Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria

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Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria. / Segbefia, Catherine; Amponsah, Seth Kwabena; Afrane, Adwoa K A; Nyarko, Mame Yaa; Brew, Yvonne; Salifu, Nihad; Ahorhorlu, Samuel Yao; Sulley, Abdul Malik; Hviid, Lars; Ofori, Michael Fokuo; Adjei, George Obeng.

In: Frontiers in Medicine, Vol. 10, 2023, p. 1291330.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Segbefia, C, Amponsah, SK, Afrane, AKA, Nyarko, MY, Brew, Y, Salifu, N, Ahorhorlu, SY, Sulley, AM, Hviid, L, Ofori, MF & Adjei, GO 2023, 'Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria', Frontiers in Medicine, vol. 10, pp. 1291330. https://doi.org/10.3389/fmed.2023.1291330

APA

Segbefia, C., Amponsah, S. K., Afrane, A. K. A., Nyarko, M. Y., Brew, Y., Salifu, N., Ahorhorlu, S. Y., Sulley, A. M., Hviid, L., Ofori, M. F., & Adjei, G. O. (2023). Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria. Frontiers in Medicine, 10, 1291330. https://doi.org/10.3389/fmed.2023.1291330

Vancouver

Segbefia C, Amponsah SK, Afrane AKA, Nyarko MY, Brew Y, Salifu N et al. Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria. Frontiers in Medicine. 2023;10:1291330. https://doi.org/10.3389/fmed.2023.1291330

Author

Segbefia, Catherine ; Amponsah, Seth Kwabena ; Afrane, Adwoa K A ; Nyarko, Mame Yaa ; Brew, Yvonne ; Salifu, Nihad ; Ahorhorlu, Samuel Yao ; Sulley, Abdul Malik ; Hviid, Lars ; Ofori, Michael Fokuo ; Adjei, George Obeng. / Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria. In: Frontiers in Medicine. 2023 ; Vol. 10. pp. 1291330.

Bibtex

@article{52bdc6cbb9c44f3c8287c5191494643e,
title = "Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria",
abstract = "INTRODUCTION: Limited information exists on any interactions between hydroxyurea (HU) and antimalarials in sickle cell disease (SCD). We evaluated changes in clinical and laboratory parameters among children with SCD on HU therapy treated with artemether-lumefantrine (AL) for acute uncomplicated malaria (UM).METHODS: A prospective, non-randomized, pilot study of 127 children with SCD (23, UM; 104, steady state) were recruited from three hospitals in Accra. UM participants were treated with standard doses of AL and followed up, on days 1, 2, 3, 7, 14, and 28. Venous blood was collected at baseline and follow-up days in participants with UM for determination of malaria parasitaemia, full blood count, reticulocytes, and clinical chemistry. Further, Plasmodium falciparum identification of rapid diagnostic test (RDT) positive samples was done using nested polymerase chain reaction (PCR).RESULTS: Among SCD participants with UM, admission temperature, neutrophils, alanine-aminotransferase, gamma-glutamyl-transferase, and haemoglobin significantly differed between HU recipients (HU+) and steady state, while white blood cell, neutrophils, reticulocytes, bilirubin, urea, and temperature differed significantly between non-HU recipients (no-HU), and steady state. Mean parasitaemia (HU+, 2930.3 vs. no-HU, 1,060, p = 0.74) and adverse events (HU+, 13.9% vs. no-HU, 14.3%), were comparable (p = 0.94). Day 28 reticulocyte count was higher in the HU+ (0.24) (0.17 to 0.37) vs. no-HU, [0.15 (0.09 to 0.27), p = 0.022]. Significant differences in lymphocyte [HU+ 2.74 95% CI (-5.38 to 58.57) vs. no-HU -0.34 (-3.19 to 4.44), p = 0.024]; bilirubin [HU+, -4.44 (-16.36 to 20.74) vs. no-HU -18.37 (-108.79 to -7.16)]; and alanine aminotransferase, [HU+, -4.00 (-48.55 to 6.00) vs. no-HU, 7.00 (-22.00 to 22.00)] were observed during follow up.CONCLUSION: Parasite clearance and adverse event occurrence were comparable between SCD children treated with AL irrespective of HU status. However, distinct patterns of changes in laboratory indices suggest the need for larger, more focused studies.",
author = "Catherine Segbefia and Amponsah, {Seth Kwabena} and Afrane, {Adwoa K A} and Nyarko, {Mame Yaa} and Yvonne Brew and Nihad Salifu and Ahorhorlu, {Samuel Yao} and Sulley, {Abdul Malik} and Lars Hviid and Ofori, {Michael Fokuo} and Adjei, {George Obeng}",
note = "Copyright {\textcopyright} 2023 Segbefia, Amponsah, Afrane, Nyarko, Brew, Salifu, Ahorhorlu, Sulley, Hviid, Ofori and Adjei.",
year = "2023",
doi = "10.3389/fmed.2023.1291330",
language = "English",
volume = "10",
pages = "1291330",
journal = "Frontiers in Medicine",
issn = "2296-858X",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Clinical and laboratory characteristics of children with sickle cell disease on hydroxyurea treated with artemether-lumefantrine for acute uncomplicated malaria

AU - Segbefia, Catherine

AU - Amponsah, Seth Kwabena

AU - Afrane, Adwoa K A

AU - Nyarko, Mame Yaa

AU - Brew, Yvonne

AU - Salifu, Nihad

AU - Ahorhorlu, Samuel Yao

AU - Sulley, Abdul Malik

AU - Hviid, Lars

AU - Ofori, Michael Fokuo

AU - Adjei, George Obeng

N1 - Copyright © 2023 Segbefia, Amponsah, Afrane, Nyarko, Brew, Salifu, Ahorhorlu, Sulley, Hviid, Ofori and Adjei.

