Meg Sullivan, MD Section of Infectious Disease.  L.M. is a 26-year old man who has sex with men  Last unprotected sexual contact 3 weeks ago  He presents.

Slides:



Advertisements
Similar presentations
Diagnosis and Management of Acute HIV Infection HIV Clinical Guidelines from the New York State Department of Health AIDS Institute January 2010 HIV CLINICAL.
Advertisements

Acute Retroviral Syndrome
David H. Spach, MD Professor of Medicine Division of Infectious Diseases University of Washington, Seattle.
Myron S. Cohen, MD Protocol Chair 6 th IAS Conference, Rome, Italy July 18, 2011 HPTN 052.
Monica Gandhi MD, MPH Associate Professor and Women’s HIV Clinic provider, HIV/AIDS Division San Francisco General Hospital/ UCSF Safe Poz Love, U.S. Positive.
Improving Retention, Adherence, and Psychosocial Support within PMTCT Services: Implementation Workshop for Health Workers All slide illustrations by Petra.
Changing Therapy Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents published October 2006 AETC NRC Slide Set.
Initiating Antiretroviral Therapy in Treatment-Naive Patients Charles B. Hicks, MD Associate Professor of Medicine, Division of Infectious Diseases and.
 After completing this session the participant should be able to:  Discuss the goals of HIV treatment.  Understand when resistance testing should be.
HIV in Texas: The Ways Forward Ann Robbins Manager of HIV/STD Prevention and Care Department of State Health Services.
Dr. Laura Guay Vice President for Research Elizabeth Glaser Pediatric AIDS Foundation J2J Global Media Training on HIV/AIDS July 14, 2010 Vienna, Austria.
BVCOG HRSA/HAB Tier 2 and 3 Performance Measures Lisa Cornelius, MD, MPH July 2010.
1 The START Trial: On the Shoulders of SMART 5 years after SMART INSIGHT Satellite Session WAC, Washington DC, July 2012.
Slide 1 of 11 From CB Hicks, MD, at Chicago, IL: May 20, 2013, IAS-USA. IAS–USA Charles B. Hicks, MD Professor of Medicine Duke University Medical Center.
WHO Guidelines for treatment monitoring Nathan Ford Dept of HIV/AIDS World Health Organization.
Critical issues for Adults with HIV: Presentation of Systematic reviews and Main recommendations WHO 2013 ARV Guidelines Launch Dr. Meg Doherty, WHO, Geneva.
Comprehensive Guideline Summary Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents December 2009 AETC NRC Slide Set.
N ORTHWEST A IDS E DUCATION AND T RAINING C ENTER 2014 IAS-USA Treatment Guidelines Brian R. Wood, MD Medical Director, NW AETC ECHO Assistant Professor.
Are people living with HIV less likely to pass HIV to others if they are on treatment? Exploring the use of treatment as prevention James Wilton Project.
HIV Early Treatment Project Groups 1 and 2 n Among HIV-infected participants in sub-Saharan Africa, does initiation of antiretroviral treatment (ART) at.
Validating five questions of antiretroviral non-adherence in a decentralized public-sector antiretroviral treatment program in rural South Africa Krisda.
October E-learn Call: Visual Design for Powerful Presentations Sophy Wong (East Bay AETC)
HIV opportunistic infections and HIV treatment Sabrina Assoumou, MD Section of Infectious Diseases.
1 Treatment Failure HAIVN Harvard Medical School AIDS Initiative in Vietnam.
IAS–USA When to Start Antiretroviral Therapy Constance A. Benson, MD Professor of Medicine University of California San Diego FINAL: Presented.
1 First Clinic Visit for Patients with HIV Infection HAIVN Harvard Medical School AIDS Initiative in Vietnam.
Background There is uncertainty regarding the frequency, predictors, and outcomes of IRIS events Prior studies on IRIS have been limited to convenience.
Management of the Treatment-Experienced Patient Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents December 2009 AETC NRC Slide.
2009 Recommendations for Antiretroviral Therapy in Adults and Adolescents Summary of WHO Rapid Advice December 2009 Source: WHO HIV/AIDS Department.
