April 2025 Br J Cardiol 2025;32(2) Online First
Anna Briggs, Louise Collier, Edith Donnelly, Becky Hyland, Hayley Rose, and Teresa O’Nwere-Tan
BSH Nurse Forum Author Board
Abstract
Early Investigator Award
The audience was treated to an impressive rapid-fire round with the three finalists for the Early Investigator Award, led by the judging panel; Dr Brian Halliday (Royal Brompton and Harefield Hospitals, London), Dr Rosita Zakeri (King’s College Hospital, London) and Rhys Williams (Cwm Taf Morgannwg University Health Board, Bridgend).
Clinical research fellow, Dr Sarah Birkhoelzer (Oxford University) presented her work on the IRON-HEART study, which aimed to determine the impact of iron repletion on cardiac and skeletal muscle energetics in patients with non-ischaemic cardiomyopathy with reduced ejection fraction. S
|
Full text
January 2025 Br J Cardiol 2025;32(1) Online First
Kaushika Rautray, Sarah M Birkhoelzer
Abstract
Professor Christopher Miller
HFpEF on the rise: navigating the heterogeneity
In an engaging opening talk, Professor Christopher Miller (University of Manchester) revealed heart failure with preserved ejection fraction (HFpEF) as the dominant form of heart failure (HF), rising by 10% every decade. Over 70% of patients with HF have HFpEF, most of whom are over 65 years of age experiencing complex comorbidities. The diagnostic challenges in heterogeneous groups were discussed against the background of the diagnostic criteria provided by European Society of Cardiology (ESC)1 as some patients with clinical signs of HFpEF show normal
|
Full text
March 2020 Br J Cardiol 2020;27:18
BJC Staff
Abstract
Tafamidis – a new treatment for amyloidosis
The European Commission (EC) has granted marketing authorisation for tafamidis (Vyndaqel®, Pfizer), a once-daily 61 mg oral capsule, for the treatment of wild-type or hereditary transthyretin amyloidosis in adult patients with cardiomyopathy (ATTR-CM). Tafamidis is the first authorised treatment in the European Union for patients with ATTR-CM. Prior to this authorisation, treatment options for patients with ATTR-CM were restricted to symptom management, and, in rare cases, heart (or heart and liver) transplant.
ATTR-CM is a rare, under-diagnosed and life-threatening disease characterised by the b
|
Full text