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Recommendations for Use of Antiretroviral Drugs in Pregnant HIV-1-Infected Women for Maternal Health and Interventions to Reduce Perinatal HIV Transmission in the United States

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Recommendations for Use of Antiretroviral Drugs During Pregnancy

Table 6. What to Start: Initial Combination Regimens for Antiretroviral-Naive Pregnant Women

Last Updated: October 26, 2016; Last Reviewed: October 26, 2016

Table 6. What to Start: Initial Combination Regimens for Antiretroviral-Naive Pregnant Women

These recommendations are for pregnant women who have never received antiretroviral therapy (ART) previously (i.e., antiretroviral-naive) and who have no evidence of significant resistance to regimen components. See Table 8 for more information on specific drugs and dosing in pregnancy. Within each drug class and recommendation category, regimens are listed alphabetically, and the order does not indicate a ranking of preference. It is recommended that women who become pregnant while on a stable ART regimen with viral suppression remain on that same regimen, with the exception of regimens containing didanosine, stavudine, or treatment-dose ritonavir.

Table 6. What to Start: Initial Combination Regimens for Antiretroviral-Naive Pregnant Women
Drug Comments
Preferred Initial Regimens in Pregnancy:
  • Drugs or drug combinations are designated as Preferred for initiating ART in ARV-naive pregnant women when clinical trial data in adults have demonstrated optimal efficacy and durability with acceptable toxicity and ease of use; pregnancy-specific PK data are available to guide dosing; and no established association with teratogenic effects (from animal and/or human studies) or clinically significant adverse outcomes for mothers, fetuses, or newborns have been reported.
Preferred Two-NRTI Backbones
ABC/3TC Available as FDC. Can be administered once daily. ABC should not be used in patients who test positive for HLA-B*5701 because of risk of hypersensitivity reaction. ABC/3TC with ATV/r or with EFV is not recommended if pretreatment HIV RNA is >100,000 copies/mL.
TDF/FTC or TDF/3TC TDF/FTC available as FDC. Either TDF/FTC (coformulated) or TDF with separate 3TC can be administered once daily. TDF has potential renal toxicity, thus TDF-based dual NRTI combinations should be used with caution in patients with renal insufficiency.
Preferred PI Regimens
ATV/r plus a Preferred Two-NRTI Backbone Once-daily administration. Extensive experience in pregnancy. Maternal hyperbilirubinemia; no clinically significant neonatal hyperbilirubinemia or kernicterus reported, but neonatal bilirubin monitoring recommended.
DRV/r plus a Preferred Two-NRTI Backbone
Better tolerated than LPV/r. PK data available. Increasing experience with use in pregnancy. Must be used twice daily in pregnancy.
Preferred Integrase Inhibitor Regimen
RAL plus a Preferred Two-NRTI Backbone PK data available and increasing experience in pregnancy. Rapid viral load reduction (potential role for women who present for initial therapy late in pregnancy). Useful when drug interactions with PI regimens are a concern. Twice-daily dosing required. If there are concerns about adherence or medication discontinuation postpartum, a PI regimen is preferred instead of an integrase inhibitor regimen, to minimize the risk of resistance.
Alternative Initial Regimens in Pregnancy:
  • Regimens with clinical trial data demonstrating efficacy in adults but one or more of the following apply: experience in pregnancy is limited, data are lacking or incomplete on teratogenicity, or regimen is associated with dosing, formulation, toxicity, or interaction issues.
Alternative Two-NRTI Backbones
ZDV/3TC Available as FDC. NRTI combination with most experience for use in pregnancy but has disadvantages of requirement for twice-daily administration and increased potential for hematologic toxicities.
PI Regimens
LPV/r plus a Preferred Two-NRTI Backbone Abundant experience and established PK in pregnancy. More nausea than with preferred agents. Twice-daily administration. Dose increase recommended in third trimester (see Table 8). Once-daily LPV/r is not recommended for use in pregnant women.
NNRTI Regimen
EFV plus a Preferred Two-NRTI Backbone Concern because of birth defects seen in primate study; data not borne out in human studies, but cautionary text remains in package insert (see Teratogenicity and Table 8). Preferred regimen in women who require coadministration of drugs with significant interactions with PIs or the convenience of coformulated, single-tablet, once-daily regimen. Screening for antenatal and postpartum depression is recommended.
RPV/TDF/FTC (or RPV plus a Preferred Two-NRTI Backbone) RPV not recommended with pretreatment HIV RNA >100,000 copies/mL or CD4 cell count <200 cells/mm3. Do not use with PPIs. PK data available in pregnancy but relatively little experience with use in pregnancy. Available in coformulated single-pill, once-daily regimen.
Insufficient Data in Pregnancy to Recommend Routine Use in Initial Regimens for ART-Naive Women:
  • Drugs that are approved for use in adults but lack adequate pregnancy-specific PK or safety data
COBI Limited data on use of COBI (including coformulations with ATV or DRV) in pregnancy.
DTG Limited data on use of DTG in pregnancy.
EVG/COBI/TDF/FTC
Fixed Drug Combination
Limited data on use of EVG/COBI component in pregnancy.
FPV
Limited data on use in pregnancy.
MVC
MVC requires tropism testing before use. Few case reports of use in pregnancy.
EVG/COBI/TAF/FTC
Fixed Drug Combination
Limited data on use of EVG/COBI; no data on use of TAF in pregnancy
TAF/FTC
Fixed Drug Combination
No data on use of TAF in pregnancy.
RPV/TAF/FTC
Fixed Drug Combination
No data on use of TAF in pregnancy.
Not Recommended for Initial ART in Pregnancy:
  • Drugs whose use is not recommended as part of initial regimens in pregnancy because of toxicity, lower rate of viral suppression or because not recommended in ART-naive populations.
Note: Drugs not recommended for initial use because of toxicity (stavudine [d4T], didanosine [ddI], treatment-dose ritonavir [RTV]) should also be stopped in women who present during pregnancy while taking these medications.

