Dysmenorrhea

Last updated
Dysmenorrhea
Other namesDysmenorrhoea, period pain, painful periods, menstrual cramps
MenstrualCycle gen.svg
Menstrual cycle and changes in hormone production
Specialty Gynecology
Symptoms Pain during first few days of menstruation, diarrhea, nausea [1] [2]
Usual onsetWithin a year of the first menstrual period [1]
DurationLess than 5 days (primary dysmenorrhea) [1]
CausesNo underlying problem, uterine fibroids, adenomyosis, endometriosis [3]
Diagnostic method Pelvic exam, ultrasound [1]
Differential diagnosis Ectopic pregnancy, pelvic inflammatory disease, interstitial cystitis, chronic pelvic pain [1]
TreatmentHeating pad, medication [3]
Medication NSAIDs such as ibuprofen, hormonal birth control, IUD with progestogen [1] [3]
Prognosis Often improves with age [2]
Frequency50–90% female adolescents and women of reproductive age [4]

Dysmenorrhea, also known as period pain, painful periods or menstrual cramps, is pain during menstruation. [4] [5] [2] Its usual onset occurs around the time that menstruation begins. [1] Symptoms typically last less than three days. [1] The pain is usually in the pelvis or lower abdomen. [1] Other symptoms may include back pain, diarrhea or nausea. [1]

Contents

Dysmenorrhea can occur without an underlying problem. [3] [6] Underlying issues that can cause dysmenorrhea include uterine fibroids, adenomyosis, and most commonly, endometriosis. [3] It is more common among those with heavy periods, irregular periods, those whose periods started before twelve years of age and those who have a low body weight. [1] A pelvic exam and ultrasound in individuals who are sexually active may be useful for diagnosis. [1] Conditions that should be ruled out include ectopic pregnancy, pelvic inflammatory disease, interstitial cystitis and chronic pelvic pain. [1]

Dysmenorrhea occurs less often in those who exercise regularly and those who have children early in life. [1] Treatment may include the use of a heating pad. [3] Medications that may help include NSAIDs such as ibuprofen, hormonal birth control and the IUD with progestogen. [1] [3] Taking vitamin B1 or magnesium may help. [2] Evidence for yoga, acupuncture and massage is insufficient. [1] Surgery may be useful if certain underlying problems are present. [2]

Estimates of the percentage of female adolescents and women of reproductive age affected are between 50% and 90%. [4] [6] It is the most common menstrual disorder. [2] Typically, it starts within a year of the first menstrual period. [1] When there is no underlying cause, often the pain improves with age or following having a child. [2]

Signs and symptoms

The main symptom of dysmenorrhea is pain concentrated in the lower abdomen or pelvis. [1] It is also commonly felt in the right or left side of the abdomen. It may radiate to the thighs and lower back. [1]

Symptoms often co-occurring with menstrual pain include nausea and vomiting, diarrhea, headache, dizziness, disorientation, fainting and fatigue. [7] Symptoms of dysmenorrhea often begin immediately after ovulation and can last until the end of menstruation. This is because dysmenorrhea is often associated with changes in hormonal levels in the body that occur with ovulation. In particular, prostaglandins induce abdominal contractions that can cause pain and gastrointestinal symptoms. [8] [9] The use of certain types of birth control pills can prevent the symptoms of dysmenorrhea because they stop ovulation from occurring.

Dysmenorrhea is associated with increased pain sensitivity and heavy menstrual bleeding. [10] [11]

For many, primary dysmenorrhea symptoms gradually subside after their mid-20s. Pregnancy has also been demonstrated to lessen the severity of dysmenorrhea, when menstruation resumes. However, dysmenorrhea can continue until menopause. 5–15% of women with dysmenorrhea experience symptoms severe enough to interfere with daily activities. [12]

Causes

There are two types of dysmenorrhea, primary and secondary, based on the absence or presence of an underlying cause. Primary dysmenorrhea occurs without an associated underlying condition, while secondary dysmenorrhea has a specific underlying cause, typically a condition that affects the uterus or other reproductive organs. [5]

Painful menstrual cramps can result from an excess of prostaglandins released from the uterus. Prostaglandins cause the uterine muscles to tighten and relax causing the menstrual cramps. This type of dysmenorrhea is called primary dysmenorrhea. [5] Primary dysmenorrhea usually begins in the teens soon after the first period. [13]

Secondary dysmenorrhea is the type of dysmenorrhea caused by another condition such as endometriosis, uterine fibroids, [5] uterine adenomyosis, and polycystic ovary syndrome. Rarely, birth defects, intrauterine devices, certain cancers, and pelvic infections cause secondary dysmenorrhea. [12] If the pain occurs between menstrual periods, lasts longer than the first few days of the period, or is not adequately relieved by the use of nonsteroidal anti-inflammatory drugs (NSAIDs) or hormonal contraceptives, this could indicate another condition causing secondary dysmenorrhea. [14]

Membranous dysmenorrhea is a type of secondary dysmenorrhea in which the entire lining of the uterus is shed all at once rather than over the course of several days as is typical. [15] Signs and symptoms include spotting, bleeding, abdominal pain, and menstrual cramps. The resulting uterine tissue is called a decidual cast and must be passed through the cervix and vagina. [16] It typically takes the shape of the uterus itself. Membranous dysmenorrhea is extremely rare and there are very few reported cases. The underlying cause is unknown, though some evidence suggests it may be associated with ectopic pregnancy or the use of hormonal contraception.

