Evidence map›Paper›PMID 39095682›Full record

Trial reportEuropean geriatric medicine2024

A descriptive analysis of drug-drug interactions and corresponding adverse drug reactions in multimorbid older inpatients: findings from the SENATOR trial.

Ine Simal, Annemie Somers, Cheima Amrouch, Andreas Capiau, Antonio Cherubini, Alfonso J Cruz-Jentoft, Adalsteinn Gudmundsson, Roy L Soiza, Denis O 'Mahony, Mirko Petrovic

Abstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in European geriatric medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
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

10 authors.

Ine SimalDepartment of Pharmacy, Ghent University Hospital, Ghent, Belgium. ine.simal@uzgent.be.ORCID 0009-0007-9570-2433
Annemie SomersDepartment of Pharmacy, Ghent University Hospital, Ghent, Belgium.ORCID 0000-0001-9245-4154
Cheima AmrouchDepartment of Internal Medicine and Paediatrics, Ghent University, Ghent, Belgium.ORCID 0000-0001-6708-7372
Andreas CapiauDepartment of Pharmacy, Ghent University Hospital, Ghent, Belgium.ORCID 0000-0003-2458-5237
Antonio CherubiniGeriatria, Accettazione Geriatrica e Centro di Ricerca per l'Invecchiamento, IRCCS INRCA, 60127, Ancona, Italy.
Alfonso J Cruz-JentoftServicio de Geriatría, Hospital Universitario Ramón y Cajal (IRYCIS), Madrid, Spain.ORCID 0000-0001-7628-4861
Adalsteinn GudmundssonDepartment of Geriatric Medicine, Landspitali University Hospital, Reykjavik, Iceland.ORCID 0009-0007-3163-4785
Roy L SoizaAgeing Clinical and Experimental Research (ACER) Group, Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.ORCID 0000-0002-1397-4272
Denis O 'MahonyDepartment of Medicine, University College Cork, Cork, Ireland.ORCID 0000-0003-2236-5222
Mirko PetrovicDepartment of Internal Medicine and Paediatrics, Ghent University, Ghent, Belgium.ORCID 0000-0002-7506-8646

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDrug-drug interactions (DDIs) are prevalent among multimorbid and polymedicated older adults and can increase the risk of adverse drug reactions (ADRs), hospital admissions, and mortality. This study describes the incidence and prevalence of 66 clinically relevant DDIs and analyses the occurrence of 12 corresponding predefined ADRs in older inpatients enrolled in the SENATOR trial.

methodsThe sub-study of the SENATOR trial that involved 1537 multimorbid older inpatients, recruited from 2016 to 2018 in six academic teaching hospitals in Belgium, Iceland, Ireland, Italy, Scotland, and Spain respectively, and analysed 66 potentially clinically significant DDIs. Descriptive analysis determined DDI and corresponding ADR prevalence/incidence.

resultsAt baseline (median age: 78 [72, 84], 52.8% male), the prevalence of patients with DDIs was high (50.9%), increased during hospitalisation (55.2%) and reduced to 49.7% after 12 weeks. The most common DDIs were: ≥ 2 potassium reducing drugs (17.1%), ≥ 3 centrally acting drugs (9.0%), and SSRI + loop/thiazide diuretic (7.2%). Of all participants, one-third experienced a prevalent (36.6%)/incident (35.8%) ADR. Major serum electrolyte disturbance had the highest incidence (10.7%)/prevalence (11.5%). Incident ADRs were more common in patients with DDIs (p = 0.013). A higher prevalence of new onset falls (p = 0.013), major constipation (p = 0.004), and major serum electrolyte disturbances (p = 0.006) was observed in patients with related and thus potentially causal DDIs.

conclusionsClinicians should, be aware of DDIs and the involved drug classes that can lead to an increased rate of ADRs in older multimorbid inpatients. Regularly reevaluating the appropriateness of the frequently prescribed drug classes and initiating judicious deprescribing is recommended.

Indexed as

Drug InteractionsDrug-Related Side Effects and Adverse ReactionsMultimorbidityAgedAged, 80 and overFemaleHospitalizationHumansIncidenceInpatientsMalePolypharmacyPrevalenceAdverse drug reactionsDrug-drug-interactionsMultimorbidityOlder adultsPolypharmacy

Identifiers

What Socratic holds

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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.