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Contraceptive Care for Women with
HIV Infection and their Partners
Kimberly McClellan, MSN, WHNP-BC, CRNP
Director Women's Health
AIDS Care Group, Chester PA
ksv23@drexel.edu
This teleconference is made possible by the
Cooperative Agreement #5U65PS000815-03 from
the Centers for Disease Control and Prevention
Special thanks to AETC, Title X and CDC EMCT partners
The views expressed by the speakers and moderators do not
necessarily reflect the official polices of the Dept. of Health and
Human Services nor does mention of trade names or
organizations imply endorsement by the U.S. Government.
Objectives
 Describe considerations for selecting appropriate
contraceptive and compare options for women living
with HIV
 Explain specific consideration related to hormonal
contraception and antiretroviral treatment
 Identify issue related to hormonal contraception and
HIV progression, transmission or acquisition
Benefits of Contraception for HIV-Positive
Women
 Prevents unintended pregnancy
 Half of all pregnancies in U.S. are unintended
 Allows women to plan a pregnancy that
 Is well timed
 Occurs in optimal health
 Minimizes risks for perinatal transmission
Special Considerations Regarding HIV
and Contraception
 Potential drug interaction with antiretrovirals (ARVs)
 Possible effects on HIV transmission
 Possible effects on HIV acquisition
 Possible effects on HIV progression
Typical Effectiveness of Contraception
HIV-positive
women generally
have the same
options as
uninfected women
US Medical Eligibility Criteria for
Contraceptive Use
US Medical Eligibility Criteria: Categories
Oral contraceptives
 Same medical criteria as for HIV-uninfected
women if woman is NOT on ART
 Drug-drug interactions are possible between ARVs
and hormonal contraceptives (HCs)
 HCs are metabolized by same pathways and cytochrome
P450 enzymes as many PIs and NNRTIs
 These interactions can cause changes in the efficacy of
the ARV or contraception
ACOG (2010), Gynecologic care for women with human
immunodeficiency virus. Practice Bulletin #117.
Hormonal Contraception: Alternate
Delivery Methods
 Combined Patch is a thin
plastic square worn on body
 Releases estrogen and
progestin through the skin
 Works by preventing
ovulation
 Efficacy
 Limited research suggests
may be more effective than
COCs
 Decreased efficacy in women
over 90 kg
Hormonal Contraception: Alternate
Delivery Methods
 Limited research suggests health risks and benefits are
similar to COCs
 Side Effects
 Skin irritation or rash where patch is applied
 Changes in bleeding pattern
 Headaches
 Nausea
 Vomiting
 Breast tenderness
 Abdominal pain
Hormonal Contraception: Alternate
Delivery Methods
 Combined Vaginal Ring is
placed into the vagina
 Releases estrogen and
progestin
 Works by preventing ovulation
 Efficacy
 Limited research suggests may
be more effective at preventing
pregnancy than COCs
Alternative Delivery Methods
 Limited research suggests risks and benefits similar to
COCs
 Side effects
 Changes in bleeding pattern
 Headaches
 Nausea
 Breast tenderness
 Vaginitis
 Leukorrhea/increase in Lactobacillus
Alternate Delivery Methods
 These delivery methods also vulnerable to drug
interactions
 One small study found significant interaction between
the estrogen and progestin hormones of the patch and
lopinavir/ritonavir
 More research needed on these delivery methods
DMPA
 Injectable (IM,SQ) progestin only
contraception
 Given every 3 months
 Works by preventing ovulation
 Efficacy
 97% effective as commonly used
 Over 99% effective when used as
directed (3 pregnancies per 1000
women)
Contraceptive Implants
 Thin rods or tubes
containing a progestin
hormone.
 Provide effective
contraception for at least
3 yrs.
 Suppresses ovulation and
changes cervical mucus.
 Menstrual irregularities in
most users.