When laparoscopy is used for diagnosis, the most common cause of dysmenorrhea is endometriosis, in approximately 70% of adolescents. [17]

Other causes of secondary dysmenorrhea include leiomyoma, [18] adenomyosis, [19] ovarian cysts, pelvic congestion, [20] and cavitated and accessory uterine mass. [21]

Risk factors

Genetic factors, stress and depression are risk factors for dysmenorrhea. [22] Risk factors for primary dysmenorrhea include: early age at menarche, long or heavy menstrual periods, smoking, and a family history of dysmenorrhea. [12]

Dysmenorrhea is a highly polygenic and heritable condition. [23] There is strong evidence of familial predisposition and genetic factors increasing susceptibility to dysmenorrhea. There have been multiple polymorphisms and genetic variants in both metabolic genes and genes responsible for immunity which have been associated with the disorder. [24]

Three distinct possible phenotypes have been identified for dysmenorrhea which include "multiple severe symptoms", "mild localized pain", and "severe localized pain". While there are likely differences in genotypes underlying each phenotype, the specific correlating genotypes have not yet been identified. These phenotypes are prevalent at different levels in different population demographics, suggesting different allelic frequencies across populations (in terms of race, ethnicity, and nationality). [25]

Polymorphisms in the ESR1 gene have been commonly associated with severe dysmenorrhea. [23] Variant genotypes in the metabolic genes such as CYP2D6 and GSTM1 have been similarly been correlated with an increased risk of severe menstrual pain, but not with moderate or occasional phenotypes. [26]

The occurrence and frequency of secondary dysmenorrhea (SD) has been associated with different alleles and genotypes of those with underlying pathologies, which can affect the pelvic region or other areas of the body. Individuals with disorders may have genetic mutations related to their diagnoses which produce dysmenorrhea as a symptom of their primary diagnosis. It has been found that those with fibromyalgia who have the ESR1 gene variation Xbal and possess the Xbal AA genotype are more susceptible to experiencing mild to severe menstrual pain resulting from their primary pathology. [27] Commonly, genetic mutations which are a hallmark of or associated with specific disorders can produce dysmenorrhea as a symptom which accompanies the primary disorder.

In contrast with secondary dysmenorrhea, primary dysmenorrhea (PD) has no underlying pathology. [28] Genetic mutation and variations have therefore been thought to underlie this disorder and contribute to the pathogenesis of PD. [29] There are multiple single-nucleotide polymorphisms (SNP) associated with PD. Two of the most well studied include an SNP in the promoter of MIF and an SNP in the tumor necrosis factor (TNF-α) gene. When a cytosine 173 base pairs upstream of macrophage migration inhibitory factor (MIF) promoter was replaced by a guanine there was an associated increase in the likelihood of the individual experiencing PD. While a CC/GG genotype led to an increase in likelihood of the individual experiencing severe menstrual pain, a CC/GC genotype led to a more significant likelihood of the disorder impacting the individual overall and increasing the likelihood of any of the three phenotypes. [30] A second associated SNP was located 308 base pairs upstream from the start codon of the TNF-α gene, in which guanine was substituted for adenine. A GG genotype at the loci is associated with the disorder and has been proposed as a possible genetic marker to predict PD. [30]

There has also been an association with mutations in the MEFV gene and dysmenorrhea, which are considered to be causative. [31] The phenotypes associated with these mutations in the MEFV genes have been better studied; individuals who are heterozygous for these mutations are more likely to be affected by PD which presents as a severe pain phenotype. [23]

Genes related to immunity have been identified as playing a significant role in PD as well. IL1A was found to be the gene most associated with primary dysmenorrhea in terms of its phenotypic impact. [23] This gene encodes a protein essential for the regulation of immunity and inflammation.15 While the mechanism of how it influences PD has yet to be discovered, it is assumed that possible mutations in IL1A or genes which interact with it impact the regulation of inflammation during menstruation. These mutations may therefore affect pain responses during menstruation which lead to the differing phenotypes associated with dysmenorrhea.

Two additionally well studied SNPs which are suspected to contribute to PD were found in ZM1Z1 (the mutant allele called rs76518691) and NGF (the mutant allele called rs7523831). Both ZMIZ1 and NGF are associated with autoimmune responses and diseases, as well as pain response. [23] The implication of these genes impacting Dysmenorrhea is significant as it suggests mutations which affect the immune system (specifically the inflammatory response) and pain response may also be a cause of primary dysmenorrhea.

Mechanism

The underlying mechanism of primary dysmenorrhea is the contractions of the muscles of the uterus which induce a local ischemia. [32]

During an individual's menstrual cycle, the endometrium thickens in preparation for potential pregnancy. After ovulation, if the ovum is not fertilized and there is no pregnancy, the built-up uterine tissue is not needed and thus shed.

Prostaglandins and leukotrienes are released during menstruation, due to the build up of omega-6 fatty acids. [33] [34] Release of prostaglandins and other inflammatory mediators in the uterus cause the uterus to contract and can result in systemic symptoms such as nausea, vomiting, bloating and headaches or migraines. [33] Prostaglandins are thought to be a major factor in primary dysmenorrhea. [35] When the uterine muscles contract, they constrict the blood supply to the tissue of the endometrium, which, in turn, breaks down and dies. These uterine contractions continue as they squeeze the old, dead endometrial tissue through the cervix and out of the body through the vagina. These contractions, and the resulting temporary oxygen deprivation to nearby tissues, are thought to be responsible for the pain or cramps experienced during menstruation.

