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QIO TRANSMITTAL SERIES 

ISSUE: Confidentiality and Disclosure of Information  -  Printable pages

Process for Disclosure of Information

 

The Foundation will disclose specific information upon receipt of an acceptable data request for such information, provided that 1) the information can be released to the requestor in accordance with confidentiality requirements and 2) the Foundation either possesses the information in the form requested or is able to produce the information from data in its possession.

 

An acceptable data request must in general be 1) in writing, 2) specific as to the precise data required and 3) accompanied by prepayment of the anticipated cost of fulfilling the request.

 

Disclosure of Nonconfidential Information

 

Non-confidential information includes any of the following:

 

1.                The norms, criteria and standards used in review activities;

2.                Winning technical proposals for contracts for the Department of Health and Human Services and winning technical proposals for subcontracts under those contracts;

3.                Copies of documents describing administrative procedures, agreed to between the QIO and institutions or between the QIO and the Medicare intermediary or Medicare carriers;

4.                Routine reports submitted by the QIO to CMS to the extent that they do not contain confidential information;

5.                Summaries of the proceedings of QIO regular and other meetings of the governing body and general membership except for those portions containing confidential information;

6.                Public information (information which has already been disclosed to the public);

7.                Aggregate statistical information that does not implicitly or explicitly identify individual patients, practitioners or reviewers;

8.                Quality review study information including summaries and conclusions from which the identification of patients, practitioners and institutions has been deleted; and

9.                Information describing the characteristics of a quality review study, including a study design and methodology.

 

If the requested data identifies an institution or institutions, the Foundation will notify each identified institution of its intent to disclose information about the institution at   least thirty (30) calendar days prior to the disclosure.  The notice will include a copy of the information to be disclosed. If the institution submits comments to the Foundation, the comments will be attached to the information when it is disclosed or, if the comments are received after disclosure, the comments will be forwarded separately to the requestor.

 

Exceptions to the 30 day comment period requirements exist in cases of imminent danger to individuals or public health and in cases to be disclosed to an agency investigating potential fraud and abuse.  In these cases, notification to the identified institution(s) will be simultaneous with the disclosure.   Any comments received on the disclosed information will be forwarded to the agency to which the information was disclosed.

 

Disclosure of Confidential Information

 

Confidential information includes any of the following:

 

1.                Information that explicitly or implicitly identifies an individual patient, practitioner or reviewer;

2.                Sanction reports and recommendations;

3.                Quality review studies which identify patients, practitioners or institutions (including HCQIP projects); and

4.                QIO deliberations.

 

The Foundation will disclose patient identified information in its possession to the identified patient or the patient's representative if the patient or patient's representative requests the information in writing and, in the case of a request by a patient's representative, the request includes the designation, by the patient, of the representative.   Fifteen days prior to direct disclosure of information to a patient, the Foundation will seek the advice of the attending practitioner who treated the patient regarding the appropriateness of direct disclosure to the patient.  If the attending practitioner states that the released information could harm the patient, the Foundation will disclose the information to the patient's designated representative.  If the patient is mentally, physically or legally unable to designate a representative, the Foundation will disclose the information to a person whom the Foundation determines is responsible for the patient, based on information provided by the medical record, attending practitioner or other reliable source.

 

If the request is in connection with a denial decision the Foundation need not seek the advise of the practitioner who treated the patient regarding the appropriateness of direct disclosure to the patient. In this case, only the information used to support the denial determination will be disclosed.

 

Procedures will be adopted to assure that a person requesting access to his own record, is, in fact, the individual on whom the record is maintained.  Minimal requirements will be put into effect to verify the identity of the individual.

 

Upon request, the Foundation will disclose to particular practitioners, reviewers and institutions, information about themselves.

 

Upon request, the Foundation must disclose to an institution information on a practitioner to the extent that the information displays practice or performance patterns of the practitioner in that institution.

 

The Foundation may disclose to any person, agency or organization, information on a particular practitioner or reviewer with the consent of the practitioner or reviewer provided the information does not identify other individuals.

 

Upon request, the Foundation must disclose to Federal and State agencies responsible for the investigation of fraud and abuse of the Medicare program and licensing and certification information that displays practice or performance patterns of a practitioner or institution.

 

Except for cases involving fraud and abuse, the Foundation will notify a practitioner or institution of the information to be disclosed (including a copy of the information) at least thirty (30) calendar days before disclosure.  Any comments submitted by the practitioner or institution will be forwarded with the information, if received before disclosure, or forwarded separately, if received after disclosure.