Intrauterine devices (IUDs)
 No known drug interactions
 No increase in shedding of HIV
2 types
 Copper (Paragard) works for 10 years,
may be associated with heavier
menses, periods regular)
 Levonorgestrel IUD (Mirena) works for
5 years, reduces menstrual blood loss
(is FDA-approved as a treatment for
menorrhagia), periods scant and not
regular
Medical Eligibility Criteria for IUD*
LNG-IUD LNG-IUD Cu-IUD Cu-IUD
Initiation Continuation Initiation Continuation
High Risk for HIV 2 2 2 2
HIV Infection 2 2 2 2
AIDS 3 2 3 2
Clinically Well on
ARV Therapy
2 2 2 2
Category 2: A condition for which the advantages of using the method generally outweigh
the theoretical or proven risks.
Category 3: A condition for which the theoretical or proven risks usually outweigh the
advantages of using the method.
*Adapted from: U.S. medical eligibility criteria for contraceptive use.
IUD and HIV Considerations
 No higher risk in HIV-positive women over
uninfected women for
 Complications
 Infections
 IUD use not associated with increased risk for
transmission to sex partners
 Women with IUD in place who develop AIDS should
be monitored for pelvic infection
Hormonal Contraception and NNRTI
Interaction Table
Efavirenz (EFV) No effect on oral ethinyl estradiol
Decreased active metabolites of
norgestimate (levonorgestrel AUC
↓ 83%; norelgestromin ↓64%)
Implant: ↓ etonogestrel
Levonorgestrel AUC ↓58%
A reliable method of barrier
contraception must be used in addition
to HC due to decreases in progestin
levels.
A reliable method of barrier
contraception must be used due to
reports of contraceptive failure.
Effectiveness of emergency
contraception may be diminished
Etravirine (ETR) Ethinyl estradiol AUC ↑22%
Norethindrone: no significant
effect
No dosage adjustment necessary
Nevirapine (NVP) Ethinyl estradiol AUC ↓20%
Norethindrone AUC ↓19%
DMPA: no significant change
Use alternative or additional methods
No dosage adjustment needed
Hormonal Contraception and Ritonavir-
boosted PI Table
Atazanavir/ritonavir (ATV/r) ↓ Ethinyl estradiol
↑ Norgestimate
Oral contraceptive should contain
at least 35 mcg of ethinyl
estradiol. OCs containing
progestins other than
norethindrone or norgestimate
have not been studied.
Darunavir/ritonavir (DRV/r) Ethinyl estradiol ↓44%
Norethindrone AUC ↓14%
Use alternative or additional
method.
Fosamprenavir/ritonavir (FPV/r) Use alternative or additional
method.
Lopinavir/ritonavir (LPV/r) Ethinyl estradiol AUC ↓42%
Norethindrone AUC ↓17%
Use alternative or additional
method.
Saquinavir/ritonavir (SQV/r) ↓Ethinyl estradiol Use alternative or additional
method.
Tipranavir/ritonavir (TPV/r) Ethinyl estradiol AUC ↓48%
Norethindrone: no significant
change
Use alternative or additional
method.
Hormonal Contraception and PIs without
Ritonavir Table
Atazanavir (ATV) Ethinyl estradiol AUC ↑48%
Norethindrone AUC ↑110%
Oral contraceptive should contain
no more than 30 mcg of ethinyl
estradiol or use alternative
method. OCs containing less than
25 mcg of ethinyl estradiol or
progestins other than
norethindrone or norgestimate
have not been studied.
Fosamprenavir (FPV) With APV: ↑Ethinyl estradiol and
↑norethindrone; ↓APV 20%
Use alternative method.
Indinavir (IDV) Ethinyl estradiol AUC ↑25%
Norethindrone AUC ↑26%
No dose adjustment.
Nelfinavir Ethinyl estradiol AUC ↓47%
Norethindrone ↓18%
Use alternative or additional
method.