Compared with non-dysmenorrheic individuals, those with primary dysmenorrhea have increased activity of the uterine muscle with increased contractility and increased frequency of contractions. [36]

Diagnosis

The diagnosis of dysmenorrhea is usually made simply on a medical history of menstrual pain that interferes with daily activities. However, there is no universally accepted standard technique for quantifying the severity of menstrual pains. [37] There are various quantification models, called menstrual symptometrics, that can be used to estimate the severity of menstrual pains as well as correlate them with pain in other parts of the body, menstrual bleeding and degree of interference with daily activities. [37]

Further work-up

Once a diagnosis of dysmenorrhea is made, further workup is required to search for any secondary underlying cause of it, in order to be able to treat it specifically and to avoid the aggravation of a perhaps serious underlying cause.

Further work-up includes a specific medical history of symptoms and menstrual cycles and a pelvic examination. [6] Based on results from these, additional exams and tests may be motivated, such as:

Management

Treatments that target the mechanism of pain include non-steroidal anti-inflammatory drugs (NSAIDs) and hormonal contraceptives. NSAIDs inhibit prostaglandin production. With long-term treatment, hormonal birth control reduces the amount of uterine fluid/tissue expelled from the uterus. Thus resulting in shorter, less painful menstruation. [38] These drugs are typically more effective than treatments that do not target the source of the pain (e.g. acetaminophen). [39] Regular physical activity may limit the severity of uterine cramps. [12] [40]

NSAIDs

Nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and naproxen are effective in relieving the pain of primary dysmenorrhea. [39] They can have side effects of nausea, dyspepsia, peptic ulcer, and diarrhea. [41] [39]

Hormonal birth control

Use of hormonal birth control may improve symptoms of primary dysmenorrhea. [42] [33] A 2009 systematic review (updated in 2023) found evidence that the low or medium doses of estrogen contained in the birth control pill reduces pain associated with dysmenorrhea. [43] In addition, no differences between different birth control pill preparations were found. [43] The review did not determine if the estrogen in birth control pills was more effective than NSAIDs. [43]

Norplant [44] and Depo-provera [45] [46] are also effective, since these methods often induce amenorrhea. The intrauterine system (Mirena IUD) may be useful in reducing symptoms. [47]

Other

A review indicated the effectiveness of transdermal nitroglycerin. [48] Reviews indicated magnesium supplementation seemed to be effective. [49] [2] A review indicated the usefulness of using calcium channel blockers. [32] Heat is effective compared to NSAIDs and is a preferred option by many patients, as it is easy to access and has no known side effects. [50]

Tamoxifen has been used effectively to reduce uterine contractility and pain in dysmenorrhea patients. [51]

There is some evidence that exercises performed 3 times a week for about 45 to 60 minutes, without particular intensity, reduces menstrual pain. [40]

Alternative medicine

There is insufficient evidence to recommend the use of many herbal or dietary supplements for treating dysmenorrhea, including melatonin, vitamin E, fennel, dill, chamomile, cinnamon, damask rose, rhubarb, guava, and uzara. [1] [52] Further research is recommended to follow up on weak evidence of benefit for: fenugreek, ginger, valerian, zataria, zinc sulphate, fish oil, and vitamin B1. A 2016 review found that evidence of safety is insufficient for most dietary supplements. [52] There is some evidence for the use of fenugreek. [53]

One review found thiamine and vitamin E to be likely effective. [54] It found the effects of fish oil and vitamin B12 to be unknown. [54] Reviews found tentative evidence that ginger powder may be effective for primary dysmenorrhea. [55] Reviews have found promising evidence for Chinese herbal medicine for primary dysmenorrhea, but that the evidence was limited by its poor methodological quality. [56] [57]

A 2016 Cochrane review of acupuncture for dysmenorrhea concluded that it is unknown if acupuncture or acupressure is effective. [58] There were also concerns of bias in study design and in publication, insufficient reporting (few looked at adverse effects), and that they were inconsistent. [58] There are conflicting reports in the literature, including one review which found that acupressure, topical heat, and behavioral interventions are likely effective. [54] It found the effect of acupuncture and magnets to be unknown. [54]

A 2007 systematic review found some scientific evidence that behavioral interventions may be effective, but that the results should be viewed with caution due to poor quality of the data. [59]

Spinal manipulation does not appear to be helpful. [54] Although claims have been made for chiropractic care, under the theory that treating subluxations in the spine may decrease symptoms, [60] a 2006 systematic review found that overall no evidence suggests that spinal manipulation is effective for treatment of primary and secondary dysmenorrhea. [61]

Valerian, Humulus lupulus and Passiflora incarnata may be safe and effective in the treatment of dysmenorrhea. [10]

TENS

A 2011 review stated that high-frequency transcutaneous electrical nerve stimulation may reduce pain compared with sham TENS, but seems to be less effective than ibuprofen. [54]

Surgery

One treatment of last resort is presacral neurectomy. [62]

