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Cardinal Health offers grants to prescription drug-abuse programs

BY Alaric DeArment

DUBLIN, Ohio — Cardinal Health’s philanthropic division is offering grants to organizations for programs to prevent abuse and misuse of prescription drugs.

The Cardinal Health Foundation said it was inviting non-profits in 18 locations around the country, as well as Puerto Rico, to apply for grant funding. The announcement marks the fourth year of the foundation’s Prescription Drug Abuse and Misuse Prevention Grant Program.

The grant program will support initiatives that increase awareness of and willingness to openly discuss prescription drug abuse, increase knowledge about how to properly dispose of prescription drugs and increase knowledge about how to reduce unlawful access to them.

Grants ranging from $5,000 to $15,000 will be given to non-profits in Albuquerque, N.M.; Atlanta; central Ohio; Delaware; Denver; El Paso, Texas; Hudson, Wis.; Lakeland and Tampa, Fla.; LaVergne, Tenn.; Little Rock, Ark.; Syracuse, N.Y., and northeast Queens in New York City; northern Chicago; Radcliff, Ky.; Seattle; St. Louis; Wheeling, W.Va.; and Puerto Rico.

 

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For patients with rare diseases, impact goes way beyond the disease itself

BY Jim Frederick

It’s tough enough to be afflicted with one of the more than 7,000 rare and poorly understood diseases that plague the world’s population, but patients who fall victim to one or more of those conditions also have to cope with the emotional, physical and financial toll that comes with them. Rare diseases afflict some 350 million people worldwide. And even in the U.S. with its relatively high standard of health care, patients with a rare condition often face a years-long odyssey of misread diagnoses, visits to multiple doctors and severe economic and emotional strain before their condition is properly diagnosed and they can begin effective treatment. That’s according to the Rare Disease Impact Report from Shire Human Genetic Therapies, presented this month at the World Orphan Drug Congress.

For the hundreds of patients polled by researchers in the U.S. and United Kingdom, “it takes on average 7.6 years in the U.S. [and] on average 5.6 years in the U.K. for a patient with a rare disease to receive a proper diagnosis,” noted the report. What’s more, researchers reported, “in order to get a proper diagnosis, a patient typically visits up to eight physicians,” including four primary care doctors and four specialists.”

Doctors, patients and caregivers are plagued by a “lack of resources and information to address rare diseases,” researchers found in their survey of more than 1,000 patients, caregivers, doctors and payers. That means serious emotional and financial hardship for patients and their families, researchers report, “particularly for those where the hope of treatment is minimal.”

The health system is just not yet equipped to handle these patients. “The entire care journey for many patients is characterized by misdiagnosis, conflicting medical opinions and emotional stress,” said Nicole Boice, CEO of Global Genes RARE Project, a patient advocacy organization that participated in the research project.

What can pharmacists in any setting do to alleviate the hardship? Participating in more collaborative-care efforts can help — both by improving the decision-making platform on which diagnostic decisions and treatment regimens are created, and by integrating points of care and patient records as those patients go through the steps required to properly assess and treat their rare diseases. And, of course, pharmacists can be the patient’s most accessible source of counseling, ongoing concern and help in managing and monitoring a condition, if the pharmacist is working in collaboration with the patient’s complete network of professional care, and is kept in the information loop.

Any other thoughts on what role pharmacists can play for patients going through “the entire care journey?” Please share your thoughts by clicking on the comment link.

 

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Medication-related waste hits poorest states harder, ESI study finds

BY Alaric DeArment

ORLANDO, Fla. — Unnecessary spending related to medications totaled nearly half a trillion dollars last year, and much of that was in the poorest states in the country, according to pharmacy benefit manager Express Scripts.

ESI said the country wasted $418 billion on bad medication-related decisions, including $55.8 billion spent on higher-priced medications when cheaper alternatives were available; and $269.4 billion went to expenses related to poor medication adherence.

On a state-by-state level, Mississippi, the poorest state in the country, had the most wasteful spending, totaling $1,622.76 per resident. Other poor states with a high degree of waste included Louisiana, Arkansas, Alabama, Kentucky, Tennessee, South Carolina, New Mexico and Oklahoma. States in the Midwest and Northeast had the lowest levels of avoidable costs, with Vermont having the lowest overall at $1,004.39 per person.

 

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