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Infectious DiseaseClinical Practice5 min read

Maternal and perinatal outcomes in pregnant women with Lassa fever: analysis from the LASCOPE prospective cohort study

However, most evidence derives from small case series with substantial limitations.

Published in The Lancet Infectious DiseasesObservational cohort study
4/5 Strong Trial
Evidence Meter · 4/5

Strong Clinical Evidence

Tested directly in patients through a prospective clinical trial or large multicenter human cohort.

Source

Clinical Outcome

33%

Although the fetal prognosis was poor, as previously reported, maternal fatality was lower than previously indicated, potentially reflecting improved supportive care and patient monitoring.

What Changes?

Infectious Disease · Clinical Practice

Current Standard

Conventional infectious disease practice relies on standard-of-care monitoring and existing regimens prior to this observational cohort study.

New Finding

These findings suggest that maternal mortality might be lower than historically reported, while confirming the urgent need for specific therapeutic interventions to improve fetal outcomes.

3 Key Takeaways

Plain English Summary
  1. 01Core Finding

    We aimed to assess maternal death and perinatal outcomes in a prospective cohort study with standardised medical care protocols.

  2. 02Study Evidence

    Tested in a observational cohort study (1006 patients) at the clinical practice stage.

  3. 03Practical Meaning

    Benefits and risks vary by individual health history — discuss with a healthcare professional.

What This Means for You

Although the fetal prognosis was poor, as previously reported, maternal fatality was lower than previously indicated, potentially reflecting improved supportive care and patient monitoring. These findings suggest that maternal mortality might be lower than historically reported, while confirming the urgent need for specific therapeutic interventions to improve fetal outcomes.

The Discovery

Lassa fever, a viral haemorrhagic fever endemic in west Africa, is usually described as associated with severe maternal and perinatal outcomes. Previous studies reported maternal mortality (whereas overall mortality is about 14% in Nigeria for patients admitted to hospital) and fetal mortality is up to 60%. However, most evidence derives from small case series with substantial limitations. We aimed to assess maternal death and perinatal outcomes in a prospective cohort study with standardised medical care protocols. We analysed data from the LASCOPE cohort from the Federal Medical Centre Owo, Nigeria, which included all patients with PCR-confirmed Lassa fever. In this analysis, non-pregnant women of childbearing age (15-45 years) were compared with pregnant women, defined as having an ongoing pregnancy during Lassa fever. The primary maternal outcome was all-cause mortality 28 days after admission and the primary pregnancy outcome was fetal death. Mortality at 28 days was compared using Kaplan-Meier estimates and a Cox proportional-hazards model, the cumulative incidence of fetal death was estimated with livebirth as a competing event, and the association between gestational age at symptom onset and fetal death was assessed by logistic regression. Between April 4, 2018, and Feb 18, 2023, of 1006 patients in the LASCOPE cohort admitted with PCR-confirmed Lassa fever, 703 were excluded for not being of childbearing age, and 303 were women of childbearing age, of whom 45 were pregnant. The median age of pregnant women was 28 years (IQR 24-32). The 28-day mortality was comparable between pregnant and non-pregnant women (four [9%; 95% CI 2-21] of 45 vs 19 [7%; 95% CI 4-11] of 258; 1·19 [95% CI 0·41-3·50]; log-rank p=0·75). Fetal case-fatality rate was 60% (27 of 45), with higher risk of fetal death if infection occurred early in the pregnancy (100% for the first trimester, 82% for the second trimester, and 25% for the third trimester). Each additional week of gestation at symptom onset was associated with a reduction in the odds of fetal death (odds ratio 0·77 [95% CI 0·61-0·90]). Among 15 liveborn infants, three (20%) died within 30 days.

How It Works, Simply

This infectious disease research focuses on pathogen neutralization & host immune priming. Researchers evaluated it using an observational cohort study (1006 patients) at the clinical practice stage of medical research.

3 Key Takeaways

Clinical Takeaways
  1. 01Core Finding

    We aimed to assess maternal death and perinatal outcomes in a prospective cohort study with standardised medical care protocols.

  2. 02Study Evidence

    Tested in a observational cohort study (1006 patients) at the clinical practice stage.

  3. 03Practical Meaning

    Benefits and risks vary by individual health history — discuss with a healthcare professional.

