Evidence map›Paper›PMID 36582903›Full record

ArticleAnnals of medicine and surgery (2012)2022

Sustained ventricular arrhythmia and sinus node dysfunction revealing a cardiac amyloidosis: A case report.

Achraf Machraa, Walid Ben Brahim, Oussama Sidaty, Rokaya Fellat, Nadia Fellat

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2022. 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
0.2field-weighted citation impact, top 51% 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, 2 citations in OpenAlex.

  1. The Arrhythmic Burden of Cardiac Amyloidosis: A Comprehensive Review.Heart views : the official journal of the Gulf Heart Association · 2026
    Review
  2. Sustained Ventricular Tachycardia as the first presentation of transthyretin amyloid cardiomyopathy.Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina) · 2024
    Article
  3. 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

5 authors at 1 institution in 1 country.

Achraf MachraaDept. of Cardiology A - National Cardiovascular League, Ibn Sina University Hospital Center, Mohammed V University, Rabat, Morocco.
Walid Ben BrahimDept. of Cardiology A - National Cardiovascular League, Ibn Sina University Hospital Center, Mohammed V University, Rabat, Morocco.
Oussama SidatyDept. of Cardiology A - National Cardiovascular League, Ibn Sina University Hospital Center, Mohammed V University, Rabat, Morocco.
Rokaya FellatDept. of Cardiology A - National Cardiovascular League, Ibn Sina University Hospital Center, Mohammed V University, Rabat, Morocco.
Nadia FellatDept. of Cardiology A - National Cardiovascular League, Ibn Sina University Hospital Center, Mohammed V University, Rabat, Morocco.
Mohammed V University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Amyloidosis is an infiltrative multisystem disease due to extracellular deposition of fibrils in tissues and organs. Cardiac involvement can result in progressive heart failure, conduction abnormalities and arrhythmias and is associated with a poor prognosis. Atrial arrhythmias and non-sustained ventricular arrhythmias are the most common arrhythmias in cardiac amyloidosis. However, the association of sinus node dysfunction and sustained ventricular arrhythmia is quite exceptional. Case presentation: A 59-year-old male patient was admitted with a gradually worsening dyspnea with a lipothymic discomfort. Upon emergency department, an initial electrocardiogram revealed a severe bradycardia related to a sinus node dysfunction. A transthoracic echocardiography and cardiac magnetic resonance imaging showed features suspicious for cardiac amyloidosis. The diagnosis of AL cardiac amyloidosis with multiple myeloma was confirmed based on histological evidence. During hospitalization, the patient presented a sustained unstable ventricular tachycardia which has been converted by electrical cardioversion. He was treated with an implantable cardioverter-defibrillator (ICD) for secondary prevention with one episode of appropriate therapy. Unfortunately, the patient died few weeks later. Clinical discussion: The AL subtype of cardiac amyloidosis is associated with higher rates of arrhythmias, especially VT. The management of arrhythmias in cardiac amyloidosis is complex and remains challenging given the lack of evidence. ICD was not associated with longer survival; these findings underscore the importance of careful patient selection for ICD. Conclusion: As prognosis improves with the advances made in the medical treatment of cardiac amyloidosis, further studies are required to guide the management of all types of arrhythmias in cardiac amyloidosis.

Indexed as

Cardiac amyloidosisImplanted cardioverter-defibrillatorInfiltrative cardiomyopathySinus node dysfunctionVentricular arrhythmia

Identifiers

PMID36582903
PMCPMC9793156
OpenAlexW4309047561

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.