(Embargoed Until: 3 P.M. (CT), Monday, September 13, 2004)
(Embargoed Until: 3 P.M. (CT), September 13, 2004)
Embargoed Until: 3 P.M. (CT), Monday, September 13, 2004
Please Note: The FOR THE MEDIA website now has a search feature to enable media to find previous JAMA/Archives news releases on specific medical topics. This search feature link is located on the home page at www.jamamedia.org
EMBARGOED FOR RELEASE UNTIL 3 P.M. (CT), MONDAY, September 13, 2004
To contact John D. Piette, Ph.D., call Kara Gavin at 734/764-2220. To contact editorialist Alex D. Federman, M.D., M.P.H., call Debra Kaplan at 212/659-9045.
MANY PATIENTS NEVER TELL THEIR HEALTH CARE CLINICIANS THEY UNDERUSE MEDICATIONS BECAUSE OF PRESCRIPTION COSTS
CHICAGOAbout one-third of chronically ill adults who underuse medications because of the costs associated with buying the drugs, never tell their health care practitioners, according to an article in the September 13 issue of the Archives of Internal Medicine, one of the JAMA/Archives journals.
Patients concerned with out-of-pocket medication costs often limit their prescription drug use, according to background information in the article. Because chronically ill patients often take multiple medications, they are especially vulnerable to the strain from drug costs, the article states. The underuse of essential medications, including cholesterol-lowering medications, heart medications, asthma medications and antipsychotics, has been associated with increased emergency department visits, nursing home admissions, acute psychiatric hospitalizations, and a decrease in self-reported health status, according to the article.
John D. Piette, Ph.D., from the University of Michigan, Ann Arbor, and colleagues surveyed 660 chronically ill adults (average age, 62.6 years) nationwide who had reported underusing medication the year before due to cost. Of those surveyed, 16 percent were nonwhite, 64 percent had at most a high school education, and 30 percent had an annual household income of $20,000 or less.
Of those surveyed, two thirds never told a clinician (doctor or nurse) in advance that they intended to underuse their medication due to cost, and 35 percent of respondents never discussed the subject at all. Of respondents who did not tell a clinician, 66 percent reported that they had not been asked about their ability to pay for prescriptions. Seventy two percent of patients who talked with their clinicians about medication costs found the conversations to be helpful. However, 31 percent said their medications were never changed to a generic or less expensive replacement. Also, only 30 percent of patients were informed of programs that help pay drug costs, and fewer people were told where to purchase less expensive medication (28 percent).
"This study suggests that most patients who fail to alert clinicians about their medication cost problems are not asked about their ability to pay for their medication, and many perceive that clinicians are unwilling or unable to help them with this problem," the authors write.
The researchers conclude: "As drug costs continue to escalate and the number of adults with chronic illnesses grows, it will be increasingly important for health care providers to take an active role in discussing patients' medication cost problems and appropriate strategies for addressing them."
(Arch Intern Med. 2004;164:1749-1755. Available post-embargo at archinternmed.com)
Editor's Note: This study was supported by grants from the Department of Veterans Affairs, Washington, DC, and the Agency for Healthcare Research and Quality, Rockville, Md.
EDITORIAL: THE STATUS OF DOCTOR-PATIENT COMMUNICATION ABOUT HEALTH CARE COSTS
In an accompanying editorial, Alex D. Federman, M.D., M.P.H., of Mount Sinai School of Medicine, New York, states that "when doctors don't ask and patients don't tell, opportunities to help are missed and patients remain at risk for underusing medications and services."
"The combination of greater cost sharing and higher prices for medical care will increasingly drive patients to forgo medications and other services," Dr. Federman writes. "As the burdens of health care costs increase, physicians have a greater responsibility to direct patients to sources of assistance with health care costs when help is needed, and to select affordable therapies whenever possible."
