Evidence map›Paper›PMID 39589584›Full record

ArticleAging clinical and experimental research2024

A newly developed method for assessing co-exposure to free dose combinations: a proof-of-concept study using antihypertensive medications in Danish registers.

Maria Antonietta Barbieri, Sidse Marie Neumann Nielsen, Andrea Rossi, Elena Olmastroni, Manuela Casula, Edoardo Spina, Maurizio Sessa

Abstract read
In one paragraph

Article in Aging clinical and experimental research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

7 authors.

Maria Antonietta BarbieriDepartment of Drug Design and Pharmacology, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Capital Region, Denmark.ORCID http://orcid.org/0000-0002-2019-4696
Sidse Marie Neumann NielsenDepartment of Drug Design and Pharmacology, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Capital Region, Denmark.
Andrea RossiDepartment of Drug Design and Pharmacology, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Capital Region, Denmark.ORCID http://orcid.org/0009-0001-6475-2418
Elena OlmastroniEpidemiology and Preventive Pharmacology Service (SEFAP), Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.ORCID http://orcid.org/0000-0001-7107-243X
Manuela CasulaEpidemiology and Preventive Pharmacology Service (SEFAP), Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.ORCID http://orcid.org/0000-0002-5124-5361
Edoardo SpinaDepartment of Clinical and Experimental Medicine, University of Messina, 98125, Messina, Italy.ORCID http://orcid.org/0000-0002-2509-7449
Maurizio SessaDepartment of Drug Design and Pharmacology, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Capital Region, Denmark. maurizio.sessa@sund.ku.dk.ORCID http://orcid.org/0000-0003-0874-4744

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundElevated blood pressure is a major risk factor for severe medical conditions. Adherence to antihypertensive medication, especially in free-dose combinations, poses a significant challenge. This study aims to develop a novel method for assessing co-exposure to free-dose antihypertensive medications using secondary data sources.

methodsA register-based cohort study was conducted on individuals aged 65 years or older in Denmark who initiated antihypertensive therapy from 1996 to 2016 and followed for 730 days from the index date. A new method was developed to assess co-exposure to antihypertensive medications through redeemed prescriptions, treatment episodes, and overlapping medication events. The method's accuracy was evaluated using a random sample of 400 individuals.

resultsA total of 1,021,819 individuals were included in the study, with a mean age of 68.8 years, and 53.7% were women. The method achieved 100% accuracy in identifying co-exposure periods. During the early stage of the follow-up (0-180 days), 54.1% of individuals were co-exposed to at least two antihypertensive medications, while 37.5% were co-exposed during the late stage of the follow-up period (181-730 days). The most frequent antihypertensive combinations included bendroflumethiazide and potassium with either amlodipine or enalapril in the early (13.2% and 12.5% of patients, respectively) and late stages (16.9% and 15.0% of patients, respectively).

conclusionsThe newly developed method effectively assesses co-exposure to antihypertensive medications, overcoming previous limitations. The findings reveal common co-exposure combinations and evolving trends in antihypertensive medication use among older individuals, reflecting changes in clinical practice and guidelines over two decades.

Indexed as

Antihypertensive AgentsHypertensionRegistriesAgedAged, 80 and overCohort StudiesDenmarkDrug MonitoringDrug Therapy, CombinationFemaleHumansMaleProof of Concept StudyAntihypertensive AgentsAntihypertensive medicationsElectronic health records databasesFree dose combinationHypertensionRegister-based cohort study

Identifiers

PMID39589584
PMCPMC11599442

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.