From Essential obstetric and newborn care › Chapter 4: Pathologies during pregnancy and pregnancy-related disorders · Médecins Sans Frontières, Current online edition, 2026
MSF clinical guideline on the diagnosis and treatment of malaria and helminth infections during pregnancy.
- Issuer
- Médecins Sans Frontières
- Edition
- Current online edition, 2026
- Audience
- Obstetricians, midwives, general practitioners, and humanitarian healthcare workers providing antenatal care
- Evidence
- Based on WHO Guidelines for the treatment of malaria, Third edition, 2015, and MSF field experience
- Reviewed
- 23 Oct 2026 · GMJ
What this guideline says
GMJ summary
This MSF guideline addresses the management of parasitic infections during pregnancy, with particular focus on malaria and helminth infections. Malaria in pregnancy is associated with low birth weight, increased anaemia risk, and in low transmission areas, increased risk of severe malaria and death. The guideline provides detailed treatment protocols for uncomplicated and severe malaria across all trimesters.
For uncomplicated falciparum malaria, artemisinin-based combination therapies (ACTs) are recommended for 3 days in all trimesters, with specific dosing tables provided for artemether/lumefantrine, artesunate/amodiaquine, artesunate/mefloquine, and dihydroartemisinin/piperaquine. Quinine remains an alternative, particularly when combined with clindamycin in South-East Asia and Amazon regions. Severe malaria requires parenteral artesunate or artemether, with specific dosing schedules and monitoring requirements.
For helminth infections, the guideline recommends albendazole 400 mg as a single dose for both ancylostomiasis (hookworms) and ascariasis, but explicitly prohibits administration during the first trimester. Associated anaemia from hookworm infection requires concurrent treatment.
Key points
For clinicians — doses and thresholds as stated in the guideline
- Uncomplicated falciparum malaria: artemisinin-based combination therapy (ACT) for 3 days in all trimesters; artemether/lumefantrine 4 tablets twice daily for 3 days (20/120 mg formulation) is one recommended option
- Severe malaria: artesunate IV/IM 2.4 mg/kg at H0, H12, H24, then once daily; or artemether IM 3.2 mg/kg loading dose then 1.6 mg/kg daily
- Quinine alternative for uncomplicated malaria: 10 mg/kg PO 3 times daily for 7 days; in South-East Asia and Amazon, combine with clindamycin 10 mg/kg twice daily for 5 days
- P. vivax, P. malariae, P. ovale, P. knowlesi: chloroquine 10 mg base/kg on days 1–2, then 5 mg base/kg on day 3, irrespective of pregnancy trimester
- Hookworms and ascariasis: albendazole 400 mg single dose, but do not administer during first trimester—wait until second trimester
- AS/SP combination is contraindicated in HIV-infected women taking co-trimoxazole prophylaxis
- IV quinine for severe malaria: loading dose 20 mg/kg over 4 hours, then maintenance 10 mg/kg every 8 hours; omit loading dose if oral quinine or mefloquine given in previous 24 hours
- After at least 24 hours of parenteral treatment for severe malaria and when oral intake tolerated, complete with 3-day ACT course
Dosage of artemisinin-based combination therapies (ACT) for uncomplicated malaria in pregnancy
Table extracted from the guideline
| ACT | Formulation | Dosage |
|---|---|---|
| artemether/lumefantrine | 20 mg artemether/120 mg lumefantrine per tablet, blister of 24 tablets | 4 tablets twice daily on D1, D2, D3 |
| artemether/lumefantrine | 80 mg artemether/480 mg lumefantrine per tablet, blister of 6 tablets | 1 tablet twice daily on D1, D2, D3 |
| artesunate + amodiaquine | 100 mg AS/270 mg AQ base per tablet, blister of 6 tablets | 2 tablets once daily on D1, D2, D3 |
| artesunate + amodiaquine | Co-blister: 12 tablets 50 mg AS + 12 tablets 153 mg AQ base | 4 tablets AS + 4 tablets AQ once daily on D1, D2, D3 |
| artesunate/mefloquine | 100 mg AS/220 mg MQ per tablet, blister of 6 tablets | 2 tablets once daily on D1, D2, D3 |
| dihydroartemisinin/piperaquine | 40 mg DHA/320 mg PPQ, blister of 9 tablets | Women 36–59 kg: 3 tablets once daily on D1, D2, D3 |
| dihydroartemisinin/piperaquine | 40 mg DHA/320 mg PPQ, blister of 12 tablets | Women 60–79 kg: 4 tablets once daily on D1, D2, D3 |
Source: Médecins Sans Frontières, Parasitic infections in pregnancy: malaria, hookworms and ascariasis — MSF Essential obstetric and newborn care. Reproduced in summary form.
From the guideline
Verbatim
“Malaria in pregnancy is associated with low birth weight, increased risk of anaemia and, in low transmission areas, an increased risk of severe malaria and death.”
