Malaria Treatment for a 70 kg Male
For a 70 kg male with uncomplicated malaria, administer artemether-lumefantrine (AL) as 4 tablets at 0 hours, 4 tablets at 8 hours on day 1, then 4 tablets twice daily on days 2 and 3, and critically, this must be taken with a fatty meal or drink to ensure adequate absorption. 1
Initial Assessment and Species Identification
Before initiating treatment, determine disease severity and identify the Plasmodium species:
- Check for severe malaria criteria: altered consciousness, seizures, respiratory distress, shock, severe anemia (Hb <4 g/dL), renal impairment, hypoglycemia, acidosis, or parasitemia >5% 2, 1
- Species matters for treatment selection: P. falciparum requires different management than P. vivax, P. ovale, or P. malariae 1
Treatment for Uncomplicated P. falciparum Malaria
First-Line: Artemether-Lumefantrine (AL)
- Dosing regimen: 4 tablets at 0 hours, 4 tablets at 8 hours on day 1, then 4 tablets twice daily on days 2 and 3 1, 3
- Critical administration requirement: AL must be taken with fatty food or a milky drink; failure to do so results in subtherapeutic drug levels and treatment failure 1, 4
- Expected outcomes: Cure rates of 98-100% with rapid parasite clearance 4, 5
- Adverse effects: Headache, vertigo, digestive disorders, and potential QTc prolongation 3
Alternative First-Line: Dihydroartemisinin-Piperaquine (DP)
- Dosing for 70 kg patient: 3 tablets daily for 3 days, taken in fasting condition 1, 3
- Advantages: Superior efficacy in preventing P. vivax recurrence (RR 0.32,95% CI 0.24-0.43) and longer half-life 1
- Caution: Also causes QTc prolongation; avoid in patients with baseline QT abnormalities or those taking QT-prolonging medications 1, 3
Second-Line Options
- Atovaquone-proguanil: 4 tablets daily for 3 days with fatty meal, reserved for ACT contraindications 1, 6
- Quinine plus doxycycline: Quinine 750 mg three times daily for 3-7 days plus doxycycline 100 mg twice daily for 7 days 1, 3
Treatment for Uncomplicated Non-Falciparum Malaria
P. vivax, P. ovale, P. malariae (Chloroquine-Sensitive Regions)
- Blood stage treatment: Chloroquine 1000 mg salt initially, then 500 mg at 6,24, and 48 hours (total 2500 mg over 3 days) 1, 4
- Alternative: ACTs (AL or DP) are equally effective 2, 1
Mandatory Radical Cure for P. vivax and P. ovale
- Test for G6PD deficiency first: This is a critical safety requirement before administering primaquine or tafenoquine 1, 4
- Primaquine (if G6PD normal): 30 mg base daily for 14 days to eliminate liver hypnozoites and prevent relapse 1, 4
- For mild-moderate G6PD deficiency (30-70% activity): Primaquine 45 mg once weekly for 8 weeks 1
- Tafenoquine alternative: Requires quantitative G6PD >70%, not widely available outside US/Australia 1
Treatment for Severe Malaria
If any severe malaria criteria are present, this is a medical emergency requiring immediate intravenous artesunate:
- IV artesunate dosing: 2.4 mg/kg IV at 0,12, and 24 hours, then daily until parasitemia <1% 2, 1
- Transition to oral therapy: Once clinically improved and able to take oral medication, complete treatment with full course of oral ACT 2, 1
- Intensive monitoring required: Check parasitemia every 12 hours until <1%, then every 24 hours until negative; monitor blood glucose, renal function, and hemoglobin daily 2
Critical Monitoring Requirements
Post-Artemisinin Delayed Hemolysis (PADH)
- Monitor hemoglobin on days 7,14,21, and 28 after treatment, as PADH occurs in 37.4% of patients using strict definitions 1, 3
Parasitemia Clearance
- Check thick blood smear every 24-48 hours until negative to confirm treatment response 2
Special Populations
Pregnant Women
- AL is safe in all trimesters with cure rates of 94.9-100% and no increased risk of adverse pregnancy outcomes 1, 4
- Primaquine and tafenoquine are absolutely contraindicated in pregnancy due to hemolysis risk 1, 4
Renal Impairment
- Atovaquone-proguanil should not be used for prophylaxis in severe renal impairment (CrCl <30 mL/min) 6
- May use cautiously for treatment if benefits outweigh risks 6
Common Pitfalls to Avoid
- Failing to ensure fatty food intake with AL is the most common cause of treatment failure 1, 4
- Not testing for G6PD deficiency before primaquine can cause life-threatening hemolysis, particularly in Asian and African populations 1, 4
- Underestimating parasitemia levels can lead to incorrect classification as uncomplicated when severe malaria is present 1
- Delayed diagnosis and treatment of P. falciparum significantly increases mortality 1
- Ignoring QTc prolongation risk with both AL and DP in susceptible patients 1, 3