laura green

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Clinical Reader in Transfusion Medicine

Queen Mary University of London

United Kingdom

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Dr. Laura Green is a Clinical Reader in Transfusion Medicine at Queen Mary University of London. Her research focuses on transfusion practices and systems, with recent work exploring bedside electronic transfusion checks, the harms associated with incompatible blood transfusions, and the development of whole blood components for traumatic hemorrhage. She is actively involved in assessing the clinical and cost-effectiveness of various blood product strategies and improving transfusion safety in NHS hospitals across England.

Recent Grants

Grant: Close

SWiFT trial mechanistic study

Open Date: 2023-03-01

Close Date: 2026-02-01

Grant: Close

Transform Trauma

Open Date: 2022-09-01

Close Date: 2025-08-01

Grant: Close

Understanding the impact of Whole Blood transfusion on haemostasis in trauma bleeding patients as part of SWiFT trial.

Open Date: 2022-08-01

Close Date: 2026-07-01

Grant: Close

Studying Whole Blood in Frontline Trauma (SWiFT), a randomised control trial

Open Date: 2022-06-01

Close Date: 2025-05-01

Grant: Close

Developing freeze dried plasma

Open Date: 2021-09-01

Close Date: 2025-09-01

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2022

NIHR Academic Clinical Lecturer

Queen Mary University of London

UNITED KINGDOM

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S. J. Stanworth

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laura green

Research Interests

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About

Recent Grants

Articles (26)

Unlocking the potential of electronic blood transfusion systems: Implementation insights from NHS hospitals in England

Implementing bedside electronic transfusion checks at Barts Health NHS Trust: A study protocol for evaluating the effectiveness and value for money

Comparison of whole blood versus red blood cells and plasma to correct trauma‐induced coagulopathy ex vivo

Quantifying Harms Associated With Red Cell ABO Incompatible Blood Transfusion: A Systematic Review of the UK SHOT Literature

Clinical, tactical and strategic benefits of a UK Spray Dried Plasma production capability

Early high-dose cryoprecipitate to reduce mortality in adult patients with traumatic haemorrhage: the CRYOSTAT-2 RCT with cost-effectiveness analysis

Understanding the benefits of universal plasma and cryoprecipitate in hospitals in England

Every minute counts: A comparison of thawing times and haemostatic quality of plasma thawed at <scp>37°C</scp> and <scp>45°C</scp> using four different methods

Use of Intravenous Albumin

The feasibility of introducing a whole blood component for traumatic haemorrhage in the <scp>UK</scp>

Harnessing the potential of data‐driven strategies to optimise transfusion practice

Early and Empirical High-Dose Cryoprecipitate for Hemorrhage After Traumatic Injury

The SWiFT trial (Study of Whole Blood in Frontline Trauma)—the clinical and cost effectiveness of pre-hospital whole blood versus standard care in patients with life-threatening traumatic haemorrhage: study protocol for a multi-centre randomised controlled trial

Definitions of massive transfusion in adults with critical bleeding: a systematic review

Renal transplant and hemostasis: early postoperative changes in recipients and donors

Association of red blood cells and plasma transfusion versus red blood cell transfusion only with survival for treatment of major traumatic hemorrhage in prehospital setting in England: a multicenter study

Haematological management of major haemorrhage: a British Society for Haematology Guideline

The CRYOSTAT2 trial: The rationale and study protocol for a multi‐Centre, randomised, controlled trial evaluating the effects of early high‐dose cryoprecipitate in adult patients with major trauma haemorrhage requiring major haemorrhage protocol activation

Assessing the risks of haemolysis as an adverse reaction following the transfusion of ABO incompatible plasma-containing components - A scoping review

Modelling the outcomes of different red blood cell transfusion strategies for the treatment of traumatic haemorrhage in the prehospital setting in the United Kingdom

UK audit of the management of major bleeding and time taken to deliver blood products

Assessing efficacy and safety of replacement fluids in therapeutic plasma exchange: A systematic scoping review of outcome measures used

Effect on haemostasis of different replacement fluids during therapeutic plasma exchange—A comparative multicentre observational study

Toward a more complete understanding of who will benefit from prehospital transfusion

Deferred consent in emergency obstetric research: findings from qualitative interviews with women and recruiters in the <i>ACROBAT</i> pilot trial for severe postpartum haemorrhage

Estimating the risks of prehospital transfusion of D‐positive whole blood to trauma patients who are bleeding in England

Collaborators (13)

Hayley Evans

Paula Dhiman

Angela Harden

Andrea Rossetto

Beverley Jane Hunt

Carolyn Doree

Jahnavi Daru

S. J. Stanworth

Helen Thomas

Yan Feng

Alison Deary

J. Benger

Nicola Curry

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