Showing posts with label progesterone. Show all posts
Showing posts with label progesterone. Show all posts

Tuesday, July 3, 2018

Vaginal progesterone scores at par with cerclage for preventing preterm births in women with previous mishap and short cervix: a comparison meta-analysis


Vaginal progesterone fares equal with cerclage for preventing preterm births in women who have a short cervix and history of previous mid-trimester miscarriage (MTM) and/or preterm labor (PTL) reports the results of an updated comparison meta-analysis published in July issue of American Journal of Obstetrics and Gynecology.

In a recent update by WHO, every year 15 million babies are born before 37 weeks of gestation and the figures continue to rise. Prematurity is the leading cause of death in children under 5 years of age and is responsible for causing about 1 million deaths worldwide.

In addition, prematurity is a major contributor towards lifelong neurological morbidities such as intellectual disability, cerebral palsy, hearing and visual impairments, and a higher risk of chronic diseases in adulthood.

Women with a previous history of PTL and a short cervix (≤25) face a 3-fold increased risk of recurrent preterm births as compared to women with a cervical length >25 mm in the midtrimester.
The efficacy of vaginal progesterone and cerclage in preventing PTL is a hotly debated topic, but to date, only 2 small RCTs have been conducted to compare these two treatment modalities. However, the sample size was too small to detect any treatment differences.

The 2016 multicenter double-blind randomized placebo-controlled OPPTIMUM trial refuted the claim that progesterone reduces the risk of PTL and helps decrease the associated neonatal morbidity and mortality.

Hence, this adjusted indirect comparison meta-analysis was performed which usually, but not always, provides results similar to head-to-head randomized controlled trials.

An updated literature search of MEDLINE, EMBASE, CINAHL, LILACS, the Cochrane Central Register of Controlled Trials, conference proceedings and research registers of ongoing trials was performed from their inception to March 31, 2018.

All the RCTs comparing vaginal progesterone to placebo/no treatment or cerclage to no cerclage in women with a singleton gestation, previous spontaneous preterm birth, and a sonographic cervical length <25 mm was included in the meta-analysis.

The researchers looked at prevention of preterm birth <35 weeks of gestation and perinatal mortality as the primary outcomes.

Five trials comparing vaginal progesterone vs placebo (265 women), 5 comparing cerclage vs no cerclage (504 women) and the OPPTIMUM study were included in the analysis.

The daily dose of vaginal progesterone used in the trials varied from 90 to 200 mg, and the treatment was administered from 18–25 to 34–36 weeks of gestation. Thirty women in two RCTs underwent a cerclage after randomization.

In direct comparison, the use of vaginal progesterone reduced the risk of preterm birth <35 weeks by 32%, <32 weeks of gestation by 40%, neonatal sepsis by 62%, neonatal morbidity by 71%, and admission to NICU by 54%.

The use of cerclage reduced the risk of preterm birth <35 weeks by 30%, <32 weeks of gestation by 34%, composite neonatal morbidity and mortality by 36%, and birthweight <1500 g by 36%.
Both interventions together were associated with a nonsignificant 36% reduction in the rate of perinatal death.

Adjusted indirect comparison meta-analyses didn’t show any differences between vaginal progesterone and cerclage in preventing preterm births and perinatal deaths.

The study has several advantages such as the use of individual patient data, similar patient demographics, and low rates of bias. There were few limitations such as the absence of data on respiratory distress syndrome in the OPPTIMUM study, some women with cerclage received 17-OHPC that could have affected the results and non-reporting of maternal side effects in the individual patient data (IPD) meta-analysis.

In the absence of adequately powered, high-quality, randomized controlled trials comparing vaginal progesterone and cerclage, our indirect comparison treatment meta-analysis provides the best available evidence regarding the comparative efficacy of the 2 interventions.

This meta-analysis results have huge implications in clinical practice. Both progesterone or cerclage show similar efficacy in preventing recurrent preterm births in patients with singleton pregnancy and short cervix. Thus, besides efficacy, the decision to use one intervention over other is based on physician preferences, cost-effectiveness, and maternal side effects.



