What are the guidelines for Nexplanon (etonogestrel) placement?

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Last updated: September 18, 2025View editorial policy

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Guidelines for Nexplanon (Etonogestrel) Placement

Nexplanon should be inserted subdermally in the inner side of the non-dominant upper arm, within the first 5 days of menstrual cycle onset for immediate contraceptive effect, or at any time if pregnancy can be reasonably excluded, with backup contraception for 7 days if inserted after day 5. 1

Timing of Insertion

The timing of Nexplanon insertion depends on the woman's current situation:

Menstruating Women

  • Insert within first 5 days since menstrual bleeding started for immediate contraceptive protection 1
  • If inserted >5 days since menstrual bleeding started, backup contraception needed for 7 days 1

Amenorrheic Women (Not Postpartum)

  • Can be inserted anytime if reasonably certain woman is not pregnant
  • Backup contraception needed for 7 days 1

Postpartum Women

  • Breastfeeding women: Can be inserted anytime (U.S. MEC 2 if <1 month postpartum; U.S. MEC 1 if ≥1 month postpartum) 1
  • Non-breastfeeding women: Can be inserted anytime, including immediately postpartum (U.S. MEC 1) 1
  • Backup contraception needed for 7 days if ≥21 days postpartum without return of menstrual cycle 1

Post-abortion

  • Can be inserted within 7 days, including immediately after abortion (U.S. MEC 1) 1
  • No backup contraception needed if placed at time of surgical abortion
  • Otherwise, backup contraception needed for 7 days 1

Switching from Another Method

  • Can be inserted immediately; waiting for next menstrual period unnecessary 1
  • Backup contraception needed for 7 days if >5 days since menstrual bleeding started 1
  • When switching from IUD, special considerations apply to prevent risk of pregnancy 1

Pre-Insertion Requirements

Among healthy women, no examinations or tests are needed before Nexplanon insertion 1:

  • No pelvic examination required
  • No liver enzyme tests required
  • Baseline weight/BMI measurement may be useful for monitoring over time 1

Insertion Procedure

Proper insertion technique is critical to prevent complications:

  • Must be performed by healthcare providers who completed the Nexplanon clinical training program 2, 3
  • Inserted subdermally in the inner side of the non-dominant upper arm
  • Proper insertion technique reduces risk of incorrect placement (12.6 per 1000 insertions) 2

Common Complications and Prevention

Complications associated with insertion and removal are rare when performed by trained clinicians 2:

  • Incorrect insertion (non-insertion, partial insertion, or deep insertion): 12.6 per 1000 insertions 2
  • Pins and needles/numbness in arm/hand/fingers: most common patient-reported event 2
  • Removal complications: encasement of implant in fibrotic tissue most common 2

Post-Insertion Care

  • Apply sterile dressing daily with local disinfection until granulation occurs (usually 1-7 days) 4
  • Counsel patients about potential side effects, particularly irregular bleeding patterns 4
  • Remind patients that Nexplanon does not protect against STIs 4

Removal Considerations

  • Nexplanon should be removed by the end of the third year of use 3
  • All removals in the NORA study were successful except one (due to deep muscle tissue location) 2
  • Mean removal time is approximately 2 minutes 5
  • Rapid return to fertility occurs after removal 3

Special Considerations

  • For women taking enzyme-inducing medications (certain antiretrovirals, anticonvulsants), additional contraceptive methods may be warranted due to potential reduced efficacy 4
  • Immediate postpartum placement is safe and effective 4

By following these guidelines for Nexplanon placement, healthcare providers can ensure high contraceptive efficacy while minimizing complications associated with insertion and removal.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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