The New HIPAA Reproductive Health Attestation: What Legal and Insurance Professionals Need to Know

Background: Post-Dobbs Privacy Protections Under HIPAA

In the wake of the Supreme Court’s Dobbs v. Jackson Women’s Health Organization decision in 2022, which removed federal abortion protections, the U.S. Department of Health & Human Services (HHS) moved to strengthen privacy for reproductive health information (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). The Biden Administration issued executive orders directing HHS to safeguard reproductive health data, leading to a new HIPAA Privacy Rule amendment in April 2024. This “HIPAA Privacy Rule to Support Reproductive Health Care Privacy” was created specifically to prevent individuals’ medical records from being used against them for lawful reproductive care (HIPAA and Reproductive Health | HHS.gov).

Under this Final Rule, covered entities (healthcare providers, health plans, clearinghouses) and their business associates are prohibited from using or disclosing protected health information (PHI) for certain purposes. In particular, they may not use or disclose PHI to investigate or punish any person for seeking, obtaining, providing, or facilitating reproductive health care if that care was lawful where and when it was provided (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). In other words, medical records can’t be turned over if the intent is to probe whether someone had an abortion or other reproductive service that was legal under the circumstances. The rule also bars disclosing PHI to identify someone for such an investigation (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). This was a direct response to concerns that state authorities or others might leverage health records to enforce new abortion bans or related laws post-Dobbs.

HHS emphasized that these changes aim to bolster patient-provider confidentiality and ensure individuals continue seeking care without fear (HIPAA and Reproductive Health | HHS.gov). The rule is narrowly tailored: it focuses on the purpose of the request (such as a law enforcement investigation into abortion) rather than broadly labeling certain records as off-limits. It does not prevent all disclosures of reproductive health information—only those attempts to use such information to pursue someone for lawful care. As HHS noted, the goal is to support privacy for lawful reproductive health care, not to obstruct legitimate law enforcement or oversight of truly unlawful activities (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). Balancing these interests, HHS introduced a new procedural safeguard: the reproductive health attestation requirement.

What Reproductive Health Information Does HIPAA Protect?

The new rule defines “reproductive health care” broadly to encompass a wide range of services and information. According to the rule, it includes “health care that affects the health of an individual in all matters relating to the reproductive system and its functions and processes.” (Reproductive Health Care: New HIPAA Restrictions & Compliance Checklist | Groom Law Group) In practical terms, this means any medical services or data related to an individual’s reproductive system or reproductive capacity. Examples of protected reproductive health information under HIPAA now include:

Because this definition is so broad, virtually any medical record could contain reproductive health information. Routine visits might mention menstrual history, contraception, or other details related to reproduction. HHS deliberately chose a broad scope to ensure privacy, noting it would be challenging to enumerate every service that falls under “reproductive health care” (Reproductive Health Care: New HIPAA Restrictions & Compliance Checklist | Groom Law Group). Therefore, covered entities should assume that any PHI might be “potentially related” to reproductive health care if it touches on pregnancy, sexual health, or similar matters (HIPAA’s New Regulations Protecting Reproductive Health Care – Wiggin and Dana LLP — Attorneys At Law).

Importantly, the enhanced protections apply only to reproductive care that is lawful or protected under the circumstances (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). If a reproductive service was unlawful (for example, an unlicensed person performing an illegal procedure), those specific privacy restrictions would not shield that information. The rule includes a presumption that reproductive care provided by someone else was lawful unless a covered entity has actual knowledge or evidence to the contrary (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov) (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). In short, HIPAA’s new safeguards are meant to protect patients and providers involved in legally provided reproductive health services.

The New Attestation Requirement: What It Is and Why It’s Needed

To implement these privacy protections, HHS introduced a new procedural step for certain disclosures of health records: an attestation requirement. An attestation in this context is a signed, written statement that a person requesting PHI affirms the request is not for any prohibited purpose (i.e. not to investigate or penalize someone for lawful reproductive care) (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). This must be obtained by the covered entity before disclosing PHI that is “potentially related” to reproductive health care.

