U.S. Medical Eligibility Criteria for Contraceptive Use, 2016
Kathryn M. Curtis, PhD; Naomi K. Tepper, MD; Tara C. Jatlaoui, MD, et al.
MMWR Recomm Rep 2016;65:1–104
The 2016 U.S. Medical Eligibility Criteria for Contraceptive Use (U.S. MEC) comprises recommendations for the use of specific contraceptive methods by women and men who have certain characteristics or medical conditions. Notable updates since the 2010 U.S. MEC include the addition of recommendations for women with cystic fibrosis, women with multiple sclerosis, and women receiving certain psychotropic drugs or St. John’s wort; revisions to the recommendations for emergency contraception, including the addition of ulipristal acetate; and revisions to the recommendations for postpartum women; women who are breastfeeding; women with known dyslipidemias, migraine headaches, superficial venous disease, gestational trophoblastic disease, sexually transmitted diseases, and human immunodeficiency virus; and women who are receiving antiretroviral therapy. These recommendations are a companion document to the CDC U.S. Selected Practice Recommendations for Contraceptive Use, 2016.
U.S. Medical Eligibility Criteria for Contraceptive Use, 2016 | MMWR
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| MMWR Recommendations and Reports Vol. 65, No. RR-3 July 29, 2016 |
U.S. Medical Eligibility Criteria for Contraceptive Use, 2016
Recommendations and Reports / July 29, 2016 / 65(3);1–104
Kathryn M. Curtis, PhD1; Naomi K. Tepper, MD1; Tara C. Jatlaoui, MD1; Erin Berry-Bibee, MD1,2; Leah G. Horton, MSPH1; Lauren B. Zapata, PhD1; Katharine B. Simmons, MD1,2; H. Pamela Pagano, MPH1; Denise J. Jamieson, MD1; Maura K. Whiteman, PhD1 (View author affiliations)
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The 2016 U.S. Medical Eligibility Criteria for Contraceptive Use (U.S. MEC) comprises recommendations for the use of specific contraceptive methods by women and men who have certain characteristics or medical conditions. These recommendations for health care providers were updated by CDC after review of the scientific evidence and consultation with national experts who met in Atlanta, Georgia, during August 26–28, 2015. The information in this report updates the 2010 U.S. MEC (CDC. U.S. medical eligibility criteria for contraceptive use, 2010. MMWR 2010:59 [No. RR-4]). Notable updates include the addition of recommendations for women with cystic fibrosis, women with multiple sclerosis, and women receiving certain psychotropic drugs or St. John’s wort; revisions to the recommendations for emergency contraception, including the addition of ulipristal acetate; and revisions to the recommendations for postpartum women; women who are breastfeeding; women with known dyslipidemias, migraine headaches, superficial venous disease, gestational trophoblastic disease, sexually transmitted diseases, and human immunodeficiency virus; and women who are receiving antiretroviral therapy. The recommendations in this report are intended to assist health care providers when they counsel women, men, and couples about contraceptive method choice. Although these recommendations are meant to serve as a source of clinical guidance, health care providers should always consider the individual clinical circumstances of each person seeking family planning services. This report is not intended to be a substitute for professional medical advice for individual patients. Persons should seek advice from their health care providers when considering family planning options.
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