BMC Research Notes | |
Effectiveness of option B highly active antiretroviral therapy (HAART) prevention of mother-to-child transmission (PMTCT) in pregnant HIV women | |
Elijah Oyoo-Okoth3  Edward Anino4  Joseph K Choge1  Eliningaya J Kweka2  Christopher Khayeka-Wandabwa5  Erastus K Ngemu4  | |
[1] School of Health Sciences, University of Eastern Africa, Baraton, PO Box 2500-30100, Eldoret, Kenya;Tropical Pesticides Research Institute, Division of Livestock and Human Diseases Vector Control, Mosquito Section, Ngaramtoni, Off Nairobi road, PO Box 3024, Arusha, Tanzania;School Natural Resources and Environmental Studies, Karatina University, PO Box 1957-10101, Karatina, Kenya;School of Science, Department of Biochemistry, University of Eldoret, PO Box 1125, Eldoret, Kenya;Institute of Tropical Medicine and Infectious Diseases (ITROMID), Jomo Kenyatta University of Agriculture and Technology (JKUAT), Nairobi, Kenya | |
关键词: Prevention of Mother-To-Child Transmission (PMTCT); Mother-To-Child Transmission (MTCT); Highly Active Antiretroviral Therapy (HAART); Early Infant Diagnosis; CD4 counts; Antiretroviral; | |
Others : 1232486 DOI : 10.1186/1756-0500-7-52 |
|
received in 2013-04-23, accepted in 2014-01-15, 发布年份 2014 | |
【 摘 要 】
Background
Ensuring that no baby is born with HIV is an essential step towards achieving an AIDS-free generation. To achieve this, strategies that decouple links between childbirth and HIV transmission are necessary. Traditional forms of prevention of mother-to-child transmission of HIV (PMTCT), has been recommended. Recognizing the importance and challenges of combination of methods to achieve rapid PMTCT, the World Health Organization (WHO) recommended option B Highly Active Antiretroviral Therapy (HAART) for all HIV-positive pregnant women. This study aimed to evaluate the effectiveness of the HAART in PMTCT. A cohort of HIV-infected pregnant women in Kenya were obtained from the DREAM Center, Nairobi. The study participants underwent adherence counselling and Option B of HAART [Nevirapine(NVP) + Lamivudine + Zidovudine] at the fourth week of gestation followed by an intravenous NVP administration intrapartum and postpartum NVP syrup to the respective infants for six weeks. Absolute pre-HAART and post-HAART CD4 counts and viral loads counts were determined. Comparison of the CD4 counts and viral loads before and after administration of HAART were done using Wilcoxon’s Matched Pairs Signed-Ranks Test.
Findings
The mean absolute CD4 cell counts in mothers after administration of HAART was significantly higher (Z = 15.664, p < 0.001) than before the administration of HAART). Also the viral load of the mothers significantly (Z = 11.324, p < 0.001) reduced following HAART treatment. Following the HAART administration in mothers, up to 90% of children were confirmed to be HIV negative.
Conclusion
Administration of HAART to mothers and children demonstrated an effective mechanism of PMTCT. However, other aspects of HAART such as adherence, costs, mothers behaviour during HAART, and the child feeding programme during the therapy should further be evaluated and ascertained how they can affect the overall efficacy of option B HAART in PMTCT.
【 授权许可】
2014 Ngemu et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20151114083653338.pdf | 747KB | download | |
Figure 2. | 38KB | Image | download |
Figure 1. | 46KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
【 参考文献 】
- [1]Bositis CM, Gashongore I, Patel DM: Updates to the World Health Organization’s recommendations for the use of antiretroviral drugs for treating pregnant women and preventing HIV infection in infants. Med J Zambia 2010, 37:111-117.
- [2]NASCOP: Guidelines for prevention of mother to child transmission (PMTCT) of HIV/AIDS in Kenya fourth edition. Kenya: Ministry of Health; 2012. Available at http://nascop.or.ke/library/pmtct/Guidelines%20for%20PMTCT%20of%20HIVAIDS%20in%20Kenya-1.pdf webcite
- [3]UNAIDS: UNAIDS Report on the global AIDS epidemic. Geneva: WHO; 2012.