Adapted from: 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.
http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf
Hormonal Contraception and CCR5
antagonist/integrase inhibitor table
CCR5 antagonist
Maraviroc (MVC) No significant effect on
ethinyl estradiol of
levonorgestrel
Safe to use in
combination
Integrase inhibitor
Raltegravir No significant drug effect No dose adjustment
necessary
Adapted from: 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.
http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf
Condoms
 Efficacy
 Pregnancy prevention as commonly used
 Male condom 85%
 Female condom 79%
 Pregnancy prevention when used correctly and consistently
 Male condom 98%
 Female condom 95%
 Male condom is 80-95% effective at preventing HIV
transmission when used correctly and consistently
Dual Contraceptive Use
 Condom use should be encouraged for women
 To prevent HIV/STI acquisition
 Condom use should be encouraged in HIV-positive
women
 To prevent HIV transmission
 Prevent STI acquisition
 As an adjuvant to contraceptives
 Condoms alone have a failure rate of 15%-21% at
preventing pregnancy
Spermicides: Not recommended
 Spermicides are not recommended by CDC
 Disrupt cervical mucosa
 Potentially increase viral shedding
 Increase transmission of HIV to uninfected partners
 Diaphragms and cervical caps are not encouraged by
the CDC due to concerns about their use with
spermicides
Female and Male Sterilization
 Contraceptive sterilization is
the most widely used
method of family planning
 Clients should be advised
that sterilization should be
considered permanent
 Male-vasectomy:
Cutting/occluding both vas
deferens
 1st yr failure rate-0%-0.5%
 Female-sterilization
 Transabdominal
 Transcervical
 Tubal sterilization
 Occlusion method
Hormonal Contraception and HIV Acquisition:
WHO Technical Statement
 Most studies found no statistically significant association
between oral contraception and HIV acquisition
 Evidence on injectable HC varied with some studies
showing increases between 48% to 100% and other studies
reporting no association
 Due to inconsistent data and limitations of the studies
performed WHO rated the current evidence as low
HIV Transmission and Hormonal Contraception:
WHO Technical Statement
 Recent observational study found a 2-3 increase in HIV
transmission in women using injectables over oral contraception
 Findings from studies assessing HC and genital HIV shedding are
not consistent
 Studies assessing HC and viral load generally showed no negative
effect
 WHO rates the evidence for HIV transmission and injectable
use as low and HIV transmission and oral contraception as very
low
HIV Disease Progression and Hormonal Contraception:
WHO Technical Statement
 None of the 10 observational studies conducted found a
significant association between hormonal contraception and
HIV progression
 One randomized controlled trial found an increased risk of
progression for HC users compared to copper IUD users
 Due to flaws in this study --- high rates of method switching and
loss to follow-up --- the evidence for HC and HIV progression is
rated as low
WHO Recommendations
 No restriction on the use of any hormonal contraceptive method for
HIV-positive women or women at high risk for HIV infection
 Critical importance must be placed on the consistent and correct use
of condoms for the prevention of HIV acquisition or transmission
 Most concern is focused on the evidence of HIV acquisition and DMPA
because a causal relationship is neither established nor ruled out
 Voluntary use of contraception by HIV positive women who wish to
prevent pregnancy continues to be an important PMTCT strategy
Thank you!
Contact the FXB Center with questions or comments, or for a
copy of the slide set:
Mary Jo Hoyt
hoyt@umdnj.edu

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contraception.ppt

  • 1. Contraceptive Care for Women with HIV Infection and their Partners Kimberly McClellan, MSN, WHNP-BC, CRNP Director Women's Health AIDS Care Group, Chester PA ksv23@drexel.edu
  • 2. This teleconference is made possible by the Cooperative Agreement #5U65PS000815-03 from the Centers for Disease Control and Prevention Special thanks to AETC, Title X and CDC EMCT partners The views expressed by the speakers and moderators do not necessarily reflect the official polices of the Dept. of Health and Human Services nor does mention of trade names or organizations imply endorsement by the U.S. Government.
