Evidence map›Paper›PMID 31430323›Full record

Observational studyPloS one2019

Dosage form suitability in vulnerable populations: A focus on paracetamol acceptability from infants to centenarians.

Fabrice Ruiz, Thibault Vallet, Amélie Dufaÿ Wojcicki, Émilie Belissa, Jean-Eudes Fontan, Loïc de Pontual, Sylvie Nathanson, Alain Chevallier, Sandra Laribe-Caget, Vincent Boudy

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.6field-weighted citation impact, top 8% of its field
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

12 citing papers in PubMed, 22 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Fabrice RuizClinSearch, Malakoff, France.ORCID 0000-0001-9167-0189
Thibault ValletClinSearch, Malakoff, France.
Amélie Dufaÿ WojcickiDépartement innovation pharmaceutique, Agence Générale des Équipements et Produits de Santé (AGEPS), Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.
Émilie BelissaDépartement innovation pharmaceutique, Agence Générale des Équipements et Produits de Santé (AGEPS), Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.
Jean-Eudes FontanHôpital Jean Verdier, Groupe Hospitalier Universitaire Paris Seine-Saint-Denis, Assistance Publique des Hôpitaux de Paris (AP-HP), Bondy, France.
Loïc de PontualHôpital Jean Verdier, Groupe Hospitalier Universitaire Paris Seine-Saint-Denis, Assistance Publique des Hôpitaux de Paris (AP-HP), Bondy, France.
Sylvie NathansonCentre Hospitalier de Versailles - André Mignot, Le Chesnay, France.
Alain ChevallierHôpital Broca, Groupe Hospitalier Universitaire Paris Centre, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.
Sandra Laribe-CagetHôpital Rothschild, Groupe Hospitalier Universitaire Est Parisien, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.
Vincent BoudyDépartement innovation pharmaceutique, Agence Générale des Équipements et Produits de Santé (AGEPS), Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.
Assistance Publique – Hôpitaux de Paris · FRAgence France-Presse · FRMonal Group (France) · FRDélégation Paris 5 · FRHôpital André Mignot · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMedicine acceptability is a multi-faceted concept driven by both product and user characteristics. Although a key factor for treatment effectiveness, especially in vulnerable populations, knowledge of those medicine features that best promote individual user acceptability remains fragmented. Focusing on paracetamol, this study has explored the appropriateness of pharmaceutical products in different dosage forms to achieve adequate patient acceptability from infants to centenarians.

methodsThis observational, multicentre, prospective study was carried out in 10 hospitals, 8 nursing homes and over 150 community dispensaries. Observers reported several behaviours/events evaluating acceptability for 1016 different pharmaceutical product uses in paediatrics (<18y.) and 1288 in the elderly (≥65y.). Using mapping and clustering, a multivariate approach offered an intelligible reference framework for each population, providing comprehensive scores: positively or negatively accepted.

resultsAmong all the evaluations supporting the acceptability reference frameworks, there were 502 reports on paracetamol products intake. Herein we focused on the 5 products with ≥30 evaluations. Although oral suspension and powder for oral solution were positively-accepted in the paediatric group, the powder had a higher rate of negative patient reaction (p<0.001). Of those that received this formulation, 72% were ≤8y., and therefore suitable to receive the better accepted oral suspension. In the elderly, patients with swallowing disorders were preferentially treated with such powders (p<0.001), which were less often fully taken than orally disintegrating tablets (p<0.001). Even in those patients ≥90y., capsule formulations appeared to be the best accepted product in patients without swallowing alterations, and thus could be a suitable alternative to the powder in this population.

conclusionsBy better integrating patient characteristics when choosing dosage forms, clinicians and caregivers may improve treatment acceptability and adherence. Moreover, hospitals and healthcare institutions could optimise purchasing to best suit their local population, disseminating information to help staff align specific dosage forms to targeted patients.

Indexed as

Dosage FormsMedication AdherenceVulnerable PopulationsAcetaminophenAdministration, OralAdolescentAgedAged, 80 and overAge FactorsChildChild, PreschoolFemaleHumansInfantInfant, NewbornProspective StudiesAcetaminophenDosage Forms

Identifiers

PMID31430323
PMCPMC6701828
OpenAlexW2969271901

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.