ReviewInternational journal of heart failure2026
Expert Consensus and Clinical Pathway Recommendations for Transthyretin Amyloid Cardiomyopathy in Malaysia.
Review in International journal of heart failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a progressive, life-threatening condition that remains under-recognised in Malaysia. Although disease-modifying therapies are available, their high cost and limited accessibility contribute to delays in diagnosis, compounded by gaps in clinical awareness, differences in diagnostic tool availability and disparities in healthcare resources. While international guidelines offer a comprehensive framework for diagnosing and managing ATTR-CM, local adaptation is essential to ensure their relevance and feasibility within the Malaysian healthcare system. This expert consensus provides practical, locally relevant recommendations to assist Malaysian clinicians in the timely identification and management of ATTR-CM. A multidisciplinary panel of clinicians from cardiology, haematology, nuclear medicine and other related specialties convened to develop tailored recommendations for national practice, drawing on international guidance, current evidence and local clinical practices. The guidance outlines key clinical features to raise early suspicion, proposes a diagnostic algorithm adaptable to different levels of care and offers recommendations on appropriate use of diagnostic tests-including imaging, laboratory investigations, tissue biopsy, and genetic testing when indicated-while emphasising the distinction between ATTR-CM and amyloid light chain amyloidosis, optimising non-invasive diagnostic approaches and fostering multidisciplinary collaboration across the care continuum. These consensus recommendations aim to enhance diagnostic accuracy, reduce variability in clinical practice and support earlier identification of ATTR-CM. By bridging global standards with local healthcare practices, this guidance equips clinicians to deliver timely, effective care for an underdiagnosed and often overlooked condition.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.