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Updated: Apr 23, 2026

Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors
Published on: April 9, 2014
Review of tenofovir use in HIV-infected children
Linda Aurpibul1, Thanyawee Puthanakit
1From the *Research Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand; †Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; and ‡HIVNAT, Thai Red Cross AIDS Research Center, Bangkok, Thailand.
Insights
Tenofovir disoproxil fumarate (TDF) is a preferred HIV medication for children and adults. While effective and convenient, ongoing monitoring for renal and bone health is crucial in pediatric patients.
Area of Science:
- Pediatric infectious diseases
- Antiretroviral therapy research
- Pharmacokinetics and drug safety
Background:
- Tenofovir disoproxil fumarate (TDF) is a widely recommended first-line antiretroviral, approved for children aged 2+ and adolescents aged 10+.
- Its efficacy against HIV and hepatitis B virus, once-daily dosing, and favorable metabolic profile make it suitable for large-scale programs.
- Unlike other nucleoside reverse transcriptase inhibitors (NRTIs), TDF does not induce multi-NRTI resistance mutations, preserving future treatment options.
Purpose of the Study:
- To review current information on the pharmacokinetics, safety, and tolerability of TDF in pediatric populations.
- To establish a weight-band-based dosing regimen for pediatric use.
- To inform clinical decision-making regarding the risks and benefits of TDF in children.
Main Methods:
- Systematic review of existing clinical data on TDF in children and adolescents.
- Analysis of pharmacokinetic and safety profiles.
- Evaluation of established dosing regimens for pediatric use.
Main Results:
- A body-weight-band dosing regimen for TDF has been established for pediatric use.
- Key safety concerns include potential effects on renal function and bone mineral density.
- Long-term data on renal and bone outcomes in HIV-infected children receiving TDF is still needed.
Conclusions:
- TDF is a valuable antiretroviral agent for children and adolescents, with established dosing guidelines.
- Regular monitoring of renal function is recommended for high-risk pediatric patients.
- Further long-term studies are necessary to fully understand the renal and bone health implications of TDF in children.
Abstract:
Tenofovir disoproxil fumarate (TDF) is approved by the Food and Drug Administration for use in children ages 2 years and older and is recommended by the World Health Organization for use as a preferred first-line nucleotide reverse transcriptase inhibitor in adults and adolescents ages 10 years and older. The simplicity of once daily dosing, few metabolic side effects and efficacy against hepatitis B virus make TDF suitable for use in a large scale program. Unlike thymidine analoge nucleoside reverse transcriptase inhibitors (NRTIs); tenofovir does not induce multi-NRTI resistance mutations, so more NRTI options are available for future second-line-regimens. Fixed-dose combinations of TDF with other ARVs as a single tablet regimen are now widely available for adults and adolescents, but none are available for young children. Current information on TDF including the pharmacokinetics, safety and tolerability in children and adolescents was reviewed. A dosing regimen according to body-weight-band has been established for pediatric use. Safety concerns of TDF mainly relate to its effects on renal function and bone mineral density. Regular monitoring of renal function in high-risk patients, including those on other nephrotoxic drugs, may be warranted to detect adverse renal effects. Long-term-data on renal and bone outcomes among HIV-infected children is needed. Lessons learned from clinical studies will help clinicians balance the risks and benefits of TDF and design appropriate antiretroviral regimens for children in different circumstances.
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