Audio-Digest Foundation: obstetrics-gynecology

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Audio-Digest FoundationObstetrics/Gynecology


Volume 55, Issue 03
February 7, 2008

The following is an abstracted summary, not a verbatim transcript, of the lectures/discussions on this audio program. If, after reviewing this written summary, you would like to hear the contents and/or earn CME/CE credit:

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CONTRACEPTION UPDATE

Highlights from the 51st Annual T. Hart Baker, MD, Obstetrics and Gynecology Symposium, presented by Southern California Permanente Medical Group, Las Vegas, NV

Anita Nelson, MD, Professor, Department of Obstetrics and Gynecology, David Geffen School of Medicine at the University of California, Los Angeles, and Chief, Women’s Healthcare Programs, Harbor-UCLA Medical Center, Torrance, CA

Introduction: speaker believes many myths, beliefs, and attitudes about mammography and prenatal care apply to pregnancy prevention; only intended and unintended pregnancies tracked; intended pregnancy considered that which is not unintended; almost 49% of all pregnancies unintended; patients restricted from higher-tier methods of contraception in some settings until oral contraceptives (OCs) fail
Tiers of contraceptive efficacy
Top tier: implants, intrauterine devices (IUDs), monthly injections; failure rate <1%; implants least used method in United States; medroxyprogesterone acetate (DMPA [eg, Depo-Provera]) failure rate 3%
Second tier: combined hormonal methods; failure rate 8%
Third tier: barrier and behavior methods; condoms at top of third tier; failure rate 15% (18% for adolescents); spermicides least effective method
Etonogestrel contraceptive implant: effective 3 yr; no pregnancies in clinical trials; Physicians’ Desk Reference states pregnancy rate of 0.38% (attributed to patient being pregnant before implant inserted or inadvertently not inserted); Food and Drug Administration attributes any conception occurring within 2 wk of stopping method to be failure of that method; rapid return to fertility; mechanism of action—ovula-tion suppression; thickens cervical mucus; contains low levels of progestin; contraindications—patient with breast cancer or breast cancer within last 5 yr; drug interaction with cytochrome P450 (efficacy affected); rare medical contraindications; side effects—unpredictable bleeding patterns; acne in 0.1% of women with no acne before using method; significant improvement in 60% of women with moderate to severe acne; no difference in weight gain compared to women using nonmedicated IUD; good method for many women with serious medical problems in which other methods contraindicated
Copper IUD: copper T 380 device marketed in 1988 under strict regulation; highly effective, especially if conception not recommended (eg, breast cancer, autoimmune diseases); approved for use <10 yr; IUD most cost-effective contraceptive method; not abortifacient (ova recovered from women using IUD not fertilized); failure rates—data show no pregnancies in women using <20 yr; risk for expulsion reduced by 50% if not inserted during menses; data show prophylactic use of nonsteroidal anti-inflammatory drugs (NSAIDs; for pain and bleeding) did not reduce removal rates; risk for infection and pelvic inflammatory disease (PID) associated with early colonization of uterus; infection develops in 1 in 1000 women; insertion no longer contraindicated by—presence of bacterial vaginosis (BV) or yeast infection (oral therapy recommended if patient has BV); history of PID; infected abortion in past 3 mo; unresolved abnormal Papanicolaou (Pap) test; untreated vaginitis; increased susceptibility to infection (eg, AIDS, leukemia); genital actinomycosis; contraindications to insertion—behavior suggesting high risk for PID; postabortion endometritis; known or suspected uterine or cervical malignancy
Levonorgestrel-releasing intrauterine system (LNG IUS): option for women considering tubal sterilization (less risky and reversible) or endometrial ablation for bleeding; failure rate—first-year failure rates equivalent to those of copper IUD; potential side effects—considerable amount of unpredictable spotting and bleeding first few months after insertion; at 4 mo, same number of bleeding days, but significantly less blood loss; by 12 mo, mean bleeding days zero; menorrhagia—LNGIUS indicated in some countries (not in United States) for treatment of menorrhagia; effective treatment for inherited bleeding disorders; data show more effective in treating menorrhagia than are NSAIDs and antifibrinolytic agents; according to Cochrane Database systematic review, as effective as ablation in controlling menorrhagia; data support use as alternative to hysterectomy
