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3–32 | <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 />

The USPHS Perinatal ARV Guidelines emphasize<br />

that <strong>the</strong> PACTG 076 regimen is effective not only <strong>for</strong><br />

women whose clinical status is similar to that <strong>of</strong> <strong>the</strong><br />

participants in <strong>the</strong> original study, but also <strong>for</strong> women<br />

with advanced <strong>HIV</strong> disease, low CD4 counts, and<br />

previous ZDV <strong>the</strong>rapy.<br />

Because <strong>the</strong> goals <strong>of</strong> ART in a pregnant woman are<br />

not only to maintain her health, but also to prevent<br />

transmission to her infant, <strong>the</strong> considerations in ART<br />

differ from those in nonpregnant adults. Because <strong>the</strong><br />

<strong>HIV</strong> viral load strongly influences <strong>the</strong> risk <strong>of</strong> <strong>HIV</strong><br />

transmission, a primary goal <strong>of</strong> <strong>the</strong>rapy should be to<br />

suppress <strong>the</strong> viral load to very low levels (preferably to<br />

undetectable levels) during pregnancy and throughout<br />

delivery; this goal guides treatment decisions. For<br />

nonpregnant adults, <strong>the</strong> Guidelines <strong>for</strong> <strong>the</strong> Use <strong>of</strong><br />

Antiretroviral Agents in <strong>HIV</strong>-1-<strong>Infected</strong> Adults and<br />

Adolescents re<strong>com</strong>mend that treatment be deferred in<br />

certain persons, depending on <strong>the</strong> CD4 cell count and<br />

<strong>the</strong> <strong>HIV</strong> viral load. (See chapter Antiretroviral Therapy.)<br />

In contrast, <strong>the</strong> USPHS Perinatal ARV Guidelines<br />

re<strong>com</strong>mend that all pregnant women, regardless <strong>of</strong> CD4<br />

cell count, receive <strong>the</strong> 3-part ZDV prophylaxis regimen<br />

used in PACTG 076, that is, ZDV orally (200 mg 3<br />

times a day or 300 mg twice a day) beginning after <strong>the</strong><br />

first trimester, intravenous ZDV during labor, and ZDV<br />

given orally to <strong>the</strong> newborn <strong>for</strong> 6 weeks. The guidelines<br />

also re<strong>com</strong>mend that women with an <strong>HIV</strong> RNA level<br />

>1,000 copies/mL (regardless <strong>of</strong> CD4 cell count) or<br />

with immunologic, virologic, or clinical indications <strong>for</strong><br />

treatment be <strong>of</strong>fered a <strong>com</strong>bination ART regimen that<br />

includes ZDV and o<strong>the</strong>r ARV drugs. Even women<br />

with <strong>HIV</strong> RNA levels 1,000 copies/mL in<br />

<strong>the</strong> weeks be<strong>for</strong>e delivery, should be counseled about<br />

<strong>the</strong> risks and benefits <strong>of</strong> cesarean section. A planned<br />

cesarean section should be scheduled <strong>for</strong> 38 weeks’<br />

gestation, because <strong>the</strong> benefits <strong>of</strong> cesarean section<br />

once <strong>the</strong> membranes have ruptured are unknown.<br />

Intravenous ZDV should be started 3 hours be<strong>for</strong>e <strong>the</strong><br />

scheduled cesarean section. Prophylactic antibiotics<br />

are re<strong>com</strong>mended at <strong>the</strong> time <strong>of</strong> cesarean section in<br />

<strong>HIV</strong>-infected women, to decrease <strong>the</strong> risk <strong>of</strong> maternal<br />

infection. The USPHS Perinatal ARV Guidelines outline<br />

4 scenarios in which <strong>the</strong> clinician must decide whe<strong>the</strong>r<br />

cesarean section is needed (Table 4). The data on <strong>the</strong><br />

benefits <strong>of</strong> cesarean section are <strong>com</strong>plex and must be<br />

balanced with <strong>the</strong> increased risk to <strong>the</strong> mo<strong>the</strong>r after<br />

surgery. The clinician may want to consult an obstetric/<br />

<strong>HIV</strong> specialist to discuss specific situations.<br />

Questions remain about <strong>the</strong> management <strong>of</strong> labor when<br />

a vaginal delivery is planned. Because <strong>the</strong> duration<br />

<strong>of</strong> ruptured membranes is a risk factor <strong>for</strong> perinatal<br />

transmission, pregnant women with <strong>HIV</strong> infection<br />

should be counseled to go to a hospital <strong>for</strong> care at<br />

<strong>the</strong> first signs <strong>of</strong> labor or rupture <strong>of</strong> membranes. If<br />

<strong>the</strong> membranes rupture spontaneously be<strong>for</strong>e labor<br />

occurs or early in labor, <strong>the</strong> clinician should consider<br />

interventions to decrease <strong>the</strong> interval to delivery, such as<br />

administration <strong>of</strong> oxytocin. Procedures that increase <strong>the</strong><br />

neonate’s exposure to maternal blood, such as <strong>the</strong> use<br />

<strong>of</strong> scalp electrodes or artificial rupture <strong>of</strong> membranes,<br />

should be avoided.

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