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Women's Health

Choosing whether—and when—to menstruate

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By Andrew M. Kaunitz, MD

Reducing the frequency of menstruation—or simply eliminating it—is a safe and effective option for many women, argues this author. Controlling when and whether menstruation occurs may even be beneficial to their health.

Menstrual disorders affect approximately 2.5 million American women between 18 and 50 years of age.1,2 Of these women, two thirds contact a doctor for relief of their ailments each year.1 Nearly one third of all the women afflicted report that their menstrual symptoms confine them to bed an average of 9.6 days per year.1 This, in turn, costs American industries—particularly the sectors that predominantly employ women—an estimated 8% of the total wage bill.2

Menstruation and its associated hormonal changes are often at the heart of these women's monthly suffering. An excessive menstrual flow, for example, can cause anemia in otherwise healthy women or worsen the condition in those with certain types of preexisting anemia. Also, hormonal changes can cause dysmenorrhea and migraine headaches, and may contribute to the aggravation of porphyria, epilepsy, and chronic pelvic pain.3,4

To alleviate menstrual symptoms, a number of interventions are available that reduce or eliminate monthly bleeding. The safety and efficacy of these methods may make them desirable to women who simply want to suppress menses for convenience sake. In this article, I will discuss the advantages to reducing or eliminating menstruation, and describe the therapeutic regimens that can contribute to a woman's overall well-being.

The benefits of suppressing menses

The idea that menstruation must occur monthly in healthy, non-pregnant women has been perpetuated by the use of oral contraceptives designed to mimic the average length of a normal menstrual cycle—21 days of active hormones followed by 7 days of placebo. The developers of the first OC—Drs. Gregory Pincus and John Rock—understood that monthly bleeding was not a necessary phenomenon but rather a response to the withdrawal of hormones. However, many of today's women and clinicians continue to believe that monthly menstruation is necessary for a woman's health.

In fact, there is evidence to suggest that frequent, regular menstruation may actually increase a woman's health risks. For example, today's Western woman has an estimated 450 menstrual periods until menopause (at approximately age 51), whereas her preagricultural ancestor had about 160 ovulations in a lifetime.5 Fewer menstrual cycles among preagricultural women is attributed to such factors as late menarche, high parity, extended periods of breastfeeding, and early menopause. These exposures, which are not typically experienced by today's women, have also been found to decrease the risk of breast, endometrial, and ovarian cancers.5,6

Certain conditions can be alleviated. A recent prospective study of 262 women—all of whom took a low-dose, combination OC containing 35 mg or less of ethinyl estradiol plus progestin—found that the women experienced headaches, pelvic pain or cramps, bloating or swelling, and breast tenderness more frequently during the 7-day, hormone-free period than during the 21 days of active hormone use.7

Drawing on these data, Sulak and colleagues conducted a prospective study of 50 patients to determine whether extended use of active hormones, for up to 12 weeks, would alleviate such problems as dysmenorrhea, menorrhagia, premenstrual syndrome, and migraines. While about one quarter of the patients (13) discontinued OCs or reverted back to the standard 21/7 regimen, nearly three quarters (37) completed the extended OC regimen without problems such as breakthrough bleeding. Within this group, 16 took active OC tablets for 84 days (12 weeks) followed by 7 days of placebo; 13 used a 63/7 regimen; and 8 used a 42/7 regimen. The investigators found that "all 37 patients reported that extending the active OCs delayed the onset and decreased the severity of their reported [menstrual] complaints." Ultimately, 27 of these patients continued with the regimen for an average of 17.2 months, completing between 5 and 13 cycles.8

 

TABLE 1
Conditions that may be remedied with reduced menstrual frequency or amenorrhea

Anemia
Dysmenorrhea
Endometriosis/chronic pelvic pain
Epilepsy

Menorrhagia associated with:

  • acquired bleeding disorders such as chronic anticoagulation and thrombocytopenia
  • inherited bleeding disorders such as von Willebrand disease, hemophilia, and factor XI deficiency
  • uterine leiomyoma/adenomyosis
Migraine headaches
Premenstrual syndrome
Porphyria

 

Amenorrhea or reduced menstrual frequency may also be use-ful in providing relief to women with other medical conditions. For example, those with endometriosis have been treated for years with medications that inhibit ovulation and menstruation.9 In addition, women who experience symptoms that are aggravated by menses may be able to avoid cyclical exacerbations of their complaints by decreasing the number of times they menstruate.