  • 3. Objectives  Describe considerations for selecting appropriate contraceptive and compare options for women living with HIV  Explain specific consideration related to hormonal contraception and antiretroviral treatment  Identify issue related to hormonal contraception and HIV progression, transmission or acquisition
  • 4. Benefits of Contraception for HIV-Positive Women  Prevents unintended pregnancy  Half of all pregnancies in U.S. are unintended  Allows women to plan a pregnancy that  Is well timed  Occurs in optimal health  Minimizes risks for perinatal transmission
  • 5. Special Considerations Regarding HIV and Contraception  Potential drug interaction with antiretrovirals (ARVs)  Possible effects on HIV transmission  Possible effects on HIV acquisition  Possible effects on HIV progression
  • 6. Typical Effectiveness of Contraception HIV-positive women generally have the same options as uninfected women
  • 7. US Medical Eligibility Criteria for Contraceptive Use
  • 8. US Medical Eligibility Criteria: Categories
  • 9. Oral contraceptives  Same medical criteria as for HIV-uninfected women if woman is NOT on ART  Drug-drug interactions are possible between ARVs and hormonal contraceptives (HCs)  HCs are metabolized by same pathways and cytochrome P450 enzymes as many PIs and NNRTIs  These interactions can cause changes in the efficacy of the ARV or contraception ACOG (2010), Gynecologic care for women with human immunodeficiency virus. Practice Bulletin #117.
  • 10. Hormonal Contraception: Alternate Delivery Methods  Combined Patch is a thin plastic square worn on body  Releases estrogen and progestin through the skin  Works by preventing ovulation  Efficacy  Limited research suggests may be more effective than COCs  Decreased efficacy in women over 90 kg
  • 11. Hormonal Contraception: Alternate Delivery Methods  Limited research suggests health risks and benefits are similar to COCs  Side Effects  Skin irritation or rash where patch is applied  Changes in bleeding pattern  Headaches  Nausea  Vomiting  Breast tenderness  Abdominal pain
  • 12. Hormonal Contraception: Alternate Delivery Methods  Combined Vaginal Ring is placed into the vagina  Releases estrogen and progestin  Works by preventing ovulation  Efficacy  Limited research suggests may be more effective at preventing pregnancy than COCs
  • 13. Alternative Delivery Methods  Limited research suggests risks and benefits similar to COCs  Side effects  Changes in bleeding pattern  Headaches  Nausea  Breast tenderness  Vaginitis  Leukorrhea/increase in Lactobacillus
  • 14. Alternate Delivery Methods  These delivery methods also vulnerable to drug interactions  One small study found significant interaction between the estrogen and progestin hormones of the patch and lopinavir/ritonavir  More research needed on these delivery methods
  • 15. DMPA  Injectable (IM,SQ) progestin only contraception  Given every 3 months  Works by preventing ovulation  Efficacy  97% effective as commonly used  Over 99% effective when used as directed (3 pregnancies per 1000 women)
  • 16. Contraceptive Implants  Thin rods or tubes containing a progestin hormone.  Provide effective contraception for at least 3 yrs.  Suppresses ovulation and changes cervical mucus.  Menstrual irregularities in most users.
  • 17. Intrauterine devices (IUDs)  No known drug interactions  No increase in shedding of HIV 2 types  Copper (Paragard) works for 10 years, may be associated with heavier menses, periods regular)  Levonorgestrel IUD (Mirena) works for 5 years, reduces menstrual blood loss (is FDA-approved as a treatment for menorrhagia), periods scant and not regular
  • 18. Medical Eligibility Criteria for IUD* LNG-IUD LNG-IUD Cu-IUD Cu-IUD Initiation Continuation Initiation Continuation High Risk for HIV 2 2 2 2 HIV Infection 2 2 2 2 AIDS 3 2 3 2 Clinically Well on ARV Therapy 2 2 2 2 Category 2: A condition for which the advantages of using the method generally outweigh the theoretical or proven risks. Category 3: A condition for which the theoretical or proven risks usually outweigh the advantages of using the method. *Adapted from: U.S. medical eligibility criteria for contraceptive use.
