Friday, 30 September 2011

Women in charge 'have less sex'

Researchers analysed data from surveys in Ghana, Malawi, Mali, Rwanda, Uganda, and Zimbabwe that asked survey participants to indicate the day, week, month and year they last had sexual intercourse.

Survey participants were also asked to indicate the person in the household who typically had the final say on the following decisions: health care, large household purchases, household purchases for daily needs and visiting family and friends. Researchers also examined socio-demographic and relationship factors such as age, wealth, parity, husband?s residence, and marital duration.

The majority of women participating in the survey reported sexual intercourse within the last month.

For men, making decisions by themselves was not related to the timing of sex.

Carie Muntifering, a co-author of the study, said: ?Understanding how women?s position in the household influences their sexual activity may be an essential piece in protecting the sexual rights of women and helping them to achieve a sexual life that is both safe and pleasurable.?

The research will be published in the October issue of the Journal of Sex Research.

Source: http://telegraph.feedsportal.com/c/32726/f/568409/s/18caca47/l/0L0Stelegraph0O0Chealth0Cwomen0Ishealth0C87833530CWomen0Ein0Echarge0Ehave0Eless0Esex0Bhtml/story01.htm

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[CDC, Office of Women's Health, Health Matters for Women] CDC?s Sudden Unexpected Infant Death Initiative

Since 1998, it appears that medical examiners and coroners are moving away from classifying deaths as SIDS and calling more deaths accidental suffocation or unknown cause, suggesting that diagnostic and reporting practices have changed. Inconsistent practices in investigation and cause-of-death determination hamper the ability to monitor national trends, ascertain risk factors, and design and evaluate programs to prevent these deaths.

As a response, CDC's Division of Reproductive Health?s (DRH) began the Sudden Unexpected Infant Death (SUID) Initiative. CDC and its partners began activities aimed at improving the investigation and reporting practices of Sudden Infant Death Syndrome (SIDS) and other SUID.

The CDC?s research on SUID and SIDS focuses on efforts to standardize and improve data collected at infant death scenes and to promote consistent classification and reporting of cause and manner of death for SUID cases.�By improving national reporting of SUID, we aim to prevent SUIDs by using improved data to monitor trends and identify those at risk.

SUID Initiative Goals and Activities

The goals of the SUID Initiative are to?

  1. Standardize and improve data collected at death scene.
  2. Promote consistent classification and reporting of cause of death.
  3. Improve national reporting of SUID.
  4. Reduce SUID by using improved data to identify those at risk.

To accomplish these objectives, the CDC SUID Initiative collaborated with a number of organizations to?

  1. Revise the 1996 Sudden Unexplained Infant Death Investigation Reporting Form (SUIDIRF).
  2. Develop a training curriculum and materials for investigators of infant deaths.
  3. Train medicolegal professionals and child advocates to conduct comprehensive infant death investigations.
  4. Develop and implement a state-based SUID Case Registry.

Sudden Unexplained Infant Death Investigation Reporting Form

In 2003, CDC led activities aimed at revising the 1996 Sudden Unexplained Infant Death Investigation Reporting Form and Guidelines for the scene investigation, as well as actively educating and disseminating training materials on infant death scene investigations.

In March 2006, a revised reporting form known as the SUIDIRF was released. Along with the revised SUIDIRF, the CDC and partners developed training materials and conducted train-the-trainer regional academies for medical examiners, coroners, investigators, and child advocates across the United States.

Training Materials

When the CDC published the 1996 SUIDIRF, an evaluation suggested that more medicolegal professionals were likely to use the form if there were training to accompany the form (Hauck, 2001).

The SUID Initiative and collaborative partners created the following training materials:

These training materials were used in conducting the five regional Sudden Unexplained Infant Death Investigation Training Academies.

Training Academies

As a means of disseminating Sudden Unexplained Infant Death Investigation training curriculum and materials, CDC conducted train-the-trainer academies in five U.S. regions from 2006 to 2008. These regional, multidisciplinary academies provided training for every state, as well as American Indian/Alaska Native teams. The academies produced more than 250 trainers, including medical examiners, coroners, law enforcement officers, child advocates, college faculty members, and medicolegal death scene investigators. Individuals participating in these academies were expected to conduct additional trainings at conferences, meetings, and courses in their respective states.

