Cargando…

Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania

BACKGROUND: Intermittent preventive treatment (IPTp) is efficacious in reducing the adverse outcomes associated with pregnancy-associated malaria, however uptake of the recommended two doses is low in Tanzania, and little is known of the timepoint during pregnancy at which it is delivered. This stud...

Descripción completa

Detalles Bibliográficos
Autores principales: Anders, Katherine, Marchant, Tanya, Chambo, Pili, Mapunda, Pasiens, Reyburn, Hugh
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396646/
https://www.ncbi.nlm.nih.gov/pubmed/18471279
http://dx.doi.org/10.1186/1475-2875-7-79
_version_ 1782155584055803904
author Anders, Katherine
Marchant, Tanya
Chambo, Pili
Mapunda, Pasiens
Reyburn, Hugh
author_facet Anders, Katherine
Marchant, Tanya
Chambo, Pili
Mapunda, Pasiens
Reyburn, Hugh
author_sort Anders, Katherine
collection PubMed
description BACKGROUND: Intermittent preventive treatment (IPTp) is efficacious in reducing the adverse outcomes associated with pregnancy-associated malaria, however uptake of the recommended two doses is low in Tanzania, and little is known of the timepoint during pregnancy at which it is delivered. This study investigated the timing of delivery of IPTp to pregnant women attending antenatal clinics (ANC), and the potential determinants of timely uptake. METHODS: Structured interviews were conducted with staff and pregnant women at antenatal clinics in northeast Tanzania, and antenatal consultations were observed. Facility-based and individual factors were analysed for any correlation with timing of IPTp uptake. RESULTS: Almost half the women interviewed first attended ANC during or before the fourth month of gestation, however 86% of these early attendees did not receive IPTp on their first visit. The timing of IPTp delivery complied closely with the national guidelines which stipulate giving the first dose at 20–24 weeks gestation. Uptake of at least one dose of IPTp among women who had reached this gestation age was 67%, although this varied considerably between clinics. At one facility, IPTp was not delivered because SP was out of stock. CONCLUSION: Early uptake of IPTp was found to be hampered by factors external to health worker performance or women's individual preferences. These include insufficient drug stocks and an apparent lack of information to health workers on the reasoning for continued use of SP for IPTp when it has been replaced as a first-line treatment. In addition, an unexpectedly high proportion of women attend antenatal clinics before 20 weeks of pregnancy. While current policy denies the use of IPTp at this time, there is emerging, but incomplete, evidence that malaria in early pregnancy may contribute considerably to the burden of pregnancy-related malaria. Current policy may thus result in a missed opportunity for maximising the benefit of this intervention, and efforts to encourage earlier attendance at ANC alone are unlikely to improve uptake of IPTp. More evidence is needed to weigh the benefits of early IPTp use against theoretical risks of antifolate drugs in early pregnancy.
format Text
id pubmed-2396646
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-23966462008-05-28 Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania Anders, Katherine Marchant, Tanya Chambo, Pili Mapunda, Pasiens Reyburn, Hugh Malar J Research BACKGROUND: Intermittent preventive treatment (IPTp) is efficacious in reducing the adverse outcomes associated with pregnancy-associated malaria, however uptake of the recommended two doses is low in Tanzania, and little is known of the timepoint during pregnancy at which it is delivered. This study investigated the timing of delivery of IPTp to pregnant women attending antenatal clinics (ANC), and the potential determinants of timely uptake. METHODS: Structured interviews were conducted with staff and pregnant women at antenatal clinics in northeast Tanzania, and antenatal consultations were observed. Facility-based and individual factors were analysed for any correlation with timing of IPTp uptake. RESULTS: Almost half the women interviewed first attended ANC during or before the fourth month of gestation, however 86% of these early attendees did not receive IPTp on their first visit. The timing of IPTp delivery complied closely with the national guidelines which stipulate giving the first dose at 20–24 weeks gestation. Uptake of at least one dose of IPTp among women who had reached this gestation age was 67%, although this varied considerably between clinics. At one facility, IPTp was not delivered because SP was out of stock. CONCLUSION: Early uptake of IPTp was found to be hampered by factors external to health worker performance or women's individual preferences. These include insufficient drug stocks and an apparent lack of information to health workers on the reasoning for continued use of SP for IPTp when it has been replaced as a first-line treatment. In addition, an unexpectedly high proportion of women attend antenatal clinics before 20 weeks of pregnancy. While current policy denies the use of IPTp at this time, there is emerging, but incomplete, evidence that malaria in early pregnancy may contribute considerably to the burden of pregnancy-related malaria. Current policy may thus result in a missed opportunity for maximising the benefit of this intervention, and efforts to encourage earlier attendance at ANC alone are unlikely to improve uptake of IPTp. More evidence is needed to weigh the benefits of early IPTp use against theoretical risks of antifolate drugs in early pregnancy. BioMed Central 2008-05-09 /pmc/articles/PMC2396646/ /pubmed/18471279 http://dx.doi.org/10.1186/1475-2875-7-79 Text en Copyright © 2008 Anders et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Anders, Katherine
Marchant, Tanya
Chambo, Pili
Mapunda, Pasiens
Reyburn, Hugh
Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania
title Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania
title_full Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania
title_fullStr Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania
title_full_unstemmed Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania
title_short Timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east Tanzania
title_sort timing of intermittent preventive treatment for malaria during pregnancy and the implications of current policy on early uptake in north-east tanzania
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396646/
https://www.ncbi.nlm.nih.gov/pubmed/18471279
http://dx.doi.org/10.1186/1475-2875-7-79
work_keys_str_mv AT anderskatherine timingofintermittentpreventivetreatmentformalariaduringpregnancyandtheimplicationsofcurrentpolicyonearlyuptakeinnortheasttanzania
AT marchanttanya timingofintermittentpreventivetreatmentformalariaduringpregnancyandtheimplicationsofcurrentpolicyonearlyuptakeinnortheasttanzania
AT chambopili timingofintermittentpreventivetreatmentformalariaduringpregnancyandtheimplicationsofcurrentpolicyonearlyuptakeinnortheasttanzania
AT mapundapasiens timingofintermittentpreventivetreatmentformalariaduringpregnancyandtheimplicationsofcurrentpolicyonearlyuptakeinnortheasttanzania
AT reyburnhugh timingofintermittentpreventivetreatmentformalariaduringpregnancyandtheimplicationsofcurrentpolicyonearlyuptakeinnortheasttanzania