An ongoing dialogue on HIV/AIDS, infectious diseases,
May 19th, 2009
Time for a Switch? Room for Debate
With first-line therapy for HIV being so astonishingly successful, much of what we do in practice is tweak regimens that are by virologic and immunologic standards, working just fine: Viral load undetectable, CD4 stable.
But not so fast — while one of my colleagues said that if he didn’t change his patients’ regimens, then he’d have nothing to do, the other said he NEVER changed a regimen that was working unless he absolutely had to.
Who’s right? Both of them, of course. The regimen might improve in convenience, tolerability, safety, etc, but new side effects could also occur, as well as virologic failure.
So consider these virologically suppressed, clinically stable patients (all recently seen) — would you switch?
- 50 year old man on ABC/3TC, EFV since 2000. No renal disease. Hyperlipidemia, on atorvastatin 80 mg a day. Father died of an MI age 48.
- 63 year old man, on EFV + LPV/r for years; past history of neuropathy on d4T and 3TC. Needs to go on inhaled steroids (preferably fluticasone) to help manage increasingly refractory asthma.
- 35 year old woman, on TDF/FTC, FPV/r BID — doing ok but missing some PM doses.
Keep in mind, all are doing fine — would you switch? If so, to what? Thanks in advance* for the consult.
(*ahem.)
3 Responses to “Time for a Switch? Room for Debate”
Paul E. Sax, MD
Associate Editor
NEJM Clinician
Biography | Disclosures & Summaries
Learn more about HIV and ID Observations.
FROM NEJM — Recent Infectious Disease Articles- The Eyes Have It March 5, 2026A 47-year-old man was brought to the ED by EMS after being found dyspneic in his car. He reported having been drinking for 6 hours before presentation. He noted a sensation of tongue swelling and difficulty breathing.
- Cabotegravir plus Rilpivirine for Persons with HIV and Adherence Challenges February 26, 2026In persons with HIV and barriers to adhering to antiretroviral therapy, a long-acting injectable treatment (monthly cabotegravir plus rilpivirine) resulted in better virologic control than standard oral ART.
- Microbial Flora in War Wounds from the Ukrainian Front Line February 26, 2026Battlefield injuries are often contaminated with potentially infecting microbes. In this study, swabs obtained in the field after injury were profiled. Microbes and potential antimicrobial-resistance genes were characterized.
- Primary Measles Infection February 26, 2026A previously healthy man presented with a 5-day history of fever, nausea, and vomiting and a 2-day history of an itchy rash. Examination showed an exanthem consisting of minute macules and subtly elevated papules.
- From Efficacy to Access in Long-Acting HIV Therapy February 26, 2026Over the past three decades, advances in antiretroviral therapy (ART) have dramatically improved life expectancy, decreased frailty, and improved quality of life for persons with human immunodeficiency virus (HIV).1,2 These gains have accrued primarily among those who can reliably access health care and adhere to daily treatment. For...
- The Eyes Have It March 5, 2026
Assuming no resistance mutations
1. Recommend a switch to tdf/ftc/efv w/ concern for potential for cardiovascular disease (abacavir) and potential for easier dosing w/ daily fixed dose atripla
2. Recommend switch to tdf/ftc/efv again. Not aware of any long term data to support this efv/lpv/r regimen and have concern for possible break through w/ only two drug regimen despite recent success. Doubt tdf/ftc would exacerbate neuropathy. Would avoid ritonavir boosted PI if the inhaled steroids are really needed.
3. Assuming a k103 is the reason for fpv/r would recommend switch to tdf/ftc/Atazanavir/r for ease of daily dosing. Also potential to lose darunavir if resistance occurs to fpv/r. If no k103 then tdf/ftc/efv would be simplest regimen and would potentially eliminate the pm missed doses
CM,
These are all very reasonable (some would say great) recommendations. For the sake of discussion, here are the counter views:
1. He’s over 60, he’s had NO side effects for 9 years on this current regimen, why risk renal/bone issues?
2. Back in the old days, I definitely had pts with bad neuropathy that worsened on 3TC … and it’s known to cause neuropathy in kids.
3. Why risk the EFV CNS side effects, and switching to a new class?
Keep in mind this isn’t necessarily what I believe on these cases … just a countering view.
I’ll let you know what I did in a separate post.
Well, the counter-arguments make some sense, but I would give my listed recommendations to the patients in question, discuss the pros and cons, and make a decision together. Having said that, I would like to get #3 off fpv/r and would feel okay about atazanavir or efv in it’s place.
I look forward to the denouement.