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Most learned people know something about the experiments done on black men in Tuskegee, AL, in the early part of the 20th century: Syphilitic men were enrolled in a study without adequate consent or understanding, and ultimately refused effective treatment in the name of science.
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In an attempt to clarify Department of Health and Human Services (HHS) regulations, the federal Office of Human Research Protections (OHRP) has issued an update to its 2000 guidance on research involving prisoners.
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The main role of a study coordinator is to act as a patient advocate, yet still maintain the integrity and progress of the trial, says Laurie Czaplewski, RN, BSN, clinical trial coordinator with the Mayo Alliance for Clinical Trials in Rochester, MN.
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Clinical trial coordinators can easily become overwhelmed by the myriad tasks they must perform during the studys duration. But the key to keeping a drug or device trial or other research study moving is to do as much advance preparation as possible, say experts.
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Dissatisfied patients. Longer wait times. Patients being treated in the hallways.
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In your ED, the color-coded Broselow Pediatric Emergency Tape, a length-based measuring tape that accurately estimates a childs weight, is probably a familiar sight. But are you using the tape correctly?
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Are you compiling and reporting performance measurement date from two core measures, as required by the Joint Commission on Accreditation of Healthcare Organizations? As of January 2004, youll need to make that three measures.
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Would you like to be responsible for a million-dollar increase in your hospitals bottom line?
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Rising patient infection rates. Adverse patient outcomes. Increased risk to staff. If these arent compelling enough reasons to comply with recent hand hygiene guidelines from the Centers for Disease Control and Prevention (CDC), consider this: The only new 2004 National Patient Safety Goal from the Joint Commission on Accreditation of Healthcare Organizations addresses this area specifically.