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Evaluation of interventions to prevent vasovagal reactions among whole blood donors: rationale and design of a large cluster randomised trial.
McMahon, Amy; Kaptoge, Stephen; Walker, Matthew; Mehenny, Susan; Gilchrist, Philippe T; Sambrook, Jennifer; Akhtar, Naim; Sweeting, Michael; Wood, Angela M; Stirrups, Kathleen; Chung, Ryan; Fahle, Sarah; Johnson, Elisha; Cullen, Donna; Godfrey, Rosemary; Duthie, Shannon; Allen, Louise; Harvey, Paul; Berkson, Michael; Allen, Elizabeth; Watkins, Nicholas A; Bradley, John R; Kingston, Nathalie; Miflin, Gail; Armitage, Jane; Roberts, David J; Danesh, John; Di Angelantonio, Emanuele.
Affiliation
  • McMahon A; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK. am2663@medschl.cam.ac.uk.
  • Kaptoge S; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK. am2663@medschl.cam.ac.uk.
  • Walker M; National Institute for Health and Care Research Blood and Transplant Research Unit in Donor Health and Behaviour, University of Cambridge, Cambridge, UK. am2663@medschl.cam.ac.uk.
  • Mehenny S; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Gilchrist PT; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.
  • Sambrook J; National Institute for Health and Care Research Blood and Transplant Research Unit in Donor Health and Behaviour, University of Cambridge, Cambridge, UK.
  • Akhtar N; Health Data Research UK Cambridge, Wellcome Genome Campus and University of Cambridge, Cambridge, UK.
  • Sweeting M; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Wood AM; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.
  • Stirrups K; NHS Blood & Transplant, Blood Donation, Barnsley, UK.
  • Chung R; National Institute for Health and Care Research Blood and Transplant Research Unit in Donor Health and Behaviour, University of Cambridge, Cambridge, UK.
  • Fahle S; School of Psychological Sciences, Macquarie University, Sydney, NSW, Australia.
  • Johnson E; Centre for Emotional Health, Macquarie University, Sydney, NSW, Australia.
  • Cullen D; Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
  • Godfrey R; National Institute for Health and Care Research BioResource, Cambridge University Hospitals NHS Foundation, Cambridge Biomedical Campus, Cambridge, UK.
  • Duthie S; NHS Blood and Transplant, Bristol, UK.
  • Allen L; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Harvey P; University of Leicester, Leicester, UK.
  • Berkson M; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Allen E; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.
  • Watkins NA; National Institute for Health and Care Research Blood and Transplant Research Unit in Donor Health and Behaviour, University of Cambridge, Cambridge, UK.
  • Bradley JR; Health Data Research UK Cambridge, Wellcome Genome Campus and University of Cambridge, Cambridge, UK.
  • Kingston N; British Heart Foundation Centre of Research Excellence, University of Cambridge, Cambridge, UK.
  • Miflin G; Cambridge Centre of Artificial Intelligence in Medicine, University of Cambridge, Cambridge, UK.
  • Armitage J; Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
  • Roberts DJ; National Institute for Health and Care Research BioResource, Cambridge University Hospitals NHS Foundation, Cambridge Biomedical Campus, Cambridge, UK.
  • Danesh J; British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Di Angelantonio E; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.
Trials ; 24(1): 512, 2023 Aug 10.
Article de En | MEDLINE | ID: mdl-37563721
ABSTRACT

BACKGROUND:

Vasovagal reactions (VVRs) are the most common acute complications of blood donation. Responsible for substantial morbidity, they also reduce the likelihood of repeated donations and are disruptive and costly for blood services. Although blood establishments worldwide have adopted different strategies to prevent VVRs (including water loading and applied muscle tension [AMT]), robust evidence is limited. The Strategies to Improve Donor Experiences (STRIDES) trial aims to reliably assess the impact of four different interventions to prevent VVRs among blood donors.

METHODS:

STRIDES is a cluster-randomised cross-over/stepped-wedge factorial trial of four interventions to reduce VVRs involving about 1.4 million whole blood donors enrolled from all 73 blood donation sites (mobile teams and donor centres) of National Health Service Blood and Transplant (NHSBT) in England. Each site ("cluster") has been randomly allocated to receive one or more interventions during a 36-month period, using principles of cross-over, stepped-wedge and factorial trial design to assign the sequence of interventions. Each of the four interventions is compared to NHSBT's current practices (i) 500-ml isotonic drink before donation (vs current 500-ml plain water); (ii) 3-min rest on donation chair after donation (vs current 2 min); (iii) new modified AMT (vs current practice of AMT); and (iv) psychosocial intervention using preparatory materials (vs current practice of nothing). The primary outcome is the number of in-session VVRs with loss of consciousness (i.e. episodes involving loss of consciousness of any duration, with or without additional complications). Secondary outcomes include all in-session VVRs (i.e. with and without loss of consciousness), all delayed VVRs (i.e. those occurring after leaving the venue) and any in-session non-VVR adverse events or reactions.

DISCUSSION:

The STRIDES trial should yield novel information about interventions, singly and in combination, for the prevention of VVRs, with the aim of generating policy-shaping evidence to help inform blood services to improve donor health, donor experience, and service efficiency. TRIAL REGISTRATION ISRCTN 10412338. Registration date October 24, 2019.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Donneurs de sang / Syncope vagale Type d'étude: Clinical_trials / Diagnostic_studies / Etiology_studies Limites: Humans Langue: En Journal: Trials Sujet du journal: MEDICINA / TERAPEUTICA Année: 2023 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Donneurs de sang / Syncope vagale Type d'étude: Clinical_trials / Diagnostic_studies / Etiology_studies Limites: Humans Langue: En Journal: Trials Sujet du journal: MEDICINA / TERAPEUTICA Année: 2023 Type de document: Article Pays d'affiliation: Royaume-Uni
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