"Because cost remains a significant barrier to care for many adults, such as the uninsured and the low-income elderly population, major policy initiatives are needed to improve access to care for these vulnerable populations. Meanwhile, physicians should work to facilitate patients' access to care using available resources. At a minimum, physicians can ask patients about problems they might have paying for health care," writes Dr. Federman.
He concludes: "Ultimately, it is the responsibility of the physician to create an atmosphere in which patients can freely discuss matters that affect their health and health care, no matter what the cause."
(Arch Intern Med. 2004;164:1723-1724. Available post-embargo at archinternmed.com)
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail mediarelations{at}jama-archives.org.
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EMBARGOED FOR RELEASE UNTIL 3 P.M. (CT), MONDAY, September 13, 2004
To contact Peter U. Heuschmann, M.D., M.P.H., e-mail: heuschma{at}uni-muenster.de.
STUDY IDENTIFIES MEDICAL AND NEUROLOGICAL COMPLICATIONS THAT INCREASE RISK OF DYING IN THE HOSPITAL AFTER STROKE
CHICAGOPatients who experience medical or neurological complications following stroke, such as pneumonia or brain swelling, are at a greater risk of dying in the hospital, according to an article in the September 13 issue of the Archives of Internal Medicine, one of the JAMA/Archives journals.
According to information in the article, stroke will be the second leading cause of death and disability in the developed world in 2020. However, there is little information on factors that may be associated with dying in the hospital and the impact of neurological complications on early outcomes for patients with stroke.
Peter U. Heuschmann, M.D., M.P.H., of the University of Muenster, Germany, and colleagues studied stroke patients who were admitted to German hospitals between January 1, 2000 and December 31, 2000 to determine factors that may predict risk of death after ischemic stroke (when a blood clot prevents blood from getting to the brain). A total of 13,440 ischemic stroke patients were included in the study.
The researchers found that overall, 4.9 percent of the stroke patients died in the hospital. In women, higher age, severity of stroke, and atrial fibrillation (heart rhythm disorder) were independent predictors for dying in the hospital. In men, diabetes and previous stroke had a significant negative influence on early outcomes after stroke in addition to the factors identified for women. Increased intracranial pressure (a building of pressure inside the skull, often due to swelling of the brain) accounted for 94 percent of deaths for patients with this complication. Pneumonia was the complication that caused the most deaths among the stroke patients, accounting for 31.2 percent of all deaths. The researchers also found that more than half of all in-hospital deaths were caused by serious medical or neurological complications.
"In our study, age, stroke severity, and atrial fibrillation were found to be independent predictors for in-hospital mortality after ischemic stroke in routine clinical care," the authors write. "Diabetes and previous stroke demonstrated a significant impact on in-hospital mortality only in men. Therefore, future studies on early stroke outcome have to consider carefully potential variations in the impact of the investigated variables between men and women."
(Arch Intern Med. 2004;164:1761-1768. Available post-embargo at archinternmed.com)
Editor's Note: The data analyses and the data pooling of the German Stroke Registers Study Group is supported by the German Federal Ministry of Research (BMBF) within the Competence Net Stroke.
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail mediarelations{at}jama-archives.org.
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EMBARGOED FOR RELEASE UNTIL 3 P.M. (CT), MONDAY, September 13, 2004
To contact Brennan M. R. Spiegel, M.D., M.S.H.S., call Rachel Champeau at 310/794-0777.
MANY FACTORS INFLUENCE QUALITY OF LIFE FOR PATIENTS WITH IRRITABLE BOWEL SYNDROME
CHICAGOThe quality of life for patients with irritable bowel syndrome is as related to non-gastrointestinal (GI) symptoms, including tiring easily and feeling tense, as it is to GI symptoms associated with the disorder, according to an article in the September 13 issue of the Archives of Internal Medicine, one of the JAMA/Archives journals.
