Scaling-up the use of sulfadoxine-pyrimethamine for the preventive treatment of malaria in pregnancy: results and lessons on scalability, costs and programme impact from three local government areas in Sokoto State, Nigeria

Nosa Orobaton, Anne M Austin, Dele Abegunde, Mohammed Ibrahim, Zainab Mohammed, Jumare Abdul-Azeez, Hakeem Ganiyu, Zwalle Nanbol, Bolaji Fapohunda, Katherine Beal, Nosa Orobaton, Anne M Austin, Dele Abegunde, Mohammed Ibrahim, Zainab Mohammed, Jumare Abdul-Azeez, Hakeem Ganiyu, Zwalle Nanbol, Bolaji Fapohunda, Katherine Beal

Abstract

Background: Intermittent preventive treatment of malaria in pregnancy with 3+ doses of sulfadoxine-pyrimethamine (IPTp-SP) reduces maternal mortality and stillbirths in malaria endemic areas. Between December 2014 and December 2015, a project to scale up IPTp-SP to all pregnant women was implemented in three local government areas (LGA) of Sokoto State, Nigeria. The intervention included community education and mobilization, household distribution of SP, and community health information systems that reminded mothers of upcoming SP doses. Health facility IPTp-SP distribution continued in three intervention (population 661,606) and one counterfactual (population 167,971) LGAs. During the project lifespan, 31,493 pregnant women were eligible for at least one dose of IPTp-SP.

Methods: Community and facility data on IPTp-SP distribution were collected in all four LGAs. Data from a subset of 9427 pregnant women, who were followed through 42 days postpartum, were analysed to assess associations between SP dosages and newborn status. Nominal cost and expense data in 2015 Nigerian Naira were obtained from expenditure records on the distribution of SP.

Results: Eighty-two percent (n = 25,841) of eligible women received one or more doses of IPTp-SP. The SP1 coverage was 95% in the intervention LGAs; 26% in the counterfactual. Measurable SP3+ coverage was 45% in the intervention and 0% in the counterfactual LGAs. The mean number of SP doses in the intervention LGAs was 2.1; 0.4 in the counterfactual. Increased doses of IPTp-SP were associated with linear increases in newborn head circumference and lower odds of stillbirth. Any antenatal care utilization predicted larger newborn head circumference and lower odds of stillbirth. The cost of delivering three doses of SP, inclusive of the cost of medicines, was US$0.93-$1.20.

Conclusions: It is feasible, safe, and affordable to scale up the delivery of high impact IPTp-SP interventions in low resource malaria endemic settings, where few women access facility-based maternal health services. ClinicalTrials.gov Identifier NCT02758353. Registered 29 April 2016, retrospectively registered.

Keywords: Community engagement; Community-based health workers; Human-centered design; IPTp-SP; Integrated MNH; Malaria in pregnancy; Nigeria; Primary health care; Scale up; Sokoto State.

Figures

Fig. 1
Fig. 1
Map of intervention and counterfactual LGAs
Fig. 2
Fig. 2
Sokoto State chlorhexidine–misoprostol distribution system
Fig. 3
Fig. 3
Decision tree for SP dosage and referral
Fig. 4
Fig. 4
Planning schema for MiPP project review meetings
Fig. 5
Fig. 5
Percentage coverage of pregnant women who took SP1 in three intervention LGAs and one counterfactual LGA, Sokoto State, Apr–Nov 2014 and Apr–Nov 2015
Fig. 6
Fig. 6
Percentage coverage of pregnant women who took SP1 in three intervention LGAs and one counterfactual LGA by source April–November 2015
Fig. 7
Fig. 7
Monthly number of pregnant women who took SP1, SP2, SP3 in three intervention LGAs and one counterfactual LGA, Sokoto State, April–November 2015
Fig. 8
Fig. 8
Mean doses of SP between April and November 2015 in the MiPP intervention and counterfactual LGAs
Fig. 9
Fig. 9
Mean head circumference in the intervention and counterfactual LGAs by birth month (April–November 2015)
Fig. 10
Fig. 10
Mean newborn head circumference in mm by number of SP doses during pregnancy, for births between April and November 2015
Fig. 11
Fig. 11
Stillbirth rate by 1, 2 and 3+ doses of SP, for births between April and November 2015