PY - 2023

Y1 - 2023

N2 - INTRODUCTION: Limited information exists on any interactions between hydroxyurea (HU) and antimalarials in sickle cell disease (SCD). We evaluated changes in clinical and laboratory parameters among children with SCD on HU therapy treated with artemether-lumefantrine (AL) for acute uncomplicated malaria (UM).METHODS: A prospective, non-randomized, pilot study of 127 children with SCD (23, UM; 104, steady state) were recruited from three hospitals in Accra. UM participants were treated with standard doses of AL and followed up, on days 1, 2, 3, 7, 14, and 28. Venous blood was collected at baseline and follow-up days in participants with UM for determination of malaria parasitaemia, full blood count, reticulocytes, and clinical chemistry. Further, Plasmodium falciparum identification of rapid diagnostic test (RDT) positive samples was done using nested polymerase chain reaction (PCR).RESULTS: Among SCD participants with UM, admission temperature, neutrophils, alanine-aminotransferase, gamma-glutamyl-transferase, and haemoglobin significantly differed between HU recipients (HU+) and steady state, while white blood cell, neutrophils, reticulocytes, bilirubin, urea, and temperature differed significantly between non-HU recipients (no-HU), and steady state. Mean parasitaemia (HU+, 2930.3 vs. no-HU, 1,060, p = 0.74) and adverse events (HU+, 13.9% vs. no-HU, 14.3%), were comparable (p = 0.94). Day 28 reticulocyte count was higher in the HU+ (0.24) (0.17 to 0.37) vs. no-HU, [0.15 (0.09 to 0.27), p = 0.022]. Significant differences in lymphocyte [HU+ 2.74 95% CI (-5.38 to 58.57) vs. no-HU -0.34 (-3.19 to 4.44), p = 0.024]; bilirubin [HU+, -4.44 (-16.36 to 20.74) vs. no-HU -18.37 (-108.79 to -7.16)]; and alanine aminotransferase, [HU+, -4.00 (-48.55 to 6.00) vs. no-HU, 7.00 (-22.00 to 22.00)] were observed during follow up.CONCLUSION: Parasite clearance and adverse event occurrence were comparable between SCD children treated with AL irrespective of HU status. However, distinct patterns of changes in laboratory indices suggest the need for larger, more focused studies.

AB - INTRODUCTION: Limited information exists on any interactions between hydroxyurea (HU) and antimalarials in sickle cell disease (SCD). We evaluated changes in clinical and laboratory parameters among children with SCD on HU therapy treated with artemether-lumefantrine (AL) for acute uncomplicated malaria (UM).METHODS: A prospective, non-randomized, pilot study of 127 children with SCD (23, UM; 104, steady state) were recruited from three hospitals in Accra. UM participants were treated with standard doses of AL and followed up, on days 1, 2, 3, 7, 14, and 28. Venous blood was collected at baseline and follow-up days in participants with UM for determination of malaria parasitaemia, full blood count, reticulocytes, and clinical chemistry. Further, Plasmodium falciparum identification of rapid diagnostic test (RDT) positive samples was done using nested polymerase chain reaction (PCR).RESULTS: Among SCD participants with UM, admission temperature, neutrophils, alanine-aminotransferase, gamma-glutamyl-transferase, and haemoglobin significantly differed between HU recipients (HU+) and steady state, while white blood cell, neutrophils, reticulocytes, bilirubin, urea, and temperature differed significantly between non-HU recipients (no-HU), and steady state. Mean parasitaemia (HU+, 2930.3 vs. no-HU, 1,060, p = 0.74) and adverse events (HU+, 13.9% vs. no-HU, 14.3%), were comparable (p = 0.94). Day 28 reticulocyte count was higher in the HU+ (0.24) (0.17 to 0.37) vs. no-HU, [0.15 (0.09 to 0.27), p = 0.022]. Significant differences in lymphocyte [HU+ 2.74 95% CI (-5.38 to 58.57) vs. no-HU -0.34 (-3.19 to 4.44), p = 0.024]; bilirubin [HU+, -4.44 (-16.36 to 20.74) vs. no-HU -18.37 (-108.79 to -7.16)]; and alanine aminotransferase, [HU+, -4.00 (-48.55 to 6.00) vs. no-HU, 7.00 (-22.00 to 22.00)] were observed during follow up.CONCLUSION: Parasite clearance and adverse event occurrence were comparable between SCD children treated with AL irrespective of HU status. However, distinct patterns of changes in laboratory indices suggest the need for larger, more focused studies.

U2 - 10.3389/fmed.2023.1291330

DO - 10.3389/fmed.2023.1291330

M3 - Journal article

C2 - 38076253

VL - 10

SP - 1291330

JO - Frontiers in Medicine

JF - Frontiers in Medicine

SN - 2296-858X

ER -

ID: 375667270