Other medications listed below may be continued in women who present during pregnancy, as long as they are well tolerated and result in sustained virologic suppression.
ABC/3TC/ZDV
Generally not recommended due to inferior virologic efficacy.
d4T* Not recommended due to toxicity.
ddI* Not recommended due to toxicity.
IDV/r Nephrolithiasis, maternal hyperbilirubinemia.
NFV
Lower rate of viral suppression with NFV compared to LPV/r or EFV in adult trials.
RTV* RTV as a single PI is not recommended because of inferior efficacy and increased toxicity.
SQV/r
Not recommended based on potential toxicity and dosing disadvantages. Baseline ECG is recommended before initiation of SQV/r because of potential PR and QT prolongation; contraindicated with preexisting cardiac conduction system disease. Limited data in pregnancy. Large pill burden. Twice-daily dosing required.
ETR Not recommended in ART-naive populations.
NVP Not recommended because of greater potential for adverse events, complex lead-in dosing, and low barrier to resistance. NVP should be used with caution when initiating ART in women with CD4 cell count >250 cells/mm3. Use NVP and ABC together with caution; both can cause hypersensitivity reactions within the first few weeks after initiation.
T20 Not recommended in ART-naive populations.
TPV/r Not recommended in ART-naive populations.
Key to Abbreviations: 3TC = lamivudine; ABC = abacavir; ART = antiretroviral therapy; ARV = antiretroviral; ATV = atazanavir; ATV/r = atazanavir/ritonavir; CD4 = CD4 T lymphocyte cell; COBI = cobicistat; d4T = stavudine; ddI = didanosine; DRV/r = darunavir/ritonavir; DTG = dolutegravir; ECG = electrocardiogram; EFV = efavirenz; ETR = etravirine; EVG = elvitegravir; FDC = fixed-drug combination; FPV = fosamprenavir; FTC = emtricitabine; IDV/r = indinavir/ritonavir; LPV/r = lopinavir/ritonavir; MVC = maraviroc; NFV = nelfinavir; NNRTI = non-nucleoside reverse transcriptase inhibitor; NRTI = nucleoside reverse transcriptase inhibitor; NVP = nevirapine; PI = protease inhibitor; PK = pharmacokinetic; PPI = proton pump inhibitor; RAL = raltegravir; RPV = rilpivirine; RTV = ritonavir; SQV/r = saquinavir/ritonavir; T20 = enfuvirtide; TAF = tenofovir alafenamide; TDF = tenofovir disoproxil fumarate; TPV = tipranavir; TPV/r = tipranavir/ritonavir; ZDV = zidovudine

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