What is the recommended follow-up schedule for a patient on Truvada (emtricitabine/tenofovir disoproxil fumarate) in the office?

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Last updated: December 22, 2025View editorial policy

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Truvada PrEP Office Follow-Up Schedule

For patients on Truvada (emtricitabine/tenofovir disoproxil fumarate) for PrEP, follow-up visits should occur every 3 months for HIV testing and STI screening, with creatinine assessment every 6 months. 1, 2

Every 3 Months (Quarterly Visits)

HIV Testing

  • Perform combination HIV antigen-antibody assay at each visit 1, 2
  • Do not prescribe more than a 90-day supply of Truvada without documented negative HIV testing 1, 2
  • If acute HIV infection is suspected based on symptoms or recent high-risk exposure, add HIV RNA testing 1, 2

STI Screening

  • Screen all potentially exposed anatomic sites (urine, throat, anal, vaginal) for gonorrhea and chlamydia using nucleic acid amplification testing 1, 2
  • Perform syphilis serology 1, 2

Adherence and Risk Assessment

  • Assess medication adherence and provide counseling 1, 2
  • Evaluate ongoing risk behaviors 2
  • Provide condoms 2

Pregnancy Testing

  • Test women of childbearing potential at each visit 2

Every 6 Months

Renal Function Monitoring

  • Measure serum creatinine and calculate estimated glomerular filtration rate (eGFR) 1, 2
  • More frequent monitoring (potentially every 3 months) is warranted for higher-risk patients: those aged >50 years, taking hypertension or diabetes medications, or with baseline eGFR near threshold 1
  • Critical pitfall: Do not continue TDF-based PrEP if creatinine clearance falls below 60 mL/min 1, 2

Annually

Hepatitis C Screening

  • Perform hepatitis C serologic testing at least once yearly 1
  • Increase frequency to every 6 months for high-risk individuals (people who inject drugs) or those with elevated transaminase levels 1, 2

Special Monitoring Situations

Initial 1-Month Visit

  • Schedule a follow-up visit at 30 days after PrEP initiation to assess adherence, tolerability, and ensure absence of primary HIV infection 1, 2

If HIV Infection Occurs During PrEP

  • Immediately add a boosted protease inhibitor (boosted darunavir) and/or dolutegravir to TDF/emtricitabine while awaiting HIV RNA and resistance testing results 1, 2
  • Order resistance testing and establish linkage to HIV care 2
  • Switch to a recommended initial antiretroviral treatment regimen once HIV is confirmed 2

Hepatitis B Co-infection

  • Monitor liver function carefully after discontinuation of Truvada in patients with active hepatitis B, due to risk of acute hepatitis flares or hepatic decompensation 2

Common Pitfalls to Avoid

  • Never prescribe >90-day supplies without documented negative HIV testing 1, 2
  • Do not use TDF-based PrEP if creatinine clearance is <60 mL/min 1, 2
  • Do not delay renal monitoring beyond 6 months in standard-risk patients or 3 months in high-risk patients 1, 2
  • Do not assume condom use prevents all STIs—comprehensive anatomic site screening is essential 1, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Truvada PrEP Monitoring Requirements

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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