References

    1. WHO. 10 facts on malaria. Geneva: World Health Organization; 2015. . Accessed 21 Feb 2016.
    1. WHO. World Malaria Report 2015. Geneva: World Health Organization; 2015. . Accessed 15 Feb 2016.
    1. Roll Back Malaria Partnership. Progress and impact series: country reports, country reports No. 4. Focus on Nigeria. 2012. . Accessed 10 Feb 2016.
    1. Nigeria population 2016. Current population of Nigeria. 2016. . Accessed 8 Oct 2016.
    1. WHO. Malaria in pregnant women. Geneva: World Health Organization; 2016. . Accessed 8 Oct 2016.
    1. Desai M, ter Kuile FO, Nosten F, McGready R, Asamoa K, Brabin B, et al. Epidemiology and burden of malaria in pregnancy. Lancet Infect Dis. 2007;7:93–104. doi: 10.1016/S1473-3099(07)70021-X.
    1. Kvinnoforum and The Rollback Malaria Forum. A guide to gender and malaria. 2010. . Accessed 8 Oct 2016.
    1. WHO. Guidelines for the treatment of malaria. 3rd ed. Geneva: World Health Organization; 2015. . Accessed 8 Oct 2016.
    1. WHO. Consensus statement: optimizing the delivery of malaria-in-pregnancy interventions. Geneva: World Health Organization; 2013. . Accessed 8 Oct 2016.
    1. McClure EM, Goldenberg RL, Dent AE, Meshnick SR. A systematic review of the impact of malaria prevention in pregnancy on low birth weight and maternal anemia. Int J Gynaecol Obstet. 2013;121:103–109. doi: 10.1016/j.ijgo.2012.12.014.
    1. Menendez C, Ordi J, Ismail MR, Ventura PJ, Aponte JJ, Kahigwa E, et al. The impact of placental malaria on gestational age and birth weight. J Infect Dis. 2000;181:1740–1745. doi: 10.1086/315449.
    1. Sreeramareddy CT, Chuni N, Patil R, Singh D, Shakya B. Anthropometric surrogates to identify low birth weight Nepalese newborns: a hospital-based study. BMC Pediatr. 2008;8:16. doi: 10.1186/1471-2431-8-16.
    1. Rijken MJ, Rijken JA, Papageorghiou AT, Kennedy SH, Visser GHA, Nosten F, et al. Malaria in pregnancy: the difficulties in measuring birthweight. BJOG. 2011;118:671–678. doi: 10.1111/j.1471-0528.2010.02880.x.
    1. Elizabeth NL, Christopher OG, Patrick K. Determining an anthropometric surrogate measure for identifying low birth weight babies in Uganda: a hospital-based cross sectional study. BMC Pediatr. 2013;13:54. doi: 10.1186/1471-2431-13-54.
    1. Villar J, Cheikh Ismail L, Victora CG, Ohuma EO, Bertino E, Altman DG, et al. International standards for newborn weight, length, and head circumference by gestational age and sex: the Newborn Cross-Sectional Study of the INTERGROWTH-21st Project. Lancet. 2014;384:857–868. doi: 10.1016/S0140-6736(14)60932-6.
    1. Blencowe H, Cousens S, Jassir FB, Say L, Chou D, Mathers C, et al. National, regional, and worldwide estimates of stillbirth rates in 2015, with trends from 2000: a systematic analysis. Lancet Glob Health. 2016;4:e98–e108. doi: 10.1016/S2214-109X(15)00275-2.
    1. Lawn JE, Blencowe H, Pattinson R, Cousens S, Kumar R, Ibiebele I, et al. Stillbirths: Where? When? Why? How to make the data count? Lancet. 2011;377:1448–1463. doi: 10.1016/S0140-6736(10)62187-3.
    1. Kerber KJ, Mathai M, Lewis G, Flenady V, Erwich JJHM, Segun T, et al. Counting every stillbirth and neonatal death through mortality audit to improve quality of care for every pregnant woman and her baby. BMC Pregnancy Childbirth. 2015;15(Suppl 2):S9. doi: 10.1186/1471-2393-15-S2-S9.
    1. Van Geertruyden J-P, Thomas F, Erhart A, D’Alessandro U. The contribution of malaria in pregnancy to perinatal mortality. Am J Trop Med Hyg. 2004;71:35–40.
    1. Radeva-Petrova D, Kayentao K, ter Kuile FO, Sinclair D, Garner P. Drugs for preventing malaria in pregnant women in endemic areas: any drug regimen versus placebo or no treatment. Cochrane Database Syst Rev. 2014;10:CD000169.
