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Crash Risk Soars When Truck Drivers Don’t Treat Sleep Apnea: Study

MONDAY, March 21, 2016 (HealthDay News) — Truck drivers with sleep apnea who don’t regularly follow their treatment program are much more likely to crash, a new study finds.

“The most surprising result of our study is the strength and robustness of the increase in the crash risk for drivers with sleep apnea who fail to adhere to mandated treatment with positive airway pressure therapy [CPAP],” said study author Stephen Burks. He’s principal investigator of the Truckers & Turnover Project at the University of Minnesota.

The research included more than 1,600 U.S. truck drivers with obstructive sleep apnea and a control group with an equal number of drivers without the condition. Those with sleep apnea were prescribed CPAP, a treatment that keeps the airways open during sleep.

The drivers with sleep apnea were given a CPAP machine that could be used both at home and in their truck’s sleeper compartment. The researchers tracked the truckers’ use of CPAP with an internal memory chip that was placed in each machine.

The rate of serious, preventable crashes was five times higher among truckers with sleep apnea who didn’t use their CPAP machine, compared to the control group. The crash rate among drivers with sleep apnea who always or sometimes used their CPAP machine was similar to that of the control group.

The study was published online March 21 in the journal Sleep.

Burks said the findings support the need for obstructive sleep apnea screening standards for all drivers. Screenings could be administered through the commercial driver’s medical exam.

Obstructive sleep apnea affects at least 25 million American adults, the researchers said.

“This study emphasizes that untreated obstructive sleep apnea is a pervasive threat to transportation safety,” American Academy of Sleep Medicine President Dr. Nathaniel Watson said in a journal news release.

“It is critical for transportation companies to implement comprehensive sleep apnea screening and treatment programs to ensure that truck drivers stay awake at the wheel,” he added.

More information

The U.S. National Heart, Lung, and Blood Institute has more on sleep apnea.





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Most Families Cherish a Child With Down Syndrome, Survey Finds

By Amy Norton
HealthDay Reporter

MONDAY, March 21, 2016 (HealthDay News) — Families of children with Down syndrome face challenges, but by and large their experiences are positive ones, a new study suggests.

Researchers found that in 87 percent of families they surveyed, everyone — parents and siblings — said they loved their family member who had Down syndrome, and almost as many families said they felt pride for the child.

Few families expressed any regret about having a child with Down syndrome, the researchers reported in the April issue of the American Journal of Medical Genetics Part A.

The findings are more than “good news” for families, said lead researcher Dr. Brian Skotko. He is co-director of the Down syndrome program at Massachusetts General Hospital, in Boston.

Skotko said the information could also help expectant parents who, through prenatal diagnosis, learn that their child will be born with Down syndrome.

“When parents come in for counseling sessions, they want to know, what will this be like for our family, for our marriage?” Skotko said.

But while many studies have focused on the developmental issues and medical conditions that affect people with Down syndrome, few have looked at families’ experiences, according to Skotko.

“We hope this study helps paint a more accurate picture of what families’ lives are like,” he said.

In the United States, about 6,000 babies are born with Down syndrome every year, according to the U.S. Centers for Disease Control and Prevention. The condition arises when a baby carries an extra copy of chromosome 21.

The effects of Down syndrome vary from one person to another, but it usually causes mild to moderate intellectual impairment. Many children also have some health issues, including heart defects, and hearing and vision problems, the CDC says.

These days, Down syndrome is often diagnosed prenatally, Skotko pointed out. Screening tests during early pregnancy — including blood tests and ultrasound — can show whether a fetus is at increased risk of Down syndrome. Invasive testing, such as amniocentesis, can then be used to confirm the diagnosis.

The latest findings are based on surveys of 283 people with Down syndrome aged 12 and older, and over 2,700 parents and siblings, from six U.S. states. Some families received the Down diagnosis prenatally, others after their child was born.

All of the families belonged to local Down syndrome nonprofits — which is a limitation of the study, said David Coe, a clinical psychologist at Nicklaus Children’s Hospital in Miami, who specializes in caring for kids with intellectual impairments.

It’s hard to know whether the families’ experiences reflect those of most U.S. families who have a member with Down syndrome, said Coe, who was not involved in the study.