- [4]Townsend CL, Cortina-Borja M, Peckham CS, de Ruiter A, Lyall H, Tookey PA: Low rates of mother-to-child transmission of HIV following effective pregnancy interventions in the United Kingdom and Ireland, 2000–2006. AIDS 2008, 22:973-981.
- [5]Cooper E, Charurat M, Mofenson L, et al.: Combination antiretroviral strategies for the treatment of pregnant HIV-1-infected women and prevention of perinatal HIV-1 transmission. Acquir Immune Defic Syndr 2002, 29:484-494.
- [6]Dorenbaum A, Cunningham CK, et al.: Two-dose intrapartum/newborn nevirapine and standard antiretroviral therapy to reduce perinatal HIV transmission: a randomized trial. JAMA 2002, 288:189-198.
- [7]WHO: Global monitoring framework and strategy for the global plan towards the elimination of new HIV infections among children by 2015 and keeping their mothers alive. Geneva: WHO; 2012.
- [8]WHO, UNAIDS and UNICEF: Towards universal access: scaling up priority HIV/AIDS interventions in the health sector. Progress report, 2005, 2006, 2007, 2008, 2009, 2010, WHO, UNAIDS, UNICEF. 2009. Available at http:/data.unaids.org/pub/Report/2009/20090930 tuapr_2009_en.pdf webcite
- [9]UNAIDS & WHO: AIDS Epidemic Update. Geneva: UNAIDS; 2009.
- [10]Coovadia H: Antiretroviral agents–how best to protect infants from HIV and save their mothers from AIDS. N Engl J Med 2004, 351:289-292.
- [11]NASCOP: Annual Health Sector HIV Report: Progress with the National Health Sector Response National AIDS/STI Control Programme. 2009. Available at: http://www.nascop.or.ke/library/3d/NASCOP%20Draft%20Annual%20Report%20for%202009.pdf webcite
- [12]Nduati R, John G, Mbori-Ngacha D, Richardson B, Overbaugh J, Mwatha A, Ndinya-Achola J, Bwayo J, Onyango FE, Hughes J, Kreiss J: Effect of breastfeeding and formula feeding on transmission of HIV-1: a randomized clinical trial. JAMA 2000, 283:1167-1174.
- [13]Lenth RV: Java applets for power and sample size [computer software]. 2010. http://www.stat.uiowa.edu/~rlenth/Power webcite
- [14]Karon JM, Fleming PL, Steketee RW, De Cock K: HIV in the United States at the turn of the century: an epidemic in transition. Am J Public Health 2001, 91:1060-1068.
- [15]Wood E, Tyndall MW, Spittal PM, Li K, Hogg RS, Montaner JS, O’Shaughnessy MV, Schechter M: Factors associated with persistent high-risk syringe sharing in the presence of an established needle exchange programme. AIDS 2002, 16:941-943.
- [16]Gayle HD: Expanding access to HIV prevention. AIDS Res Ther 2006, 3:2. BioMed Central Full Text
- [17]Kerr T, Kaplan K, Suwannawong P, Jürgens R, Wood E: The global fund to fight AIDS, tuberculosis and malaria: funding for unpopular public-health programmes. Lancet 2004, 364:11-12.
- [18]Markel H: The search for effective HIV vaccines. N Engl J Med 2005, 353:753-757.
- [19]Siliciano JD, Siliciano RF: A long-term latent reservoir for HIV-1: discovery and clinical implications. J Antimicrob Chemother 2004, 54:6-9.
- [20]Furtado MR, Callaway DS, Phair JP, Kunstman KJ, Stanton JL, Macken CA, Perelson AS, Wolinsky S: Persistence of HIV-1 transcription in peripheral-blood mononuclear cells in patients receiving potent antiretroviral therapy. N Engl J Med 1999, 340:1614-1622.
- [21]Pomerantz R: Residual HIV-1 disease in the era of highly active antiretroviral therapy. N Engl J Med 1999, 340:1672-1674.
- [22]Montaner JS, Harris M, Mo T, Harrigan P: Rebound of plasma HIV viral load following prolonged suppression with combination therapy. AIDS 1998, 12:1398-1399.