Irritable bowel syndrome (IBS) is a chronic disorder of the gastrointestinal tract characterized by frequent abdominal pain and abnormal bowel habits. IBS affects 15 percent of the general adult population, results in 3.6 million physician visits annually, and costs more than $8 billion per year. Patients with IBS have worse health-related quality of life (HRQOL) than patients with diabetes or severe kidney disease, the article states. However, data suggest that many physicians do not adequately assess the impact of IBS symptoms and non-disease-related symptoms on their patients' lives and health status.
Brennan M. R. Spiegel, M.D., M.S.H.S., of The David Geffen School of Medicine at the University of California, Los Angeles, and colleagues identified several factors that play a role in the HRQOL in patients with IBS.
The researchers examined 770 patients, 18 years and older (69.1 percent female), with IBS at a university-based referral center. Participants completed a 90-item questionnaire on their symptoms, and a 36-item health survey.
The researchers found seven factors were related to patients' HRQOL: making more than five physician visits per year, tiring easily, low energy, severe symptoms, predominantly painful symptoms, feeling that there is "something seriously wrong with my body," and symptom flares lasting longer than 24 hours. The researchers found that eight factors were related to mental HRQOL: feeling tense, feeling nervous, feeling hopeless, difficulty sleeping, tiring easily, low sexual interest, IBS symptoms interfering with sexual function, and low energy.
"... we have identified specific clinical predictors of mental and physical HRQOL that may facilitate efficient assessment and targeted treatment in patients with IBS," the researchers write. "Whereas physical HRQOL is associated with symptom severity, symptom periodicity, and pain, mental HRQOL is associated with abnormalities in sexuality, mood, and anxiety."
"These findings suggest that rather than focusing on physiological epiphenomena (stool characteristics and subtype of IBS) and potentially misleading clinical factors (age and disease duration), physicians might be better served to gauge global symptom severity, address anxiety, and eliminate factors contributing to chronic stress in patients with IBS."
(Arch Intern Med. 2004;164:1773-1780. Available post-embargo at archinternmed.com)
Editor's Note: This study was supported by a training grant (Dr. Spiegel), a Career Development Award (Drs. Dulai and Mayer), and a grant from the National Institutes of Health, Bethesda, Md., and by an Advanced Career Development Award from the VA HSR&D, Washington, DC (Dr. Gralnek).
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail mediarelations{at}jama-archives.org.
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EMBARGOED FOR RELEASE UNTIL 3 P.M. (CT), MONDAY, September 13, 2004
To contact Eliot L. Berson, M.D., call Mary Leach at 617/573-4170.
USE OF OMEGA-3 FATTY ACID THERAPY DOES NOT SLOW THE PROGRESSION OF RETINITIS PIGMENTOSA IN PATIENTS RECEIVING VITAMIN A TREATMENT
CHICAGOPatients with retinitis pigmentosa, a progressive eye disease that can cause vision loss, who were treated with vitamin A and docosahexaenoic acid (DHA), a kind of omega-3 fatty acid, did not experience slowing of the progression of their disease, according to two articles in the Archives of Ophthalmology, one of the JAMA/Archives journals.
Retinitis pigmentosa is a disorder of the light-collecting cells on the retina-the layer at the back of the eye that collects light-and can cause vision loss. According to the article, retinitis pigmentosa affects about one in 4,000 people worldwide. Previous studies have shown that patients treated with vitamin A have a slower decline in retinal function and vision loss compared to patients who do not take vitamin A. Other studies have found that patients with retinitis pigmentosa tend to have lower blood levels of docosahexaenoic acid (DHA), an omega-3 fatty acid found in the photoreceptor cells.
Eliot L. Berson, M.D., of the Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, and colleagues investigated whether giving oral DHA to patients already receiving vitamin A treatment could halt or slow the course of their retinitis pigmentosa.
The researchers studied 221 patients with retinitis pigmentosa aged 18 to 55 years who were followed over a four year period. Patients were given either 1,200 milligrams per day of DHA or control capsules (placebo), and all were given 15,000 IU/d (international units per day) of vitamin A.
