Antiretroviral Use for HIV Prevention During Pregnancy: The Need to Strengthen Regulatory and Surveillance Systems in Africa

被引:0
|
作者
Schaefer, Robin [1 ]
Donaldson, L. [1 ]
Chigome, A. [2 ]
dos Santos, M. Escudeiro [3 ]
Lamprianou, S. [4 ]
Ndembi, N. [5 ]
Nwokike, J. I. [6 ]
Nyambayo, P. [7 ]
Palmi, V. [8 ]
Renaud, F. [9 ]
Tome, M. Gonzalez [3 ]
Miller, V. [1 ]
机构
[1] Univ Calif Berkeley, Forum Collaborat Res, Berkeley, WA 20036 USA
[2] South African Hlth Prod Regulatory Author, Pretoria, South Africa
[3] European Med Agcy, Human Med Div, Vaccines & Therapies Infect Dis, Amsterdam, Netherlands
[4] WHO, Pharmacovigilance Team, Dept Regulat & Prequalificat, Geneva, Switzerland
[5] Africa Ctr Dis Control & Prevent, Addis Ababa, Ethiopia
[6] United States Agcy Int Dev USAIDs Promoting Qual M, United States Pharmacopeia, Rockville, MD USA
[7] Med Control Author Zimbabwe, Harare, Zimbabwe
[8] European Med Agcy, Int Affairs Dept, Amsterdam, Netherlands
[9] WHO, Global HIV Hepatitis & STIs Programmes, Geneva, Switzerland
关键词
BREAST-FEEDING WOMEN; DRUG; PHARMACOVIGILANCE; COUNTRIES; FOOD;
D O I
10.1007/s40264-024-01494-6
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
HIV-prevention efforts focusing on women of child-bearing potential are needed to end the HIV epidemic in the African region. The use of antiretroviral drugs as pre-exposure prophylaxis (PrEP) is a critical HIV prevention tool. However, safety data on new antiretrovirals during pregnancy are often limited because pregnant people are excluded from drug development studies. Calls from communities, healthcare professionals, and regulators to improve the information supporting decision-making around the use of medical products during pregnancy have been increasing. Post-marketing safety surveillance is an essential tool for detecting adverse outcomes and evaluating real-world, longer-term effects of drugs. Detecting and evaluating uncommon pregnancy outcomes requires large sample sizes, highlighting the benefits of and need for safety surveillance. Surveillance systems vary widely across Africa, and the need for enhanced surveillance of PrEP use during pregnancy highlights the limitations of current regulatory and surveillance systems. Challenges include weak regulation and insufficient resources. Pooling of resources and regulatory harmonization could address resource challenges. The African Medicines Agency, as a specialized agency of the African Union, has the potential to improve African medical product regulation, including post-marketing safety surveillance. This can strengthen regulation and ensure that market authorization holders meet their responsibility to invest in post-marketing surveillance systems, such as pregnancy registries. At the same time, independent post-marketing studies are needed to ensure generation of essential safety data. The Forum for Collaborative Research has initiated a project to facilitate interactions between regulators in Africa, the USA, and Europe, as well as other stakeholders, and to work toward consensus on safety data generation from PrEP during pregnancy before and after marketing authorization.
引用
收藏
页码:209 / 216
页数:8
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