Medroxyprogesterone acetate (DMPA; Depo-Provera): highly effective; good method for women with seizure disorders (maintains therapeutic level despite interaction with anticonvulsants; slight anticonvulsant effect); potential side effects—one double-blind placebo-controlled study showed no increase in weight from baseline and no difference in weight gain between users of DMPA and those receiving placebo injection, but profound weight gain observed (patient should be counseled about possible weight gain); concerns about bone mineral density (BMD)—2004 “Black Box” warning states DMPA should be used >2 yr only if other methods inadequate; American College of Obstetricians and Gynecologists’ (ACOG) position is that concerns about BMD should not restrict initiation or continuation of DMPA in adults or teens; adequate calcium intake should be encouraged
DMPA administration protocol: quick start or same-day start endorsed; offer patient emergency contraception (EC; Plan B) if indicated (ie, unprotected intercourse within last 5 days); administer DMPA and advise use of backup method for 7 days; obtain pregnancy test or repeat test in 2 to 3 wk; 40% of pregnancies in women using DMPA not diagnosed until second trimester; DMPA does not adversely affect fetus, but delays diagnosis of pregnancy
Lower-dose DMPA (DMPA-SC): new formulation (new concentration and new buffers); 104 mg/0.65 mL; administered subcutaneously every 14 wk (provides extra month per year in same number of injections); potential for self administration; approved for treatment of endometriosis pain (reduction in pain score same as with gonadotropin-releasing hormone [GnRH] agonist); zero pregnancies in 20,000 woman-cycles of exposure; efficacy not affected by body mass index (BMI)
Oral contraceptives: only 30% of women using prescribed OCs by third cycle; body weight and OC failure—data show women in upper quartile of weight more likely to have OC failure with low-dose formulation; recommend shortening of pill-free interval, rather than prescribing higher-dose formulation; hormone withdrawal symptoms—data show no increase in many hormone-related side effects associated with OCs; data show 3 times as many problems during hormone-free interval than during active-pill week; drospirenone (24/4 dosing regimen) shown effective for symptoms of premenstrual dysphoric disorder; new develop-ments—extended or continuous use; quick start and first-day start each cycle
Quick-start protocol: evidence that with conventional start, up to 25% of women do not fill prescription (particularly adolescents); start with first pill in pack; provide EC if indicated; provide backup method for 7 days; data show by third cycle, 54% of women missing >2 pills every cycle
Transdermal contraceptive systems (patches): failure rate—30% of pregnancies occurred in 3% of women weighing >198 lb; data show compliance higher than with OCs; extended use possible (speaker less enthusiastic about extended use for patch); no long-term data on episodic use or “use for indication”; pharmacokinetic profile for patch—different from pharmacokinetic profile for OCs; serum level of estrogen in patch 60% higher than in OCs, but peak concentration 25% lower (misses intestinal first-pass metabolism); no convincing evidence of increased thrombosis; ACOG guidelines do not recommend estrogen-containing methods of birth control for women >35 yr of age with BMI >30
Contraceptive vaginal rings: once-a-month method; easily placed by woman; discreet; lowest estrogen dose among combined hormonal methods; constant serum concentrations; avoid gastrointestinal interference with absorption; avoid hepatic first-pass metabolism; patient concerns—associated pain, displacement, partner’s ability to sense; can be placed anywhere in vagina; cycle control better than with comparator OC (Nordette 28); can initiate quick-start and extended cycles; increase in vaginal discharge; 2 studies show decrease in recurrence of BV
Condoms: marketing targeting women; array of choices in sizes and characteristics (eg, flavors, scents, colors, textures, climax control); polyurethane condoms recommended if woman using antifungal agents
Barrier methods
Lea’s shield: no fitting needed; prescription only (available over-the-counter in Europe); one-way valve allows exit for cervical secretions and air
FemCap: 2 sizes (eg, parous and nulliparous); spermicide applied inside bow; clinical trials looking at microbicides on brim of cap
Contraceptive sponge: discreet and less messy than other spermicides
Cycle beads: color-coded string of beads; helps woman identify days of cycle when pregnancy likely and unlikely; mechanism easy to understand
Emergency contraception: single-dose regimen recommended vs 2-dose regimen taken within 12 hr; can be taken up to 120 hr after unprotected intercourse; provide prescription in advance; more effective when taken sooner; data support concept that EC has little or no effect on postovulation event, but highly effective when taken before ovulation