  • 19. IUD and HIV Considerations  No higher risk in HIV-positive women over uninfected women for  Complications  Infections  IUD use not associated with increased risk for transmission to sex partners  Women with IUD in place who develop AIDS should be monitored for pelvic infection
  • 20. Hormonal Contraception and NNRTI Interaction Table Efavirenz (EFV) No effect on oral ethinyl estradiol Decreased active metabolites of norgestimate (levonorgestrel AUC ↓ 83%; norelgestromin ↓64%) Implant: ↓ etonogestrel Levonorgestrel AUC ↓58% A reliable method of barrier contraception must be used in addition to HC due to decreases in progestin levels. A reliable method of barrier contraception must be used due to reports of contraceptive failure. Effectiveness of emergency contraception may be diminished Etravirine (ETR) Ethinyl estradiol AUC ↑22% Norethindrone: no significant effect No dosage adjustment necessary Nevirapine (NVP) Ethinyl estradiol AUC ↓20% Norethindrone AUC ↓19% DMPA: no significant change Use alternative or additional methods No dosage adjustment needed
  • 21. Hormonal Contraception and Ritonavir- boosted PI Table Atazanavir/ritonavir (ATV/r) ↓ Ethinyl estradiol ↑ Norgestimate Oral contraceptive should contain at least 35 mcg of ethinyl estradiol. OCs containing progestins other than norethindrone or norgestimate have not been studied. Darunavir/ritonavir (DRV/r) Ethinyl estradiol ↓44% Norethindrone AUC ↓14% Use alternative or additional method. Fosamprenavir/ritonavir (FPV/r) Use alternative or additional method. Lopinavir/ritonavir (LPV/r) Ethinyl estradiol AUC ↓42% Norethindrone AUC ↓17% Use alternative or additional method. Saquinavir/ritonavir (SQV/r) ↓Ethinyl estradiol Use alternative or additional method. Tipranavir/ritonavir (TPV/r) Ethinyl estradiol AUC ↓48% Norethindrone: no significant change Use alternative or additional method.
  • 22. Hormonal Contraception and PIs without Ritonavir Table Atazanavir (ATV) Ethinyl estradiol AUC ↑48% Norethindrone AUC ↑110% Oral contraceptive should contain no more than 30 mcg of ethinyl estradiol or use alternative method. OCs containing less than 25 mcg of ethinyl estradiol or progestins other than norethindrone or norgestimate have not been studied. Fosamprenavir (FPV) With APV: ↑Ethinyl estradiol and ↑norethindrone; ↓APV 20% Use alternative method. Indinavir (IDV) Ethinyl estradiol AUC ↑25% Norethindrone AUC ↑26% No dose adjustment. Nelfinavir Ethinyl estradiol AUC ↓47% Norethindrone ↓18% Use alternative or additional method. Adapted from: 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. http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf
  • 23. Hormonal Contraception and CCR5 antagonist/integrase inhibitor table CCR5 antagonist Maraviroc (MVC) No significant effect on ethinyl estradiol of levonorgestrel Safe to use in combination Integrase inhibitor Raltegravir No significant drug effect No dose adjustment necessary Adapted from: 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. http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf
  • 24. Condoms  Efficacy  Pregnancy prevention as commonly used  Male condom 85%  Female condom 79%  Pregnancy prevention when used correctly and consistently  Male condom 98%  Female condom 95%  Male condom is 80-95% effective at preventing HIV transmission when used correctly and consistently
  • 25. Dual Contraceptive Use  Condom use should be encouraged for women  To prevent HIV/STI acquisition  Condom use should be encouraged in HIV-positive women  To prevent HIV transmission  Prevent STI acquisition  As an adjuvant to contraceptives  Condoms alone have a failure rate of 15%-21% at preventing pregnancy
  • 26. Spermicides: Not recommended  Spermicides are not recommended by CDC  Disrupt cervical mucosa  Potentially increase viral shedding  Increase transmission of HIV to uninfected partners  Diaphragms and cervical caps are not encouraged by the CDC due to concerns about their use with spermicides