Epidemiology

Dysmenorrhea is one of the most common gynecological problems, regardless of age or race. It is one of the most frequently identified causes of pelvic pain in those who menstruate. Dysmenorrhea is estimated to affect between 50% and 90% of female adolescents and women of reproductive age. [4] Another report states that estimates can vary between 16% and 91% of surveyed individuals, with severe pain observed in 2% to 29% of menstruating individuals. [50] Reports of dysmenorrhea are greatest among individuals in their late teens and 20s, with reports usually declining with age. The prevalence in adolescent females has been reported to be 67.2% by one study [63] and 90% by another. [64] It has been stated that there is no significant difference in prevalence or incidence between races, [64] although one study of Hispanic adolescent females indicated an elevated prevalence and impact in this group. [65] Another study indicated that dysmenorrhea was present in 36.4% of participants, and was significantly associated with lower age and lower parity. [66] Childbearing is said to relieve dysmenorrhea, but this does not always occur. One study indicated that in nulliparous individuals with primary dysmenorrhea, the severity of menstrual pain decreased significantly after age 40. [67]

A survey in Norway showed that 14 percent of females between the ages of 20 to 35 experience symptoms so severe that they stay home from school or work. [68] Among adolescent girls, dysmenorrhea is the leading cause of recurrent short-term school absence. [69]

A study from India conducted by Dr RimJhim Kumari found that painful menstruation affected 66.7% of the girls, out of which only 27% sought medical advice from a doctor. [70]

Related Research Articles

<span class="mw-page-title-main">Menstruation</span> Shedding of the uterine lining

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<span class="mw-page-title-main">Endometriosis</span> Disease of the female reproductive system

Endometriosis is a disease in which cells like those in the endometrium, the layer of tissue that normally covers the inside of the uterus, grow outside the uterus. It occurs in humans and a limited number of menstruating mammals. Lesions can be found on ovaries, fallopian tubes, tissue around the uterus and ovaries (peritoneum), intestines, bladder, and diaphragm; and may also occur in other parts of the body. Symptoms include pelvic pain, heavy and painful periods, pain with bowel movements, painful urination, pain during sexual intercourse and infertility. Nearly half of those affected have chronic pelvic pain, while 70% feel pain during menstruation. Up to half of affected individuals are infertile. About 25% of individuals have no symptoms and 85% of those seen with infertility in a tertiary center have no pain. Endometriosis can have both social and psychological effects.

<span class="mw-page-title-main">Menstrual cycle</span> Natural changes in the human female reproductive system

The menstrual cycle is a series of natural changes in hormone production and the structures of the uterus and ovaries of the female reproductive system that makes pregnancy possible. The ovarian cycle controls the production and release of eggs and the cyclic release of estrogen and progesterone. The uterine cycle governs the preparation and maintenance of the lining of the uterus (womb) to receive an embryo. These cycles are concurrent and coordinated, normally last between 21 and 35 days, with a median length of 28 days. Menarche usually occurs around the age of 12 years; menstrual cycles continue for about 30–45 years.

<span class="mw-page-title-main">Hysterectomy</span> Surgical removal of the uterus

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<span class="mw-page-title-main">Adenomyosis</span> Extension of endometrial tissue into the myometrium

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<span class="mw-page-title-main">Vaginal bleeding</span> Medical condition

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<span class="mw-page-title-main">Endometrial polyp</span> Mass on the interior lining of the uterus

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<span class="mw-page-title-main">Pelvic pain</span> Medical condition

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<span class="mw-page-title-main">Uterine prolapse</span> Medical condition

Uterine prolapse is a form of pelvic organ prolapse in which the uterus and a portion of the upper vagina protrude into the vaginal canal and, in severe cases, through the opening of the vagina. It is most often caused by injury or damage to structures that hold the uterus in place within the pelvic cavity. Symptoms may include vaginal fullness, pain with sexual intercourse, difficulty urinating, and urinary incontinence. Risk factors include older age, pregnancy, vaginal childbirth, obesity, chronic constipation, and chronic cough. Prevalence, based on physical exam alone, is estimated to be approximately 14%.

<span class="mw-page-title-main">Postpartum bleeding</span> Loss of blood following childbirth

Postpartum bleeding or postpartum hemorrhage (PPH) is often defined as the loss of more than 500 ml or 1,000 ml of blood following childbirth. Some have added the requirement that there also be signs or symptoms of low blood volume for the condition to exist. Signs and symptoms may initially include: an increased heart rate, feeling faint upon standing, and an increased breathing rate. As more blood is lost, the patient may feel cold, blood pressure may drop, and they may become restless or unconscious. In severe cases circulatory collapse, disseminated intravascular coagulation and death can occur. The condition can occur up to twelve weeks following delivery in the secondary form. The most common cause is poor contraction of the uterus following childbirth. Not all of the placenta being delivered, a tear of the uterus, or poor blood clotting are other possible causes. It occurs more commonly in those who already have a low amount of red blood, are Asian, have a larger fetus or more than one fetus, are obese or are older than 40 years of age. It also occurs more commonly following caesarean sections, those in whom medications are used to start labor, those requiring the use of a vacuum or forceps, and those who have an episiotomy.

<span class="mw-page-title-main">Hematometra</span> Medical condition

Hematometra is a medical condition involving collection or retention of blood in the uterus. It is most commonly caused by an imperforate hymen or a transverse vaginal septum.

