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Must All Test Results Be Sent to and Reviewed by a Patient's Primary Care Physician?

Learning Objectives
1. Describe the myth or issue that impacts physicians and their care teams
2. Explain the facts that debunk the myth or issue that impacts physicians and their care teams
3. Explain the way in which physicians should handle and communicate about the tests they order
0.25 Credit CME
Abstract

“Closing the loop” on test results—ensuring test results are communicated with patients and acted on by care teams in a timely manner—helps prevent missed or delayed diagnosis and protects patient safety. However, when test results are reported to multiple clinicians, there can be confusion concerning whose responsibility it is to review test results, communicate them with patients, and initiate follow-up: the ordering physician/allowed non-physician practitioner or the patient's PCP. This iteration of the DRM series explains guidance surrounding which physician is responsible for reviewing and following up on test results.

To earn full credit for this activity, you must review all accompanying resources, which have been curated to support your learning of the subject matter.

The Myth

All test results must be sent to and reviewed by a patient's primary care physician (PCP).

Debunking the Myth

To the best of our knowledge, there is no federal regulatory policy mandating that all test results be sent to and reviewed by patients' PCPs. In fact, the results reporting standards of the Clinical Laboratory Improvement Amendments, a Centers for Medicare and Medicaid Services program that ensures quality laboratory testing, requires that laboratory results be released to the ordering clinician and—as mandated by the 21st Century Cures Act—the patient.1,2 As the AMA STEPS Forward® EHR Inbox Reduction Checklist phrases it, “You order it, you own it”.3

To support this transparency, the Office of the National Coordinator for Health Information Technology guidance emphasizes that the ordering clinician should be identifiable on all ordered tests and test reports in the electronic health record (EHR). This guidance also stresses that, if available, the clinician responsible for follow-up should be listed as well.4,5 Unless the patient's PCP is the ordering physician or the physician responsible for follow-up, they do not need to be notified of test results. However, if the patient's PCP requests a copy of a test result from another clinician or health system, this request should be honored because an unnecessary delay could be considered information blocking under federal regulation.2

Background

Studies have demonstrated that EHR inbox burden significantly contributes to physician burnout and decisions to reduce clinical hours or leave medicine altogether.6 In an analysis of PCP inbox management, findings showed that most inbox time is spent on addressing test results.7 Further, in cases where multiple tests are ordered for a single patient, each individual result is often sent as a separate inbox notification, unnecessarily increasing the inbox volume.

The delivery of test results to a physician's inbox is a critical part of the diagnostic and treatment process. The Joint Commission identified closed-loop communication as a National Patient Safety Goal in 2005.8 “Closing the loop” on test results—ensuring test results are communicated with patients and acted on by care teams in a timely manner—helps prevent missed or delayed diagnosis and protects patient safety. However, when test results are reported to multiple clinicians, there can be confusion concerning whose responsibility it is to review test results, communicate them with patients, and initiate follow-up: the ordering physician/allowed non-physician practitioner or the patient's PCP.

Health systems have begun developing standards and policies that guide staff on how diagnostic test results should be reviewed and followed up on. For example, Veterans Health Administration policy places responsibility upon the ordering clinician for initiating follow-up of abnormal test results unless another qualified clinician was authorized to receive test results in the ordering clinician's absence.4,9

Case Example

Physicians and other staff at a large not-for-profit regional hospital medical center became inundated with lab result alerts to the point they were no longer meaningful nor manageable and contributed to burnout. A message for each individual result was sent at the exact time the result was generated, even when it was part of a test panel. This meant that multiple alerts for one test could be sent to staff inboxes nearly simultaneously or hours apart.

To find a solution to this issue, the hospital worked with a healthcare data integration company to implement a new message delivery system that automated the generation, consolidation, and delivery of certain message types. Through their solution, all results for a single order, including a panel, were aggregated into one result message. The consolidated messages were then sent to the EHR on a specified schedule, preventing physicians from being overwhelmed with a constant stream of lab result alerts. With consolidated patient results delivery, physicians could better focus on diagnosing and providing informed medical care to patients.

