BMC Infectious Diseases (Nov 2010)

Hypoglycaemia in severe malaria, clinical associations and relationship to quinine dosage

  • Kivaya Esther,
  • Boga Mwanamvua,
  • Jemutai Julie,
  • Akech Samuel,
  • Ogetii Gilbert N,
  • Fegan Greg,
  • Maitland Kathryn

DOI
https://doi.org/10.1186/1471-2334-10-334
Journal volume & issue
Vol. 10, no. 1
p. 334

Abstract

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Abstract Background Hypoglycaemia is an independent risk factor for death in severe malaria and a recognized adverse treatment effect of parenteral quinine. In 2006 our hospital changed quinine treatment policy from 15 mg/kg loading (plus 10 mg/kg 12-hourly) to 20 mg/kg loading (plus 10 mg/kg 8-hourly) to comply with new WHO guidelines. This presented us with the opportunity to examine whether there was any dose relationship of quinine and hypoglycaemia occurrence. Methods Retrospective case notes review of all children admitted to hospital with severe falciparum malaria between April 2002 - July 2009, before and after the introduction of the new WHO quinine regimen. Four-hourly bedside glucose levels were measured until intravenous quinine was discontinued. Clinical events immediately preceding or concurrent with each episode of hypoglycaemia (glucose Results 954 children received the old quinine regime and 283 received the new regime. We found no evidence of an increased prevalence of hypoglycaemia ( Conclusion There was no evidence to indicate a dose relationship between quinine and occurrence of hypoglycaemia. Hypoglycaemia concurred with severity features, disruption of glucose infusion and transfusion. Careful glucose monitoring should be targeted to these complications where resources are limited.