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2014 IAS-USA Treatment Guidelines 2014 IAS-USA Treatment Guidelines

2014 IAS-USA Treatment Guidelines - PowerPoint Presentation

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2014 IAS-USA Treatment Guidelines - PPT Presentation

Brian R Wood MD Medical Director NW AETC ECHO Assistant Professor of Medicine University of Washington Presentation prepared by Presenter Last Updated 101614 International Antiviral SocietyUSA Guidelines ID: 760191

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Slide1

2014 IAS-USA Treatment Guidelines

Brian R. Wood, MDMedical Director, NW AETC ECHOAssistant Professor of Medicine, University of Washington

Presentation prepared by:

Presenter

Last Updated:

10/16/14

Slide2

International Antiviral Society-USA Guidelines Updated July 2014

Prevention Guidelines – Dr. Marrazzo will discuss 11/6/14Treatment Guidelines

Slide3

Rating Scale

Strength of Recommendations:

A: Strong support

B: Moderate support

C: Limited support

Quality of Evidence:

I

a:

>

1 RCTs published in peer-reviewed literature

Ib:

>

1 RCTs presented at peer-reviewed scientific meetings

IIa: non-RCT’s, cohort, or case-control studies published

IIb: non-RCT’s, cohort, or case-control studies presented

III: panel’s analysis of accumulated available evidence

Slide4

When to Start

Slide5

What to Start: Recommended Initial Regimens

Anchor

BackboneCommentsDolutegravirTenofovir-emtricitabineMay increase serum creatinineDolutegravir^Abacavir-lamivudineAbacavir not inferior to tenofovir at high HIV RNA levels if given with dolutegravirElvitegravir/cobicistat^Tenofovir-emtricitabineMay increase serum creatinine; similar drug interactions as ritonavirRaltegravirTenofovir-emtricitabineRaltegravir twice dailyEfavirenz^Tenofovir-emtricitabineCNS/psych SE’s; no longer contraindicated in pregnancy but avoid in woman of child-bearing potentialEfavirenzAbacavir-lamivudineSame as aboveRilpivirine^Tenofovir-emtricitabineAvoid if HIV RNA >100,000 copies or on PPI; taken with full mealAtazanavir/ritonavirTenofovir-emtricitabineMay cause cholelithiasis/nephrolithiasis; consider H2 blocker/PPI interactionsDarunavir/ritonavirTenofovir-emtricitabineOnce-daily dosing for initial therapy

^

Single tablet regimen (STR) option

Slide6

Additional Considerations

Tenofovir: Potential for renal and bone toxicityAbacavir:Associated with cardiovascular events, though data conflictingHLA-B*5701 must be negativeAbacavir/lamivudine:Less efficacious than tenofovir/emtricitabine when given with efavirenz or boosted atazanavir if baseline HIV RNA >100,000

Slide7

What to Start: Alternatives

Anchor

Backbone

Comments

Raltegravir

Abacavir-lamivudine

Abacavir not inferior to tenofovir at high HIV RNA levels if given with raltegravir

Nevirapine

2 NRTI’s

Severe hepatotoxicity may occur if CD4 >250 in women

or >400 in men; more severe rash than other NNRTI’s

Rilpivirine

Abacavir-lamivudine

Not recommended if HIV RNA

>100,000 copies

Atazanavir-cobicistat

2 NRTI’s

Atazanavir

levels equivalent with cobicistat or ritonavir

Darunavir-cobicistat

2 NRTI’s

Darunavir levels equivalent with cobicistat or ritonavir

Lopinavir-ritonavir

2 NRTI’s

May be less tolerable and have increased CV

toxicity

Darunavir-ritonavir

Abacavir-lamivudine

Single randomized study available

Darunavir-ritonavir

Raltegravir

Inferior if CD4 <200 or

HIV RNA >100,000

copies

Lopinavir-ritonavir

Raltegravir

Single study

available with significant limitations

Lopinavir-ritonavir

Lamivudine

Single study available with significant limitations

Slide8

Estimated Patent Expiration Dates for Branded Antiretrovirals

Year

Antiretrovirals

2012

Zidovudine, lamivudine, stavudine, didanosine, saquinavir, nevirapine

2013

Ritonavir, efavirenz, zidovudine/lamivudine

2016

Abacavir, lopinavir/ritonavir (softgel)

2017

Tenofovir,

ata

zanavir, darunavir

2019

Etravirine, abacavir/lamivudine

2024

Tenofovir/emtricitabine

2025

Raltegravir

2026

Tenofovir/emtricitabine/efavirenz,

tenofovir/emtricitabine/rilpivirine, dolutegravir

Slide9

Initiating ART in Special Circumstances

Slide10

Initiating in Setting of an Acute OI or Tuberculosis

Slide11

ART Monitoring

“There are

insufficient data

to make general recommendations

for

the management of

patients with sustained viremia of 50 to 200 copies

/mL.”