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1 Symptoms  





2 Risk factors  





3 Diagnosis  





4 Etiology (Causes)  





5 Treatment  





6 Prognosis  





7 Epidemiology  





8 History  





9 Alternative views  





10 References  





11 External links  














Premenstrual syndrome: Difference between revisions






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Undid revision 296416755 by 24.109.50.138 (talk)previous version preferable
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Line 86: Line 86:

* [[Non-steroidal anti-inflammatory drugs]] (NSAIDs; eg ibuprofen) have been used.

* [[Non-steroidal anti-inflammatory drugs]] (NSAIDs; eg ibuprofen) have been used.

* [[Evening Primrose Oil]], which contains [[gamma-Linolenic acid]] (GLA), has been advocated but lacks scientific support.

* [[Evening Primrose Oil]], which contains [[gamma-Linolenic acid]] (GLA), has been advocated but lacks scientific support.

*Clonidine has been reported to successfully treat a significant number of women whose PMS symptoms coincide with a steep decline in serum beta-endorphin on a monthly basis.<ref>{{cite journal |author=Giannini AJ, Sullivan B, Sarachene J, Loiselle RH |title=Clonidine in the treatment of premenstrual syndrome: a subgroup study |journal=J Clin Psychiatry |volume=49 |issue=2 |pages=62–3 |year=1988 |month=February |pmid=2962993 |doi= |url=}}</ref>

* [[Clonidine]] has been reported to successfully treat a significant number of women whose PMS symptoms coincide with a steep decline in serum beta-endorphin on a monthly basis.<ref>{{cite journal |author=Giannini AJ, Sullivan B, Sarachene J, Loiselle RH |title=Clonidine in the treatment of premenstrual syndrome: a subgroup study |journal=J Clin Psychiatry |volume=49 |issue=2 |pages=62–3 |year=1988 |month=February |pmid=2962993 |doi= |url=}}</ref>



==Prognosis==

==Prognosis==


Revision as of 01:09, 17 June 2009

Premenstrual syndrome
SpecialtyGynaecology Edit this on Wikidata

Premenstrual Syndrome (PMS) (sometimes referred to as PMTorPremenstrual Tension) is a collection of physical, psychological, and emotional symptoms related to a woman's menstrual cycle. While most women (about 80 percent) of child-bearing age have some symptoms of PMS,[1] the official definition limits the scope to having symptoms of "sufficient severity to interfere with some aspects of life".[2] Such symptoms are usually predictable and occur regularly during the two weeks prior to menses. Generally, symptoms may vanish both before or after the start of menstrual flow.

While some experts claim that virtually all menstruating women experience PMS, a more recent and intermediate position shows that only a small percentage of women (2 to 5%) have significant premenstrual symptoms that are separate from the discomfort associated with menstruation.[3] Culturally, the abbreviation PMS is widely understood in the United States (and other countries, for example Australia) to refer to difficulties associated with menses, and the abbreviation is used frequently even in casual and colloquial settings, without regard to medical rigor. In these contexts, the syndrome is rarely referred to without abbreviation, and the connotations of the reference are frequently more broad than the clinical definition.

Symptoms

PMS is a collection of symptoms. More than 200 different symptoms have been identified, but the three most prominent symptoms are irritability, tension, and dysphoria (unhappiness).[2] The exact symptoms and their intensity vary from woman to woman. Most women with premenstrual syndrome experience only a few of the problems. The following symptoms can also be attributed to PMS: [4][5] [6][7]

Risk factors

Family history is often a good predictor of the probability of premenstrual syndrome; studies have found that the occurrence of PMS is twice as high among identical twins compared with fraternal twins.[2] Although the presence of premenstrual syndrome is high among women with affective disorders such as depression and bipolar disorder,[citation needed] a causal relationship has not been established.

Vitamin B can also assist with unstable emotions.[citation needed]

Diagnosis

There is no laboratory test or unique physical findings to verify the diagnosis of PMS. To establish a pattern, a woman's physician may ask her to keep a prospective record of her symptoms on a calendar for at least two menstrual cycles.[4] This will help to establish if the symptoms are, indeed, premenstrual and predictably recurring. A number of standardized instruments have been developed to describe PMS, including the Calendar of Premenstrual syndrome Experiences (COPE), the Prospective Record of the Impact and Severity of Menstruation (PRISM), and the Visual Analogue Scales (VAS).[2]

In addition, other conditions that may explain symptoms better must be excluded.[2] A number of medical conditions are subject to exacerbation at menstruation, a process called menstrual magnification. These conditions may lead the patient to believe that she may have PMS, when the underlying disorder may be some other problem. A key feature is that these conditions may also be present outside of the luteal phase. Conditions that can be magnified perimenstrually include depression, migraine, seizure disorders, fatigue, irritable bowel syndrome, asthma, and allergies.[2]