- [23]Zhang L, Ramratnam B, Tenner-Racz K, He Y, Vesanen M, Lewin S, Talal A, Racz P, Perelson AS, Korber BT, Markowitz M, Guo Y, Duran M, Hurley A, Tsay J, Huang Y-C, Wang C-C, Ho DD: Quantifying residual HIV-1 replication in patients receiving combination antiretroviral therapy. New Eng J Med 1999, 340:1605-1613.
- [24]Taylor GP, Clayden P, Dhar J, Gandhi K, Gilleece Y, Harding K, Hay P, Kennedy J, Low-Beer N, Lyall H, Palfreeman A, Tookey P, Welch S, Wilkins E, de Ruiter A: British HIV association guidelines for the management of HIV infection in pregnant women 2012. HIV Med 2012, 13:87-157.
- [25]UNAIDS: Report on the global AIDS epidemic. Annex 2: HIV/AIDS estimates and data, 2005. Geneva: WHO; 2006.
- [26]UNAIDS: Financing the expanded response to AIDS: HIV vaccine and microbicide research and development, 2005. Geneva: UNAIDS; 2006.
- [27]UNAIDS: Resource needs for an expanded response to AIDS in low- and middle-income countries, 2005. Geneva: UNAIDS; 2006.
- [28]Hogg RS, Rhone SA, Yip B, Sherlock C, Conway B, Schechter MT, O’Shaughnessy MV, Montaner J: Antiviral effect of double and triple drug combinations amongst HIV- infected adults: lessons from the implementation of viral load-driven antiretroviral therapy. AIDS 1998, 12:279-284.
- [29]Biesma RG, Brugha R, Harmer A, Walsh A, Spicer N, Walt G: The effects of global health initiatives on country health systems: a review of the evidence from HIV/AIDS control. Health Policy Plan 2009, 24:239-252.
- [30]Cu-Uvin S, Caliendo AM, Reinert S, Chang A, Juliano-Remollino C, Flanigan TP, Mayer KH, Carpenter CC: Effect of highly active antiretroviral therapy on cervicovaginal HIV-1 RNA. AIDS 2000, 14:415-421.
- [31]Vernazza PL, Gilliam BL, Flepp M, et al.: Effect of antiviral treatment on the shedding of HIV-1 in semen. AIDS 1997, 11:1249-1254.
- [32]Quinn TC, Wawer MJ, Sewankambo N, Serwadda D, Li C, Wabwire-Mangen F, Meehan MO, Lutalo T, Gray RH: Viral load and heterosexual transmission of human immunodeficiency virus type 1. New Eng J Med 2000, 342:921-929.
- [33]Tovanabutra S, Robison V, Wongtrakul J, et al.: Male viral load and heterosexual transmission of HIV-1 subtype E in northern Thailand. J Acquir Immune Defic Syndr 2002, 29:275-283.
- [34]Fang CT, Hsu HM, Twu SJ, Chen MY, Chang YY, Hwang JS, Wang JD, Chuang C: Decreased HIV transmission after a policy of providing free access to highly active antiretroviral therapy in Taiwan. J Infect Dis 2004, 190:879-885.
- [35]Musicco M, Lazzarin A, Nicolosi A, et al.: For the Italian study group on HIV heterosexual transmission. Antiretroviral treatment of men infected with human immunodefi ciency virus type 1 reduces the incidence of heterosexual transmission. Arch Intern Med 1994, 154:1971-1976.
- [36]Study EC: Mother-to-child transmission of HIV infection in the era of highly active antiretroviral therapy. Clin Infect Dis 2005, 40:458-465.
- [37]Fang G, Burger H, Grimson R, et al.: Maternal plasma human immunodefi ciency virus type 1 RNA level: a determinant and projected threshold for mother-to-child transmission. Proc Natl Acad Sci USA 1995, 92:100-104.
- [38]Guay LA, Musoke P, Fleming T, et al.: Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVNET 012 randomised trial. Lancet 1999, 354:795-802.
- [39]De Cock KM, Fowler MG, Mercier E, et al.: Prevention of mother-to-child HIV transmission in resource-poor countries: translating research into policy and practice. JAMA 2000, 283:1175-1182.