Monthly Archives: October 2022

A win for stem cells | Washington Examiner

Posted: October 4, 2022 at 2:30 am

The stem cell industry has scored a major victory in its efforts to keep patient treatments exempt from Food and Drug Administration regulations, brushing aside the regulatory agencys concerns that the therapies are unproven and could be dangerous.

The FDA made that argument in 2018 when it sought court orders to stop the Beverly Hills and Rancho Mirage offices of the California Stem Cell Treatment Center from administering the treatments. The move was part of a yearslong FDA crackdown on clinics nationally claiming that stem cells can treat or cure conditions including orthopedic injuries, Alzheimers and Parkinsons diseases, multiple sclerosis, and erectile dysfunction.

Federal Judge Jesus G. Bernal of the U.S. District Court for the Central District of California oversaw a seven-day trial in May 2021 based on the FDAs lawsuit against CSCTC. More than a year later, on Sept. 1, Bernal issued a ruling siding with CSCTC. Bernal effectively rejected the FDA's argument that the clinics were selling unapproved drug products in the form of adipose cell mixtures, or connective tissue that is mainly composed of fat cells called adipocytes.

Industry attorneys say the FDA is likely to appeal the ruling by Bernal, who is based in Riverside, California, and was nominated to the federal bench in 2012 by then-President Barack Obama and confirmed by the Senate. But for now, it makes more difficult the agencys efforts to regulate some stem cell clinics. And it gives a green light to people seeking to use personal stem cells as part of medical treatments.

The FDAs lawsuits named as defenders CSCTCs founders, Dr. Elliot Lander and the late Dr. Mark Berman, who died in April. Lander said in a statement that Bernals ruling was a vindication of his companys scientific and medical bona fides.

We appreciate the Court's clear and unequivocal ruling, which affirms what we have been saying for 12 years: that our innovative surgical approach to personal cell therapy is safe and legal, Lander said. With this victory behind us, we look forward to refocusing our energy on our practice and harnessing life-changing stem cell treatments to support doctors and benefit patients across the country.

In a request for comment, a spokesperson for the regulatory agency said, The FDA is reviewing the courts decision and does not have further comment at this time.

Long-running battle

The FDA has long been skeptical of stem therapies. The agency also brought a similar suit against a Florida stem cell company. In 2015, at least three patients came forward stating they lost their eyesight after the material extracted by the Florida company, U.S. Stem Cell Clinic, was injected directly into their eyes to treat macular degeneration. The Florida clinic lost its suit in 2019, and its appeal request was subsequently denied.

In the case of CSCTC, the FDAs complaint said the treatments violated current good manufacturing practice requirements, including some that could impact the sterility of their products, putting patients at risk. The FDA argued that physician use of a patients own stem cells was equal to manufacturing a biological drug product that would, therefore, be subject to regulation.

CSCTC was founded in 2010 by Lander, a surgeon and board-certified urologist, and Berman, a board-certified otolaryngologist and cosmetic surgeon.

Berman returned from Japan in 2010 with technology that could isolate stem cells from a bodys fat from the bedside. After discovering the technology, Berman and Lander began to study the efficacy and safety of these cells. In 12 years, the team learned that stem cells are another source of repair cells, similar to bone marrow cells.

In 2012, the Cell Surgical Network, the research branch of CSCTC, was founded to teach these SVF technologies to qualified physicians across the globe who also sought to bring regenerative medicine into their own practices.

The approach quickly found adherents.

Laurie Hanna, an independent certified registered nurse anesthetist who worked previously with Berman, said stem cells relieved significant health problems.

I was living in pain with decreased quality of life. Over the course of 12 years, I was facing the prospect of a complete knee replacement and experienced a significant exacerbation of my chronic regional pain syndrome that was resistant to conventional medical treatment, Hanna told the Washington Examiner.

After surgery and chemotherapy for breast cancer, I developed lymphedema and chemo neuropathy. Through treatments with Cell Surgical Network, I was able to receive my own stem cells, Hanna said. My lymphedema significantly improved, neuropathy resolved, and quality of life was restored. Little did I know when I started personal cell therapy with CSN in 2010 that in 2022 stem cells would still be making me whole.

According to Lander, stem cell therapies are incredibly safe. They allow clinics to help patients by using their own bodies to heal in a way that is in harmony with nature, he added. Lander said that despite the intermission in treatments and research due to the suit, he and colleagues remain optimistic about the future of stem cell therapies.

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California court creates regulatory uncertainty over the FDA regulation of stem cell therapies – BioEdge

Posted: October 4, 2022 at 2:29 am

In a recent lawsuit brought by the Food and Drug Administration (FDA), a California judge entered a judgment in favour of the California Stem Cell Treatment Center (CSCTC).

The decision was that the use of patients own stem cells to treat various diseases and conditions does not fall under the purview of the FDAs authority.

This is a massive win for private stem cell clinics. Critics say that the ruling by Judge Jesus Bernal of the Central District of California is regarded as flawed. They warn that it creates opportunities for unscrupulous for-profit private clinics to provide stem cell treatments that are scientifically unproven and potentially risky.

