Evidence map›Paper›PMID 37548755›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2024

Pilot study on the probability of drug-drug interactions among direct oral anticoagulants (DOACs) and antiseizure medications (ASMs): a clinical perspective.

Federica Ranzato, Roberta Roberti, Cristina Deluca, Mariarosa Carta, Alessia Peretti, Diana Polo, Francesco Perini, Emilio Russo, Gianfranco Di Gennaro

Abstract read
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Review
  3. Observational
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

9 authors.

Federica Ranzato *Regional Epilepsy Center, Neurology Unit, San Bortolo Hospital, Vicenza, Italy.
Roberta Roberti *Science of Health Department, School of Medicine, Magna Graecia University of Catanzaro, Via T. Campanella, 115, 88100, Catanzaro, Italy.
Cristina DelucaStroke Unit, Neurology, San Bortolo Hospital, Vicenza, Italy.
Mariarosa CartaLaboratory Unit, San Bortolo Hospital, Vicenza, Italy.
Alessia PerettiRegional Epilepsy Center, Neurology Unit, San Bortolo Hospital, Vicenza, Italy.
Diana PoloRegional Epilepsy Center, Neurology Unit, San Bortolo Hospital, Vicenza, Italy.
Francesco PeriniRegional Epilepsy Center, Neurology Unit, San Bortolo Hospital, Vicenza, Italy.
Emilio RussoScience of Health Department, School of Medicine, Magna Graecia University of Catanzaro, Via T. Campanella, 115, 88100, Catanzaro, Italy. erusso@unicz.it.ORCID http://orcid.org/0000-0002-1279-8123
Gianfranco Di GennaroScience of Health Department, School of Medicine, Magna Graecia University of Catanzaro, Via T. Campanella, 115, 88100, Catanzaro, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is little and controversial information about changes in plasma concentrations (PCs) or clinical events during coadministration of antiseizure medications (ASMs) and direct oral anticoagulants (DOACs). We aimed to explore possible determinants of dosage class among DOACs trough PCs when ASMs are co-administered and the relative risks. We also provided some clinical examples of patients' management.

methodsData on adult patients concomitantly treated with ASMs (grouped in enzyme-inducing [I-ASMs], non-inducing [nI-ASMs], and levetiracetam [LEV]) and DOACs with at least one measurement of DOACs' PC were retrospectively collected. The role of DOAC-ASM combinations in predicting PC class (ranging from I at ischemic/thromboembolic risk to IV at increased bleeding risk) was investigated by an ordered logit model, and the marginal probabilities of belonging to the four dosage classes were calculated.

resultsWe collected 46 DOACs' PCs out of 31 patients. There were 5 (10.9%) determinations in class I (4 out of 5 with concomitant I-ASMs) and 5 (10.9%) in class IV. The rivaroxaban/I-ASM combination was associated with lower DOAC dosages than rivaroxaban/LEV (OR: 0.00; 95% CI: 0.00-0.62). Furthermore, patient's probability of being in class I was approximately 50% with the rivaroxaban/I-ASM combination, while apixaban, dabigatran, and edoxaban had the highest cumulative probability of being in class II or III despite the ASM used.

conclusionThese preliminary results confirm the reduction of DOAC's PC by I-ASMs and suggest a better manageability of apixaban, dabigatran, and edoxaban independently from the concomitant ASM, whereas rivaroxaban seems the most liable to PC alterations with I-ASMs.

Indexed as

Atrial FibrillationStrokeAdministration, OralAdultAnticoagulantsDabigatranDrug InteractionsHumansPilot ProjectsProbabilityPyridinesPyridonesRetrospective StudiesRivaroxabanThiazolesAnticoagulantsDabigatranedoxabanPyridinesPyridonesRivaroxabanThiazolesApixabanDabigatranEdoxabanPlasma concentrationsRivaroxaban

Identifiers

PMID37548755
PMCPMC10761387

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.