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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
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Intrapartum management and infant prophylaxis for pregnant women with HIV in resource-rich settings

Intrapartum management and infant prophylaxis for pregnant women with HIV in resource-rich settings
Treatment and VL status of the mother Received antepartum ART with no adherence concerns
  • No antepartum ART*
  • ART adherence concerns
  • Unknown HIV RNA
  • HIV diagnosis made in labor
  • Acute/primary HIV during pregnancy
Undetectable VL (<50 copies/mL) within 4 weeks of delivery Detectable (≥50 copies/mL) but ≤1000 copies/mL within 4 weeks of delivery >1000 copies/mL within 4 weeks of delivery
Risk for HIV transmission Low risk High risk High risk High risk
Preferred delivery mode Determined by obstetric indications Determined by obstetric indications Scheduled cesarean delivery at 38 weeks Individualized based on HIV viral level (if known) and presentationΔ
Intrapartum antiretrovirals Continue baseline ART regimen
  • Continue baseline ART regimen
  • Consider intrapartum intravenous zidovudine
  • Continue baseline ART regimen
  • Intrapartum intravenous zidovudine
  • Continue baseline ART regimen if receiving ART
  • Intrapartum intravenous zidovudine§
Other intrapartum interventions Avoid fetal scalp electrodes
  • Avoid artificial rupture of membranes
  • Avoid operative delivery with forceps or vacuum extractor
  • Avoid fetal scalp electrodes
Avoid fetal scalp electrodes
  • Avoid artificial rupture of membranes (if not undergoing cesarean)
  • Avoid operative delivery with forceps or vacuum extractor (if not undergoing cesarean)
  • Avoid fetal scalp electrodes
Infant antiretroviral prophylaxis¥ 2 to 4 weeks of zidovudine Presumptive HIV therapy Presumptive HIV therapy Presumptive HIV therapy
This table reflects the general principles of intrapartum management and infant antiretroviral prophylaxis for pregnant women with HIV.

ART: antiretroviral therapy; VL: viral load.

* Women who present in labor with unknown HIV status (or a prior negative test with subsequent risk factors for HIV infection) should undergo rapid combination antibody/antigen HIV testing. If this test is positive, the woman and her infant should be managed as high risk for HIV transmission (having had no antepartum ART) while awaiting confirmatory testing.

¶ Primary HIV infection refers to the first 6 months of infection.

Δ In the United States, clinicians can consult with the National Perinatal HIV/AIDS Clinical Consultation Center at 1-888-448-8765 to help rapidly develop an individualized plan for individuals who present in labor or with ruptured membranes.

◊ Clinicians may reasonably add intrapartum zidovudine for such patients, particularly if there were concerns about adherence to ART during pregnancy. We typically use intrapartum zidovudine at this VL range.

§ Intrapartum zidovudine is administered intravenously with a 2 mg/kg dose followed by a continuous infusion of 1 mg/kg/hour until delivery. For women undergoing scheduled cesarean delivery, zidovudine is initiated 3 hours before the procedure. For women who present in labor and have not received antepartum ART, intravenous zidovudine should be administered immediately.

¥ Refer to other UpToDate content for specifics on regimens and dosing for infant antiretroviral prophylaxis.
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