The First Successful Haematopoietic Stem Cell Transplantation for a Patient with Sickle Cell Disease in a Private Hospital in a Low Resource Country, Nigeria: A Case Report

Authors

  • G. N. Bazuaye Department of Haematology, University of Benin Teaching Hospital, Benin, Nigeria Author
  • B. Nwogoh Department of Haematology, University of Benin Teaching Hospital, Benin, Nigeria Author
  • Y. T. Israel-Aina Department of Child Health, University of Benin Teaching Hospital, Nigeria Author
  • B. Ogunlere Department of Nursing, University of Benin Teaching Hospital, Nigeria Author
  • X. Yamah Department of Haematology, University of Benin Teaching Hospital, Benin, Nigeria Author
  • G. Agbonkhese Department of Anaesthesia, University of Benin Teaching Hospital, Nigeria Author
  • K. N. Bazuaye Department of Optometry, University of Benin, Nigeria Author
  • M. U. Nwagu Department of Haematology, Edo University Iyamho, Nigeria Author
  • I. N. Ojiemhangbe Stem Cell Transplant Unit, Celltek Healthcare Medical Center, Benin City, Nigeria Author
  • J. O. Omonlumhen Stem Cell Transplant Unit, Celltek Healthcare Medical Center, Benin City, Nigeria. Author

Keywords:

private medical centre, haematopoietic stem cell transplantation (HSCT), Sickle cell disease

Abstract

Background꞉ Sickle cell disease (SCD) is a chronic debilitating disease and is highly prevalent in Nigeria. Despite documented challenges in setting up stem cell transplant centres in developing  resource  poor  countries,  the  first successful haematopoietic stem cell transplant (HSCT) in Nigeria was performed at the University  of  Benin  Teaching  Hospital,  Benin City (a Federal Centre) in 2011. Despite more challenges, we present the first successful HSCT in a private centre in Nigeria for a patient with SCD.

Case Report꞉ Patient was a 15 year old male with sickle cell anaemia (SCA) who had recurrent acute chest syndrome, stable haemoglobin  (Hb)  of  7g/dl and pentazocine addicted. The donor was an 18 year-old HLA matched (10/10) sister with haemoglobin phenotype AS.  The  patient  had reduced intensity conditioning (RIC), 2 fludarabine  160  mg/m ,  busulphan  14mg/kg (Flu/Bu) and anti-thymocyte globulin (ATG; ATGAM) 22.73 mg/kg. Graft versus host disease (GvHD) prophylaxis was with cyclosporin A and mycophenolate mofetil.
A total of 6.1 x 10 /kg nucleated cells, i.e. stem cells from the bone marrow, were transfused on day 0. Neutrophil and platelet engraftment occurred on days +16 and +22 respectively. By day +30, donor chimerism was 68 % and there was no graft versus host disease (GvHD). The patient was clinically stable and was discharge on day +66. The full blood count result showed haemoglobin  of 11.5  g/dl,  white  cell  count  of 6,200  /ul,  platelet  count  of  113,000  /ul  and haemoglobin phenotype was AS (as the donor). One year later, the patient had a 100 % donor chimerism and had not experienced any sickle cell crises.

Conclusion꞉ A  private  hospital  in  a  low  income  country  in collaboration  with  trained  personnel  from  a Federal Teaching Hospital performed a successful HSCT for a patient with SCA despite several documented challenges. There is need for private public partnership to drive and sustain HSCT activities in low income countries like Nigeria.

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Published

2023-08-20

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Articles

How to Cite

Bazuaye , G. N., Nwogoh , B., Israel-Aina , Y. T., Ogunlere , B., Yamah , X., Agbonkhese , G., Bazuaye , K. N., Nwagu , M. U., Ojiemhangbe , I. N., & Omonlumhen , J. O. (2023). The First Successful Haematopoietic Stem Cell Transplantation for a Patient with Sickle Cell Disease in a Private Hospital in a Low Resource Country, Nigeria: A Case Report. Nigerian Journal of Haematology, 4(1&2), 57-62. https://njhaem.org.ng/index.php/home/article/view/52

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