    1. National Federal Ministry of Health (FMOH). National guidelines and strategies for malaria prevention and control during pregnancy. A publication of the Federal Ministry of Health, Nigeria; Malaria Control Programme. Abuja: FMOH; 2005.
    1. National Federal Ministry of Health (FMOH), WHO. National drug policy—Nigeria: 5.0. Targets of the National Drug Policy. 2005. . Accessed 8 Oct 2016.
    1. Amoran OE, Ariba AA, Iyaniwura CA. Determinants of intermittent preventive treatment of malaria during pregnancy (IPTp) utilization in a rural town in Western Nigeria. Reprod Health. 2012;9:12. doi: 10.1186/1742-4755-9-12.
    1. National Population Commission (NPC), Nigeria, and ICF International. Nigeria demographic ands health survey 2013. Abuja: NPC and ICF International; 2013. . Accessed 8 Oct 2016.
    1. WHO Global Malaria Programme. WHO Policy brief for the implementation of intermittent preventive treatment of malaria in pregnancy using sulfadoxine-pyrimethamine (IPTp-SP). Geneva: World Health Organization; 2013 . Accessed 8 Oct 2016.
    1. WHO. Evidence Review Group: Intermittent preventive treatment of malaria in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP). Geneva: WHO Headquarters; 2012. . Accessed 8 Oct 2016.
    1. Okeibunor JC, Orji BC, Brieger W, Ishola G, Otolorin E, Rawlins B, et al. Preventing malaria in pregnancy through community-directed interventions: evidence from Akwa Ibom State, Nigeria. Malar J. 2011;10:227. doi: 10.1186/1475-2875-10-227.
    1. World Bank. Improving primary health care delivery in Nigeria: evidence from Four States, 2010, Working Bank Paper. 2010. . Accessed 8 Oct 2016.
    1. Sokoto State Government, Sokoto State Ministry of Health. Strategic Health Development Plan (2010–2015). 2010. revised 05.01.2011.pdf. Accessed 8 Oct 2016.
    1. National Federal Ministry of Health (FMOH). Nigeria Health Management Information System. . Accessed 10 Feb 2016.
    1. Uauy R, Casanello P, Krause B, Kuzanovic JP, Corvalan C. Conceptual basis for prescriptive growth standards from conception to early childhood: present and future. BJOG. 2013;120(Suppl 2):3–8. doi: 10.1111/1471-0528.12057.
    1. Meuris S, Piko BB, Eerens P, Vanbellinghen AM, Dramaix M, Hennart P. Gestational malaria: assessment of its consequences on fetal growth. Am J Trop Med Hyg. 1993;48:603–609.
    1. National Population Commission [Nigeria] and ICF Macro. Nigeria Demographic and Health Survey 2008. Abuja: NPC and ICF International; 2009. . Accessed 8 Oct 2016.
    1. Peters PJ, Thigpen MC, Parise ME, Newman RD. Safety and toxicity of sulfadoxine/pyrimethamine: implications for malaria prevention in pregnancy using intermittent preventive treatment. Drug Saf. 2007;30:481–501. doi: 10.2165/00002018-200730060-00003.
    1. Brabin BJ, Romagosa C, Abdelgalil S, Menéndez C, Verhoeff FH, McGready R, et al. The sick placenta-the role of malaria. Placenta. 2004;25:359–378. doi: 10.1016/j.placenta.2003.10.019.
    1. Hill J, Hoyt J, van Eijk AM, D’Mello-Guyett L, ter Kuile FO, Steketee R, et al. Factors affecting the delivery, access, and use of interventions to prevent malaria in pregnancy in sub-Saharan Africa: a systematic review and meta-analysis. PLoS Med. 2013;10:e1001488. doi: 10.1371/journal.pmed.1001488.
    1. Kibusi SM, Kimunai E, Hines CS. Predictors for uptake of intermittent preventive treatment of malaria in pregnancy (IPTp) in Tanzania. BMC Public Health. 2015;15:540. doi: 10.1186/s12889-015-1905-0.
    1. Sangaré LR, Stergachis A, Brentlinger PE, Richardson BA, Staedke SG, Kiwuwa MS, et al. Determinants of use of intermittent preventive treatment of malaria in pregnancy: Jinja, Uganda. PLoS ONE. 2010;5:e15066. doi: 10.1371/journal.pone.0015066.
    1. WHO. Stillbirths. Geneva: World Health Organization; 2015. . Accessed 8 Oct 2016.

Source: PubMed

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