Women with inherited bleeding disorders may also benefit from suppressed menses because they frequently suffer from menorrhagia, which impairs their quality of life. One study of 99 patients with von Willebrand disease, hemophilia, and factor XI deficiency found that, during menstruation, 47% felt that they accomplished less, 40% thought it took more effort to perform their work, 39% reported cutting down on the amount of time they spent on work or other activities, and 38% felt limited as to the kind of work and activities they could do.10 The study also found that 51% experienced moderate to very severe dysmenorrhea.10 Combination OCs in the standard 21/7 regimen have been shown to reduce menorrhagia in women with von Willebrand disease.11 One can only imagine the benefits that patients with von Willebrand disease and other inherited bleeding disorders may experience through an extended OC regimen.

Infrequent menses provides convenience. A number of studies, dating back to 1977, have shown that women favor infrequent menses. For example, a 1996 telephone survey of Dutch women found that, if women could create an OC to change how often they menstruated, the majority—regardless of age—would eliminate menses completely or reduce the frequency to less than once a month (Table 2).12

 

TABLE 2
A Dutch woman’s view on ideal menstruation

  Age of women
  15-19
(N=321)
25-34
(N=324)
45-49
(N=319)
Once a month 26.2 33.3 28.8
Once every 3 months 38.3 25.0 21.3
Once every 6 months 7.8 6.8 4.4
Once a year 4.0 3.4 6.6
Never 21.8 25.0 26.3
Not inclined to use OCs 1.9 6.5 12.5
  x2 (4df)
P value
21.1
0.001
13.3
0.02
 
Source: Adapted from den Tonkelaar I, Oddens BJ.12

 

The survey also found that among those who were currently using or had previously used OCs, 69% of adolescents (ages 15 to 19) and 63% of reproductive-age women (ages 25 to 34) had used the pills to postpone menstrual bleeding. The study investigators noted that the preferences of these women contrast with current medical practice in that combination OCs are designed to mimic monthly menstruation and clinicians often change formulations of OCs to produce monthly bleeding when amenorrhea occurs.12

In general, young teens and perimenopausal women have much to gain from reducing menstrual frequency. For example, American teens, whose age of menarche continues to decline, must cope with the pain and inconvenience of menstruation.13 Moreover, they often experience dysmenorrhea and iron-deficiency anemia.14 Prescribing OCs using the standard 21/7 regimen can provide relief for dysmenorrhea and reduce menstrual flow by nearly 50%.14 However, extended use of active OCs may improve their quality of life more dramatically.

Similarly, perimenopausal women can find relief from irregular menses and vasomotor symptoms by taking combination OCs in the standard 21/7 regime.15,16 But because hot flashes and other vasomotor symptoms may still occur during the hormone-free period, these women may benefit from an extended OC regimen that reduces the number of times per year that they must endure symptoms.

Finally, women in the military and female athletes may find it useful to suppress menstruation to improve performance. For example, according to a recent survey, more than 60% of 158 female cadets enrolled at the United States Military Academy at West Point reported that menstrual-related symptoms interfered with required physical activities—not to mention the difficulties the cadets experienced in maintaining menstrual hygiene.17 An extended OC regimen could help these cadets function more optimally in the military setting. Moreover, female athletes have used standard OCs to manipulate their cycle and control premenstrual symptoms—actions that may enhance their athletic abilities.18 Again, an extended OC regimen may be a more effective way of improving performance.

Contraceptive efficacy may improve. Unintended pregnancies often result because a woman is confused about when to start the next pill pack, does not take the pill at the same time every day, or forgets to start the next pill pack at the correct time.19,20 Arguably, an extended OC regimen may help improve contraceptive efficacy by limiting the chance that a woman will forget to start a new pill pack: For example, a woman who uses an extended OC regimen that contains 87 days of active hormones must only start a new pack four times—rather than 13 times—per year.

