Levonorgestrel Intrauterine System

Key Points

  • The levonorgestrel-releasing intrauterine contraception (LNG-IUS/LNG-IUC) is a T-shaped device inserted into the uterus that releases low-dose progestin locally — the most effective reversible contraception available (99.8% perfect and typical use).
  • Brand options by duration: Mirena (7 years), Liletta (6 years), Kyleena (5 years), Skyla (3 years — smaller frame for adolescents/nulliparous).
  • Dual indications: (1) Long-term contraception; (2) treatment of heavy menstrual bleeding (menorrhagia) — Mirena FDA-approved for up to 5 years for menorrhagia.
  • Key complications: increased risk of ectopic pregnancy, IUC expulsion or misplacement, PID risk elevated in first 3 weeks after insertion, uterine perforation (rare).
  • Patient education: check strings monthly at the cervix, attend early placement follow-up (commonly 4-6 weeks), and understand fertility returns immediately after removal.

Mechanism of Action

The LNG-IUS releases levonorgestrel (progestin) locally into the uterine cavity:

  1. Endometrial suppression: Prevents proliferation of the endometrium — thin lining reduces menstrual bleeding and endometrial cancer risk
  2. Cervical mucus thickening: Progestin thickens cervical mucus, preventing sperm penetration
  3. Suppression of ovulation (partial, depending on dose): Higher-dose devices (Mirena) may partially suppress ovulation
  4. Foreign body effect: The plastic T-frame creates a local inflammatory response that is spermicidal

Brand Comparison

BrandDurationFrame SizeNotes
MirenaUp to 7 yearsStandardApproved for menorrhagia treatment (up to 5 years); 20 mcg/day initial release
LilettaUp to 6 yearsStandardSimilar to Mirena; lower cost option
KyleenaUp to 5 yearsSmallerLower hormone dose; suitable for adolescents and nulliparous patients
SkylaUp to 3 yearsSmallestLowest dose (14 mcg/day); best for adolescents or short-term use

Indications

IndicationNotes
Long-term contraceptionHighly effective for up to 7 years; immediate return to fertility after removal
Menorrhagia (heavy menstrual bleeding)Mirena FDA-approved for treatment of menorrhagia — thins endometrium, reduces blood loss
Dysmenorrhea associated with endometriosisReduces menstrual pain and bleeding
PerimenopauseLNG-IUS during perimenopause controls abnormal and heavy bleeding; not contraindicated

Benefits

  • Highest effectiveness: Perfect and typical use effectiveness equal at 99.8% — no adherence required
  • Amenorrhea: 6%–20% of users develop amenorrhea (absence of periods), depending on device hormone dose
  • Reduced endometrial cancer risk: Prevents endometrial thickening
  • No estrogen-related risks: Safe for patients who cannot use estrogen (smokers, hypertension, DVT history)
  • Privacy: No visible packaging; nothing to do before intercourse
  • Immediate return to fertility after removal

Complications

ComplicationDescriptionNursing Action
Ectopic pregnancy riskProgestin slows cilia in fallopian tubes, increasing ectopic risk if pregnancy occursEducate to report pregnancy symptoms immediately; check strings monthly
Expulsion or misplacementDevice expelled from uterus — especially high rate if placed immediately after placenta deliveryEducate patient to check strings monthly; contact provider if strings not felt or if can’t locate device
Pelvic inflammatory disease (PID)Risk elevated in first 3 weeks after insertion; not significantly higher overallScreen for STIs before insertion; educate to report fever, abnormal discharge, pelvic pain
Uterine perforationRare during insertion — device may extrude into peritoneal cavityEducate to report heavy vaginal bleeding, severe cramping, fever after insertion
Abnormal bleedingIrregular spotting common in first 3–6 months, especially with MirenaReassure patient; menstrual pattern typically improves after 3 months

Contraindications

  • Pregnancy (known or suspected)
  • Uterine anomalies that distort the uterine cavity
  • Current pelvic infection (PID, endometritis, cervicitis)
  • Unexplained vaginal bleeding
  • Reproductive tract cancers (cervical, uterine, ovarian)
  • Breast cancer (hormone-sensitive)
  • Liver disease or hepatic tumor

Pre-Insertion Nursing Responsibilities

  • Screen for STIs (gonorrhea, chlamydia) before insertion — reduces PID risk
  • Confirm no current pregnancy
  • Obtain informed consent — discuss benefits, risks, complications, and alternative methods
  • Assess for uterine anomalies (may require imaging prior to insertion)
  • Educate patient about expected cramping and bleeding during and after insertion
  • Arrange follow-up to confirm placement stability, commonly about 4-6 weeks after insertion

Patient Education

NCLEX Focus

Key patient education priorities: (1) check strings monthly at the cervix — contact provider if cannot feel them; (2) report pregnancy symptoms immediately (ectopic risk); (3) return to fertility is immediate after removal; (4) LNG-IUS does NOT protect against STIs; (5) irregular bleeding in first 3–6 months is expected.

  • String check: Reach inside vagina to locate strings hanging from cervix — check monthly after menstruation
  • Follow-up timing: Keep early postinsertion visit (often 4-6 weeks) to confirm continued correct placement
  • STI protection: LNG-IUS does NOT protect against sexually transmitted infections — condoms recommended
  • Pregnancy symptoms: Report nausea, breast tenderness, missed period — check for ectopic pregnancy
  • Menstrual changes: Expect irregular spotting initially; amenorrhea is expected and normal with Mirena

Self-Check

  1. A patient with an LNG-IUS reports she cannot feel the strings during her monthly check. What is the priority nursing instruction?
  2. A patient asks why the nurse is recommending condom use when she already has an LNG-IUS. How should the nurse respond?
  3. What is the advantage of Kyleena or Skyla over Mirena for an adolescent patient requesting an IUC?