Virginia Mason Franciscan Health and Seattle Children's expand pediatric, neonatal partnership
The new strategic affiliation builds on nearly 15 years of collaboration between the two organizations and aims to improve access to expert physicians, specialized care teams, and seamless coordination for families, according to a joint statement.
Access to high-quality health care remains a significant challenge in the Puget Sound region, VMFH and Seattle Children's noted.
By joining resources and leveraging their combined network of care sites, both groups say they hope to bring advanced medical services closer to home for more patients.
'This affiliation marks a significant step forward in our mission to improve health care access for mothers, babies and children,' said Ketul J. Patel, CEO of Virginia Mason Franciscan Health and President of CommonSpirit Health's Northwest Region. 'Seattle Children's is a globally recognized leader in pediatric medicine, and we're honored to work alongside them to further elevate the standard of care in our communities.'
Seattle Children's consistently ranks among the top ten children's hospitals in the United States, while VMFH hospitals are also nationally recognized for quality care.
Their partnership has already brought neonatologists to VMFH Family Birth Centers, offering 24/7 onsite and remote support to care for the region's most vulnerable newborns without the need to transfer them to different facilities.
The collaboration has also connected patients at VMFH's St. Joseph Medical Center in Tacoma to Seattle Children's pediatric cardiologists and infection prevention teams, allowing for on-site assessments of complex maternal and newborn conditions.
Jeff Sperring, MD, Chief Executive Officer of Seattle Children's, said the expanded affiliation aligns with the hospital's broader mission. 'We are proud of our long-standing reputation for excellence in pediatric and neonatal care,' Sperring said. 'Virginia Mason Franciscan Health is a recognized leader in quality care and clinical excellence, and we're excited to work together to continue fulfilling our vision of helping every child live their healthiest and most fulfilling life possible.'
As part of the expanded affiliation, perinatal, neonatal, and specialty services will grow across VMFH Birth Centers located in King, Pierce, and Kitsap counties.
The goal is to support thousands of families while minimizing the separation of mothers and their newborns after delivery.
The partnership will also focus on improving access to pediatric specialists across VMFH's nearly 300 care sites, strengthening connections between primary, specialty, ambulatory, and urgent care services.
Officials said this effort will ensure children can get the right care at the right time, with seamless referrals to Seattle Children's specialists when needed.

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Medscape
29-07-2025
- Medscape
Preterm Birth Predicts Adult Health Problems
Adults born preterm were significantly more likely to have cardiometabolic risk factors and internalized mental health issues than full-term peers, according to an ongoing preterm birth cohort study in the US. 'This study addresses a significant gap in understanding the long-term health effects of preterm birth in the US,' said lead author Amy D'Agata, PhD, of the College of Nursing, The University of Rhode Island, Kingston, Rhode Island, in an interview. Although the annual preterm birth rate in the US has held at a relatively stable 10%-12% for decades, since the 1970s, more preterm infants are surviving because of advances in neonatal intensive care, D'Agata said. Millions of individuals born preterm are aging into adulthood, but few data are available on their long-term health outcomes, she noted. In the new study, published in JAMA Network Open , D'Agata and colleagues reviewed data from a cohort of individuals who received level III neonatal intensive care at a single center between 1985 and 1989. The study population included 158 preterm-born and 55 full-term born adult control individuals. Preterm was defined as weighing under 1850 g at birth with various neonatal diagnoses; critically ill infants and those with major congenital abnormalities were excluded. The mean age across the groups was 35 years; 50% were women. The researchers used latent growth curve models to show changes over time. Overall, the preterm individuals who had higher medical risk in early life were significantly more likely to have a range of health problems at 35 years of age, notably, higher triglycerides than control individuals (beta value, 53.97; P = .03). Measures of systolic blood pressure and central adiposity also were significantly higher in the preterm birth group (beta values of 7.15 and 0.22, respectively), whereas bone density and high-density lipoprotein cholesterol were lower (beta values of -1.14 and -13.07, respectively). In addition, internalizing mental health problems were significantly more common in the preterm cohort than in the control individuals (beta value, 0.85; P = .01) but no difference in externalizing mental health problems was noted between the groups. The researchers also reviewed the impact of social protection and childhood socioeconomic status and found no association between these and physical or psychological health risks in adults born preterm. The Long View of Preterm Birth The population of adults born preterm remains largely invisible to the US healthcare system and its clinicians, highlighting critical issues of health equity and quality of care, D'Agata told Medscape Medical News . 'Much of the existing research in this area has focused on international, homogeneous populations, creating a need for rigorous, US-based longitudinal data to guide healthcare policy and clinical practice,' she added. 'These findings generally confirmed what has been observed internationally, that there is a link between higher early life medical risk and increased likelihood of mental health issues, elevated systolic blood pressure, unfavorable cholesterol and triglyceride levels, body fat distribution, and lower bone density among adults born preterm, and it was notable to see these clear and consistent associations replicated in a US cohort using a prospective, longitudinal design,' said D'Agata. The study findings emphasized the need to inquire about birth history in adult care settings and suggest that those born preterm and their families must be their own health advocates, if necessary, said D'Agata. 'Even if a patient isn't asked about their birth history, they should share it,' she noted. Clinicians work hard to provide the best care, but it takes time for evidence-based research to inform clinical practice, she said. 'Although our birth cohort is small and comes from a single geographic region, the results generally align with international findings,' D'Agata told Medscape Medical News . However, future studies should include more racially and ethnically diverse cohorts from multiple clinical settings, she said. Research is needed not only to examine which subgroups of preterm individuals are most at risk but also to differentiate between those with varying degrees of early life complications, she added. Long Follow-Up Strengthens Findings The 35-year duration of the preterm birth cohort study was impressive and valuable, said Tim Joos, MD, a clinician with a combination internal medicine/pediatrics practice at Neighborcare Health in Seattle. 'We don't often have the long game in mind, in healthcare as well as in other parts of our society,' said Joos, who was not involved in the study. 'We don't tend to follow pediatric conditions into adulthood,' he noted. The current study findings demonstrated a long-term psychological and physical impact of prematurity on adult health that was humbling, Joos told Medscape Medical News . Looking ahead, the results highlight not only the need to continue to prevent preterm birth but also to the importance of asking older patients about preterm birth as part of their health history, he said.


