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Doctors overlook current postpartum depression treatment in favor of expensive synthetic drugs


A Postpartum Depression Drug Is Hitting The Market, But A ‌Better Alternative Already Exists

The first⁤ FDA-approved‍ drug in pill form to treat⁤ postpartum depression, Zurzuvae, is expected to hit the market⁣ next month,​ with pricing starting at nearly $16,000 for a two-week course of treatment. ⁤Meanwhile, progesterone replacement⁤ therapy, a ‍safe, ⁤cheap, and ⁤effective‌ treatment, available on the market for as low‍ as 36​ cents ‌per capsule, continues to be ⁢ignored by most ​U.S. doctors.

Pharmaceuticals can’t solve what traditional American health care is plagued by — a lack of ​individualized, high-quality‌ care for women, especially around fertility,‌ pregnancy, and postpartum.

“Women’s health care in America is an insult to women,” said Dr. Timothy ‍Millea, orthopedic surgeon and Health Care Policy ‌Committee chair for the Catholic Medical Association, in⁢ an interview.

No⁤ other developed nation comes‍ close to America’s rising ⁣maternal death rate; next in ⁤line, ⁤France, has three times fewer deaths per live birth each year.

Data gathered in‍ 2021 and published⁤ in the ‌American Journal of Obstetrics and Gynecology found nearly 20 percent of women suffer from postpartum depression, or⁢ PPD. The current line of treatment is psychotherapy and slow-acting selective serotonin reuptake inhibitors (SSRIs), ⁢which are low-risk but can take several weeks to be effective.

“Women​ really‍ need a lot of care postpartum,” said Dr. Teresa Hilgers, ⁢ OB-GYN at the Saint Paul VI Institute in Omaha, Nebraska. “We need to be monitoring for PPD. ⁣It can occur in anyone who ⁣has no‌ risk factors. The ‌risk goes up naturally for all women.”

Costly New Drug

On Nov. ​7, Sage Therapeutics, in partnership with ​Biogen, announced⁣ long-anticipated pricing and market availability for their new drug. Zurzuvae, found to reduce depression symptoms within days​ for most women, with continued psychiatric benefits for four to six weeks, was approved by the FDA in August and ‍classified as a Schedule ⁤IV drug by the⁤ Drug Enforcement Agency.

Sage’s first‌ attempt ‍at the postpartum market, Zulresso, was considered successful, but the drug was too costly and cumbersome for widespread use, requiring a multi-day intravenous administration and costing about $34,000.

Long-Term Concerns

A drug’s real value can only be determined‍ compared to the current ‌standard of care, said Gregg​ Girvan, a Foundation for Research on⁣ Equal Opportunity⁤ scholar. Subjects in the⁢ Zurzuvae⁢ trial were given either a drug or placebo and stratified based on whether the participant was also ⁣taking an antidepressant at the ⁤time of the study.

“Payers need to aggressively negotiate with Sage based on the⁣ fact‍ that, after a certain time period, the results between Zurzuvae‌ and⁤ SSRIs appear to converge,” Girvan said.

Furthermore, Sage’s studies ⁢on Zurzuvae​ are ⁢short-term.⁢ There is limited long-term⁣ data on the drug. Hormone​ fluctuations, particularly ‌present in ‌breastfeeding ⁢mothers⁣ and those with thyroid ⁤disease, can exacerbate ​mental health conditions ​for several months postpartum, ⁢far beyond the Zurzuvae trials.

“If you ‌look at it from ⁤the 30,000-foot view, that’s ⁢problematic,” Millea said. “It’s ‌really, really good that ‍you have women feeling better after a ⁢few days, but⁣ what about‍ a few weeks? What ‌happens after six weeks?”

Bioidentical‍ Hormone Treatment

The superiority of bioidentical hormone therapy⁣ over synthetics is evident. The side effects ​of synthetics include breast cancer, strokes, ⁤and heart disease, with many lesser, uncomfortable symptoms ‍reported.

Zuranolone is a synthetic of allopregnanolone, a ‌neurosteroid ⁣the body derives ​from progesterone. Pharmaceutical companies cannot patent bioidentical⁣ hormones, just⁣ synthetic versions. Women are ‍left to suffer the difference in⁤ cost and treatment.

Doctors at the Paul VI Institute have a postpartum protocol using bioidentical progesterone to treat depression, anxiety,⁣ and hormone imbalances, that is inexpensive, safe, and readily‌ available on‌ the market, but not ‍widely used.

“With the use of ‍progesterone postpartum, typically women feel better within hours, even 24 ⁤hours,” Hilgers said. “Only 3.3 percent of⁤ women did not have‍ improvement in⁢ their symptoms. The vast​ majority ​have ‌moderate to marked improvement, mostly marked. Some women only need one dose.”

But a strong cancel culture ⁢and lack ⁤of pharmaceutical backing​ in women’s care contribute to progesterone treatment not making it to the mainstream, Millea said.

“Cancel culture for things outside the politically, medically ‘correct’ environment has been around a long time, especially in response to Catholic doctors,” Millea said.

With current women’s health policy focused on abortion and synthetic hormones, health care providers ​need to buck the trend and speak up, offering ⁤the ‍best treatment options to women.

