Patient access to records: the invisible confidentiality right
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Patient access to records: the invisible confidentiality right Author: Bruce Borkosky, Psy.D.1 Journal: The National Psychologist, 22(5), 9-10. Cite: Borkosky, B. G. (2013). Patient access to records: The invisible confidentiality right. The National Psychologist, 22(5), 9- 10. CONFIDENTIALITY WAS ALWAYS REQUIRED, BUT ACCESS IS NEW Confidentiality1 has been around since Hippocrates. In contrast, the patient’s right to obtain a copy of her records (patient access2) is a relatively recent concept. This may be a surprise, be- cause patients have had a legal right to their records for 30+ years. However, prior to the 1970’s, patients had no right to access their records. No state or federal statutes required it, and profes- sional associations3 advocated denial. Some patients had to obtain a court order to gain access4. The APA has been a laggard here. The first mention of access rights occurred in 19925, but only in regards to test data, and only as an exception to confidentiality (2.02). Psychologists could withhold records, except to patients; but psychologists were permitted to withhold access if they determined the access was “inappropriate”. It wasn’t until the enactment of HIPAA6, that the eth- ics code began to address access rights. ACCESS IS NOT REQUIRED BY THE APA Although HIPAA mandates access, official APA policy sees things differently. Here is a sam- pling: - The Forensic Guidelines7 - a forensic patient has no right of access. - The Record Keeping Guidelines8, ASPPB Code of Conduct9, ASPPB Model Act10, Rights and Responsibilities of Test Takers11, and Guidelines for Test User Qualifications12 each refer to confidentiality, but do not mention access rights. - Although the 2002 ethics code13 requires release of test data with a written release (9.04a), records can be withheld by institutional policy or legal proceedings (3.05c), courts (9.04b), and organizational clients (4.05a). Finally, psychologists are not required to release records (using the permissive “may” 4.05a). 1 Independent Practice. forensicpsychologist@outlook.commailto:drborkosky@gmail.com, 800-919-9008, skype: Bruce- Borkosky Page 1
PRACTITIONERS OFTEN REFUSE ACCESS This position by the APA may be part of the reason that access to records has been14, and continues to be15, controversial16, and a topic of heated listserve discussions17. Psychologists re- fuse to release records to patients18, third parties19, the courts20, non-psychologists21, and attor- neys22, sometimes enlisting the Court in their efforts23 (although courts are rarely supportive24). Denial of access is a top Health Insurance Portability and Accountability Act (HIPAA) complaint against healthcare providers.25,26 Many states have laws that prohibit release of test data to nonpsychologists.27 HOWEVER, ACCESS IS REQUIRED BY LAW This denial or access is surprising, because state and federal laws require access. Every state except for three (NC, IA, WY) has laws requiring access28,29,30,31. Further, for the vast ma- jority of psychologists who are regulated by HIPAA, HIPAA preempts any state laws that might limit access32. Finally, patient access is ethical: AUTONOMY The EPPCC uses an unusual wording for Principle E (normally referred to as autonomy33), perhaps to emphasize that respect for autonomy requires more than acquiescence to the patient’s choices – it’s a positive obligation. One should actively enable the patient’s capacity for free choice, including disclosing information to the patient that increases understanding, fosters deci- sion making, and nurtures their capacity as a free agent. Privacy, confidentiality, privilege, informed consent and access comprise these infor- mation-based facets of the autonomy right. Patients decide to consent to services. Then they choose to share private information with the psychologist, and finally, determine whether (and with whom) to disclose that information to third parties. Psychologists demonstrate respect for these rights by obtaining written informed consent to treatment and written authorization to re- lease information. Exactly as we demonstrate respect for the patient in handling their information in these ways, we should also respect the patient enough to let them know what information is contained in those records. Further, access is consistent with informed consent – a patient must know what information is going to be released, so they can determine whether to release the rec- ords. NONMALEFICENCE A number of scholarly arguments have offered as reasons to withhold access34. Some scholars be- lieve that the patient might be harmed by the information in the records.35,36,37 However, there is little empirical evidence of such harm38, and there is evidence of no harm.39,40 On the other hand, patients may be harmed when access is refused. Records may contain errors, other professionals may need the records to perform their jobs, and the patient may need access in order to make im- portant decisions. If the information is needed by the patient or others, refusing to release the rec- ords can result in harm to the patient. HONESTY (INTEGRITY) Honesty refers to comprehensive, accurate, and objective transmission of information, in- cluding patient understanding. When we withhold information, we convert our relationship with the patient from one of respect to paternalism; we make the patient dependent vulnerable to a Page 2