AMA policy

Resources

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The AMA Debunking Medical Practice Regulatory Myths series provides physicians and their care teams with regulatory clarification to streamline clinical workflow processes and improve patient outcomes. Learn more

Article Information

AMA CME Accreditation Information

CME Disclosure Statement: Unless noted, all individuals in control of content reported no relevant financial relationships.

If applicable, all relevant financial relationships have been mitigated.

Disclaimer: The AMA's Debunking Regulatory Myths (DRM) series is intended to convey general information only, based on guidance issued by applicable regulatory agencies, and not to provide legal advice or opinions. The contents within DRM should not be construed as, and should not be relied upon for, legal advice in any particular circumstance or fact situation. An attorney should be contacted for advice on specific legal issues.

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References
1.
Hamilton  T.  Clinical Laboratory Improvement Amendments of 1988 (CLIA) – Issuance of Revised Survey Procedures and Interpretive Guidelines for Laboratories and Laboratory Services in Appendix C of the State Operations Manual to Facilitate the Electronic Exchange of Laboratory Information.  Published online March 1 , 2010. Accessed March 26, 2023.
2.
Office of the National Coordinator for Health Information Technology, Health and Human Services Departments.  21st Century Cures Act: Interoperability, Information Blocking, and the ONC Health IT Certification Program.; 2020. Accessed March 26, 2023.
3.
AMA STEPS Forward®.  EHR Inbox Reduction Checklist for Health Care Organizations.  In:  AMA STEPS Forward® Playbook Series. Taming the Electronic Health Record Playbook—EHR Inbox Reduction Checklist for Health Care Organizations.; 2023. Accessed March 26, 2023. https://www.ama-assn.org/system/files/ehr-inbox-reduction-checklist.pdfGoogle Scholar
4.
Kwan  JL, Singh  H.  Assigning responsibility to close the loop on radiology test results.  Diagnosis (Berl). 2017;4(3):173–177.Google ScholarCrossref
5.
The Office of the National Coordinator for Health Information Technology,  Safety Assurance Factors for EHR Resilience.  Self-Assessment: Test Results Reporting and Follow-Up.; 2016. Accessed March 26, 2023.Google Scholar
6.
Sinsky  CA, Shanafelt  TD, Ripp  JA.  The Electronic Health Record Inbox: Recommendations for Relief.  Journal of General Internal Medicine. 2022;37(15):4002–4003.Google ScholarCrossref
7.
Akbar  F, Mark  G, Warton  EM,  et al.  Physicians' electronic inbox work patterns and factors associated with high inbox work duration.  Journal of the American Medical Informatics Association. 2021;28(5):923–930.Google ScholarCrossref
8.
Ward  B.  Close the Loop on Test Results.  Patient Safety & Quality Healthcare. Published February 18 , 2020. Accessed March 27, 2023. https://www.psqh.com/analysis/close-the-loop-on-test-results/
9.
Department of Veterans Affairs.  Communicating Test Results to Providers and Patients.; 2022. Accessed March 26, 2023. https://www.va.gov/vhapublications/ViewPublication.asp?pub_ID=3148
AMA CME Accreditation Information

Credit Designation Statement: The American Medical Association designates this Enduring Material activity for a maximum of 0.25  AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to:

  • 0.25 Medical Knowledge MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program;;
  • 0.25 Self-Assessment points in the American Board of Otolaryngology – Head and Neck Surgery’s (ABOHNS) Continuing Certification program;
  • 0.25 MOC points in the American Board of Pediatrics’ (ABP) Maintenance of Certification (MOC) program;
  • 0.25 Lifelong Learning points in the American Board of Pathology’s (ABPath) Continuing Certification program; and
  • 0.25 credit toward the CME of the American Board of Surgery’s Continuous Certification program

It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting MOC credit.

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