HIV viraemia during pregnancy in women receiving preconception antiretroviral therapy in KwaDukuza, KwaZulu-Natal

Vuyokazi Ntlantsana, Richard J Hift, Wendy P Mphatswe, Vuyokazi Ntlantsana, Richard J Hift, Wendy P Mphatswe

Abstract

Background: Preconception antiretroviral therapy (PCART) followed by sustained viral suppression is effective in preventing mother-to-child transmission of HIV. The rates of persistent and transient viraemia in such patients have not been prospectively assessed in South Africa.

Objectives: We determined the prevalence of transient and persistent viraemia in HIV-positive women entering antenatal care on PCART and studied variables associated with viraemia.

Methods: We performed a prospective cross-sectional observational study of HIV-positive pregnant women presenting to a primary healthcare facility in KwaZulu-Natal. All had received at least 6 months of first-line PCART. Viral load (VL) was measured, patients were interviewed, adherence estimated using a visual analogue scale and adherence counselling provided. Viral load was repeated after 4 weeks where baseline VL exceeded 50 copies/mL.

Results: We enrolled 82 participants. Of them, 59 (72%) pregnancies were unplanned. Fifteen participants (18.3%) were viraemic at presentation with VL > 50 copies/mL. Of these, seven (8.5%) had viral suppression (VL < 50 copies/mL), and eight remained viraemic at the second visit. Adherence correlated significantly with viraemia at baseline. Level of knowledge correlated with adherence but not with lack of viral suppression at baseline. Socio-economic indicators did not correlate with viraemia. No instances of vertical transmission were observed at birth.

Conclusions: Approximately 20% of women receiving PCART may demonstrate viraemia. Half of these may be transient. Poor adherence is associated with viraemia, and efforts to encourage and monitor adherence are essential. The rate of unplanned pregnancies is high, and antiretroviral therapy programmes should focus on family planning needs of women in the reproductive age group to prevent viral non-suppression prior to pregnancy.

Keywords: Preconception Antiretroviral Therapy; HIV; Viraemia; Antenatal Care; Adherence.

Conflict of interest statement

The authors declare that they have no financial or personal relationship(s) that may have inappropriately influenced them in writing this article.

Figures

FIGURE 1
FIGURE 1
Evolution of viral load in 15 participants who were viraemic at the initial visit over the subsequent 4 weeks. The lower, middle and upper red lines represent viral load measurements of 50, 400 and 1000 copies/mL, respectively.
FIGURE 2
FIGURE 2
Distribution of knowledge scores among 82 participants. The maximum obtainable score is 32.

