Combined hormonal contraceptives contain both estrogen and a progestin. This contraceptive category includes combined oral contraceptives, transdermal patches and vaginal rings. They are effective when taken as directed, reversible and can be used by women of all ages. It is important to alert women that they will not protect against STDs and other preventative measures will be required to protect against infections. The following assumes there are no contraindications to estrogen component (e.g., breast cancer, hyperlipidemia, liver disease etc.). Only BP is “essential and mandatory” and when BP cannot be measured by a provider, a measurement obtained in other setting can be reported by the woman to her provider. The following are highlights from the CDC recommendations on initiation:
Initiation – Criteria and Timing
Patient with Amenorrhea (Not Postpartum)
Postpartum (Not Breastfeeding)
Postabortion (Spontaneous or Induced)
Switching from Another Contraceptive Method
CDC Criteria to determine with ‘reasonable certainty’ that woman is not pregnant (≥1 of the following)
Timing
Back-Up Contraception
There may be times there is uncertainty whether a woman is pregnant. According to the CDC, “the benefits of starting combined hormonal contraceptives likely exceed any risk; therefore, starting combined hormonal contraceptives should be considered at any time, with a follow-up pregnancy test in 2–4 weeks.” In a situation where a woman needs to use additional contraceptive protection when making the switch to combined hormonal contraception, consider continuing previous contraceptive methods for 7 days after starting combined hormonal contraception
The following factors elevate risk of VTE sufficiently to classify as 3 or 4 and alternate methods should be used
CDC: U.S. Selected Practice Recommendations for Contraceptive Use, 2016
CDC MEC: Classifications for Combined Hormonal Contraceptives
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