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Hereditary Angioedema: Reduce Time to Diagnosis With Appropriate Work-Up

Clinical Thought

In this commentary, Chrystal Lewis, PhD, RN discusses how a thorough patient history and laboratory testing can reduce the time to a hereditary angioedema (HAE) diagnosis and initiation of treatment, and result in an improvement in the patient’s quality of life.

Released: September 26, 2022

Expiration: September 25, 2023

No longer available for credit.

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Faculty

Chrystal Lewis

Chrystal Lewis, PhD, RN

Nurse Scientist
Office of Research and Patient Care Services
Stanford Health Care
Menlo Park, California

Acknowledgement

This activity is supported by educational grants from BioCryst Pharmaceuticals, Inc. and Takeda Pharmaceuticals U.S.A., Inc.

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Supporters

BioCryst Pharmaceuticals, Inc.

Takeda Pharmaceuticals U.S.A., Inc.

Target Audience

NPs and PAs in primary care

Disclosure

Chrystal Lewis, PhD, RN: consultant/advisor/speaker: Pharming.

Format

ClinicalThought

Disclaimer

The opinions or views expressed in this CE/CME activity do not necessarily reflect the opinions or recommendations of Practicing Clinicians Exchange or any educational supporter.

Additional Information

Program Medium

This program has been made available online.