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Two separate surveys found that 66 percent of Americans would be willing to donate their genetic material for medical research (Genetics & Public Policy Center, 2007; Research!America, 2007). However, despite this apparent positive view of genetic research, 92 percent of Americans reported they were concerned about their genetic information being used in a “harmful way” (Genetics & Public Policy Center, 2007). The U.S. healthcare system has significant problems including nursing and physician shortages, massive healthcare costs, poor patient care and reduced revenues, which often lead to organizational mergers. As a result of this and other reasons, IT healthcare is more important than ever and the need for IT experts has expanded exponentially in this area. The IT healthcare infrastructure within the U.S. is especially in need of revamping due to archaic infrastructures, remnant architectures and colossal computer applications.

A review of survey questions to gauge the public willingness to allow their medical records to be used in research can be found in Chapter 2. If the research enterprise is impeded, or if it is less robust, important societal interests are affected. In addition to defining health research and delineating its value to individuals and society, this chapter provides an overview and historical perspective of federal research regulations that were in place long before the Privacy Rule was implemented.

Therefore, tracking clinical experience with the drug is important for identifying relatively rare adverse effects and for determining the effectiveness in different populations or in various circumstances. It is also vital to record and assess experience in clinical practice in order to develop guidelines for best practices and to ensure high-quality patient care. Physicians tend to frequently ignore alerts from clinical decision support systems. A study13 evaluated 18,115 drug alerts in the Boston area and found that 33% of alerts were ignored by the ordering physician. Several clinical trials14,15 have studied the effect of different CDS system modifications to improve physician’s compliance to alerts and have found that “tiering” and “automation of alerts” resulted in improved physician’s compliance to CDS alerts.

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Several studies suggest that the low participation rates by racial and ethnic minority groups are due to their strong distrust of the medical research community compared to the general population (Braunstein et al., 2008; Corbie-Smith et al., 1999; Farmer et al., 2007; Grady et al., 2006; Shavers et al., 2002). Other reasons driving the IT healthcare movement include the desire for more efficient and productive communication between medical entities such as treating physicians, hospitals, private practices and laboratories. Marketing Tech provides digital marketing news and jobs, industry analysis and digital media insight around numerous marketing disciplines; mobile strategy, email marketing, SEO, analytics, social media and much more. All articles are shared with our audience ofover 700,000 marketing and digital media professionalsmaking it a great profile raiser for both yourself and your company. We also add writer’s profiles to our homepage and every article includes a writer biography and a link to your company website.

We’re open to guest contributions There’s always the possibility of becoming regular contributors to the blog. Devine EB, Hansen RN, Wilson-Norton JL, Lawless NM, Fisk AW, Blough DK, et al. The impact of computerized provider order entry on medication errors in a multi specialty group practice. The National Committee on Vital and Health Statistics has noted that “secondary uses” of health data is an ill-defined term, and urges abandoning it in favor of precise description of each use . Trauth JM, Musa D, Siminoff L, Jewell IK, Ricci E. Public attitudes regarding willingness to participate in medical research studies. Shavers VL, Lynch CF, Burmeister LF. Racial differences in factors that influence the willingness to participate in medical research studies.

As noted by the National Committee on Vital and Health Statistics, “Clinically rich information is now more readily available, in a more structured format, and able to be electronically exchanged throughout the health and health care continuum. As a result, the information can be better used for quality improvement, public health, and research, and can significantly contribute to improvements in health and health care for individuals and populations” . The informatics grid recently developed with support from the National Cancer Institute is an example of a how information technologies can facilitate health research by enabling broader sharing of health data while still ensuring regulatory compliance and protecting patient privacy (Box 3-2).

However, many patients probably are not aware that their medical records are being used in information-based research. Some members of the health care community have proposed requiring that all prospective quality improvement activities go through external review , while others have outlined specific criteria to differentiate quality improvement activities from research. Organizations need to identify areas that health information technology might aid in improving patient safety namely, medication safety, guideline adherence, and so forth. To address these difficulties, a number of models have been proposed that outline the criteria IRBs and Privacy Boards should use to distinguish practice and research.