Suggested Reading

Holt VL et al: Body mass index, weight, and oral contraceptive failure risk. Obstet Gynecol 105:46, 2005; Jick S et al: Further results on the risk of nonfatal venous thromboembolism in users of the contraceptive transdermal patch compared to users of oral contraceptives containing norgestimate and 35 microg of ethinyl estradiol. Contraception 76:4, 2007; Marjoribanks J et al: Surgery versus medical therapy for heavy menstrual bleeding. Cochrane Database Syst Rev 10:DC003855, 2006; Potter LS: How effective are contraceptives? The determination and measurement of pregnancy rates. Obstet Gynecol 88:13S, 1996; Lahteenmaki P et al: BMJ 316:1122, 1998; Nelson AL: Contraindications of IUD and IUS use: Contraception 75:S76, 2007; Novikova N et al: Effectiveness of levonorgestrel emergency contraception given before or after ovulation—a pilot study. Contraception 75:112, 2007; Sulak PJ et al: Hormone withdrawal symptoms in oral contraceptive users. Obstet Gynecol 95:261, 2000; Sivin I: Utility and drawbacks of continuous use of a copper T IUD for 20 years. Contraception 75:S70, 2007; Stewart FH et al: Extended use of transdermal norelgestromin/ethinyl estradiol: a randomized trial. Obstet Gynecol 105:1389, 2005.

Educational Objectives

The goal of this program is to present evidence supporting the use of contraceptive options. After hearing and assimilating this program, the clinician will be better able to:
1. Discuss reasons why women may not use contraception for pregnancy prevention.
2. Identify contraceptive methods that comprise the top tier of efficacy.
3. Counsel patients about contraceptive options.
4. Discuss mechanisms of action, potential side effects and noncontraceptive benefits associated with some contraceptives.
5. Describe new approaches to older contraceptive methods.

Faculty Disclosure

In adherence to ACCME Standards for Commercial Support, Audio-Digest requires all faculty and planning committee members to disclose relevant financial relationships within the past 12 months that might create any personal conflicts of interest. Any identified conflicts were resolved to ensure that this educational activity promotes quality in health care and not a proprietary business or commercial interest. For this program, the following has been disclosed: Dr. Nelson has received research grants from Barr (Duramed), Bayer Healthcare (Berlex), and Wyeth Pharmaceuticals, and either acts as a consultant or is on the advisory board for Barr, Bayer, and Wyeth. Dr. Nelson has received honoraria or is on the Speaker’s Bureaus of Barr, Bayer, and Wyeth. The planning committee reported nothing to disclose.

Acknowledgment

Dr. Nelson was recorded at the 51st Annual T. Hart Baker, MD, Obstetrics and Gynecology Symposium, sponsored by Kaiser Permanente Southern California and held on November 9-10, 2007, in Las Vegas, NV.

Reproduction of this summary in whole or in part in any form or medium without express written permission is prohibited.

If, after reviewing this written summary, you would like to hear the contents and/or earn CME/CE credit:

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