Evidence map›Paper›PMID 33125663›Full record

ArticleDrug safety2021

Patterns of Benzodiazepine Use and Excess Risk of All-Cause Mortality in the Elderly: A Nationwide Cohort Study.

Clément Mathieu, Pierre Joly, Hélène Jacqmin-Gadda, Mathilde Wanneveich, Bernard Bégaud, Antoine Pariente

Abstract read
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Article in Drug safety, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Clément MathieuUniv. Bordeaux, INSERM, BPH, U1219, Team Pharmacoepidemiology, Univ. Bordeaux, F-33000, Bordeaux, France.
Pierre JolyUniv. Bordeaux, INSERM, BPH, U1219, Team Biostatistics, Univ. Bordeaux, F-33000, Bordeaux, France.
Hélène Jacqmin-GaddaUniv. Bordeaux, INSERM, BPH, U1219, Team Biostatistics, Univ. Bordeaux, F-33000, Bordeaux, France.
Mathilde WanneveichUniv. Bordeaux, INSERM, BPH, U1219, Team Biostatistics, Univ. Bordeaux, F-33000, Bordeaux, France.
Bernard BégaudUniv. Bordeaux, INSERM, BPH, U1219, Team Pharmacoepidemiology, Univ. Bordeaux, F-33000, Bordeaux, France.
Antoine ParienteUniv. Bordeaux, INSERM, BPH, U1219, Team Pharmacoepidemiology, Univ. Bordeaux, F-33000, Bordeaux, France. antoine.pariente@u-bordeaux.fr.ORCID 0000-0002-7873-5483

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite the risks associated with their use, benzodiazepines remain used more widely than wisely. In this context, a better understanding of how their patterns of use can be associated with an increased risk of death appears essential. Indeed, the studies that investigated this association so far are inconsistent and question the influence of potential biases.

objectiveThe objective of this study was to investigate the association of various patterns of benzodiazepine use with all-cause mortality.

methodsA nationwide cohort of non-prevalent benzodiazepine users aged ≥ 65 years was identified using French healthcare insurance system claims databases. Exposure to benzodiazepines considered short-term, chronic (defined as a cumulated ≥ 6-month period over the previous 12 months), ongoing, and discontinued use. Using a Cox model, adjusted hazard ratios for all-cause mortality were estimated according to benzodiazepine patterns of use; exposure and confounders were treated as time-dependent variables.

resultsIn the cohort of 54,958 individuals aged ≥ 65 years, adjusted hazard ratios for all-cause mortality and benzodiazepines were 2.26 (95% confidence interval 1.96-2.61) for short-term use, 3.86 (3.04-4.90) for chronic use-discontinued, and 3.05 (2.17-4.29) for chronic use-ongoing. At age 80 years, these were 1.62 (1.48-1.79), 2.00 (1.82-2.19) and 1.13 (1.02-1.26), respectively. Adjusted hazard ratios show similar decreases with age for all patterns of benzodiazepine use.

conclusionsThese findings confirm the existence of an excess risk of mortality associated with benzodiazepine use and provide pattern- and age-specific estimates. Higher risks were observed for patients aged < 80 years, short-term use, or chronic use recently interrupted. If the two latter can relate to an indication bias, the associations found for ongoing chronic use and short-term use conversely support a potential causal hypothesis.

Indexed as

BenzodiazepinesAgedAged, 80 and overBiasCohort StudiesDatabases, FactualHumansProportional Hazards ModelsBenzodiazepines

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.