Friday, January 13, 2017

Luteal Start Vaginal Micronized Progesterone ups the rate of ongoing pregnancy in RPL.



vaginal micronized progesterone

Recurrent pregnancy loss (RPL) is one of the most traumatic and frustrating experience for patients and consulting obstetricians. It is an area of obstetrics lacking in evidence based diagnostic and treatment strategies. As per data by American Society for Reproductive Medicine(ASRM) it affects 15-25% of all pregnancies and in nearly 50% of cases the cause is not known.


Courtesy:Dr.Malpani Blog

Therapeutic interventions are generally based on the cause of RPL and data from observational studies and clinical experiences of the treating obstetrician. Treatment options range from active interventions in the form of hormonal supplementation to masterly inactivity (= reassurance).[i]

Progesterone (P) has long been used in the treatment of infertility because of its immunomodulator action on endometrium but it’s use is largely empirical along with other treatment regimen.  Cochrane review and meta-analysis concluded that P supplementation could improve the reproductive outcome in women with 3 or more pregnancy loss.

But, in none of these studies P was started after LH surge (luteal start) and varied route and dosing of P administration was used. [ii]

A new study published on line on January 9, 2017 in Fertility & Sterility international journal of the American Society for Reproductive Medicine assessed the effectiveness of luteal start vaginal micronized P in a recurrent pregnancy loss (RPL) cohort.

In this observational, cohort study 116 women with a history of RPL were recruited and followed prospectively. Vaginal micronized progesterone was supplemented in dose of 100–200 mg every 12 hours starting 3 days after LH surge (luteal start corresponding to day 13 of the cycle) with or without >20% increase in levels of nuclear cyclin E (nCyclinE) expression. The controls did not receive P and had normal nCyclinE (≤20%). P was continued till 10 weeks of pregnancy.

The research team lead by Dr. Mary D. Stephenson tested Nuclear cyclin E (nCyclinE) levels to assess the state of endometrium. It is an endometrial molecular marker(EFT) and a cell cycle regulator, levels more than 20% after day 20 of the menstrual cycle correlates with a history of infertility. NCyclinE expression was determined by an EB was performed 9–11 days after the LH surge in previous cycle.

Of 116 women tested, 59 had high levels of nCyclinE and 57 had normal levels.
The results of the test were very promising with 68% pregnancy rate in study group as compared to women who did not take P. The chances of successful pregnancy increased from 6% to 69% in treatment group.

Six women needs to be treated with P to achieve one additional successful pregnancy.( Number need to treat). 

This observational study cannot establish causality, the researchers believe that P is beneficial in changing the endometrial milieu and benefitting the developing embryo.   

Dr. Stephenson said “The positive results show us that next we need to study progesterone as a treatment for recurrent pregnancy loss with a prospective randomized trial to validate the findings." 





[i] http://blog.drmalpani.com/2016/08/pgs-for-recurrent-pregnancy-loss-forget.html
[ii] Haas, M.D. and Ramsey, P.S. Progestogen for preventing miscarriage. Cochrane Database Syst Rev. 2013;: CD003511

Wednesday, February 24, 2016

Large randomized trial does not support the use of progesterone in recurrent miscarriage.



Recurrent miscarriage affects about 1% of all women of child bearing age.

50% of all early pregnancy loss are due to chromosomal aberration, most common being aneuploidy.  

Progestogens play an important role in implantation, cytokine balance, natural killer cell activity, arachidonic acid release and myometrial contractility. It is secreted by corpus luteum till 7-8 weeks, when the function is taken over by developing placenta. Lack of progesterone support in the luteal phase increases the chances of early pregnancy loss; hence progesterone is often used specially in women with history of recurrent pregnancy loss!

Results of a recent large RCT published in the November issue of  New England Journal of Medicine concluded that Progesterone Doesn't Improve Outcomes After Recurrent Miscarriages.

This large multicenter, double-blind, placebo-controlled, randomized trial recruited 1568 women aged 18-39 years with a history of three or more consecutive or nonconsecutive first-trimester pregnancy losses. Women with anatomical, medical or hematological causes that explain the reason behind miscarriages were excluded from the study.

