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A response to minister of health on mother to child transmission11 September, 2007 - 00:00 — moderatorThe Minister of Health has made statements to the media that the Department of Health has long been prepared to implement dual therapy regimens in all the provinces in South Africa, but has been prohibited by the 2001 Constitutional Court judgment in Minister of Health and Others v TAC and Others. She states that the judgment limited the Department of Health to implementing only 'monotherapy' nevirapine (NVP) to mothers with HIV to reduce mother-to-child transmission. This is a gross distortion of the truth. The facts are as follows:
We welcome yesterday's announcement by the Department of Health at SANAC of the imminent approval of dual therapy as a minimum treatment regimen for PMTCT. We call for the urgent and proper implementation of this policy. For more information contact:
Heather Mangwiro (011) 356 4117 or
Adila Hassim (011) 356 4116
Nosisa Mhlathi (021) 788 3507 Extract from speech by the Minister of Health to Parliament =96 We are not responsible for the errors in the text.From http://www.info.gov.za/speeches/1999/0001131124a1002.htm The fifth clinical trial was done, both with AZT, and with a new drug called Nivirapine The trial was done as a joint Uganda/United States study. The drugs were given to the women once during labour and delivery and the babies were given one dose within three days of being born. The final results of the study have not been published yet, but in the interim analysis, the team looked at 308 women who had taken AZT and 310 who had taken Nivirapine, and the Nivirapine was markedly more effective. Nivirapine was also safer, less expensive and more practical than AZT or any other drug tested so far, in preventing MTCT. Nevertheless, Nivirapine is still not registered in Uganda for mass administration for the prevention of MTCT. In terms of affordability, the cost of the short course of AZT, as given in the Thai study that showed a 50% reduction in transmission, would be approximately R400 per mother. The cost of Nivirapine, by comparison, would be approximately R30 per mother and child. This will mean that many countries that could not adopt drug strategies that involved AZT, because of the cost, could now adopt a strategy with Nivirapine, that could lower the rate of MTCT. Comparative studies are currently underway in South Africa to look at Nivirapine as compared to the short course in AZT (the Thai Trial) and the short course in AZT plus 3TC (the PETRA Trial). The findings of these cost-effectiveness studies are expected in March 2000.
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