Evidence map›Paper›PMID 29223434›Full record

Trial reportAmerican heart journal2017

Durability of quality of life benefits of transcatheter aortic valve replacement: Long-term results from the CoreValve US extreme risk trial.

Suzanne J Baron, Suzanne V Arnold, Matthew R Reynolds, Kaijun Wang, Michael Deeb, Michael J Reardon, James Hermiller, Steven J Yakubov, David H Adams, Jeffrey J Popma and 2 more

Open access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in American heart journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 32 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

12 authors at 9 institutions in 1 country.

Suzanne J BaronSaint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO.
Suzanne V ArnoldSaint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO.
Matthew R ReynoldsThe Baim Institute, Boston, Massachusetts and Lahey Hospital and Medical Center, Burlington, MA.
Kaijun WangSaint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO.
Michael DeebUniversity of Michigan Health System, Ann Arbor, MI.
Michael J ReardonHouston-Methodist-DeBakey Heart and Vascular Center, Houston, TX.
James HermillerSt. Vincent Medical Group, Indianapolis, IN.
Steven J YakubovOhioHealth Heart and Vascular Physicians, Columbus, OH.
David H AdamsMount Sinai Hospital, New York City, NY.
Jeffrey J PopmaBeth Israel Deaconess Medical Center, Boston, MA.
David J CohenSaint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO. Electronic address: dcohen@saint-lukes.org.
US CoreValve Investigators
University of Missouri–Kansas City · USBeth Israel Deaconess Medical Center · USHouston Methodist · USLahey Medical Center · USMichigan Medicine · USMount Sinai Hospital · USOhioHealth · USSaint Luke's Hospital · USSt. Vincent Hospital · US

Funding

Optimal Decision Making in Aortic Valve ReplacementK23HL116799 · NHLBI · SAINT LUKE'S HOSPITAL · PI ARNOLD, SUZANNE VICTORIA · 2014 to 2018
$635k
NHLBI NIH HHS K23 HL116799
6 · The paper itself

Abstract

backgroundFor patients with severe aortic stenosis (AS) at extreme surgical risk, transcatheter aortic valve replacement (TAVR) leads to improved survival and health status when compared with medical therapy. Whether the early health status benefits of TAVR in these patients are sustained beyond 1 year of follow-up is unknown. METHODS AND

resultsSix hundred thirty-nine patients with severe AS at extreme surgical risk underwent TAVR in the CoreValve US Extreme Risk Pivotal trial. Health status was evaluated at baseline and at 1, 6, 12, 24, and 36 months using the Kansas City Cardiomyopathy Questionnaire (KCCQ), the Short-Form-12, and the EuroQoL-5D. Analyses were performed using pattern mixture models to account for both death and missing data and were stratified by iliofemoral (IF) and non-iliofemoral (non-IF) access. After TAVR, there was substantial health status improvement in disease-specific and generic scales by 6 to 12 months. Although there were small declines in health status after 12 months, the initial benefits of TAVR were largely sustained through 3 years for both IF and non-IF cohorts (change from baseline in KCCQ Overall Summary score 19.0 points in IF patients and 14.9 points in non-IF patients; P<.01 for both comparisons). Among surviving patients, clinically meaningful (≥10 point) improvements in the KCCQ Overall Summary Score at 3 years were observed in 85.0% and 83.4% of IF and non-IF patients respectively.

conclusionsAmong extreme risk patients with severe AS, TAVR resulted in large initial health status benefits that were sustained through 3-year follow-up. Although late mortality was high in this population, these findings demonstrate that TAVR offers substantial and durable health status improvements for surviving patients.

Indexed as

Health StatusQuality of LifeAged, 80 and overAortic ValveAortic Valve StenosisFemaleFollow-Up StudiesHumansMaleRetrospective StudiesRisk FactorsSeverity of Illness IndexSurveys and QuestionnairesSurvival RateTime FactorsTranscatheter Aortic Valve Replacement

Identifiers

PMID29223434
PMCPMC5821894
OpenAlexW2749669371

What OpenQuestion holds

Textmetadata
LicenceTDM
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.