An epidemic of redundant meta-analyses.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
05 2021
Historique:
revised: 05 02 2021
received: 01 12 2020
accepted: 19 02 2021
pubmed: 5 3 2021
medline: 22 5 2021
entrez: 4 3 2021
Statut: ppublish

Résumé

Meta-analyses are widely used to strengthen available evidence and obtain more precise estimates of treatment effect than any individual trial. Paradoxically, multiplication of meta-analyses on the same topic can lead to confusion as practitioners no longer benefit from a rapid and synthetic response. This phenomenon may appear disproportionate when the number of published meta-analyses exceeds the number of original studies. To describe an example of redundant meta-analyses published in the same area with the same randomized clinical trials (RCTs). A systematic review was performed to identify all published meta-analyses of original RCTs that compared direct oral anticoagulants with low molecular weight heparins in cancer patients with venous thromboembolism (VTE). Forest plots were used to represent the meta-analyses results for efficacy (VTE recurrence) and safety (major bleeding) endpoints. An authors' network was constructed to explore the links between the authors of the published meta-analyses. In the past 3 years, four original RCTs were the subject of 20 published meta-analyses by 142 authors: five, four, and 11 meta-analyses pooled the data of two, three, and four RCTs, respectively. The results of meta-analyses were similar regarding the risks of VTE recurrence and major bleeding. The 11 meta-analyses of four RCTs were published within 6 months of the publication of the last RCT. The epidemic proportions of such redundant literature and authorship could be moderated by developing "living" meta-analyses and encouraging authors of new RCTs to update the corresponding meta-analysis in the same paper as their original research.

Sections du résumé

BACKGROUND
Meta-analyses are widely used to strengthen available evidence and obtain more precise estimates of treatment effect than any individual trial. Paradoxically, multiplication of meta-analyses on the same topic can lead to confusion as practitioners no longer benefit from a rapid and synthetic response. This phenomenon may appear disproportionate when the number of published meta-analyses exceeds the number of original studies.
OBJECTIVES
To describe an example of redundant meta-analyses published in the same area with the same randomized clinical trials (RCTs).
METHODS
A systematic review was performed to identify all published meta-analyses of original RCTs that compared direct oral anticoagulants with low molecular weight heparins in cancer patients with venous thromboembolism (VTE). Forest plots were used to represent the meta-analyses results for efficacy (VTE recurrence) and safety (major bleeding) endpoints. An authors' network was constructed to explore the links between the authors of the published meta-analyses.
RESULTS
In the past 3 years, four original RCTs were the subject of 20 published meta-analyses by 142 authors: five, four, and 11 meta-analyses pooled the data of two, three, and four RCTs, respectively. The results of meta-analyses were similar regarding the risks of VTE recurrence and major bleeding. The 11 meta-analyses of four RCTs were published within 6 months of the publication of the last RCT.
CONCLUSIONS
The epidemic proportions of such redundant literature and authorship could be moderated by developing "living" meta-analyses and encouraging authors of new RCTs to update the corresponding meta-analysis in the same paper as their original research.

Identifiants

pubmed: 33660901
doi: 10.1111/jth.15280
pii: S1538-7836(22)00758-9
doi:

Substances chimiques

Anticoagulants 0
Heparin, Low-Molecular-Weight 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1299-1306

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2021 International Society on Thrombosis and Haemostasis.

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Auteurs

Céline Chapelle (C)

Unité de Recherche Clinique, Innovation, Pharmacologie, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France.
SAINBIOSE U1059, Université Jean Monnet, Univ. Lyon, INSERM, Saint-Etienne, France.

Edouard Ollier (E)

Unité de Recherche Clinique, Innovation, Pharmacologie, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France.
SAINBIOSE U1059, Université Jean Monnet, Univ. Lyon, INSERM, Saint-Etienne, France.

Philippe Girard (P)

Institut Mutualiste Montsouris, Paris, France.
F-CRIN INNOVTE network, Saint Etienne, France.

Corinne Frere (C)

Sorbonne Université, INSERM UMRS1166, ICAN - Institute of CardioMetabolism and Nutrition, Hôpital Pitié-Salpêtrière, Paris, France.

Patrick Mismetti (P)

Unité de Recherche Clinique, Innovation, Pharmacologie, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France.
SAINBIOSE U1059, Université Jean Monnet, Univ. Lyon, INSERM, Saint-Etienne, France.
F-CRIN INNOVTE network, Saint Etienne, France.
Service de Médecine Vasculaire et Thérapeutique, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France.

Michel Cucherat (M)

Service de Pharmacologie, HCL, UMR CNRS 5558 Evaluation et Modélisation des Effets Thérapeutiques, Université Claude Bernard Lyon 1, Lyon, France.

Silvy Laporte (S)

Unité de Recherche Clinique, Innovation, Pharmacologie, CHU Saint-Etienne, Hôpital Nord, Saint-Etienne, France.
SAINBIOSE U1059, Université Jean Monnet, Univ. Lyon, INSERM, Saint-Etienne, France.
F-CRIN INNOVTE network, Saint Etienne, France.

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