Table 4.
Guideline source | DHHS [37] | EACS [8] | WHO [10,11] |
---|---|---|---|
Date of revision | 2015 | 2015 | 2015f
2013g |
Timing of ART | For women already on ART who present in the first trimester, continue current regimen if it is well tolerated and virological suppression has been achieved
For women not on ART who present in the first trimester, consider initiating ART as soon as possible |
For pregnant women already on ART continue current regimen unless that regimen is contra-indicated in pregnancy
For women not on ART who present in pregnancy, initiate ART as soon as possible and no later than the beginning of the second trimester |
ART should be initiated in all pregnant and breastfeeding women with HIV, regardless of CD4 count or WHO clinical stage (option B+) |
Preferred regimens for ART initiation in pregnancy | NRTI backbones:
Third agent: |
Generally the same as for non-pregnant women but:
|
Same as for non-pregnant adults:
|
Post-partum | ART is recommended for all HIV-infected individuals regardless of CD4 cell count
Increase supports in immediate post-partum period as this represents a vulnerable time for ART adherence |
ART is recommended for all HIV-infected individuals regardless of CD4 cell count | ART should be continued lifelong for all HIV-infected women |
DHHS: Department of Health and Human Services; EACS: European AIDS Clinical Society; WHO: World Health Organization; ART: antiretroviral therapy; NRTI: nucleoside reverse transcriptase inhibitor; ABC: abacavir; 3TC: lamivudine; TDF: tenofovir disoproxil fumarate; ZDV: zidovudine; ATV/r: ritonavir-boosted atazanavir; DRV/r: ritonavir-boosted darunavir; EFV: efavirenz; RAL: raltegravir; PI: protease inhibitor; NVP: nevirapine; LPV/r: ritonavir-boosted lopinavir; d4T: stavudine; ddI: didanosine.
For patients who are HLA-B*5701 negative.
Based on extensive experience in pregnancy; once-daily dosing.
Twice-daily dosing required.
Only if initiated after 8 weeks' gestational age.
Associated with rapid virological suppression; twice-daily dosing required.
Publication of timing of initiation recommendation.
Publication of recommended regimens.