Original article

Blood Transfusion - 5 2020 (September-October)

Bacterial contamination of blood products for transfusion in the Democratic Republic of the Congo: temperature monitoring, qualitative and semi-quantitative culture

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Key words: bacterial contamination, blood safety, blood transfusion, Africa South of the Sahara, Democratic Republic of the Congo
Publication Date: 2020-08-06

Abstract

Background - Bacterial contamination of blood for transfusion is rarely investigated in low-income countries. We determined the contamination rate of blood products in the Democratic Republic of the Congo.
Material and methods - In this prospective observational study, blood products in one rural and two urban hospitals (paediatric and general) contained a satellite sampling bag by which blood was sampled for culture in a blood culture bottle (4 mL) and on an agar-coated slide to estimate colony forming units (CFU/mL). Bacteria were identified with biochemical tests and MALDI-TOF (Bruker). Exposure time >10 °C was assessed on a subset of blood products.
Results - In total, 1.4% (41 of 2,959) of blood products were contaminated with 48 bacterial isolates. Skin (e.g., Staphylococcus spp.) and environmental (e.g., Bacillus spp.) bacteria predominated (97.8% of 45 isolates identified). Bacterial counts were ≤10³ CFU/mL. Contamination rates for the urban paediatric, urban general and rural hospitals were 1.6%, 2.4% and 0.3%, respectively (p=0.004). None of the following variables was significantly associated with contamination: (i) donor type (voluntary 1.6%, family 1.2%, paid 3.9%); (ii) type of blood product (red cells 1.6%, whole blood 0.6%); (ii) season (dry season 2.4%, rainy season 1.8%); (iv) age of blood product (contaminated 8 days vs non-contaminated 6 days); and (v) exposure time >10 °C (median for contaminated and non-contaminated blood reached maximum test limit of 8 hours).
Discussion - A bacterial contamination rate of 1.4% of whole blood and red cells is similar to results from high-income countries. Implementation of feasible risk-mitigation measures is needed.

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Authors

Anne-Sophie Heroes - Institute of Tropical Medicine, Department of Clinical Sciences, Antwerp, Belgium; KU Leuven, Department of Microbiology, Immunology and Transplantation, Leuven, Belgium

Natacha Ndalingosu - Centre National de Transfusion Sanguine, Hemovigilance Department, Kinshasa, Democratic Republic of the Congo

Jocelyne Kalema - Institut National de Recherche Biomédicale, Department of Microbiology, Kinshasa, Democratic Republic of the Congo; Cliniques Universitaires, Department of Clinical Biology, Kinshasa, Democratic Republic of the Congo

Aimée Luyindula - Hôpital Saint-Luc, Blood bank, Kisantu, Democratic Republic of the Congo

Dorothée Kashitu - Hôpital Provincial Général de Référence, Blood bank, Kinshasa, Democratic Republic of the Congo

Catherine Akele - Hôpital Pédiatrique Kalembe Lembe, Head Office, Kinshasa, Democratic Republic of the Congo

Jeff Kabinda - Centre National de Transfusion Sanguine, Head Office, Kinshasa, Democratic Republic of the Congo; Université Pédagogique Nationale, Department of Health Science, Kinshasa, Democratic Republic of the Congo

Katrien Lagrou - KU Leuven, Department of Microbiology, Immunology and Transplantation, Leuven, Belgium; University Hospitals Leuven, Department of Laboratory Medicine and National Reference Centre for Mycosis, Leuven, Belgium

Philippe Vandekerckhove - Belgian Red Cross-Flanders, Blood service, Mechelen, Belgium; KU Leuven, Department of Public Health and Primary Care, Leuven, Belgium

Jan Jacobs - Institute of Tropical Medicine, Department of Clinical Sciences, Antwerp, Belgium; KU Leuven, Department of Microbiology, Immunology and Transplantation, Leuven, Belgium

Octavie Lunguya - Institut National de Recherche Biomédicale, Department of Microbiology, Kinshasa, Democratic Republic of the Congo; Cliniques Universitaires, Department of Clinical Biology, Kinshasa, Democratic Republic of the Congo

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