Evidence map›Paper›PMID 36611101›Full record

ArticleCardiology and therapy2023

Detection and Diagnosis of Cardiac Amyloidosis in Egypt.

Mohamed Abdelghany, Magdy Abdelhamid, Adel Allam, Adel El Etriby, Sherif Hafez, Hany Ragy, Mohamed Sobhy

Open access · goldAbstract read
In one paragraph

Article in Cardiology and therapy, 2023. 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
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Unraveling cardiac amyloidosis in Egypt: diagnostic challenges and disease outcomes.The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology · 2026
    Article
  2. 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

7 authors at 6 institutions in 1 country.

Mohamed AbdelghanyDepartment of Cardiology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Magdy AbdelhamidDepartment of Cardiology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Adel AllamDepartment of Cardiology, Faculty of Medicine, Azhar University, Cairo, Egypt.
Adel El EtribyDepartment of Cardiology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Sherif HafezPfizer Egypt Medical Affairs, Cairo, Egypt.
Hany RagyNational Heart Institute, Giza, Egypt. hanyragy@gmail.com.ORCID http://orcid.org/0000-0001-5409-9745
Mohamed SobhyDepartment of Cardiology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Cairo University · EGAin Shams University · EGAl-Azhar University · EGAlexandria University · EGNational Heart Institute · EGWorld Health Organization - Egypt · EG

Funding

Pfizer Medical writing and publication fees were funded by Pfizer, Egypt
6 · The paper itself

Abstract

Cardiac amyloidosis is a life-threatening disease that occurs when amyloid proteins, most commonly immunoglobulin light chain or transthyretin, mutate or become unstable, misfold, deposit as amyloid fibrils, and accumulate in the myocardium. Early diagnosis of cardiac amyloidosis is hindered by insufficient awareness, specifically regarding clinical red flags and diagnostic pathways. Cardiac amyloidosis diagnosis comprises two important phases, clinical suspicion (phase one) followed by definitive diagnosis (phase two). Each phase is associated with specific clinical techniques. For example, clinical features, electrocardiography, echocardiography, and cardiac magnetic resonance imaging serve to raise suspicion of cardiac amyloidosis and facilitate early diagnosis, whereas laboratory tests (i.e., blood or urine electrophoresis with immunofixation), biopsy, scintigraphy-based nuclear imaging, and genetic testing provide a definitive diagnosis of cardiac amyloidosis. In Egypt, both the lack of cardiac amyloidosis awareness amongst healthcare providers and the unavailability of clinical expertise for the use of diagnostic techniques must be overcome to improve the prognosis of cardiac amyloidosis in the region. Previously published diagnostic algorithms for cardiac amyloidosis have amalgamated techniques that can raise clinical suspicions of cardiac amyloidosis with those that definitively diagnose cardiac amyloidosis. Though such algorithms have been successful in developed countries, diagnostic tools like echocardiography, scintigraphy, and cardiac magnetic resonance imaging are not ubiquitously available across Egyptian facilities. This review presents the current state of knowledge regarding cardiac amyloidosis in Egypt and outlines a new diagnostic algorithm which leverages regional nuclear imaging expertise. Importantly, the proposed diagnostic algorithm guides accurate amyloid-typing to mitigate misdiagnosis and erroneous treatment selection and improve the cardiac amyloidosis diagnostic accuracy in Egypt.

Indexed as

AlgorithmCardiac amyloidosisCardiac MRIDiagnosis and subtypingEchocardiographyEgyptElectrocardiographyEndomyocardial biopsyImmunoelectrophoresisScintigraphy

Identifiers

PMID36611101
PMCPMC9986164
OpenAlexW4313681480

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.