  • 27. Female and Male Sterilization  Contraceptive sterilization is the most widely used method of family planning  Clients should be advised that sterilization should be considered permanent  Male-vasectomy: Cutting/occluding both vas deferens  1st yr failure rate-0%-0.5%  Female-sterilization  Transabdominal  Transcervical  Tubal sterilization  Occlusion method
  • 28. Hormonal Contraception and HIV Acquisition: WHO Technical Statement  Most studies found no statistically significant association between oral contraception and HIV acquisition  Evidence on injectable HC varied with some studies showing increases between 48% to 100% and other studies reporting no association  Due to inconsistent data and limitations of the studies performed WHO rated the current evidence as low
  • 29. HIV Transmission and Hormonal Contraception: WHO Technical Statement  Recent observational study found a 2-3 increase in HIV transmission in women using injectables over oral contraception  Findings from studies assessing HC and genital HIV shedding are not consistent  Studies assessing HC and viral load generally showed no negative effect  WHO rates the evidence for HIV transmission and injectable use as low and HIV transmission and oral contraception as very low
  • 30. HIV Disease Progression and Hormonal Contraception: WHO Technical Statement  None of the 10 observational studies conducted found a significant association between hormonal contraception and HIV progression  One randomized controlled trial found an increased risk of progression for HC users compared to copper IUD users  Due to flaws in this study --- high rates of method switching and loss to follow-up --- the evidence for HC and HIV progression is rated as low
  • 31. WHO Recommendations  No restriction on the use of any hormonal contraceptive method for HIV-positive women or women at high risk for HIV infection  Critical importance must be placed on the consistent and correct use of condoms for the prevention of HIV acquisition or transmission  Most concern is focused on the evidence of HIV acquisition and DMPA because a causal relationship is neither established nor ruled out  Voluntary use of contraception by HIV positive women who wish to prevent pregnancy continues to be an important PMTCT strategy
  • 32. Thank you! Contact the FXB Center with questions or comments, or for a copy of the slide set: Mary Jo Hoyt hoyt@umdnj.edu

Editor's Notes

  1. Centers for Disease Control and Prevention. (2010, April 30). Unintended pregnancy prevention: Home. Retrieved from http://www.cdc.gov/reproductivehealth/unintendedpregnancy/ Panel on Treatment of HIV-Infected Pregnant Women and Prevention of Perinatal Transmission. (2011, September 14). 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. Retrieved from http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf.
  2. Talking Points One of the most important strategies to decrease the proportion of unintended pregnancies is the use of effective family planning methods. This chart shows the relative typical effectiveness of various family planning methods – typical effectiveness refers to how effective the different methods are at preventing pregnancy during actual use, including inconsistent or incorrect use. At the top you will find male and female sterilization, along with long acting reversible contraceptives or LARCS, which include intrauterine devices or IUDs and contraceptive implants. More commonly used, and less effective methods, are listed below such as injectables and oral contraceptives shown in the second row from the top and condoms shown in the third row from the top. References Adapted from: WHO. Family Planning: A Global Handbook
  3. World Health Organization Department of Reproductive Health and Research (WHO/RHR) and Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs (CCP), INFO Project. (2007) Family planning: A global handbook for providers. Baltimore and Geneva: CCP and WHO.
  4. World Health Organization Department of Reproductive Health and Research (WHO/RHR) and Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs (CCP), INFO Project. (2007) Family planning: A global handbook for providers. Baltimore and Geneva: CCP and WHO.