This decision was not entirely surprising. Earlier, Judge Bernal had ruled against requests by the FDA and the Department of Justice for a summary judgment (a decision entered by a judge on one party and against another party summarily, i.e., without a full trial).

The FDA injunction case was pursued against the CSCTC, the Cell Surgical Network Corporation and their founders, Dr Elliot Lander, a surgeon and board-certified urologist, and the late Dr Mark Berman, a board-certified otolaryngologist and cosmetic surgeon. Since 2010 CSCTC has performed stem cell treatments for thousands of patients. Its doctors remove fat tissue to isolate stem cells. The treatments use the patients own cells.

The FDA alleged that the defendants manufactured products without first obtaining FDAs approval for a new drug. The company responded that a patients stem cells are not drugs and are not subject to regulation by the FDA.

The court ruled that the CSCTCs treatments are surgical procedures and do not create a new drug. It declared: The adipose tissue Defendants remove from patients clearly consists of human cells. And whatever is injected back into patients as part of Defendants SVF Surgical Procedure and Expanded MSC Surgical Procedure certainly contains such cells.

The defendants SVF procedure but not the expanded MSC procedure qualifies for a surgical procedure exception.

The International Society for Cell & Gene Therapy (ISCT) said that the ruling will have negative consequences for the cell and gene therapy field and patients safety.

Its president, Jacques Galipeau, said: This ruling introduces regulatory uncertainty into the CGT market, and unscrupulous clinics prey on this uncertainty to market unproven interventions to patients. The ruling reinforces the imperative market need for informative resources that establish scientific consensus, standards, and best practices. ISCT will continue to work with FDA and other like-minded national and international organisations and regulatory agencies to achieve ISCTs mission to drive clinical translation of cell and gene therapies worldwide.

It is critical that the therapies provided by clinics are evidence-based and the FDA plays a crucial role in ensuring this.

Judge Bernals judgment also conflicts with an earlier decision on a similar case in Florida. In that case, the state district court awarded summary judgment against the defendants, US Stem Cell clinics.

Now there is regulatory uncertainty.

It is not clear whether the FDA will appeal against this controversial decision. I hope that it does. The grave worry is that some clinics may be encouraged by this court judgment and continue to market untested stem cell treatments to vulnerable patients.

Dr Patrick Foong is a senior law lecturer at Western Sydney University. His research interest lies in bioethics and health law.

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Scientists have created a mechanical womb that can grow life in the lab – Inverse

Posted: October 4, 2022 at 2:29 am

The dystopian universe of Blade Runner features replicants, or genetically bioengineered people with sci-fi powers, like super-strength and advanced intelligence, that far outstrip any ordinary individual (albeit with a limited lifespan). Their invention is considered a colossal feat of scientific achievement (and the basis for a pretty messed-up society).

But off of the silver screen, weve yet to come close to making any organism let alone a human entirely from scratch. Until now.

In a study published last month in the journal Nature, scientists in the U.S., U.K., and Israel successfully created a synthetic mouse embryo without using any eggs or sperm. Instead, they used an assortment of stem cells.

Compared to natural embryos maturing alongside them, these lab-grown counterparts developed similar features seen nearly nine days after fertilization, such as a beating heart, a very early-stage brain, and a gut tube before they abruptly halted growth.

Essentially, the big question that we are addressing in the lab is how do we start our lives? said Magdalena Zernicka-Goetz, the studys lead researcher and a stem cell biologist at the University of Cambridge and California Institute of Technology, during a press briefing.

When a sperm fertilizes an egg, the fusion sets off a cascade of changes that cause the single cell to multiply, specialize, and organize into distinct cell types, tissues, organs, and other structures that constitute a complete organism.

For the last several decades, scientists have tried recreating models of embryonic development in the lab to learn how the primordial phenomenon proceeds in real time. But this feat has proven extremely challenging. After all, we cant just peer into a live uterus in the lab to directly observe the microscopic goings-on.

Specifically, researchers dont know what exactly happens in the womb between around 14 days and a month into development, says Max Wilson, a molecular biologist at the University of California, Santa Barbara, who was not involved in the study.

During this mystery period, the brain gets built and the heart is laid down. Its called the black box of human development, he explains.

Recent efforts to untangle these mysteries have involved coaxing human embryonic stem cells into blastocysts, a thin-walled, hollow ball of dividing cells that gives rise to the embryo during natural development.

This blastoid method didnt exactly bring scientists closer to seeing how cells self-organize and specialize into organs. But in 2021, researchers at the Weizmann Institute of Science in Israel who also worked on the new Nature study developed a sort of mechanical womb (picture an axolotl tank la Frank Herberts Dune).

This device took seven grueling years of engineering. It included an incubator, which floated and spun the embryos in vials filled with special nutrient-rich liquid. Meanwhile, a ventilator provided oxygen and carbon dioxide, meticulously controlling the gasses flow and pressure.

With this setup, the Weizmann researchers managed to make stem cell-derived synthetic mouse embryos thrive in their artificial mommy for about six days until they managed to extend it further, according to a study published earlier this month in the journal Cell.