The researchers write that "No significant differences in decline in ocular function were found between the docosahexaenoic acid plus vitamin A (DHA+A) group and control plus vitamin A (control + A) group over a four-year interval."
"In patients assigned to receive 15,000 IU/d of vitamin A, this randomized trial showed that 1,200 milligrams per day of docosahexaenoic acid supplementation over a four-year interval did not, on average, slow the course of disease in patients with retinitis pigmentosa," the researchers conclude.
(Arch Ophthalmol. 2004;122:1297-1305. Available post-embargo at archophthalmol.com)
In a separate analysis from the same study also reported in this issue of The Archives of Ophthalmology, Dr. Berson and colleagues investigated the effect of DHA and vitamin A treatment in the patients with retinitis pigmentosa according to whether or not patients were taking vitamin A before enrolling in the study. Thirty percent of those patients were not taking vitamin A prior to entering the study.
The researchers found that "Among patients not taking vitamin A prior to entry, those in the DHA+A group [30 patients] had a slower decline in [vision loss] than those in the control +A group [35 patients] over the first two years; these differences were not observed in years three and four of follow-up or among patients taking vitamin A prior to entry."
The researchers conclude: "For patients with retinitis pigmentosa beginning vitamin A therapy, addition of docosahexaenoic acid, 1,200 milligrams per day, slowed the course of disease for two years. Among patients on vitamin A for at least two years, a diet rich in omega-3 fatty acids (0.20 grams per day or more) slowed the decline in [vision loss]."
"The present study also supports a previous recommendation that most adults with the typical forms of retinitis pigmentosa should continue to take 15,000 IU/d of vitamin A palmitate under medical supervision to slow the course of their condition," the authors write. "It should be noted that the precursor of vitamin A, betacarotene, is not predictably converted into vitamin A; therefore, betacarotene is not a suitable substitute for vitamin A palmitate in the context of this treatment regimen."
(Arch Ophthalmol. 2004;122:1306-1314. Available post-embargo at archophthalmol.com)
Editor's Note: Both studies were supported by a grant from the National Eye Institute, Bethesda, Md., and in part by the Foundation Fighting Blindness, Owings Mills, Md.
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail mediarelations{at}jama-archives.org.
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EMBARGOED FOR RELEASE UNTIL 3 P.M. (CT), MONDAY, September 13, 2004
To contact corresponding author James C. Tsai, M.D., call Elizabeth Streich at 212/305-6535.
CORNEAL THICKNESS MAY INFLUENCE DECISION REGARDING TREATMENT OPTIONS FOR PATIENTS WITH GLAUCOMA
CHICAGOThickness of the cornea, the thin, transparent layer covering the eye, may be an important factor in considering treatment options for patients with glaucoma, according to an article appearing in the September issue of the Archives of Ophthalmology, one of the JAMA/Archives journals.
According to information in the article, central corneal thickness (CTT) can effect the accuracy of intraocular pressure (IOP) measurements. Elevated intraocular pressure (pressure inside the eyeball) is a strong indicator of glaucoma, a disease of the optic nerve that can cause vision loss. Patients with decreased CCT measurements are at an increased risk for developing glaucoma, the article states.
Carolyn Y. Shih, M.D., of the Edward S. Harkness Eye Institute, Columbia University, New York, and colleagues evaluated the effect of CCT measurements on decisions regarding clinical management of 188 patients with glaucoma or suspected glaucoma.
The researchers measured CCT and IOP for each participant. Using an algorithm, the researchers adjusted the IOP measurements based on their findings from the CCT measurements. Adjustments in therapy-use of eye drops, or addition or cancellation of laser therapy or surgery-were recorded for patients whose IOP was adjusted by 1.5 mm Hg (millimeters of mercury, the unit of measurement for pressure inside the eye) or more based on the CCT findings (referred to in the paper as "measurement-significant adjustment").