Topics covered at the training academy included how to?

  • Complete the SUIDIRF.
  • Interview families.
  • Conduct death scene investigations including doll reenactments.
  • Assess infant growth and development.

The SUIDIRF and training curriculum have been endorsed by several national organizations representing law enforcement, medical examiners, and coroners. More than 20,000 individuals have been trained, and many jurisdictions report that they are using the new SUIDIRF. View map SUIDI Training Academies.

SUID Surveillance System Feasibility Study

In 2007, CDC conducted a SUID surveillance feasibility study with seven states in collaboration with CDC?s National Violent Death Reporting System (NVDRS). NVDRS is a state-based surveillance system that links data from law enforcement, coroners and medical examiners, and vital statistics, etc. The feasibility study indicated that the most efficient way to develop a surveillance system would be to use the Child Death Review (CDR) system already in place. CDC partners suggested calling a future surveillance system the SUID Case Registry.

SUID Case Registry

Planning and Development

In 2008, partners with an interest in SIDS and SUID came together to discuss the logistics of the SUID Case Registry and Surveillance System. Partners supported the idea of building upon and enhance the CDR system, as it would strengthen multidisciplinary team reviews already in place and avoid duplication of efforts. Discussion also focused around creating a program model, delineating objectives, and questions that a SUID Case Registry could answer, and defining a limited set of variables.

The SUID Case Registry aims to generate public health surveillance information about SUID at the national, state, and local levels that is more detailed than what is currently available. Instead of creating an entirely new system, the SUID Case Registry enhances the National Center for Child Death Review program and their Case Reporting System.

The SUID Case Registry generates public health surveillance information that can comprehensively describe the circumstances and events surrounding SUID cases. This will allow researchers, medicolegal investigators, and program prevention planners to better understand characteristics associated with SUID, evaluate case investigation practices, and ultimately prevent infant deaths.

The SUID Case Registry?s objectives are to?

  1. Create state-level surveillance systems that build upon Child Death Review activities.
  2. Categorize SUID using standard definitions.
  3. Monitor the incidence of different types of SUID and describe demographic and environmental factors.
  4. Determine similarities and differences among SUID unexplained by autopsy.
  5. Inform interventions and potentially save lives.

In July 2009, five state participants were announced to receive funding for the SUID Case Registry Pilot Study as part of a cooperative agreement. Colorado, Georgia, Michigan, New Jersey, and New Mexico began entering information about SUID cases in January 2010. They use a modified version of the National Center for Child Death Review?s Web-based data collection system already place specific to SUID. An additional two states (New Hampshire and Minnesota) were added to the SUID Case Registry in July 2010.

Hauck F. Final Report: National Survey to Evaluate Use of the Sudden Unexplained Infant Death Investigation Report Form (SUIDI RF). Charlottesville, VA: University of Virginia Health System; 2001 (unpublished).

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Source: http://www2c.cdc.gov/podcasts/download.asp?af=h&f=8621107

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Costs of cancer treatments questioned

The Daily Mail has reported that doctors do not support giving life-extending drugs to patients with terminal cancer. The newspaper says that a new report has said the treatments ?give false hope and are too costly for the public purse?.

The news story is based on an extensive international report that examined the cost and value of cancer care in developed countries. In the report doctors, health economists and patient advocates voice their opinions and suggest potential policy changes that could make cancer care more affordable�for both patients and society.�However, the report does not actually suggest that life-extending drugs should be withheld from terminal cancer patients, rather that there is a greater need to understand whether treatments at this stage will actually extend life, and whether resources would be better directed at improving patients? quality of life through options such as palliative care. The report also suggests several policy areas that could be targeted to improve quality of care while reducing its cost.

This report is likely to stimulate discussions on policy relating to cancer care, but it is not policy itself. The report is of great interest but a broad agreement within the health service would be needed if it were to change the manner in which care is provided in the UK.

Where did the story come from?

