Electonic Health Record Paper

811 Words2 Pages

Electronic Health Record Paper

Introduction

According to the Centers for Medicare & Medicaid Services (CMS), “an EHR is an electronic version of a patients medical history, that is maintained by the provider over time, and may include all of the key administrative clinical data relevant to that persons care under a particular provider, including demographics, progress notes, problems, medications, vital signs, past medical history, immunizations, laboratory data and radiology reports”. (www.cms.gov, 2012). EHRs will replace paper health care records, in aid to help health caregivers provide quality patient care. It is supposed to improve quality care, reduce cost, and help resolve medication errors to help achieve best outcomes for the patient overall health care. In this paper I will discuss about the national electronic health record (EHR) mandate. I will then describe the current plan and status of my health care facility of employment in implementing this mandate. I will also analyze the plan, progress, and challenges to patient confidentiality and patient self-determination.

National EHR Mandate

The idea of mandating EHR began in 2004 when President Bush introduced his plan to have americans health records digital by 2014 to ensure safe medical practices. Having EHR would promote less medical errors, more collaboration amongst health care professionals, and reduce costs in providing quality care. It was later decided under the Obama administration in 2009 to continue with President Bush goals of EHRs and then link quality of care and payment to improve medical care and control cost of ...

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...s to dealing with EHRs. “Because practitioners, including nurses, cannot completely control access to computerized databases, concern arises that patients may withhold important health information or refrain from seeking care due to fear that their records will not remain private”. (Burkhart & Nathaniel, 2008, p. 285). Patients have the right to know who has access to their medical information and how it is being used. “It suggests that while health systems hold confidential information about patients, it is not the system’s right to use this information as it chooses. Rather, the system needs to secure patients’ consent to transfer records or data to a third party, even it is another medical caretaker”. (Elwyn & Miron-Shatz, 2011). Therefore patients should have the ability to control what is going in and out of their health records and grant access to it.

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