Assessing the control of the disease on current treatments available in Romania for hereditary angioedema patients

1 Cicardi M, Aberer W, Banerji A, et al. Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group. Allergy. 2014;69(5):602-616. doi:10.1111/all.12380. Search in Google Scholar

2 Magerl M, Sala-Cunill A, Weber-Chrysochoou C, Trainotti S, Mormile I, Spadaro G. Could it be hereditary angioedema? -Perspectives from different medical specialties. Clin Transl Allergy. 2023;13(9):e12297. doi:10.1002/clt2.12297. Search in Google Scholar

3 Bork K, Anderson JT, Caballero T, et al. Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report. Allergy Asthma Clin Immunol. 2021;17(1):40. doi:10.1186/s13223-021-00537-2. Search in Google Scholar

5 Maurer M, Magerl M, Betschel S, et al. The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update. World Allergy Organ J. 2022;15(3):100627. doi: 10.1016/j.waojou.2022.100627. Search in Google Scholar

6 Maurer M, Magerl M, Ansotegui I, et al. The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and update. Allergy. 2018;73(8):1575-1596. doi:10.1111/all.13384. Search in Google Scholar

7 Germenis AE, Speletas M. Genetics of Hereditary Angioedema Revisited. Clin Rev Allergy Immunol. 2016;51(2):170-182. doi:10.1007/s12016-016-8543-x. Search in Google Scholar

8 Cicardi M, Zuraw BL. Angioedema Due to Bradykinin Dysregulation. J Allergy Clin Immunol Pract. 2018;6(4):1132-1141. doi: 10.1016/j. jaip.2018.04.022. Search in Google Scholar

9 Bork K, Wulff K, Steinmüller-Magin L, et al. Hereditary angioedema with a mutation in the plasminogen gene [published correction appears in Allergy. 2018 Dec;73(12):2412]. Allergy. 2018;73(2):442-450. doi:10.1111/all.13270. Search in Google Scholar

10 Bork K, Wulff K, Rossmann H, et al. Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin. Allergy. 2019;74(12):2479-2481. doi:10.1111/all.13869. Search in Google Scholar

11 Ariano A, D’Apolito M, Bova M, et al. A myoferlin gain-of-function variant associates with a new type of hereditary angioedema. Allergy. 2020;75(11):2989-2992. doi:10.1111/all.14454. Search in Google Scholar

12 Bork K, Wulff K, Möhl BS, et al. Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation. J Allergy Clin Immunol. 2021;148(4):1041-1048. doi: 10.1016/j.jaci.2021.01.011. Search in Google Scholar

13 Bork K, Machnig T, Wulff K, Witzke G, Prusty S, Hardt J. Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence. Orphanet J Rare Dis. 2020;15(1):289. doi:10.1186/s13023-020-01570-x. Search in Google Scholar

14 Weller K, Donoso T, Magerl M, et al. Validation of the Angioedema Control Test (AECT)-A Patient-Reported Outcome Instrument for Assessing Angioedema Control. J Allergy Clin Immunol Pract. 2020;8(6):2050-2057.e4. doi: 10.1016/j.jaip.2020.02.038. Search in Google Scholar

15 Weller K, Donoso T, Magerl M, et al. Development of the Angioedema Control Test-A patient-reported outcome measure that assesses disease control in patients with recurrent angioedema. Allergy. 2020;75(5):1165-1177. doi:10.1111/all.14144. Search in Google Scholar

16 Mendivil J, Murphy R, de la Cruz M, et al. Clinical characteristics and burden of illness in patients with hereditary angioedema: findings from a multinational patient survey. Orphanet J Rare Dis. 2021;16(1):94. doi:10.1186/s13023-021-01717-4. Search in Google Scholar

17 Banerji A, Davis KH, Brown TM, et al. Patient-reported burden of hereditary angioedema: findings from a patient survey in the United States. Ann Allergy Asthma Immunol. 2020;124(6):600-607. doi: 10.1016/j.anai.2020.02.018. Search in Google Scholar

18 Gabos G, Nadasan V, Mihaly E, Dobru D. Hereditary Angioedema Due to C1-Inhibitor Deficiency in Romania: First National Study, Diagnostic and Treatment Challenges. Iran J Immunol. 2020;17(3):226-235. doi:10.22034/iji.2020.85416.1709. Search in Google Scholar

19 Zarnowski J, Rabe M, Kage P, Simon JC, Treudler R. Prophylactic Treatment in Hereditary Angioedema Is Associated with Reduced Anxiety in Patients in Leipzig, Germany. Int Arch Allergy Immunol. 2021;182(9):819-826. doi:10.1159/000514973. Search in Google Scholar

20 Fijen LM, Vera C, Buttgereit T, et al. Sensitivity to change and minimal clinically important difference of the angioedema control test. Clin Transl Allergy. 2023;13(9):e12295. doi:10.1002/clt2.12295. Search in Google Scholar