2019
DOI: 10.1001/amajethics.2019.8
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Should Immigration Status Information Be Included in a Patient's Health Record?

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Cited by 29 publications
(9 citation statements)
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References 12 publications
(11 reference statements)
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“…This approach was used when HIV infection and AIDS first emerged; during this period, clinicians were hesitant to record the HIV status of patients because of the potential for stigma and discrimination. In the past, practitioners were also reluctant to share patients’ DNA pedigrees and other genetic information that could be used by insurance companies or employers to target asymptomatic patients based on their genetic susceptibilities …”
Section: Discussionmentioning
confidence: 99%
“…This approach was used when HIV infection and AIDS first emerged; during this period, clinicians were hesitant to record the HIV status of patients because of the potential for stigma and discrimination. In the past, practitioners were also reluctant to share patients’ DNA pedigrees and other genetic information that could be used by insurance companies or employers to target asymptomatic patients based on their genetic susceptibilities …”
Section: Discussionmentioning
confidence: 99%
“…Fourth, EDs must have a systematic process for whether or not to screen for patient status. Asking patients about their status can induce fear, and in general, the literature does not recommend documenting status in order to protect the identity of patients [22,27]. However, in practice, physicians or, more commonly, social workers often do ask.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, sharing sensitive patient information outside of the scope of the provider and patient runs the risk of stigmatization and discrimination in vulnerable populations and law enforcement involvement, such as in cases of immigration status. Physicians in cases such as these must balance the professional and ethical responsibilities of justice to provide quality care to all people regardless of their background [7].…”
Section: Legal Considerations For Patient Data In the United Statesmentioning
confidence: 99%