» Articles » PMID: 18992140

Implementation of Intermittent Preventive Treatment in Pregnancy with Sulphadoxine/pyrimethamine (IPTp-SP) at a District Health Centre in Rural Senegal

Overview
Journal Malar J
Publisher Biomed Central
Specialty Tropical Medicine
Date 2008 Nov 11
PMID 18992140
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Intermittent preventive treatment with sulphadoxine-pyrimethamine (SP) is recommended for reducing the risk of malaria in pregnancy and its consequences on mothers and babies (IPTp-SP). Indicators of implementation and effects of IPTp-SP were collected in a rural clinic in Southern Senegal.

Methods: Women seen routinely at the antenatal clinic (ANC) of a rural dispensary during 2000-2007. Deployment of IPTp-SP started in January 2004. Inspection of antenatal and outpatient clinic registries of the corresponding period.

Results: Between 1st January 2000 and 30th April 2007, 1,781 women of all gravitidities and parities attended the ANC with 965 deliveries (606 and 398 respectively since 1st January 2004, when IPTp-SP was started.) 69% of women were seen > or = 3 times; 95% received at least one dose and 70% two doses of SP (from 61% in 2004 to 86% in 2007). The first visit, first and second dose of SP occurred at a median week 20, 22 and 31. The probability of receiving two doses was > 80% with > or = 3 antenatal visits and a first dose of SP by week 20.The prevalence of maternal malaria was low and similar pre- (0.7%) and during IPTp (0.8%). Effects on of low birth weight (LBW, < 2.5 kg) were non-statistically significant. The prevalence of LBW was 10.8% pre- and 7.7% during IPTp deployment (29% risk reduction, p = 0.12).Unfavourable pregnancy outcomes numbered 72 (7.5% of pregnancies with known outcome), including 30 abortions and 42 later deaths (late foetal deaths, stillbirth, peri-natal) of which 13 with one or more malformations (1.35% of all recorded deliveries).

Conclusion: The implementation of IPTp-SP was high. Early attendance to ANC favours completion of IPTp-SP. The record keeping system in place is amenable to data extraction and linkage. A model was developed that predicts optimal compliance to two SP doses, and could be tested in other settings. Maternal malaria was infrequent and unaffected by IPTp-SP. The risk of LBW was lower during IPT implementation but the difference was non-significant and could have other explanations.

Citing Articles

Factors associated with the uptake of intermittent preventive treatment of malaria in pregnancy in the Bamenda health districts, Cameroon.

Diengou N, Nambile Cumber S, Nkfusai C, Mbinyui M, Viyoff V, Bede F Pan Afr Med J. 2020; 35:42.

PMID: 32499857 PMC: 7245972. DOI: 10.11604/pamj.2020.35.42.17600.


Determinants of intermittent preventive treatment of malaria among women attending antenatal clinics in primary health care centers in Ogbomoso, Oyo State, Nigeria.

Adewole A, Fawole O, Ajayi I, Yusuf B, Oladimeji A, Waziri E Pan Afr Med J. 2019; 33:101.

PMID: 31489079 PMC: 6713488. DOI: 10.11604/pamj.2019.33.101.14800.


Intermittent preventive treatment of malaria in pregnancy: a cross-sectional survey to assess uptake of the new sulfadoxine-pyrimethamine five dose policy in Ghana.

Owusu-Boateng I, Anto F Malar J. 2017; 16(1):323.

PMID: 28797296 PMC: 5553599. DOI: 10.1186/s12936-017-1969-7.


Prevalence of intermittent preventive treatment with sulphadoxine-pyrimethamine (IPTp-SP) use during pregnancy and other associated factors in Sekondi-Takoradi, Ghana.

Orish V, Onyeabor O, Boampong J, Afoakwah R, Nwaefuna E, Acquah S Afr Health Sci. 2016; 15(4):1087-96.

PMID: 26958008 PMC: 4765396. DOI: 10.4314/ahs.v15i4.6.


Probabilistic record linkage for monitoring the safety of artemisinin-based combination therapy in the first trimester of pregnancy in Senegal.

Dellicour S, Brasseur P, Thorn P, Gaye O, Olliaro P, Badiane M Drug Saf. 2013; 36(7):505-13.

PMID: 23673815 DOI: 10.1007/s40264-013-0059-1.


References
1.
Villar J, Baaqeel H, Piaggio G, Lumbiganon P, Miguel Belizan J, FARNOT U . WHO antenatal care randomised trial for the evaluation of a new model of routine antenatal care. Lancet. 2001; 357(9268):1551-64. DOI: 10.1016/s0140-6736(00)04722-x. View

2.
Correa-Villasenor A, Cragan J, Kucik J, OLeary L, Siffel C, Williams L . The Metropolitan Atlanta Congenital Defects Program: 35 years of birth defects surveillance at the Centers for Disease Control and Prevention. Birth Defects Res A Clin Mol Teratol. 2004; 67(9):617-24. DOI: 10.1002/bdra.10111. View

3.
White N . Intermittent presumptive treatment for malaria. PLoS Med. 2005; 2(1):e3. PMC: 545196. DOI: 10.1371/journal.pmed.0020003. View

4.
Agnamey P, Brasseur P, Cisse M, Gaye O, Dumoulin J, Rigal J . Economic evaluation of a policy change from single-agent treatment for suspected malaria to artesunate-amodiaquine for microscopically confirmed uncomplicated falciparum malaria in the Oussouye District of south-western Senegal. Trop Med Int Health. 2005; 10(9):926-33. DOI: 10.1111/j.1365-3156.2005.01482.x. View

5.
Hill J, Kazembe P . Reaching the Abuja target for intermittent preventive treatment of malaria in pregnancy in African women: a review of progress and operational challenges. Trop Med Int Health. 2006; 11(4):409-18. DOI: 10.1111/j.1365-3156.2006.01585.x. View