The study group (n=404) were assigned to receive 400mg of vaginal micronized progesterone , while the control group ( n=432) received a similar looking placebo as soon as the pregnancy were confirmed till 12 weeks of naturally conceived pregnancy.

The live birth rate in progesterone group was 65.8% vs. 63.3% in placebo group. The rate of ectopic pregnancy, congenital anomalies, miscarriage and still birth rates were also comparable in both the groups.  

A Cochrane review in 2013 based on smaller number of trials and subject reported lower rate of miscarriage with progesterone support. This large RCT lead us to a different conclusion.

Management of women with RPL is a challenge in itself, as these women are very anxious and apprehensive and ask for some form of ‘therapy’ to avert a loss again. Over the years many other modalities like heparin, aspirin and acupuncture have been evaluated with mixed results.

There are many unanswered question in therapy of RPL, including the definition of RPL, the evaluation and the timing of starting treatment. Progesterone is an important part of regimen offered, being having endometrial supportive and immune-modulating effects.
Different studies have come up with different results; the study also differed in patient population, mode and type of progesterone and the initiation of treatment since pregnancy confirmation.

Whatever the results and conclusions of different trials may be, the psychological and placebo effect of the progesterone cannot be overlooked for patients who have a high level of anxiety and are afraid of another loss.


References:

Thursday, December 31, 2015

Few decisive articles in obstetrics from 2015




Role of progesterone in preventing recurrent preterm births (PTB)

It is widely accepted that progesterone supplementation in pregnancy reduces the risk of recurrent preterm birth. But, according to a secondary analysis of data  from Maternal-Fetal Medicine Units Network Trial of hydroxyprogesterone caproate for prevention of recurrent preterm birth before 37wks concluded that the drug may not be effective in women with a BMI>30 kg/m2. The cut off weight is 168 pounds or 75 kg. This finding may be due to subtherapeutic serum levels in women with increased BMI or weight. Further larger and planned studies in women with BMI >30 kg/m2 are warranted and also the universal use of progesterone in women independent of BMI also deserves reassessment.
Heyborne KD et al - Does 17-alpha hydroxyprogesterone caproate prevent recurrent preterm birth in obese women?
Am J Obstet Gynecol. 2015 Aug;



Maternal Hypertension in Pregnancy predisposes the offspring for higher risks of Congenital Heart Disease

According to a systemic review and metaanalysis published in the journal of pediatric cardiology robust associations were observed between maternal hypertension and overall CHDs, irrespective of being treated or untreated. The authors identified 16 studies that met the study criteria. The effect was also uniform across all the subtypes of CHDs. The results were also similar for various type of antihypertensive medications used.
The authors propose to understand the mechanisms to design strategies to reduce the risks..
Ramakrishnan A et al- Maternal Hypertension During Pregnancy and the Risk of Congenital Heart Defects in Offspring: A Systematic Review and Meta-analysis.
Pediatr Cardiol. 2015 Oct;36(7):1442-51. Epub 2015 May 8.


The downside of improved control of malaria.

We are recently seeing improved malaria control in many endemic areas worldwide, leading to a decrease in immunity in the population. A large observational study carried out in Mozambique assessed the prevalence of Plasmodium falciparum infection among 1819 Mozambican women who delivered infants between 2003 and 2012.
A major decline in maternal level of antimalarial IgG antibodies were seen in pregnant women both for pregnancy specific parasitic lines as well as general parasitic lines.
It was also seen that those women who developed malaria antenatally had a larger reduction in hemoglobin levels as well as the neonatal birthweight as the immunity declined.
Mayor A et al- Changing Trends in P. falciparum Burden, Immunity, and Disease in Pregnancy. N Engl J Med. 2015 Oct 22;373(17):1607-17.


Uterine exteriorization at cesarean delivery

Uterine exteriorization vs in situ repair has always been a topic of debate among obstetricians.  In A large meta-analysis of 16 studies amounting to a total of 19,439 subjects 9,736 underwent exteriorization, 9,703 had in situ uterine repair. It was seen that the estimated blood loss was not statistically significant between the two groups as well as other perioperative outcomes. Individual preferences and individual intraoperative circumstances should guide the decision.
Zaphiratos V et al- Uterine exteriorization compared with in situ repair for Cesarean delivery: a systematic review and meta-analysis.
Can J Anaesth. 2015 Nov;62(11):1209-1220.

