Evaluation of interventions to prevent vasovagal reactions among whole blood donors: rationale and design of a large cluster randomised trial

被引:1
|
作者
McMahon, Amy [1 ,2 ,3 ]
Kaptoge, Stephen [1 ,2 ,3 ,4 ,5 ]
Walker, Matthew [1 ,2 ]
Mehenny, Susan [6 ]
Gilchrist, Philippe T. [3 ,7 ,8 ]
Sambrook, Jennifer [9 ,10 ]
Akhtar, Naim [11 ]
Sweeting, Michael [1 ,12 ]
Wood, Angela M. [1 ,2 ,3 ,4 ,5 ,13 ,14 ]
Stirrups, Kathleen [9 ,10 ]
Chung, Ryan [1 ,2 ]
Fahle, Sarah [1 ,2 ,3 ]
Johnson, Elisha [1 ,2 ,3 ]
Cullen, Donna [15 ]
Godfrey, Rosemary [6 ]
Duthie, Shannon [1 ,2 ,3 ]
Allen, Louise [16 ]
Harvey, Paul [1 ,2 ,3 ]
Berkson, Michael [1 ,2 ,3 ]
Allen, Elizabeth [1 ,2 ,3 ]
Watkins, Nicholas A. [17 ]
Bradley, John R. [10 ]
Kingston, Nathalie [9 ,10 ]
Miflin, Gail [11 ]
Armitage, Jane [18 ]
Roberts, David J. [3 ,15 ,19 ,20 ]
Danesh, John [1 ,2 ,3 ,4 ,5 ,13 ,21 ]
Di Angelantonio, Emanuele [1 ,2 ,3 ,4 ,5 ,13 ,22 ,23 ]
机构
[1] Univ Cambridge, British Heart Fdn Cardiovasc Epidemiol Unit, Dept Publ Hlth & Primary Care, Cambridge, England
[2] Univ Cambridge, Victor Phillip Dahdaleh Heart & Lung Res Inst, Cambridge, England
[3] Univ Cambridge, Natl Inst Hlth & Care Res, Blood & Transplant Res Unit Donor Hlth & Behav, Cambridge, England
[4] Wellcome Genome Campus, Hlth Data Res UK Cambridge, Cambridge, England
[5] Univ Cambridge, Cambridge, England
[6] NHS Blood & Transplant, Blood Donat, Barnsley, England
[7] Macquarie Univ, Sch Psychol Sci, Sydney, NSW, Australia
[8] Macquarie Univ, Ctr Emot Hlth, Sydney, NSW, Australia
[9] Univ Cambridge, Dept Haematol, Cambridge Biomed Campus, Cambridge, England
[10] Cambridge Univ Hosp NHS Fdn, Natl Inst Hlth & Care Res BioResource, Cambridge Biomed Campus, Cambridge, England
[11] NHS Blood & Transplant, Bristol, England
[12] Univ Leicester, Leicester, England
[13] Univ Cambridge, British Heart Fdn Ctr Res Excellence, Cambridge, England
[14] Univ Cambridge, Cambridge Ctr Artificial Intelligence Med, Cambridge, England
[15] John Radcliffe Hosp, NHS Blood & Transplant, Oxford, England
[16] NHS Blood & Transplant, Ashford, England
[17] UK Hlth Secur Agcy, Data Analyt & Surveillance, Nobel House, London, England
[18] Univ Oxford, Nuffield Dept Populat Hlth, MRC Populat Hlth Res Unit, Oxford, England
[19] Univ Oxford, Radcliffe Dept Med, Oxford, England
[20] Univ Oxford, BRC Haematol Theme, Oxford, England
[21] Wellcome Sanger Inst, Dept Human Genet, Hinxton, England
[22] Human Technopole, Hlth Data Sci Ctr, I-20157 Milan, Italy
[23] NHS Blood & Transplant, Cambridge, England
关键词
Vasovagal reactions; Blood donors; Blood donation; Cluster randomised trial; Cross-over; Stepped-wedge; Factorial design; DONATION; HYDRATION;
D O I
10.1186/s13063-023-07473-z
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundVasovagal 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.MethodsSTRIDES 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.DiscussionThe 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.
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页数:13
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