When to Initiate ART in Adults and Adolescents (2009 WHO Guidelines) Target PopulationClinical conditionRecommendation Asymptomatic Individuals (including.
Transition Program of HIV-infected adolescents to Adult HIV care in Buenos Aires, Argentina S. Arazi Caillaud 1, D. Mecikovsky 1, A.Bordato.
Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection DR. S.K CHATURVEDI DR. KANUPRIYA CHATURVEDI.
1 Starting ART in the Context of Opportunistic Infections HAIVN Harvard Medical School AIDS Initiative in Vietnam.
Office of Overseas Programming & Training Support (OPATS) Treatment Adherence HIV Care, Support, and Treatment.
HIV i-Base: SMART Study & CROI Feedback UK-CAB - Feb 2006 UK-CAB 24 February 2006 CROI Feedback: SMART Study Simon Collins.
Guidelines for the use of antiretroviral agents in HIV infections in Taiwan, revised in 2002 by Infectious Diseases Society of the ROC and Taiwan AIDS.
BHIVA Clinical Audit Management of patients who switch therapy; re-audit of patients starting therapy from naïve.
I. Jean Davis, PhD, PA, AAHIVS Manager - Clinical Services Desert AIDS Project.
1 Introduction to ARV Therapy HAIVN Harvard Medical School AIDS Initiative in Vietnam.
Implementation of HIV Treatment as Prevention in China Yan Zhao MD National Center for AIDS/STD Control & Prevention Chinese Center for Disease Control.
Immigration Removal Centres and HIV Clinical Care Jane Anderson Homerton University Hospital NHS Foundation Trust.
HIV-infected subjects with CD4 350 to 550 cells/mm serodiscordant couples HPTN 052 Study Design Immediate ART CD Delayed ART CD4
Prevention of Mother to Child HIV Transmission Dr. Laura Guay Vice President for Research Elizabeth Glaser Pediatric AIDS Foundation July 15, 2009 Cape.
ART: When to Start? – Case Discussion Roy M. Gulick, MD, MPH Professor of Medicine Chief, Division of Infectious Diseases Weill Medical College of Cornell.
ANTEPARTUM CARE. Pregnant Women Who Are ARV Naive (1)  Pregnant women with HIV infection should receive standard clinical, immunologic, and virologic.
Providing Treatment, Restoring Hope Secondary Prevention as part of HIV Clinical Care Martine Etienne, MPH, DrPH University of Maryland School of Medicine.
Module 3: Management of Patients on Antiretroviral Therapy Unit 2: Initiation and Monitoring of ART in Adults and Adolescents.
Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.
SPECIAL CONSIDERATIONS August
Prophylaxis of Opportunistic Infections
WORLD AIDS DAY Zero new HIV infections Zero discrimination Zero AIDS-related deaths.
PRECONCEPTION COUNSELING AND CARE FOR HIV-INFECTED WOMEN OF CHILDBEARING AGE.
1 Adherence to ARV Therapy and Resistance HAIVN Havard Medical School AIDS Initiative in Vietnam.
Strategies for Management of Antiretroviral Therapy Study Wafaa El-Sadr and James Neaton for the SMART Study Team.
Treatment Failure HAIVN Harvard Medical School AIDS Initiative in Vietnam.
N ORTHWEST A IDS E DUCATION AND T RAINING C ENTER Major Changes to the HHS Adult and Adolescent HIV Treatment Guidelines: April 2015 Brian R. Wood, MD.
Kimberly Y. Smith, MD, MPH Associate Professor of Medicine Division of Infectious Diseases Rush University Medical Center Chicago, Illinois Putting the.
Response to Antiretroviral Treatment In an Ethiopian Hospital Samuel Hailemariam, MD, MPH; J Allen McCutchan, MD, MSc Meaza Demissie, MD, PMH, PHD; Alemayehu.
HAART Initiation Within 2 Weeks of Seroconversion Associated With Virologic and Immunologic Benefits Slideset on: Hecht FM, Wang L, Collier A, et al. A.
1 Chapter 35 HIV- and AIDS-Related Drugs Copyright © 2015, 2012, 2009, 2006, 2003, 2000, 1997, 1993 by Saunders, an imprint of Elsevier Inc.
Switch to PI/r monotherapy
TREATMENT OF HIV.
2017 Key Considerations for adolescents and children & Key populations
Comprehensive Guideline Summary
Pharmacokinetics: HIV Drugs
What’s New in the Perinatal Guidelines
When to START During an OI
Diagnosis and Management of Acute HIV
HIV.
Undetectable = Untransmittable
Presentation transcript:

Meg Sullivan, MD Section of Infectious Disease

 L.M. is a 26-year old man who has sex with men  Last unprotected sexual contact 3 weeks ago  He presents with a 1 week history of fever, rash, headache, sore throat, and diarrhea  HIV EIA reactive, HIV Western blot indeterminate, HIV RNA > 10 million copies/ml; CD4+ lymphocyte count 880/ml February 2013www.aidsetc.org2

 C.A. is a 56-year-old Haitian woman  Presented to PCP with dysphagia  EGD demonstrated esophageal candidiasis  HIV EIA and WB reactive  CD4+ lymphocyte count 7/ml February 2013www.aidsetc.org3

 N.C. is a 35-year-old homeless man  No regular shelter use  Recent IV heroin relapse  HIV test performed by OBOT provider  HIV EIA and WB reactive  CD+ lymphocyte count 418/ml February 2013www.aidsetc.org4

 For which of these patients is antiretroviral therapy indicated?  What benefit would accrue to each?  For which might ART be postponed? Why? February 2013www.aidsetc.org5

February 2013www.aidsetc.org6 Developed by the Department of Health and Human Services (DHHS) Panel on Antiretroviral Guidelines for Adults and Adolescents – A Working Group of the Office of AIDS Research Advisory Council (OARAC)

 Reduce HIV-related morbidity; prolong duration and quality of survival  Restore and/or preserve immunologic function  Maximally and durably suppress HIV viral load  Prevent HIV transmission February 2013www.aidsetc.org7

 Effective ART with virologic suppression improves and preserves immune function, regardless of baseline CD4 count ◦ Earlier ART may result in better immunologic responses and clinical outcomes  Reduction in AIDS- and non-AIDS-associated morbidity and mortality  Reduction in HIV-associated inflammation and associated complications  ART can significantly reduce risk of HIV transmission- ”Treatment as Prevention”  Recommended ARV combinations are effective and well tolerated February 2013www.aidsetc.org8

 Exact CD4 count at which to initiate therapy not known, but evidence points to starting at higher counts  Current recommendation: ART for all February 2013www.aidsetc.org9

ART is recommended for treatment:  “ART is recommended for all HIV- infected individuals to reduce the risk of disease progression.” ◦ The strength of this recommendation varies on the basis of pretreatment CD4 count (stronger at lower CD4 levels) February 2013www.aidsetc.org10

 Strength of recommendation: ◦ A: Strong ◦ B: Moderate ◦ C: Optional  Quality of evidence: ◦ I: ≥1 randomized controlled trials ◦ II: ≥1 well-designed nonrandomized trials or observational cohort studies with long-term clinical outcomes ◦ III: Expert opinion February 2013www.aidsetc.org11

 Recommended for all CD4 counts:  CD4 count <350 cells/µL (AI)  CD4 count cells/µL (AII)  CD4 count >500 cells/µL (BIII) February www.aidsetc.org

 CD4 count  350 cells/µL or history of AIDS- defining illness: ◦ Randomized control trial (RCT) data show decreased morbidity and mortality with ART  CD4 count cells/µL: ◦ RCT data as well as nonrandomized trials and cohort data support morbidity and perhaps mortality benefit of ART February 2013www.aidsetc.org13

 CD4 count >500 cells/µL ◦ Cohort study data are not consistent; some show survival benefit if ART initiated ◦ Other considerations (eg, potential benefit of ART on non-AIDS complications, HIV transmission risk) support recommendation for ART February 2013www.aidsetc.org14

◦ Untreated HIV may be associated with development of AIDS and non-AIDS- defining conditions  Earlier ART may prevent HIV-related end- organ damage; deferred ART may not reliably repair damage acquired earlier ◦ Increasing evidence of direct HIV effects on various end organs and indirect effects via HIV- associated inflammation ◦ End-organ damage occurs at all stages of infection February 2013www.aidsetc.org15

 Potential decrease in risk of many complications, including: ◦ HIV-associated nephropathy ◦ Liver disease progression from hepatitis B or C ◦ Cardiovascular disease ◦ Malignancies (AIDS defining and non-AIDS defining) ◦ Neurocognitive decline ◦ Blunted immunological response owing to ART initiation at older age ◦ Persistent T-cell activation and inflammation February 2013www.aidsetc.org16

 Pregnancy  AIDS-defining condition  Acute opportunistic infection  Lower CD4 count (eg, <200 cells/µL)  Acute/recent infection  Rapid decline in CD4  Higher viral load (eg, >100,000 copies/mL)  HIVAN  HBV coinfection  HCV coinfection February 2013www.aidsetc.org17

 ARV-related toxicities  Nonadherence to ART  Drug resistance  Cost February 2013www.aidsetc.org18

ART is recommended for Prevention:  “ART also is recommended for HIV- infected individuals for the prevention of transmission of HIV.”  “Treatment as Prevention” February 2013www.aidsetc.org19

Stable, healthy, serodiscordant couples, sexually active CD4+ count: 350 to 550 cells/mm 3 Primary Transmission Endpoint Virologically-linked transmission events Primary Clinical Endpoint WHO stage 4 clinical events, pulmonary tuberculosis, severe bacterial infection and/or death HPTN 052 Study Design Immediate ART CD Delayed ART CD4 <250 Randomization

Total HIV-1 Transmission Events: 39 HPTN 052: HIV-1 Transmission Breakdown Linked Transmissions: 28 Unlinked or TBD Transmissions: 11 (p < 0.001) 96% efficacy Immediat e Arm: 1 Delayed Arm: 27 23/28 (82%) transmissions in sub-Saharan Africa 18/28 (64%) transmissions from female to male partners