Genital leiomyomas are leiomyomas that originate in the dartos muscles, or smooth muscles, of the genitalia, areola, and nipple. They are a subtype of cutaneous leiomyomas that affect smooth muscle found in the scrotum, labia, or nipple. They are benign tumors, but may cause pain and discomfort to patients. Genital leiomyoma can be symptomatic or asymptomatic and is dependent on the type of leiomyoma. In most cases, pain in the affected area or region is most common. For vaginal leiomyoma, vaginal bleeding and pain may occur. Uterine leiomyoma may exhibit pain in the area as well as painful bowel movement and/or sexual intercourse. Nipple pain, enlargement, and tenderness can be a symptom of nipple-areolar leiomyomas. Genital leiomyomas can be caused by multiple factors, one can be genetic mutations that affect hormones such as estrogen and progesterone. Moreover, risk factors to the development of genital leiomyomas include age, race, and gender. Ultrasound and imaging procedures are used to diagnose genital leiomyomas, while surgically removing the tumor is the most common treatment of these diseases. Case studies for nipple areolar, scrotal, and uterine leiomyoma were used, since there were not enough secondary resources to provide more evidence.

Endometriosis and its complications are a major cause of female infertility. Endometriosis is a dysfunction characterized by the migration of endometrial tissue to areas outside of the endometrium of the uterus. The most common places to find stray tissue are on ovaries and fallopian tubes, followed by other organs in the lower abdominal cavity such as the bladder and intestines. Typically, the endometrial tissue adheres to the exteriors of the organs, and then creates attachments of scar tissue called adhesions that can join adjacent organs together. The endometrial tissue and the adhesions can block a fallopian tube and prevent the meeting of ovum and sperm cells, or otherwise interfere with fertilization, implantation and, rarely, the carrying of the fetus to term.

Fundal massage, also called uterine massage, is a technique used to reduce bleeding and cramping of the uterus after childbirth or after an abortion. As the uterus returns to its nonpregnant size, its muscles contract strongly, which can cause pain. Fundal massage can be performed with one hand over the pubic bone, firmly massaging the uterine fundus, or with the addition of one hand in the vagina compressing the two uterine arteries. Routine use of fundal massage can prevent postpartum or post-abortion hemorrhage and can reduce pain; it may also reduce the need for uterotonics, medications that cause the uterus to contract. It is used to treat uterine atony, a condition where the uterus lacks muscle tone and is soft to the touch instead of firm.

Menstrual suppression refers to the practice of using hormonal management to stop or reduce menstrual bleeding. In contrast to surgical options for this purpose, such as hysterectomy or endometrial ablation, hormonal methods to manipulate menstruation are reversible.