Therapeutic options to reduce or halt menstruation

Historically, hysterectomy has been the only definitive treatment to attain amenorrhea for women with severe problems associated with menstruation. In the 1980s, endometrial ablation was developed. Although this alternative procedure costs less, requires little if any hospitalization, and has a shorter recovery period than hysterectomy, menorrhagia may recur within 3 years and amenorrhea is achieved in less than 50% of patients. Still, among the successful cases, 85% are cured of menorrhagia at 3 years.21

Today there are a number of alternative therapies for women with menstrual disorders. These alternatives, which either reduce menstrual frequency or completely eliminate it, are well tolerated and often have the added bonus of protecting against pregnancy (Table 3).

 

TABLE 3
Therapeutic options for suppressing menses

  Extended OC regimen* DMPA* Levonorgestrel IUD Norethisterone acetate Danocrine GnRH agonist
Dosage <35 µg estrogen monophasic continuous; Seasonale (investigational drug): extended 84/7 regimen Depo-Provera:
150 mg IM every
3 months
Mirena: Releases 20 µg levonorgestrel daily, effective for 5 years Aygestin: 5 mg, 1–3 times daily Danazol: 800 mg twice a day (optional titration to lowest dose sufficient to maintain amenorrhea) Leuprolide acetate (Lupron Depot):
3.75 mg monthly or 11.25 mg every 3 months
Medical uses Menorrhagia, dysmenorrhea, endometriosis, anemia, premenstrual syndrome, menstrual migraines Menorrhagia, dysmenorrhea, endometriosis, anemia, premenstrual syndrome, menstrual migraines Menorrhagia Menorrhagia, dysmenorrhea, endometriosis, anemia, premenstrual syndrome, menstrual migraines Endometriosis, menorrhagia Menorrhagia dysmenorrhea endometriosis anemia premenstrual syndrome menstrual migraines
Contraception
provided
Yes Yes Yes Yes No No
Adverse effects Breakthrough bleeding or spotting Irregular bleeding or spotting Intermenstrual bleeding Progestin side effects such as bloating or mood changes Androgenic and hypoestrogenic side effects Hypoestrogenic side effects that can be counteracted with estrogen supplementation
Cost-
effectiveness
Cost-effective if the use of sanitary products is high Cost-effective Initial high cost, but becomes cost-effective with extended use More costly than extended OC regimen Expensive Very expensive
*None of the medical uses listed are FDA-approved indications.
† Approved for the treatment of endometriosis.
 Approved for the treatment of endometriosis and menorrhagia-induced anemia in women with fibroids. Other GnRH agonists approved for the treatment of endometriosis include Synarel and Zoladex.
DMPA—depot medroxyprogesterone acetate

 

Extended OC regimen. Sulak argues that women who suffer from menstrual symptoms obtain only limited relief when they use the standard 21/7 OC regimen. She notes that these women still experience menstrual symptoms during the 7-day hormone-free period. Extending the use of active hormones over several cycles, based on the individual woman's tolerance level, decreases the number of times that she must suffer during the hormone-free period.22

In addition, Sulak contends that shortening the hormone-free period from 7 to 4 or 5 days—in addition to extending the active-hormone period—provides greater ovarian suppression. This, in turn, helps reduce the occurrence of symptoms associated with hormone withdrawal, as well as the risk of ovulation that can lead to pregnancy.22

A new OC formulation--known as Seasonale--was approved by the FDA in September 2003. It is a 91-day OC regimen of ethinyl estrodiol and levonorgestrel for 84 days and 7 days of placebo.

Depot medroxyprogesterone acetate (DMPA). Between 50% and 73% of women who use DMPA (Depo-Provera) for 1 year experience amenorrhea. As the duration of use increases, amenorrhea—and the reduction of menstrual symptoms—becomes more common.23,24 DMPA works by inhibiting ovulation, providing highly effective contraception as well.

