What are the benefits and risks of Depo-Provera (medroxyprogesterone acetate) birth control for a woman of reproductive age?

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Depo-Provera Birth Control: Key Information

Effectiveness

Depo-Provera (depot medroxyprogesterone acetate, DMPA) is a highly effective contraceptive with a typical-use failure rate of approximately 6% in the first year, comparable to modern IUDs and superior to many other methods. 1 The contraceptive efficacy exceeds 99% with perfect use. 2

  • DMPA is administered as 150 mg intramuscularly or 104 mg subcutaneously every 13 weeks (up to 15 weeks). 1
  • Ovulation is suppressed for at least 14 weeks after a single 150 mg dose. 2
  • The method can be initiated mid-cycle with a "quick start" approach if pregnancy is reasonably excluded, with backup contraception needed for the first 7 days. 1
  • Self-administration of the subcutaneous formulation is now supported, with studies showing 12-month continuation rates of 1.27 times higher than provider-administered methods. 1

Major Benefits

  • Convenience: Requires only quarterly injections rather than daily adherence, eliminating the "fear of forgetting" associated with daily methods. 3
  • Menstrual benefits: Reduces menstrual blood loss, improves dysmenorrhea, and protects against iron-deficiency anemia. 1
  • Cancer protection: Provides prolonged protective effect against endometrial cancer with no increased overall risk of breast, ovarian, liver, or cervical cancer in long-term surveillance studies. 4
  • Medical advantages: Safe for lactating women, may raise seizure threshold in epilepsy, may decrease sickle cell crises, and reduces risk of pelvic inflammatory disease. 1, 2
  • Cardiovascular safety: No appreciable effects on blood pressure or thrombosis risk, making it suitable for women who cannot use combined hormonal contraceptives. 3

Critical Risks and Side Effects

Bone Mineral Density Loss (Most Serious Concern)

The FDA issued a black box warning in 2004 regarding significant bone mineral density (BMD) loss with DMPA use, though subsequent evidence shows substantial recovery after discontinuation. 1, 4

  • Adult women using DMPA for 5 years show spine and hip BMD decreases of 5-6%, with the most pronounced decline in the first 2 years. 4
  • Adolescents show even greater concern: at 4.6 years of use, lumbar spine BMD decreased 4.17% while untreated controls gained 5.12%. 4
  • BMD partially recovers after discontinuation, but recovery may be incomplete with longer duration of use. 1, 4
  • The American College of Obstetricians and Gynecologists does NOT recommend limiting use to 2 years or routine BMD monitoring, as preventing unwanted pregnancy outweighs bone density concerns. 1, 5
  • DMPA should be used long-term (>2 years) only if other methods are inadequate, per FDA labeling. 4

All patients must receive counseling on skeletal health measures: 1300 mg calcium daily, 600 IU vitamin D, regular weight-bearing exercise, and smoking cessation. 1, 5

Menstrual Irregularities

  • Nearly all users experience menstrual disruption initially, typically irregular spotting and bleeding. 1, 4
  • By 12 months, 55% of women experience amenorrhea; by 24 months, 68% have amenorrhea. 4
  • Counseling about menstrual changes BEFORE the first injection significantly improves continuation rates. 1
  • Irregular bleeding typically improves over time and rarely requires surgical intervention. 3

Weight Gain

  • Weight gain is common, though not universal. 1, 5
  • Weight gain status at 6 months strongly predicts future excessive weight gain: patients gaining >5% body weight at 6 months are at high risk for significant BMI increases with continued use. 1, 5
  • Studies show 21% of adolescents experience early excessive weight gain. 1

Delayed Return to Fertility

  • Return to fertility typically takes 9-18 months after discontinuation, regardless of subcutaneous or intramuscular formulation. 1, 5, 2
  • This delay occurs while the endometrial lining recovers and ovulatory function returns. 5
  • DMPA does not cause permanent infertility. 2

Other Side Effects

  • Headache, breast tenderness (mastalgia), hair loss, and changes in libido may occur. 1, 5
  • Injection site reactions are more common with self-administered subcutaneous formulations. 1

Contraindications

Absolute contraindications include: 6

  • History of stroke or myocardial infarction
  • Current or history of pulmonary embolism or deep vein thrombosis
  • History of neurofibromas or meningiomas (DMPA may stimulate tumor growth)

Relative contraindications/special precautions: 1, 6

  • Positive antiphospholipid antibodies
  • High risk for osteoporosis (metabolic bone disease, chronic corticosteroid use, anorexia nervosa, strong family history)
  • Active smoking combined with other risk factors

NOT contraindications: 6

  • Past history of pelvic inflammatory disease (only current PID is contraindicated)
  • HIV infection or immunosuppression
  • Adolescent age (though bone density concerns require thorough counseling)

Special Populations

Adolescents

  • DMPA is appropriate for adolescents with proper counseling about bone density effects. 1
  • Particularly useful for those with complex medical conditions requiring menstrual suppression when estrogen is contraindicated. 1
  • Scheduling visits every 11-12 weeks (rather than 13) allows buffer for missed appointments. 1

Women with Rheumatic Diseases

  • Safe in most women with rheumatic and musculoskeletal diseases, with 3% typical-use failure rate. 1
  • Exceptions: positive antiphospholipid antibodies or high osteoporosis risk. 1

Postpartum and Lactating Women

  • Safe for breastfeeding women with no adverse effects on lactation. 7
  • Provides advantage over combined hormonal methods in this population. 7

Clinical Pitfalls to Avoid

  • Do not assume amenorrhea after 3 years is solely due to DMPA: Rule out pregnancy and other causes, especially if amenorrhea persists beyond 18 months post-discontinuation. 8
  • Do not fail to counsel about menstrual changes before initiation: Pre-injection counseling dramatically improves continuation rates. 1, 3
  • Do not ignore early weight gain: Patients gaining >5% at 6 months need counseling about risk of continued excessive weight gain. 1
  • Do not automatically limit use to 2 years: ACOG does not recommend this restriction, though FDA labeling suggests using long-term only if other methods inadequate. 1, 5, 4
  • Do not forget STI protection counseling: DMPA provides no protection against sexually transmitted infections; condoms must be used concurrently for STI prevention. 1

Monitoring Recommendations

  • No routine BMD monitoring is recommended by ACOG, though BMD evaluation should be considered when women need to continue long-term use. 4
  • For adolescents, BMD interpretation must account for patient age and skeletal maturity. 4
  • Evaluate for other osteoporosis risk factors when considering long-term use. 5
  • If abnormal bleeding persists or is severe, investigate to rule out organic pathology. 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Long-acting injectable contraception with depot medroxyprogesterone acetate.

American journal of obstetrics and gynecology, 1994

Research

Depo Provera. Position paper on clinical use, effectiveness and side effects.

The British journal of family planning, 1999

Guideline

Risks of Long-Term Depo Provera Use Beyond 2 Years

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Contraindications and Precautions for Depo-Provera Use

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Experience with medroxyprogesterone acetate (Depo-Provera) as an injectable contraceptive.

International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 1977

Guideline

Workup for Secondary Amenorrhea Following Depo Provera Use

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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