Although there is no universal agreement about what qualifies as PMS, two definitions are commonly used in research programs:

Etiology (Causes)

The exact causes of PMS are not fully understood. While PMS is linked to the luteal phase, measurements of sex hormone levels are within normal levels. PMS tends to be more common among twins, suggesting the possibility of some genetic component.[2] Current thinking suspects that central-nervous-system neurotransmitter interactions with sex hormones are affected.[2] It is thought to be linked to activity of serotonin (a neurotransmitter) in the brain.[6] [9][10]

Genetic factors also seem to play a role, as the concordance rate is two times higher in monozygotic twins than in dizygotic twins. [11] Preliminary studies suggest that up to 40% of women with symptoms of PMS, have a significant decline in their circulating serum levels of beta-endorphin. Beta endorphin is a naturally occurring opioid neurotransmitter which has an affinity for the same receptor that is accessed by heroin and other opiates. Some researchers have noted similarities in symptom presentation between PMS symptoms and opiate withdrawal symptoms. [12]

A variety of evolutionary rationales for the syndrome have been offered, including that it is an epiphenomenon due to the selective advantage accruing to other phases of the hormonal cycle[13], that it leads to "intensification of male ardour during the next onset of fertility"[14], and that it prompts females to reject infertile males (who cause PMS due to not impregnating the female). "... an infertile male/potentially fertile female partnership would tend to break down, thus allowing a new pair-bond to be formed. The greater the degree of premenstrual hostility of the female, the sooner a fertile mating could ensue."[15] Any theory would have to account for the persistence of PMS over substantial evolutionary time, as it appears to afflict baboons as well[16].

Treatment

Many treatments have been suggested for PMS, including diet or lifestyle changes, and other supportive means. Medical interventions are primarily concerned with hormonal intervention and use of selective serotonin reuptake inhibitors (SSRIs).

Prognosis

PMS is generally a stable diagnosis, with susceptible women experiencing the same symptoms at the same intensity near the end of each cycle for years.[21]

Treatment for specific symptoms is usually effective at controlling the symptoms. Even without treatment, symptoms tend to decrease in perimenopausal women, and disappear at menopause.[22]

Women who have PMS have an increased risk for clinical depression.

Epidemiology

The number of women who experience PMS depends entirely on the stringency of the definition of PMS.[23] While 80% of menstruating women have experienced at least one symptom that could be attributed to PMS, estimates of prevalence range from as low as 3%[24] to as high as 30%.[23]

Mood symptoms such as emotional lability are both more consistent and more disabling than somatic symptoms such as bloating.[25] A woman who experiences mood symptoms is likely to experience these symptoms consistently and predictably, whereas physical symptoms may come and go. Most women find that physical symptoms related to PMS are less disruptive than emotional symptoms

History

PMS was originally seen as an imagined disease.[citation needed] When women first started reporting these symptoms, they were often told it was "all in their head". Interest in PMS began to increase after it was used as a criminal defense in Britain during the early 1980s. [citation needed]

The study of PMS was brought about by many characters in society. Physicians and researchers study and treat recognized medical conditions. In order to have an impact, the existence, and importance of a disease needs to be socially accepted. Women have contributed to the rise of interest in PMS and society's acceptance of it as an illness. It is argued that women are partially responsible for the medicalization of PMS.[26] By legitimizing this disorder, women have contributed to the social construction of PMS as an illness. It has also been suggested that the public debate over PMS and PMDD was impacted by organizations who had a stake in the outcome including feminists, the APA, physicians and scientists.[27]

The study of PMS symptoms is not a new development. Debates about the definition and validity of this syndrome have a long history. As stated above, growing public attention was given to PMS starting in the 1980’s. [citation needed] Up until this point, there was little research done surrounding PMS and it was not seen as a social problem. Through clinical trials and the work of feminists, viewing PMS in a social context had begun to take place.

Alternative views

Some medical professionals suggest that PMS might be a socially constructed disorder.[28]

Supporters of PMS' medical validity claim support from work on the similar problem, premenstrual dysphoric disorder ("PMDD"). In women with PMDD, studies have shown a correlation between self-reported emotional distress and levels of a serotonin precursor as measured by positron emission tomography (PET).[29] PMDD also has a consistent treatment record with SSRIs, when compared with placebos.[30] However, the diagnosis has been controversial (including in regard to the pharmaceutical company influence, see below) and questioned on scientific grounds as medicalization.[31]

However, most supporters of PMS as a social construct do not dispute PMDD's medical status. Rather, they believe PMDD and PMS to be unrelated issues: one a product of brain chemistry, the other a product of a hypochondriatic culture. There has not been enough debate between the two views to come to any sound conclusion. [citation needed] Part of the reason the validity of the emotional aspects of PMS is being doubted is the lack of scientifically-sound studies on the matter. Many Western studies on PMS (PMS is primarily seen in Western Europe and North America) rely solely on self-reporting, and since Western women are socially conditioned to expect PMS or to at least know of its purported existence, they report their symptoms accordingly.[32]. Many women, however, find this an insulting view, suggesting that they are unable to know their own minds, or recognise patterns in their behaviour [citation needed] .

