logo
Mobile help for opioid overdoses rolls into south suburbs with aid of Cook County $1M grant

Mobile help for opioid overdoses rolls into south suburbs with aid of Cook County $1M grant

Chicago Tribune2 days ago

Through a clinic in Harvey, Family Guidance Centers offers medications to people meant to counteract the effects of opioid overdoses.
But whether it's access to transportation, child care needs or physical limitations, the nonprofit knows there are many people who need the lifesaving drugs but can't get to the clinic, said Ron Vlasaty, Family Guidance Centers' chief operating officer.
With the help of a Cook County grant of nearly $1 million, Vlasaty and county officials celebrated the rollout of a van that will bring the medications, used to revive people suffering the effects of an opioid overdose, to more than two dozen south suburbs.
The program was announced Friday during a news conference outside the Posen Fire Department's headquarters, with the new van and another already in use by Family Guidance Centers parked outside.
Cook County Board President Toni Preckwinkle said while opioid overdose fatalities are 'trending in the right direction,' the problem is still of major concern.
'This crisis is everywhere,' Preckwinkle said. 'This is a challenge we have all over the country, not just in Cook County.'
With the rollout of the van, which is a refurbished ambulance, residents will no longer need to overcome transportation or access issues, she said.
We are 'able to deliver the care and services right where they are,' Preckwinkle said.
The mobile van is equipped with a nurse, peer recovery support specialist and outreach staff to deliver care directly to communities most affected by the opioid crisis, according to the county.
It carries methadone, buprenorphine and naltrexone, FDA-approved medications for opioid and other drug overdoses. Family Guidance Centers' other van delivers naloxone, also known as Narcan, which can revive a person suffering an opioid overdose, Vlasaty said.
Posen police Chief William Alexander said opioid overdoses are one of the most urgent challenges faced by first responders.
'We are losing far too many lives to addiction and senseless violence,' Alexander said.
Preckwinkle said, with the rollout of the van, health care officials are working to operate in a backdrop of possible federal spending cuts that would help their efforts.
The nearly $1 million grant to Family Guidance Centers comes from the county's allocation of federal American Rescue Plan Act, a $1.9 trillion economic stimulus package passed in response to the COVID-19 pandemic.
'We see at the federal level a discouraging and alarming willingness to cut health care services,' Preckwinkle said, vowing Cook County will continue to provide services to those in need.
'If someone needs help we want to make sure they get it,' she said.
Deborah Sims, former Cook County commissioner for the 5th District, which includes many south suburbs, said 'this is a good day.'
Sims said that in delivering health care, agencies 'always want people to come to us.'
'If we can take it to the community it's always better for us and better for the residents,' she said.
The grant program is part of the county's Stronger Together initiative, a countywide effort focused on behavioral health equity, system coordination and the expansion of community-based care, according to the county.
The county grant to Family Guidance Centers is spread over three years, and the mobile unit will operate Monday through Friday.
Tom Nutter, chief behavioral health officer with the Cook County Office of Behavioral Health, said opioid addiction affects people from the very start, creating a dependency that requires increasing amounts of drugs.
For those with addictions, Nutter said their day 'begins with how will I get the drug and how will I pay for it?'
Nutter praised Family Guidance Centers for its work, saying they bring 'unquestionable dedication' to the job.
The Cook County Office of Behavioral Health was established by the county in 2023 to address the behavioral health needs of county residents, particularly those from historically marginalized and underserved populations.
Vlasaty said that the Family Guidance Centers operates 14 locations in Illinois, including eight in Cook County.
He said the Harvey clinic takes in residents from many south suburbs, but people can't always get to that location.
Vlasaty said the van will be able to go to patients' homes or central locations, such as village halls and police and fire stations, to distribute medications.
He said the nonprofit already distributes naloxone, which can help revive someone suffering an opioid overdose, to south suburban police departments through a smaller van it purchased with help of a previous county grant.
Family Guidance Centers also has a naloxone distribution point at Harvey's Pace bus station, established about a year ago. He said it needs to be refilled every couple of days and was done in conjunction with the county and Pace.
Vlasaty said Family Guidance Centers will put up informational posters at municipal buildings, liquor stores, gas stations and food pantries 'and wherever people congregate' to publicize the new mobile unit.
'We need to get the word out to where people are at to let them know this is available,' he said.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Subtle Differences Emerge Between FDA And CDC On COVID Vaccine Advice
Subtle Differences Emerge Between FDA And CDC On COVID Vaccine Advice

