03.12.2012 Views

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

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Section 3—Antiretroviral Therapy | 3–27<br />

Table 2. Antiretroviral Drug Use in Pregnant <strong>HIV</strong>-<strong>Infected</strong> Women: Pharmacokinetics, Toxicity Data, and Re<strong>com</strong>mendations<br />

Nucleoside/ Nucleotide Reverse Transcriptase Inhibitors<br />

Antiretroviral Drug Pharmacokinetics during Pregnancy Concerns during Pregnancy Rationale <strong>for</strong> Re<strong>com</strong>mended<br />

Use during Pregnancy<br />

NRTI class concerns and<br />

<strong>com</strong>ments<br />

Re<strong>com</strong>mended Agents<br />

Zidovudine<br />

(Retrovir, AZT, ZDV)<br />

Lamivudine<br />

(Epivir, 3TC)<br />

Alternative Agents<br />

Didanosine<br />

(Videx, ddI)<br />

Emtricitabine<br />

(Emtriva, FTC)<br />

Stavudine<br />

(Zerit, d4T)<br />

Abacavir<br />

(Ziagen, ABC)<br />

Insufficient Data to Re<strong>com</strong>mend Use<br />

Ten<strong>of</strong>ovir DF<br />

(Viread)<br />

Not Re<strong>com</strong>mended<br />

Zalcitabine<br />

(Hivid, ddC)<br />

Note: zalcitabine has<br />

been discontinued by <strong>the</strong><br />

manufacturer.<br />

Pharmacokinetics not significantly<br />

altered in pregnancy; no change in<br />

dose indicated.<br />

Pharmacokinetics not significantly<br />

altered in pregnancy; no change in<br />

dose indicated.<br />

Pharmacokinetics not significantly<br />

altered in pregnancy; no change in<br />

dose indicated.<br />

See text <strong>for</strong> discussion <strong>of</strong> potential maternal<br />

and infant mitochondrial toxicity.<br />

No evidence <strong>of</strong> human teratogenicity. Welltolerated,<br />

short-term safety demonstrated <strong>for</strong><br />

mo<strong>the</strong>r and infant.<br />

No evidence <strong>of</strong> human teratogenicity. Welltolerated,<br />

short-term safety demonstrated <strong>for</strong><br />

mo<strong>the</strong>r and infant.<br />

Cases <strong>of</strong> lactic acidosis, some fatal, have<br />

been reported in pregnant women receiving<br />

didanosine and stavudine toge<strong>the</strong>r.<br />

NRTIs are re<strong>com</strong>mended <strong>for</strong> use as part <strong>of</strong><br />

<strong>com</strong>bination regimens, usually including 2 NRTIs with<br />

ei<strong>the</strong>r an NNRTI or 1 or more PIs. Use <strong>of</strong> single or dual<br />

NRTIs alone is not re<strong>com</strong>mended <strong>for</strong> treatment <strong>of</strong><br />

<strong>HIV</strong> infection (zidovudine alone may be considered<br />

<strong>for</strong> prophylaxis <strong>of</strong> perinatal transmission in pregnant<br />

women with <strong>HIV</strong> RNA

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!