The embryos underwent gastrulation (when an early embryo transforms into a multilayered structure) over the course of eight and a half days, but then stalled for unknown reasons. (A mouse pregnancy lasts for about 20 days.)

But the experiment wasnt entirely a dud. It set the mammoth task for the latest study: to show it was entirely possible to grow mammalian embryos outside the uterus.

Zernicka-Goetz and her colleagues used embryonic stem cells, along with those that give rise to the placenta and yolk sac, to grow synthetic embryos.Jose A. Bernat Bacete/Moment/Getty Images

Zernicka-Goetz, one of the authors behind the new Nature study, has spent the last decade investigating ways to develop synthetic embryos. She said her lab only initially used embryonic stem cells to mimic early development.

But in 2018, she and her colleagues discovered that if they tossed in two other stem cells that give rise to the placenta (the organ that provides nutrients and removes wastes) and the yolk sac (a structure that provides nourishment during early development), the embryos were better prepared for self-assembly.

Heres the thing about science: theres always competition. After their 2018 Nature paper, Zernicka-Goetzs team was surprised when the Weizmann group came out with an incubator-ventilator system, along with later experiments that forged embryos without sperm or eggs just as they were attempting.

But science is also about collaboration. The two groups eventually teamed up to see whether combining their techniques could culminate in the life-creating golden ticket.

The results were impressive: Zernicka-Goetz and her colleagues watched the artificially wombed cells grow into synthetic embryoids without any sort of external modifications or guidance.

Compared to the natural mouse embryos that were grown separately, these embryonic mice went through the same stages of development up to eight and half days after fertilization (just like the Weizmann teams earlier work) which is equivalent to day 14 of human embryonic development.

The embryo model developed a head and heart parts of the body researchers were never able to study in vitro, said Zernicka-Goetz.

This is really the first demonstration of the forebrain in any models of embryonic development, and thats been a Holy Grail for the field, co-author David Glover, a research professor of biology and biological engineering at Caltech, said during the press briefing.

Zernicka-Goetzs team also tinkered with a gene called Pax6, which appears to be a key player in brain development and function. After removing Pax6 from the mouse stem cell DNA with the help of CRISPR, Zernicka-Goetz and her colleagues observed that the heads of these synthetic embryos didnt develop correctly, mimicking whats seen when natural embryos lack this gene.

In humans, rare mutations or deletions of Pax6 can lead to abnormal development of the fetus and death. They can also spur conditions like aniridia (absence of the eyes colored part, the iris) or Peters anomaly, which hinders the development of eye structures like the cornea.

Concocting synthetic embyros from human stem cells could prove a technical (and ethical) challenge.Westend61/Westend61/Getty Images

The detailed glimpse into early embryonic development could be a boon to human health. For instance, it could help scientists grasp why many pregnancies, whether naturally conceived or via assisted reproductive means, fail in the early trimester.

Zernicka-Goetz said the research might also advance regenerative medicine. It could help scientists learn how to make viable, full-functioning replacement organs for a transplant patient using their own stem cells (potentially eliminating the need for lifelong use of immunosuppressants).

Currently, we have a broad sense of organogenesis or the development of an organ from embryo to birth but we dont know all the microscopic steps and cellular interactions that culminate in a fully-fledged, functional organ.

The model system could aid the development of new drugs: It may reveal which medications are safe to take during pregnancy without harming the fetus. Now, researchers can potentially test them out on synthetic embryos, Zernicka-Goetz said.

This is an advance but at a very early stage of development, a rare event which while superficially looking like an embryo, bears defects which should not be overlooked, Alfonso Martinez Arias, a developmental biologist at Pompeu Fabra University in Spain who wasnt involved in the study, said in a press release.

One glaring challenge: While the synthetic mouse embryos appear identical to their natural counterparts, their stalled development at eight and a half days makes it tough to say whether theyd continue to grow right on course.

So despite its enormous potential, fashioning synthetic embryos from stem cells just isnt possible right now.

This blockade is not understood and needs to be overcome if one desires to grow mouse synthetic embryos past day eight, Christophe Galichet, a stem cell biologist at Francis Crick Institute in London who also wasnt involved in the new work, said in the same press release.

Since humans and mice dont exactly share all the same characteristics when it comes to embryonic development, the next step is to eventually concoct synthetic embryos from human stem cells.

That likely will prove complicated, more so ethically than technique-wise. But Wilson thinks this research marks a major scientific milestone and tool to add to humanitys technological toolbox.

This is very strong evidence that we will one day have this power, and it will be possible [to create synthetic life], Wilson says. Whether we decide to do that or not because of ethics or even the potential upsides thats a question for society at large.

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Hormone replacement therapy (HRT) – Benefits and risks – NHS

Posted: October 4, 2022 at 2:28 am

When deciding whether to havehormone replacement therapy (HRT), it's important to understand the benefits and risks.

Many studies on HRTpublished over the past 15 yearshighlight the potential risks. As a result, some women and doctors have been reluctant to use HRT.

But recent evidence says that the risks of HRT are small and are usually outweighed by the benefits.

