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Enregistrement W2316013226 · doi:10.1097/ede.0b013e3181f56fc0

Accounting for Center Effects in Multicenter Trials

2010· letter· en· W2316013226 sur OpenAlexafffund
Navdeep Tangri, Georgios D. Kitsios, Shi Su, David M. Kent

Notice bibliographique

RevueEpidemiology · 2010
Typeletter
Langueen
DomaineMathematics
ThématiqueAdvanced Causal Inference Techniques
Établissements canadiensBC Studies
Organismes subventionnairesCanadian Institutes of Health Research
Mots-clésConfoundingMedicineRandomized controlled trialPopulationMEDLINEObservational studySample size determinationClinical trialFamily medicineInternal medicineStatisticsEnvironmental health

Résumé

récupéré en direct d'OpenAlex

To the Editors: Individual patients in multicenter trials may not represent truly independent observations. Center characteristics and practice patterns, particularly in cases with substantial between-center variability in outcome rates, can lead to potentially misleading conclusions, if ignored. More specifically, failure to consider the center can lead to incorrect standard errors and P values (due to clustering), biased estimates (from uncontrolled confounding), and unrecognized heterogeneity across centers (from effect modification).1–3 Although statistical methods for dealing with center-level clustering in the analysis of randomized controlled trials (RCTs) have been well-described and advocated,1–5 there is some evidence that the application of these methods is limited.6,7 We believe that accounting for center effects is of crucial importance in RCTs of medicinal products, particularly in large multicenter studies.2,3 Because the extent of center-effect adjustment has not previously been described for medicinal products, we performed an empirical evaluation of adjustment for center-level clustering in reports of multicenter RCTs in 4 major medical journals. A systematic search for RCTs published during the year 2007 in 4 prominent medical journals (British Medical Journal, Journal of the American Medical Association, Lancet, and New England Journal of Medicine) was conducted in PubMed. We evaluated the retrieved articles for the following inclusion criteria: adult human study population enrolled, use of randomized design, multicenter enrollment, and testing for efficacy/effectiveness of medicinal products. The main characteristics of the 101 included RCTs are shown in the Table. The majority of the trials used a superiority study design; cardiovascular and oncology disorders were the most commonly studied conditions (32% and 25%, respectively); and binary and time-to-event outcomes were examined in almost equal proportions.TABLE: Characteristics of RCTs Included in the Analysis (n = 101)The number of centers included in the RCTs ranged from 2–707 (median = 64, interquartile range = 22–117), representing 70–22,949 patients. Of the 101 studies, 36 (36%) performed random allocation stratified by center. Statistical analysis adjusting for the clustering of patients by center was present in 18% of the reports. Of these, only 1 used a random term for the center-effect, whereas the remaining used a fixed-effects model. Thus, a total of 82% did not adjust for center effects. Previous investigators have studied RCTs of surgical interventions; they reported similar results for allocation stratification on center (38%) and adjusted statistical analysis (6%).6–8 Our literature sample is more contemporary and focused on 4 major medical journals publishing RCTs of medical interventions. Studies published in these journals are expected to be of high quality and have the potential to disproportionately influence clinical practice. Nonetheless, the similarities between our results and those of previous investigators highlight the lack of accounting for center effects in RCTs as a widespread problem. Our analysis has some limitations. Our results may not be generalizable to the entire medical literature. (The proportion of RCTs accounting for center effects is likely to be even lower among the less prestigious journals.) Second, our conclusions regarding center effect accounting were based on the published statistical methods. It is possible that appropriate accounting was performed, but not reported due to space constraints. In summary, using a contemporary sample of RCTs from 4 major medical journals, we find that center effects are not accounted for in the recruitment stage or in the statistical analysis of the majority of RCTs evaluating medical interventions. The recent extension of the CONSORT statement advocates center-effect reporting and adjustment for trials, involving nonpharmacologic interventions. Our analysis highlights the need for similar recommendations in trials of medical therapies. Navdeep Tangri Georgios D. Kitsios Shi Hann Su David M. Kent Tufts Clinical and Translational Science Institute Institute for Clinical Research and Health Policy Studies Tufts Medical Center Boston, MA [email protected]

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 distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,011
score de la tête « metaresearch » (Gemma)0,171
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesMétarecherche, Méta-épidémiologie (sens strict), Intégrité de la recherche
Catégories consensuellesIntégrité de la recherche
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Sans objet · Signal consensuel: aucune
GenreSignal candidat: Commentaire · Signal consensuel: Commentaire
Score de désaccord entre enseignants0,504
Score d'incertitude au seuil1,000

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0110,171
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0030,001
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0000,000
Science ouverte0,0010,000
Intégrité de la recherche0,0040,005
Charge utile insuffisante (le modèle a refusé de juger)0,0000,000

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 Opus0,368
Tête enseignante GPT0,517
Écart entre enseignants0,149 · 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; les deux têtes enseignantes s’accordent sur ce qui est montré ici.

Devis d'étudeSans objet
Domainenon disponible
GenreCommentaire

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

En bref

Citations10
Publié2010
Routes d'admission2
Résumé présentoui

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