Initial injections of DMPA should be administered within 5 days of the onset of menses and every 3 months thereafter. The usual dose is 150 mg. Reinjecting DMPA at an earlier time (8 or 10 weeks) to reduce bleeding was found to be ineffective and to cause weight gain.25 Similarly, there is little evidence to support the use of supplemental estrogen to accelerate the onset of amenorrhea.26

Likewise, while monthly injections of medroxyprogesterone acetate/estradiol cypionate (Lunelle) is associated with regular withdrawal bleeding similar to spontaneous menstruation, there is no evidence to indicate that changing the injection interval of this monthly contraceptive will create an amenorrhic state.27

Levonorgestrel intrauterine device (IUD). A recent study of 30 patients with refractory recurrent hypermenorrhea found that the levonorgestrel IUD (Mirena) was as effective at reducing bleeding over 12 to 24 months as roller-ball endometrial ablation. Investigators believe that the Mirena system, which received FDA approval last year for contraceptive use, will replace approximately 75% of endometrial ablation.28

Another recent study of women with idiopathic menorrhagia found that this progestin-releasing IUD reduced menstrual blood loss by 94% after 3 months. Nearly one third of the women who used the IUD experienced amenorrhea during this study period. At the end of the study, investigators found that more than three quarters of those using the IUD wanted to continue with the treatment.29

Norethisterone. The same study that examined the use of levonorgestrel IUD in women with idiopathic menorrhagia also found that a 5-mg oral dose of norethisterone taken three times a day reduces menstrual blood loss by 87%. However, none of the women treated with norethisterone experienced amenorrhea during the 3-month study, and only about one quarter elected to continue with the treatment once the study ended.29

In my experience, a lower dose of norethisterone (5 mg, once a day) can produce amenorrhea in patients suffering from menorrhagia, including those with uterine fibroids. However, even at this low dose, there seem to be more side effects, including bloating and mood swings, than with OCs, DMPA, or the levonorgestrel IUD. Moreover, norethisterone is more costly than OCs or DMPA.

Danocrine and GnRH agonists. To induce amenorrhea, decrease menorrhagia, and shrink uterine fibroids, danocrine (Danazol) and GnRH agonists are also effective treatments.21 However, they are costly and may not universally suppress ovulation; therefore, a nonhormonal contraceptive may be necessary. Moreover, this class of medications produces hypoestrogenic side effects. For example, leuprolide acetate, a GnRH agonist, may cause breast tenderness or pain, vaginal dryness, and a loss of bone density.

As additional therapeutic options to suppress menses become available, many women will choose whether and when to bleed. Clinicians are in an ideal position to educate their patients about ways to reduce the frequency of menstruation or to eliminate this burden altogether.

REFERENCES

1. Kjerulff KH, Erickson BA, Langenberg PW. Chronic gynecological conditions reported by U.S. women: findings from the National Health Interview Survey, 1984 to 1992. Am J Public Health. 1996;86:195-199.

2. Thomas SL, Ellertson C. Nuisance or natural and healthy: should monthly menstruation be optional for women? Lancet. 2000;355:922-924.

3. Couthino EM, Segal SJ. Is Menstruation Obsolete? New York, NY: Oxford University Press; 1999.

4. MacGregor EA. Menstruation, sex hormones, and migraine. Neurol Clin. 1997;15:125-141.

5. Eaton SB, Pike MC, Short RV, et al. Women's reproductive cancers in evolutionary context. Q Rev Biol. 1994;69:353-367.

6. Gladwell M. John Rock's error. The New Yorker. 2000;(Mar. 13):52-63.

7. Sulak PJ, Scow RD, Preece C, et al. Hormone withdrawal symptoms in oral contraceptive users. Obstet Gynecol. 2000;95:261-266.

8. Sulak PJ, Cressman BE, Waldrop E, et al. Extending the duration of active oral contraceptive pills to manage hormone withdrawal symptoms. Obstet Gynecol. 1997;89:179-183.

9. Speroff L, Glass RH, Kase NG. Clinical Gynecologic Endocrinology and Infertility. 6th ed. Baltimore, MD: Lippincott Williams & Wilkins, 1999:1063-1064.

10. Kadir RA, Sabin CA, Pollard D, et al. Quality of life during menstruation in patients with inherited bleeding disorders. Haemophilia. 1998;4:836-841.

11. Ward CL. Hemorrhaging at menarche: a case report. J Fam Pract. 1992;34:351-354.

12. den Tonkelaar I, Oddens BJ. Preferred frequency and characteristics of menstrual bleeding in relation to reproductive status, oral contraceptive use, and hormone replacement therapy use. Contraception. 1999;59:357-362.