The report was created by researchers from a variety of institutions from the UK, US, Australia, Canada and across Europe. These institutions include King?s College London, CancerPartnersUK, North of England Cancer Network, Northumbria Healthcare, the Institute of Nuclear Medicine, the Association of the British Pharmaceutical Industry, the University of London and Oxford University.

The Lancet states that the commission was peer reviewed and funded by The Lancet Oncology, where it was published.

The media focused on futile care, which is a particular issue highlighted in the report. This is addressed under the issue of ?overutilisation? in general, and is not the primary focus of the report. That said, the report does recommend that special attention should be paid to end of life cancer care. They say that improving the ability to predict the effectiveness of treatment could spare patients side effects and false hope from ineffective care, and also spare the healthcare system the cost of ineffective care. However, some life-extending drugs are valuable for people with terminal illness and the authors do not say that all of these give false hope or are too expensive.

What kind of research was this?

This is a discursive policy report written by a panel of international cancer experts. The report is intended to guide public debate on cancer care in developed countries, including the UK. The report attempts to identify the drivers of high-cost cancer care, as well as to propose solutions for these issues.

The extensive report looks at many of the different factors that drive the cost of cancer care. It gathers opinions from a variety of experts, including clinicians, patient advocates, policy makers and cancer survivors. The authors examined the cost and effectiveness of cancer care, and identified issues that drive up the cost of care but that may not provide great improvements in health outcomes. Among the issues examined are the economics of cancer care, the individual and societal impact of cancer treatments, areas where new technology could be improved or developed, predicted rates of cancer in the years to come and whether current methods for evaluating evidence are appropriate.

What did the research involve?

The authors collected opinions from a wide variety of experts on the status of cancer care costs and the effectiveness of cancer treatment in developed countries.�They examined the role that cost drivers, evolving patterns of disease and trends in the provision of care play in determining the amount of money spent on cancer care. They then examined the value of cancer care from various perspectives, including the role played by:

  • health research and research into cost-effectiveness
  • available treatment options, such as surgery, radiation and imaging technologies
  • the possibilities offered by new testing technologies, including genetic testing
  • anti-cancer drugs, the pharmaceutical industry and the processes for developing new drugs
  • patients? involvement in treatment and their ability to express their wishes

They also examined current approaches to addressing the affordability of cancer care in different countries.

The authors say that there are several areas that could be addressed to reduce cost and improve the quality of cancer care. These are as follows.

Cost of care

The authors first examined the cost of cancer care, and specifically ?cost drivers?. These are those interventions that account for most of the costs. They examined the cost of cancer from the perspective not only of the price paid for treatments, but also in terms of the economic impact of patients not being able to function normally due to illness or early death.

Burden of disease

The authors also looked at the patterns of disease, the complexity of illness and how research accounted for these patterns. They then examined how this burden of disease translates into the cost of treating individual patients and�the cost of treating cancer in society as a whole.

Technological development

The authors next highlight the process by which technologies are developed and the cost of this process, and suggest ways in which these costs could be reduced without forfeiting benefits in terms of health outcomes.

Overutilisation

The report looks at how ?overutilisation? of cancer technologies and services can drive costs without adding any additional benefit in terms of health outcomes, for example the use of expensive diagnostic tests that provide no greater benefit than cheaper alternatives. The authors identified areas of care that could be reduced without reducing health outcomes.

What were the basic results?

The study is extensive so the following section only provides a very brief overview of its findings. The authors identified multiple sources of high cancer costs, and outlined recommendations for improving care and reducing costs in each of the identified areas.

Cost of care

The authors found that the absolute amount spent on cancer care is increasing in all developed countries, and that the rate of this increase is going up year by year. They say that this is not simply due to the increasing number of cancer cases seen, but that the rise is also driven by factors such as the use of increasingly individualised treatments that are expensive to develop and the use of inappropriate cancer products (although they say this is more of an issue in the US than in the UK). They found that in 2009-2010, the NHS spent �5.86 billion on cancer care, which is 5.6% of the UK?s total health spend.

They recommend that countries attempt to drive the development of new low-cost technologies by increasing the use of off-patent products and rethinking the pathway of care that patients follow when they have cancer.