Still, he said it’s important for researchers to delve into not only parents’ feelings about raising a child with intellectual impairments, but siblings’ emotions as well.

In this survey, when problems with family relationships did appear, they often involved younger siblings — kids aged 9 to 11. About 13 percent of them did not “feel proud” of their brother or sister with Down syndrome, for example.

It’s not surprising that younger siblings would have a tougher time than older brothers and sisters would, according to Coe. “Those younger children are going through their own developmental issues, and it can be hard to process their siblings’ issues, too,” he said.

Skotko agreed that it’s not surprising. In some cases, he said, younger children might be jealous of the attention their sibling with Down syndrome receives. Other times, children might be embarrassed; that was more likely, the survey found, if parents acknowledged that they themselves felt embarrassed.

Skotko said he thinks the younger children’s feelings were often “pretty typical” for kids their age.

But, he added, if parents think their child is really struggling with having a sibling with Down syndrome, they can ask for help — from their health provider or a local support group.

“Sometimes you just need to talk to other families, and get some kind of validation,” Skotko said.

There was one surprise finding from the survey, according to Skotko: Families’ feelings about their experiences seemed unrelated to the severity of their child’s intellectual disability.

Coe stressed that kids with Down syndrome are all different — with a range of abilities and special needs — just like all families are different. So there’s no way to predict what your family’s experience will be based on other people’s.

The researchers agree that there’s no single “playbook” for family relationships.

But, Skotko said, the feelings of families in his survey do paint a portrait that’s different from what many people may believe.

“These families were overwhelming happy and content,” he said. “And many felt their lives have been enriched.”

More information

The National Down Syndrome Society has more on caring for the whole family.





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Can I Wear My Colored Contacts Every Day?

Photo: Getty Images

Photo: Getty Images

Q: Are cosmetic contacts safe to wear every day?

Yes, as long as they aren’t a random pair picked off the rack at the Halloween store. Just like contact lenses that correct your vision, decorative contacts are overseen by the FDA and require a prescription. While there may be vendors out there selling colored, vampire, or cat-eye lenses without requiring an Rx, buying from these folks isn’t safe. Go through a reputable eye-care professional to get the lenses properly prescribed and fitted for your eyes.

RELATED: 9 Worst Eye Care Mistakes You’re Making

You should also follow the same safety and hygiene guidelines that you do with regular prescription contact lenses. Make sure you clean and disinfect them according to the instructions and take them out after the recommended length of time. If redness or pain occurs or you notice any discharge, remove them and call your eye doctor right away.

RELATED: Colored Contacts Can Be Totally Safe, As Long As You Take These 3 Steps

Health’s medical editor, Roshini Rajapaksa, MD, is assistant professor of medicine at the NYU School of Medicine.




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Blooming Trees Can Bring Misery to Allergy Sufferers

SUNDAY, March 20, 2016 (HealthDay News) — Tree pollen season has arrived, but there are a number of ways allergy sufferers can prevent or control their symptoms, an expert says.

Mid-February is when blooming trees begin to flower. By the time the blossoms have fallen in April, grass pollen season is well underway. This is followed by mid-summer and fall allergens, such as ragweed, according to Dr. Jeffrey Culp. He is an assistant professor of medicine and an allergist in the asthma, sinus and allergy program at Vanderbilt University Medical Center, in Nashville, Tenn.

Some allergens stick around all year long, such as pet dander, dust mites and mold, he added.

Most people aren’t allergic to everything, Culp said, and there are a number of ways people can deal with both indoor and outdoor allergens.

The first is doing everything possible to avoid allergens, he suggested.

“This can take different forms. If you are allergic to dust mites, you need to wash your bedding in hot water once a week, get new pillows, use dust mite covers on your pillows and mattress, vacuum regularly and use HEPA air filters,” Culp said in a Vanderbilt news release.

“If pollen is a problem, you should avoid being outside on high pollen-count days and keep the windows closed. Run your air conditioning in your home and car,” Culp said.

“I recommend showering and washing your hair after being outside. Hair is a pollen magnet,” he explained.

“Pollen counts are highest in the morning and rain helps to lower pollen counts, so keep these factors in mind when planning outdoor activities,” Culp advised.

