptomatic/incidentally diagnosed VTE were excluded from analysis. Results: Forty-seven (4.356±0.01%) of the 1079 patients had sVTE. The mean age at diagnosis for sVTE patients was 10.142 years. The mean age at diagnosis of the remaining patients (n=1032) was 7.451 years. The difference in the mean ages in the 2 categories was statistically significant (p=0.001). The gender ratio was M:F: 1.765:1 in patients with sVTE as compared to M:F: 1.123:1 in the remainder of the patients (p=0.336). Central veins were the most common location for sVTE (72.3%, n=34). Other less common locations included 1 each of sinovenous, mesenteric, cardiac, renal vein thrombosis and pulmonary embolism. On univariate analysis for risk factors, age > 10 years at diagnosis (P = 0.021), type of cancer (P = 0.028) and non-O blood group (P = 0.043) were associated with sVTE, while gender (p=0.336) and use of asparaginase (p=0.663) were not. On multivariate analysis, age > 10 years at diagnosis (odds ratio [OR]: 1.737 [1.066-2.831], p=0.027), and type of cancer (non-brain tumor; OR: 11.154 [1.527-81.451], P=0.017) were associated with sVTE. The association of non-O blood group with sVTE trended towards significance (OR: 1.886 [0.962-3.695], p=0.065) likely due to small numbers and difficulty identifying sVTE retrospectively. Conclusion: In a large population-based cohort of patients, we established incidence of sVTE in pediatric cancer patients. The study identified that sVTE occur in central veins in almost 3/4th of the patients. As well, we evaluated easily available and independent risk factors for sVTE in pediatric cancer patients. Further larger prospective and multicenter studies are needed to validate these observations and develop a risk prediction model for sVTE in pediatric cancer patients. Disclosures No relevant conflicts of interest to declare.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,001
score de la tête « metaresearch » (Gemma)0,002
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: Observationnel
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,022
Score d'incertitude au seuil0,143

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0010,002
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,001
Bibliométrie0,0020,006
Études des sciences et des technologies0,0020,001
Communication savante0,0010,000
Science ouverte0,0010,001
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0010,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,027
Tête enseignante GPT0,321
Écart entre enseignants0,294 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations1
Publié2015
Routes d'admission2
Résumé présentoui

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