Burden of disease

The report says that one of the main drivers of cancer care costs is the ageing population (more people are being diagnosed with cancer) and the increasing complexity of disease, including patients with multiple illnesses. They say that the increase in cancer care costs is due both to the amount spent per patient and the number of patients diagnosed.

The authors found that current clinical research often fails accurately to reflect the burden of disease seen in the real world. Patients with multiple illnesses are often excluded from clinical trials, so that the evidence base for new technologies does not accurately reflect the way in which cancer occurs and will be treated in the real world. The researchers recommend that clinical research into new treatments be reflective of this real-world burden of disease for society, and take into account patient frailty and multiple illnesses.

Technology development

The authors found that many technologies that provide little additional benefit are taken all the way through the technology development phase, which becomes increasingly expensive the further along it goes. They recommend that the technology development process be changed, and that the design of early clinical trials be improved. They say that technologies that show little additional benefit should be halted earlier in the development process so that they do not reach the most expensive phases. The researchers say that this should result not only in reduced research costs, but also in more rigorous standards of evidence.

Overutilisation

The report found that overutilisation of cancer services is an issue in all areas of care. The authors say that the need to treat cancer promptly plays a role in overutilisation as it may be quicker and easier for medical staff to discuss a plan for treatment than to discuss why other treatments may not be suitable for use. They say that clinicians are also increasingly relying on technology and scans to assess new symptoms rather than physical examinations, but that the costs of using imaging techniques are also increasing per patient. The sheer amount of information on new technologies may also prevent clinicians from thoroughly understanding the evidence base needed to decide on the most appropriate treatment plan for a patient.

The report recommends six indicators of when interventions may be suitable for reduction, where cutting the use would have minimal effect on health outcomes. These include interventions that:

  • provide no benefit
  • result in little increased benefit
  • have no clearly defined benefit
  • are not desired by patients
  • are duplicates of other tests or services
  • are more expensive than an equally effective alternative treatment

How did the researchers interpret the results?

The authors say that ?in general, there are two primary mechanisms to control costs. We can lower the cost of cancer-care services or interventions, or we can reduce [their use]?. They say that examining current policy can result in decreased utilisation of ineffective services, and increased utilisation of effective services. This, they say, is the way to improve efficiency and value of cancer care. They further say that rethinking how research, policy and clinical practice interact can result in reduced costs and improved quality of cancer care.

Conclusion

This is an extensive expert opinion piece looking at the high cost of cancer care. The authors examined cost drivers from a variety of policy and clinical perspectives ? from epidemiology to research to technology development and health economics. The report identifies key areas that they feel could be addressed to reduce the cost and improve the quality of cancer care. Although the paper discusses specific treatments and national healthcare systems (including the NHS) it is not a specific analysis of where changes in individual systems would be beneficial. Instead, the document raises many issues pertaining to whether cancer care strategies need to be examined and reformed in terms of both cost-effectiveness and clinical benefit.

However, the media generally focused on one specific recommendation outlined in the report - the suggestion that attempts to use cancer-fighting therapies to lengthen the lives of terminal-stage cancer patients may not always be appropriate. Newspaper coverage may not fully reflect the tone and context of the report, which arguably raises questions on the issue rather than attempting to provide a definitive verdict on the current situation.

For example, rather than suggesting that medical care should be withdrawn from cancer patients within their last few weeks of life, the report says that continuing care strategies such as chemotherapy may be problematic for patients, and that focusing on palliative care may improve their quality of life and possibly prolong their survival. In short, the researchers question whether spending could be directed at cheaper, potentially better methods for helping people with late-stage cancer, and (contrary to some news coverage) do not suggest that they should not be helped at all.

The researchers also suggest that there is a need for clinical measures that can accurately determine which late-stage patients would and would not benefit from further disease-fighting therapy, highlighting that they are not advocating the withdrawal of appropriate care options for terminal patients.

The authors say that each health system now needs to consider how much is spent on cancer care and prevention compared with other healthcare priorities. This should include funding the most effective interventions, and insistence on a strong evidence base before adopting newly available medical technology.