When must an attestation be obtained? The requirement applies to requests for PHI in four scenarios commonly associated with investigations or legal proceedings (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov):

  1. Health oversight activities – e.g. a state medical board or insurance regulator requesting records.

  2. Judicial and administrative proceedings – e.g. a subpoena or court order in a lawsuit or hearing.

  3. Law enforcement purposes – e.g. police or prosecutors seeking records during an investigation.

  4. Disclosures to coroners or medical examiners – e.g. for determining a cause of death that might involve reproductive health information.

In these cases, if the records could relate to reproductive health care, the covered entity or business associate must first obtain a signed attestation from the requestor stating that the use or disclosure of the PHI is not for a prohibited investigative or punitive purpose (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov) (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). This attestation is in addition to any other HIPAA requirements for the disclosure. For example, if a subpoena is required under HIPAA’s usual rules, the subpoena is still needed – but now the attestation must accompany it for the disclosure to proceed (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render).

Why did HHS add this attestation step? It serves a few critical functions:

  • Written assurance: It provides covered entities with a formal, written representation from the requestor that they are not seeking the information to enforce anti-reproductive laws (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). This helps the entity document its compliance and decision-making.

  • Puts requestors on notice: By signing, the requesting party is made explicitly aware of the legal boundaries and penalties. HHS noted that the attestation reminds requestors that knowingly obtaining or disclosing health information in violation of HIPAA can carry criminal penalties (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). It effectively warns, “if you lie about your purpose, you could face serious consequences.”

  • Deterrence of improper requests: The extra step may deter fishing expeditions. If someone’s true intent is to pursue an abortion-related charge in violation of the rule, they would have to commit fraud on paper to do so. This risk is meant to discourage misuse of medical data.

The attestation must meet certain standards to be valid. It should be a stand-alone statement (not buried in another document) and written in plain language with all required elements, with no extraneous commitments or waivers (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). HHS has provided a model attestation form and instructions to help organizations implement this requirement consistently (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). Electronic signatures are acceptable as long as they comply with e-signature laws (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). Notably, an attestation is required for each separate request/disclosure – there is no blanket attestation covering multiple requests (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). If a requestor refuses to sign an attestation when one is required, the covered entity must decline the disclosure.

Covered entities are generally allowed to rely on a signed attestation in good faith and are not expected to investigate the veracity of the requestor’s claim, absent clear reasons to doubt it (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). However, if they discover that an attestation was materially false, they must cease any further disclosures relying on that attestation (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). In practice, this means if evidence later shows the requestor was actually using records to pursue someone for a lawful abortion (despite attesting otherwise), the covered entity should stop cooperating and report the violation as appropriate.

Overall, the attestation requirement introduces a safeguard and accountability layer for third parties requesting medical records. It ensures everyone involved formally acknowledges the sensitive nature of reproductive health information and the heightened privacy protections now in place.

Federal Guidance and Compliance Expectations

Federal health authorities have issued guidance to help implement these changes. HHS’s Office for Civil Rights (OCR) published a detailed Fact Sheet and hosted webinars explaining the new rule’s provisions, and it has released a Model Attestation Form for covered entities to use (HIPAA and Reproductive Health | HHS.gov) (HIPAA and Reproductive Health | HHS.gov). Key points from federal guidance include:

Federal officials have stressed that these modifications to HIPAA are intended to build trust in the healthcare system. Patients, especially those in states with restrictive reproductive laws, had expressed fear that their conversations and records with doctors could be turned over to authorities (HIPAA and Reproductive Health | HHS.gov). By implementing a formal attestation process and limiting certain disclosures, HHS aims to reassure patients that their lawful reproductive health decisions will remain private. This, in turn, supports open communication between patients and providers, which is critical for quality care (HIPAA and Reproductive Health | HHS.gov).

