Showing posts with label VMS. Show all posts
Showing posts with label VMS. Show all posts

Wednesday, January 23, 2019

NAMS video series 2019: Understanding the etiology and mechanism of vasomotor symptoms


The North American Menopause Society (NAMS) regularly posts comprehensive videos for clinicians about important midlife health topics. All interviews in the series are hosted by NAMS Board of Trustees Member and Past-President Dr. Marla Shapiro, a Canadian physician who led this exciting initiative. Dr. Shapiro is also a medical consultant for CTV News.

In this first video of 2019, Dr. Rebecca Thurston, Director of the Women’s Biobehavioral Health Laboratory and Professor of Psychiatry, Psychology, Epidemiology, and Clinical and Translational Science at the University of Pittsburgh throws some light on the why and how about vasomotor symptoms (VMS).

The natural history of vasomotor symptoms is still evolving. It is estimated that about 75% of women experiencing menopause will have hot flashes. A substantial number of women seen in everyday gynecological practice or specialty menopause clinic report VMS well past the age of 60 and some well into the 80s.


Hot flashes considerably reduce the quality of life and hamper the day to day activities. Prevalence of VMS is generally associated with increased risk of CVD due to endothelial dysfunction. Hence, women with VMS could be screened for CVD risk factor and offered lifestyle modifications and frequent screening for early diagnosis and prevention.

Saturday, September 2, 2017

Endocrine Society issues guidelines for management of menopausal symptoms in breast cancer survivors


Women experiencing menopausal symptoms after receiving treatment for breast cancer should be managed with life-style changes instead of hormonal therapy says the first ever set of professional guidelines issued by the Endocrine Society.

Increasing incidence of breast cancer and improved survival have led to increasing number of women survivors who have a long life ahead, while experiencing the side effects of cancer chemotherapy.  
It is estimated that there are 9.3 million breast cancer survivors worldwide, who experience menopausal symptoms or clinical manifestations of estrogen deficiency.

The comprehensive review was published August 02, 2017 in Endocrine Society’s Journal of Clinical Endocrinology & Metabolism.

Premenopausal women diagnosed with breast cancer experience abrupt onset of estrogen depletion symptoms after treatment with chemotherapy. Just like women experiencing natural menopause these women develop vulvovaginal atrophy (VVA), vasomotor symptoms (VMS), osteopenia, and osteoporosis, CVDs and psychological symptoms like sleep disorders, mood changes and depression.

These women cannot be treated with Hormonal Replacement Therapy (HRT) like their counterparts with natural menopause.

The study’s first author, Richard J. Santen, M.D., of the University of Virginia Health System in Charlottesville, VA said in a News Release by Endocrine Society “Following breast cancer, women should generally not be treated with menopausal hormone therapy but should instead focus on lifestyle modifications such as smoking cessation, weight loss, and regular physical activity.”

“Pharmacologic agents are also available to treat women with severe symptoms. The most important thing to remember is that therapy must be individualized based on each woman’s needs and goals,” he further added.

The author and his colleagues reviewed randomized controlled clinical trials (RCTs), observational studies, evidence- based guidelines, and expert opinion from professional societies to formulate the guidelines.

1) Life style modification advised for all breast cancer survivors include weight management, regular physical activity, smoking and alcohol cessation, vitamin D and calcium supplementation and eating healthy diet.

2) Sleep and other psychomotor symptoms should be treated with mind-brain-behavior or nonhormone, pharmacologic therapy.

3) Vasomotor symptoms respond well to selective serotonin /noradrenaline reuptake inhibitors and gabapentenoid agents.

4) A variety of non-hormonal treatments are available for treating osteoporosis like bisphosphonates, including zoledronic acid (Reclast) and denosumab (Prolia).

5) Treatment of VVA is a grey zone, low dose estrogen applied vaginally is absorbed in blood and although the blood levels are within normal limits, it could still potentially stimulate occult breast cancer cells. Hence, it is not generally advised, especially those on aromatase inhibitors.