 Perinatal transmission  Recommended for all HIV-infected pregnant women (AI)  Sexual transmission  Recommended for all who are at risk of transmitting HIV to sexual partners (AI for heterosexuals, AIII for other transmission risk groups) February www.aidsetc.org

 Young MSM  Acute HIV infection  CD4 count preserved  Very high viral load  Should we treat him?  Why? February 2013www.aidsetc.org23

 Preservation of CD4 count in normal range  ? Prevention of CV risk, HAND, malignancy  ? Prevention of transmission ◦ High viral load associated with increased infectiousness ◦ Prevention by ART not as well established for MSM as for heterosexual couples February 2013www.aidsetc.org24

 “Patients starting ART should be willing and able to commit to treatment and should understand the benefits and risks of therapy and the importance of adherence.”  Patients may choose to postpone ART  Providers may elect to defer ART, based on an individual patient’s clinical or psychosocial factors February www.aidsetc.org

February 2013www.aidsetc.org26

 Clinical or personal factors may support deferral of ART ◦ If CD4 count is low, deferral should be considered only in unusual situations, and with close follow-up  When there are significant barriers to adherence  If comorbidities complicate or prohibit ART  “Elite controllers” and long-term nonprogressors February 2013www.aidsetc.org27

 A major determinant of degree and duration of viral suppression  Poor adherence associated with virologic failure  Optimal suppression requires 90-95% adherence  Suboptimal adherence is common 10/06

 Regimen complexity and pill burden  Poor clinician-patient relationship  Active drug use or alcoholism  Unstable housing  Mental illness (especially depression)  Lack of patient education  Medication adverse effects  Fear of medication adverse effects 10/06

 Age, race, sex, educational level, socioeconomic status, and a past history of alcoholism or drug use do NOT reliably predict suboptimal adherence.  Higher SES and education levels and lack of history of drug use do NOT reliably predict optimal adherence. 10/06

 Emotional and practical supports  Convenience of regimen  Understanding of the importance of adherence  Belief in efficacy of medications  Feeling comfortable taking medications in front of others  Keeping clinic appointments  Severity of symptoms or illness 10/06

 Establish readiness to start therapy  Provide education on medication dosing  Review potential side effects  Anticipate and treat side effects  Utilize educational aids including pictures, pillboxes, and calendars 10/06

 Simplify regimens, dosing, and food requirements  Engage family, friends  Utilize team approach with nurses, pharmacists, and peer counselors  Provide accessible, trusting health care team 10/06

 Older Haitian woman with OI  CD4 very low  Should we treat her?  Why? February 2013www.aidsetc.org34

 Immunologic recovery ◦ Likely somewhat blunted secondary to AIDS and low nadir count  Decreased risk for further OI  Decreased AIDS-related mortality  Except for tuberculous and cryptococcal meningitis, early ART reduces M/M especially if CD4 <50 February 2013www.aidsetc.org35

 Young middle-aged homeless man  Irregular housing  Recent IDU relapse  CD4 low, but > 350  Should we treat him?  Why? February 2013www.aidsetc.org36

 Benefits ◦ Decreased HIV morbidity ◦ ? Decreased mortality  But NC is at high risk for nonadherence  How can we help him with that? February 2013www.aidsetc.org37

February 2013www.aidsetc.org38

 Allows effective, durable viral suppression  3 standard combinations ◦ 2 NRTI + 1 NNRTI ◦ 2 NRTI+ 1 PI ◦ 2 NRTI+ 1 II February 2013www.aidsetc.org39

 Preferred ◦ Randomized controlled trials show optimal efficacy and durability ◦ Favorable tolerability and toxicity profiles  Alternative ◦ Effective but have potential disadvantages ◦ May be the preferred regimen for individual patients  Other ◦ May be selected for some patients but are less satisfactory than preferred or alternative regimens February 2013www.aidsetc.org40

 TDF/FTC preferred ◦ What coinfection is also treated by this combination? ◦ What cormorbidities might make this combination a suboptimal choice?  ABC/3TC alternative ◦ What test should be performed prior to using abacavir? Why? February 2013www.aidsetc.org41

 EFV preferred ◦ In what population should EFV NOT be used?  RPV alternative ◦ Is RPV an optimal choice if VL > 100K? ◦ What class of drugs is contraindicated in combination with RPV? February 2013www.aidsetc.org42

 ATV/r and DRV/r preferred ◦ What drug class must be used with caution in combination with ATV?  FPV/r and LPV/r alternative  Which comorbidities might make PI a suboptimal choice?  What drug classes interact with PIs? February 2013www.aidsetc.org43

 RAL preferred  EVG alternative ◦ What comorbidity contraindicates EVG? February 2013www.aidsetc.org44

  February 2013www.aidsetc.org45