Impact of a post‐donation hemoglobin testing strategy on efficiency and safety of whole blood donation in England: A modeling study

Author:

Kim Lois G.12ORCID,Bolton Thomas23,Sweeting Michael J.4,Bell Steven5,Fahle Sarah12,McMahon Amy12,Walker Matthew12,Ferguson Eamonn16ORCID,Miflin Gail7,Roberts David J.189,Di Angelantonio Emanuele12101112,Wood Angela M.12101113

Affiliation:

1. Blood and Transplant Research Unit in Donor Health and Behaviour Cambridge UK

2. Dept of Public Health & Primary Care University of Cambridge Cambridge UK

3. BHF Data Science Centre Health Data Research UK

4. Dept of Health Sciences University of Leicester Leicester UK

5. Dept of Clinical Neurosciences University of Cambridge Cambridge UK

6. School of Psychology University of Nottingham Nottingham UK

7. NHS Blood & Transplant Bristol UK

8. NHS Blood & Transplant John Radcliffe Hospital Oxford UK

9. Radcliffe Dept of Medicine University of Oxford Oxford UK

10. British Heart Foundation Centre of Research Excellence University of Cambridge Cambridge UK

11. Health Data Research UK Cambridge, Wellcome Genome Campus and University of Cambridge Cambridge UK

12. Health Data Science Research Centre Human Technopole Milan Italy

13. Cambridge Centre of Artificial Intelligence in Medicine Cambridge UK

Abstract

AbstractBackgroundDeferrals due to low hemoglobin are time‐consuming and costly for blood donors and donation services. Furthermore, accepting donations from those with low hemoglobin could represent a significant safety issue. One approach to reduce them is to use hemoglobin concentration alongside donor characteristics to inform personalized inter‐donation intervals.Study Design and MethodsWe used data from 17,308 donors to inform a discrete event simulation model comparing personalized inter‐donation intervals using “post‐donation” testing (i.e., estimating current hemoglobin from that measured by a hematology analyzer at last donation) versus the current approach in England (i.e., pre‐donation testing with fixed intervals of 12‐weeks for men and 16‐weeks for women). We reported the impact on total donations, low hemoglobin deferrals, inappropriate bleeds, and blood service costs. Personalized inter‐donation intervals were defined using mixed‐effects modeling to estimate hemoglobin trajectories and probability of crossing hemoglobin donation thresholds.ResultsThe model had generally good internal validation, with predicted events similar to those observed. Over 1 year, a personalized strategy requiring ≥90% probability of being over the hemoglobin threshold, minimized adverse events (low hemoglobin deferrals and inappropriate bleeds) in both sexes and costs in women. Donations per adverse event improved from 3.4 (95% uncertainty interval 2.8, 3.7) under the current strategy to 14.8 (11.6, 19.2) in women, and from 7.1 (6.1, 8.5) to 26.9 (20.8, 42.6) in men. In comparison, a strategy incorporating early returns for those with high certainty of being over the threshold maximized total donations in both men and women, but was less favorable in terms of adverse events, with 8.4 donations per adverse event in women (7.0, 10,1) and 14.8 (12.1, 21.0) in men.DiscussionPersonalized inter‐donation intervals using post‐donation testing combined with modeling of hemoglobin trajectories can help reduce deferrals, inappropriate bleeds, and costs.

Funder

British Heart Foundation

Medical Research Council

National Institute for Health and Care Research

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

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