Thank you very much.
The Canadian Medical Association, CMA, is pleased to be here today to participate in your review of the Personal Information Protection and Electronic Documents Act, or PIPEDA. The CMA has had a long-standing interest in privacy-related matters, including enhancing measures to protect and promote the privacy of health information. We welcome the opportunity to share our policies and thoughts on these vital matters.
As a pediatric oncologist from Winnipeg and chair of the CMA's committee on ethics, I come here today with one bottom line. Physicians have always taken, and continue to take, their patients' privacy very seriously. This is the cornerstone of the special bond between patients and their doctor and has been thus since the time of Hippocrates. In recognition of the importance of privacy, the CMA has produced such documents as the CMA code of ethics and the CMA health information privacy code to guide our more than 64,000 members across the country. These documents existed before the federal government introduced PIPEDA. We speak to you today out of our concern for protecting and ensuring the privacy of medical information.
We would like to raise three specific issues. The first is recognition in law of the unique nature of health care, the second is physician information as work product, and the third is emerging privacy and health information issues.
To the first point, recognition in law of the unique nature of health care, I would like to highlight the importance of recognizing in law the special circumstances of protecting health information. In fact, when PIPEDA was first being debated, CMA posed questions about the scope of the act and was told the legislation, originally designed for commerce and the private sector, would not capture health information. We were also told that even if it did, PIPEDA wouldn't change how we practised medicine.
The passing of PIPEDA generated enough concern and uncertainty that government agreed to delay its application to health for three years. For example, PIPEDA failed to clarify the issue of implied consent for the sharing of patient information among health professionals providing care. For example, when the family physician says to a patient they're going to be sent to see an oncologist to run some tests and the patient agrees and follows that course of action, then clearly there is consent to the sharing of their health information with others. As an oncologist, I assume there is consent to send the test results to other specialists I may need to consult to advance the patient's care in a timely fashion. This, however, needed to be addressed before PIPEDA was applied to health care.
The delayed application allowed the federal government and the health care community to work together and develop a set of guidelines to apply PIPEDA. The resulting PIPEDA awareness-raising tools, known as PARTs, contain a series of questions and answers that make up guidelines for health care providers. They answered many of our concerns, provided necessary definitions, and allowed for the implied consent model to continue to be used within the circle of care. The CMA applauds the government for this collaborative effort. The results and guidelines have been used by health care providers ever since.
However, we remain concerned that the PARTs guidelines have no legal status. This limitation creates a degree of uncertainty that the CMA would like this legislative review to see addressed by ensuring the PARTs series of questions and answers are referenced in PIPEDA. In addition to participating in the PARTs initiative since PIPEDA's implementation, the CMA has designed practical tools for physicians and patients. We've adopted the CMA policy, “Principles Concerning Physician Information”, to address the importance of protecting the privacy of physician information. We've produced Privacy in Practice: A Handbook for Canadian Physicians to help physicians maintain best practices in the protection of patient health information. Finally, CMA PrivacyWizard™ was created to help physicians record their current privacy practices, communicate these to patients, and identify possible areas for enhancement.
The second issue I'd like to address is physician practice information as “work product”. I referred earlier to CMA's policy document on physician information. The CMA strongly believes physicians have legitimate privacy concerns about the use by third parties of information such as prescribing and other practice data for commercial purposes. Currently deemed “work product”, this information can be collected, used, and disclosed without consent.
We feel that PIPEDA inadequately protects this information. We recognize that it is information generated out of the patient-physician relationship. We disagreed with findings of the previous Privacy Commissioner that physician prescribing information is not subject to PIPEDA's privacy protection provisions for personal information. The CMA has consistently advocated that physician prescribing data and other practice information is personal information, and appeared as an intervenor in a Federal Court review of this issue that was ultimately settled by the main parties.
As well, insufficient regard for the privacy of prescribing and other physician data could have a negative impact on the sanctity of the physician-patient relationship. Patients confide highly sensitive information to physicians with the expectation that this information will be kept in the strictest confidence. This expectation exists because they know that physicians are under ethical and regulatory dictates to safeguard their information and that physicians take these responsibilities very seriously. The perceived and indeed actual loss of control by physicians over information created in the patient encounter, such as prescribing data, could undermine the confidence and faith of our patients that we are able to safeguard their health information.
This concern is not hypothetical. For physicians, so-called work product information also encompasses such practice patterns as discharge rates, referral rates, billing patterns, hospital lengths of stay, complaints, peer review results, mortality, and readmittance rates.
With the advent of electronic medical records and growth in pay-for-performance and outcome-based incentive programs for physicians, there is an enormous potential for the resulting physician performance data or work product to be mined by other parties and used to influence performance review—traditionally the purview of the medical licensing authorities—as well as decisions around treatment funding and system planning.
The lack of transparency in the sale and compilation of physicians' prescribing and other performance data means that physicians might find themselves to be the unwitting subjects and targets of marketing research. We believe practice decisions must be made in the best interests of patients, not the bottom-line interests of business and marketers.
CMA therefore recommends a legislative change to include physician information as personal information under PIPEDA. Legislation in Quebec provides an example that is consistent with CMA's approach, since it requires regulatory oversight and gives individuals the right to opt out of the collection, use, and disclosure of professional information.
Finally, I would like to address emerging privacy and health information issues. With budgetary and demographic pressures, our health care system is under strain. Physicians are striving to deliver timely quality care to patients, often with competing and multiple demands. Physicians are therefore seeking assurances from lawmakers that any amendments to PIPEDA will take into account the potential impact on them and their patients.
Therefore, we seek assurances that, one, health care is recognized as unique when it comes to the disclosure of personal information before the transfer of a business, such as one physician transferring his or her practice to another. This is already regulated at the provincial level through the appropriate licensing bodies. As a general rule, physicians must give notice to the public, whether via a newspaper ad or a notice in the office, about the change in practice.
Secondly, we would like the federal government to consider the impact of the transborder flow of personal information on telehealth and electronic health record activities. Communications between patients and physicians via electronic means are likely to increase and to move across geographic boundaries with increasing frequency.
Finally, we would like the federal government to study the issue of international cross-border data flows, particularly among Canadian researchers who receive funding from U.S. drug companies. These arrangements should be governed by Canadian law, PIPEDA, not American, such as HIPAA or the U.S. Patriot Act.
In closing, the privacy protection of personal health information is a responsibility that my colleagues and I do not take lightly. It is a key pillar of our relationship with Canadians. They not only expect it, they deserve it.
I look forward to taking questions from committee members.
Thank you.