13. Kaplowitz PB, Oberfield SE. Reexamination of the age limit for defining when puberty is precocious in girls in the United States: implications for evaluation and treatment. Drug and Therapeutics and Executive Committees of the Lawson Wilkins Pediatric Endocrine Society. Pediatrics. 1999;104:936-941.

14. ACOG Educational Bulletin. No. 256. Oral Contraceptives for Adolescents: Benefits and Safety. 1999(Dec):1-8.

15. Davis A, Lippman J, Godwin A, et al. Triphasic norgestimate-ethinyl estradiol for treating dysfunctional uterine bleeding. Obstet Gynecol. 2000;96:913-920.

16. Casper RF, Dodin S, Reid RL, and study investigators. The effect of 20 µg ethinyl estradiol/1 mg norethindrone acetate (MinestrinTM), a low-dose oral contraceptive, on vaginal bleeding patterns, hot flashes, and quality of life in symptomatic perimenopausal women. Menopause. 1997;4:139-147.

17. Schneider MB, Fisher M, Friedman SB, et al. Menstrual and premenstrual issues in female military cadets: a unique population with significant concerns. J Pediatr Adolesc Gynecol. 1999;12:195-201.

18. Bennell K, White S, Crossley K. The oral contraceptive pill: a revolution for sportswomen? Br J Sports Med. 1999;33:231-238.

19. Rosenberg MJ, Waugh MS, Meehan TE. Use and misuse of oral contraceptives: risk indicators for poor pill taking and discontinuation. Contraception. 1995;51:283-288.

20. Rosenberg MJ, Burnhill MS, Waugh MS, et al. Compliance and oral contraceptives: a review. Contraception. 1995;52:137-141.

21. Stabinsky SA, Einstein M, Breen JL. Modern treatments of menorrhagia attributable to dysfunctional uterine bleeding. Obstet Gynecol Survey. 1998;54:61-72.

22. Sulak PJ, Cressman BE, Waldrop E, et al. Extending the duration of active oral contraceptive pills to manage hormone withdrawal symptoms. Obstet Gynecol. 1997;89:179-183.

23. Kaunitz AM. Long-acting contraceptive options. Int J Fertil Menopausal Stud. 1996;41:69-76.

24. Kaunitz AM. Injectable contraception. New and existing options. Obstet Gynecol Clin North Am. 2000;27:741-780.

25. Harel Z, Biro FM, Kollar LM. Depo-Provera in adolescents: effects of early second injection or prior oral contraception. J Adolesc Health. 1995;16:379-384.

26. Said S, Sadek W, Rocca M, et al. Clinical evaluation of the therapeutic effectiveness of ethinyl oestradiol and oestrone sulphate on prolonged bleeding in women using depot medroxyprogesterone acetate for contraception. World Health Organization, Special Programme of Research, Development and Research Training in Human Reproduction, Task Force on Long-acting Systemic Agents for Fertility Regulation. Hum Reprod. 1996;11(Suppl 2):1-13.

27. Kaunitz AM, Garceau RJ, Cromie MA, et al. Comparative safety, efficacy, and cycle control of Lunelle monthly contraceptive injection (medroxyprogesterone acetate and estradiol cypionate injectable suspension) and Ortho-Novum 7/7/7 oral contraceptive (norethindrone/ethinyl estradiol triphasic). Contraception. 1999;60:179-187.

28. Römer T. Prospective comparison study of levonorgestrel IUD versus Roller-Ball endometrial ablation in the management of refractory recurrent hypermenorrhea. Eur J Obstet Gynecol Reprod Biol. 2000;90:27-29.

29. Irvine GA, Campbell-Brown MB, Lumsden MA, et al. Randomised comparative trial of the levonorgestrel intrauterine system and norethisterone for treatment of idiopathic menorrhagia. Br J Obstet Gynaecol. 1998;105:592-598.

Dr. Kaunitz is Professor and Assistant Chairman, Department of Obstetrics and Gynecology, University of Florida Health Science Center, Jacksonville, Fla.

 



Choosing whether--and when--to menstruate. JAAPA March 2004;17:Web.

Copyright © 2004, Advanstar Medical Economics Healthcare Communications at Montvale, NJ 07645-1742. All rights reserved.





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