Texas-Specific Legal Considerations and State Challenges

Not everyone welcomes the new federal rules. Texas, in particular, has been at the center of opposition to the HIPAA reproductive health privacy changes. Texas is among the states that enacted a near-total abortion ban after Dobbs (with only narrow exceptions for the life of the patient), imposing criminal and civil penalties on those who violate the ban (Texas Challenges HHS’s HIPAA Rule Protecting Reproductive Health Information from State Investigative Bodies | Mintz). Texas authorities therefore have a keen interest in obtaining medical records for any evidence of unlawful abortions or related care. The new HIPAA rule creates a potential roadblock for such efforts, especially if a Texas patient traveled to another state where an abortion was legal (making the care “lawful under the circumstances” and thus protected from disclosure (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov)).

In September 2024, the Texas Attorney General filed a lawsuit against HHS challenging the validity of the new reproductive health privacy rule (Texas Challenges HHS’s HIPAA Rule Protecting Reproductive Health Information from State Investigative Bodies | Mintz). Texas’s complaint argues that HHS overstepped its authority with these HIPAA amendments and seeks to have the rule struck down (vacated) (Texas Challenges HHS’s HIPAA Rule Protecting Reproductive Health Information from State Investigative Bodies | Mintz). Some key points of the Texas legal challenge and related state considerations:

As of early 2025, these legal challenges are ongoing. No final court ruling has yet invalidated the HIPAA reproductive health rule, so it remains in effect (2024 HIPAA Reproductive Privacy Rule Status Update  –). However, the litigation does introduce uncertainty. It’s possible that a court could pause enforcement of the rule or that a future administration might reconsider it. For now, covered entities in Texas (and other states) must carefully navigate the tension between state demands and federal requirements. Generally, HIPAA (a federal law) will preempt any contrary state law unless the state law is more privacy-protective. In this case, the HIPAA rule is more protective of privacy than Texas law, suggesting that Texas providers should follow the federal rule to avoid HIPAA violations.

Texas healthcare providers and legal counsel should watch the progress of Texas v. HHS in the Northern District of Texas. That court has, in other cases, been sympathetic to state challenges against federal health regulations (Reproductive Health Care: New HIPAA Restrictions & Compliance Checklist | Groom Law Group). Until and unless the rule is blocked, the safest course for covered entities is to comply with the attestation requirement and prohibition – even if that means denying a request from Texas law enforcement – and document the legal rationale. Texas requestors, on the other hand, should be prepared for new hurdles in obtaining information and may need to tailor their strategies (for example, clearly demonstrating if an investigation concerns unlawful reproductive care, which would fall outside HIPAA’s new protection).

Best Practices for Compliance

Both those requesting medical records and those disclosing them need to adjust their practices under this new attestation requirement. Below are some recommended best practices for compliance, tailored to requestors (e.g., attorneys, insurers, law enforcement) and covered entities (healthcare providers, health plans, and their Release of Information staff or vendors):

For Requestors of Medical Records:

  • Anticipate the Attestation: If you are seeking records in a context of litigation, investigation, or oversight, assume you will need to sign an attestation when reproductive health information might be involved. Plan for this extra step in your record request process. Failing to include a required attestation will likely result in delays or outright denials of the records request.

  • Be Clear and Specific in Your Request: When requesting PHI, be explicit about the purpose. Vague or broad requests are more likely to raise red flags. Clearly state the legitimate purpose (e.g., “health oversight – Medicaid fraud investigation” or “judicial proceeding – malpractice lawsuit”) so the covered entity can see it’s not a fishing expedition for abortion-related infractions. This context will also help you assert that the request is not for any prohibited purpose on the attestation itself.

  • Only Request What You Need (Minimum Necessary): Under HIPAA’s Minimum Necessary standard, even with an attestation, you should request only the information genuinely needed for your inquiry (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). Tailor your records subpoena or request to exclude extraneous sensitive information. For example, if you need records of a specific surgery, avoid a blanket request for “all gynecological records” which could encompass reproductive services unrelated to your case. A focused request is more likely to be honored and viewed as good faith.