Fox News
27-07-2025
- Fox News
Inside the male birth control study showing promising results
Fox News medical contributor Dr. Nicole Saphier joins 'Fox & Friends Weekend' to discuss a male birth control study and the side effects of women's birth control.
Yahoo
23-07-2025
- Yahoo
Male birth control pill passes early safety test, with more trials underway
When you buy through links on our articles, Future and its syndication partners may earn a commission. An experimental, hormone-free male birth control pill has just passed its first safety test in humans. The trial included 16 people and was only intended to test whether the drug reached adequate levels in the body, as well as whether it triggered any serious side effects, such as concerning changes in heart rate, hormone function, inflammation, mood or sexual function. Across the doses tested, no significant side effects were observed. That result tees up the pill to be tested in larger trials that will now look at both safety and efficacy. The results of the early safety trial, published Tuesday (July 22) in the journal Communications Medicine, are a critical first step toward getting the pill approved, Dr. Stephanie Page, an endocrinologist at the University of Washington School of Medicine who wasn't involved in the study, told Scientific American. "We really need more reversible contraceptive methods for men," she added. For the moment, the only male birth control options are condoms and vasectomies. The latter can be reversed, but the actual success rate of the reversal procedure varies widely in terms of how likely a person is to conceive a child afterward. If approved, the new pill would be the first drug in its class. "A safe and effective male pill will provide more options to couples for birth control," Gunda Georg, a professor in the University of Minnesota College of Pharmacy, where the drug molecule was developed, said in a statement released earlier this year following promising preclinical testing of the pill. Columbia University was also involved in the drug's development, along with the company YourChoice Therapeutics, which is overseeing the trials. Related: Why is there still no male birth control pill? "It will allow a more equitable sharing of responsibility for family planning and provide reproductive autonomy for men," Georg said. How the male birth control pill works The experimental pill, called YCT-529, is designed to pause sperm production by interrupting specific signals in the body. Specifically, the drug works by blocking a protein called "retinoic acid receptor alpha," which is known to play a key role in the formation and maturation of sperm. In the testes, the receptor would usually be activated by the insertion of a "key" — a vitamin A metabolite — but the drug stops this key from clicking into place. That, in turn, prevents the chain reaction that ends with sperm being made. Finding a compound with this effect required the scientists to closely examine the structure of the receptor when it's bound to its key, as well as test dozens of molecules to see which could block the interaction. In preclinical tests with male lab mice, the drug "elicited profound effects" on sperm production. It triggered reversible infertility within four weeks of use, showing 99% effectiveness at preventing pregnancy in the female mice the treated males mated with. When taken off the drug, the male mice's fertility was restored within about four to six weeks. Further tests in nonhuman primates returned similar results, with sperm counts falling dramatically within two weeks of starting the drug and fully recovering within 10 to 15 weeks of stopping the drug. These preclinical tests set the stage for the recent clinical trial in people. The trial included 16 males ages 32 to 59, all of whom had previously undergone vasectomies. This was done out of an abundance of caution, in case the experimental drug was to have any lasting impacts on fertility, Nadja Mannowetz, co-founder and chief science officer of YourChoice Therapeutics, told Scientific American. The participants were split into groups who received either placebo pills or a low or high dose of the drug. Most of the participants took the pill only after a period of fasting, but a subset were also given doses after a large meal, to see if that affected levels of the drug in the body. Across all of the doses and conditions tested, the levels of the drug in the body reached decent levels, but Mannowetz anticipates that, if approved, the final dose would be closest to the highest one tested: 180 milligrams. RELATED STORIES —Hormonal birth control may double risk of stroke, study finds —1st over-the-counter birth control pill approved by FDA —Blood clot risk linked to taking common painkillers alongside certain hormonal birth control Both the animal study and the human trial results suggest that the approved pill would likely be taken once a day, but further trials will confirm that dosing. And although no notable side effects emerged in this small trial, future trials with larger study cohorts will still need to monitor for these effects. "The positive results from this first clinical trial laid the groundwork for a second trial, where men receive YCT-529 for 28 days and 90 days, to study safety and changes in sperm parameters," the study authors wrote in their paper. That trial is already underway and again is looking at males who have already had vasectomies or who have made a firm decision not to father children. This article is for informational purposes only and is not meant to offer medical advice.