6) Intravaginal DHEA and oral ospemiphene is often prescribed to relieve dyspareunia but their safety is still not established in breast cancer survivors.

7) Vaginal laser therapy is being used, but still more data is needed to document its efficacy.

8) Researchers are looking into other therapies in near future like lasofoxifene, neurokinin B inhibitors, stellate ganglion blockade, vaginal testosterone, and estetrol.

9) The most important recommendation is treatment should be individualized according to need of each patient.

Friday, July 7, 2017

NAMS updates its position statement on HRT, clearing five critical areas of confusion.

courtesy: www.renewedvitalitymd.com
The North American Menopause Society has updated its position statement regarding menopausal and post-menopausal hormone therapy, replacing the earlier statement issued in 2012.

Instead of prescribing, “lowest dose for the shortest period of time” which may be harmful for some women, the new emphasis is on “appropriate dose, duration, regimen, and route of administration that provides the most benefit with the minimal amount of risk.”

The new position statement was published online June 21 in NAMS’s Journal Menopause.

Hormone Replacement Therapy remains the most effective treatment for vasomotor symptoms (VMS) and Genitourinary symptoms of menopause (GSM) and helps prevent osteoporosis and fractures.

The US FDA approved indications for starting HRT are bothersome vasomotor symptoms and genitourinary symptoms, Estrogen deficient states caused by premature ovarian insufficiency (POI), hypogonadism and castration and prevention of bone loss.

Women who are seeking relief for bothersome vasomotor symptoms are offered conjugated equine estrogen (CEE) if they already had hysterectomy or it is paired with a progestogen or with bazedoxifene, a selective estrogen-receptor modulator (SERM), to protect users against endometrial cancer.


The statement authors also suggest that micronized progesterone at a dose of 300 mg at bedtime can be an effective treatment to reduce hot flashes and night sweats and improves sleep.

Low dose, intravaginal estrogen preparation is the treatment of choice for women with vulvovaginal atrophy (VVA), because of minimum systemic absorption. For women who are intolerant to estrogen, ospemifene or intravaginal DHEA is equally effective in relieving the symptoms of atrophy. This preparation also bring relief from urinary symptoms.

Systemic Hormonal therapy is not effective in improving urinary incontinence and on the other hand may exacerbate stress incontinence.

HRT in women who have undergone surgical menopause or POI should be started early and at least continued till the age of 52 years.

An important update in this statement was about starting HRT in women with BRCA 1/2 mutation. Dr. JoAnn V. Pinkerton, NAMS executive director said, "For BRCA-positive women without breast cancer who have undergone risk-reducing bilateral salpingoophorectomy, observational data suggest that systemic HRT to the median age of menopause may decrease health risks associated with premature loss of estrogen without increasing breast-cancer risk. "

Physician should be cautious in starting HRT in women who are 10 years past menopause or 60 years old at the time of initiating HRT. In these group of women, the benefit/risk ration is less favorable than for younger women because of increased risk of stroke, CVD, venous thromboembolism and dementia.

If the women are already on HRT, the therapy need not be discontinued abruptly at age 60 or 65 years. It may be continued past 65 years of age for persistent hot flashes, prevention of osteoporosis, and quality-of-life issues, with an open dialogue with the patients about the risk and benefits of HRT at this age.

Once HRT is stopped, in 50% of women, vasomotor symptoms will recur, irrespective of age of starting the therapy or duration of therapy quoted the authors of the statement.

And, nearly all women, will lose [bone-mineral density], with increased risk of bone fractures and excess mortality from hip fracture," they also point out.

Dr Pinkerton added "And the risks of longer use of HRT may be minimized with the use of lower doses of both estrogen and progestogens, the use of transdermal therapies to avoid hepatic first-pass effect, or the combination of conjugated estrogen paired with the SERM bazedoxifene, which provides endometrial protection without the need for a progestogen."

NAMS has also released a patient information sheet called ‘MenoNote’ that simplify the facts and help women to decide using HRT. The ‘MenoNote’ is available on NAMS website. It can be accessed here.