The main benefit of HRT is that it can help relieve most menopausal symptoms, such as:

HRT can also help prevent thinning of the bones, which can lead to fracture (osteoporosis). Osteoporosis is more common after the menopause.

The benefits of HRT usually outweigh the risks for most women.

The risks are usually very small, and depend on the type of HRT you take, how long you take it and your own health risks.

Speak to a GP if you're thinking about starting HRT or you're already taking it, and you're worried about any risks.

There is little or no change in the risk of breast cancer if you take oestrogen-only HRT.

Combined HRT can be associated with a small increase in the risk of breast cancer.

The increased risk is related to how long you take HRT, and it falls after you stop taking it.

Because of therisk of breast cancer, it's especially important to attend all yourbreast cancer screening appointments if you're taking HRT.

The evidence shows that:

HRT does not significantly increase the risk ofcardiovascular disease (includingheart disease andstrokes)when started before 60 years of age, and may reduce your risk.

TakingHRT tablets is associated with a small increase in the risk of stroke, but the risk of stroke for women under age 60 is generally very low, so the overall risk is still small.

Page last reviewed: 09 September 2019Next review due: 09 September 2022

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Thyroid Hormone Replacement Therapy | Johns Hopkins Medicine

Posted: October 4, 2022 at 2:28 am

What is thyroid hormone replacement therapy?

Thyroid hormone therapy is the use of manmade thyroid hormones to raise abnormally low levels of natural thyroid hormones in the body. Thyroid hormone is usually given in pill form and is often used to treat an underactive thyroid that is secreting little or no thyroid hormones. The most commonly prescribed thyroid hormone replacement is pure synthetic thyroxine (T4).

Thyroid hormone therapy is generally prescribed when your thyroid is not making enough thyroid hormone naturally. This is a condition referred to as hypothyroidism. Other reasons for using thyroid hormone therapy may rarely include:

To control the growth of the enlarged thyroid gland (also called goiter)

To control the growth of nodules on the thyroid gland

Treatment after the removal of the thyroid for benign or malignant disease

After treatment of hyperthyroidism by radioactive iodine ablation

Healthcare providers do careful blood testing to find the proper dose of hormone replacement therapy for each person.The blood tests reveal levels of thyroid hormones in the blood, as well as thyroid-stimulating hormone (TSH)released by the pituitary gland. The pituitary gland plays an integral role in the functioning of the thyroid gland. It controls how much thyroid hormone is released by making TSH that "stimulates" the thyroid. Increased levels of TSH may indicate that you have an underactive thyroid or that thyroid hormone replacement needs to be increased.

You will have lab tests to measure levels of thyroid hormones and TSH. Hypothyroidism can be a progressive disease. This needs dosage increases over time.

To make sure that your thyroid hormone replacement works properly, consider the following recommendations:

Maintain regular visits to your healthcare provider.

Take your thyroid medicine at least 1 hour before breakfast and any calcium or iron medicines you may take. Or take at bedtime, or at least 3 hours after eating or taking any calcium or iron medicines.

Tell your healthcare providerof your thyroid hormone treatment before beginning treatment for any other disease. Some treatments for other conditions or diseases can affect the dosage of thyroid hormone therapy.

Let your healthcare provider know if you become pregnant.

Tell your healthcare provider of any new symptoms that may arise.

Tellall healthcare providers of your thyroid condition and medicine dosage.

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Prescribing HRT in women with migraine The Medical Republic – The Medical Republic

Posted: October 4, 2022 at 2:28 am

Two in three perimenopausal women may not report headache, so doctors are urged to ask patients about symptoms.

A headache specialist has urged doctors to ask perimenopausal patients about headache symptoms, because migraines are often undiagnosed and poorly managed in these women.

There were also important considerations for women taking HRT, the headache and womens health specialist Professor Anne MacGregor told the Australasian Menopause Society Congress in Cairns last month.

Migraine symptoms become more common when women reach menopause and can have severe impacts on quality of life, but few women report migraine as a symptom of menopause. Among women who attended a menopause clinic, 62% experienced headache but did not spontaneously report it, Professor MacGregor told the conference.

And among women at the clinic who experienced migraine, 79% reported very severe or substantial disability, said Professor MacGregor, from the Queen Mary University of London.

Our research of women with migraine attending amenopauseclinic suggests that women are not receiving optimal treatment for symptomatic treatment of migraine attacks, she said.

Migraine with or without aura does not contraindicate the use of hormone replacement therapy, but transdermal HRT was preferable, Professor MacGregor said.

Hormone replacement therapy could help migraine symptoms, but only in the context of prescribing HRT for management of vasomotor symptoms in women with migraine, she said.

Migraine can be worsened by changes in hormones, so providing stable hormone levels using transdermal oestrogen and ideally continuous progestogen is best.

Professor MacGregor told the conference that if patients experienced a new-onset migraine with aura, doctors should firstly exclude transient ischemic attack and reassure the patient.

She then recommended changing the patients HRT to a transdermal form and prescribing the lowest effective dose of estrogen to control vasomotor symptoms, and consider non-hormonal options if aura does not resolve or increases in frequency.

Professor MacGregor told TMR there were several alternatives to HRT that may also be helpful when patients experience migraine.

