Frequently Asked Questions

Information Blocking

Electronic Health Information

When information blocking is no longer limited to the subset that is represented by data elements in the United States Core Data for Interoperability (USCDI), what information will be covered by information blocking regulations as “electronic health information (EHI)”?

We have focused the EHI definition on terms that are used in the HIPAA Rules and that are widely understood in the health care industry as well as on a set of health information that is currently collected, maintained, and made available for access, exchange, and use by actors. On and after October 6, 2022, the definition of information blocking will apply to the full scope of EHI (as defined in 45 CFR 171.102):  

Electronic health information (EHI) means electronic protected health information as defined in 45 CFR 160.103 to the extent that it would be included in a designated record set as defined in 45 CFR 164.501regardless of whether the group of records are used or maintained by or for a covered entity as defined in 45 CFR 160.103, but EHI shall not include:

     (1) Psychotherapy notes as defined in 45 CFR 164.501; or

     (2) Information compiled in reasonable anticipation of, or for use in, a civil, criminal, or administrative action or proceeding.” (emphasis added)

EHI as defined for the purposes of information blocking is information that is consistent with the definitions of electronic protected health information (ePHI) and the designated record set (DRS) regardless of whether they are maintained by or for an entity covered by the Health Insurance Portability and Accountability Act (HIPAA) Rules. Just like ePHI, the data that constitutes EHI is not tied to a specific system in which the EHI is maintained. We also noted in our final rule that health information that is de-identified consistent with the requirements of 45 CFR 164.514(b) is not included in the definition of EHI for the purposes of information blocking (85 FR 25804). Thus, any individually identifiable health information that is transmitted by or maintained in electronic media is EHI to the extent that the information would be included in the designated record set.

As defined in the HIPAA Rules, the designated record set comprises:

  • medical records and billing records about individuals;
  • enrollment, payment, claims adjudication, and case or medical management record systems maintained by or for a health plan;
  • other records that are used, in whole or in part, to make decisions about individuals.

The term “record” means any item, collection, or grouping of information that includes protected health information. (45 CFR 164.501)

ID:IB.FAQ39.1.2021NOV

For the period of time when information blocking is limited to the United States Core Data for Interoperability, what constitutes a progress note for the purposes of information blocking?

As stated in the United States Core Data for Interoperability Version 1 (July 2020 Errata) (“USCDI v1”), a progress note “represents a patient’s interval status during a hospitalization, outpatient visit, treatment with a LTPAC provider, or other healthcare encounter.” Any note that meets the above definition is considered a progress note for the purposes of the information blocking regulations codified in 45 CFR part 171.

From April 5, 2021 through October 5, 2022, the definition of information blocking is limited to the subset of EHI that is represented by data elements in the USCDI v1. The initial limitation of information blocking to the subset of EHI that is described in USCDI v1 was established to create a transparent, predictable starting point for sharing EHI while actors prepare for the sharing of all EHI (85 FR 25794).        

In our final rule, we noted that clinical note types identified in the USCDI are content exchange standard agnostic, and thus they should not necessarily be only interpreted or associated with the specific C-CDA Document Templates that may share the same name (85 FR 25674-5).

For more information on EHI including clinical notes, please review the other FAQs under the Electronic Health Information heading.

This FAQ is specific to the information blocking regulations codified in 45 CFR part 171. For more information about certification of health IT under the ONC Health IT Certification Program, including certification to criteria that include the USCDI as a standard, please see the About The ONC Health IT Certification Program and 2015 Edition Cures Update Test Method pages of ONC’s website, HealthIT.gov.

ID:IB.FAQ40.1.2021NOV

Are nursing, pharmacy, or other professions’ clinical notes included in the definition of “electronic health information”?

Yes. Electronic health information (EHI), as defined in 45 CFR 171.102, does not specifically include or exclude notes or other clinical observations based on the type or specialty of the professional who authors them.