The best time to perform External Cephalic Version (ECV)

The optimum age to perform ECV has always been a debatable issue.
External cephalic version (ECV) of the breech fetus at term (after 37 weeks) has been shown to be effective in reducing the number of breech presentations and caesarean sections, but the rates of success are relatively low. This systemic review of Cochrane Data base examines studies initiating ECV prior to term (before 37 weeks' gestation).
Pooled results suggested that early ECV reduced the risk of non-cephalic presentation at birth, failure to achieve vaginal cephalic birth, and vaginal breech delivery. However there was no statistical significant difference in Caesarean Section rate between the two groups. There was evidence that risk of preterm labour was increased with early ECV compared with ECV after 37 weeks. Future research reporting infant morbidity outcomes in these late preterm births is warranted.
Hutton E.K et al- External cephalic version for breech presentation before term.
Cochrane Database Syst Rev. 2015 Jul 29;7:CD000084.


Limited value of fetal ST-segment analysis

STAN S31 is a one-of-a-kind fetal monitor which exclusively combines standard CTG technology with ST-Analysis of the fetal ECG (FECG) during labour. The combined analysis of the CTG and fetal ECG helps to detect a fetus that is exposed to hypoxia and which needs remedial action, and also provides reassurance when no intervention is required.
However, It is not clear whether use of STAN 31 as an adjunct to other conventional fetal heart rate monitor improves the intrapartum and neonatal outcome.
This Multicenter RCT of about 11,108 subjects included women with a single fetus undergoing vaginal delivery at more than 36 weeks of gestation with cervical dilation of 2 to 7 cm. They were randomly assigned to "open" or "masked" monitoring with fetal ST-segment analysis. The masked system functioned as a normal fetal heart-rate monitor (FHR). The open system functioned as both FHR as well as fetal ECG monitor.
The primary outcome was a composite of intrapartum fetal death, neonatal death, an Apgar score of 3 or less at 5 minutes, neonatal seizure, an umbilical-artery blood pH of 7.05 or less with a base deficit of 12 mmol per liter or more, intubation for ventilation at delivery, or neonatal encephalopathy.
It was observed that fetal ECG monitoring along with FHR  did not improve perinatal outcome or decreased the rate of caesarean delivery. The primary outcome occurred in 52 fetuses or neonates of women in the Fetal ECG group  and 40 fetuses or neonates of women in the FHR  group.
Belfort M.A- A Randomized Trial of Intrapartum Fetal ECG ST-Segment Analysis.
N Engl J Med. 2015 Aug 13;373(7):632-41.

Expectant management of mild preeclampsia near term is feasible.

There is little guidelines for the management of women with mild preeclampsia with stable maternal and fetal conditions at 34 to 36 weeks of gestation. The study by Broekhuijsen K et al in Lancet 2015, investigated the effect of immediate delivery versus expectant monitoring on maternal and neonatal outcomes in such women. This open-label, randomised controlled trial, in seven academic hospitals and 44 non-academic hospitals in the Netherlands confirmed that most patients will reach term without progressing into severe disease and the expectant management buys us valuable time for optimum neonatal maturity without any harm to the mother.

References:


  • Relation of body mass index to frequency of recurrent preterm birth in women treated with 17-alpha hydroxyprogesterone caproate.Co AL, Walker HC, Hade EM, Iams JD. Am J Obstet Gynecol. 2015 Aug; 213(2):233.e1-5
  • Ramakrihnan A et al- Maternal Hypertension During Pregnancy and the Risk of Congenital Heart Defects in Offspring: A Systematic Review and Meta-analysis.Pediatr Cardiol. 2015 Oct;36(7):1442-51
  • Mayor A et al- Changing Trends in P. falciparum Burden, Immunity, and Disease in Pregnancy. N Engl J Med. 2015 Oct 22;373(17):1607-17.
  • Zaphiratos V et al- Uterine exteriorization compared with in situ repair for Cesarean delivery: a systematic review and meta-analysis.Can J Anaesth. 2015 Nov;62(11):1209-1220.

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