Thursday, April 13, 2017

New natural (bioidentical) 17ß-estradiol-progesterone combination available as single soft gel capsules effective in treating postmenopausal symptoms: News from ENDO17

Courtesy: TherapeuticsMD

An innovative, investigational combination of 17ß-estradiol and progesterone in a single, oral softgel, was found effective for the treatment of moderate to severe vasomotor symptoms (VMS) due to menopause. The results of the study were presented at the ENDO 2017, the annual meeting of the Endocrine Society in Orlando, Florida, April 1-4.

TherapeuticsMD, Inc which specializes in developing women’s health products has developed this combination drug named as TX-001HR. TherapeuticsMD is using the unique technology called ‘SYMBODA’ in manufacturing the softgel capsules. SYMBODA, meaning “similar to the body,” is a solubilized female hormone technology for formulation of estradiol and progesterone identical in chemical structure to the estradiol and progesterone that women naturally produce.

Robert G. Finizio, Chief Executive Officer of TherapeuticsMD. "There are currently no FDA-approved oral bio-identical estradiol and progesterone combination products for women experiencing hot flushes and night sweats. Approximately 1 million to 2.5 million women are currently estimated to use non-FDA-approved compounded menopausal hormone therapy (CBHT) in the U.S. 
TherapeuticsMD seeks to address the unmet needs of post-menopausal women as we develop potentially the first FDA-approved 17β-estradiol plus progesterone combination softgel capsule in the United States."

If the drug gets approved by FDA, it represents first single combined bioidentical estradiol and progesterone formulation in the market. Till now bioidentical hormones are custom made at compounding pharmacies which are ‘not regulated by FDA.’ Many women choose these because they think they are natural, plant based, safer and do not have any side effects.

Many Societies like The Endocrine Society, the North American Menopause Society, the American College of Obstetricians and Gynecologists (ACOG) and the British Menopause Society have all raised concern regarding the hazards of using custom-compounded hormones to treat menopausal symptoms.



The positive results of Replenish Trial, a phase 3 study that evaluated the safety and efficacy of four doses of TX-001HR were presented at the conference by Rogerio Lobo, M.D., professor of Obstetrics and Gynecology and Director of the Reproductive Endocrinology Program at Columbia University.

Replenish trial is a prospective, randomized, double-blind, placebo-controlled, parallel-group, multicenter study evaluating four doses of TX-001HR with an objective of evaluating the drug’s effectiveness in relieving hot flashes in post-menopausal women.

The study enrolled 1835 healthy women between 40−65 years with intact uterus having ≥7/day or ≥50/week hot flushes. They were randomized to 5 groups receiving either of this 4-dose combination of TX-001HR:  E2/P 1.0 mg/100 mg; E2/P 0.5 mg/100 mg; E2/P 0.5/50; E2/P 0.25/50 or a placebo.

The efficacy of the drug was assessed by changes in number and intensity of hot flushes while on drug at end of 1 and 3 months.

Another subset of women who did not fit the criteria for VMS were randomized to receive either of the 4-dose combination of the drug to evaluate endometrial hyperplasia. All women underwent biopsy at the start of therapy and at the end of1 year. The safety end point was ≤1% incidence of endometrial hyperplasia at end of 12 months.

The results showed that TX-001HR combinations of E2/P 1.0 mg/100 mg or 0.5 mg/100 mg was most effective in controlling VMS without any unacceptable side effects.

Incidence of endometrial hyperplasia was 0%, with no reported case of endometrial cancer with any of the dose combination at the end of 12 months which is unlike reported cases of endometrial hyperplasia with compounded bio-identical hormone therapy (CBHT).

Dr Lobo concluded his talk saying “TX-001HR, "if approved," would be a new oral hormone-therapy option for postmenopausal women with moderate to severe vasomotor symptoms who have an intact uterus.

It may be a new option for the estimated millions of women currently using less regulated and unapproved compounded bioidentical hormone therapy."

The combination hormone pill Replenish Trial is the second clinical trial completed by TherapeuticsMD, which last December announced results from its Rejoice trial where it tested its softgel successfully in relieving vaginal dryness associated with menopause.