References

    1. Joint United Nations Programme on HIV/AIDS The gap report. Geneva, Switzerland: Joint United Nations Programme on HIV/AIDS; 2014.
    1. Joint United Nations Programme on HIV/AIDS UNAIDS data 2017. Geneva, Switzerland: Joint United Nations Programme on HIV/AIDS; 2017.
    1. Joint United Nations Programme on HIV/AIDS Global report: UNAIDS report on the global AIDS epidemic 2010. Geneva, Switzerland: Joint United Nations Programme on HIV/AIDS; 2010. Report No.: 9291738719.
    1. South African National Department of Health The 2012 national antenatal sentinel HIV & Herpes simplex type-2 prevalence survey in South Africa. Pretoria, South Africa: South African National Department of Health; 2013.
    1. Myer L, Phillips T, Manuelli V, et al. . Evolution of antiretroviral therapy services for HIV-infected pregnant women in Cape Town, South Africa. J Acquir Immune Defic Syndr. 2015;69:e57–e65. 10.1097/QAI.0000000000000584
    1. Laut KG, Shepherd LC, Pedersen C, et al. . Associations between HIV-RNA-based indicators and virological and clinical outcomes. AIDS. 2016;30:1961–1972. 10.1097/QAD.0000000000001144
    1. Hermans LE, Moorhouse MA, Carmona S, et al., editors. Increased risk of cART failure after low-level viremia under WHO guidelines. Conference on retroviruses and opportunistic infections; 2017. February 13–16; Seattle, WA.
    1. Nachega JB, Uthman OA, Anderson J, et al. . Adherence to antiretroviral therapy during and after pregnancy in low-income, middle-income, and high-income countries: A systematic review and meta-analysis. AIDS. 2012;26:2039–2052. 10.1097/QAD.0b013e328359590f
    1. Jordan MR, Bennett DE, Bertagnolio S, Gilks CF, Sutherland D. World Health Organization surveys to monitor HIV drug resistance prevention and associated factors in sentinel antiretroviral treatment sites. Antivir Ther. 2008;13:15.
    1. Gallant JE. Making sense of blips. J Infect Dis. 2007;196:1729–1731. 10.1086/523705
    1. Sorstedt E, Nilsson S, Blaxhult A, et al. . Viral blips during suppressive antiretroviral treatment are associated with high baseline HIV-1 RNA levels. BMC Infect Dis. 2016;16:305 10.1186/s12879-016-1628-6
    1. Tobin NH, Learn GH, Holte SE, et al. . Evidence that low-level viremias during effective highly active antiretroviral therapy result from two processes: Expression of archival virus and replication of virus. J Virol. 2005;79:9625–9634. 10.1128/JVI.79.15.9625-9634.2005
    1. Gandhi RT, McMahon DK, Bosch RJ, et al. . Levels of HIV-1 persistence on antiretroviral therapy are not associated with markers of inflammation or activation. PLoS Pathog. 2017;13:e1006285 10.1371/journal.ppat.1006285
    1. Elvstam O, Medstrand P, Yilmaz A, et al. . Virological failure and all-cause mortality in HIV-positive adults with low-level viremia during antiretroviral treatment. PLoS One. 2017;12:e0180761 10.1371/journal.pone.0180761
    1. Ryscavage P, Kelly S, Li JZ, Harrigan PR, Taiwo B. Significance and clinical management of persistent low level viremia and very low level viremia in HIV-1 infected patients. Antimicrob Agents Chemother. 2014;58(7):3585–98. 10.1128/AAC.00076-14
    1. Joint United Nations Programme on HIV/AIDS 90-90-90: An ambitious treatment target to help end the AIDS epidemic. Geneva, Switzerland: Joint United Nations Programme on HIV/AIDS; 2014.
    1. Peters R, Kekana M, Cole-Hamilton S, Mongwe MW, Railton J. Towards the HIV 90-90-90 target: A simple and low-cost intervention to improve viral load completion. HIV Nurs Matt. 2016;7:35–39.
    1. Mzingwane ML, Tiemessen C, Richter KL, et al. . Pre-treatment minority HIV-1 drug resistance mutations and long term virological outcomes: Is prediction possible? Virol J. 2016;13:170. 10.1186/s12985-016-0628-x
    1. Bull L, Khan AW, Barton S. Management of HIV infection in pregnancy. Obstet Gynaecol Reprod Med. 2015;25:273–278. 10.1016/j.ogrm.2015.07.004
    1. Mandelbrot L, Tubiana R, Le Chenadec J, et al. . No perinatal HIV-1 transmission from women with effective antiretroviral therapy starting before conception. Clin Infect Dis. 2015;61:1715–1725. 10.1093/cid/civ578
    1. Reliquet V, Winer N, Chereau N, et al. . The spectrum of HIV mother-to-child transmission risk. J Int AIDS Soc. 2014;17:19703 10.7448/IAS.17.4.19703
