Clinical Manual for Management of the HIV-Infected ... - myCME.com
Clinical Manual for Management of the HIV-Infected ... - myCME.com
Clinical Manual for Management of the HIV-Infected ... - myCME.com
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1–34 | <strong>Clinical</strong> <strong>Manual</strong> <strong>for</strong> <strong>Management</strong> <strong>of</strong> <strong>the</strong> <strong>HIV</strong>-<strong>Infected</strong> Adult/2006<br />
A: Assessment and Plan<br />
Patients with primary <strong>HIV</strong> infection will need<br />
additional medical evaluation, baseline laboratory testing,<br />
and intensive support, counseling, and education about<br />
<strong>HIV</strong> infection. See chapters Initial History, Initial<br />
Physical Examination, and Initial and Interim Laboratory<br />
and O<strong>the</strong>r Tests <strong>for</strong> detailed in<strong>for</strong>mation on <strong>the</strong> initial<br />
evaluation <strong>of</strong> <strong>HIV</strong>-infected patients.<br />
Laboratory<br />
The initial laboratory work should include <strong>the</strong><br />
following:<br />
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The CD4 count and <strong>HIV</strong> viral load should be<br />
checked on 2 occasions within several weeks.<br />
A baseline <strong>HIV</strong> genotype test should be obtained <strong>for</strong><br />
all patients with primary <strong>HIV</strong> infection, even those<br />
who do not choose to start antiretroviral treatment<br />
(ART). In some cities in <strong>the</strong> United States and<br />
Europe, up to 15-20% <strong>of</strong> individuals infected in<br />
recent years have acquired <strong>HIV</strong> virus strains with<br />
mutations that confer resistance to antiretroviral<br />
medications. These resistance mutations may be<br />
identified by early resistance testing, but later may<br />
not be detectable. (See chapter Resistance Testing.)<br />
The <strong>HIV</strong> antibody test should be repeated in 4-6<br />
weeks to document <strong>the</strong> <strong>HIV</strong> status <strong>of</strong> patients who<br />
are presumed to have primary <strong>HIV</strong> infection.<br />
Treatment<br />
It is reasonable to consider starting <strong>com</strong>bination ART in<br />
patients with acute <strong>HIV</strong> infection, because some limited<br />
evidence suggests that treatment initiated during primary<br />
<strong>HIV</strong> infection may preserve <strong>HIV</strong>-specific immune<br />
function that would o<strong>the</strong>rwise be lost as <strong>the</strong> infection<br />
progresses. However, it is not yet clear whe<strong>the</strong>r initiating<br />
early treatment yields long-term immunologic, virologic,<br />
or clinical benefits. The potential advantages <strong>of</strong> ART <strong>for</strong><br />
primary infection must be weighed against <strong>the</strong> possibility<br />
<strong>of</strong> short- and long-term toxicities, <strong>the</strong> possibility <strong>of</strong><br />
developing drug resistance, and <strong>the</strong> adherence challenges<br />
associated with starting antiretrovirals quickly in newly<br />
diagnosed patients. These issues are <strong>com</strong>plex, and consultation<br />
with an <strong>HIV</strong> expert or referral to a clinical trial is<br />
re<strong>com</strong>mended.<br />
For patients who choose to start <strong>the</strong>rapy during<br />
primary <strong>HIV</strong> infection, <strong>the</strong> choice <strong>of</strong> agents and <strong>the</strong><br />
monitoring <strong>of</strong> patients on treatment are similar to those<br />
in <strong>the</strong> treatment <strong>of</strong> chronic <strong>HIV</strong> infection (see chapter<br />
Antiretroviral Therapy). The initial goal <strong>of</strong> <strong>the</strong>rapy in<br />
primary <strong>HIV</strong> infection is to suppress <strong>the</strong> <strong>HIV</strong> viral load<br />
to undetectable levels.<br />
<strong>Clinical</strong> trials across <strong>the</strong> country currently are recruiting<br />
individuals to evaluate both <strong>the</strong> natural history <strong>of</strong><br />
primary <strong>HIV</strong> infection and <strong>the</strong> possible benefits <strong>of</strong><br />
treatment <strong>of</strong> acute <strong>HIV</strong> infection. In<strong>for</strong>mation on<br />
clinical studies <strong>of</strong> primary <strong>HIV</strong> may be obtained<br />
through <strong>the</strong> AIDS <strong>Clinical</strong> Trials In<strong>for</strong>mation Service<br />
(ACTIS) on its Web site at http://www.aidsinfo.nih.<br />
gov/clinicaltrials or by telephone at 800-<strong>HIV</strong>-0440.<br />
Issues concerning <strong>the</strong> possible treatment <strong>of</strong> primary<br />
<strong>HIV</strong> infection also are reviewed in <strong>the</strong> U.S. Department<br />
<strong>of</strong> Health and Human Services Guidelines <strong>for</strong> <strong>the</strong> Use<br />
<strong>of</strong> Antiretroviral Agents in <strong>HIV</strong>-1-<strong>Infected</strong> Adults and<br />
Adolescents.<br />
Patient Education<br />
Patients with primary <strong>HIV</strong> infection need support and<br />
counseling, as do all newly diagnosed patients. Intensive<br />
education about <strong>HIV</strong> infection, <strong>the</strong> course <strong>of</strong> disease,<br />
prognosis, and <strong>the</strong> risks and benefits <strong>of</strong> ART must<br />
be undertaken. Counseling about safer sex and drug<br />
injection techniques, as indicated, is especially important<br />
<strong>for</strong> <strong>the</strong>se patients because <strong>the</strong>y may have ongoing highrisk<br />
behaviors <strong>for</strong> <strong>HIV</strong> transmission and because <strong>the</strong>y<br />
may be highly infectious during <strong>the</strong> primary infection<br />
period. (See chapter Preventing <strong>HIV</strong> Transmission /<br />
Prevention with Positives <strong>for</strong> more in<strong>for</strong>mation about<br />
patient support and counseling in <strong>the</strong>se areas.)<br />
References<br />
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Daar ES, Little, S, et al. Diagnosis <strong>of</strong> primary <strong>HIV</strong>-<br />
1 infection. Los Angeles County Primary <strong>HIV</strong><br />
Infection Recruitment Network. Ann Intern Med.<br />
2001 Jan 2;134(1):25-9.<br />
Schacker T, Collier AC, Hughes J, et al. <strong>Clinical</strong> and<br />
epidemiologic features <strong>of</strong> primary <strong>HIV</strong> infection. Ann<br />
Intern Med. 1996 Aug 15;125(4):257-64.<br />
Smith DE, Walker BD, Cooper DA, et al. Is<br />
antiretroviral treatment <strong>of</strong> primary <strong>HIV</strong> infection<br />
clinically justified on <strong>the</strong> basis <strong>of</strong> current evidence?<br />
AIDS. 2004 Mar 26;18(5):709-18.<br />
U.S. Department <strong>of</strong> Health and Human Services.<br />
Guidelines <strong>for</strong> <strong>the</strong> Use <strong>of</strong> Antiretroviral Agents in <strong>HIV</strong>-<br />
1-<strong>Infected</strong> Adults and Adolescents. October 10, 2006.<br />
Available online at aidsinfo.nih.gov/Guidelines/<br />
GuidelineDetail.aspx?GuidelineID=7. Accessed July<br />
7, 2007.