Until October 6, 2022, EHI’s scope for purposes of the information blocking definition (45 CFR 171.103) is limited to that information represented by data classes and elements within the United States Core Data for Interoperability (USCDI). Therefore, until October 6, 2022, only those notes that map to any of the eight types specified in the “Clinical Notes” data class within the USCDI would be required to be included in a response to a request for legally permissible access, exchange, or use of EHI. However, actors (health care providers, health IT developers of certified health IT, and health information networks or health information exchanges) should bear in mind that none of the eight types of clinical notes currently represented within the USCDI are limited based on the type or specialty of the professional who authors them.

Please review the other questions under this heading for more information.

ID:IB.FAQ15.1.2021JAN

Does the “electronic health information” definition’s exclusion of psychotherapy notes apply to notes of sessions conducted by a type of mental health professional other than a psychiatrist?

It depends. To the extent the content of any particular note meets the definition of “psychotherapy notes” in the HIPAA Rules (see 45 CFR 164.501), that note would be considered a psychotherapy note for purposes of information blocking. The information blocking regulations do not specify types of health care providers to be mental health professionals for purposes of applying the “psychotherapy notes” definition under the information blocking regulations. Thus, all notes that are “psychotherapy notes” for purposes of the HIPAA Rules are also “psychotherapy notes” for purposes of the information blocking regulations in 45 CFR part 171, and are therefore excluded from the definition of EHI for purposes of the information blocking regulations.  

ID:IB.FAQ16.1.2021JAN

Is non-final clinical information, such as draft clinical notes or incomplete test results that are pending confirmation, included in the definition of electronic health information (EHI) for purposes of the information blocking regulations?

It depends. Draft clinical notes and laboratory results pending confirmation are, as we discussed in the ONC 21st Century Cures Act Final Rule, examples of data points that may not be appropriate to disclose or exchange until they are finalized. However, if such data are used to make health care decisions about an individual then that data would fall within the definition of “designated record set” (see 45 CFR § 164.501), and therefore within the definition of EHI. To the extent a data point falls within the definition of EHI, practices likely to interfere with legally permissible access, exchange or use of that EHI could implicate the information blocking definition.

From April 5, 2021 through October 5, 2022, EHI’s scope for purposes of the information blocking definition is limited to the EHI that is represented by data classes and elements within the United States Core Data for Interoperability (USCDI). Therefore, during this period, interference with a request for legally permissible access, exchange, or use of non-final data points would potentially implicate the information blocking regulations only to the extent noted in the above paragraph and only to the extent that the data are within both the definition of EHI and the data classes and elements represented within the USCDI.

ID:IB.FAQ17.1.2021JAN

For the period of time when EHI is “limited to the United States Core Data for Interoperability (USCDI),” does that mean the information blocking regulations apply only to EHI that is recorded or requested according to the applicable standards within the USCDI?

No. The definition of electronic health information in 45 CFR 171.102 is not limited by whether the data is recorded or could be exchanged using any particular technical functionality or standard. The information blocking definition (45 CFR 171.103) provides that before October 6, 2022, electronic health information (EHI) is limited to the subset of EHI represented by the data elements identified by the USCDI standard. This limitation of EHI for purposes of the information blocking definition is not contingent on whether those data elements are recorded or represented using the specific content and vocabulary standards in the USCDI standard at 45 CFR 171.213. On and after October 6, 2022, the information blocking regulations in 45 CFR part 171 pertain to all EHI as defined in 45 CFR 171.102.

ID:IB.FAQ18.1.2020NOV

For the period of time when information blocking was “limited to the United States Core Data for Interoperability (USCDI),” how was an actor expected to fulfill a request for the USCDI if they did not yet have certified health IT in place that includes an API with the USCDI standard?