Non-hormonal options that benefit both migraine and vasomotor symptoms ofmenopauseinclude losing weight if obese, exercise, cognitive behavioural therapy and prescribed medications including SSRIs and SNRIs, particularly venlafaxine.

Professor MacGregor told the conference that migraine was a risk factor for the onset of menopause and could predict more frequent vasomotor symptoms associated with anxiety, depression and sleep disturbance.

Professor MacGregor wrote in a review in Maturitas that perimenstrual estrogen withdrawal is implicated in thepathophysiologyof menstrual migraine, with increased prevalence of migraine in perimenopause associated with unpredictable estrogen fluctuations.

Professor MacGregor said general practitioners should ask women about migraine symptoms, particularly sinus headache.

Perimenopausal women should routinely be asked about symptoms suggestive of migraine bearing in mind that the most common misdiagnosis is sinusitis which should then be managed appropriately according to national guidelines.

Professor MacGregor said for most women, migraine developed during their teens and 20s, became more prevalent during perimenopause and gradually improved with time after menopause. A few women develop migraine for the first time during perimenopause, she said.

Migraine has a global prevalence of 19% in women and 9% in men, she wrote.

Migraine without aura is the most prevalent type, affecting 70-80% of people with migraine.

The three best predictors for diagnosing migraine without aura are photophobia, disability and nausea: people who report two of these symptoms have an 81% probability of migraine, with the presence of three symptoms increasing the probability to 93%.

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Caring for the gynecologic needs of the adolescent patient – Contemporary Obgyn

Posted: October 4, 2022 at 2:28 am

Carri Holton, MSN, WHNP-BC, Department of Pediatric & Adolescent Gynecology at Childrens Hospital Colorado, gave a presentation on gynecologic care for adolescent patients at the NPWH 25th Annual Premier Women's Healthcare Conference in Houston, Texas, from September 29 to October 2.1

Holton first outlined how health care providers can provide preventive health screenings and offer guidance to adolescents, teens, and parents in pediatric gynecology. Conditions such as pediatric vulvovaginitis, lichen sclerosis, genital injuries, labial adhesions, congenital anomalies in the reproductive system, menstrual suppression, tumors, premenstrual syndrome and premenstrual dysphoric disorder, and breast problems in youths are treated via pediatric gynecology, as is fertility preservation or hormone replacement.

During an office evaluation, there should be a welcoming environment for adolescent patients, according to Holton. Health care providers will require technical skills to complete hymen exams, single-digit exams, and smaller speculums. They will also need to have the patience to listen to adolescents and parents, along with learning the history of their patients.

Confidentiality was also discussed. Holton noted that adolescents must be made aware of instances when information is not confidential, such as suicidal or homicidal thoughts. Minor consent laws should be known, as many states allow minors to consent to family planning, pregnancy care, substance use related care, and outpatient mental health services. All states allow minors to consent to sexually transmitted infection testing.

When arranging and performing an adolescent exam, the decision should be between the adolescent and the provider, though there should be a chaperone present. Providers should explain all components of the exam to the patient and parent. Patients should be reassured that they are in control of their body and the exam can be stopped at any time.

When moving onto the next step, providers should ask permission to pull the sheet back. Holton reminded them to be explaining female anatomy with proper terms, educating parents and patients. Breasts and pubic hair should be examined for Tanner staging, and external genitalia should be examined for normal anatomy.

In the presentation, Holton discussed normal pubertal development along with abnormalities, and encouraged attendees to learn this information so that they may recognize signs of abnormal development. Providers need to first identify the cause then determine treatment. This could include hormone replacement therapy in cases of primary ovarian insufficiency.

Holton also outlined instances of physiologic anovulationwhen slow maturation occurs in anovulatory cycles. This can lead to noncyclic, unpredictable, and inconsistent bleeding. In cases where bleeding is too much, adolescents should see an oncologist for testing, especially in cases of concerning history with bleeding disorders in the individual or family.

In cases of mild bleeding without anemia, providers should reassure patients, provide them with prophylactic iron supplementation, and offer hormonal contraceptives if desired. In moderate bleeding with anemia, providers should give patients combined oral contraceptives, micronized oral progesterone, depo Provera injection, levonorgestrel (LNg) intrauterine device (IUD), and iron supplementation.

Further treatments, along with hospitalization and blood transfusion, may be needed in cases of severe bleeding. In all cases, Holton stated that iron supplementation should be given.

Holton also discussed polycystic ovary syndrome (PCOS), reminding attendees that every case is different. Holton also noted that PCOS is not caused by ovarian cysts or being overweight, and that much is still unknown about PCOS. Diagnoses may be given as irregular periods, and can present as amenorrhea, oligomenorrhea, and chaotic periods.

Treatment for PCOS will vary based on concerns, as it can lead to metabolic concerns, acne, dermatologic concerns, and nutrition concerns. When these concerns arise, screenings should establish a rapport in the first visit. Repeated screenings should at first take place every 3 months, then every 3 to 12 months depending on the patient.