Key Numbers

Quantitative Study Readout
14%
Clinical Outcome
60%
Clinical Outcome
01

Biological Mechanism & Study Design

Study Design & Cohort

Observational cohort study

Observational cohort study (1006 patients) · Clinical Practice

Biological Pathway & Modality

Pathogen neutralization & host immune priming

Intervention: Maternal and perinatal outcomes in pregnant women with Lassa fever: analysis from

02

Experimental Findings & Endpoints

Lassa fever, a viral haemorrhagic fever endemic in west Africa, is usually described as associated with severe maternal and perinatal outcomes.

Previous studies reported maternal mortality (whereas overall mortality is about 14% in Nigeria for patients admitted to hospital) and fetal mortality is up to 60%. However, most evidence derives from small case series with substantial limitations.

We aimed to assess maternal death and perinatal outcomes in a prospective cohort study with standardised medical care protocols. We analysed data from the LASCOPE cohort from the Federal Medical Centre Owo, Nigeria, which included all patients with PCR-confirmed Lassa fever.

In this analysis, non-pregnant women of childbearing age (15-45 years) were compared with pregnant women, defined as having an ongoing pregnancy during Lassa fever. The primary maternal outcome was all-cause mortality 28 days after admission and the primary pregnancy outcome was fetal death.

Mortality at 28 days was compared using Kaplan-Meier estimates and a Cox proportional-hazards model, the cumulative incidence of fetal death was estimated with livebirth as a competing event, and the association between gestational age at symptom onset and fetal death was assessed by logistic regression. Between April 4, 2018, and Feb 18, 2023, of 1006 patients in the LASCOPE cohort admitted with PCR-confirmed Lassa fever, 703 were excluded for not being of childbearing age, and 303 were women of childbearing age, of whom 45 were pregnant.

The median age of pregnant women was 28 years (IQR 24-32). The 28-day mortality was comparable between pregnant and non-pregnant women (four [9%; 95% CI 2-21] of 45 vs 19 [7%; 95% CI 4-11] of 258; 1·19 [95% CI 0·41-3·50]; log-rank p=0·75).

Fetal case-fatality rate was 60% (27 of 45), with higher risk of fetal death if infection occurred early in the pregnancy (100% for the first trimester, 82% for the second trimester, and 25% for the third trimester). Each additional week of gestation at symptom onset was associated with a reduction in the odds of fetal death (odds ratio 0·77 [95% CI 0·61-0·90]).

Among 15 liveborn infants, three (20%) died within 30 days.

03

Clinical Translation & Practice Context

Although the fetal prognosis was poor, as previously reported, maternal fatality was lower than previously indicated, potentially reflecting improved supportive care and patient monitoring.

These findings suggest that maternal mortality might be lower than historically reported, while confirming the urgent need for specific therapeutic interventions to improve fetal outcomes.

03

The Bottom Line · Clinical Pearl

“Although the fetal prognosis was poor, as previously reported, maternal fatality was lower than previously indicated, potentially reflecting improved supportive care and patient monitoring.”

Published in The Lancet Infectious Diseases · Current Stage: Clinical Practice

Infectious Disease · Clinical Practice
Study Type
Observational cohort study

Observational cohort study (1006 patients)

Evidence Score
4/5 · Strong Clinical Evidence
Evidence Meter · 4/5

Strong Clinical Evidence

Tested directly in patients through a prospective clinical trial or large multicenter human cohort.

Tested directly in patients through a prospective clinical trial or large multicenter human cohort.

Who It Applies To
Pregnant women with Lassa fever: analysis from the LASCOPE prospective cohort
Intervention & Mechanism
Maternal and perinatal outcomes in pregnant women with Lassa fever: analysis from

Pathogen neutralization & host immune priming

Key Limitation
Benefits and risks vary by individual health history — discuss with a healthcare professional.

Translational Stage

LEVEL 1 · Clinical Practice

Classified as Observational cohort study along the clinical evidence continuum

  1. Lab & Discovery
  2. Early Trials
  3. Human Evidence
  4. 4Clinical PracticeActive

Original Publication & AMA Citation

Maternal and perinatal outcomes in pregnant women with Lassa fever: analysis from the LASCOPE prospective cohort study. The Lancet Infectious Diseases. Published 2026;Nov 10. Accessed November 15, 2026. https://pubmed.ncbi.nlm.nih.gov/43008760/

The Lancet Infectious Diseases

https://pubmed.ncbi.nlm.nih.gov/43008760/

Read Original Paper

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