“To the Biden administration’s⁣ FDA, an abortion ‍is an expression of freedom, not the bondage⁤ of mental health issues‌ and depression,” Millea said. “Eighty percent or higher of ⁢women report mental health problems after abortion. To me this [drug] ‍is ​a small project,‌ a ​small success, but also⁤ a glaring ⁣deficiency in recognizing ‌post-pregnancy mental health‌ issues.”


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What are⁣ the potential long-term concerns and limitations of‌ the Zurzuvae drug, and how does it compare to the benefits of progesterone replacement ⁤therapy in the long⁢ run

A Postpartum ⁣Depression Drug⁢ Is Hitting ‌The ​Market, But A Better Alternative Already‍ Exists

The first FDA-approved drug in​ pill form to treat⁣ postpartum depression,‍ Zurzuvae, is expected to hit the market next month, with ⁤pricing starting at nearly $16,000 for a two-week course ​of ​treatment. Meanwhile, progesterone replacement ⁣therapy, a safe, cheap,​ and effective treatment,‍ available on the market for as low as 36 cents per capsule, continues to be ignored by most U.S. doctors.

Pharmaceuticals ⁣can’t solve what traditional American ​health care is plagued ⁢by‍ — a⁤ lack of individualized, high-quality care for women, especially ⁢around fertility,‍ pregnancy, and postpartum.

“Women’s health care‍ in America is an‍ insult to women,” said Dr. ⁤Timothy Millea, orthopedic surgeon and Health Care Policy Committee ⁣chair⁣ for the Catholic Medical Association, in an interview.

No other developed nation⁢ comes close to America’s​ rising maternal death rate; next in line, France, has three times fewer‍ deaths per live birth each ⁢year.

Data gathered in 2021 and published in the American Journal of Obstetrics and ⁣Gynecology found nearly ​20 percent⁢ of women suffer from postpartum depression, or⁣ PPD.​ The current line of treatment is psychotherapy and slow-acting selective serotonin reuptake inhibitors (SSRIs), which are⁢ low-risk but can take several weeks to be effective.

“Women really need a lot of care postpartum,” said Dr. ‍Teresa Hilgers, OB-GYN at the Saint Paul VI⁣ Institute in Omaha, Nebraska. “We need⁤ to be monitoring for PPD.​ It can occur in anyone who has no risk factors. The risk ⁢goes‍ up⁤ naturally for ⁣all women.”

Costly New Drug

On Nov. 7, ‍Sage Therapeutics, in partnership with Biogen, announced long-anticipated pricing ‍and ‌market⁢ availability for their new drug. ​Zurzuvae, found to⁣ reduce depression symptoms within days for most women,⁣ with continued psychiatric benefits for four to‍ six weeks,‌ was approved by the FDA in August and classified as a Schedule IV drug by the Drug Enforcement Agency.

Sage’s first⁢ attempt at the postpartum⁤ market, ⁢Zulresso, was considered successful, but the drug was too ​costly and cumbersome ‍for widespread ⁣use, requiring a multi-day intravenous administration and costing about $34,000.

Long-Term Concerns

A drug’s real value can only be determined compared to the current standard of care,⁣ said Gregg Girvan, a Foundation for Research on Equal ‍Opportunity scholar. Subjects in the Zurzuvae trial were given ‍either a drug or placebo and stratified based on whether the participant ⁢was also taking an antidepressant at the ‌time of the study.

“Payers need ‌to aggressively negotiate with Sage based on the fact that, after a certain time period, the results between Zurzuvae and SSRIs appear to converge,” Girvan ‌said.

Furthermore, Sage’s studies on Zurzuvae are​ short-term. There⁤ is limited long-term data⁤ on the ‌drug. Hormone fluctuations, particularly present in breastfeeding mothers⁤ and ​those with thyroid disease, can exacerbate mental ‍health conditions for several months postpartum, ‍far beyond the Zurzuvae trials.

“If you look at it from ⁣the 30,000-foot⁤ view, that’s problematic,” Millea said. “It’s really, ⁢really good that you have women feeling better after a few ​days, but what about a few weeks? What happens ​after‍ six weeks?”

Bioidentical Hormone Treatment

The superiority of bioidentical⁤ hormone therapy over ‍synthetics is evident. The side effects of ‌synthetics ⁣include ⁣breast cancer, strokes, and heart disease, ⁣with​ many lesser, uncomfortable symptoms reported.

Zuranolone is ⁣a ‍synthetic of allopregnanolone, a neurosteroid the body​ derives ​from ⁣progesterone. Pharmaceutical‍ companies are often driven by profits, leading them to develop and market new drugs rather than promoting ​existing, safer alternatives.

In conclusion, while the FDA-approved postpartum depression drug Zurzuvae is making ⁣its way to the market, it is crucial to acknowledge the availability‍ of a ⁣better alternative – progesterone replacement‌ therapy. Traditional American health care needs to prioritize individualized, ‍high-quality care for women’s health, especially during the crucial phases of fertility, pregnancy, and postpartum. It’s time for doctors‍ and​ medical professionals ⁤to⁢ explore ​and embrace safer and ‌more affordable ⁢options like progesterone replacement therapy for the well-being‌ of ⁣women.



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