Holton lastly talked about dysmenorrhea and endometriosis. Dysmenorrhea is painful menstruation, often increasing risk of anxiety and depression. It can be managed with dietary, vitamin, and herbal treatments along with exercise and yoga, or with pharmacologic interventions.

Dysmenorrhea is often caused by endometriosis. Risk factors of endometriosis include earlier menarche, nulliparity, shorter menstrual cycles, childhood sexual and physical abuse, and more. To treat endometriosis, Holton recommended both surgical and medical treatments. Complementary and alternative therapies may also reduce symptoms.

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Im a GP heres the best way to treat acne and when to see a doctor… – The US Sun

Posted: October 4, 2022 at 2:28 am

EVEN if you like a bit of alone time, being lonely is very different, and can be very damaging.

In fact, loneliness can significantly affect your health and wellbeing and its something none of us should learn to live with.

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Luckily, there is lots of help out there, and there are small changes you can make yourself to tackle it, from speaking to the Samaritans to joining a club to meet new people.

Youre never truly alone!

Here are this weeks reader questions...

Q: IS there help for someone in their late 30s starting to go through perimenopause?

A: Premature ovarian failure insufficiency is a condition that occurs when your ovaries are no longer working properly and youre under the age of 40.

This affects approximately one per cent of women. It usually means that your periods stop or become irregular, and you may also experience menopause symptoms.

The term early menopause is used when periods stop between the ages of 40 and 45.

You say that youre in your late thirties, so its possible that you could fall into either of these groups.

The most important thing is for you to seek medical help here and get a diagnosis.

While its not normally recommended for women over the age of 45 to have blood tests to look for menopause, for women under 45 who are having symptoms it is.

This is because its important to make the diagnosis because its vital that women receive the correct hormonal replacement therapy, or HRT.

We often talk about how HRT is safe for most women and the benefits outweigh the risks, but that calculation is different in women under 45, where almost definitely there are huge benefits to taking HRT that massively outweigh any risk.

The next step for you is to see your GP, and keep a log of the symptoms youve been having, and Id expect your GP to do a series of blood tests spread out over time to find out your levels of FSH, or follicular stimulating hormone.

If these levels are high, it would suggest youre experiencing premature ovarian insufficiency.

Q: MY metronidazole prescription finished today. Ive had two days of awful abdominal pain, sweats and now kidney pain.

A: It sounds possible youve had an allergic reaction to the metronidazole.

Serious side effects from this antibiotic medication are rare and happen in fewer than one in 1,000 people, however the symptoms you describe after taking metronidazole suggest an adverse reaction, and this requires medical attention.

If all of your symptoms have now resolved, it may be that your GP decides further tests arent necessary, but if your symptoms are still ongoing youll need blood tests to check things like the health of your liver and kidneys and you should be monitored.

Metronidazole is a slightly unusual antibiotic, as it affects our bodys ability to metabolise alcohol.

So whenever it is prescribed, you should receive information and advice not to drink alcohol when taking the medicine, and to wait for two days afterwards before drinking alcohol, as this allows the metronidazole to leave your body.

Q: NO one has helped me in a long time what should I do? Ive had cancer, I cant speak to my family about it, I have no help or support.

Im scared, alone and getting depressed.

A: Anybody who has cancer should be able to access help and support from the cancer specialist nurse.

The team looking after you for your cancer should be able to put you in touch if you havent been given their contact details already.

Usually there are also charities which provide peer support, such as online chat rooms. A diagnosis of cancer is a life-changing event which not only affects our physical health but our mental health too.

It impacts our relationships, our ability to do our jobs and every aspect of our social life.

Nobody should feel that they are on the cancer journey alone, as there is always help and support available.

The first port of call if youre feeling confused and overwhelmed is just to speak to your GP and let them help you in creating a support system, as you will need this.

It also opens up the conversation around loneliness, which we can think of as a health condition on its own now, thanks to new and ongoing research.

We know loneliness affects every aspect of a persons physical and mental health.

It has even been said that loneliness is as risky to a persons health as smoking.

Loneliness requires treatment.

Your GP will be able to let you know about what befriending services are available locally, and you can usually get some advice from the charity Age UK as well.

Please dont suffer alone or in silence. A problem shared is a problem halved I really believe that saying to be true.

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Q: CAN you give me some advice on how to treat adult acne?

Acne can be a real pain for adults.

We tend to think of it as a condition that affects teenagers, but especially in women it is quite common for acne to persist into adulthood.

Acne over the age of 25 is termed adult acne, while some people get it for the first time as an adult, and this is termed adult-onset acne.

It can range from a few spots on the face, neck, back or chest, to more severe cases, and acne which is causing scarring should be treated by a healthcare professional without delay.

For more simple acne which is white, and blackheads with no scarring, its fine to try over-the-counter remedies first.

But if these arent helping its a good idea to see your GP.It is caused by the glands in the skin producing too much oil and at the same time dead skin cells build up and plug the pores, causing blockages.

A type of bacteria which lives on everyones skin can then cause you some further problems.

Whenever treating acne, the first things to think of are the basics.

Simple things such as cleansing your skin well twice a day, eating healthy and nutritious foods, maintaining good hydration levels, and using a simple oil-free moisturiser are all important.

