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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3–2 | <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 />
O: Objective<br />
Per<strong>for</strong>m <strong>the</strong> following objective tests:<br />
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Complete physical examination (see chapter Initial<br />
Physical Examination)<br />
Current CD4 count and <strong>HIV</strong> viral load: preferably<br />
2 or more separate results approximately 1 month<br />
apart<br />
Drug resistance test. To try to detect <strong>the</strong> presence <strong>of</strong><br />
transmitted ARV resistance mutations, a genotype<br />
should be per<strong>for</strong>med in all patients be<strong>for</strong>e initiating<br />
ART. This should be done as early in <strong>the</strong> course <strong>of</strong><br />
infection as possible, because mutations may revert<br />
to wild type. Review <strong>the</strong> results <strong>of</strong> previous resistance<br />
testing or obtain a baseline resistance test, if this was<br />
not done earlier. (See chapter Resistance Testing.)<br />
Complete blood count (CBC) and platelet count,<br />
liver function tests (LFTs), renal function tests,<br />
fasting lipid panel (see chapter Initial and Interim<br />
Laboratory and O<strong>the</strong>r Tests) fasting glucose, rapid<br />
plasma reagin (RPR), tuberculin skin test, hepatitis<br />
serologies<br />
A: Assessment<br />
Make <strong>the</strong> following basic decisions:<br />
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The patient is or is not likely to benefit from ART<br />
at this time (ie, do potential benefits outweigh <strong>the</strong><br />
risks)? See <strong>the</strong> Adult and Adolescent ARV Guidelines<br />
noted above, which thoroughly address <strong>the</strong> issue.<br />
A brief summary is included in <strong>the</strong> tables in <strong>the</strong><br />
chapter Determining Risk <strong>of</strong> <strong>HIV</strong> Progression and in<br />
<strong>the</strong> chapter CD4 Monitoring and Viral Load Testing.<br />
The patient is or is not willing to start ARVs at<br />
this time (<strong>the</strong> choice to accept or decline <strong>the</strong>rapy<br />
ultimately lies with <strong>the</strong> patient).<br />
The patient is or is not likely to adhere to an ARV<br />
regimen (an adherence counselor, with or without<br />
a mental health clinician, may be able to assist<br />
with this assessment and should be called upon<br />
if available). No patient should be automatically<br />
excluded from consideration <strong>of</strong> ART; <strong>the</strong> likelihood<br />
<strong>of</strong> adherence must be discussed and determined<br />
individually.<br />
P: Plan<br />
After educating <strong>the</strong> patient about <strong>the</strong> purpose and<br />
logistics <strong>of</strong> <strong>the</strong> proposed regimen and assessing <strong>the</strong><br />
patient’s potential <strong>for</strong> adherence, <strong>the</strong> ART regimen can<br />
be initiated, changed, or postponed accordingly.<br />
The goals <strong>of</strong> <strong>the</strong>rapy are to achieve maximal and durable<br />
viral suppression, restore or preserve immune function,<br />
improve quality <strong>of</strong> life, and reduce <strong>HIV</strong>-related<br />
morbidity and mortality.<br />
Considerations be<strong>for</strong>e Initiating ART<br />
No “average patient” exists. Some patients will do better<br />
during treatment and some will do worse than clinical<br />
studies would predict. Health care providers must<br />
work with each patient to develop a treatment strategy<br />
that is both clinically sound and appropriate <strong>for</strong> that<br />
individual’s needs, priorities, and circumstances <strong>of</strong> daily<br />
life. Not all patients will be able to tolerate all drugs,<br />
and <strong>the</strong> patients understanding, readiness to <strong>com</strong>mit<br />
to <strong>the</strong> regimen, and history <strong>of</strong> adherence to previous<br />
regimens must be considered when choosing ARV<br />
<strong>com</strong>binations. Major considerations are as follows:<br />
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Willingness <strong>of</strong> <strong>the</strong> individual to begin <strong>the</strong>rapy,<br />
coupled with understanding <strong>of</strong> <strong>the</strong> purpose and <strong>the</strong><br />
mechanics <strong>of</strong> <strong>the</strong> planned regimen, and how it will<br />
fit into his or her life<br />
Degree <strong>of</strong> immunodeficiency and risk <strong>of</strong> disease<br />
progression as reflected by <strong>the</strong> CD4 count and <strong>HIV</strong><br />
RNA level (see tables in <strong>the</strong> chapter Determining<br />
Risk <strong>of</strong> <strong>HIV</strong> Progression and <strong>the</strong> chapter CD4<br />
Monitoring and Viral Load Testing)<br />
Potential benefits and risks <strong>of</strong> ARV drugs<br />
Likelihood <strong>of</strong> adherence to <strong>the</strong> prescribed regimen<br />
Resistance, if any, to ARV medications (obtain<br />
resistance testing prior to ARV initiation in ARVnaive<br />
patients)<br />
The patient has <strong>the</strong> right to decline or postpone ART.<br />
This decision should not affect any o<strong>the</strong>r aspect <strong>of</strong><br />
care, and ART should be <strong>of</strong>fered again at each visit to<br />
patients who meet <strong>the</strong> criteria <strong>for</strong> treatment. If mental<br />
health issues, addiction, or <strong>the</strong> patient's social situation<br />
are barriers to adherence, initiate appropriate referrals<br />
and reassess adherence barriers at regular intervals.