Evidence map›Paper›PMID 39077150›Full record

ReviewReviews in cardiovascular medicine2022

Emerging from the Darkness. Sudden Cardiac Death in Cardiac Amyloidosis.

Valeria Cammalleri, Valeria Maria De Luca, Giorgio Antonelli, Ombretta Annibali, Annunziata Nusca, Simona Mega, Myriam Carpenito, Danilo Ricciardi, Fiorella Gurrieri, Giuseppe Avvisati and 2 more

Abstract readReview
In one paragraph

Review in Reviews in cardiovascular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Valeria CammalleriFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.
Valeria Maria De LucaDepartment of Cardiovascular Science, Università Campus Bio-Medico di Roma, 00128 Roma, Italy.
Giorgio AntonelliDepartment of Cardiovascular Science, Università Campus Bio-Medico di Roma, 00128 Roma, Italy.
Ombretta AnnibaliDepartment of Haematology, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.
Annunziata NuscaFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.
Simona MegaFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.
Myriam CarpenitoFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.
Danilo RicciardiFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.
Fiorella GurrieriLaboratory of Medical Genetics, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.
Giuseppe AvvisatiDepartment of Haematology, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.
Gian Paolo UssiaFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.
Francesco GrigioniFondazione Policlinico Universitario Campus-Biomedico, Operative Research Unit of Cardiovascular Science, 00128 Roma, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac amyloidosis (CA) manifests as infiltrative cardiomyopathy with a hypertrophic pattern, usually presenting with heart failure with a preserved ejection fraction. In addition, degenerative valvular heart disease, particularly severe aortic stenosis, is commonly seen in patients with CA. However, amyloid fibril deposition might also infiltrate the conduction system and promote the development of electrical disorders, including ventricular tachyarrhythmias, atrio-ventricular block or acute electromechanical dissociation. These manifestations can increase the risk of sudden cardiac death. This review summarises the pathophysiological mechanisms and risk factors for sudden cardiac death in CA and focuses on the major current concerns regarding medical and device management in this challenging scenario.

Indexed as

cardiac amyloidosisimplantable cardioverter defibrillatormonoclonal immunoglobulin light chainssudden cardiac deathtransthyretin amyloidosisventricular arrhythmia

Identifiers

PMID39077150
PMCPMC11267335

What OpenQuestion holds

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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.