Investigadores del estado de Washington están destacando una población que a menudo se pasa por alto: los adultos con demencia sin parientes.
Esta población suele ser difícil de estudiar por diversos motivos. Marlaine Figueroa-Gray es antropóloga del Instituto de Investigación Médica de Kaiser Permanente en Washington que ha participado en esta investigación.
Ella dice que cuando las personas con demencia no tienen cónyuge o hijos, a menudo no hay nadie que actúe como punto de contacto para los estudios. Figueroa-Gray señala que también hay otras consecuencias.
"Cuando las personas con demencia acaban viviendo como personas sin familia," dice Figueroa-Gray, "no tienen ese apoyo de quien los lleve a recibir atención médica."
Figueroa-Gray afirma que los investigadores querían averiguar qué les ocurre a estas personas cuando no cuentan con el apoyo de un cuidador. Así que adoptaron un enfoque único y buscaron en los registros administrativos adultos con demencia sin parentesco.
En otro estudio, Figueroa-Gray afirma que los investigadores encontraron que esta población tenía dificultades para realizar las actividades cotidianas y necesitaba ayuda para bañarse, vestirse y administrar la medicación.
"Tuvieron problemas para conducir y experimentaron cambios para mantener la vida cotidiana, a menudo se vieron incapaces de mantenerse al día con el aumento de los alquileres en sus vecindarios," asegura Figueroa-Gray. "Y todas estas necesidades son obviamente más difíciles de gestionar sin un apoyo cercano."
Figueroa-Gray señala que una red de vecinos a veces puede proporcionar cuidados a pacientes con demencia, pero estas relaciones pueden ser frágiles. Dice que muchas personas pueden encontrarse en esta situación, por lo que es importante que todos lo entiendan.
"Pensando realmente en el sistema y sus políticas: ¿qué podemos hacer para apoyar a las personas a medida que envejecen y pueden, estar fuera de las relaciones familiares simplemente por haber sobrevivido a otras muertes?", se cuestiona Figueroa-Gray.
Divulgación: El Proyecto Kaiser Health Plan of Washington contribuye a nuestro fondo para informar sobre la prevención del abuso de alcohol y drogas, problemas de salud, hambre/alimentación/nutrición y problemas de personas mayores. Si desea ayudar a respaldar noticias de interés público,
haga clic aquí.
get more stories like this via email
After more than 50 years of use, some Michigan lawmakers say naloxone may not be the best choice in an overdose situation.
Naloxone is sometimes called the "Lazarus drug" because of its powerful ability to seemingly resurrect people after a drug overdose.
Sen. Kevin Hertel, D-St. Clair Shores, and some of his colleagues have introduced a bill which would open the door for what they say are more costly, but more powerful, antidotes.
"Given the prevalence of fentanyl in our communities, and how much stronger some of these drugs that we're now seeing are, we believe -- and in talking with others -- that there should be other tools to respond to an overdose," Hertel explained. "To make sure we're doing everything we can to save somebody's life."
Not everyone is on board with the proposed legislation, Senate Bill 542. Opponents argued the more expensive naloxone alternatives are not necessary, and using them would only increase profits for the pharmaceutical industry.
Jonathan Stoltman, director of the Opioid Policy Institute in Grand Rapids, said while the naloxone alternatives do help in overdose situations, they can also cause nasty side effects.
"The newer approaches, they put people into more severe withdrawal," Stoltman pointed out. "That's a pretty profound negative side effect. The one approach is very inexpensive and works great; the other approach is far more expensive and has this strong negative side effect."
Sponsors of the bill say they're hoping to give Michigan residents a chance to chime in on the issue in a public hearing sometime in June. Michigan saw more than 3,000 opioid overdose deaths in 2021.
get more stories like this via email
New Mexico saw record enrollment numbers for the Affordable Care Act this year and is now setting its sights on lowering out-of-pocket costs - those not reimbursed by insurance. More than 56,000 New Mexicans are enrolled in a medical health insurance plan on the state exchange - an increase of 12,000 people overall.
Colin Baillio, deputy superintendent with the state's Office of Insurance, said the state has boosted its outreach and made efforts to improve the overall consumer experience.
"We saw a 40% year-over-year increase, and New Mexico saw the biggest percentage increase during the open-enrollment period among all of the state-based marketplaces," he explained
Part of the enrollment increase is due to what's called the "unwinding" - a federal directive that required all states to redetermine Medicaid eligibility following a three-year pause on checks during the COVID pandemic. He said by using expanded tools made available by the federal and state government, 8% of New Mexico's population is now uninsured - down from 23% in 2010.
Following approval by lawmakers in the 2024 legislative session, the New Mexico governor signed seven health care-related bills into law - one of which requires annual reporting of prescription drug pricing. Baililo said the Affordable Care Act built the foundation that has allowed the state to pursue additional affordability initiatives.
"I'm really glad to see that there's so much interest in the next step of health reform, really leaning into these out-of-pocket cost issues and making it easier for people to afford to stay covered and see their doctors," he continued.
Two years ago, the state also passed a one-of-a-kind law that did away with behavioral health co-pays for people in certain insurance plans.
get more stories like this via email
New York's medical aid-in-dying bill is gaining further support. The Medical Society of the State of New York is supporting the bill. New York's bill allows terminally ill people with only six months to live to use this option, with safeguards requiring two physicians' approval.
The bill's Assembly sponsor Amy Paulin, D-Westchester, said despite the growing support, other hurdles lie ahead.
"Now we have what I believe, if it came to the floor, a majority. There's still a hesitation on the part of leadership. You know, we need members to assure leadership that they no longer have reservations," she said.
Other newly resolved concerns center on making sure insurance companies and doctors who don't support this aren't held liable. She's optimistic the bill will pass after nine years in the Legislature. New York would be the 11th state along with Washington, D.C. to have medical aid in dying legislation.
Corinne Carey, senior New York campaign director with Compassion and Choices finds the pandemic drew a vivid picture of a person's end-of-life experience. There were images of people dying on ventilators, apart from loved ones, and unable to communicate. She said people began thinking about a "good death."
"And, what is a good death is being surrounded by loved ones, having some measure of control, experiencing the touch of your loved ones, and being the one in the driver's seat," she explained.
Now people have different options for end-of-life care, each of which presents various challenges. Polls show medical aid in dying has garnered considerable support since being introduced in 2015. A 2022 Compassion and Choices poll finds 57% of nurses support medical aid in dying professionally, although fewer support it personally.
Disclosure: Compassion & Choices contributes to our fund for reporting on Civic Engagement, Health Issues, Senior Issues, Social Justice. If you would like to help support news in the public interest,
click here.
get more stories like this via email