Attack rates are shown across three clinical management phases: T0 (2016–September 2019, no prophylaxis), T1 (September 2019–April 2021, long-term prophylaxis with plasma-derived C1-INH), and T2 (April 2021–present, long-term prophylaxis with lanadelumab). Variations were −38.50% from T0 to T1 and −88.50% from T0 to T2. Data before T2 were retrospectively collected from the patient’s clinical history and medical records. C1-INH: C1 inhibitor.
Declarations
Author contributions
MBG: Conceptualization, Validation, Writing—review & editing. SS: Investigation, Writing—original draft. MR: Investigation, Writing—original draft. AZ: Validation, Writing—review & editing, Supervision. All authors read and approved the submitted version.
Conflicts of interest
Andrea Zanichelli received speaker/consultancy fees from and/or was a member of advisory boards for Astria Therapeutics, BioCryst, CSL Behring, KalVista Pharmaceuticals, Pharming, Pharvaris, Otsuka, and Takeda. The other authors declare no conflicts of interest.
Ethical approval
The study complies with the Declaration of Helsinki. Ethical approval is not required for a case report study according to the local ethics committee.
Consent to participate
Informed consent to participate in the study was obtained from the participant.
Consent to publication
Informed consent to publication was obtained from the participant.
Availability of data and materials
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Open Exploration maintains a neutral stance on jurisdictional claims in published institutional affiliations and maps. All opinions expressed in this article are the personal views of the author(s) and do not represent the stance of the editorial team or the publisher.
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