Everything you need to know about the contraceptive implant
FDA approval means US women now have a progestin-only implant among their birth control options
IN THIS ARTICLE
On July 17, the US Food and Drug Administration (FDA) approved what may be the most effective hormonal contraceptive ever developed, a single-rod implant that goes by the trade name Implanon. The implant contains 68 mg of etonogestrel (ENG), the active metabolite of desogestrel, in a membrane of ethylene vinyl acetate. In clinical trials involving 20,648 cycles of exposure, only 6 pregnancies occurred, for a cumulative Pearl Index of 0.38 per 100 woman-years.1
This article reviews:
- the 2 contraceptive mechanisms
- indications and patient selection
- pharmacology, safety, adverse effects
- patient satisfaction and discontinuation rates
- insertion and removal
- key points of patient counseling
Unlike Norplant, a multi-rod implant which garnered a million American users before it was removed from the market, the single-rod implant is easy to insert and remove. Before you can order the implant, you must complete a manufacturer-sponsored training program.
Which patients are suitable candidates?
Because the subdermal implant contains only progestin, provides up to 3 years of protection, and requires no daily, weekly, or even monthly action on the part of the user, it is well-suited for:
- Women who wish to or need to avoid estrogen
- Teens who find adherence to a contraceptive regimen difficult
- Healthy adult women who desire long-term protection
- Women who are breastfeeding
Pros and cons
- Cost. A study2 of 15 contraceptive methods found the implant cost-effective compared to short-acting methods, provided it was used long-term. As of press time, the manufacturer had not released the price.
- Short fertility-recovery time.
- No serious cardiovascular effects.3
Drawbacks. Progestin-only contraceptives also have disadvantages:
- Implants require a minor surgical procedure by trained clinicians for insertion and removal.
- Cost-effectiveness depends on duration of use; early discontinuation negates this benefit.2
- The implant does not protect against sexually transmitted infections—this is a disadvantage of all contraceptive methods except condoms and, perhaps, other barrier methods.
A forgettable contraceptive—that’s its allure
After Implanon is inserted just below the dermis 6 to 8 cm above the elbow crease on the inner aspect of the arm, it remains effective for up to 3 years. To remove it, make a 2-mm incision at the distal tip of the implant and push on the other end of the rod until it pops out.
The implant resides beneath the dermis but above the subcutaneous fat. It remains palpable but invisible, releasing about 60 μg of etonogestrel per day
Images: Rich Larocco
The Norplant experience
Research and development of progestin-only subdermal implants began more than 35 years ago, but early research involving very-low-dose implants found that they did not prevent ectopic pregnancies. This problem ended with Norplant, a 6-capsule implant using the potent progestin levonorgestrel (LNG).
Norplant was highly effective. Over 7 years of use, fewer than 1% of women became pregnant.4 Despite low pregnancy rates and few serious side effects, limitations in component supplies and negative media coverage on complications with removal led to its withdrawal in 2002, leaving no implant available in the US.5
The antiestrogenic effect
Long-acting, progestin-only contraceptives such as the new implant, the LNG-releasing intrauterine system (Mirena), and injectable methods (Depo-Provera) are safer than oral contraceptives (OCs) because they lack estrogen, which can provoke deep venous thrombosis.6,7
LNG, the gonane progestin used in Norplant, binds with high affinity to the progesterone, androgen, mineralocorticoid, and glucocorticoid receptors, but not to estrogen receptors. ENG, also known as 3-keto-desogestrel, demonstrates no estrogenic, anti-inflammatory, or mineralocorticoid activity, but has shown weak androgenic and anabolic activity, as well as strong antiestrogenic activity.
Unlike LNG, which binds mainly to sex hormone-binding globulin, ENG binds mainly to albumin, which is not affected by varying endogenous or exogenous estradiol levels. The safety of ENG has been demonstrated in studies of combined estrogen-progestin OCs and progestin-only OCs that use desogestrel as a component.
How the progestin-only implant prevents fertilization
The progestin-only implant has 2 primary mechanisms:
- Inhibition of ovulation
- Restriction of sperm penetration of cervical mucus28
Ovulation is suppressed. LNG implants disrupt follicular growth and inhibit ovulation by exerting negative feedback on the hypothalamic–pituitary axis, causing a variety of changes, from anovulation to insufficient luteal function. A few women using LNG implants have quiescent ovaries, but most begin to ovulate as LNG blood concentrations gradually fall.29 The ENG implant suppresses ovulation by altering the hypothalamic–pituitary–ovarian axis and down-regulating the luteinizing hormone surge, which is required to support the production, growth, and maturation of ovarian follicles.11
Oocytes are not fertilized, even if follicles grow during use of the progestin implant. If the follicle ruptures, abnormalities of the ovulatory process prevent release of a viable egg.
Sperm cannot penetrate the cervical mucus. The antiestrogenic action of the progestin renders the cervical mucus viscous, scanty, and impenetrable by sperm.12
Contraceptive effects occur before fertilization
No signs of embryonic development have been found among implant users, indicating the implant lacks abortifacient properties.
Desogestrel in combination with ethinyl estradiol may slightly increase the attributable risk of deep venous thrombosis, but this response has not been shown without estrogen.
The single-rod design means little discomfort for patients at insertion or removal, an unobtrusive implant, and almost no scarring. Insertion and removal are predictably brief. In US and European trials, which began 10 years ago, average insertion time was 1 minute, and removal time was 3 minutes. In contrast, Norplant required up to 10 minutes to insert and 1 hour to remove.8
Because only 1 rod is implanted, there is no risk of dislocating previously placed capsules.9 Nor is it necessary, as it was with Norplant, to create channels under the skin, which made implants difficult to palpate after insertion.
