User profiles for "author:Sara Trompeter"

Sara Trompeter

UCL
Verified email at nhs.net
Cited by 1797

[HTML][HTML] Challenges of blood transfusions in β-thalassemia

FT Shah, F Sayani, S Trompeter, E Drasar, A Piga - Blood reviews, 2019 - Elsevier
Patients with β-thalassemia major (BTM) require regular blood transfusions, supported by
appropriate iron chelation therapy (ICT), throughout their life. β-thalassemia is a global …

Noncontrast myocardial T1 mapping using cardiovascular magnetic resonance for iron overload

DM Sado, V Maestrini, SK Piechnik… - Journal of magnetic …, 2015 - Wiley Online Library
Purpose To explore the use and reproducibility of magnetic resonance‐derived myocardial
T1 mapping in patients with iron overload. Materials and Methods The research received …

Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID‐19 pandemic

NBA Roy, P Telfer, P Eleftheriou… - British journal of …, 2020 - Wiley Online Library
With the developing COVID‐19 pandemic, patients with inherited anaemias require specific
advice regarding isolation and changes to usual treatment schedules. The National …

Safety and efficacy of voxelotor in pediatric patients with sickle cell disease aged 4 to 11 years

JH Estepp, R Kalpatthi, G Woods… - Pediatric blood & …, 2022 - Wiley Online Library
Background Sickle cell disease (SCD) is a devastating, multisystemic disorder that affects
millions of people worldwide. The earliest clinical manifestations of SCD can affect infants as …

Haemoglobin F modulation in childhood sickle cell disease

S Trompeter, I Roberts - British journal of haematology, 2009 - Wiley Online Library
While supportive care remains the best option for most well children with sickle cell disease
(SCD), increasing awareness of early signs of chronic organ damage in childhood has …

[HTML][HTML] Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients

P Telfer, J De la Fuente, M Sohal, R Brown… - …, 2020 - ncbi.nlm.nih.gov
Faced with the rapidly evolving COVID-19 pandemic, in March 2020 the UK Government
advocated strict self-isolation ('shielding') to protect extremely vulnerable patient groups …

Development and validation of a universal blood donor genotyping platform: a multinational prospective study

NS Gleadall, B Veldhuisen, J Gollub… - Blood …, 2020 - ashpublications.org
Each year, blood transfusions save millions of lives. However, under current blood-matching
practices, sensitization to non–self-antigens is an unavoidable adverse side effect of …

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

DC Rees, Y Kilinc, S Unal, C Dampier… - Blood, The Journal …, 2022 - ashpublications.org
Excessive intravascular release of lysed cellular contents from damaged red blood cells
(RBCs) in patients with sickle cell anemia (SCA) can activate the inflammasome, a …

Autophagic vesicles on mature human reticulocytes explain phosphatidylserine-positive red cells in sickle cell disease

TJ Mankelow, RE Griffiths, S Trompeter… - Blood, The Journal …, 2015 - ashpublications.org
During maturation to an erythrocyte, a reticulocyte must eliminate any residual organelles
and reduce its surface area and volume. Here we show this involves a novel process …

Position paper on International Collaboration for Transfusion Medicine (ICTM) Guideline 'Red blood cell specifications for patients with hemoglobinopathies: a …

S Trompeter, E Massey, S Robinson… - British Journal of …, 2020 - Wiley Online Library
Summary The International Collaboration for Transfusion Medicine Guidelines (ICTMG) has
published guidance on transfusion for haemoglobinopathies. To give a UK perspective on …