Information Assurance in E-Healthcare

Information Assurance in E-Healthcare

Sherrie D. Cannoy (The University of North Carolina at Greensboro, USA) and A. F. Salam (The University of North Carolina at Greensboro, USA)
Copyright: © 2006 |Pages: 8
DOI: 10.4018/978-1-59140-799-7.ch096
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There is growing concern that the healthcare industry has not adopted IT systems as widely and effectively as other industries. Healthcare technological advances generally emerge from the clinical and medical areas rather than clerical and administrative. The healthcare industry is perceived to be 10 to 15 years behind other industries in its use of information technology (Raghupathi & Tan, 1997). Incorporating new technology into the healthcare organization’s processes is risky because of the potential for patient information being disclosed. The purpose of this study is to investigate the information assurance factors involved with security regulations and electronic medical record initiatives—a first necessary step in making the healthcare industry more efficient. Noncompliance of a healthcare organization’s employees with security and privacy policies (i.e., information assurance) can result in legal and financial difficulties, as well as irreparable damage to an organization’s reputation. To implement electronic medical initiatives, it is vital that an organization has compliance with security and privacy policies. E-health technology is a relatively current phenomenon. There are two types of distance-related healthcare that are technology driven. Telehealth is known for involving telemedicine—medicine practiced over a distance, with the impetus of control being in the physician’s hands (Maheu, 2000). E-health involves the patient or physician actively searching for information or a service, usually via the Internet (Maheu). Electronic medical records fall into the e-health category because the physician, healthcare partners, and patient would be able to access the information through an Internet connection. Security and information assurance are critical factors in implementing e-health technologies. There is a lack of a well-developed theoretical framework in which to understand information assurance factors in e-healthcare. The theory of reasoned action (TRA) and technology acceptance model (TAM) enable a conceptual model of information assurance and compliance to be formed in the context of healthcare security and privacy policy. The relationship between behavior and intentions, attitudes, beliefs, and external factors has been supported in previous research and will provide a framework for ensuring compliance to security and privacy policies in healthcare organizations so that HIPAA (Health Insurance Portability and Accountability Act) regulations are enforced and electronic medical records (EMRs) can be securely implemented. Traditionally, records in the healthcare industry have been paper based, enabling strict accessibility to records. This allowed for confidentiality of information to be practically ensured. The uniqueness of healthcare records and the sensitive information they contain is specific to the industry. Over the many years that medical records have been kept, those involved in the field have undertaken a self-imposed rule of stringently protecting the patient information while providing quality care. The patient’s expectation for confidentiality of personally identifiable medical records is also critical. According to Rindfleisch (1997, pp. 95-96), in his study of healthcare IT privacy, the threats to patient information confidentiality are inside the patient-care institution; from within secondary user settings which may exploit data; or from outsider intrusion into medical information. Rindfleisch (1997) examined specific disclosures which could release sensitive information such as emotional problems, fertility and abortions, sexually transmitted diseases, substance abuse, genetic predispositions to disease—all of which could cause embarrassment and could affect insurability, child custody cases, and employment. The process of healthcare treatment includes not only the patient and physician but also nurses, office staff who send out bills and insurance claims, the insurance company, billing clearinghouses, pharmacies, and any other companies to which these processes can be outsourced. There is an estimate that states as many as 400 people may have access to your personal medical information throughout the typical care process (Mercuri, 2004). The government is also a partner in national health concerns, and also maintains databases containing information on contagious diseases, cancer registries, organ donations, and other healthcare information of national interest. (See for a listing of the databases.) With the advent of government mandates such as EMRs and HIPAA regulations, the increased accessibility of sensitive records requires intense effort to create policies that limit access for those who are authorized. Although there is an area of information economics which views information as an asset that can be numerically valued for its benefit, the same perspective has not been adopted in healthcare. Especially in the United States, clinical information and patient care are considered proprietary (Hagland, 2004). There is no specific associated cost with one’s medical information—what damage is done when one’s medical information has been utilized improperly? Even though damages are ill-defined, there are regulations and standards for emerging technology in healthcare. The two most current important security and privacy issues involve HIPAA regulation and the government mandate for EMRs.

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