References

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 Osayande AS, Mehulic S (March 2014). "Diagnosis and initial management of dysmenorrhea". American Family Physician. 89 (5): 341–346. PMID   24695505.
  2. 1 2 3 4 5 6 7 8 American College of Obstetricians and Gynecologists (Jan 2015). "FAQ046 Dynsmenorrhea: Painful Periods" (PDF). Archived (PDF) from the original on 27 June 2015. Retrieved 26 June 2015.
  3. 1 2 3 4 5 6 7 "Menstruation and the menstrual cycle fact sheet". Office of Women's Health. December 23, 2014. Archived from the original on 26 June 2015. Retrieved 25 June 2015.
  4. 1 2 3 4 McKenna KA, Fogleman CD (August 2021). "Dysmenorrhea". Am Fam Physician. 104 (2): 164–170. PMID   34383437.
  5. 1 2 3 4 "Period Pain". MedlinePlus. National Library of Medicine. March 1, 2018. Retrieved November 7, 2018.
  6. 1 2 3 4 5 "Dysmenorrhea and Endometriosis in the Adolescent". ACOG. American College of Obstetricians and Gynecologists. 20 November 2018. Retrieved 21 November 2018.
  7. "Dysmenorrhea". www.hopkinsmedicine.org. 13 May 2019. Retrieved 2019-10-04.
  8. "Period pain". nhs.uk. 2017-10-19. Retrieved 2019-10-04.
  9. "Using Foods Against Menstrual Pain". Physicians Committee for Responsible Medicine. Retrieved 2019-10-04.
  10. 1 2 Gomathy N, Dhanasekar KR, Trayambak D, Amirtha R (November 2019). "Supportive therapy for dysmenorrhea: Time to look beyond mefenamic acid in primary care". Journal of Family Medicine and Primary Care. 8 (11): 3487–3491. doi: 10.4103/jfmpc.jfmpc_717_19 . PMC   6881953 . PMID   31803641.
  11. Payne LA, Rapkin AJ, Seidman LC, Zeltzer LK, Tsao JC (2017). "Experimental and procedural pain responses in primary dysmenorrhea: a systematic review". Journal of Pain Research. 10: 2233–2246. doi: 10.2147/JPR.S143512 . PMC   5604431 . PMID   29066929.
  12. 1 2 3 4 [ better source needed ] "Dysmenorrhea - Gynecology and Obstetrics". Merck Manuals Professional Edition. Archived from the original on 10 September 2017.
  13. "Period problems | Office on Women's Health". www.womenshealth.gov. Retrieved 14 November 2022.
  14. Carlson KJ, Eisenstat SA, Ziporyn TD (2004). The New Harvard Guide to Women's Health. Harvard University Press. p. 479. doi:10.2307/j.ctv1b9f66x. ISBN   978-0-674-01282-0. JSTOR   j.ctv1b9f66x.
  15. "How to manage a decidual cast, aka shedding your entire uterus lining in one go". 3 November 2020.
  16. "What is a Decidual Cast?".
  17. Janssen EB, Rijkers AC, Hoppenbrouwers K, Meuleman C, D'Hooghe TM (2013). "Prevalence of endometriosis diagnosed by laparoscopy in adolescents with dysmenorrhea or chronic pelvic pain: a systematic review". Human Reproduction Update. 19 (5): 570–582. doi: 10.1093/humupd/dmt016 . PMID   23727940.
  18. Hilário SG, Bozzini N, Borsari R, Baracat EC (January 2009). "Action of aromatase inhibitor for treatment of uterine leiomyoma in perimenopausal patients". Fertility and Sterility. 91 (1): 240–243. doi: 10.1016/j.fertnstert.2007.11.006 . PMID   18249392.
  19. Nabeshima H, Murakami T, Nishimoto M, Sugawara N, Sato N (2008). "Successful total laparoscopic cystic adenomyomectomy after unsuccessful open surgery using transtrocar ultrasonographic guiding". Journal of Minimally Invasive Gynecology . 15 (2): 227–230. doi:10.1016/j.jmig.2007.10.007. PMID   18312998.
  20. Hacker, Neville F., J. George Moore, and Joseph C. Gambone. Essentials of Obstetrics and Gynecology, 4th ed. Elsevier Saunders, 2004. ISBN   0-7216-0179-0 [ page needed ]
  21. Acién P, Acién M, Fernández F, José Mayol M, Aranda I (November 2010). "The cavitated accessory uterine mass: a Müllerian anomaly in women with an otherwise normal uterus". Obstetrics and Gynecology. 116 (5): 1101–1109. doi:10.1097/AOG.0b013e3181f7e735. PMID   20966695. S2CID   20532705.
  22. Ju H, Jones M, Mishra G (2014). "The prevalence and risk factors of dysmenorrhea". Epidemiologic Reviews. 36: 104–113. doi: 10.1093/epirev/mxt009 . PMID   24284871.
  23. 1 2 3 4 5 Li Z, Chen J, Zhao Y, Wang Y, Xu J, Ji J, et al. (April 2017). "Common variants in ZMIZ1 and near NGF confer risk for primary dysmenorrhoea". Nature Communications. 8 (1): 14900. Bibcode:2017NatCo...814900L. doi:10.1038/ncomms14900. PMC   5414039 . PMID   28447608.
  24. Ju H, Jones M, Mishra G (2014-01-01). "The prevalence and risk factors of dysmenorrhea". Epidemiologic Reviews. 36 (1): 104–113. doi: 10.1093/epirev/mxt009 . PMID   24284871.
  25. Chen CX, Carpenter JS, Ofner S, LaPradd M, Fortenberry JD (January 2021). "Dysmenorrhea Symptom-Based Phenotypes: A Replication and Extension Study". Nursing Research. 70 (1): 24–33. doi:10.1097/NNR.0000000000000477. PMC   7736149 . PMID   32956256.
  26. Wu D, Wang X, Chen D, Niu T, Ni J, Liu X, Xu X (November 2000). "Metabolic gene polymorphisms and risk of dysmenorrhea". Epidemiology. 11 (6): 648–653. doi: 10.1097/00001648-200011000-00006 . PMID   11055624. S2CID   27774699.
