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Table 1 Characteristics of included studies

From: Safety and tolerability of repeated doses of dihydroartemisinin-piperaquine for intermittent preventive treatment of malaria in pregnancy: a systematic review and an aggregated data meta-analysis of randomized controlled trials

Author, publication year

Setting

Sample size (n)

Intervention (n of patients)

Comparator (n of patients)

Important patient outcomes

Desai et al. 2015 [23]

Kenya

n = 1546

IPT DP (n = 516)

IPT SP (n = 515)

IST DP (n = 515)

Incidence of SAEs

Mlugu et al. 2021 [33]

Tanzania

n = 956

IPT DP (n = 478)

IPT SP (n = 478)

Prevalence of vomiting within 30 min after study drug administration

Kajubi et al. 2019 [10]

Uganda

n = 782

IPT DP (n = 391)

IPT SP (n = 391)

Mean change in QTc interval

Incidence of SAEs

Incidence of grade 3 or 4 AEs possibly related to study drug

Prevalence of vomiting within30 minutes after study drug administration

Kakuru et al. 2016 [24]

Uganda

N = 300

IPT DP 3 doses (n = 94)

IPT DP Monthly (n = 100)

IPT SP 3 doses (n = 106)

Median change in QTc interval

Incidence of SAEs

Incidence of grade 3 or 4 AEs possibly related to study drug

Prevalence of vomiting within 30 min after study drug administration

Natureeba et al. 2017 [32]

Uganda

n-200

IPT DP

Monthly + TMP/SMX Daily (n = 100)

TMP/SMX

Daily(n = 100)

Mean change in QTc interval

Incidence of SAEs

Prevalence of vomiting within 30 min after study drug administration

Madanitsa et al. 2023 [34]

Kenya, Malawi, Tanzania

N = 4680

IPT DP (n = 1561)

IPT DP + Azithromycin (1558)

IPT SP (n = 1561)

Incidence of SAEs

Vomiting within 30 min after study drug administration

  1. IPT intermittent preventive treatment, SP sulfadoxine−pyrimethamine, DP dihydroartemisinin−piperaquine, TMP trimethoprim, SMX sulfamethoxazole, n number, SAE serious adverse events