If you do develop allergy symptoms, try saline nasal sprays and/or over-the-counter allergy medications. If these don’t help, the next step is prescription nasal sprays and medications. After that, your best option is allergy shots, Culp said.

More information

The American Academy of Family Physicians has more about allergies.





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Gene Tests May Help Predict Outcomes in Advanced Ovarian Cancer

SATURDAY, March 19, 2016 (HealthDay News) — A special genetic test might help gauge outcomes for women diagnosed with ovarian cancer, a new study suggests.

As researchers at the University of Washington in Seattle explained, advanced ovarian cancer doesn’t progress as rapidly in women who have mutations in certain “DNA repair” genes, known as homologous recombination (HR) genes.

Women with the disease who also have these mutations may survive longer, said a team led by gynecologic oncologist Dr. Barbara Norquist.

The finding may also someday help guide treatment, the researchers said.

Experts said the findings highlight the increasing role of DNA tests in cancer care.

There’s a “wealth of new information that is being generated with regard to the genetics of ovarian cancer, and this study shows how useful such information can be in the everyday management of patients,” said Dr. Mitchell Maiman, chair of obstetrics and gynecology at Staten Island University Hospital in New York City.

The new study came out of a phase 3 clinical drug trial involving Norquist’s team.

The researchers wondered if having mutations in DNA repair genes might affect a woman’s response to combination drug therapy for ovarian cancer.

The study found that the mutations did not affect whether or not a patient would respond to the treatment, but they did affect patient outcomes — including how long the women might live and remain disease-free.

“This is important prognostic information for patients, and highlights the importance of knowing genetic status in clinical trials in ovarian cancer,” Norquist said in a news release from the Society of Gynecologic Oncology.

For the study, the researchers sequenced DNA from blood or tumors or both from nearly 1,200 women using a gene panel test called BROCA-HR.

They found that close to 26 percent of the women had a mutation in at least one of a number of genes predicted to affect DNA repair.

For women without mutations, the median progression-free survival (meaning no progression of disease) was just over a year, while the overall survival was about 3.5 years, the study found.

Carrying a DNA repair gene mutation seemed to extend survival, Norquist’s team found.

For example, for women with mutations in the BRCA1 gene, the outlook was greatly improved. Average progression-free survival was 15.7 months, while their overall survival was 55.3 months (about 4.5 years).

For those with BRCA2 mutations, median progression-free survival was just under 22 months, while overall survival was a little more than 75 months (more than six years).

All of the women who carried mutations in DNA repair genes “had significantly better progression-free and overall survival when compared to those with no mutations,” Norquist noted.

“This underscores the message that women with any type of ovarian cancer should have genetic testing, and they should be included in clinical trials of drugs that work best in the setting of HR [gene] defects,” she said.

For his part, Maiman said the results of the study are “obviously dramatically pertinent for both clinicians and patients alike.

“Although the findings in this study do not directly alter treatment guidelines, the dramatic differences in prognosis with regard to both overall and progression-free survival in mutation-carrier groups can now provide a bit of optimism in those affected,” he said.

Dr. David Fishman directs the Cancer Center at NewYork-Presbyterian/Queens hospital in New York City. He agreed that the study “demonstrates the rapidly evolving use of genetics to optimize and individualize cancer care.

“We are now entering the era of molecular [classification] of cancer which will allow us to optimize patient care,” Fishman said.

The findings were expected to be presented on Saturday in San Diego at the Society of Gynecologic Oncology’s annual meeting. Findings presented at medical meetings are typically considered preliminary until published in a peer-reviewed journal.

More information

The U.S. National Cancer Institute provides more information on ovarian cancer.





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Maria Menounos Snapchats Her Egg-Retrieval Procedure

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

It looks like Maria Menounos and fiancé Keven Undergaro are getting ready to be parents.

Yesterday, the 37-year-old E! News host shared a series of videos and photos on Snapchat while in the hospital having an egg-retrieval procedure. During this medical procedure, patients are sedated while a doctor removes eggs for future in vitro fertilization treatments.