The authors say that focusing on areas of care that provide little or no benefit, increasing the use of low-cost technologies and refocusing care pathways on high-quality, cost-effective and value-based care can reduce the cost of cancer care without sacrificing benefits. They also say that countries could further address cancer care costs by developing new ways of financing cancer care, including evaluating the pricing of drugs.

Overall, this is a valuable and intriguing exploration of the nature of current cancer treatment and, contrary to the impression given by media reports, these authors do not suggest that all end of life care should be stopped. Instead the report focuses on value, saying that the benefits of cancer care should be weighed from both an individual and societal perspective, and that the cost of care, in terms of price as well as side effects, should be balanced against the benefits, including quality as well as extension of life.

Links To The Headlines

Dying cancer patients should not be given 'futile' drugs. The Daily Telegraph, September 27 2011

Don't give out cancer drugs if it's just to extend life: Treatment costs can't be justified, say experts. Daily Mail, September 27 2011

Cancer cost 'crisis' warning from oncologists. BBC News, September 27 2011

Links To Science

Sullivan R, Peppercorn J, Sikora K et al. Delivering affordable cancer care in high-income countries. The Lancet Oncology, Volume 12, Issue 10, Pages 933 - 980, September 2011

Source: http://www.nhs.uk/news/2011/09September/Pages/cost-of-advanced-cancer-drugs-questioned.aspx

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Thursday, 29 September 2011

Ovarian Cysts, Fibroids, and Polyps

Women's Health Forum: After having a very bad pain a few days ago, on my left side, I had a vaginal ultrasound. They found various problems, like intramuraual fibroids, suserours fibroids, follicles, polyps and the thing that is worrying me the most, a couple of cysts. One is said to be "avascular complex cystic" "low level echoes"... I don't have a clue what this means. What are the chances of this being malignant?

I would like to hear from someone that has a some information that could help me understand this, before seeing the gynecologist. I have to make an appointment to see him, and would like to have some questions ready when I go. Thanks to anyone that can help me better understand this...What would you ask the doctor?

Source: http://womenshealth.about.com/b/2011/09/21/ovarian-cysts-fibroids-and-polyps.htm

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Check Plastic Surgeon's Credentials or Risk Tragic Results, Experts Warn

By Alan Mozes
HealthDay Reporter

MONDAY, Sept. 26 (HealthDay News) -- "I was in shock," recalled 40-year old Dinora Rodriguez. "It was a nightmare."

Rodriguez had woken up from cosmetic surgery only to find that she could not move her arms or even close her eyes. And so begins a harrowing account of plastic surgery, in her case involving breast implants and a facial scar, gone terribly wrong.

As a cautionary tale, Rodriguez' experience highlights the urgency behind a new safety campaign launched this week by the American Society of Plastic Surgeons (ASPS).

The goal: to draw attention to the physical disfigurement and emotional torment that can follow when patients fail to check a surgeon's credentials before they go under the scalpel.

"I already had implants put in five years earlier, in Mexico," explained Rodriguez, who lives in Los Angeles. "And that time, the first time, I had no problems. But I wondered if they were still OK, or if it was time to replace them."

"So I had this friend who recommended this doctor to me," she continued. "She said she had had liposuction done on herself, and both her daughters also went to this woman. So I went. I never checked on her background or if she was certified. I just went."

"And she told me," remembers Rodriguez, "that I needed a mammogram [to check the implant]. And after, she told me that it showed that one of the implants was leaking, and I needed to replace them right away because it was not good for my health."

It would be months before Rodriguez would find out the truth: her doctor had lied. There was no leakage, and thus no need for new implants.

"But that wasn't all," she said. "That day she also discussed a scar I had on my face [near the eyes], because of an accident. She said she could fix it. And I said I would think about it. On the day of the implant surgery she asked again, about my eyes. She said she could fix it at the same time. That it was simple. But I said no. I said, 'I don't want to deal with two pains at the same time.'"

"But when I woke up I found that she had operated on my eye, on both my eyes, without my permission! I was shocked and upset. And in pain. So much pain."

As it turns out, Rodriguez's physician had removed so much skin from around the eyes that Rodriguez was no longer able to fully close them. What's more, the breast surgery had been botched as well, the result of two breast implants having been inserted into one packet.