Of 188 patients, 105 (55.9 percent) had a measurement-significant adjustment in their IOP measurements, with 67 patients (35.6 percent) having adjustments between 1.5 and 3.0 mm Hg, with 38 patients (20.2 percent) having an outcomes-significant IOP adjustment. Sixteen patients (8.5 percent) had a change in eye drop therapy, four (2.1 percent) had a change regarding laser therapy, and six (3.2 percent) had a decision change regarding glaucoma surgery.
"Although some authors have reported that patients may be misdiagnosed because of the absence of CCT determination or the subsequent adjustment of IOP, we are not aware of any studies that have assessed the effect of CCT-associated IOP adjustments on glaucoma clinical management," write the researchers.
"Based on our analysis, there appears to be clinical usefulness in the IOP corrections, as approximately 8 percent to 10 percent of the patients had a change in their medication therapy, about 2 percent had a change in the recommendation (or deferment) of laser procedures, and about 3 percent had a change in the recommendation (or deferment) of glaucoma incisional surgery," write the authors.
They conclude: "… central corneal thickness has a significant effect on the clinical management of patients with glaucoma and glaucoma suspect [suspected glaucoma]."
(Arch Ophthalmol. 2004;122:1270-1275. Available post-embargo at archophthalmol.com)
Editor's Note: This study was supported by the Columbia University Homer McK. Rees Scholar Award (Dr. Tsai) and Eye Surgery Fund (Dr. Tsai) and by an unrestricted departmental grant from Research to Prevent Blindness, New York.
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail mediarelations{at}jama-archives.org.
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EMBARGOED FOR RELEASE UNTIL 3 P.M. (CT), MONDAY, September 13, 2004
To contact Perminder Sachdev, M.D., Ph.D., F.R.A.N.Z.C.P., e-mail: p.sachdev{at}unsw.edu.au.
ELEVATED HOMOCYSTEINE LEVELS MAY BE RELATED TO CHANGES IN DEEP BRAIN TISSUE
CHICAGOHigher blood levels of homocysteine (HCY), an amino acid in the body, may be associated with changes in deep brain tissue in middle-aged men, according to an article in the September issue of the Archives of Neurology, one of the JAMA/Archives journals.
According to the article, high HCY levels have been associated with an increased risk for vascular diseases, and some studies have suggested that HCY may also increase the risk for brain atrophy and Alzheimer disease. Other studies have shown an inverse relationship between elevated HCY levels and cognitive functioning, the article states.
Perminder Sachdev, M.D., Ph.D., F.R.A.N.Z.C.P., of the University of New South Wales, Sydney, Australia, and colleagues examined the relationship between HCY levels and findings from brain magnetic resonance imaging (MRI) and cognitive function among healthy individuals aged 60 to 64 years old. There were 196 men and 189 women included in the study.
Blood samples from each participant were used to measure HCY levels. Participants also had MRI of their brains and underwent a battery of cognitive tests administered within three months of the MRI and blood examinations.
The researchers found that HCY levels did not have a significant relationship with brain atrophy, but high HCY levels in men were related to changes in deep white matter hyperintensities in the brain, which appeared on the MRI.
"Total HCY level is independently related to leukoaraiosis [deep white matter hyperintensities] in middle-aged men, and this may be functionally relevant in the form of mild cognitive impairment," write the authors.
"Contrary to expectation and based on our finding in a previous study involving somewhat older individuals, tHCY [total HCY] levels did not relate with brain atrophy," the researchers write. "The subjects in our current study were younger than in the previously reported studies, and it is possible that the effect of tHCY levels on brain structure does not manifest until later in life, possibly at age 70 years and older."
(Arch Neurol. 2004;61:1369-1376. Available post-embargo at archneurol.com)
Editor's Note: This study was supported by grants from the National Health and Medical Research Council of Australia, Canberra.
For more information, contact JAMA/Archives media relations at 312/464-JAMA (5262) or e-mail mediarelations{at}jama-archives.org.
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