The recommendation LGK-974 solubility dmso from the Writing Group

is that in constructing an optimized background, continuing/commencing NRTIs may contribute partial ARV activity to a regimen, despite drug resistance [55, 56]. For those drugs with a novel mode of action (integrase and fusion inhibitors, and CCR5 antagonists), the absence of previous exposure indicates susceptibility although MVC is only active against patients harbouring CCR5 tropic virus. For DRV, TPV and ETV, the number and type of mutations inform the degree to which these drugs are active [56-58]. The potential for DDIs is also important. ETV can be paired with DRV/r (but not TPV/r) and MVC dosing is variable depending on the other drugs in the new regimen; however, RAL and enfuvirtide require no alteration. Some patients can have a successfully suppressive fully active three-drug regimen constructed without a PI/r [59]. Nevertheless, where feasible, a PI/r such as DRV/r should be included because of its protective effect on emergent resistance to the other drugs in the regimen although this can be given DRV/r 800 mg/100 mg once

daily in treatment-experienced patients without DRV resistance associated mutations [60]. Enfuvirtide is an option in some patients despite the inconvenience of subcutaneous injection and injection site reactions. With the availability of the newer agents, dual PI/r are not recommended [61]. The same principles Sirolimus supplier Dabrafenib purchase regarding reviewing adherence, tolerability/toxicity issues, DDIs/food interactions, and mental health/drug dependency problems

apply. Additional adherence support is important in these patients as the reason triple-class failure has occurred often relates to past poor adherence. Additionally, the pill burden is increased and careful discussion with the patient should take place. We recommend accessing newer agents through research trials, expanded access and named patient programmes (GPP). We suggest continuing/commencing NRTIs as this may contribute partial ARV activity to a regimen, despite drug resistance (2C). We recommend the use of 3TC or FTC to maintain a mutation at codon position 184 of the RT gene (1B). We recommend against discontinuing or interrupting ART (1B). We recommend against adding a single, fully active ARV because of the risk of further resistance (1D). We recommend against the use of MVC to increase the CD4 cell count in the absence of CCR5 tropic virus (1C). This situation usually occurs following attempts in patients with triple-class failure to achieve virological suppression with the newer agents and often indicates adherence issues have not been addressed successfully or sequential addition of the newer agents has occurred without incomplete viral suppression and selection of resistance to the new drug.