Depending on the type of acne you have, and the pattern whether it flares up during your period and what treatments youve unsuccessfully tried the treatment strategy will differ for different people.

Talk to your pharmacist, who can assess what would be a good next step based on what youve tried already and if this isnt helping, the next step is to see your GP.

Sometimes people require an oral medication called Roaccutane, which can only be prescribed by a dermatologist.

I cannot stress enough that if you have acne which is causing scarring, you should see your GP without delay.

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Im a GP heres the best way to treat acne and when to see a doctor... - The US Sun

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State-by-state prevalence of the 5 most common types of cancer – KFOR Oklahoma City

Posted: October 4, 2022 at 2:28 am

(STACKER) In his 2010 book, The Emperor of Maladies, Siddhartha Mukherjee called cancer not one disease but many diseases sharing a fundamental feature: the abnormal growth of cells. What was at one point in history (not so far removed from our own), a whispered-about illness has become the target of a global effort to thwart its onset.

Certain forms of cancer are more common than others, notably in late-stage development.Stacker analyzed cancer incidence data from the National Cancer Institute and CDC to look at where the five most common forms of cancer are most prevalent.

The annual averages in each slide are calculated from data compiled between 2014 and 2018, and have been adjusted for patient age. The data was adjusted to account for the increased likelihood of older people developing cancer, and the state-by-state maps reflect the rates of each type of cancer per 100,000 people.

The following list is derived from the National Institutes of Healths 2022 projection estimates for the most commonly diagnosed cancers in the U.S., though the projection totals themselves are not included as a data point; a direct comparison would be misleading because this dataset uses compiled and age-adjusted historical data.

Cancer incidence, survival, and mortality rates are population-based indicators of progress against cancer. The mortality-to-incidence ratio can be broadly defined as the percentage of death certificates that include the persons cancer diagnosis and specify the type of cancer. However, the mortality-to-incidence ratio should not necessarily be interpreted as the survival rate. A cancer diagnosis on a death certificate could have happened at any point in the past and does not necessarily mean the person died of cancer.

Stacker also looked at risk factors for these common cancers, ways to reduce risk, and methods for cancer screening.

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Average national incidences per year: 49,438 Percent of incidences in late-stage: 15.0% Average annual mortality count: 5,428 Mortality-to-incidence ratio: 11.0%

The word melanoma means black tumor. Its development begins in melanocytesthe cells that produce the pigment melanin. Most people think of melanoma as a type of skin cancer, because it can form in moles on the skin. But it can also form in other pigmented tissues, such as those in the eye or intestine.

Melanoma is less common than other types of skin cancer, but it is more likely than other types of skin cancer to grow and metastasize, or spread to other organs. The most common risk factors for melanoma include exposure to ultraviolet light, having many moles or freckles, having lighter hair, and having a family or personal history of melanoma. The use of tanning beds and sun lamps also increases melanoma risk.

The best ways to prevent melanoma are using sunscreen, wearing sun protective clothing and sunglasses, and seeking shade during midday, when the sun is at its strongest.

Average national incidences per year: 75,374 Percent of incidences in late-stage: 57.4% Average annual mortality count: 27,717 Mortality-to-incidence ratio: 36.8%

Colorectal cancer develops as malignant cells grow and accumulate in the colon rectum, and usually present as a growth called a polyp. Risk factors for colorectal cancer include smoking, obesity, age, and family history.

Physical activity, combination hormone replacement therapy, and aspirin reduce the risk of colon cancer. Procedures such as colonoscopy and sigmoidoscopy can find polyps, so the doctor can remove them before they become cancerous. The recommended age for men to begin regular colonoscopies, once 50, is now 45. Fecal occult blood tests screen for blood hidden in the stool, which may be a sign of colorectal cancer.

Average national incidences per year: 115,218 Percent of incidences in late-stage: 70.4% Average annual mortality count: 78,841 Mortality-to-incidence ratio: 68.4%

Lung cancer is the third most common kind of cancer in the U.S., according to the NIH, and the leading cause of cancer death in both men and women. Smoking and exposure to secondhand smoke are the most common risk factors associated with lung cancer. Although most cases of lung cancer are caused by smoking, nonsmokers can get lung cancer, too.

There are two types of lung cancer: small cell lung cancer and non-small cell lung cancer. The bronchi, the two tubes that lead from the trachea to the lungs, are sometimes also involved in lung cancer. Screening tests for lung cancer are in clinical trials, though LDCT scans have been shown to decrease the risk of death in heavy smokers.

Average national incidences per year: 200,677 Percent of incidences in late-stage: 20.6% Average annual mortality count: 30,566 Mortality-to-incidence ratio: 15.2%

Prostate cancer is the second most common cancer among men in the U.S. One in eight men in the U.S. will be diagnosed with this type of cancer. The biggest risk factors for prostate cancer are age, race, and family history. It is more common in men over 50, and in Black men compared to white men. Most men diagnosed with prostate cancer do not die of it, because the majority of prostate cancers grow and spread slowly.

