Evidence map›Paper›PMID 34622668›Full record

ArticleJournal of the American Heart Association2021

Cardiovascular Diseases That Have Emerged From the Darkness.

Barry J Maron, Martin S Maron, Mathew S Maurer, Ethan J Rowin, Bradley A Maron, Nazzareno Galiè

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. The Relationship between Changes inJournal of cardiovascular development and disease · 2023
    Review
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

6 authors.

Barry J MaronDivision of Cardiology HCM Institute Tufts Medical Center Boston MA.ORCID 0000-0002-1710-8670
Martin S MaronDivision of Cardiology HCM Institute Tufts Medical Center Boston MA.ORCID 0000-0002-9923-3853
Mathew S MaurerCardiac Amyloidosis Center Columbia University Irving Medical CenterNew York-Presbyterian Hospital New York NY.ORCID 0000-0002-1867-0526
Ethan J RowinDivision of Cardiology HCM Institute Tufts Medical Center Boston MA.ORCID 0000-0002-3953-0143
Bradley A MaronDivision of Cardiovascular Medicine Brigham & Women's Hospital and Harvard Medical School Boston MA.ORCID 0000-0002-6784-764X
Nazzareno GalièAlma Mater Studiorum University of Bologna Bologna Italy.

Funding

SCAN-MP (Screening for Cardiac Amyloidosis with Nuclear imaging in Minority Populations) COVID-19 SuppplementR01HL139671 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAURER, MATHEW S, RUBERG, FREDERICK LIEF · 2019 to 2023
$7.4M
Midcareer Mentoring Award for Patient Oriented Research in Geriatric CardiologyK24AG036778 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAURER, MATHEW S · 2010 to 2020
$1.6M
Analysis of Lumbar Spine Stenosis Speciments for Early Identification of TTR Cardiac AmyloidosisR21AG058348 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAURER, MATHEW S · 2018 to 2019
$456k
NHLBI NIH HHS R01 HL139671NIA NIH HHS K24 AG036778NIA NIH HHS R21 AG058348
6 · The paper itself

Abstract

It is important for both the patient and physician communities to have timely access to information recognizing rapid progress in the diagnosis and treatment of familiar but relatively uncommon cardiovascular diseases. Patients with 3 cardiovascular diseases (ie, hypertrophic cardiomyopathy, pulmonary arterial hypertension, and transthyretin (TTR) cardiac amyloidosis (ATTR)]), once considered rare without effective management options and associated with malignant prognosis, have now benefited substantially from the development of a variety of innovative therapeutic strategies. In addition, in each case, enhanced diagnostic testing has expanded the patient population and allowed for more widespread administration of contemporary treatments. In hypertrophic cardiomyopathy, introduction of implantable defibrillators to prevent sudden death as well as high-benefit:low-risk septal reduction therapies to reverse heart failure have substantially reduced morbidity and disease-related mortality (to 0.5% per year). For pulmonary arterial hypertension, a disease once characterized by a particularly grim prognosis, prospective randomized drug trials with aggressive single (or combined) pharmacotherapy have measurably improved survival and quality of life for many patients. In cardiac amyloidosis, development of disease-specific drugs can for the first time reduce morbidity and mortality, prominently with breakthrough ATTR-protein-stabilizing tafamidis. In conclusion, in less common and visible cardiovascular diseases, it is crucial to recognize substantial progress and achievement, given that penetration of such information into clinical practice and the patient community can be inconsistent. Diseases such as hypertrophic cardiomyopathy, pulmonary arterial hypertension, and ATTR cardiac amyloidosis, once linked to a uniformly adverse prognosis, are now associated with the opportunity for patients to experience satisfactory quality of life and extended longevity.

Indexed as

Amyloid Neuropathies, FamilialAmyloidosisCardiomyopathy, HypertrophicCardiovascular DiseasesPulmonary Arterial HypertensionDarknessHumansProspective StudiesQuality of Lifeamyloiddrug therapyheart failurehypertrophic cardiomyopathyimplantable cardioverter‐defibrillatorpulmonary hypertensionsudden death

Identifiers

PMID34622668
PMCPMC8751898

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.