The 2 abstracts from the ENDO 17 conference can be accessed here: Abstract 1 and Abstract 2.


Thursday, December 17, 2015

Guidelines advocate a more tailored approach in management of Menopause!



Guidelines advocate a more tailored approach in management of Menopause!


photo courtesy -dreams time

The evaluation and treatment of menopause has undergone a sea change in last two decades, but this was not always backed up by evidence.

The Endocrine Society has updated the latest guidelines, and the recommendations are all backed by solid clinical research. The guidelines were published online October 7 and appeared in the November issue of the Journal of Clinical Endocrinology & Metabolism.

The article is primarily derived from the journal articleTreatment of Symptoms of the Menopause: An Endocrine Society Clinical Practice Guideline.” In the November issue of The Journal of Clinical Endocrinology & Metabolism 2015 100:11, 3975-4011

In 2002, a large government study called the Women’s Health Initiative study generated intense scrutiny on the practice of menopausal hormone therapy due to concerns about increased risk for blood clots, stroke, breast cancer and heart attacks. Since then, physicians all over the world are very cautious in prescribing hormones as a therapy for management of menopausal symptoms.

The guidelines advocates that the individual risk is lower in younger women who have recently gone through menopause, and varies based on a woman’s health history, age and other factors. Developed by Endocrine Society menopause experts, the guideline provides recommendations on how to tailor treatments to suit a woman’s individual symptoms, health history and preferences and how to assess which women could consider menopausal hormone therapy.

The guidelines were developed by a panel of six experts on the subjects and were chaired by Cynthia Stuenkel, MD. She is a founding member of The North American Menopause Society (NAMS) and also a clinical professor of medicine at the University of California, San Diego School of Medicine and an attending physician for the university’s Endocrinology and Metabolism Service.

“There is no need for a woman to suffer from years of debilitating menopausal symptoms, as a number of therapies, both hormonal and non-hormonal are now available,” said Cynthia A. Stuenkel, MD, in a press release .She also said that “Every woman should be full partners with her health care providers in choosing whether treatment is right for her and what treatment option best suits her needs. The decision should be based on available evidence regarding the treatment’s safety and effectiveness, as well as her individual risk profile and personal preferences.”




