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A Guide to Primary Care of People with HIV/AIDS - Canadian Public ...

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A <strong>Guide</strong> <strong>to</strong> <strong>Primary</strong> <strong>Care</strong> <strong>of</strong> <strong>People</strong> <strong>with</strong> <strong>HIV</strong>/<strong>AIDS</strong><br />

Chapter 11: Postexposure Prophylaxis<br />

11<br />

Table 11-5. Labora<strong>to</strong>ry Evaluation and<br />

Followup <strong>of</strong> Exposed Health <strong>Care</strong> Personnel<br />

Lab tests Comment Frequency<br />

<strong>HIV</strong> antibody test<br />

HBV<br />

Anti HCV<br />

Liver enzymes<br />

CBC, renal<br />

function, and<br />

hepatic function<br />

Test HCP if source<br />

patient is <strong>HIV</strong><br />

positive regardless<br />

<strong>of</strong> whether PEP is<br />

given<br />

Test if source<br />

patient is HBsAg or<br />

HBeAg positive<br />

Test if source<br />

patient is HCV<br />

positive<br />

Test if source<br />

patient is HCV<br />

positive<br />

If PEP is warranted<br />

Baseline, 6 weeks,<br />

12 weeks, 6<br />

months (rapid<br />

test at baseline, if<br />

possible)<br />

Baseline and 4-6<br />

months ( or 1-2<br />

months after last<br />

HBV vaccine)<br />

Baseline and 4-6<br />

months; HCV RNA<br />

at 4-6 weeks is<br />

optional<br />

Baseline and 4-6<br />

months<br />

Prior <strong>to</strong> initiating<br />

PEP and repeated<br />

in 2 weeks<br />

Are there special considerations for PEP in<br />

dental settings?<br />

Although the number <strong>of</strong> exposures is relatively high<br />

in dental settings, the risk <strong>of</strong> transmission is low and<br />

no different from other HCP settings. Fac<strong>to</strong>rs that are<br />

associated <strong>with</strong> increased risk <strong>of</strong> transmission are<br />

failure <strong>to</strong> follow PEP pro<strong>to</strong>cols, failure <strong>to</strong> use puncturepro<strong>of</strong><br />

containers, treating >20 patients per day, failure<br />

<strong>to</strong> use eye protection or masks, and male gender. For<br />

more information, see Suggested Resources.<br />

INTERVENTIONS FOR<br />

NONOCCUPATIONAL PEP<br />

(NPEP)<br />

What is the role <strong>of</strong> nPEP for nonoccupational<br />

exposure?<br />

PEP for nonoccupational exposure <strong>to</strong> <strong>HIV</strong> (nPEP) is<br />

routinely being administered in cases <strong>of</strong> sexual assault<br />

in hospital emergency departments and is increasingly<br />

being made available during other cases <strong>of</strong> sexual<br />

exposure or injection drug use exposure and in nonhospital<br />

settings. This issue is particularly relevant in<br />

the care <strong>of</strong> <strong>HIV</strong> discordant couples. Research on risk<br />

<strong>of</strong> <strong>HIV</strong> transmission from a single nonoccupational<br />

exposure is relatively lacking compared <strong>with</strong><br />

occupational exposures (see Table 11-6). A national<br />

registry has been developed <strong>to</strong> gather the data <strong>with</strong><br />

which <strong>to</strong> develop a CDC recommendation for <strong>HIV</strong> PEP<br />

in the nonoccupational setting. Information about this<br />

registry can be found at http://www.hivpepregistry.org.<br />

In general, PEP for non-HCP is modeled after PEP<br />

interventions and procedures for HCP.<br />

Table 11-6. Estimated Risk <strong>of</strong> <strong>HIV</strong> Transmission<br />

Following Different Types <strong>of</strong> Exposures<br />

Type <strong>of</strong> exposure<br />

Needle-sharing exposure <strong>with</strong><br />

an infected source<br />

Receptive anal intercourse <strong>with</strong><br />

an infected source<br />

Receptive vaginal intercourse<br />

<strong>with</strong> an infected source<br />

Insertive anal intercourse <strong>with</strong><br />

an infected source<br />

Insertive vaginal intercourse<br />

<strong>with</strong> an infected source<br />

Oral sex <strong>with</strong> ejaculation <strong>with</strong><br />

an infected source<br />

0.67%<br />

Estimated risk<br />

0.5%-3.0%<br />

0.1%<br />

0.065%<br />

0.05%<br />

Conflicting data; however,<br />

risk is considered <strong>to</strong> be<br />

extremely low<br />

(

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