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Table 1 Summary table of studies examining the effect of malaria treatment during pregnancy on low birth weight infants

From: The impact of malaria during pregnancy on low birth weight in East-Africa: a topical review

Authors

Country

Study design (year)

Sample size

Treatment; frequency

Method for determining malaria infection

Results/comment

Braun et al. [11]

Western Uganda

Cross-sectional study (2013)

915

IPTp, SP;

Start in 2nd trimester, then with every ANC visit

Polymerase chain reaction of parasite DNA

P. falciparuma infection was significantly associated with LBWb

IPTpc—> no significant influence on the presence of P. falciparum infection

Mbonye et al. [12]

Mukono district, Uganda

Non-randomized community trial (2003–2005)

2785

IPTp, SP;

One dose in 2nd and one in 3rd trimester

Self-reported (based on fever, headache, joint pain, general weakness)

Lower prevalence of LBW (6%) with the new delivery system vs. with health units (p < 0.03)

Mikomangwa et al. [13]

Dar-es-Salaam, Tanzania

Facility-based observational cross-sectional study (2018)

631

IPTp, SP;

Start in 2nd trimester, then with every ANC visit

Rapid antigen-based test

The prevalence of LBW was 6.5%. Malaria positive women had 11 times increased risk of LBW compared to those who were negative (p = 0.04)

 ≥ 3 doses of IPTp-SPd—> 83% decreased risk of LBW compared to those who did not use IPTp-SP (p = 0.05)

Mosha et al. [14]

Moshi and Rufiji, Tanzania

Prospective observational study (2012)

350

IPTp;

Start in 2nd trimester, then monthly

Polymerase chain reaction of parasite DNA

No significant association between IPTp use and reduced risk of LBW

Ndeserua et al. [15]

Rufiji, Tanzania

Cross-sectional study (2012)

350

2 doses SP; One dose in 2nd and one in 3rd trimester

Quantification of parasites in blood smear

Two doses SP during pregnancy was insignificantly associated with risk of LBW (p = 0.73)

Ndyomugyenyi et al. [16]

Kabale, Uganda

Randomized controlled trial (2004–2007)

5775

ITNe + placebo

or

ITN + IPTp

or

IPTp;

Start in 2nd trimester, then with every ANC visit

Quantification of parasites in blood smear

There was no significant difference between the three intervention groups in the prevalence of LBW (p = 0.802)

Van Eijk et al. [17]

Kenya

Cohort study (1999–2000)

889

IPTp, SP;

Start in 2nd trimester, then with every ANC visit

Quantification of parasites in blood smear

1 dose IPTp—> associated with a mean increased BWf of 54 g (p = 0.11)

 ≥ 2 doses IPTp- > associated with a mean increased BW of 128 g (p = 0.004) compared with mothers who had not used IPTp

  1. aPlasmodium falciparum, bLow birth weight, cIntermittent preventive treatment during pregnancy, dIntermittent preventive treatment during pregnancy with sulfadoxine-pyrimethamine, eInsecticide-treated nets, fBirth weight. Note, all papers used the WHO definition of LBW (birth weight < 2.5 kg)