Forbes

timean hour ago

  • Forbes

Subtle Differences Emerge Between FDA And CDC On COVID Vaccine Advice

An illustration picture shows vials with Covid-19 vaccine stickers attached and syringes with the ... More logo of the company Novavax. (Photo by JUSTIN TALLIS / AFP) (Photo by JUSTIN TALLIS/AFP via Getty Images) In a major policy shift last month, Food and Drug Administration officials proposed requiring new clinical trial research with respect to the effectiveness of COVID-19 vaccines in healthy people under 65, including pregnant women, before issuing an updated approval for a broader population. At the same time, in an update to its immunization schedule posted May 29th, the Centers for Disease Control and Prevention include the option of COVID-19 vaccines for healthy children and pregnant women. Based on the language used by CDC, it suggests the agency aims for a shared decision-making approach in which individuals consult with their doctor prior to getting a shot. We witnessed a preview of the new FDA approach when the agency made an unusual decision to limit the approval of the nation's only non-mRNA coronavirus vaccine, Novavax's nuvaxovid, for use only in adults 65 and older or those 12 to 64 who have at least one health problem that puts them at increased risk from COVID-19. To be indicated for a broader population, the FDA plans to require that vaccine makers conduct booster trials to demonstrate effectiveness in people under 65 or without certain risks. These trials could take a year to complete, according to a STAT report. As such, it's not something that can be accomplished prior to the autumn, even if Novavax, Pfizer, or Moderna, wished to pursue this pathway. Similar to annual flu shots, which adapt to new strains, COVID-19 boosters update immunity to target evolving variants. Data from several years of booster campaigns show lower hospitalization and death rates for boosted individuals compared to unvaccinated people or those who haven't gotten boosters. This particularly applies to the vulnerable subpopulations, stratified by age and underlying health conditions. The COVID-19 vaccines, both mRNA and non-mRNA, are recommended for anyone who is over 65 or who has a medical condition that can increase the risk of severe illness or death. Underlying conditions include, among other things, obesity, 'physical inactivity,' diabetes, clinical depression and being immunocompromised. It's estimated that between 100 and 200 million Americans will still be eligible for vaccination due to having such health issues. Nevertheless, this raises questions for people who don't have underlying health conditions and are under 65 but would like to get a COVID-19 shot this fall. The FDA and CDC appear to differ subtly in terms of their current advice for healthy individuals under 65. Is it possible for these folks to obtain a jab at the pharmacy with no questions asked? Or will they have to go to their doctor and be granted de facto permission to get the shot? Perhaps equally important, will their insurer pay for it? As the New York Times explains, insurance companies may serve as the 'gatekeepers by demanding medical documentation of an underlying condition before agreeing to cover the cost.' The out-of-pocket cost to patients could be as much $140 a shot. Top FDA officials Prasad and Makary advocate an 'evidence-based' approach to COVID-19 vaccination. They also write of aligning policy with Europe. Indeed, in most instances, European public health authorities have adopted a targeted approach that aims at ensuring the elderly and those with underlying health conditions get boosted. This means that outreach campaigns in European countries only target subpopulations for which the vaccine is recommended by the respective public health authority. This is unlike the universal recommendations previously issued by the CDC that didn't differentiate by age or risk factors. However, the European agencies in charge of vaccine approval, the EMA and MHRA, haven't suggested marketing authorization changes, such as narrowing the indication based on age, for any of the approved COVID-19 vaccines.

Blood test-guided treatment with AstraZeneca pill cut risk of breast cancer progression, study finds
Blood test-guided treatment with AstraZeneca pill cut risk of breast cancer progression, study finds

Yahoo

time2 hours ago

  • Yahoo

Blood test-guided treatment with AstraZeneca pill cut risk of breast cancer progression, study finds

