Evidence map›Paper›PMID 27053716›Full record

SynthesisNeurology2016

Association between oral fluoroquinolones and seizures: A self-controlled case series study.

Celine S L Chui, Esther W Chan, Angel Y S Wong, Adrian Root, Ian J Douglas, Ian C K Wong

Abstract readMeta-Analysis
In one paragraph

Synthesis in Neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

  1. Seizures and quinolone antibiotics in children: a systematic review of adverse events.European journal of hospital pharmacy : science and practice · 2020
    Pooled it
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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.

Celine S L ChuiFrom the Centre for Safe Medication Practice and Research (C.S.L.C., E.W.C., A.Y.S.W., I.C.K.W.), Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, PR China; Department of Non-communicable Disease Epidemiology (A.R., I.J.D.), Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine; Research Department of Practice and Policy (I.C.K.W.), UCL School of Pharmacy, London, UK.
Esther W ChanFrom the Centre for Safe Medication Practice and Research (C.S.L.C., E.W.C., A.Y.S.W., I.C.K.W.), Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, PR China; Department of Non-communicable Disease Epidemiology (A.R., I.J.D.), Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine; Research Department of Practice and Policy (I.C.K.W.), UCL School of Pharmacy, London, UK.
Angel Y S WongFrom the Centre for Safe Medication Practice and Research (C.S.L.C., E.W.C., A.Y.S.W., I.C.K.W.), Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, PR China; Department of Non-communicable Disease Epidemiology (A.R., I.J.D.), Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine; Research Department of Practice and Policy (I.C.K.W.), UCL School of Pharmacy, London, UK.
Adrian RootFrom the Centre for Safe Medication Practice and Research (C.S.L.C., E.W.C., A.Y.S.W., I.C.K.W.), Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, PR China; Department of Non-communicable Disease Epidemiology (A.R., I.J.D.), Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine; Research Department of Practice and Policy (I.C.K.W.), UCL School of Pharmacy, London, UK.
Ian J DouglasFrom the Centre for Safe Medication Practice and Research (C.S.L.C., E.W.C., A.Y.S.W., I.C.K.W.), Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, PR China; Department of Non-communicable Disease Epidemiology (A.R., I.J.D.), Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine; Research Department of Practice and Policy (I.C.K.W.), UCL School of Pharmacy, London, UK.
Ian C K WongFrom the Centre for Safe Medication Practice and Research (C.S.L.C., E.W.C., A.Y.S.W., I.C.K.W.), Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, PR China; Department of Non-communicable Disease Epidemiology (A.R., I.J.D.), Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine; Research Department of Practice and Policy (I.C.K.W.), UCL School of Pharmacy, London, UK. i.wong@ucl.ac.uk.

Funding

Medical Research Council G0802403Medical Research Council MR/M014649/1
6 · The paper itself

Abstract

objectivesThe aim of this study was to investigate the association and to estimate the crude absolute risk of seizure among patients exposed to fluoroquinolones (FQs) in Hong Kong and the United Kingdom.

methodsA self-controlled case series study was conducted. Data were collected from the Hong Kong Clinical Data Analysis and Reporting System database and the Clinical Practice Research Datalink. Patients who were prescribed any oral FQ and had an incident seizure diagnosis from 2001 to 2013 were included. The risk windows were defined as pre-FQ start, FQ-exposed, and post-FQ completion. Incidence rate ratios were estimated in all risk windows and compared with baseline periods. A post hoc subgroup analysis was conducted to examine the effect of patients with a history of seizure.

resultsAn increased incidence rate ratio was found in the pre-FQ start periods and no association was found in the post-FQ completion periods in both databases. The crude absolute risk of an incident seizure in 10,000 oral FQ prescriptions was 0.72 (95% confidence interval 0.47-1.10) in the Clinical Data Analysis and Reporting System and 0.40 (95% confidence interval 0.30-0.54) in the Clinical Practice Research Datalink. The rate ratio during treatment was not higher than pre-FQ start periods among patients with a history of seizure, therefore the results did not raise serious concerns.

conclusionsThis study does not support a causal association between the use of oral FQs and the subsequent occurrence of seizure. An increased risk before the FQ exposure period suggests that the clinical indication for which FQ was prescribed may have contributed to the development of seizure rather than the drug itself.

Indexed as

Administration, OralAgedAnti-Bacterial AgentsFemaleFluoroquinolonesFollow-Up StudiesHong KongHumansIncidenceMaleMiddle AgedRiskSeizuresSensitivity and SpecificityUnited KingdomAnti-Bacterial AgentsFluoroquinolones

Identifiers

PMID27053716
PMCPMC4854590

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.