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
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
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.