Women are eligible for HRT if they are younger than 60 years old and are no more than 10 years into menopause, Dr Stuenkel emphasized.
Before putting a patient on Menopausal Hormone Therapy (MHT), clinicians need to assess a patient's baseline risk for cardiovascular disease or breast cancer -- a high risk for either condition can constitute a contraindication to use of HRT.
Standard cardiovascular disease risk-assessment scores from organizations such as the American Heart Association has Standard cardiovascular disease risk-assessment scores for women who are at moderate or low risk for cardiovascular events; women falling into both of these categories can be considered for HRT.
 National Cancer Institute Breast Cancer Risk Assessment Tool is utilized by clinicians to calculate a woman's 5-year risk for invasive breast cancer, whereas the International Breast Intervention Study calculator predicts a woman's 10-year and lifetime risk.
The Updated guidelines specifically targets vasomotor symptoms (hot flushes/flashes/night sweats) and genitourinary tract symptoms (vaginal dryness or discharge, pain, burning or itching, urinary frequency, recurrent urinary tract infections).
Menopausal symptoms typically start a year before the last period and can be very bothersome for unpredictable time period; it could be as little as few months or 10-14 years after the last period.
"The most effective therapy [for both sets of symptoms] is HRT," Dr Stuenkel said.
"But we have listed many other nonhormonal and over-the-counter [OTC] options that physicians can use as well, and each of these options can be discussed with patients."
Current evidence does not justify the use of MHT to prevent coronary heart disease, breast cancer, or dementia.
These guidelines emphasize safety in identifying which late perimenopausal and recently postmenopausal women are candidates for various therapeutic agents.
Dr Stuenke advocates that women for HRT can receive estrogen replacement alone if they are without a uterus; if women have a uterus, they require the combination of estrogen plus progestogen to prevent endometrial hyperplasia and cancer.
Additional hormonal options for women with a uterus include estrogen combined with bazedoxifene and tibolone where available.
Women in the United States and some other countries have a broader range of therapeutic choices than ever before, including: MHT dose, type, and route of administration; new selective estrogen receptor modulators (SERMs) as solo or combination therapies; and expanded choices of nonhormonal prescription medications.
Other medical options recommended by the Endocrine Society include
  • Transdermal estrogen therapy by patch, gel or spray is recommended for women who request menopausal hormone therapy and have an increased risk of venous thromboembolism – a disease that includes deep vein thrombosis.
  • Progestogen treatment prevents uterine cancer in women taking estrogen for hot flash relief. For women who have undergone a hysterectomy, it is not necessary.
  • If a woman on menopausal hormone therapy experiences persistent unscheduled vaginal bleeding, she should be evaluated to rule out endometrial cancer or hyperplasia.
  • Medications called selective serotonin reuptake inhibitors (SSRIs), serotonin-norepinephrine reuptake inhibitors (SNRIs), gabapentin or pregabalin are recommended for women who want medication to manage moderate to severe hot flashes, but either prefer not to take hormone therapy or have significant risk factors that make hormone therapy inadvisable.
  • Low-dose vaginal estrogen therapy is recommended to treat women for genitourinary symptoms of menopause, such as burning and irritation of the genitalia, dryness, discomfort or pain with intercourse; and urinary urgency or recurrent infections. This treatment should only be used in women without a history of estrogen-dependent cancers.
Impact on quality of Life
The impact of severe menopausal symptoms on quality of life may be substantial," Dr Stuenkel noted.
In light of this, there are circumstances under which a woman with a history of coronary artery disease or even breast cancer might choose to accept a degree of risk that initially might outweigh the benefits of HRT.
Nevertheless, patients should be fully informed about the risks and benefits associated with HRT to enable them to make a decision that best balances these risk and benefits, Dr Stuenkel emphasized.
"We in the Endocrine Society were dismayed by the incredible drop-off in the use of HRT [following the Women's Health Initiative study]," she noted.
A 2012 Endocrine Society survey found that 72% of women currently experiencing menopausal symptoms had not received any treatment for them.
"And while we don't blame the average clinician for being confused or frustrated by all the contradictory data that have emerged over the past decade, we wanted to take a strong stance to simplify these data and to say that in carefully selected women, HRT will be the most effective therapy we have for menopausal symptoms," Dr Stuenkel added.
"So...the data we present in our guidelines help substantiate why HRT is a reasonable approach for carefully selected women, and physicians should be revisiting this question annually with their patients to discuss their decision regarding HRT and perhaps modify it if other health concerns have arisen in the preceding year."
Stopping the MHT
The guidelines also state that the approach to discontinuation of HRT is an individual choice, too.
Menopausal symptoms and joint pain can recur when HRT is discontinued, and depending on the severity of the symptoms, women may elect to restart HRT, perhaps at a lower dose, or seek relief with nonhormonal therapies.
