Background
- Vertical transmission of HIV occurs in 25 to 35% of patients if untreated, but less than 1% if treated
- Risk of transmission is proportional to viral load at delivery and goes down with treatment
Epidemiology
- An increasing problem with the increase in effectiveness of antiretroviral therapy
- Decreasing vertical transmission over time
Management
Antepartum Management
- Start a pregnancy-safe antiretroviral regimen (discussed below)
- Monitor viral load monthly during pregnancy
- Routine HIV management including vaccinations (including TDaP)
Regimens for Treatment-Naive Women
- NRTI backbones
- INSTI-based regimens
- PI regimens
Antiretroviral Safety in Pregnancy
Drug | Starting | Continuing | Restarting | Conceiving |
---|---|---|---|---|
NRTIs | ||||
ABC | Preferred | Continue | Preferred | Preferred |
FTC | Preferred | Continue | Preferred | Preferred |
3TC | Preferred | Continue | Preferred | Preferred |
TDF | Preferred | Continue | Preferred | Preferred |
ZDV | Alternative | Continue | Alternative | Alternative |
TAF | No data | Continue | No data | No data |
Integrase Inhibitors | ||||
DTG | Avoid in T1, then preferred |
Avoid in T1 | Avoid in T1 | Not recommended |
RAL | Preferred | Continue | Preferred | Preferred |
BIC | No data | No data | No data | No data |
EVG-COBI | Not recommended | Consider switch | Not recommended | Not recommended |
Protease Inhibitors | ||||
ATV/r | Preferred | Continue | Preferred | Preferred |
DRV/r | Preferred | Continue | Preferred | Preferred |
LPV/r | Alternative | Continue | Alternative | Alternative |
ATV/COBI | Not recommended | Consider switch | Not recommended | Not recommended |
DRV/COBI | Not recommended | Consider switch | Not recommended | Not recommended |
NNRTIs | ||||
EFV | Alternative | Continue | Alternative | Alternative |
RPV | Alternative | Continue | Alternative | Alternative |
DOR | No data | No data | No data | No data |
ETR | Not recommended | Continue | Not recommended | Not recommended |
NVP | Not recommended | Continue | Not recommended | Not recommended |
Entry Inhibitors & Fusion Inhibitors | ||||
IBA | No data | No data | No data | No data |
MVC | Not recommended | Continue | Not recommended | Not recommended |
T-20 | Not recommended | Continue | Not recommended | Not recommended |
Fixed Drug Combinations | ||||
ABC-DTG-3TC | Avoid T1 (DTG), then preferred |
Consider switch if T1 | Avoid T1 (DTG), then preferred |
Not recommended (DTG) |
EFV-FTC-TDF | Alternative (EFV) | Continue | Alternative (EFV) | Alternative (EFV) |
EFC-3TC-TDF | Alternative (EFV) | Continue | Alternative (EFV) | Alternative (EFV) |
FTC-RPV-TDF | Alternative (RPV) | Continue (RPV) | Alternative (RPV) | Alternative (RPV) |
BIC-FTC-TAF | No data (BIC/TAF) | No data (BIC) | No data (BIC/TAF) | No data (BIC/TAF) |
DOR-3TC-TDF | No data (DOR) | No data (DOR) | No data (DOR) | No data (DOR) |
FTC-RPV-TAF | No data (TAF) | Continue (RPV/TAF) | No data (TAF) | No data (TAF) |
EVG/COBI-FTC-TDF | Not recommended (EVG/c) | Consider switch | Not recommended (EVG/c) | Not recommended (EVG/c) |
EVG/COBI-FTC-TAF | Not recommended (EVG/c) | Consider switch | Not recommended (EVG/c) | Not recommended (EVG/c) |
DRV/COBI-FTC-TAF | Not recommended (DRV/c) | Consider switch | Not recommended (DRV/c) | Not recommended (DRV/c) |
DTG-RPV | Not recommended | Consider switch | Not recommended | Not recommended |
- Starting = ART for Pregnant Women Who Have Never Received ARV Drugs and Who Are Initiating ART for the First Time
- Continuing = Continuing ART for Women Who Become Pregnant on an ART Regimen that has been Well Tolerated and Virologically Suppressive
- Restarting = ART for Pregnant Women Who Have Received ARV Drugs in the Past and Who Are Restarting ART
- Conceiving = ART for Nonpregnant Women Who Are Trying to Conceive
Intrapartum Management
- HIV-positive women are managed with standard antiretrovirals (discussed above), intravenous zidovudine during labour, and consideration of Cesarean section, followed by management of the neonate
- If viral load is unknown, get a STAT viral load
- Dose of intrapartum zidovudine is 2 mg/kg IV given over 1 hour, followed by 1 mg/kg/hour infusion until delivery
- They oral antiretrovirals should be continued during labour
Viral Load | Management of Mother | Management of Infant | ||
---|---|---|---|---|
ART | Zidovudine | C-section | ||
<40 | yes | yes | no | zidovudine for 4 to 6 weeks |
40-999 | yes | yes | consider | combination ART, or zidovudine monotherapy for 4-6 weeks |
≥1000 | yes | yes | yes | combination ART |
unknown | yes | yes | yes | combination ART, adjusted based on results of maternal viral load |
- If serostatus is unknown but they are at risk, then get STAT serology
- If positive, manage as above for HIV-positive women
- If negative, then assess risk that they are in the window period
- If high risk, then manage as above for HIV-positive women, and repeat serology or get viral PCR
- High risk includes ongoing commercial sex work or intravenous drug use
- If not high risk, then no further management required
- If high risk, then manage as above for HIV-positive women, and repeat serology or get viral PCR
Postpartum Management
- Generally recommend against breastfeeding for HIV-positive mothers in Canada, even if HIV is well-controlled
- Transmission is 10-20% risk if breastfeeding and uncontrolled; less than 1% if fully and reliably suppressed
- As well as risk of HIV transmission, it could theoretically expose child's HIV to low-level antivirals which could induce resistance
- If they won't be breastfeeding, give cabergoline 1 mg po once within 24 hours of delivery to prevent lactation
- Discuss plans for contraception
- Monitor for post-partum depression
- Counsel on the risks of pre-chewing food as a method of transmission (if applicable)