Tag Archives: Maureen Salamon

Want happy, healthy kids? Be involved

It’s common sense, but it’s a good reminder: A supportive environment makes for happier kids. (Courtesy Spectrum Health Beat)

By Maureen Salamon, HealthDay


Teenagers living in cohesive neighborhoods—where trusted neighbors get involved in monitoring each other’s children—experience fewer symptoms of depression and anxiety, a study suggests.


The researchers also found consistent results across different cities regardless of family composition and neighborhood income, indicating strong neighborhoods help teen mental health across various populations.


Along with common risk factors, neighborhood environments should probably be given more attention when looking for potential factors linked to teen mental health problems, said study author Louis Donnelly. He’s a postdoctoral research associate at the Bendheim-Thoman Center for Research on Child Wellbeing at Princeton University in Princeton, N.J.


“Notably, whether a child grew up in a higher- or lower-income household, the associations were similar. The findings can be generalized across different city contexts,” he added.


About 14 percent of adolescents in the United States have had depression or a mood disorder. Eight percent have been severely impaired from an anxiety disorder, the study said.


The study included information on more than 2,200 children born in large U.S. cities. The information was collected between 1998 and 2000.


The study authors wanted to see if “neighborhood collective efficacy”—a blend of social cohesion and shared expectations for social control—was linked to better teen mental health.


The teens evaluated their own mental health at age 15. Parents provided “collective efficacy” information when their children were 3, 5 and 9. Parents ranked their agreement with statements such as, “People around here are willing to help their neighbors,” or “People in this neighborhood generally don’t get along with each other.”


Another scale asked parents to express their belief in statements demonstrating that neighbors would be likely to intervene or get involved in scenarios such as, “Children were spray-painting buildings with graffiti,” or “Children were showing disrespect to an adult.”


The researchers found that the “neighborhood effect” offered a protective effect similar to depression prevention programs targeting teens.


“There are really two (measurements) that are distinct, one being social cohesion and mutual trust. This is the idea of believing that people in your neighborhood share similar values and can be relied on for support,” Donnelly explained.


“The second dimension relies on informal social control,” he added. “We measured that based on the extent to which families and other adults can be relied upon to intervene … (such as) if a fight broke out in the street or children are not attending school.”


Maurice Elias said he wasn’t at all surprised by the study findings. He’s a professor of psychology at Rutgers University in Piscataway, N.J.


“The idea that being in a supportive environment would be good for children’s mental health shouldn’t be a revolution,” said Elias, also director of the Rutgers Social-Emotional and Character Development Lab. “It’s always nice when research helps confirm common sense. I see this as one of those examples.”


Reprinted with permission from Spectrum Health Beat.





Caregiver challenge: Needs double as end of life nears

By Maureen Salamon, HealthDay

 

Reliance on caregivers doubles as people near death, and half of those caregivers—typically unpaid family members—report having no time for themselves, a new study indicates.

 

The research used a nationally representative sample of about 2,400 older adults in the United States. The study authors found that caregivers provided nearly twice the number of hours of help each week to dying individuals than to those not at the end of life.

 

“We were certainly aware when dealing with end-of-life care that families are mostly involved, but we couldn’t quantify that prior to this [research],” said study author Dr. Katherine Ornstein. She’s an assistant professor of geriatrics and palliative medicine at the Icahn School of Medicine at Mount Sinai in New York City.

 

More than 34 million Americans provided unpaid care to an adult aged 50 or older in the past 12 months, according to 2015 figures from the National Alliance for Caregiving and AARP. Most caregivers are female.

 

Ornstein and her team drew from two nationally representative surveys in which caregivers in the United States reported their experiences caring for dying adults over age 65. The researchers contrasted this data with that of other caregivers providing ongoing care.

 

Older adults were classified as being at the end of life if they died within 12 months of the surveys’ completion.

 

The study found that dying adults had an average of 2.5 caregivers assisting them. Those near the end of life received 61 hours of help per week compared to 35 hours of help per week for older adults who weren’t at the end of life.

 

More than one-third of the end-of-life caregivers reported physical difficulty related to their duties. Just over half reported having no time for themselves. These figures were 21 percent and 40 percent, respectively, for other caregivers.

 

Nearly nine in 10 caregivers are unpaid, according to the study. For end-of-life caregivers who were spouses, nearly two-thirds reported receiving no help from family or friends.

 

“What we see now is, on average, there are 2.5 people helping someone at the end of life. You can imagine if they don’t have that, it’s much more difficult,” Ornstein said. “When spouses are serving as caregivers, the majority are reporting doing it alone and have the [most challenging] consequences.”

 

Barbara Coombs Lee is president of Compassion & Choices, a Washington, D.C.-based advocacy organization for patients’ rights and end-of-life issues. She pointed out that the caregivers surveyed in the new study didn’t necessarily know ahead of time that the person they were caring for was at the end of life.

 

This lack of awareness may have increased caregivers’ stress levels, she said.

 

“This told me the caregivers were probably struggling, not knowing this was an end-of-life situation. Our [organization’s] research indicates that uncertainty about decision-making is an inherent and extremely powerful source of stress,” Lee said.

 

“I would guess that many of these people didn’t know they were dying … so they pursued heroic, torturous, futile treatment,” she added. “Often the default decision [to continue treatment] increases the caregiver burden.”

 

Ornstein said she hopes greater awareness of the family burden of caregiving, especially at the end of life, comes from her research.

 

“We need to think about expanding access to palliative care services, which can help facilitate the delivery of supportive services to families earlier,” she added. “And we can see how we need to provide more paid family leave so families can provide the support we’re pretty much expecting them to provide.”

 

Lee agreed with the need for expanded access to hospice and palliative care.

 

“One of the big barriers to access to hospice is [an] information gap,” Lee said. “People don’t understand that hospice is appropriate to them in their journey in their illness. Palliative care utilization would go up if people had more candid conversations and were privy to information that physicians have but aren’t sharing.”

 

The study was published in the journal Health Affairs.

 

Reprinted with permission from Spectrum Health Beat.