Evidence map›Paper›PMID 42201639›Full record

ArticleCardiology and therapy2026

Patient Perspectives on Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Treatment Attributes.

Nisith Kumar, Joshua Coulter, Alexandra Haddad-Angulo, Louis Baig, Haechung Chung, Sanjana Mahalakshmi Chandrasekar, Caroline Vass, Jayne Galinsky, Anne Marie Carr, Katharine McIntosh and 1 more

Abstract read
In one paragraph

Article in Cardiology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Nisith KumarPfizer Inc., New York, NY, USA.
Joshua CoulterPfizer Inc., New York, NY, USA.
Alexandra Haddad-AnguloPfizer Inc., New York, NY, USA.
Louis BaigPfizer UK, Tadworth, UK.
Haechung ChungPfizer Inc., New York, NY, USA.
Sanjana Mahalakshmi ChandrasekarPfizer Inc., New York, NY, USA.
Caroline VassRTI-HS, Manchester, UK.
Jayne GalinskyRTI-HS, Manchester, UK.
Anne Marie CarrHereditary Amyloidosis Canada, Hagersville, ON, Canada.
Katharine McIntoshCardiomyopathy UK, Buckinghamshire, UK.
Brett HauberPfizer Inc., New York, NY, USA. albert.hauber@rti.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTransthyretin amyloid cardiomyopathy (ATTR-CM), a progressive disease characterized by the accumulation of misfolded transthyretin amyloid proteins in the myocardium, often leads to heart failure. The experiences and treatment priorities of individuals living with ATTR-CM have not been evaluated in depth.

methodsThis multinational patient advisory board qualitatively explored patients' experiences with ATTR-CM and their preferences for the attributes of current and emerging treatments for heart failure caused by ATTR-CM. In a pre-advisory board survey, participants answered benefit-risk scaling questions to gauge the importance of treatment side effects, treatment benefits, and modes of administration. The results of the survey were then discussed during the advisory board.

resultsOf the 13 participants who completed the survey (two in Australia, two in Canada, one in Switzerland, four in the United Kingdom, and four in the United States), 11 participated in the advisory board discussion and two in follow-up discussions. The survey results and advisory board discussion revealed tiredness and fatigue to be the most bothersome and injection site pain to be the least bothersome of the side effects evaluated. Lowering the risk of death was the most important and being able to easily take a bath or a shower was the least important of the treatment benefits evaluated. On average, once-daily oral administration was the most preferred mode of administration tested, over twice-daily oral administration, subcutaneous injection, and infusion, although participants' preferences were heterogeneous. Although the length of life was important, quality of life was also important to participants: they especially valued spending time doing the activities they enjoyed and prioritized these activities over basic functioning and self-care routines.

conclusionsIndividuals living with ATTR-CM have heterogeneous preferences. As the ATTR-CM treatment landscape expands to include treatments with distinct attributes, patients and care teams should participate in shared decision-making to prioritize patients' preferences and goals.

Indexed as

Advisory boardATTR-CMBest–worst scalingCardiac amyloidosisCardiomyopathyMode of administrationPatient preferences, qualitativeTransthyretin

Identifiers

PMID42201639
PMCPMC13221513

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LicenceCC BY-NC
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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 OpenQuestion graph.