Another view holds that PMS is too frequently or wrongly diagnosed in many cases. A variety of problems, such as chronic depression, infections, and outbursts of frustration can be mis-diagnosed as PMS if they happen to coincide with the premenstrual period. Often, says this theory, PMS is used as an explanation for outbursts of rage or sadness, even when it is not the primary cause. [33]

Some feminists have suggested that viewing PMS as a disease is born out of a patriarchal society. They assert that the symptoms that are associated with PMS are often in conflict with the way a woman "should" behave, contending that anger, irritability and increased sex drive are patterns of behavior which go against social norms for women. Some people believe that PMS, along with other female-attributed disorders, are used to enforce gender stereotypes.[34]. This does not mean that the expression of these behaviours does not vary cyclically in many women, but that it does not necessarily constitute a problem that needs curing, being rather a part of normal variation in female behaviour.

Some feminists [who?] assert that the emergence of PMS as a disorder occurred during a time when women's roles in society were changing. Particularly, women were beginning to enter the work force at increasing numbers. They argue that this may not be mere coincidence, asserting a belief that PMS is used as a method of social control.

The use of multiple SSRI's to treat PMS has caused some controversy. The makers of Prozac began marketing the generic form, fluoxetine, under the name Sarafem to treat PMS. This coincided with their loss of patent on Prozac, which has led to suggestions that their motivations are not completely benign.[35] Recently an oral contraceptive named Drospirenone (Yaz) has become the only birth control pill approved to treat PMDD. The marketing of Yaz centers on this aspect of the drug.[36]

