PMID- 36065111 OWN - NLM STAT- MEDLINE DCOM- 20220908 LR - 20221212 IS - 1539-6304 (Electronic) IS - 1088-5412 (Linking) VI - 43 IP - 5 DP - 2022 Sep 1 TI - Longitudinal experience with treatment of acquired angioedema using tranexamic acid. PG - 413-418 LID - 10.2500/aap.2022.43.220043 [doi] AB - Background: Acquired angioedema (AAE) is a rare form of angioedema (AE) and is often associated with lymphoproliferative conditions and/or anti-C1 esterase inhibitor (C1-INH) antibodies without clear treatment consensus. Current treatments have been reported to have variable effectiveness with different safety concerns. A large Italian cohort of patients with AAE was previously found to respond well to tranexamic acid (TXA). Herein, we report our experience treating AAE with TXA used as prophylaxis. Objective: The objective was to describe clinical characteristics of patients with AAE and to report our experience with treating AAE with TXA. Methods: A retrospective chart review of patients with AAE (N = 13) from a large practice was conducted to assess characteristics and treatment responses. Patient demographics in addition to C1-INH quantitative, C1-INH functional, C4, and C1q levels; the presence of C1-INH antibodies; and a history of lymphoproliferative disease were extracted. The patients were also characterized by their treatment response to TXA. Results: All the patients were white, with a mean age at diagnosis of 67 years, an average body mass index of 31.3 kg/m(2), and a male-to-female ratio of 7:6. Nine patients had positive C1-INH antibodies. The patients were on various prophylaxis treatments before TXA, including chemotherapy that targeted malignancy, cyclophosphamide, rituximab, and plasmapheresis. Ultimately, 11 of the 13 patients were on TXA for prophylaxis. At 1, 12, and 24 months after TXA treatment, attacks decreased by 97, 86, and 99%, respectively. One patient developed a deep vein thrombosis and TXA was stopped. Conclusion: These findings demonstrated that treatment of AAE with TXA was effective as prophylaxis for AE attacks. However, potential adverse effects remain a concern, which emphasizes the need for additional options. FAU - Kesh, Susamita AU - Kesh S AD - From the Division of Immunology and Allergy, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio. FAU - Singh, Umesh AU - Singh U AD - Division of Immunology/Allergy Section, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio; and. FAU - Bernstein, Jonathan A AU - Bernstein JA AD - Division of Immunology/Allergy Section, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio; and. LA - eng PT - Journal Article PL - United States TA - Allergy Asthma Proc JT - Allergy and asthma proceedings JID - 9603640 RN - 0 (Complement C1 Inhibitor Protein) RN - 6T84R30KC1 (Tranexamic Acid) RN - Acquired angioedema SB - IM MH - *Angioedema/diagnosis MH - *Angioedemas, Hereditary/diagnosis MH - Complement C1 Inhibitor Protein/therapeutic use MH - Female MH - Humans MH - *Lymphoproliferative Disorders MH - Male MH - Retrospective Studies MH - *Tranexamic Acid/therapeutic use EDAT- 2022/09/07 06:00 MHDA- 2022/09/09 06:00 CRDT- 2022/09/06 00:32 PHST- 2022/09/06 00:32 [entrez] PHST- 2022/09/07 06:00 [pubmed] PHST- 2022/09/09 06:00 [medline] AID - 10.2500/aap.2022.43.220043 [doi] PST - ppublish SO - Allergy Asthma Proc. 2022 Sep 1;43(5):413-418. doi: 10.2500/aap.2022.43.220043.