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optimalanddurablevirologicefficacy,favorabletolerabilityandtoxicityprofiles,andeaseofuse.
            “Alternativeregimens”arethoseregimensthatareeffectivebuthavepotentialdisadvantageswhen
            comparedwithpreferredregimens.Incertainsituationsandbasedonindividualpatientcharacteristicsand
            needs,aregimenlistedasanalternativemayactuallybethepreferredregimenforaspecificpatient.
            Comparedwithpreferredoralternativeregimens,someregimensareclassifiedas“acceptableregimens”
            becauseofreducedvirologicactivity,lackofefficacydatafromlargeclinicaltrials,orotherfactors(suchas
            greatertoxicities,pillburden,druginteractionpotential,orneedforadditionaltesting).

            Lastly,thePanelclassifiedsomeregimensas“regimensthatareacceptablebutshouldbeusedwithcaution”
            becauseofcertainsafetyorefficacyconcernsexplainedinTable5b.

            Factors to Consider When Selecting an Initial Regimen

            Regimenselectionshouldbeindividualizedonthebasisofanumberoffactors,includingthefollowing:

            •  comorbidconditions(e.g.,cardiovasculardisease[CVD],chemicaldependency,liverdisease,psychiatric
               disease,renaldiseases,ortuberculosis[TB]);
            •  potentialadversedrugeffects;
            •  potentialdruginteractionswithothermedications;
            •  pregnancyorpregnancypotential;
            •  resultofgenotypicdrug-resistancetesting;

            •  genderandpretreatmentCD4countifconsideringnevirapine(NVP);
            •  HLA-B*5701testingifconsideringabacavir(ABC);
            •  coreceptortropismassayifconsideringmaraviroc(MVC);
            •  patientadherencepotential;and
            •  convenience(e.g.,pillburden,dosingfrequency,andfoodandfluidconsiderations).

            Considerations for Therapies

            AppendixB,Tables1–6 providealistingofcharacteristics,suchasformulations,dosingrecommendations,
            pharmacokinetics(PKs),andcommonadverseeffects,ofindividualARVagents.Additionally,AppendixB,
            Table7 providesclinicianswithARVdosingrecommendationsforpatientswhohaverenalorhepatic
            insufficiency.

            AninitialARVregimengenerallyconsistsoftwoNRTIsincombinationwithanNNRTI,aPI(preferably
            boostedwithritonavir[RTV]),anINSTI(namelyraltegravir[RAL]),oraCCR5antagonist(namelyMVC).
            Inclinicaltrials,NNRTI-,PI-,INSTI-,orCCR5antagonist-basedregimenshaveallresultedinHIVRNA
            decreasesandCD4cellincreasesinalargemajorityofpatients. 1-7
            Tables5aand5b includethePanel’srecommendationsforinitialtherapy.



















            Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents          F-2

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