Editor’s perspective
Why this matters for Georgia and the region
Prof. Giorgi Pkhakadze, MD, MPH, PhD
Editor-in-Chief, Georgian Medical Journal · Chair, Public Health Institute of Georgia · WHO consultant, health and migration
As Editor-in-Chief of the Georgian Medical Journal, I recognise that while Georgia achieved malaria elimination in 2010, this MSF guideline remains essential for our clinicians working in humanitarian missions and for managing imported cases in travellers. The clear treatment algorithms for severe malaria with specific artesunate dosing—2.4 mg/kg at H0, H12, H24—provide critical decision support that could prove lifesaving in emergency settings. The helminth treatment protocols are directly relevant: hookworm and ascariasis persist in rural areas of Georgia and neighbouring countries, and the strict contraindication of albendazole in the first trimester must be emphasised to primary care providers integrating deworming into antenatal care. The main implementation challenge for Georgian programmes will be ensuring artemisinin-based combination therapies are maintained in emergency drug stocks despite low domestic malaria incidence, balanced against expiry and cost considerations.
ORCID 0000-0001-7609-4515 · Perspective written for the GMJ Guidelines Library, 23 Oct 2026
Applicability
Georgia and the South Caucasus
Georgia is a malaria-free country since 2010, following WHO certification of elimination, though imported cases from endemic regions remain a consideration given migration patterns to and from Central Asia, Middle East and Africa. For Georgian clinicians, this guideline is most relevant for travel medicine consultations and for healthcare workers deployed in humanitarian settings. The helminth treatment protocols are directly applicable: hookworm and ascariasis remain endemic in parts of rural Georgia and neighbouring Armenia and Azerbaijan, particularly in areas with inadequate sanitation. National maternal health programmes should integrate second-trimester albendazole administration into routine antenatal care protocols in endemic areas, while ensuring first-trimester screening identifies women requiring deferred treatment.
Questions this guideline answers
Quick answers
Can artemisinin-based combination therapies be safely used in the first trimester of pregnancy?
Yes. This MSF guideline recommends ACTs as the treatment of choice in all trimesters for uncomplicated falciparum malaria. While quinine was historically preferred in the first trimester, current evidence supports ACT use throughout pregnancy.
When should I use IV artesunate versus artemether for severe malaria in pregnancy?
Artesunate IV (or IM if IV not feasible) is the first choice at 2.4 mg/kg at H0, H12, H24, then daily. Artemether IM (3.2 mg/kg loading, then 1.6 mg/kg daily) is used only if artesunate is not available. Both require completion with oral ACT after at least 24 hours of parenteral therapy.
Why is albendazole contraindicated in the first trimester for hookworms or ascariasis?
The guideline explicitly states 'Do not administer during the first trimester of pregnancy.' Treatment should be deferred until the second trimester. This precaution relates to theoretical teratogenic risk during organogenesis, though the document does not provide detailed justification.
What special considerations apply when treating malaria in HIV-infected pregnant women?
The combination artesunate/sulfadoxine-pyrimethamine (AS/SP) is contraindicated in HIV-infected women taking co-trimoxazole preventive therapy due to the sulfonamide overlap. Use alternative ACT combinations such as artemether/lumefantrine or artesunate/amodiaquine instead.
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- Bacterial infections in pregnancy (MSF Essential obstetric and newborn care) — MSF Essential obstetric and newborn careChapter 4: Pathologies during pregnancy and pregnancy-related disorders
- Iron deficiency anaemia — MSF Essential obstetric and newborn careChapter 4: Pathologies during pregnancy and pregnancy-related disorders
- Diagnosis of bleeding during the second half of pregnancy (summary) — MSF Essential obstetric and newborn careChapter 3: Bleeding during the second half of pregnancy
- Uterine rupture — MSF Essential obstetric and newborn careChapter 3: Bleeding during the second half of pregnancy
- Abruptio placentae — MSF Essential obstetric and newborn careChapter 3: Bleeding during the second half of pregnancy
- Placenta praevia — Essential obstetric and newborn care — MSF Essential obstetric and newborn careChapter 3: Bleeding during the second half of pregnancy
Other guidelines on this topic
- Bacterial infections in pregnancy (MSF Essential obstetric and newborn care) — MSF Essential obstetric and newborn care
- Iron deficiency anaemia — MSF Essential obstetric and newborn care
- Diagnosis of bleeding during the second half of pregnancy (summary) — MSF Essential obstetric and newborn care
- Uterine rupture — MSF Essential obstetric and newborn care
- Abruptio placentae — MSF Essential obstetric and newborn care
- Issuer
- Médecins Sans Frontières
- Guideline
- Essential obstetric and newborn care
- Chapter
- Chapter 4: Pathologies during pregnancy and pregnancy-related disorders
- Type
- Clinical guideline (chapter)
- Edition
- Current online edition, 2026
- Status
- Current
- Published
- 2026-10-14
- Scope
- Parasitic infections in pregnancy: malaria (all species) and helminth infections (hookworms, ascariasis)
- Audience
- Obstetricians, midwives, general practitioners, and humanitarian healthcare workers providing antenatal care
- Evidence
- Based on WHO Guidelines for the treatment of malaria, Third edition, 2015, and MSF field experience
- Record history
- Created 23 Oct 2026 · updated 23 Oct 2026 · next check Apr 2027
Médecins Sans Frontières. Parasitic infections. In: Essential obstetric and newborn care [Internet]. Paris: MSF; 2026 [cited 2026 Oct 14]. Chapter 4, Section 4.3. Available from: https://medicalguidelines.msf.org/GMJ Guidelines Library records are original summaries written by the GMJ editorial team from the issuer’s published document and reviewed by a physician. They do not replace the full guideline. The document is the copyright of its issuer and is linked, not hosted. Spotted an error or a newer edition? Tell the Guidelines Desk.
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