"We hear these stories over and over again," warned ASPS president Dr. Malcolm Z. Roth. "And worse. Situations arising from 'my friend who gave me the reference.' And to that I say: you spend time researching buying a car. You look for a safe car, and you put on your seatbelt. You take it seriously. But unfortunately people often think that getting cosmetic surgery is something else. It's not. It's serious. You're taking your life into your hands."

"Because these are not emergency procedures, you have an opportunity to do the homework," noted Roth, who is also chief of plastic surgery at the Albany Medical Center in Albany, NY. "You make sure that the person you're considering going to is first off a physician, of course. And most important, that they're board-certified in plastic surgery by the ASPS. Not in some other field."

Because appearances can be misleading. Part of the new ASPS campaign is focused on a problem the group calls "white coat deception": the fact that just because a doctor has a medical license does not mean he or she is properly trained and qualified to perform plastic surgery.

The problem stems from the fact that only four states (California, Florida, Louisiana, and Texas) have laws on the books requiring that physicians take steps to disclose the specifics of their medical background. In all other states, no such regulations exist. That leaves a pediatrician or a gastroenterologist, for example, free to cross over into the role of plastic surgeon at will and without disclosure.

"And because cosmetic surgery by it's nature can be done in an outpatient facility, doctors can -- and do -- promote themselves as a plastic surgeon, even if they have never held a knife in their life, and there's no one there to stop them," Roth said.

Some so-called plastic surgeons may not even be doctors at all, but con artists preying on vulnerable individuals. Last July a 22-year-old California woman died after being given silicone injections in the buttocks in an operation run by two sisters who did not have medical licenses to practice in the United States, according to Los Angeles Times.

To avoid such potentially deadly scenarios, the ASPS calls on patients to search for certification credentials at the organization's website (www.plasticsurgery.org), and confirm that properly sealed credentials are readily viewable in the physician's office.

"All our members have a minimum of six years of surgical training in plastic surgery," Roth said. "All have completed oral and written examinations, and continue to pursue 50 hours a year of continuing education, with an important emphasis on patient safety. And none operate in a facility unless it is accredited with all the bells and whistles needed for the rare occasion when there is a problem."

Unfortunately, Rodriguez was not so lucky.

"I looked deformed" after the surgery, Rodriguez said. The uncertified surgeon "tore skin from my cleavage, and I looked like I only had one breast. But she told me that she had done nothing wrong, that my breasts were only swollen, that I needed a couple of months to heal, and that my eye scar had looked so ugly that I 'needed' the surgery."

Unable to fully move her arms or even lay down comfortably, Rodriguez returned to the doctors a few months later, still racked with pain and unable to close her eyes. But the physician turned her away, declaring: 'I don't want to see you; you are not my patient anymore. I can fix it, but there's nothing I can do until you pay me more money.'"

That was four years ago. In the intervening years, Rodriguez said enduring pain has been accompanied by deep and recurring bouts of depression, at one point culminating in a suicide attempt.

On a positive note, reconstructive surgery conducted at a different facility has done much to restore the appearance of Rodriguez's breasts. But nerve and muscle damage lingers. And to date her eyes remain, in her words, "a permanent mess."

"This should be a wake-up call to anyone considering plastic surgery," stressed Roth. "The most important thing is patient safety. You don't want plastic surgery to be a game of Russian roulette."

MedicalNewsCopyright � 2011 HealthDay. All rights reserved.

SOURCES: Malcolm Z. Roth, MD, president, American Society of Plastic Surgeons (ASPS), and chief, division of plastic surgery, Albany Medical Center, Albany, NY; Dinora Rodriguez, Los Angeles


Source: http://www.medicinenet.com/guide.asp?s=rss&a=149824&k=Womens_Health_General

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Do Women's Voices Really Allow Men To Detect Ovulation?

Main Category: Sexual Health / STDs
Also Included In: Women's Health / Gynecology
Article Date: 23 Sep 2011 - 0:00 PDT email icon email to a friendprinter icon printer friendlywrite icon opinions

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The voice can reveal a lot about a person - their sex, their age, how they are feeling - and recent studies have even suggested that women's voices might also contain cues that men can read about how close they are to ovulation. A new study, however, published in the journal PLoS ONE, challenges the view that women broadcast reproductive information in their voice.