  27. Arslan HS, Nursal AF, Inanir A, Karakus N, Yigit S (2021-08-26). "Influence of ESR1 Variants on Clinical Characteristics and Fibromyalgia Syndrome in Turkish Women". Endocrine, Metabolic & Immune Disorders Drug Targets. 21 (7): 1326–1332. doi:10.2174/1871530320666200910110915. PMID   32914729. S2CID   221623106.
  28. Osayande AS, Mehulic S (March 2014). "Diagnosis and initial management of dysmenorrhea". American Family Physician. 89 (5): 341–346. PMID   24695505.
  29. Osonuga A, Ekor M (December 2019). "Risk factors for dysmenorrhea among Ghanaian undergraduate students". African Health Sciences. 19 (4): 2993–3000. doi:10.4314/ahs.v19i4.20. PMC   7040311 . PMID   32127874.
  30. 1 2 Dogru HY, Ozsoy AZ, Karakus N, Delibas IB, Isguder CK, Yigit S (August 2016). "Association of Genetic Polymorphisms in TNF and MIF Gene with the Risk of Primary Dysmenorrhea". Biochemical Genetics. 54 (4): 457–466. doi:10.1007/s10528-016-9732-2. PMID   27105877. S2CID   86975436.
  31. Erten S, Altunoglu A, Keskin HL, Ceylan GG, Yazıcı A, Dalgaci AF, et al. (September 2013). "Increased frequency of MEFV gene mutations in patients with primary dysmenorrhea". Modern Rheumatology. 23 (5): 959–962. doi:10.3109/s10165-012-0779-6. PMID   23053724. S2CID   75848809.
  32. 1 2 Fenakel K, Lurie S (December 1990). "The use of calcium channel blockers in obstetrics and gynecology; a review". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 37 (3): 199–203. doi: 10.1016/0028-2243(90)90025-v . PMID   2227064.
  33. 1 2 3 Harel Z (December 2006). "Dysmenorrhea in adolescents and young adults: etiology and management". Journal of Pediatric and Adolescent Gynecology. 19 (6): 363–371. doi:10.1016/j.jpag.2006.09.001. PMID   17174824.
  34. Bofill Rodriguez M, Lethaby A, Farquhar C (September 2019). "Non-steroidal anti-inflammatory drugs for heavy menstrual bleeding". The Cochrane Database of Systematic Reviews. 2019 (9): CD000400. doi:10.1002/14651858.CD000400.pub4. PMC   6751587 . PMID   31535715.
  35. Wright, Jason and Solange Wyatt. The Washington Manual Obstetrics and Gynecology Survival Guide. Lippincott Williams and Wilkins, 2003. ISBN   0-7817-4363-X [ page needed ]
  36. Rosenwaks Z, Seegar-Jones G (October 1980). "Menstrual pain: its origin and pathogenesis". The Journal of Reproductive Medicine. 25 (4 Suppl): 207–212. PMID   7001019.
  37. 1 2 Wyatt KM, Dimmock PW, Hayes-Gill B, Crowe J, O'Brien PM (July 2002). "Menstrual symptometrics: a simple computer-aided method to quantify menstrual cycle disorders". Fertility and Sterility. 78 (1): 96–101. doi: 10.1016/s0015-0282(02)03161-8 . PMID   12095497.
  38. Miller L, Notter KM (November 2001). "Menstrual reduction with extended use of combination oral contraceptive pills: randomized controlled trial". Obstetrics and Gynecology. 98 (5 Pt 1). LWW Journals: 771–778. doi:10.1016/s0029-7844(01)01555-1. PMID   11704167. S2CID   23668483.
  39. 1 2 3 Marjoribanks J, Ayeleke RO, Farquhar C, Proctor M (July 2015). "Nonsteroidal anti-inflammatory drugs for dysmenorrhoea". The Cochrane Database of Systematic Reviews. 2015 (7): CD001751. doi:10.1002/14651858.CD001751.pub3. PMC   6953236 . PMID   26224322.
  40. 1 2 Armour M, Ee CC, Naidoo D, Ayati Z, Chalmers KJ, Steel KA, et al. (September 2019). "Exercise for dysmenorrhoea". The Cochrane Database of Systematic Reviews. 2019 (9): CD004142. doi:10.1002/14651858.CD004142.pub4. PMC   6753056 . PMID   31538328.
  41. Rossi S, editor. Australian Medicines Handbook 2006. Adelaide: Australian Medicines Handbook; 2006. ISBN   0-9757919-2-3
  42. Archer DF (November 2006). "Menstrual-cycle-related symptoms: a review of the rationale for continuous use of oral contraceptives". Contraception. 74 (5): 359–366. doi:10.1016/j.contraception.2006.06.003. PMID   17046376.
  43. 1 2 3 Schroll JB, Black AY, Farquhar C, Chen I (July 2023). "Combined oral contraceptive pill for primary dysmenorrhoea". The Cochrane Database of Systematic Reviews. 2023 (7): CD002120. doi:10.1002/14651858.CD002120.pub4. PMC   10388393 . PMID   37523477.
  44. Power J, French R, Cowan F (July 2007). Power J (ed.). "Subdermal implantable contraceptives versus other forms of reversible contraceptives or other implants as effective methods of preventing pregnancy". The Cochrane Database of Systematic Reviews. 2007 (3): CD001326. doi:10.1002/14651858.CD001326.pub2. PMC   7025801 . PMID   17636668.
  45. Glasier A (2006). "Contraception". In DeGroot LJ, Larry JJ (eds.). Endocrinology (5th ed.). Philadelphia: Elsevier Saunders. pp.  2993–3003. ISBN   978-0-7216-0376-6.
  46. Loose DS, Stancel GM (2006). "Estrogens and Progestins". In Brunton LL, Lazo JS, Parker KL (eds.). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11th ed.). New York: McGraw-Hill. pp.  1541–1571. ISBN   978-0-07-142280-2.
  47. Gupta HP, Singh U, Sinha S (July 2007). "Laevonorgestrel intra-uterine system--a revolutionary intra-uterine device". Journal of the Indian Medical Association. 105 (7): 380, 382–380, 385. PMID   18178990.
  48. Morgan PJ, Kung R, Tarshis J (May 2002). "Nitroglycerin as a uterine relaxant: a systematic review". Journal of Obstetrics and Gynaecology Canada. 24 (5): 403–409. doi:10.1016/S1701-2163(16)30403-0. PMID   12196860.
