What is the treatment for cerebral malaria with cerebrospinal fluid (CSF) pleocytosis?

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Last updated: October 9, 2025View editorial policy

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Treatment of Cerebral Malaria with CSF Pleocytosis

Intravenous artesunate is the first-line treatment for cerebral malaria with CSF pleocytosis, administered at 2.4 mg/kg at 0,12,24, and 48 hours until clinical improvement and parasitemia is <1%. 1

Initial Management

  • Immediate hospitalization is required for patients with suspected cerebral malaria, with prompt diagnostic tests including thick blood film, hemoglobin measurement, blood glucose, and lumbar puncture 2, 1
  • If artesunate is unavailable, administer intravenous quinine: initial dose of 20 mg(salt)/kg body weight in 10 mL/kg 5% dextrose infused over 3 hours, followed by 10 mg/kg every 12 hours 2
  • For patients who have already received quinine before admission, the initial dose should be reduced to 10 mg/kg 2
  • Switch to oral medications as soon as the patient's condition allows 2
  • For patients returning from malaria-endemic areas, rapid blood malaria antigen tests and three thick and thin blood films should be examined for malaria parasites 2

Management of CSF Pleocytosis

  • Perform lumbar puncture to rule out other causes of meningitis or encephalitis, as cerebral malaria can present with CSF pleocytosis 2, 3
  • Despite the presence of CSF pleocytosis, continue antimalarial treatment as the primary intervention 1, 4
  • Do NOT administer steroids, as they have an adverse effect on outcomes in cerebral malaria 2, 1

Supportive Care and Management of Complications

  • Carefully manage fluid therapy to prevent fluid overload, which can precipitate pulmonary edema or ARDS and worsen cerebral edema 2, 3
  • Use 5% dextrose with 1/2 normal saline as the IV fluid of choice to prevent hypoglycemia and minimize salt leakage into pulmonary and cerebral tissues 2, 3
  • Monitor blood glucose levels regularly, as hypoglycemia is a common complication and risk factor for fatal outcome 2
  • Treat hypoglycemia with 50 mL of 50% IV dextrose 2
  • For seizures, administer paraldehyde 0.2 mL/kg by IM injection, and repeat if convulsions recur 3
  • For persistent convulsions, give phenobarbital 10 mg/kg IM 1, 3
  • Provide blood transfusion when hemoglobin is below 4 g/dL, or below 6 g/dL with signs of heart failure 2

Monitoring and Follow-up

  • Monitor parasitemia every 12 hours until decline to <1%, then every 24 hours until negative 1
  • Monitor for post-artemisinin delayed hemolysis (PADH) at days 7,14,21, and 28 1
  • Start antibiotics if concomitant bacterial infection is suspected, but continue only if blood cultures are positive 1
  • Monitor for renal failure by tracking fluid intake and output 2
  • In case of oliguria, a fluid challenge followed by furosemide injection can help differentiate acute renal failure from prerenal causes 2

Special Considerations

  • For patients with cerebral malaria who cannot swallow or have persistent vomiting, use IV antimalarial therapy 2
  • Despite advances in treatment, cerebral malaria can still result in long-term neurological sequelae even with appropriate treatment 4, 5
  • Exchange blood transfusion is no longer indicated with the availability of artesunate 1

References

Guideline

Treatment of Cerebral Malaria

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Severe Malaria

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Severe malaria: update on pathophysiology and treatment.

Current opinion in infectious diseases, 2019

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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