In vitro fertilization (often referred to as IVF) is a type of assisted reproductive technology in which a woman’s eggs are fertilized with sperm in a laboratory to create embryos, which are then implanted in the woman’s womb. Some women choose to undergo this procedure when they’re having trouble getting pregnant (for example, if they have a medical condition such as endometriosis or uterine fibroids). About 165,00 IVF procedures are performed in the U.S. each year, according to a 2014 report from the Society for Assisted Reproductive Technology.

RELATED: Maria Menounos on Her Mom’s Best Cooking Advice: “There Are No Mistakes”

In one of the Snapchat videos, Menounos could be seen lying in a hospital bed with Undergaro by her side as the medication takes effect. “They’re starting to drug me, it feels good,” she says. Other photos showed the actress and author about to undergo the procedure (she captioned a video of her IV bag “egg retrieval time”) and leaving the hospital afterward with sunglasses on.

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

Photo: Maria Menounos/Snapchat

RELATED: Maria Menounos’ Secrets to Success

Although Menounos has yet to share her timeline for a possible pregnancy, she’s openly discussed her desire to start a family in the past.

In 2011, she appeared on Good Morning America with her fertility specialist and said that while she and Undergaro weren’t yet ready to have children, she was planning on freezing her eggs as an “insurance policy” for the future.

“To me, parenting is the most difficult job in the entire world,” she said. “And when I do it, I want to be committed and I want to be 100% ready to take it on and be the best mom I can be. Right now, I don’t see myself to be in that position.”

In an interview with Redbook magazine last year, Menounos opened up about her fertility struggles.

“On my reality show last year, I was talking about freezing my eggs,” she said. “I started the process, but I wasn’t successful, and it’s still not happening. So let’s call it what it is—not a good situation.”

RELATED9 Things Every Woman Must Know About Her Fertility

Undergaro proposed to Menounos just last week when she was a guest on Howard Stern’s SiriusXM radio show. The couple, who started dating in 1998, have been together for nearly 19 years.

“I’ve never been so shocked or surprised in my life,” Menounos said of the engagement on The Jimmy Kimmel Show earlier in the week. “You can see in the video, I’m just in utter shock, my jaw is on the ground the entire time.”

In a 2014 interview with Health, Menounos gushed about her longtime boyfriend. “[If you want to make a change], be smart about it, but just do it. I ask, What’s my worst-case scenario? Keven taught me that,” she said. “Even if everything went away tomorrow, we’d open up a little pizza place and be so happy together.”




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Exercise Helps Ease Psychosis Symptoms

FRIDAY, March 18, 2016 (HealthDay News) — Exercise can reduce symptoms in teens and young adults who had a first psychosis episode, a new study says.

“Establishing an exercise regime for people with psychosis is likely to be much more effective when they are younger, and in the earliest stages of treatment. Getting people into a routine early on also helps set habits for life, which can make a huge difference to their long-term physical and mental health,” study author Joseph Firth, from the University of Manchester in the United Kingdom, said in a university news release.

Young people diagnosed with psychosis typically face a difficult future, with high rates of relapse, unemployment and premature death. And, drugs they may need to take can cause rapid weight gain, the researchers said.

The study included 31 people who had a first psychosis episode. They were between 18 and 35 years old. The study volunteers did personalized workout regimens for 10 weeks under the supervision of a researcher. The participants did 107 minutes of vigorous exercise each week.

At the end of 10 weeks, the patients in the exercise program had a 27 percent reduction in psychiatric symptoms. That was significantly better than how the control group of 7 psychosis patients did, researchers said. The control group received mental health treatment but weren’t given a workout program.

The patients in the exercise group also showed improvement in brain functions and lost some weight, the researchers said.

Previous research has shown that exercise can benefit people with schizophrenia.

The study was published recently in the journal Early Intervention in Psychiatry.

More information

The National Alliance on Mental Illness has more about psychosis.





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Heart Defects at Birth May Raise Risk for PTSD Later in Life

FRIDAY, March 18, 2016 (HealthDay News) — Adults born with heart defects may be at increased risk for post-traumatic stress disorder (PTSD), researchers say.

The reason? High levels of mental stress associated with their condition and treatments, the study authors suggested.

The study included 134 adults who had been born with heart defects, known as congenital heart disease (CHD). The investigators found that 11 percent to 21 percent of these adults had PTSD, depending on the method used to assess symptoms of the disorder.