References

  1. ^ "Apotek1: PMS". 2007. Retrieved 2007-02-02. {{cite web}}: Text "publisher: Apotek 1" ignored (help)
  • ^ a b c d e f g h i j k l m Lori M. Dickerson, Pharm. D., Pamela J. Mazyck, Pharm. D., and Melissa H. Hunter, M.D. (2003). "Premenstrual Syndrome". Premenstrual Syndrome. American Academy of Family Physicians. Retrieved 2008-01-10. {{cite web}}: Italic or bold markup not allowed in: |publisher= (help)CS1 maint: multiple names: authors list (link) Cite error: The named reference "ACOG" was defined multiple times with different content (see the help page).
  • ^ Matlin, Margaret W., The Psychology of Women: Sixth Edition 2008.
  • ^ a b "MayoClinic.com: Premenstrual syndrome syndrome (PMS): Signs and symptoms". 2006-10-27. Retrieved 2007-02-02. {{cite web}}: Text "publisher: MayoClinic.com" ignored (help)
  • ^ "Always: Tips and information". 2007. Retrieved 2007-02-02. {{cite web}}: Text "publisher: Always" ignored (help)
  • ^ a b "Merck Manual Professional - Menstrual Abnormalities". 2005-11. Retrieved 2007-02-02. {{cite web}}: Check date values in: |date= (help)
  • ^ a b Johnson S, PHD. "Premenstrual Syndrome (Premenstrual Tension)". Menstrual Abnormalities and Abnormal Uterine Bleeding. Armenian Health Network, Health.am. Retrieved 2008-01-10.
  • ^ Amy Scholten, MPH. "What are the risk factors for premenstrual syndrome?". Premenstrual Syndrome (PMS). Harvard Medical school. Retrieved 2008-01-10.
  • ^ "NHS Direct: Premenstrual syndrome - Causes". 2005-11-09. Retrieved 2007-02-02. {{cite web}}: Text "publisher: NHS Direct" ignored (help)
  • ^ "Causes of PMS". 2007. Retrieved 2007-02-11. {{cite web}}: Text "publisher: Always" ignored (help)
  • ^ Kendler KS, Karkowski LM, Corey LA, Neale MC (1998). "Longitudinal population-based twin study of retrospectively reported premenstrual symptoms and lifetime major depression". Am J Psychiatry. 155 (9): 1234–40. PMID 9734548. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  • ^ Giannini AJ, Martin DM, Turner CE (1990). "Beta-endorphin decline in late luteal phase dysphoric disorder". Int J Psychiatry Med. 20 (3): 279–84. PMID 2265889.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ Reiber C (2008). "An evolutionary model of premenstrual syndrome". Med Hypotheses. 70 (5): 158–65. doi:10.1016/j.mehy.2007.08.031. PMID 18053655.
  • ^ Rosseinsky DR, Hall PG (1974). "Letter: An evolutionary theory of premenstrual tension". Lancet. 7887 (2): 1024. doi:10.1016/S0140-6736(74)92132-1. PMID 4138262.
  • ^ Morriss GM, Keverne, EB (1974). "Letter: Premenstrual tension". Lancet. 7892 (2): 1317–8. PMID 4139547.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ Erik Eckholm (1985). "Premenstrual Problems Seem To Beset Baboons". {{cite web}}: Unknown parameter |retrieved= ignored (|access-date= suggested) (help)
  • ^ a b "familydoctor.org: PMS: What you can do to ease your symptoms?". 2005. Retrieved 2007-02-02. {{cite web}}: Text "publisher: familydoctor.org" ignored (help)
  • ^ a b Shah NR, Jones JB, Aperi J, Shemtov R, Karne A, Borenstein J (2008). "Selective serotonin reuptake inhibitors for premenstrual syndrome and premenstrual dysphoric disorder: a meta-analysis" ([dead link]Scholar search). Obstet Gynecol. 111 (5): 1175–82. doi:10.1097/AOG.0b013e31816fd73b. PMID 18448752. {{cite journal}}: External link in |format= (help); Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  • ^ "U.S. Department of Health & Human Services: Premenstrual syndrome". 2006-09. Retrieved 2007-02-02. {{cite web}}: Check date values in: |date= (help); Text "publisher: U.S. Department of Health & Human Services" ignored (help)
  • ^ Giannini AJ, Sullivan B, Sarachene J, Loiselle RH (1988). "Clonidine in the treatment of premenstrual syndrome: a subgroup study". J Clin Psychiatry. 49 (2): 62–3. PMID 2962993. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  • ^ Roca CA, Schmidt PJ, Rubinow DR (1999). "A follow-up study of premenstrual syndrome". J Clin Psychiatry. 60 (11): 763–6. PMID 10584765.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ "LifeWatch - Women's Health - Women's Reproductive Health: PMS". Retrieved 2008-01-13.
  • ^ a b Dean BB, Borenstein JE, Knight K, Yonkers K (2006). "Evaluating the criteria used for identification of PMS". J Womens Health (Larchmt). 15 (5): 546–55. doi:10.1089/jwh.2006.15.546. PMID 16796482.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ "NIH Press Release-Hormones Trigger PMS Symptoms - 01/21/1998". Retrieved 2008-02-28.
  • ^ Bloch M, Schmidt PJ, Rubinow DR (1997). "Premenstrual syndrome: evidence for symptom stability across cycles". Am J Psychiatry. 154 (12): 1741–6. PMID 9396955.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • ^ Markens, Susan. “The Problematic of ‘Experience’ A Political and Cultural Critique of PMS.” Gender & Society. 10.1 (February 1996): 42-58.
  • ^ Figert, Anne E. “The Three Faces of PMS: The Professional, Gendered, and Scientific Structuring of a Psychiatric Disorder.” Social Problems. 42.1 (February 1995): 56-73.
  • ^ Rodin M (1992). "The social construction of premenstrual syndrome". Soc Sci Med. 35 (1): 49–56. doi:10.1016/0277-9536(92)90118-A. PMID 1496412.
  • ^ Eriksson O, Wall A, Marteinsdottir I; et al. (2006). "Mood changes correlate to changes in brain serotonin precursor trapping in women with premenstrual dysphoria". Psychiatry Res. 146 (2): 107–16. doi:10.1016/j.pscychresns.2005.02.012. PMID 16515859. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • ^ Eriksson E (1999). "Serotonin reuptake inhibitors for the treatment of premenstrual dysphoria". Int Clin Psychopharmacol. 14 Suppl 2: S27–33. PMID 10471170.
  • ^ Does PMDD Belong in the DSM? Challenging the Medicalization of Women's Bodies Journal article by Alia Offman, Peggy J. Kleinplatz; The Canadian Journal of Human Sexuality, Vol. 13, 2004
  • ^ Carol Tavris, The Mismeasure of Woman (New York: Simon & Schuster, 1992), 144.
  • ^ Carol Tavris, The Mismeasure of Woman (New York: Simon & Schuster, 1992), 142.
  • ^ Rittenhouse, C. Amanda. "The Emergence of Premenstrual Syndrome as a Social Problem". Social Problems. 38.3 (August 1991): 412-425.
  • ^ Lorber, Judith and Lisa Jean Moore. Gender and the Social Construction of Illness. 2nd ed. Walnut Creek, CA: Altamira Press, 2002.
  • ^ http://www.yaz.com/html/index.html
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