  • Understand “Lawful vs. Unlawful” Care: If your investigation involves potentially unlawful reproductive health care (e.g., an alleged illegal abortion or unlicensed practice), recognize that the HIPAA rule’s prohibition might not apply in the same way. You may need to provide the covered entity with facts indicating illegality to overcome the presumption of lawfulness (Reproductive Health Care: New HIPAA Restrictions & Compliance Checklist | Groom Law Group) (Texas Challenges HHS’s HIPAA Rule Protecting Reproductive Health Information from State Investigative Bodies | Mintz). For instance, a law enforcement request could include a statement of probable cause that a crime was committed. This can help the provider determine that the request is outside the scope of “lawful reproductive care” protections. In such cases, an attestation might still be used but would affirm that the purpose is not to target lawful care (since the care is believed unlawful). Always consult legal counsel on the proper wording if you believe an exception applies.

  • Do Not Misrepresent Your Purpose: This may sound obvious, but it’s crucial – never lie on an attestation. Knowingly obtaining health information under false pretenses is a violation of federal law, and the attestation form makes it easier to prove such intent (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). The attestation is a legally binding statement. Perjury or HIPAA enforcement action (with potential fines and criminal charges) could result if you misuse the attestation. If your true goal is something prohibited (e.g. enforcing a state abortion ban for a procedure that was legal), recognize that HIPAA now bars that request. Seeking an alternate route or court order won’t change the HIPAA restriction, unless the law itself changes.

For Covered Entities and ROI Specialists:

  • Update Policies and Procedures: Immediately revise your HIPAA privacy policies to incorporate the new prohibitions and attestation requirements (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). Develop a standard operating procedure for handling any request that could involve reproductive health information. This includes flagging the need for an attestation and a process for reviewing the completed attestation. Ensure your release-of-information (ROI) departments or third-party ROI vendors know the new rules and have updated forms (consider using HHS’s model form for consistency).

  • Train Your Workforce: Provide targeted training to staff, especially those who handle subpoenas, law enforcement requests, or interact with investigators (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). Frontline employees should be trained to recognize requests that might trigger the reproductive health protections. For example, if a police officer shows up asking for records related to a pregnancy or a miscarriage, staff must know not to release anything on the spot and instead to involve your privacy office for an attestation and legal review. Role-play scenarios so staff know how to politely say, “Our policy requires a signed attestation before we can release those records, due to federal privacy regulations.” Training should also cover how to handle pushback or urgent requests – emphasize that “required by law” disclosures still must go through this filter unless it’s truly an emergency.

  • Implement Data Identification or Flagging: Because “reproductive health care” can permeate many parts of a medical record, consider ways to identify PHI that falls under this category in your systems (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). This might involve tagging certain diagnosis codes (e.g., pregnancy, IVF, abortion, contraception) or using keywords to flag records. Realistically, you may not catch everything, so the safest approach is to treat requests contextually: focus on the purpose of the request rather than trying to cherry-pick which records contain reproductive info. Nonetheless, educating your HIM (Health Information Management) teams on typical records that often include reproductive health data (OB/GYN records, fertility clinic files, etc.) can help them be extra vigilant with those.

  • Incorporate Attestations into Release Workflow: Adjust your release-of-information workflow so that no PHI leaves for the covered scenarios without an attestation on file. You may need to coordinate with legal counsel when a request comes in. Have a template attestation ready to send to requestors if they haven’t provided one. When an attestation is returned, verify it is properly completed and signed (and meets the required elements as per the rule). Keep these attestations on record – they should be retained as part of the disclosure documentation, and any disclosure made under an attestation should be logged for accounting of disclosures purposes (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render).