  5. World Health Organization Department of Reproductive Health and Research (WHO/RHR) and Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs (CCP), INFO Project. (2007) Family planning: A global handbook for providers. Baltimore and Geneva: CCP and WHO.
  6. Vogler, M.A., Patterson, K. et al. (2010, December 1). Contraceptive efficacy of oral and transdermal hormones when co-administered with protease inhibitors in HIV-1 infected women: Pharmacokinetic results of ACTG trial A5188. J Acquir Immune Defic Syndr, 55(4), 473-82.
  7. World Health Organization Department of Reproductive Health and Research (WHO/RHR) and Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs (CCP), INFO Project. (2007) Family planning: A global handbook for providers. Baltimore and Geneva: CCP and WHO.
  8. Centers for Disease Control and Prevention. (2010, May 28). U.S. medical eligibility criteria for contraceptive use, 2010: Adapted from the World Health Organization medical eligibility criteria for contraceptive use, 4th edition. MMWR Early Release, 59.
  9. Centers for Disease Control and Prevention. (2010, May 28). U.S. medical eligibility criteria for contraceptive use, 2010: Adapted from the World Health Organization medical eligibility criteria for contraceptive use, 4th edition. MMWR Early Release, 59.
  10. Panel on Treatment of HIV-Infected Pregnant Women and Prevention of Perinatal Transmission. (2011, September 14). 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. Retrieved from http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf.
  11. Panel on Treatment of HIV-Infected Pregnant Women and Prevention of Perinatal Transmission. (2011, September 14). 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. Retrieved from http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf.
  12. Panel on Treatment of HIV-Infected Pregnant Women and Prevention of Perinatal Transmission. (2011, September 14). 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. Retrieved from http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf.
  13. Panel on Treatment of HIV-Infected Pregnant Women and Prevention of Perinatal Transmission. (2011, September 14). 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. Retrieved from http://aidsinfo.nih.gov/ContentFiles/PerinatalGL.pdf.
  14. World Health Organization Department of Reproductive Health and Research (WHO/RHR) and Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs (CCP), INFO Project. (2007) Family planning: A global handbook for providers. Baltimore and Geneva: CCP and WHO.
  15. American College of Obstetricians and Gynecologists (ACOG). (2010, December). Gynecologic care for women with human immunodeficiency virus. Obstetrics and Gynecology, 116(6), 1492-1509. World Health Organization Department of Reproductive Health and Research (WHO/RHR) and Johns Hopkins Bloomberg School of Public Health/Center for Communication Programs (CCP), INFO Project. (2007) Family planning: A global handbook for providers. Baltimore and Geneva: CCP and WHO.
  16. Centers for Disease Control and Prevention. (2010, May 28). U.S. medical eligibility criteria for contraceptive use, 2010: Adapted from the World Health Organization medical eligibility criteria for contraceptive use, 4th edition. MMWR Early Release, 59. World Health Organization. (2009). Medical eligibility criteria for contraceptive use fourth edition, 2009. Retrieved from http://whqlibdoc.who.int/publications/2010/9789241563888_eng.pdf
  17. World Health Organization. (2012, February 16). Hormonal contraception and HIV: Technical statement. Retrieved from http://whqlibdoc.who.int/hq/2012/WHO_RHR_12.08_eng.pdf
  18. World Health Organization. (2012, February 16). Hormonal contraception and HIV: Technical statement. Retrieved from http://whqlibdoc.who.int/hq/2012/WHO_RHR_12.08_eng.pdf
  19. World Health Organization. (2012, February 16). Hormonal contraception and HIV: Technical statement. Retrieved from http://whqlibdoc.who.int/hq/2012/WHO_RHR_12.08_eng.pdf
  20. World Health Organization. (2012, February 16). Hormonal contraception and HIV: Technical statement. Retrieved from http://whqlibdoc.who.int/hq/2012/WHO_RHR_12.08_eng.pdf