An actor is not automatically required to fulfill a request using the specific content and vocabulary standards identified in the United States Core Data for Interoperability (USCDI) standard for the representation of data classes and data elements, nor are they required to use certified technology or any specific functionality. The information blocking definition (45 CFR 171.103) provides that before October 6, 2022, electronic health information (EHI) is limited to the subset of EHI represented by the data elements identified by the USCDI standard. This limitation of EHI for purposes of the information blocking definition is not contingent on whether those data elements are recorded or represented using specific content and vocabulary standards in the USCDI standard in 45 CFR 171.213. On and after October 6, 2022, the information blocking regulations in 45 CFR part 171 pertain to all EHI as defined in 45 CFR 171.102.

Again, the information blocking regulations do not require the use of any specific standard or functionality. Instead, the “Manner” exception (45 CFR 171.301) outlines a process by which an actor may prioritize the use of standards in fulfilling a request for EHI in a manner that supports and prioritizes the interoperability of the data. This means that, for the purposes of information blocking, before October 6, 2022, an actor may have fulfilled a request with the EHI identified by the data elements represented in the USCDI standard, first in the manner requested and, if not, in an alternate manner agreed upon with the requestor, following the order of priority specified in the exception.

Updated:

This FAQ has been updated to reflect the effective date of the HTI-1 Final Rule.

ID:IB.FAQ19.2.2020NOV

Is electronic health information (EHI) that is covered by the information blocking regulations limited by when the information was generated?

No, the definition of electronic health information (EHI) is not limited by when the information was generated. Before October 6, 2022, an actor must respond to a request to access, exchange, or use EHI with, at a minimum, the requested EHI that they have and that can be identified by the data elements represented in the United States Core Data for Interoperability (USCDI), regardless of when the information was generated. On and after October 6, 2022, an actor must respond to a request to access, exchange, or use EHI with EHI as defined in 45 CFR 171.102, regardless of when the information was generated. For example, an actor who has the necessary technical capability to do so is required to fulfill a request to access, exchange or use EHI that they have and could appropriately disclose in response to that request even if the EHI was generated before the ONC Cures Act Final Rule was published and even if the EHI was generated before the Cures Act was enacted by Congress.

ID:IB.FAQ20.1.2020NOV

Is an actor required to fulfill a request for access, exchange or use of EHI with all the EHI they have for a patient or should the amount of EHI be based on the details of the request? In addition, what if an actor only maintains some of the requested information electronically?

The fulfillment of a request for access, exchange or use of EHI, including what EHI is shared, should be based on the request. However, any activity by the actor that seeks to artificially restrict or otherwise influence the scope of EHI that may be requested may constitute interference and could be subject to the information blocking regulation in 45 CFR part 171.

In terms of fulfilling requests for EHI, it is important to remember that the requirement to fulfill requests for access, exchange, and use of EHI is in any case limited to what the actor may, under applicable law, permissibly disclose in response to a particular request. Under the information blocking regulations in 45 CFR part 171, the actor is only required to fulfill a request with the requested EHI that they have and that can be permissibly disclosed to the requestor under applicable law. However, for protected health information they have, but do not maintain electronically, all HIPAA requirements would still be applicable, including the right of access.

ID:IB.FAQ21.1.2020NOV

Privacy Exception

Would it be information blocking if an actor does not fulfill a request to access, exchange, or use EHI in order to comply with federal privacy laws that require certain conditions to have been met prior to disclosure?**

No, it would not be information blocking if the actor’s practice of not fulfilling a request in such circumstances meets the Privacy Exception (45 CFR 171.202). All actors remain responsible for disclosing EHI only when the disclosure is allowed under all applicable federal laws. For example, actors who are HIPAA covered entities or business associates must comply with the HIPAA Privacy Rule and any other applicable federal laws that limit access, exchange, or use of EHI in particular circumstances. Adherence to such federal laws is not information blocking, if the other conditions of the Privacy Exception are also met.*

In particular, where federal law such as the HIPAA Privacy Rule does not permit EHI to be used or disclosed unless certain requirements (“preconditions”) are met, then an actor’s practice of not fulfilling a request to access, exchange, or use EHI when these preconditions are not met is not information blocking.*** The Precondition Not Satisfied (45 CFR 171.202(b)) sub-exception of the Privacy Exception outlines a framework for actors to follow so that the actors’ practices of not fulfilling requests to access, exchange, or use EHI would not constitute information blocking when a precondition of applicable law has not been satisfied.

