Evidence map›Paper›PMID 42664265›Full record

ArticlePloS one2026

Enhancing patient involvement through shared decision-making: Are we there yet in multiple myeloma? Findings from a cross-country survey.

Charlotte Verbeke, Jolien Broekmans, Elise Schoefs, Silène Ten Seldam, Kate Morgan, Katie Joyner, Eilidh Duncan, Ariel Aviv, Varda Shoham, Michel Delforge and 4 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Charlotte VerbekeDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-7149-2239
Jolien BroekmansDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0009-0008-3663-0334
Elise SchoefsDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Silène Ten SeldamMyeloma Patients Europe, Brussels, Belgium.
Kate MorganMyeloma Patients Europe, Brussels, Belgium.
Katie JoynerMyeloma Patients Europe, Brussels, Belgium.
Eilidh DuncanMyeloma Patients Europe, Brussels, Belgium.
Ariel AvivDepartment of Hematology, Ha'Emek medical center, Afula, Israel.
Varda ShohamDepartment of Hematology, Ha'Emek medical center, Afula, Israel.
Michel DelforgeDepartment of Hematology, University Hospital Leuven, Leuven, Belgium.
Anneleen VanhellemontDepartment of Hematology, University Hospital Leuven, Leuven, Belgium.
Rosanne JanssensDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Alexandre BohynDepartment of Public Health and Primary Care, Leuven Biostatistics and Statistical Bioinformatics Centre, KU Leuven, Leuven, Belgium.
Isabelle HuysDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionShared decision-making (SDM) can enhance patient involvement in treatment and care decisions. Still, questions remain on how multiple myeloma (MM) patients perceive and evaluate their current and desired roles in these decisions and whether characteristics influence their willingness to be involved. This study aimed to identify I) the current knowledge of the concept SDM among MM patients and healthcare professionals (HCPs) involved in MM care, II) how MM patients are and want to be involved in decisions, and III) differences in the willingness to be involved in view of participants' characteristics (e.g., age, gender, health literacy).

methodsAn online survey for MM patients and HCPs involved in MM care was launched in October and December 2023, respectively. The data was statistically analyzed.

results558 patients and 89 HCPs completed the survey. Most patients lived in the Netherlands (28.7%), Israel (23.5%) and Belgium (15.8%), and most HCPs lived in France (39.3%) and Israel (24.7%). 56.6% of the patients and 28.1% of the HCPs had not previously heard of SDM. Almost all patients (96.1%) indicated wanting to be involved in treatment decisions. 3.9% of patients indicated not wanting to be involved, because they did not know whether they would have enough knowledge to decide or because they were used to the HCP deciding. All HCPs believed that MM patients should be involved if they want to. Patients had higher involvement scores at recent consultations and desired to be more involved in initial decisions following diagnosis. The survey revealed no significant differences in participants' involvement and their characteristics.

conclusionMM patients want to be involved in decisions and HCPs are willing to involve MM patients. However, challenges remain concerning the practical implementation of involvement and SDM. This highlights the importance of understanding SDM and patient involvement and assessing the individual needs and preferences of MM patients.

Indexed as

Decision Making, SharedMultiple MyelomaPatient ParticipationAdultAgedAged, 80 and overDecision MakingFemaleHealth PersonnelHumansMaleMiddle AgedSurveys and Questionnaires

Identifiers

PMID42664265
PMCPMC13524276

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.