    1. Kennedy CE, Yeh PT, Pandey S, Betran AP, Narasimhan M. Elective cesarean section for women living with HIV: A systematic review of risks and benefits. AIDS. 2017;31:1579 10.1097/QAD.0000000000001535
    1. Henegar CE, Westreich DJ, Maskew M, et al. . The effect of pregnancy and the postpartum period on adherence to antiretroviral therapy among HIV-infected women established on treatment. J Acquir Immune Defic Syndr. 2015;68:477 10.1097/QAI.0000000000000501
    1. Hoffmann CJ, Cohn S, Mashabela F, et al. . Treatment failure, drug resistance, and CD4 T-cell count decline among postpartum women on antiretroviral therapy in South Africa. J Acquir Immune Defic Syndr. 2016;71:31–37.
    1. Myer L, Phillips T, McIntyre J, et al. . HIV viraemia and mother-to-child transmission risk after antiretroviral therapy initiation in pregnancy in Cape Town, South Africa. HIV Med. 2017;18:80–88. 10.1111/hiv.12397
    1. Myer L, Dunning L, Lesosky M, et al. . Frequency of viremic episodes in HIV-infected women initiating antiretroviral therapy during pregnancy: A cohort study. Clin Infect Dis. 2017;64:422–427.
    1. Townsend CL, Byrne L, Cortina-Borja M, et al. . Earlier initiation of ART and further decline in mother-to-child HIV transmission rates, 2000–2011. AIDS. 2014;28:1049–1057. 10.1097/QAD.0000000000000212
    1. Mnyani CN, Simango A, Murphy J, Chersich M, McIntyre JA. Patient factors to target for elimination of mother-to-child transmission of HIV. Global Health. 2014;10:36 10.1186/1744-8603-10-36
    1. Cragg CD. Evaluating viral load monitoring in antiretroviral-experienced HIV-positive pregnant women accessing antenatal care in Khayelitsha, Cape Town [doctoral dissertation]. Cape Town, South Africa: University of Cape Town; 2015.
    1. Sagna T, Bisseye C, Compaore TR, et al. . Prevention of mother-to-child HIV-1 transmission in Burkina Faso: Evaluation of vertical transmission by PCR, molecular characterization of subtypes and determination of antiretroviral drugs resistance. Glob Health Action. 2015; 8:26065 10.3402/gha.v8.26065
    1. Omole OB, Semenya M-AM. Treatment outcomes in a rural HIV clinic in South Africa: Implications for health care. S Afr J HIV Med. 2016;17:1–6. 10.4102/sajhivmed.v17i1.414
    1. Calvert C, Ronsmans C. Pregnancy and HIV disease progression: A systematic review and meta-analysis. Trop Med Int Health. 2015;20:122–145. 10.1111/tmi.12412
    1. Heffron R, Donnell D, Kiarie J, et al. . A prospective study of the effect of pregnancy on CD4 counts and plasma HIV-1 RNA concentrations of antiretroviral-naive HIV-1 infected women. J Acquir Immune Defic Syndr. 2014;65:231 10.1097/QAI.0000000000000013
    1. Myer L, Phillips TK, Hsiao N-Y, et al. . Plasma viraemia in HIV-positive pregnant women entering antenatal care in South Africa. J Int AIDS Soc. 2015;18:20045 10.7448/IAS.18.1.20045
    1. Chesney M, Ickovics J. ACTG Adherence baseline questionnaire. San Francisco, CA: AIDS Clinical Trial Group, University of California San Francisco; 1997.
    1. Muzigaba M, Kolbe-Alexander TL, Wong F. The perceived role and influencers of physical activity among pregnant women from low socioeconomic status communities in South Africa. J Phys Act Health. 2014;11:1276–1283. 10.1123/jpah.2012-0386
    1. Solarin I, Black V. ‘They told me to come back’: Women’s antenatal care booking experience in inner-city Johannesburg. Matern Child Health J. 2013;17:359–367. 10.1007/s10995-012-1019-6
    1. Cloete A, Strebel A, Simbayi L, et al. . Challenges faced by people living with HIV/AIDS in Cape Town, South Africa: Issues for group risk reduction interventions. AIDS Res Treat [serial online]. 2010. [cited 2018 Jan 26];2010:420270: Available from:
    1. Chetty T, Newell ML, Thorne C, Coutsoudis A. Viraemia before, during and after pregnancy in HIV-infected women on antiretroviral therapy in rural KwaZulu-Natal-South Africa, 2010–2015. Trop Med Int Health. 2018;23(1):79–91. 10.1111/tmi.13001
    1. Hoffmann CJ, Charalambous S, Sim J, et al. . Viremia, resuppression, and time to resistance in human immunodeficiency virus (HIV) subtype C during first-line antiretroviral therapy. Clin Infect Dis. 2009;49:1928–1935. 10.1086/648444
    1. El-Khatib Z, Ekström AM, Ledwaba J, et al. . Viremia and drug resistance among HIV-1 patients on antiretroviral treatment – A cross-sectional study in Soweto, South Africa. AIDS. 2010;24:1679 10.1097/QAD.0b013e32833a097b