range of future harms.41 Others may wonder what we have to hide. Conversely, access to records increases openness and transparency, and is itself clarifying. JUSTICE Justice is a broad topic, far too wide-ranging for our discussion here. However, in part, jus- tice refers to fairness, protection of civil liberties,42 equal treatment,43 equitable distribution of services, and guarding against bias and prejudice44. Under various theories of justice, it can be ar- gued that patient control over, and access to, their records is just. According to formal justice, equals should be treated equally; when some patients are permitted access to their records but oth- ers are not (e.g., clinical vs. forensic), equals are treated disparately and unjustly.45 Under Liber- tarian views of justice, control over the distribution of one’s records affirms an individual’s lib- erty and property rights.46 Courts have established the patient’s common law property right to the information in their records47. The transfer of this informational ‘property’, is only just if it is freely chosen by the patient. In summary, although required by law, psychologists often refuse to release records. Alt- hough permitting access is the more ethical path, it’s surprisingly absent from APA ethical guide- lines. Psychologists who believe that refusing to release records is ethical may face (in additional to legal sanctions), a serious ethical dilemma, when organizations such as the Veteran Admin- istration make access easier by placing records online. The APA should clarify this issue in future guidelines. REFERENCES 1. Bersoff, Donald N. (2000). Confidentiality. In (A. E. Kazdin, Ed.) Encyclopedia of psychology. Washington, D.C.: American Psychological Association. doi: 10.1037/10517-097 2. Westin, Alan F. (1977). Medical records: should patients have access? Hastings Center Re- port, 7(6), 23-28. DOI: 10.2307/3560879 3. Rosenman H. (1997). Patients’ Rights to Access their Medical Records: An Argument for Uni- form Recognition of a Right of Access in the United State and Australia. Fordham International Law Journal. 21(4). p. 1500–1557. Available from: http://ir.lawnet.fordham.edu/cgi/viewcon- tent.cgi?article=1571&context=ilj 4. Ross, S. E., & Chen-Tan, L. (2003). Effects of Promoting Patient Access to Medical Records: A Review, The. Journal of the American Medical Informatics Association, 10(2), 129–138. doi:10.1197/jamia.M1147 5. American Psychological Association Ethics Committee. (1992). Ethical Principles of Psycholo- gists and Code of Conduct 1992. American Psychologist, 47(12), 1597–1611. doi:10.1037/0003- 066X.47.12.1597 6. Office for Civil Rights Department of Health and Human Services. (2002). Standards for Privacy of Individually Identifiable Health Information: final rule. Federal Register, 67(157), 53182– 53273. Available from: http://www.gpo.gov/fdsys/pkg/FR-2002-08-14/pdf/02-20554.pdf Page 3
7. American Psychological Association. (2013). Specialty guidelines for forensic psychology. The American Psychologist, 68(1), 7–19. doi:10.1037/a0029889 8. American Psychological Association. (2007). Record keeping guidelines. The American psycholo- gist, 62(9), 993–1004. doi:10.1037/0003-066X.62.9.993 9. http://www.ok.gov/OSBEP/documents/ASPPB_Code_of_Conduct_2005[1].pdf 10. http://c.ymcdn.com/sites/www.asppb.net/resource/resmgr/guidelines/final_approved_mlra_no- vember.pdf 11. Test Taker Rights and Responsibilities Working Group of the Joint Committee on Testing Prac- tices. (1998). Rights and Responsibilities Of Test Takers. Guidelines and Expectations. doi: 10.1037/e302942004-001 12. Turner, S. M., DeMers, S. T., Fox, H. R., & Reed, G. (2001). APA's guidelines for test user quali- fications: An executive summary. American Psychologist, 56(12), 1099-1113. doi:10.1037/0003- 066X.56.12.1099 13. American Psychological Association. (2002). Ethical Principles of Psychologists and Code of Conduct. American Psychologist, 57(12), 1060–1073. doi:10.1037//0003-066X.57.12.1060 14. Vane, J. (1972). Getting Information from School and Clinical Psychologists. Professional Psy- chology, 3(3), 205–208. Doi: 10.1037/h0021362 15. Erard, R. E. (2013). An Ethical Prohibition that Isn’t And Never Really Was. National Psycholo- gist, 22(2), 8–9. Retrieved from http://nationalpsychologist.com/2013/03/an-ethical-prohibition- that-isnt-and-never-really-was/101860.html 16. Bush, S. S., Rapp, D. L., & Ferber, P. S. (2010). Maximizing test security in forensic neuropsy- chology. In A. M. J. Horton & lawrence C. Hartlage (Eds.), The Handbook of Forensic Neuropsy- chology (2nd ed., pp. 177–196). New York: Springer Publishing Co. 17. psylaw-l@listserv.unl.edu, bestinterests-talk@lists.washlaw.edu, FORENSICNP@listserv.ua.edu 18. Bush, S. S., Connell, M. A., & Denney, R. L. (2006). Documentation of findings and opinions. In Ethical practice in forensic psychology: A systematic model for decision making (pp. 91–112). Washington, D.C.: American Psychological Assn. doi: 10.1037/11469-005 19. Bush, S. S., & Martin, T. A. (2010). The Ethical and Clinical Practice of Disclosing Raw Test Data : Addressing the Ongoing Debate. Applied Neuropsychology : Adult, 13(2), 115–124. Doi: 10.1207/s15324826an1302_6 20. Lees-Haley, P. R., & Courtney, J. C. (2000). Disclosure of tests and raw test data to the courts: a need for reform. Neuropsychology Review, 10(3), 169–174; discussion 175–182. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/10983900 21. Kaufmann, Paul M. (2005). Protecting the objectivity, fairness, and integrity of neuropsychologi- cal evaluations in litigation. A privilege second to none? The Journal of legal medicine, 26(1), 95– 131. doi: 10.1080/01947640590918007 Page 4
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