  49. Parazzini F, Di Martino M, Pellegrino P (February 2017). "Magnesium in the gynecological practice: a literature review". Magnesium Research. 30 (1): 1–7. doi: 10.1684/mrh.2017.0419 . PMID   28392498.
  50. 1 2 Nagy, H.; Khan MAB (2020). "Dysmenorrhea". StatPearls. PMID   32809669. CC-BY icon.svg Text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  51. Thomas B, Magos A (2009). "Modern management of dysmenorrhoea". Trends in Urology, Gynaecology & Sexual Health. 14 (5): 25–29. doi: 10.1002/tre.120 .
  52. 1 2 Pattanittum P, Kunyanone N, Brown J, Sangkomkamhang US, Barnes J, Seyfoddin V, Marjoribanks J (March 2016). "Dietary supplements for dysmenorrhoea". The Cochrane Database of Systematic Reviews. 2016 (3): CD002124. doi:10.1002/14651858.CD002124.pub2. PMC   7387104 . PMID   27000311.
  53. Nagulapalli Venkata KC, Swaroop A, Bagchi D, Bishayee A (June 2017). "A small plant with big benefits: Fenugreek (Trigonella foenum-graecum Linn.) for disease prevention and health promotion". Molecular Nutrition & Food Research. 61 (6): 1600950. doi:10.1002/mnfr.201600950. PMID   28266134. S2CID   23539394.
  54. 1 2 3 4 5 6 Latthe PM, Champaneria R, Khan KS (February 2011). "Dysmenorrhoea". BMJ Clinical Evidence. 2011. PMC   3275141 . PMID   21718556.
  55. Daily JW, Zhang X, Kim DS, Park S (December 2015). "Efficacy of Ginger for Alleviating the Symptoms of Primary Dysmenorrhea: A Systematic Review and Meta-analysis of Randomized Clinical Trials". Pain Medicine. 16 (12): 2243–2255. doi: 10.1111/pme.12853 . PMID   26177393.
  56. Zhu X, Proctor M, Bensoussan A, Wu E, Smith CA (April 2008). Zhu X (ed.). "Chinese herbal medicine for primary dysmenorrhoea". The Cochrane Database of Systematic Reviews (2): CD005288. doi:10.1002/14651858.CD005288.pub3. PMID   18425916.
  57. Gao L, Jia C, Zhang H, Ma C (October 2017). "Wenjing decoction (herbal medicine) for the treatment of primary dysmenorrhea: a systematic review and meta-analysis". Archives of Gynecology and Obstetrics. 296 (4): 679–689. doi:10.1007/s00404-017-4485-7. PMID   28791471. S2CID   32573698.
  58. 1 2 Smith CA, Armour M, Zhu X, Li X, Lu ZY, Song J (April 2016). "Acupuncture for dysmenorrhoea". The Cochrane Database of Systematic Reviews. 2016 (4): CD007854. doi:10.1002/14651858.CD007854.pub3. PMC   8406933 . PMID   27087494.
  59. Proctor ML, Murphy PA, Pattison HM, Suckling J, Farquhar CM (July 2007). Proctor M (ed.). "Behavioural interventions for primary and secondary dysmenorrhoea". The Cochrane Database of Systematic Reviews. 2007 (3): CD002248. doi:10.1002/14651858.CD002248.pub3. PMC   7137212 . PMID   17636702.
  60. Chapman-Smith D (2000). "Scope of practice". The Chiropractic Profession: Its Education, Practice, Research and Future Directions. West Des Moines, IA: NCMIC. ISBN   978-1-892734-02-0.[ page needed ]
  61. Proctor ML, Hing W, Johnson TC, Murphy PA (July 2006). Proctor M (ed.). "Spinal manipulation for primary and secondary dysmenorrhoea". The Cochrane Database of Systematic Reviews. 3 (3): CD002119. doi:10.1002/14651858.CD002119.pub3. PMC   6718213 . PMID   16855988.
  62. Ramirez C, Donnellan N (August 2017). "Pelvic denervation procedures for dysmenorrhea". Current Opinion in Obstetrics & Gynecology. 29 (4): 225–230. doi:10.1097/GCO.0000000000000379. PMID   28683027. S2CID   205607600.
  63. Sharma P, Malhotra C, Taneja DK, Saha R (February 2008). "Problems related to menstruation amongst adolescent girls". Indian Journal of Pediatrics. 75 (2): 125–129. doi:10.1007/s12098-008-0018-5. PMID   18334791. S2CID   58327516.
  64. 1 2 Holder A, Edmundson LD, Mert E (31 December 2009). "Dysmenorrhea". eMedicine. Archived from the original on 2011-02-22.
  65. Banikarim C, Chacko MR, Kelder SH (December 2000). "Prevalence and impact of dysmenorrhea on Hispanic female adolescents". Archives of Pediatrics & Adolescent Medicine. 154 (12): 1226–1229. doi: 10.1001/archpedi.154.12.1226 . PMID   11115307.
  66. Sule ST, Umar HS, Madugu NH (June 2007). "Premenstrual symptoms and dysmenorrhoea among Muslim women in Zaria, Nigeria". Annals of African Medicine. 6 (2): 68–72. doi: 10.4103/1596-3519.55713 . hdl: 1807/44286 . PMID   18240706.
  67. Juang CM, Yen MS, Horng HC, Cheng CY, Yuan CC, Chang CM (October 2006). "Natural progression of menstrual pain in nulliparous women at reproductive age: an observational study". Journal of the Chinese Medical Association. 69 (10): 484–488. doi: 10.1016/S1726-4901(09)70313-2 . PMID   17098673. S2CID   24518670.
  68. "Mozon: Sykemelder seg på grunn av menssmerter". Mozon. 2004-10-25. Archived from the original on 2007-03-17. Retrieved 2007-02-02.
  69. French L (2008). "Dysmenorrhea in adolescents: diagnosis and treatment". Paediatric Drugs. 10 (1): 1–7. doi:10.2165/00148581-200810010-00001. PMID   18162003. S2CID   33563026.
  70. Kumari R (2019). "Perspectives on adolescent girls' health-seeking behaviour in relation to reproductive health in Rohats, Bihar, India" (PDF). Ann. Int. Med. Den. Res. 5 (3): 17–20.