Finally, ethylene vinyl acetate, the plastic from which Implanon is made, is less likely than Norplant’s Silastic to form a fibrous sheath that can prolong removal.10
Pharmacology of Implanon
Implanon is a single nonbiodegradable rod of 40% ethylene vinyl acetate and 60% ENG (40 mm×2 mm) covered with a membrane of rate-controlling ethylene vinyl acetate 0.06 mm thick.
The 68 mg of ENG contained in the rod are initially absorbed by the body at a rate of 60 μg per day, slowly declining to 30 μg per day after 2 years.
The steady release of ENG into the circulation avoids first-pass effects on the liver.
The bioavailability of ENG remains nearly 100% throughout 2 years of use. The elimination half-life of ENG is 25 hours, compared with 42 hours for Norplant’s LNG.
Rapid return to ovulation
Efficacy and safety
Liver enzyme-inducing drugs lower ENG levels
Like other contraceptive steroids, serum levels of ENG are reduced in women taking liver enzyme-inducing drugs such as rifampin, griseofulvin, phenylbutazone, phenytoin, and carbamazepine, as well as anti-HIV protease inhibitors. Pregnancies were reported among Australian women using Implanon along with some of these antiepileptic drugs.13
Equal efficacy in obese women?
The efficacy of the single-rod implant was studied in clinical trials involving 20,648 cycles of use.1 Only 6 pregnancies occurred in this population—2 each in years 1, 2, and 3 of use. None of the women who weighed 154 lb (70 kg) or more became pregnant.12
However, questions remain as to whether the new implant will maintain its high efficacy in obese women, as it has not been studied in women weighing more than 130% of their ideal body weight. Serum levels of ENG are inversely related to body weight and diminish over time, but increased pregnancy rates in obese women have not been reported.
Potential for ectopic pregancy
Suspect ectopic pregnancy in the rare event that a woman becomes pregnant or experiences lower abdominal pain.1 The reason: Pregnancies in women using contraceptive implants are more likely to be ectopic than are pregnancies in the general population. Ovulation is possible in the third year of use, but intrauterine pregnancies are very rare.1
Limited metabolic effects
Published studies indicate that the metabolic effects of the ENG implant are unlikely to be clinically significant, including its effects on lipid and carbohydrate metabolism, liver function, hemostasis, blood pressure, and thyroid and adrenal function.14-17
Adverse event rates
Overall, implants, including the ENG implant, appear to be safe. The rate of adverse events is comparable to rates in nonusers18 (death, neoplastic disease, cardiovascular events, anemia, hypertension, bone-density changes, diabetes, gall bladder disease, thrombocytopenia, and pelvic inflammatory disease).
In a study comparing 42 lactating mother–infant pairs using the ENG implant, compared with 38 pairs using intrauterine devices, there were no significant differences in milk volume, milk constituents, timing and amount of supplementary food, or infant growth rates.19
Because it contains no estrogen, Implanon is a good choice for immediate postpartum contraception.
Insertion and removal
The disposable trocar comes preloaded,22 and the needle tip has 2 cutting edges with different slopes. The extreme tip has a greater angle and is sharp to allow penetration through the skin. The second upper angle is smaller, and the corresponding edge is unsharpened to reduce the risk of placing the implant in muscle tissue.
Subdermal placement is imperative for efficacy and easy removal.
Have the patient lie on the examination table with her nondominant arm flexed at the elbow and her hand next to her ear. Identify and mark the insertion site using a sterile marker, and apply any necessary local anesthetic. The insertion site should be 6 to 8 cm above the elbow crease on the inner aspect of the arm. Also mark the skin 6 to 8 cm proximal to the first mark; this serves as a guide during insertion.
Remove Implanon from its package and, with the shield still on the needle, confirm the presence of the implant (a white cylinder) within the needle tip. Remove the needle shield, holding the inserter upright to prevent the implant from falling out. Apply countertraction to the skin at the insertion point and, holding the inserter at an angle no greater than 20 degrees, insert the needle tip into the skin with the beveled side up. Lower the inserter to a horizontal position, lifting the skin with the needle tip without removing the tip from the subdermal connective tissue, and insert the needle to its full length.
Next, break the seal of the applicator by pressing the obturator support, and rotate the obturator 90% (in regard to the needle) in either direction. At this point, the insertion process is the opposite of an injection: Hold the obturator in place and retract the cannula.
After insertion, the implant may not be visible but must remain palpable.1
Timing the insertion. Placement should occur at one of the following times:
- For women who have not been using contraception or who have been using a nonhormonal method, insert the implant between days 1 and 5 of menses.
- For women changing from a combination or progestin-only OC, insert the implant any time during pill-taking.
- For women changing from injectable contraception, insert the implant on the date the next injection is scheduled.
- For women using the IUD, insertion can take place at any time.
Additional birth control for 7 days
Advise all women to use an additional barrier method of contraception for 7 days following insertion, unless insertion directly follows an abortion (in which case, no additional contraception is needed).
In all cases, exclude pregnancy before inserting the implant, although there is no evidence that hormonal contraceptives cause birth defects.
The ENG implant can be removed at any time at the woman’s discretion, but will remain effective for 3 years.
Removal requires a 2-mm incision at the distal tip of the implant. The other end of the rod is then pushed until the rod pops out of the incision.9