Intermittent Preventive Treatment The challenge of implementation

  • Allison Bell Technical Officer , Malaria consortium East and Southern Africa

الملخص

The Direct consequences of malaria during pregnancy are more prevalent in unstable transmission areas. In those areas pregnant women have little or on immunity. In those women malaria causes hyperpyrexia, hypoglycaemia, severe haemolytic anaemia, cerebral malaria and pulmonary oedema and maternal death if not treated. (Looareesuwan et al 1985). Fever in pregnancy may bring about abortion or intrauterine foetal death. The average malaria in pregnancy case fatality varies from 1% in low endemic areas to 13.1% in epidemics (Brabin 7003).


          The indirect consequences of malaria during pregnancy are more prevalent in stable transmission areas. In such settings the main maternal effect is anaemia, which is frequently severe and a risk factor for maternal death. The contribution of malaria to maternal mortality is estimated as 0.5-23% of hospital based deaths and 2.9-17.6% of community based maternal deaths. The second important effect of malaria in pregnancy in areas of stable transmission is low birth weight (LBW). 20% of children born in Malawi are LBW; malaria was most important contributory factor to LBW (verhoef et al 1988). LBW in Malawi contributed to 80% of all neonatal deaths and 38% of infant mortality (MC Dermott et al 1996). LBW is the single biggest risk factor for neonatal mortality and major contributor to infant mortality (Mc Cormick 1985).

المراجع

• Brabin, B (2003) Presentation to Royal College of Physicians, London.
• Looareesuwan et al., 1985
• Luxemburger,C. McGready, R Kham, A et al (2001) Effects of malaria during pregnancy on infant mortality in an area of low transmission American J of Epidemiology; 154:459-65
• McCormick, M.C (1985) The contribution of low birth weight to infant mortality and childhood mortality. New England Journal of Medicine; 312:82-90
• McDermott et al 1996
• Newman et al (2003) Burden of malaria during pregnancy in areas of stable & unstable transmission in Ethiopia during a non-epidemic year. The Journal of Infectious Diseases 187: 1765-72
• Parise,M. E et al. (1998) Efficacy of SP for prevention of placental malaria in an area of Kenya with a high prevalence of malaria and HIV infection. American Journal of Tropical Medicine & Hygiene. 59 (5): 813-22.
• Schultz, L.J et al (1994) The efficacy of antimalarial regimens containing SP and/or Chloroquine in preventing peripheral & placental Plasmodium falciparum infection among pregnant women in Malawi. American Journal of Tropical medicine & Hygiene 51(5):512-22
• Shulman ,C et al. (1999) Intermittent SP to prevent severe anaemia secondary to malaria in pregnancy: a randomised placebo-controlled trial. Lancet 353 (9153): 632-6
• Verhoeff et al (1999) malaria in pregnancy and its consequences for the infant in rural Malawi. Annals of Tropical Medicine and Parasitology. 93 Suppl 1:S25-33.
• WHO (2002) Strategic Framework for Malaria Control During Pregnancy in the Africa Region
منشور
2004-01-01
كيفية الاقتباس
BELL, Allison. Intermittent Preventive Treatment The challenge of implementation. مجلة الجزيرة للعلوم الصحية, [S.l.], v. 1, n. 1, jan. 2004. ISSN 1810-5386. متوفر في: <http://37.60.236.48/index.php/gjhs/article/view/168>. تأريخ الوصول: 03 june 2026.
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