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Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research
BACKGROUND: Plasmodium falciparum infection may cause severe anaemia, particularly in children. When planning a diagnostic study on children suspected of severe malaria in sub-Saharan Africa, it was questioned how much blood could be safely sampled; intended blood volumes (blood cultures and EDTA bl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890332/ https://www.ncbi.nlm.nih.gov/pubmed/27251128 http://dx.doi.org/10.1186/s12936-016-1356-9 |
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author | Kuijpers, Laura Maria Francisca Maltha, Jessica Guiraud, Issa Kaboré, Bérenger Lompo, Palpouguini Devlieger, Hugo Van Geet, Chris Tinto, Halidou Jacobs, Jan |
author_facet | Kuijpers, Laura Maria Francisca Maltha, Jessica Guiraud, Issa Kaboré, Bérenger Lompo, Palpouguini Devlieger, Hugo Van Geet, Chris Tinto, Halidou Jacobs, Jan |
author_sort | Kuijpers, Laura Maria Francisca |
collection | PubMed |
description | BACKGROUND: Plasmodium falciparum infection may cause severe anaemia, particularly in children. When planning a diagnostic study on children suspected of severe malaria in sub-Saharan Africa, it was questioned how much blood could be safely sampled; intended blood volumes (blood cultures and EDTA blood) were 6 mL (children aged <6 years) and 10 mL (6–12 years). A previous review [Bull World Health Organ. 89: 46–53. 2011] recommended not to exceed 3.8 % of total blood volume (TBV). In a simulation exercise using data of children previously enrolled in a study about severe malaria and bacteraemia in Burkina Faso, the impact of this 3.8 % safety guideline was evaluated. METHODS: For a total of 666 children aged >2 months to <12 years, data of age, weight and haemoglobin value (Hb) were available. For each child, the estimated TBV (TBVe) (mL) was calculated by multiplying the body weight (kg) by the factor 80 (ml/kg). Next, TBVe was corrected for the degree of anaemia to obtain the functional TBV (TBVf). The correction factor consisted of the rate ‘Hb of the child divided by the reference Hb’; both the lowest (‘best case’) and highest (‘worst case’) reference Hb values were used. Next, the exact volume that a 3.8 % proportion of this TBVf would present was calculated and this volume was compared to the blood volumes that were intended to be sampled. RESULTS: When applied to the Burkina Faso cohort, the simulation exercise pointed out that in 5.3 % (best case) and 11.4 % (worst case) of children the blood volume intended to be sampled would exceed the volume as defined by the 3.8 % safety guideline. Highest proportions would be in the age groups 2–6 months (19.0 %; worst scenario) and 6 months–2 years (15.7 %; worst case scenario). A positive rapid diagnostic test for P. falciparum was associated with an increased risk of violating the safety guideline in the worst case scenario (p = 0.016). CONCLUSIONS: Blood sampling in children for research in P. falciparum endemic settings may easily violate the proposed safety guideline when applied to TBVf. Ethical committees and researchers should be wary of this and take appropriate precautions. |
format | Online Article Text |
id | pubmed-4890332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48903322016-06-03 Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research Kuijpers, Laura Maria Francisca Maltha, Jessica Guiraud, Issa Kaboré, Bérenger Lompo, Palpouguini Devlieger, Hugo Van Geet, Chris Tinto, Halidou Jacobs, Jan Malar J Research BACKGROUND: Plasmodium falciparum infection may cause severe anaemia, particularly in children. When planning a diagnostic study on children suspected of severe malaria in sub-Saharan Africa, it was questioned how much blood could be safely sampled; intended blood volumes (blood cultures and EDTA blood) were 6 mL (children aged <6 years) and 10 mL (6–12 years). A previous review [Bull World Health Organ. 89: 46–53. 2011] recommended not to exceed 3.8 % of total blood volume (TBV). In a simulation exercise using data of children previously enrolled in a study about severe malaria and bacteraemia in Burkina Faso, the impact of this 3.8 % safety guideline was evaluated. METHODS: For a total of 666 children aged >2 months to <12 years, data of age, weight and haemoglobin value (Hb) were available. For each child, the estimated TBV (TBVe) (mL) was calculated by multiplying the body weight (kg) by the factor 80 (ml/kg). Next, TBVe was corrected for the degree of anaemia to obtain the functional TBV (TBVf). The correction factor consisted of the rate ‘Hb of the child divided by the reference Hb’; both the lowest (‘best case’) and highest (‘worst case’) reference Hb values were used. Next, the exact volume that a 3.8 % proportion of this TBVf would present was calculated and this volume was compared to the blood volumes that were intended to be sampled. RESULTS: When applied to the Burkina Faso cohort, the simulation exercise pointed out that in 5.3 % (best case) and 11.4 % (worst case) of children the blood volume intended to be sampled would exceed the volume as defined by the 3.8 % safety guideline. Highest proportions would be in the age groups 2–6 months (19.0 %; worst scenario) and 6 months–2 years (15.7 %; worst case scenario). A positive rapid diagnostic test for P. falciparum was associated with an increased risk of violating the safety guideline in the worst case scenario (p = 0.016). CONCLUSIONS: Blood sampling in children for research in P. falciparum endemic settings may easily violate the proposed safety guideline when applied to TBVf. Ethical committees and researchers should be wary of this and take appropriate precautions. BioMed Central 2016-06-02 /pmc/articles/PMC4890332/ /pubmed/27251128 http://dx.doi.org/10.1186/s12936-016-1356-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Kuijpers, Laura Maria Francisca Maltha, Jessica Guiraud, Issa Kaboré, Bérenger Lompo, Palpouguini Devlieger, Hugo Van Geet, Chris Tinto, Halidou Jacobs, Jan Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research |
title | Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research |
title_full | Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research |
title_fullStr | Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research |
title_full_unstemmed | Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research |
title_short | Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research |
title_sort | severe anaemia associated with plasmodium falciparum infection in children: consequences for additional blood sampling for research |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890332/ https://www.ncbi.nlm.nih.gov/pubmed/27251128 http://dx.doi.org/10.1186/s12936-016-1356-9 |
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