Previous studies in this area have typically relied on the comparison of voices recorded in just two phases in the cycle: high conception risk vs. low conception risk. This new work, on the other hand, looked at variation in the voice throughout the entire menstrual cycle - a crucial step to evaluate the potential information contained in any observed voice changes.

Their results showed that the overall variation in women's vocal quality throughout the whole cycle precludes unequivocal identification of the period with the highest conception risk. Specifically, while they found that the women studied spoke with the highest tone (suggested by previous studies to be associated with attractiveness) just prior to ovulation, the tone rose again to levels indistinguishable from pre-ovulation shortly after ovulation, making it a very poor mating clue. Furthermore, they found that the men studied showed only a very slight preference for pre-ovulation voices relative to voices recorded during ovulation.

The authors conclude that women's voices do not provide reliable information about the timing of ovulation, confirming the view that information about reproductive state is 'leaked' rather than broadcast. In an interesting further finding, the study found that women's voice were harsher and more irregular during menstruation, providing scientific data to explain why female opera singers may be granted 'grace days' during menstruation.

Funding: The authors have no support or funding to report.

Competing Interests: The authors have declared that no competing interests exist.

The international collaborative study was led by Prof Julia Fischer (German Primate Centre), Dr Stuart Semple (Roehampton University, London) and Dr Ofer Amir (Tel-Aviv University).
Citation: Citation: Fischer J, Semple S, Fickenscher G, Jurgens R, Kruse E, et al. (2011) Do Women's Voices Provide Cues of the Likelihood of Ovulation? The Importance of Sampling Regime. PLoS ONE 6(9): e24490. doi:10.1371/journal.pone.0024490
LINK TO THE SCIENTIFIC ARTICLE: http://dx.plos.org/10.1371/journal.pone.0024490
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Source: http://www.medicalnewstoday.com/releases/234829.php

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Glee Season Premiere Is Tonight! WH Talks to Lea Michele And Heather Morris

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GLEE SEASON 3

Susan Rinkunas

Glee Season 3 Lea MicheleGlee Season 3 Heather Morris

Attention Gleeks: Season 3 of Glee kicks off tonight at 8/7 central on Fox! In honor of the highly anticipated premiere, we revisited WH's interviews with two of the show's leading ladies!

The Broadway Veteran
Lea Michele plays Rachel Berry, the star singer of William McKinley High School's glee club, New Directions. Lea?a Broadway veteran whose credits include Les Mis�rables, Fiddler on the Roof, and Spring Awakening?appeared on our cover in June 2010 (left, above).

The Bronx native stays in shape with rock climbing, hiking, and yoga. She switches between vegan and macrobiotic diets, so she eats fish, but no other animal products. Her favorite indulgences? "I love organic wine and dark chocolate!"

Video: Go behind the scenes with Lea Michele at her WH cover shoot!

The Dancing Queen
Heather Morris, who graced our June 2011 cover, plays Cheerio [cheerleader] Brittany Pierce. Fun fact: As a former backup dancer for Beyonce, Heather was initially called in to teach the cast the "Single Ladies" choreography, only to be hired for a small role on the show.

"Between takes, Heather would do these hysterical impersonations," recalls Zach Woodlee, Glee coproducer and choreographer. "The writers began to latch on to her, and that's how [Brittany] came to be a speaking part."

Heather, who grew up in Scottsdale, Arizona, still takes dance classes, mostly because they keep her mentally tough. She also loves piloxing, a turbo-charged interval program that combines Pilates, boxing, and dance moves. "I went to Piloxing before the Golden Globes because I'm crazy!" she explains with a laugh. "I was wearing a skintight dress, and I wanted to look hot."

Video: Go behind the scenes with Heather Morris at her WH cover shoot!

Tell us: Which female cast member of Glee would you like us to interview next?

RELATED: Get the Dancer's Body Workout!

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Source: http://www.womenshealthmag.com/health/glee-season-3

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