What is Copper T (intrauterine device, IUD), its method of insertion, types, mechanism of action, contraindications, and indications?

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Copper T Intrauterine Device (IUD): Comprehensive Overview

What is the Copper T IUD?

The Copper T380-A (ParaGard) is a T-shaped intrauterine device containing 380 mm² of copper that provides highly effective, long-acting reversible contraception for 10 years with a failure rate of less than 1%. 1

The device is used by over 150 million women worldwide, making it the most widely used reversible contraceptive method globally. 2

Types of Copper IUDs

Available Copper IUDs

  • TCu380A (Copper T380-A, ParaGard): The most effective copper IUD, approved for 10 years of use in the United States 1
  • TCu380S: Slightly more effective than TCu380A after the first year, though associated with higher expulsion rates 3
  • MLCu375, MLCu250, TCu220, TCu200, NovaT: Older generation devices that are less effective than TCu380A 4, 3

TCu380A and TCu380S are superior to all other copper IUDs in preventing pregnancy. 3 TCu380A demonstrated significantly better efficacy than MLCu375 (rate difference 1.70% after 4 years), MLCu250, TCu220, and TCu200. 4

Mechanism of Action

The copper IUD prevents pregnancy primarily by preventing fertilization, not by preventing implantation. 5

Specific Mechanisms:

  • Spermicidal effect: Copper ions create a toxic environment for sperm, inhibiting sperm motility and viability 6
  • Inflammatory response: Creates a sterile inflammatory reaction in the endometrium that is toxic to sperm and ova 5
  • Cervical mucus alteration: Thickens cervical mucus, creating a barrier to sperm penetration 6
  • All mechanisms occur before fertilization, making this a true contraceptive rather than an abortifacient 7

Method of Insertion

Timing of Insertion

  • Immediate effectiveness: No backup contraception is required after insertion, as the device is effective immediately 8, 9
  • Can be inserted at any time during the menstrual cycle if pregnancy can be reasonably excluded 1
  • Postpartum insertion: Safe at ≥4 weeks after delivery, or can be inserted immediately postpartum (though with higher expulsion rates) 1

Insertion Procedure Considerations

  • STI screening: Can be performed on the day of insertion; treatment can be provided afterward without device removal if needed 1, 9
  • Pain at insertion: Less than 1.5% of women experience significant problems such as difficult insertion, pain, bleeding, or syncope 6
  • Perforation risk: Occurs in 0.6 to 16 cases per 1000 insertions; risk is higher when inserted less than 4-6 weeks postpartum or post-abortion 6
  • Nulliparous women: Experience more pain during insertion but are otherwise appropriate candidates 6, 3

Post-Insertion Monitoring

  • Infection risk window: The risk of pelvic infection is confined to the first 20-21 days after insertion 1, 2
  • Expulsion rates: Occur in 5-10% of cases within 5 years, with higher rates in younger nulliparous women 1, 6

Indications

Primary Indication

  • Long-term contraception for women seeking highly effective, reversible, non-hormonal birth control for up to 10 years 1

Special Populations Where Copper IUD is Particularly Indicated

  • Women with contraindications to estrogen: First-line choice for women with history of deep venous thrombosis, pulmonary embolism, or coronary events 6
  • Breastfeeding women: Safe to use immediately postpartum 6
  • Women with diabetes or HIV infection: No contraindications 6
  • Nulliparous adolescents: Safe and effective despite past concerns 1
  • Women requiring emergency contraception: Can be inserted within 5 days of unprotected intercourse as highly effective emergency contraception 1

Additional Clinical Scenarios

  • Immediate postpartum period: Can be inserted while still in the hospital, supported by ACOG and CDC 1
  • History of ectopic pregnancy: Not a contraindication 6
  • During NSAID therapy: Safe to use 6

Contraindications

Absolute Contraindications (Category 4)

Pregnancy is the only absolute contraindication to copper IUD insertion due to risk of severe pelvic infection and septic spontaneous abortion. 8, 9

Relative Contraindications (Category 3)

  • Current purulent cervicitis 1
  • Active gonorrhea or chlamydia infection: Increased risk of pelvic inflammatory disease with insertion 1, 8, 9
  • Current pelvic inflammatory disease 1
  • Other current pelvic infections 1

Important: NOT Contraindications

  • Past PID: Not a contraindication to IUD use 1
  • HIV infection: Not a contraindication 1, 9
  • Immunosuppression: Not a contraindication 1
  • Nulliparity: Not a contraindication 1

Common Pitfalls and Caveats

Infection Management

The critical window for infection risk is the first 20-21 days post-insertion; beyond this period, IUDs do not increase rates of STIs or PID. 1 If STIs or PID develop, they can be treated with the IUD in place as long as the patient improves with treatment. 1

Pregnancy Considerations

  • Ectopic pregnancy: While ectopic pregnancies are rarer in IUD users than in women using no contraception, about 1 in 20 pregnancies that occur with an IUD in place is ectopic 6
  • Intrauterine pregnancy with IUD: If pregnancy occurs, about 25% end in live birth if the device is left in place, compared to 90% if removed 6

Side Effects

  • Increased menstrual bleeding: Copper IUDs increase menstrual blood loss by approximately 50%, often associated with dysmenorrhea 6, 5
  • Most common reasons for discontinuation: Menstrual bleeding and pain 2
  • However, continuation rates are high: Approximately 50% of women continue use after 5 years, which is higher than many other contraceptive methods 2

STI Protection

The copper IUD does not protect against sexually transmitted infections or HIV; condoms must be used consistently if there is STI/HIV risk. 9

Expulsion

  • Higher in younger women: Expulsion may occur more frequently in adolescents and younger nulliparous women, though overall rates remain below 5% 8
  • Recurrence: Expulsion recurs in approximately 30% of women who experience it once 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Copper containing, framed intra-uterine devices for contraception.

The Cochrane database of systematic reviews, 2007

Research

Modern intra-uterine devices.

Bailliere's clinical obstetrics and gynaecology, 1996

Guideline

Levonorgestrel Intrauterine Device (IUD) Contraception and Therapeutic Benefits

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Copper T IUD Contraindications and Risks

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Contraindications for the Use of Copper Intrauterine Devices

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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