In comparison, PTSD rates are just 3.5 percent in the general population, the study authors noted. PTSD is a psychiatric disorder that can arise after experiencing life-threatening events such as military combat, natural disasters or personal trauma.

The findings indicate that doctors and caregivers need to watch for signs of PTSD in adult patients with congenital heart disease.

“Although the life expectancy of adults living with CHD has improved, ongoing care may include multiple surgeries and procedures,” study senior author Dr. Yuli Kim, a cardiologist at the Children’s Hospital of Philadelphia, said in a hospital news release. Kim is also director of the Philadelphia Adult Congenital Heart Center.

“These patients remain at risk for both cardiac and non-cardiac effects of their chronic condition, and face unique life stressors that may place them at elevated risk for psychological stress,” Kim explained.

The study was published in the March issue of the American Journal of Cardiology.

Heart defects are the most common type of birth defect in the United States. Surgical and medical advances mean there are more American adults living with congenital heart defects than the number of children born with them each year, the researchers said.

Among the patients in the study with PTSD symptoms, less than half were being treated for the disorder, the researchers said.

“We need to conduct more research to identify measures along the lifespan to support our patients and ensure that they have a good quality of life,” study corresponding author Lisa Deng, also from the Children’s Hospital of Philadelphia, said in the news release.

More information

The U.S. National Heart, Lung, and Blood Institute has more about congenital heart defects.





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CDC: 116 Cases of Zika in U.S. Residents in First 2 Months of Year

By Steven Reinberg
HealthDay Reporter

FRIDAY, March 18, 2016 (HealthDay News) — During the first two months of this year, 116 U.S. residents have tested positive for infection with the Zika virus, and all but one were linked to travel to regions endemic for the virus.

That’s according to a report released Friday by the U.S. Centers for Disease Control and Prevention. Experts there say that of the 116 cases confirmed between Jan. 1 and Feb. 26, 110 involved travel by the patient to a Zika-endemic area, while five involved sexual contact with a person who had recently traveled to such areas.

The remaining case of infection occurred when a mother passed the virus to her child in pregnancy. No details were given on that case.

Zika is a mosquito-borne virus that’s been tied to thousands of cases — mainly in Brazil — of a severe birth defect called microcephaly. In microcephaly, a newborn’s head is smaller than normal, with the potential for long-term neurological damage.

“Among the 115 [U.S.] patients with travel-associated infection, all patients reported clinical illness,” the CDC said. In the majority of cases, symptoms included rash (97 percent of cases), fever and joint pain.

“Zika virus disease should be considered in patients with acute onset of fever, rash, arthralgia [joint pain], or conjunctivitis [pink eye] who traveled to areas with ongoing Zika virus transmission or who had unprotected sex with someone who traveled to one of those areas and developed compatible symptoms within 2 weeks of returning,” the CDC said.

The findings were reported in the March 18 issue of the agency’s Morbidity and Mortality Weekly Report.

Earlier this week, scientists reported more evidence supporting a link between the Zika virus and microcephaly.

Researchers report that one in every 100 pregnant women infected with the virus during the first trimester will give birth to a baby with the birth defect.

The new risk analysis did have one important caveat, however.

“The findings are from the 2013-14 outbreak [of Zika] in French Polynesia, and it remains to be seen whether our findings apply to other countries in the same way,” study co-author Dr. Simon Cauchemez said in a news release from The Lancet. The findings were published in the journal on March 15.

“Data from French Polynesia are particularly important since the outbreak is already over,” said study co-author Arnaud Fontanet, a colleague of Cauchemez at the Institut Pasteur in France.

“This provides us with a small — yet much more complete — dataset than data gathered from an ongoing outbreak,” Fontanet added.

His team believes that the findings strengthen the notion that maternal infection during the first trimester of pregnancy may be especially linked to microcephaly in babies.

Last week, U.S. health officials said they were learning much about the virus. However, the more they learn, the more they realize how much they don’t know, Dr. Anthony Fauci, director of the U.S. National Institute of Allergy and Infectious Diseases, said during a media briefing.

“Unfortunately, the more we learn, the worse things seem to get,” Fauci said.