 

The Foundation's deliberations concerning patients, practitioners and facilities, which serve as a basis of the Foundation's QIO decisions, shall not be disclosed outside the Foundation, except to the Health Care Financing Administration, the Office of the Inspector General, or the General Accounting Office, as specified in the regulations governing disclosure of QIO information.

 

Redisclosure of Confidential Information by Recipient

 

Disclosure of confidential information by the Foundation will be accompanied by a written statement informing recipient about unauthorized redisclosure.

 

The Foundation will identify those individuals who improperly disclose information to the Office of the Inspector General.

 

Individuals convicted of unauthorized disclosure could be fined up to $1,000 or be imprisoned up to six months or both and liable for costs of prosecution.

 

Redisclosure of confidential information by a recipient is permitted under the following conditions:

 

1.                If QIO approval for redisclosure is given.

2.                If CMS approval is given in order to carry out specific responsibilities of the Secretary.

3.                If it is necessary for CMS to carry out specific responsibilities for appeals.

4.                If a patient has more than one source of reimbursement for health services, the sources (including Medicare and private insurers) may exchange confidential information among themselves as necessary for the payment of claims.

5.                If the person who receives the information can also obtain the information on his/her own from the original source, that individual may redisclose the information in accordance with the confidentiality rules or the originator of the data.

6.                If it is necessary for the General Accounting Office to carry out audit responsibilities.

7.                Information pertaining to a patient or practitioner may be disclosed by that individual provided it does not identify any other patient or practitioner.

8.                An institution may disclose information pertaining to itself providing it does not identify an individual patient or practitioner.

9.                A Government fraud and abuse agency, state licensing or certification agencies, and Federal and state health planning agencies recognized by CMS may disclose information as necessary in a judicial, administrative or other formal legal proceeding resulting from an investigation conducted by the agency and if necessary for state and local public health officials to carry out their responsibilities to protect against an imminent danger to public health.

10.           If it is necessary for the Office of the Inspector General to carry out its statutory responsibilities.

 

Request for Onsite Inspection of Existing Information

 

The Foundation office will be open to the public from 10:00 a.m. to 12:00 noon and from 2:00 p.m. to 4:00 p.m. for inspection of existing information.

 

An appointment will be required.  The appointment may be made by telephone if the request is to inspect any of the following:

 

·   The norms, criteria and standards used in review activities;

·   Winning technical proposals for contracts for the Department of Health and Human Services;

·   Copies of documents describing administrative procedures, agreed to between the Foundation and institutions or between the Foundation and the Medicare intermediary;

·   Public information (information which has already been disclosed to the public).

 

Medicare beneficiaries who have had a QIO denial have the right to review all information used by the Foundation in connection with the denial determination; the beneficiary may designate a representative to examine the information.  (The appointment to review this information may be made by telephone.)  The information to be made available includes the complete medical record in the Foundation's possession, any additional information provided by the physician or provider and any correspondence between the Foundation and the physician and provided that was used in the denial determination.  However, records of Foundation deliberations and any identification of Foundation reviewers or consultants cannot be made available to anyone outside of the Foundation/QIO system.

 

A written request for an appointment must be made in order to inspect any information other than that described above.  Upon receipt of the written request, the Foundation must determine whether the requestor has the right to view the data (if the information is confidential), whether time is required to prepare the information (e.g., to remove identifiers or to collate materials) and whether a comment period is required prior to releasing the information.  The Foundation will respond in writing to the requestor, indicating its determination on the above items and establishing a date and time for the requestor to inspect the data.

 

No staff member will be available to answer questions concerning the information being reviewed or to make copies of any materials.  Requests for copies must be made in writing in accordance with the procedures described above. The procedure for making inquiries regarding data are described below.

 

Inquiries Concerning Information Furnished by the Northeast Health Care Quality Foundation

 

All inquiries regarding any information furnished by the Foundation, whether reviewed onsite at the Foundation office or received in written form, must be made in writing and must be as specific as possible.  Inquiries should be addressed to the Director of Review, who will forward them to the appropriate staff member for response.  Responses to inquiries which do not require the provision of additional data will be made within 10 calendar days of receipt of the inquiry, unless the Foundation requires written clarification from the Health Care Financing Administration or some other source in order to answer the inquiry.  If additional data is required to satisfy the inquiry or if copies of materials viewed onsite are desired, procedures described above will be in effect.

 

November 2002

 

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