Average national incidences per year: 249,261 Percent of incidences in late-stage: 31.9% Average annual mortality count: 41,951 Mortality-to-incidence ratio: 16.8%

Breast cancer is the second most common type of cancer in women in the U.S. It is the second leading cause of cancer death in women, after lung cancer. Older age, a family or personal history of breast cancer, dense breast tissue, obesity, and the use of hormone replacement therapy for the treatment of menopausal symptoms can increase the risk of breast cancer.

Mammography can detect tumors in the breast, even before they have spread to other organs. Mammograms are recommended for women ages 45-54 yearly, and every two years thereafter, except in cases of higher risk factors.

You may also like: 25 facts about food allergies

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State-by-state prevalence of the 5 most common types of cancer - KFOR Oklahoma City

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QC Kinetix (Columbia) Offers Regenerative Medicine Treatments to Treat Different Types of Physical Pain and Injuries – Yahoo Finance

Posted: October 4, 2022 at 2:24 am

COLUMBIA, MO - (NewMediaWire) - October 3, 2022 - via QC Kinetix - QC Kinetix (Columbia) therapies work by stimulating the body's natural healing abilities to heal damaged tissues much faster than normal.

Although unpleasant, pain is many times useful to our bodies as it signals us about body parts that need more attention and care. However, some pain can persist for several weeks, months, or even years and negatively affect the quality of life. In many cases, physicians recommend surgery or prescription medication when other interventions have failed. These recommendations often come unwelcome by patients. Fortunately, technology and innovation have led to the discovery of new, effective ways of treating pain naturally, such as through regenerative medicine.

QC Kinetix (Columbia) treats different types of mild and severe pain naturally using regenerative medicine. The clinic has a wide spectrum of treatments that do not involve surgery or prescription of addictive medications. The therapies work by stimulating the body's natural healing abilities to heal damaged tissues much faster than normal, resulting in pain relief and reduced inflammation. They treat many conditions, including pain in the knee, back, wrist, shoulder, ankle, hip, and other body parts. They also treat pain in the large joints like the legs and small joints like fingers and toes caused by degenerative conditions like arthritis.

The pain control clinic offers customized treatment plans that are tailor-made to meet patients' unique health needs. They begin each treatment with a free consultation that diagnoses patients' conditions and informs on patients' eligibility for regenerative medicine. The consultation involves a thorough analysis of the patient's medical history and may require additional tests to improve accuracy in diagnosis. This is followed by a recommendation of the most useful therapies based on the diagnosis. The physician takes time to explain to patients what regenerative medicine entails and how it can help them to improve their condition.

QC Kinetix (Columbia)'s treatments help relieve many symptoms, including limited joint mobility, swelling, redness, stiffness, bone-on-bone grinding, knee cracking, popping, and many more. The procedures allow patients to get back to their normal lives fast, as they barely have any downtime once the healing process begins. They are minimally invasive, have long-lasting results, and improve function and quality of life. The clinic offers a personalized concierge-level service that provides logistical support to patients receiving treatment at the facility. The physicians keep patients informed every step of the process.

The pain control clinic has an entire division dedicated to providing regenerative medicine for sports and accident injuries. The therapies are ideal for when patients have tried the common advice of rest, ice, compression, and elevation but have failed in rehabilitating the injuries. The clinic steps in to offer a full recovery regime that combines traditional sports injury treatments, rest, and bracing with regenerative medicine for the best possible results. The therapies do not only heal the injured areas but also strengthen the tendons, ligaments, and cartilage to avoid re-injury. Some of the sports injuries they treat include golfer's elbow, torn Meniscus, torn rotator cuff, torn ACL/MCL, and joint and musculoskeletal pain from a thrown-out joint or muscle.

QC Kinetix (Columbia) has invested in advanced technologies and modern equipment that improves paint outcomes. Regenerative medicine remains one of the fastest growing industries, which has led them to adopt a continuous learning culture that allows easy adoption of new, well-researched techniques that match industry trends. Treatments are administered by a team of board-certified physicians with extensive experience in the industry. They use a patient-centered approach that focuses on meeting patient needs and encouraging patient engagement.

The clinic representative had this to say about their services,

"When you visit our facility in Columbia, MO, an orthopedic specialist from our Team Will evaluate you and review your symptoms and previous treatments. QC Kinetix (Columbia) has several regenerative protocols that we use to create customized treatment plans for every patient. Our natural pain treatments can address joint pain and produce long-lasting results."

QC Kinetix (Columbia) is located at 3700 I-70 Dr. SE, Suite 106, Columbia, MO, 65201, US. For consultation and booking, contact their staff by calling (573) 545-5588. Visit the company website to learn more about their Columbia office and their non-surgical regenerative medicine treatments for mild and severe pains and injuries.

Media Contact:

Company Name: QC Kinetix (Columbia)

Contact Person: Scott Hoots

Phone: (573) 545-5588

Address: 3700 I-70 Dr SE, Suite 106

City: Columbia

State: MO

Postal Code: 65201

Country: US

Website: https://qckinetix.com/mid-missouri/

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QC Kinetix (Columbia) Offers Regenerative Medicine Treatments to Treat Different Types of Physical Pain and Injuries - Yahoo Finance

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