Detailed Medical Treatment of Malaria
Artemisinin-based combination therapy (ACT) is the first-line treatment for uncomplicated Plasmodium falciparum malaria, with artemether-lumefantrine being highly effective with cure rates exceeding 95%, while intravenous artesunate is the treatment of choice for severe malaria. 1
Diagnosis
- Microscopy: Gold standard for malaria diagnosis, allows calculation of parasitemia percentage and monitoring treatment response
- Rapid Diagnostic Tests (RDTs): Use when qualified microscopists are unavailable
- Nucleic Acid Amplification Tests (NAATs): 10-100 times more sensitive than microscopy or RDTs
Treatment of Uncomplicated Malaria
P. falciparum and P. knowlesi
First-line treatment: Artemisinin-based Combination Therapy (ACT)
- Artemether-lumefantrine: Total of 24 tablets for adults >35kg, taken with food
- Atovaquone-proguanil: Alternative for patients with QT prolongation risk or from Southeast Asia with high ACT resistance
Alternative regimens (when ACTs unavailable or contraindicated):
P. vivax, P. ovale, P. malariae
Blood stage treatment:
Radical cure (for P. vivax and P. ovale to eliminate liver hypnozoites):
Treatment of Severe Malaria
- First-line treatment: Intravenous artesunate 1, 4
- Monitor parasitemia every 12 hours until <1%, then every 24 hours until negative 1
- Monitor for post-artesunate delayed hemolysis (PADH) at days 7,14,21, and 28 1
Special Populations
Pregnant Women
- Artemether-lumefantrine is endorsed for use in all trimesters of pregnancy 1
- Primaquine and tafenoquine are contraindicated during pregnancy 1
- Defer anti-relapse therapy until after pregnancy 1
- Chloroquine is safe during pregnancy for blood-stage treatment 1, 3
Renal Impairment
- For quinine: Loading dose of 648 mg followed 12 hours later by maintenance doses of 324 mg every 12 hours 1
- Atovaquone-proguanil should not be used for malaria prophylaxis in severe renal impairment (creatinine clearance <30 mL/min) 2
- Atovaquone-proguanil may be used with caution for treatment in severe renal impairment if benefits outweigh risks 2
Hepatic Impairment
- Avoid quinine in severe hepatic impairment 1
- Monitor closely if mild to moderate hepatic impairment 1
- No dosage adjustments needed for atovaquone-proguanil in mild to moderate hepatic impairment 2
Monitoring Treatment Response
- For uncomplicated malaria: Monitor parasitemia every 24 hours until negative 1
- For severe malaria: Monitor parasitemia every 12 hours until <1%, then every 24 hours until negative 1
- Check hemoglobin, haptoglobin, and lactate dehydrogenase levels to monitor for hemolysis 1
Resistance Considerations
- P. falciparum has developed resistance to chloroquine in most regions worldwide 1
- Increasing artemisinin resistance in Greater Mekong sub-region and parts of Africa requires vigilant monitoring 1
- In areas with known resistance, use alternative regimens based on local resistance patterns 1
Pediatric Considerations
- ACT regimens are effective in children, with dosing based on weight 1, 5
- The six-dose regimen of artemether-lumefantrine has shown high efficacy (>93% when PCR-corrected) in African children 5
- Children are at higher risk for severe malaria and require prompt treatment 4
Prevention
- Travelers to endemic areas should take preventive measures:
- Insecticide-treated bed nets
- Protective clothing
- Insect repellents
- Appropriate chemoprophylaxis 1
The treatment of malaria requires prompt diagnosis and species-specific therapy to ensure optimal outcomes. ACTs remain the cornerstone of treatment for uncomplicated P. falciparum malaria, while chloroquine plus primaquine/tafenoquine is essential for P. vivax and P. ovale infections to prevent relapse. Severe malaria requires immediate intravenous artesunate and intensive monitoring.