  • Assess Business Associate Compliance: If you use any business associates to handle health information or release records (for example, an outsourced ROI service or a health information exchange), update your Business Associate Agreements (BAAs) to obligate compliance with these new requirements (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). You may need to communicate with BAs about how to forward or handle any requests they receive. They too must obtain attestations and abide by the prohibitions when acting on your behalf. Ensure they have a copy of the model attestation and understand the circumstances that require one. It may be prudent to review all BA relationships to ensure none are improperly disclosing reproductive health PHI for prohibited reasons (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render) (for instance, a data exchange might unknowingly fulfill a law enforcement request unless they’re made aware of the rule).

  • Plan for NPP Updates and Patient Communication: Though the deadline is later, start drafting updates to your Notice of Privacy Practices to include a statement about the new reproductive health protections (HIPAA-Regulated Entities Required to Comply with New Rules to Support Reproductive Health Care Privacy by the End of the Year | Hall Render). This will involve explaining that certain disclosures of reproductive health information will only be made with additional safeguards or may not be made at all without patient authorization. It’s also wise to train patient-facing staff (like front desk or patient relations) on how to answer questions from patients who may have heard about these protections. Patients may ask, “Will you keep my abortion information private?” Staff should be able to reassure them that your organization follows new HIPAA rules that further protect reproductive health records and will not release that information for investigatory purposes without strict conditions. This can bolster patient trust and satisfaction.

In summary, maintaining compliance in this evolving landscape means staying proactive. Keep abreast of HHS guidance updates (OCR may issue FAQs or clarifications as stakeholders pose questions). Also monitor the outcome of the Texas and multi-state lawsuits, as a court decision could change the requirements. For now, both requestors and covered entities should operate under the assumption that the rule is here to stay – and adjust their practices accordingly to avoid violations or penalties.

Conclusion

The introduction of the HIPAA reproductive health attestation requirement marks a significant development in healthcare privacy law. It reflects the federal government’s response to a shifting legal climate around reproductive rights, aiming to ensure that medical privacy is not eroded by new state abortion restrictions. Legal professionals and insurance companies must understand these changes, as they will influence how medical records can be obtained in investigations, litigation, or oversight activities. Healthcare providers and Release of Information specialists, meanwhile, carry the responsibility of implementing the new protections on the ground, balancing compliance with requests against their duty to safeguard patient confidentiality.

While the requirements add complexity to the records disclosure process, they also provide clarity and reassurance in a sensitive area: if the care was lawful, patients and providers should not fear that health records will be used against them (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). By obtaining a simple attestation, covered entities can document that any disclosure of reproductive health information is above-board and not for a prohibited purpose (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov). This practice ultimately protects all parties – patients, providers, and even requestors acting in good faith – by drawing a bright line that certain uses of health data are off-limits.

As with any major regulatory change, it will take time for workflows to adapt. Some states (like Texas) are pushing back, creating a dynamic legal environment that warrants close observation (2024 HIPAA Reproductive Privacy Rule Status Update  –). Nevertheless, organizations would be wise to proceed with compliance efforts. Prioritize updating your policies, training your teams, and communicating with requestors about the new rules. By doing so, you not only reduce legal risk but also affirm your commitment to patient privacy in an era when it needs reinforcement. In the end, protecting sensitive health information – especially about deeply personal decisions – is foundational to the trust that underpins our healthcare and insurance systems. The new HIPAA reproductive health attestation requirement is a tool to help preserve that trust in a post-Dobbs world, and all stakeholders should treat it as an essential element of modern health information governance.

Sources: The information above is based on guidance from the U.S. Department of Health & Human Services and analyses by healthcare legal experts (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov) (HIPAA Privacy Rule Final Rule to Support Reproductive Health Care Privacy: Fact Sheet | HHS.gov) (Reproductive Health Care: New HIPAA Restrictions & Compliance Checklist | Groom Law Group) (Texas Challenges HHS’s HIPAA Rule Protecting Reproductive Health Information from State Investigative Bodies | Mintz) (2024 HIPAA Reproductive Privacy Rule Status Update  –), as linked throughout this post. These authoritative sources provide further detail and can be consulted for a deeper dive into the regulatory text and its interpretation.

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