4.3 Article

Establishment of haematological and immunological reference values for healthy Tanzanian children in Kilimanjaro Region

Journal

TROPICAL MEDICINE & INTERNATIONAL HEALTH
Volume 15, Issue 9, Pages 1011-1021

Publisher

WILEY
DOI: 10.1111/j.1365-3156.2010.02585.x

Keywords

CD4-positive T-lymphocyte; child; haematology; infant; Tanzania; reference values

Funding

  1. NIH [AI062563]
  2. Duke Clinical Trials Unit and Clinical Research Sites [U01 AI069484]
  3. Fogarty International Center [D43 PA03018]
  4. Duke University Center for AIDS Research (CFAR) [P30 AI 64518]
  5. International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT)
  6. National Institute of Allergy and Infectious Diseases (NIAID) [U01 AI068632]
  7. Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  8. National Institute of Mental Health (NIMH) [AI068632]
  9. National Institute of Allergy and Infectious Diseases (NIAID)
  10. NICHD [N01-DK-9-001/HHSN267200800001C]

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OBJECTIVE To determine the normal haematological and immunological reference intervals for healthy Tanzanian children. METHODS We analysed data from 655 HIV-seronegative, healthy children from 1 month to 18 years of age from the Kilimanjaro Region of Tanzania for this cross-sectional study. Median and 95% reference ranges were determined for haematological and immunological parameters and analysed by age cohorts, and by gender for adolescents. RESULTS Median haemoglobin (Hb) and haematocrit (Hct) for all age groups were higher than established East African reference intervals. Compared to U.S. intervals, reference ranges encompassed lower values for Hb, Hct, mean corpuscular volume, and platelets. Applying the U.S. National Institute of Health Division of AIDS (DAIDS) adverse event grading criteria commonly used in clinical trials to the reference range participants, 128 (21%) of 619 children would be classified as having an adverse event related to Hb level. CD4-positive T-lymphocyte absolute counts declined significantly with increasing age (P < 0.0001). For those aged under five years, CD4-positive T-lymphocyte percentages are lower than established developed country medians. CONCLUSIONS Country-specific reference ranges are needed for defining normal laboratory parameters among children in Africa. Knowledge of appropriate reference intervals is critical not only for providing optimal clinical care, but also for enrolling children in medical research. Knowledge of normal CD4-positive T-lymphocyte parameters in this population is especially important for guiding the practice of HIV medicine in Tanzania.

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