One example that highlights the alignment between the HIPAA Privacy Rule and the information blocking regulations is when a law enforcement official requests records of abortions performed from a clinic. As explained in the “HIPAA Privacy Rule and Disclosures of Information Relating to Reproductive Health Care” guidance issued by the Office for Civil Rights, there are certain preconditions that must be met before this disclosure can be made: “If the request is not accompanied by a court order or other mandate enforceable in a court of law, the Privacy Rule would not permit the clinic to disclose PHI in response to the request. Therefore, such a disclosure would be impermissible and constitute a breach of unsecured PHI requiring notification to HHS and the individual affected.” In this example, federal law does not permit the disclosure of EHI unless certain requirements are met, and therefore, the actor’s practice not to disclose EHI would not be information blocking. We note that this is just one example of how the HIPAA Privacy Rule gives individuals confidence that their protected health information, including information relating to abortion and other sexual and reproductive health care, will be kept private. Please see the guidance from the Office for Civil Rights for additional information and examples.

A second example of the alignment between the HIPAA Privacy Rule and the information blocking regulations is in circumstances where the HIPAA Privacy Rule permits a covered entity to use or disclose EHI only following receipt of a valid HIPAA authorization from the individual (patient) or the individual’s personal representative. If an actor does not have a valid HIPAA authorization from the individual or their personal representative that permits the use or disclosure of EHI for the requested purpose, then a precondition for disclosure is not satisfied. Accordingly, the actor’s practice of not disclosing EHI would not be considered information blocking if it is consistent with the requirements of the Precondition Not Satisfied sub-exception.

To emphasize, wherever any federal law requires the authorization of the individual to disclose the EHI, an individual may always choose not to give such authorization, and an actor who does not disclose the EHI would not be information blocking if the actor meets all applicable requirements of the Privacy Exception.

* For more information on how practices would be evaluated to determine whether the unique facts and circumstances constitute information blocking, please see the following FAQ: How would any claim or report of information blocking be evaluated? (IB.FAQ46.1.2022FEB)

** It is important to remember that the information blocking exceptions defined in 45 CFR part 171 subparts B and C are voluntary, offering actors certainty that any practice meeting the conditions of one or more exceptions would not be considered information blocking. An actor’s practice that does not meet the conditions of an exception would not automatically constitute information blocking. Rather, such practices will be evaluated on a case-by-case basis to determine whether information blocking has occurred. (See, e.g., IB.FAQ29.1.2020NOV).

*** “EHI” as defined in 45 CFR 171.102 is a subset of protected health information (PHI). See 45 CFR 160.103 (definition of “protected health information”). For more information on the HIPAA Privacy Rule, who must comply with it, and its conditions for disclosures of protected health information (PHI), please see resources of the Office for Civil Rights at HHS.gov/HIPAA.

ID:IB.FAQ48.1.2023APR

If an individual requests that their EHI not be disclosed, is it information blocking if an actor does not disclose the EHI based on the individual’s request?*

No, if the actor’s conduct satisfies the requirements of the information blocking regulations, such as the Privacy Exception (45 CFR 171.202). For example, the sub-exception Respecting an Individual’s Request Not to Share Information permits an actor, unless the disclosure is required by law, to honor an individual’s request not to provide access, exchange, or use of the individual’s EHI, which aligns with the individual’s right to request a restriction on disclosures of their protected health information under the HIPAA Privacy Rule (45 CFR 164.522(a)(1)).

Separately, if an actor has privacy or security concerns about disclosing EHI to an app/app developer with which an individual may choose to share their EHI, an actor may educate the individual about such concerns consistent with the following FAQ: Will educating patients about the privacy and security risks posed by third-party apps that the patient chooses be considered interference?

