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SSRIs increase the risk of falls in patients with Dementia


January 19, 2012 - Nursing home residents with dementia who are selected using serotonin inhibitors reuptake (SSRIs), a decline that SSRIs, new research shows do not use the injury as compared withrisk is increased.In addition, the risk is dose dependent, average nonusers, authors, Rotterdam, Erasmus University Medical Centre, Netherlands, reported in S. Carolyn Sterke, MSc, lead 3 times the risk compared with those using food with.

 
Carolyn Sterke
"Even at low doses, SSRIs in nursing home residents with dementia fall hazards are associated with a growing danger," the authors write.A hypnotic or sedative SSRI use with increased risk include even more.The study, published online January 18 in the British Journal of Clinical Pharmacology are.Vulnerable population"The poor are elderly patients," Josepha A. I Cheong, MD, University of Florida College of Medicine, Gainesville, Florida, who was not involved in the research professor of psychiatry, Medscape Medical News has reported.reaction or is likely to potentiate the side effects, including increased sedation, which may predispose a patient is definitely lacking, "he said.The study investigators analyzed the daily drug use and comes on every 2-year period, 248 nursing home residents with dementia January 1, 2006 January 1, 2008. The average age of participants was 82 years.Falls investigators SSRIs and antipsychotics, anxiolytics, hypnotics, sedatives, antidiabetic drugs, beta-blocker eyedrops, cardiovascular drugs, analgesics, anticholinergics, antihistamines, and antivertigo drug is known to increase risk, including other drugs and foods produced using , copies of medical records from the database.The most common SSRI citalopram, followed by paroxetine,,,, sertraline, and fluvoxamine was from. tricyclic antidepressants amitriptyline and nortriptyline were also used, including other antidepressants trazodone and mirtazapine.Need for new treatment protocolsDuring the study period, 152 residents (61.5%) had 683 falls. Thirty eight residents (15.4%) fell once, 114 (46.2%) fell often, authors are reported.Of falls (220 or 32.2%) resulted in a third of an injury. These falls, 10 (1.5%) resulted in a hip fracture, 11 injured in the (1.6%) were other fractures. One resident died as a result of a fall.Furthermore, the 198 falls (30.0%) injuries in other types of open wounds, sprains, bruises, swellings and other results.The study showed that the resulting reduction in the risk of injury increased with age (hazard ratio [HR], 1.05, 95% confidence interval [CI] 1.01 - 1.09), and use of antipsychotics (HR 1.76, 1.18 inCI 95% - 2,63).Increased risk of falls only SSRIs, was seen with the authors of the report. Overall, SSRIs associated with the use of HR 2.50 (- 4.19 95% CI, 1.50) did.The risk of dose dependence is seen with high doses of SSRI was with. Less than a quarter of defined daily doses, the risk increased 31 percent, half the risk in defined daily dose is increased by 73 percent and total daily dose, 198% increase risk (2.98 HR; 95 % CI, 1,94 - 4.57).The authors list several limitations of the study. The different characteristics of the patient, possible talks cytochrome P450, and other drug use, such as benzodiazepines, antihypertensives, and antipsychotics are, concomitantly SSRs with include.Caution when prescribingDevelopment should consider, "he said in a statement that Ms. Sterke."The reason that people fall more often when using these drugs, including SSRIs. Think," he told Medscape Medical News."Central nervous system adverse effects have been other studies, such as daytime drowsiness, sedation, dizziness, extrapyramidal symptoms and Orthostatic hypotension and syncope, which affects the motor system is increased risk of falls with SSRI use To link has been proposed as possible explanations., "he said.Ms. Sterke also believe that doctors prescribe SSRIs to patients before they should be very careful.should be., he said. ""The study results of depression in nursing home professionals to help residents and residents with positive investment activities initiated and helped to demonstrate the least bit worried," he said."The authors take into account other drugs, but how do you say that the falls were due to SSRIs and other drugs can not," Dr. Cheong is the point."We already know that SSRIs and other medications to prevent drug metabolism in small quantities, or may be less than SSRIs authors also say that several factors may be responsible. Study if they had a strong age . nondemented people who were on the same drug combination, "he said.Dr Cheong also said that depression and dementia in nursing home patients, SSRIs may be wrong to prevent a major factor."The most clinicians approach patients on multiple medication regimen when adding an SSRI to monitor the alarm is due, he said.''

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The placebo-controlled ATLAS ACS 2 showed rivaroxaban reduced the risk of both all-cause and cardiovascular mortality while increasing the risk of bleeding and intracranial hemorrhage, but the studies were hindered by early patient withdrawals and missing data. We Don't Know What We're Missing Based on the ATLAS ACS 2 results, FDA reviewer Dr Karen Hicks recommended approval of rivaroxaban for the requested indications except all-cause mortality. However, another FDA reviewer, Dr Thomas Marciniak, was adamant that the trial results are not interpretable because about 12% of the patients had incomplete follow-up, far higher than the 1% to 1.5% differences in the end-point rates between rivaroxaban and placebo. A total of 1294 subjects discontinued the trial prematurely, and the company was only able to contact 183, of which 177 were confirmed to be alive. Because of the patient dropouts, the company adopted a "modified intention-to-treat analysis," whereby patients were observed for 30 days after randomization or the global end date for the trial, instead of observing all the patients until the end of the trial as the FDA originally suggested. Marciniak criticized the sponsor's efforts to follow the patients and said that three patient deaths not counted in the modified intention-to-treat analysis may just be the "tip of the iceberg." Because the percentage of patients whose ultimate vital status remains unknown is much greater than the reported differences in mortality rates, the claimed mortality benefits are not reliable. The majority of the panel sided with Marciniak. For example, Dr Sanjay Kaul (University of California, Los Angeles) voted "no" because "there was enough uncertainty in the quality and robustness of the data that dissuaded me from voting yes. . . . 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