By Julie Steenhuysen CHICAGO (Reuters) -Treating breast cancer patients with AstraZeneca's experimental pill camizestrant at the first sign of resistance to standard treatments cut the risk of disease progression or death by half, a finding that could change the way such cancers are treated, cancer experts said on Sunday. The results, presented at the American Society of Clinical Oncology meeting in Chicago, mark the first use of a blood test called a liquid biopsy to indicate the need for a change in treatment in women with a common form of breast cancer, even before tumor growth can be detected on imaging. The early switch approach in women with hormone receptor-positive, HER2-negative breast cancer resulted in a 56% reduction in the risk of disease progression or death, said Dr. Eleonora Teplinsky, an oncologist at Valley-Mount Sinai Comprehensive Cancer Care and an ASCO breast cancer expert. "When patients progress on scans, we're already behind," Teplinsky said at a media briefing. She said an early switch approach, before disease progression, allows doctors "to essentially stay ahead of the curve." Camizestrant is not yet FDA-approved, but Teplinsky believes the data will likely result in a new treatment paradigm. The trial involved 3,256 patients with advanced hormone receptor-positive, HER2-negative breast cancer, the most common type in which hormones such as estrogen fuel cancer growth. These cancers lack high levels of HER2, another cancer driver. Women in the trial had at least six months of treatment with aromatase inhibitors that block hormones fueling the cancer, as well as targeted drugs called CDK4/6 inhibitors such as Novartis' Kisqali, Pfizer's Ibrance or Lilly's Verzenio, which block an enzyme that fuels cancer growth. About 40% of patients treated with aromatase inhibitors develop mutations in the estrogen receptor 1 gene called ESR1 mutations, a sign of early drug resistance. Camizestrant and similar drugs called Selective Estrogen Receptor Degraders (SERDS) block estrogen receptor signaling in cancer cells. In the trial, researchers used blood tests to look for ESR1 mutations until 315 patients were identified. They were randomly assigned to either switch to camizestrant plus the CDK4/6 inhibitor (157 patients) or continue with standard treatment plus a placebo (158 patients). The researchers found that it took 16 months for the disease to progress in women who got camizestrant, compared with 9.2 months in those who continued on standard therapy, a statistically significant difference in progression-free survival. No new side effects were reported and few patients from either group dropped out due to side effects. "This is going to be very impactful for our patients," said Dr. Hope Rugo, head of breast medical oncology at City of Hope in Duarte, California. The question, she said, is how do doctors incorporate the testing into clinical practice. Separately, adding AstraZeneca's immunotherapy durvalumab to standard treatment before and after surgery in patients with early-stage stomach and esophageal cancers helped extend the time patients had without cancer progression or recurrence compared to chemotherapy alone. The global study of nearly 950 patients tested durvalumab, sold under the brand Imfinzi, in combination with a chemotherapy regimen called FLOT given around the time of initial cancer surgery. Patients in the durvalumab plus FLOT arm experienced a 29% better event-free survival than those who received the chemotherapy regimen. "We demonstrate that immunotherapy works in early-stage disease, which is great," lead study author Dr. Yelena Jarnigan of Memorial Sloan Kettering Cancer Center in New York told reporters at the meeting. "We did not see any new safety signals, so this will change practice for our patients, which is exciting to see." Both studies were published on Sunday in the New England Journal of Medicine.

F.D.A. Updates Recall of Tomatoes, Warning of a High Risk of Illness or Death
F.D.A. Updates Recall of Tomatoes, Warning of a High Risk of Illness or Death

New York Times

time5 hours ago

  • New York Times

F.D.A. Updates Recall of Tomatoes, Warning of a High Risk of Illness or Death

The Food and Drug Administration has updated an ongoing recall of tomatoes distributed in three states to its most severe warning, saying there is a higher probability that potential salmonella contamination could lead to 'serious adverse health consequences or death.' It is unlikely that consumers will encounter any fresh tomatoes from the recalled batch, but the bacteria can survive for weeks in dry environments and months in wet ones, such as the freezer, according to the F.D.A. The tomatoes, which were sold in packages as small as a three-pack and as large as 25 pounds, were distributed between April 23 and 28 to Georgia, North Carolina and South Carolina under the name H&C Farms Label. They were first voluntarily recalled at the beginning of May for possible salmonella contamination. No illnesses were reported at the time, according to the F.D.A. The recall was updated on Wednesday to Class I, which the F.D.A. describes as 'a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.' The potential source of contamination was not immediately known. Williams Farms Repack, the South Carolina-based firm that distributed the tomatoes, did not immediately respond to a request for comment on Saturday. H&C Farms declined to comment on Saturday. Exposure to salmonella, a bacteria, can be deadly, especially in adults over 65, children under 5 and people with compromised immune systems, who have the highest risk of severe illness. But healthy people should also avoid eating the tomatoes. Exposure to salmonella, usually from contaminated foods, sickens more than one million people in the United States each year and it is responsible for more than 400 deaths annually. The infection caused by salmonella can trigger symptoms including fever, diarrhea and abdominal pain that may last for days.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store