"Anecdotally, some women find that a very low dose...maintains adequate symptom relief and well-being and prefer that to complete discontinuation," state the recommendations.
Resources for patients are available at www.menopausemap.org. The Hormone Health Network also offers a digital toolkit for healthcare providers.
Summary of Recommendations
·        The clinical symptoms, menstrual history, history of surgery (Hysterectomy with Bilateral oophorectomy) are sufficient to make the diagnosis of menopause for the majority of women. Laboratory studies are not a prerequisite for the diagnosis but may be used when necessary.
·        Menopausal Transition is also a good time for addressing other health issues   such as bone health, smoking cessation, alcohol use, cardiovascular risk assessment and management, and cancer screening and prevention.
·        For menopausal women < 60 years of age or < 10 years past menopause with bothersome VMS (with or without additional climacteric symptoms) who do not have contraindications or excess cardiovascular or breast cancer risks and are willing to take menopausal hormone therapy (MHT), the study suggest initiating estrogen therapy (ET) for those without a uterus and estrogen plus progestogen therapy (EPT) for those with a uterus.
·        Women at high risk for CVD, should receive nonhormonal therapies to alleviate bothersome VMS (with or without climacteric symptoms) over MHT.
·        Women at moderate risk  for CVD should  be started on transdermal estradiol as first-line treatment, alone for women without a uterus or combined with micronized progesterone(or another progestogen that does not adversely modify metabolic parameters) for women with a uterus, because these preparations have less untoward effect on blood pressure, triglycerides, and carbohydrate metabolism.
·        Non-oral estrogen is also preferred in the treatment of menopausal women with an elevated risk for venous thromboembolic disease. These patients should also receive a progestogen, such as progesterone or dydrogestone, which is more neutral in its effects on coagulation.
·        Women at high or intermediate risk of breast cancer considering MHT for menopausal symptom relief, the guideline suggest nonhormonal therapies over MHT to alleviate bothersome VMS.
·        The treatment plan should be reviewed annually, estimating the risk and benefits.
·        The taskforce also called on physicians to advise women about the uncertainty of over the counter medicines for menopause.
·        The study also  recommend informing women about the possible increased risk of breast cancer during and after discontinuing EPT and emphasizing the importance of adhering to age-appropriate breast cancer screening.
·        For young women with primary ovarian insufficiency (POI), premature or early menopause, without contraindications, we suggest taking MHT until the time of anticipated natural menopause, when the advisability of continuing MHT can be reassessed.
·        Stopping the MHT should be a shared decision-making approach to elicit individual preference about adopting a gradual taper vs abrupt discontinuation.
·        For women seeking pharmacological management for moderate to severe VMS for whom MHT is contraindicated, or who choose not to take MHT, we recommend selective serotonin reuptake inhibitors (SSRIs)/serotonin-norepinephrine reuptake inhibitors (SNRIs) or gabapentin or pregabalin (if there are no contraindications).In  women not responding to these drugs  a trial of clonidine is suggested.
·        This new term “genitourinary syndrome of menopause” (GSM) combines the conditions of VVA and urinary tract dysfunction.
  • Women with symptoms of vulvovaginal atrophy may be treated initially with a trial of vaginal moisturizers at least twice weekly. Low-dose vaginal estrogen therapy can be introduced if initial treatment is insufficient.
  • Women with a history of endometrial or breast cancer may initiate treatment with vaginal estrogen therapy, but this decision-making process should involve the treating oncologist.
  • Low-dose vaginal estrogen therapy does not require co-treatment with a progestogen.
·        Women with moderate to severe dyspareunia and vaginal atrophy may be offered a trial of ospemifene, which has been demonstrated to reduce dyspareunia and improve sexual satisfaction in randomized controlled trials.
·        Diabetes is considered by the AHA to be a CHD risk equivalent , which would suggest that women with diabetes should not take MHT. The evidence at this time is inadequate to make firm recommendations. An individualized approach to treating menopausal symptoms could be considered, with a low threshold to recommend nonhormonal therapies, particularly in women with concurrent CVD.

The Hormone Health Network, the Endocrine Society’s public education arm, developed an interactive digital resource called the Menopause MapTM for women to explore the stages of menopause and learn about symptoms they may experience. The Menopause MapTM related resources are available at
http://www.hormone.org/menopausemap/postmenopause.html

The Hormone Health Network also offers a digital toolkit for health care providers.

References :
http://press.endocrine.org/doi/citedby/10.1210/jc.2015-2236
http://www.medscape.org/viewarticle/853793
https://www.endocrine.org/membership/email-newsletters/endocrine-insider/2015/october-16-2015#/9
http://menopausehealthmatters.com/hormone-replacement-therapy/
http://answers.webmd.com/expert/39928/cynthia-stuenkel-north-american-menopause-society
https://www.endocrine.org/news-room/current-press-releases/experts-recommend-assessing-individual-benefits-risks-of-menopausal-therapies