    1. Boulle A, Van Cutsem G, Hilderbrand K, et al. . Seven-year experience of a primary care antiretroviral treatment programme in Khayelitsha, South Africa. AIDS. 2010;24:563–572. 10.1097/QAD.0b013e328333bfb7
    1. Solomon SS, Mehta SH, McFall AM, et al. . Community viral load, antiretroviral therapy coverage, and HIV incidence in India: A cross-sectional, comparative study. Lancet HIV. 2016;3:e183–e190. 10.1016/S2352-3018(16)00019-9
    1. Gregson J, Kaleebu P, Marconi VC, et al. . Occult HIV-1 drug resistance to thymidine analogues following failure of first-line tenofovir combined with a cytosine analogue and nevirapine or efavirenz in sub Saharan Africa: A retrospective multi-centre cohort study. Lancet Infect Dis. 2017;17:296–304. 10.1016/S1473-3099(16)30469-8
    1. Gregson J, Tang M, Ndembi N, et al. . Global epidemiology of drug resistance after failure of WHO recommended first-line regimens for adult HIV-1 infection: A multicentre retrospective cohort study. Lancet Infect Dis. 2016;16:565–575. 10.1016/S1473-3099(15)00536-8
    1. Bulage L, Ssewanyana I, Nankabirwa V, et al. . Factors associated with virological non-suppression among HIV-positive patients on antiretroviral therapy in Uganda, August 2014–July 2015. BMC Infect Dis. 2017;17:326 10.1186/s12879-017-2428-3
    1. Dharan NJ, Cooper DA. Long-term durability of HIV viral load suppression. Lancet HIV. 2017;4(7):e279–e280. 10.1016/S2352-3018(17)30063-2
    1. Burch LS, Smith CJ, Anderson J, et al. . Socioeconomic status and treatment outcomes for individuals with HIV on antiretroviral treatment in the UK: Cross-sectional and longitudinal analyses. Lancet Public Health. 2016;1:e26–e36. 10.1016/S2468-2667(16)30002-0
    1. Azia IN, Mukumbang FC, Van Wyk B. Barriers to adherence to antiretroviral treatment in a regional hospital in Vredenburg, Western Cape, South Africa. S Afr J HIV Med. 2016;17:1–8. 10.4102/sajhivmed.v17i1.476
    1. Matthews LT, Ribaudo HB, Kaida A, et al. . HIV-infected Ugandan women on antiretroviral therapy maintain HIV-1 RNA suppression across periconception, pregnancy, and postpartum periods. J Acquir Immune Defic Syndr. 2016;71:399–406. 10.1097/QAI.0000000000000874
    1. Mekuria LA, Nieuwkerk PT, Yalew AW, Sprangers MAG, Prins JM. High level of virological suppression among HIV-infected adults receiving combination antiretroviral therapy in Addis Ababa, Ethiopia. Antivir Ther. 2016;21:385–396. 10.3851/IMP3020
    1. McMahon JH, Elliott JH, Bertagnolio S, Kubiak R, Jordan MR. Viral suppression after 12 months of antiretroviral therapy in low-and middle-income countries: A systematic review. Bull World Health Organ. 2013;91:377–85. 10.2471/BLT.12.112946
    1. Stirratt MJ, Dunbar-Jacob J, Crane HM, et al. . Self-report measures of medication adherence behavior: Recommendations on optimal use. Trans Behav Med. 2015;5:470–482. 10.1007/s13142-015-0315-2
    1. Chaiyachati K, Hirschhorn LR, Tanser F, Newell M-L, Bärnighausen T. Validating five questions of antiretroviral nonadherence in a public-sector treatment program in rural South Africa. AIDS Patient Care STDs. 2011;25:163–170. 10.1089/apc.2010.0257
    1. Mindry DL, Milford C, Greener L, et al. . Client and provider knowledge and views on safer conception for people living with HIV (PLHIV). Sex Reprod Healthc. 2016;10:35–40. 10.1016/j.srhc.2016.03.005
    1. Haffejee F, Ports KA, Mosavel M. Knowledge and attitudes about HIV infection and prevention of mother to child transmission of HIV in an urban, low income community in Durban, South Africa: Perspectives of residents and health care volunteers. Health SA Gesondheid. 2016;21:171–178. 10.4102/hsag.v21i0.949
    1. Pillay Y. Implementation of the universal test and treat strategy for HIV positive patients and differentiated care for stable patients. Department of Health, South Africa; 2016. Avaiable from
    1. Crankshaw TL, Smit JA, Beksinska ME. Placing contraception at the centre of the HIV prevention agenda. Afr J AIDS Res. 2016;15:157–162. 10.2989/16085906.2016.1204330
    1. South African National Department of Health National consolidated guidelines for the prevention of mother-to-child transmission of HIV (PMTCT) and the management of HIV in children, adolescents and adults. Pretoria: South African National Department of Health; 2015. Contract No.: 11 December.

Source: PubMed

3
Předplatit