* For more information on how practices would be evaluated to determine whether the unique facts and circumstances constitute information blocking, please see the following FAQ: How would any claim or report of information blocking be evaluated? (IB.FAQ46.1.2022FEB)

ID:IB.FAQ47.1.2023APR

If an actor, such as a health care provider, operates in more than one state, is it consistent with the information blocking regulations for the health care provider to implement practices to uniformly follow the state law that is the most privacy protective (more restrictive) across all the other states in which it operates?

Yes, if the actor satisfies the requirements of the information blocking regulations, such as the Precondition Not Satisfied sub-exception of the Privacy Exception (45 CFR 171.202(b)).** For purposes of the information blocking regulations, health care providers and other information blocking actors operating under multiple state laws, or state and tribal laws, with inconsistent legal requirements for EHI disclosures may choose to adopt uniform policies and procedures so that the actor only makes disclosures of EHI that meet the requirements of the state law providing the most protection to individuals’ privacy (45 CFR 171.202(b)).** Essentially, the Precondition Not Satisfied sub-exception establishes conditions under which an actor may adopt policies to satisfy state laws with more restrictive preconditions and apply those policies in all the jurisdictions in which they operate. 

To illustrate, consider a scenario in which an actor operates in two states, “State A” and “State B.” State A forbids disclosure of certain EHI, such as EHI specific to reproductive health care, to another health care provider, who is also currently treating the individual, without first obtaining written authorization from the individual. This scenario assumes State B’s law does not require authorization from the individual for disclosure of reproductive health care EHI for treatment purposes. In this scenario, an actor subject to the laws of both State A and State B can, consistent with the Privacy Exception (see 45 CFR 171.202(b)(3)), adopt uniform privacy policies and procedures that result in the actor disclosing EHI only when the individual has provided written authorization for a specific disclosure (consistent with the more privacy-protective requirements of State A’s law) of EHI about them for treatment purposes across the actor’s operations in both State A and State B. If the actor’s policies, procedures, and actions are consistent with the requirements of the Precondition Not Satisfied sub-exception (45 CFR 171.202(b)), the actor’s practices would not be considered information blocking – even though the actor’s uniform privacy policies and procedures may deny or delay access, exchange, or use of EHI in State B that (under laws in force in State B) would not require specific written authorization.

In a second, similar scenario, State A’s law sets more privacy protective or more “stringent”  requirements (“preconditions”) than both State B’s law and the HIPAA Privacy Rule for disclosures of EHI[1] for particular purposes (such as disclosing information related to reproductive health care for law enforcement purposes[2]). An actor operating in States A and B can meet the requirements of the Precondition Not Satisfied sub-exception (45 CFR 171.202(b)(1) through (3)) in order to have confidence that disclosing EHI only when the disclosure is consistent with the most privacy protective (most restrictive or most “stringent”) preconditions (in this example, State A’s) across all their operations in both State A and State B would not be considered information blocking.

[1]EHI” as defined in 45 CFR 171.102 is a subset of protected health information (PHI). See 45 CFR 160.103 (definition of “protected health information”). For more information on the HIPAA Privacy Rule and its conditions for disclosures of protected health information (PHI), please see resources of the Office for Civil Rights at HHS.gov/HIPAA.

[2] For example, see “HIPAA Privacy Rule and Disclosures of Information Relating to Reproductive Health Care,” which discusses the permissibility of disclosures for law enforcement purposes under the HIPAA Privacy Rule.

** It is important to remember that the information blocking exceptions defined in 45 CFR part 171 subparts B and C are voluntary, offering actors certainty that any practice meeting the conditions of one or more exceptions would not be considered information blocking. An actor’s practice that does not meet the conditions of an exception would not automatically constitute information blocking. Rather, such practices will be evaluated on a case-by-case basis to determine whether information blocking has occurred. (See, e.g., IB.FAQ29.1.2020NOV).

ID:(IB.FAQ49.1.2023APR)