Haematological quality and age of donor blood issued for paediatric transfusion to four hospitals in sub-Saharan Africa.


Journal

Vox sanguinis
ISSN: 1423-0410
Titre abrégé: Vox Sang
Pays: England
ID NLM: 0413606

Informations de publication

Date de publication:
May 2019
Historique:
received: 01 10 2018
revised: 28 12 2018
accepted: 28 01 2019
pubmed: 7 3 2019
medline: 23 7 2019
entrez: 7 3 2019
Statut: ppublish

Résumé

Paediatric blood transfusion for severe anaemia in hospitals in sub-Saharan Africa remains common. Yet, reports describing the haematological quality of donor blood or storage duration in routine practice are very limited. Both factors are likely to affect transfusion outcomes. We undertook three audits examining the distribution of pack types, haematological quality and storage duration of donor blood used in a paediatric clinical trial of blood at four hospitals in Africa (Uganda and Malawi). The overall distribution of whole blood, packed cells (plasma-reduced by centrifugation) and red cell concentrates (RCC) (plasma-reduced by gravity-dependent sedimentation) used in a randomised trial was 40·7% (N = 1215), 22·4% (N = 669) and 36·8% (N = 1099), respectively. The first audit found similar median haematocrits of 57·0% (50·0,74·0), 64·0% (52·0,72·5; P = 0·238 vs. whole blood) and 56·0% (48·0,67·0; P = 0·462) in whole blood, RCC and packed cells, respectively, which resulted from unclear pack labelling by blood transfusion services (BTS). Re-training of the BTS, hospital blood banks and clinical teams led to, in subsequent audits, significant differences in median haematocrit and haemoglobins across the three pack types and values within expected ranges. Median storage duration time was 12 days (IQR: 6, 19) with 18·2% (537/2964) over 21 days in storage. Initially, 9 (2·8%) packs were issued past the recommended duration of storage, dropping to 0·3% (N = 7) in the third audit post-training. The study highlights the importance of close interactions and education between BTS and clinical services and the importance of haemovigilance to ensure safe transfusion practice.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
Paediatric blood transfusion for severe anaemia in hospitals in sub-Saharan Africa remains common. Yet, reports describing the haematological quality of donor blood or storage duration in routine practice are very limited. Both factors are likely to affect transfusion outcomes.
MATERIALS AND METHODS METHODS
We undertook three audits examining the distribution of pack types, haematological quality and storage duration of donor blood used in a paediatric clinical trial of blood at four hospitals in Africa (Uganda and Malawi).
RESULTS RESULTS
The overall distribution of whole blood, packed cells (plasma-reduced by centrifugation) and red cell concentrates (RCC) (plasma-reduced by gravity-dependent sedimentation) used in a randomised trial was 40·7% (N = 1215), 22·4% (N = 669) and 36·8% (N = 1099), respectively. The first audit found similar median haematocrits of 57·0% (50·0,74·0), 64·0% (52·0,72·5; P = 0·238 vs. whole blood) and 56·0% (48·0,67·0; P = 0·462) in whole blood, RCC and packed cells, respectively, which resulted from unclear pack labelling by blood transfusion services (BTS). Re-training of the BTS, hospital blood banks and clinical teams led to, in subsequent audits, significant differences in median haematocrit and haemoglobins across the three pack types and values within expected ranges. Median storage duration time was 12 days (IQR: 6, 19) with 18·2% (537/2964) over 21 days in storage. Initially, 9 (2·8%) packs were issued past the recommended duration of storage, dropping to 0·3% (N = 7) in the third audit post-training.
CONCLUSION CONCLUSIONS
The study highlights the importance of close interactions and education between BTS and clinical services and the importance of haemovigilance to ensure safe transfusion practice.

Identifiants

pubmed: 30838664
doi: 10.1111/vox.12764
pmc: PMC6563499
doi:

Substances chimiques

Hemoglobins 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

340-348

Subventions

Organisme : Medical Research Council
ID : MC_UU_12023/17
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12023/26
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/J012483/1
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2019 The Authors. Vox Sanguinis published by John Wiley & Sons Ltd on behalf of International Society of Blood Transfusion.

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Auteurs

Sophie Uyoga (S)

KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.

Ayub Mpoya (A)

KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.

Peter Olupot-Olupot (P)

Mbale Clinical Research Institute, Mbale, Uganda.
Faculty of Health Sciences, Busitema University, Mbale Campus, Mbale, Ugandas.

Sarah Kiguli (S)

Department of Paediatrics, Mulago Hospital, Makerere University, Kampala, Uganda.

Robert O Opoka (RO)

Department of Paediatrics, Mulago Hospital, Makerere University, Kampala, Uganda.

Charles Engoru (C)

Department of Paediatrics, Soroti Regional Referral Hospital, Soroti, Uganda.

Macpherson Mallewa (M)

Department of Paediatrics and Child Health, College of Medicine, University of Malawi, Blantyre, Malawi.

Neil Kennedy (N)

Department of Paediatrics and Child Health, College of Medicine, University of Malawi, Blantyre, Malawi.
School of Medicine, Dentistry and Biomedical Science, Queen's University, Belfast, UK.

Bridon M'baya (B)

Malawi Blood Transfusion Service, Blantyre, Malawi.

Dorothy Kyeyune (D)

Uganda Blood Transfusion Service, Kampala, Uganda.

Benjamin Wabwire (B)

Mbale Regional Blood Bank, Mbale, Uganda.

Imelda Bates (I)

Liverpool School of Tropical Medicine and Hygiene Pembroke Place, Liverpool, UK.

Diana M Gibb (DM)

MRC Clinical Trials Unit, Institute of Clinical Trials & Methodology, University College London, London, UK.

Ann Sarah Walker (AS)

MRC Clinical Trials Unit, Institute of Clinical Trials & Methodology, University College London, London, UK.

Elizabeth C George (EC)

MRC Clinical Trials Unit, Institute of Clinical Trials & Methodology, University College London, London, UK.

Thomas N Williams (TN)

KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Department of Medicine, St Mary's Campus Imperial College, London, UK.

Kathryn Maitland (K)

KEMRI/Wellcome Trust Research Programme, Kilifi, Kenya.
Department of Medicine, St Mary's Campus Imperial College, London, UK.

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Classifications MeSH