The Zika virus is suspected of causing an epidemic that started last spring in Brazil, where there have been more than 5,600 suspected or confirmed cases of microcephaly.

Zika has also been linked to Guillain-Barre syndrome, an immune system disorder that can occasionally lead to a fatal form of paralysis.

Dr. Tom Frieden, director of the U.S. Centers for Disease Control and Prevention, said: “We are learning more about Zika every day. The link with microcephaly and other possibly serious birth defects is growing stronger every day. The link to Guillain-Barre syndrome is likely to be proven in the near future, and the documentation that sexual transmission is possible is now proven.”

First discovered in Uganda in 1947, the Zika virus wasn’t thought to pose major health risks until last year, when it became clear that it posed potentially devastating threats to pregnant women.

But, for most other people the virus offers little threat — approximately 80 percent of people who become infected never experience symptoms.

Meanwhile, the virus continues to spread in Latin America and the Caribbean.

It is not expected to pose a significant threat to the United States mainland, federal health officials have said in the past.

In Puerto Rico, however, the situation is “of great concern,” Frieden said.

“Puerto Rico is on the frontline of the battle against Zika,” said Frieden, who had just returned from the island. “And it’s an uphill battle.”

By next year, Frieden said, there could be hundreds of thousands of cases of Zika in the territory, and “thousands of infected pregnant women.”

Last month, President Barack Obama asked Congress for $1.9 billion to fight the Zika virus. To date, Congress has not approved the funding and both Frieden and Fauci expressed concern that efforts to fight Zika are in jeopardy if the funds aren’t forthcoming.

One goal is to create a vaccine that can be given to children before they reach puberty to prevent Zika infection, Fauci said. “We cannot do what needs to be done in a sustained way without those resources,” he said.

The CDC currently has this advice for pregnant women:

  • Consider postponing travel to any area where Zika virus transmission is ongoing.
  • If you must travel to or live in one of these areas, talk to your health-care provider first and strictly follow steps to prevent mosquito bites.
  • If you have a male partner who lives in or has traveled to an area where Zika transmission is ongoing, either use condoms the right way every time, or do not have sex during your pregnancy.

The Zika virus has now spread to over 33 countries and territories in Latin America and the Caribbean. The World Health Organization estimates there could be up to 4 million cases of Zika in the Americas in the next year.

More information

For more on Zika virus, visit the U.S. Centers for Disease Control and Prevention.

To see the CDC list of sites where Zika virus is active and may pose a threat to pregnant women, click here.





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Black Smokers Less Likely to Get Lung Cancer Screening

FRIDAY, March 18, 2016 (HealthDay News) — Differences in smoking habits between black and white Americans may lead to lower lung cancer screening rates for blacks, new research suggests.

Researchers reviewed federal government data from 1965 to 2012. They found that blacks are less likely than whites to start smoking in their late teens, but also less likely to quit as they get older.

The study also found that black smokers use fewer cigarettes a day than white smokers.

These racial differences result in important and somewhat contradictory differences in lifetime cigarette exposure, the Yale School of Public Health team said.

While blacks tend to continue smoking into their later years, the fact that they tend to smoke fewer cigarettes means that have fewer average “pack-years,” calculated by multiplying the number of packs smoked per day by years of smoking, the researchers noted.

“Pack-years” is one of the ways to determine eligibility for lung cancer screening. But, while black smokers may have fewer pack-years, they may have a longer exposure to smoking. That means it’s possible that fewer at-risk black smokers would be targeted for lung cancer screening, the experts said.

This is a problem because black smokers face a similar, possibly even higher risk of death from tobacco-related diseases, the researchers noted.

The study was published online recently in the journal Nicotine & Tobacco Research.

“Racial differences in smoking initiation, cessation, and intensity give rise to substantial differences in risk for tobacco-related diseases,” study author Theodore Holford, a professor of public health at Yale in New Haven, Conn., said in a university news release.

More research is needed, but “this study shows that commonly used measures may give rise to disparities in access to lifesaving interventions,” added Holford, a member of Yale Cancer Center’s Cancer Prevention and Control Program.

More information

The U.S. National Cancer Institute has more on lung cancer screening.





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