Evidence map›Paper›PMID 35898273›Full record

ArticleFrontiers in cardiovascular medicine2022

Beta-Adrenergic Antagonist Tolerance in Amyloid Cardiomyopathy.

Stuart Ramsell, Carlos Arias Bermudez, Cyril Ayuk Mbeng Takem Baiyee, Brandon Rodgers, Samir Parikh, Salem Almaani, Nidhi Sharma, Samantha LoRusso, Miriam Freimer, Elyse Redder and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

15 authors at 4 institutions in 1 country.

Stuart RamsellCollege of Medicine, The Ohio State University, Columbus, OH, United States.
Carlos Arias BermudezCollege of Medicine, The Ohio State University, Columbus, OH, United States.
Cyril Ayuk Mbeng Takem BaiyeeCollege of Medicine, The Ohio State University, Columbus, OH, United States.
Brandon RodgersCollege of Medicine, The Ohio State University, Columbus, OH, United States.
Samir ParikhDivision of Nephrology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Salem AlmaaniDivision of Nephrology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Nidhi SharmaDivision of Hematology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Samantha LoRussoDepartment of Neurology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Miriam FreimerDepartment of Neurology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Elyse RedderDepartment of Oncology Rehabilitation, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Naresh BummaDivision of Hematology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Ajay VallkatiDivision of Cardiology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Yvonne EfeberaDivision of Hematology/Oncology, OhioHealth, Columbus, OH, United States.
Rami KahwashDivision of Cardiology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Courtney M CampbellDivision of Cardiology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
The Ohio State University Wexner Medical Center · USThe Ohio State University · USOhioHealth · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Beta-adrenergic antagonists or blockers (BB) are a cornerstone of cardiac therapy for multiple indications. However, BB are considered relatively contraindicated in amyloid cardiomyopathy due to poor tolerance. This intolerance is hypothesized to be due to concomitant neuropathy and significant restrictive cardiomyopathy. This study analyzes the incidence and characteristics of BB tolerance in patients with amyloid cardiomyopathy. Methods: Through a single-center retrospective chart review, patients with amyloid cardiomyopathy, confirmed by endomyocardial biopsy or technetium-99 pyrophosphate scan, were identified and clinical data was collected. Statistical methods included Chi-square test and two sample Results: Of 135 cardiac amyloidosis patients, 27 patients (20.0%) had no BB use, 56 patients (41.5%) were current BB users, and 52 patients (38.5%) were prior BB users. The most frequent indications for BB use were heart failure, hypertension, coronary artery disease, and arrhythmia. The most common reason for stopping BB therapy was hypotension (62.8%) followed by fatigue, bradycardia, and orthostasis. Neurologic symptoms at the initial BB prescription or most recent evaluation were not significantly different between current and prior BB users. Their cardiovascular profiles were similar by ejection fraction, wall thickness, troponin I, and brain natriuretic peptide. There was no association for BB discontinuation based on amyloid subtype, sex, or race. Conclusion: The majority of patients with amyloid cardiomyopathy were prescribed BB, and over half of these patients still tolerated BB therapy. Current and prior BB users had similar profiles from a cardiovascular and neurologic perspective, with no association identified to predict BB discontinuation.

Indexed as

amyloidosisheart failurelight chainpharmacologytransthyretin

Identifiers

PMID35898273
PMCPMC9309481
OpenAlexW4285005026

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.