Publication: Understanding how long people with transthyretin amyloid cardiomyopathy (ATTR-CM) live when they take tafamidis as part of their regular healthcare: a plain language summary.
| dc.contributor.author | Garcia-Pavia, Pablo | |
| dc.contributor.author | Kristen, Arnt V | |
| dc.contributor.author | Drachman, Brian | |
| dc.contributor.author | Carlsson, Martin | |
| dc.contributor.author | Amass, Leslie | |
| dc.contributor.author | Maurer, Mathew S | |
| dc.date.accessioned | 2026-04-20T08:29:56Z | |
| dc.date.available | 2026-04-20T08:29:56Z | |
| dc.date.issued | 2025-06 | |
| dc.description.abstract | This summary describes results from a called the ( for short). In this study from THAOS, researchers looked at people with a heart condition called ( for short). Some people from this study took an approved treatment for ATTR-CM called and some did not. Researchers looked at how many people with ATTR-CM were alive after two and a half years and three and a half years. They also looked at the people had when they took tafamidis.In people who took tafamidis, an estimated 8 in 10 people (84%) were alive after two and a half years, and an estimated 8 in 10 people (77%) were alive after three and a half years. In people who did not take tafamidis, an estimated 7 in 10 people (70%) were alive after two and a half years, and an estimated 6 in 10 people (59%) were alive after three and a half years. The side effects people had while taking tafamidis in the THAOS study were similar to what has been reported in clinical studies.This real-world study supports the use of tafamidis for improving survival in people with ATTR-CM[Box: see text]. | |
| dc.description.peerreviewed | Sí | |
| dc.identifier.citation | Future Cardiol. 2025 Jun;21(7):433-445. | |
| dc.identifier.journal | Future Cardiology | |
| dc.identifier.pubmedID | 40391408 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12105/27433 | |
| dc.language.iso | eng | |
| dc.publisher | TAYLOR & FRANCIS LTD | |
| dc.relation.isreferencedby | PubMed | |
| dc.relation.publisherversion | 10.1080/14796678.2025.2492958 | |
| dc.repisalud.institucion | CNIC | |
| dc.rights.accessRights | open access | |
| dc.rights.license | Attribution-NonCommercial-NoDerivatives 4.0 International | en |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.title | Understanding how long people with transthyretin amyloid cardiomyopathy (ATTR-CM) live when they take tafamidis as part of their regular healthcare: a plain language summary. | |
| dc.type | research article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication |
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