Treatment
Treatment
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Introduction to combination therapy - June 2008
Although UK guidelines recommend starting with an NNRTI-based combination, PI-based combinations can be just as good at getting your viral load to undetectable.
PI regimens can be less vulnerable to resistance. Some people start on a PI regimen and then switch to an NNRTI regimen that requires fewer pills later.
UK guidelines only recommend using ritonavir-boosted PIs.
Lopinavir/r (Kaletra) is the most widely used PI.
Fosamprenavir/r is an alternative to Kaletra that is used less frequently.
Atazanavir/r is a once-daily PI. It is not approved in Europe for first-time therapy, but is still used widely for this. Atazanavir/r is recommended if you want to switch drugs because of side effects. The daily dose is 300mg, boosted by 100mg of ritonavir.
If this dose causes side-effects, the ritonavir can sometimes be stopped and a slightly higher atazanavir dose (400mg) used instead. A recent study suggested you get better drug levels with unboosted atazanavir by taking 200mg twice-daily.
Unboosted atazanavir should not be used in a combination that includes tenofovir.
Darunavir/r is a PI used for secondline PI therapy. However, a recent study showed that darunavir achieved better results compared to Kaletra in people using treatment for the first time. Guidelines may therefore recommend darunavir for first-line treatment in the future.
Saquinavir/r is an alternative to Kaletra that is used less frequently.
Tipranavir/r is a PI that is only used by people with PI-resistance.
Nelfinavir is not recommended in UK guidelines for first-line therapy but it is sometimes chosen as the third drug if someone cannot tolerate ritonavir or for use during pregnancy.
This is the web edition of the i-Base guide Introduction to
combination therapy. This guide is available in UK clinics.
Decisions relating to your treatment should always be taken in consultation with your doctor. Information in this guide is intended to support those discussions.
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