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Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

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Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010
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Page 1: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Mary Lawrence Hicks, FNP

Positive Health Program

October 21, 2010

Page 2: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

What is your field?

1 2 3 4

25% 25%25%25%

1. Family Medicine

2. General Medicine

3. HIV/AIDS

4. Midwifery/gynecology

Page 3: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

I see HIV+ patients in my practice?

Yes No

50%50%

1. Yes

2. No

Page 4: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Historical Perspectives: the 80’s Average lifespan from time of diagnosis:

18 months AZT licensed March 1987 as

monotherapeutic agent Goals of therapy: prevent opportunistic

infections; improve quality of life with decreased symptomatology

Page 5: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Course of HIV Infection

Page 6: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Historical Perspectives: the 00’s Delay ARV start until CD4 350 or below Resistance: save ARVs ‘til you really

need them (resistance assays available) Restoration of immune function

demonstrated Why subject healthy person to SEs?

Page 7: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Historical Perspectives: the 90’s Early 90’s: serial monotherapy Mid 90’s: Protease Inhibitors usher in

the HAART (Highly Active Antiretroviral Therapy) Era

Hit Early Hit Hard: begin ARVs when CD4 count drops below 500

Lost immune function can’t be recovered Viral load testing becomes available

Page 8: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

2010 December 1, 2009 new DHHS Guidelines

recommend ARV start with CD4 of 500* Rationale: Inflammation caused by

unsuppressed virus damaging to cardiac, brain, liver and renal tissue

Other considerations: new classes and new agents give more options if resistance develops

*SFDPH recommends ARVs @ any CD4 count

Page 9: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Guidelines for the Use of AntiretroviralAgents in HIV-1-Infected Adults and Adolescents

December 1, 2009

Developed by the DHHS Panel on Antiretroviral Guidelines for Adults and Adolescents – A

Working Group of the Office of AIDS Research Advisory Council (OARAC)

Page 10: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Initiation of Antiretroviral Therapy

• ART should be initiated: history of an AIDS-defining illness or with CD4 count < 350 cells.

• Initiate ART, any CD4 count: pregnancy, HIV-associated nephropathy, and HBV co-infection when treatment of HBV is indicated.

• ART recommended CD4 counts 350 - 500 cells. The panel was divided: 55% of panel members for strong recommendation (A) and 45% for moderate recommendation

• For patients with >500 CD4 cells, 50% of panel members favor starting antiretroviral therapy ; the other 50% of members view treatment as optional in this setting

Page 11: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

500 500

350

Page 12: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Case Study

35 yo male diagnosed 1 year ago

CD4 498; VL 78,000

Pt ambivalent re ARV start

Page 13: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

What would you recommend?

1 2 3

33% 33%33%1. Experts must know what they’re talking about; start ARVs

2. CD4 is high; pt is ambivalent; slow down and assess pt readiness.

3. Why use ARVs; HIV doesn’t cause AIDS

Page 14: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

Panel members favoring earlier initiation of therapy base their recommendation on several recent developments

(1) a recent cohort study demonstrating survival benefit with initiation of antiretroviral therapy at CD4 count >500

(2) untreated HIV infection associated with development of non-AIDS-defining diseases: cardiovascular disease, kidney disease, liver disease, and malignancy

(3) availability of more effective, more convenient, and better tolerated ARVs

(4) increasing evidence that effective ARV therapy reduces HIV transmission

Page 15: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

NA-ACCORD Study Two analyses: 17,517 asx ARV naïve HIV+ pts

receiving care 1996-2005 in US & Canada

1st analysis: 8362 pts. 2084 (25%) started ART @ CD4 351-500; 6278 (75%) deferred ART. After adjusting for multiple variables, deferring group found to have 69% higher risk of death.

2nd analysis: 9155 pts. 2220 (24%) started ART @ CD4 > 500; 6935 (76%) deferred ART. Among deferred-therapy group, increased risk of death was 94%

Kitahata et al. Effect of Early versus Deferred Antiretroviral Therapy for HIV on Survival. N Eng J Med 2009; 360: 1815-1826

Page 16: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

The SMART Study Multinational trial: 5472 pts with CD4

>350 Pts randomized into continuous ART vs.

episodic TX interruption guided by CD4 count.

Study enrollment halted 2o TX interruption group had incr risk AIDS and non-AIDS related events (CV, liver and kidney diseases).

The New England Journal of Medicine; November 30, 2006. Vol. 355 No. 22

Page 17: Mary Lawrence Hicks, FNP Positive Health Program October 21, 2010.

City Endorses New Policy for Treatment of H.I.V.By SABIN RUSSELL, NY TimesPublished: April 3, 2010

San Francisco public health doctors have begun to advise patients to start taking antiviral medicines as soon as they are found to be infected, rather than waiting ……..

“It’s just too risky,” said Dr. Jay Levy, the U.C.S.F. virologist ……

Dr. Capaldini recognizes that today’s drugs are a vast improvement ..“is not ready for prime time.”

‘ living in happy symbiosis with this virus is delusional,” Dr. Follansbee


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