Sub-microscopic infections and long-term recrudescence of Plasmodium falciparum in Mozambican pregnant women

Malar J. 2009 Jan 9:8:9. doi: 10.1186/1475-2875-8-9.

Abstract

Background: Control of malaria in pregnancy remains a public health challenge. Improvements in its correct diagnosis and the adequacy of protocols to evaluate anti-malarial drug efficacy in pregnancy, are essential to achieve this goal.

Methods: The presence of Plasmodium falciparum was assessed by real-time (RT) PCR in 284 blood samples from pregnant women with clinical complaints suggestive of malaria, attending the maternity clinic of a Mozambican rural hospital. Parasite recrudescences in 33 consecutive paired episodes during the same pregnancy were identified by msp1 and msp2 genotyping.

Results: Prevalence of parasitaemia by microscopy was 5.3% (15/284) and 23.2% (66/284) by RT-PCR. Sensitivity of microscopy, compared to RT-PCR detection, was 22.7%. Risk of maternal anaemia was higher in PCR-positive women than in PCR-negative women (odds ratio [OR] = 1.92, 95% confidence interval [CI] 1.09-3.36). Genotyping confirmed that recrudescence after malaria treatment occurred in 7 (21%) out of 33 pregnant women with consecutive episodes during the same pregnancy (time range between recrudescent episodes: 14 to 187 days).

Conclusion: More accurate and sensitive diagnostic indicators of malaria infection in pregnancy are needed to improve malaria control. Longer follow-up periods than the standard in vivo drug efficacy protocol should be used to assess anti-malarial drug efficacy in pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Antigens, Protozoan / genetics
  • Antimalarials / therapeutic use
  • Chloroquine / therapeutic use
  • Drug Combinations
  • Female
  • Genotype
  • Humans
  • Malaria, Falciparum / drug therapy
  • Malaria, Falciparum / epidemiology
  • Malaria, Falciparum / parasitology*
  • Merozoite Surface Protein 1 / genetics
  • Mozambique / epidemiology
  • Parasitemia / drug therapy
  • Parasitemia / epidemiology
  • Plasmodium falciparum / drug effects
  • Plasmodium falciparum / genetics*
  • Plasmodium falciparum / isolation & purification*
  • Polymerase Chain Reaction
  • Pregnancy
  • Pregnancy Complications, Parasitic / drug therapy
  • Pregnancy Complications, Parasitic / epidemiology
  • Pregnancy Complications, Parasitic / parasitology*
  • Prevalence
  • Protozoan Proteins / genetics
  • Pyrimethamine / therapeutic use
  • Recurrence*
  • Sensitivity and Specificity
  • Sulfadoxine / therapeutic use

Substances

  • Antigens, Protozoan
  • Antimalarials
  • Drug Combinations
  • Merozoite Surface Protein 1
  • Protozoan Proteins
  • merozoite surface protein 2, Plasmodium
  • fanasil, pyrimethamine drug combination
  • Sulfadoxine
  • Chloroquine
  • Pyrimethamine