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Tranexamic acid for angiotensin converting enzyme inhibitor induced angioedema: A retrospective multicenter study.
Lindauer, Kristen E; Lo, Bruce M; Weingart, Gregory S; Karpov, Matvey V; Gartman, Grace H; Neubauer, Lexie E; Kaplan, Marcus C.
Afiliación
  • Lindauer KE; Pharmacy, Sentara Health, Virginia, United States. Electronic address: k_ingold2@yahoo.com.
  • Lo BM; Pharmacy, Sentara Health, Virginia, United States; Department of Emergency Medicine, Eastern Virginia Medical School, 825 Fairfax Ave, Norfolk, United States; Emergency Physicians of Tidewater, Virginia, Norfolk, United States.
  • Weingart GS; Pharmacy, Sentara Health, Virginia, United States; Department of Emergency Medicine, Eastern Virginia Medical School, 825 Fairfax Ave, Norfolk, United States; Emergency Physicians of Tidewater, Virginia, Norfolk, United States.
  • Karpov MV; Research and Infrastructure Service Enterprise, Eastern Virginia Medical School, 825 Fairfax Ave, Norfolk, United States.
  • Gartman GH; Department of Emergency Medicine, Eastern Virginia Medical School, 825 Fairfax Ave, Norfolk, United States; Emergency Physicians of Tidewater, Virginia, Norfolk, United States.
  • Neubauer LE; Department of Emergency Medicine, Eastern Virginia Medical School, 825 Fairfax Ave, Norfolk, United States; Emergency Physicians of Tidewater, Virginia, Norfolk, United States.
  • Kaplan MC; Pharmacy, Sentara Health, Virginia, United States.
Am J Emerg Med ; 79: 33-37, 2024 05.
Article en En | MEDLINE | ID: mdl-38340480
ABSTRACT

BACKGROUND:

Angiotensin converting enzyme inhibitors (ACE-Is) prevent the breakdown of bradykinin and can lead to life threatening angioedema. Tranexamic acid is an antifibrinolytic that inhibits formation of precursors involved in bradykinin synthesis and, in case reports, has been described as a potential treatment for ACE-I angioedema.

METHODS:

This retrospective study included patients who presented to the emergency department (ED) from January 2018 to August 2021 with angioedema while taking an ACE-I. Patients who received tranexamic acid (treatment group) were compared with patients who did not receive tranexamic acid (control group). Primary outcome was length of stay (LOS). Secondary outcomes evaluated included ICU admissions, intubations, and safety events.

RESULTS:

A total of 262 patients were included in this study (73 treatment; 189 control). Overall, the median ED LOS was longer in the treatment group than controls (20.9 h vs 4.8 h, p < 0.001). ICU admission rates were higher in the treatment group (45% vs 16%, p < 0.001). More patients were intubated in the treatment group (12% vs 3%, p = 0.018). No difference was seen between the treatment group and the controls for return within 7 days, complications related to thrombosis, and death. In patients presenting with severe angioedema symptoms who were admitted to the hospital, median LOS was not different between the two groups (58.7 h vs 55.7 h, p = 0.61).

CONCLUSIONS:

Patients who received tranexamic acid had increased ED LOS, rates of ICU admission, and need for intubation. This finding may be related to the severity of presentation. Administration of tranexamic acid appears safe to use in ACE-I angioedema. Prospective randomized controlled studies should be considered to determine whether tranexamic acid is an effective treatment for ACE-I angioedema.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácido Tranexámico / Angioedema Tipo de estudio: Clinical_trials / Observational_studies Límite: Humans Idioma: En Revista: Am J Emerg Med Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácido Tranexámico / Angioedema Tipo de estudio: Clinical_trials / Observational_studies Límite: Humans Idioma: En Revista: Am J Emerg Med Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos