Detailed Information on Publication Record
2018
Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy
HAKL, Roman, Pavel KUKLÍNEK, Irena KRČMOVÁ, Pavlína KRÁLÍČKOVÁ, Tomáš FREIBERGER et. al.Basic information
Original name
Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy
Authors
HAKL, Roman (203 Czech Republic, guarantor, belonging to the institution), Pavel KUKLÍNEK (203 Czech Republic), Irena KRČMOVÁ (203 Czech Republic), Pavlína KRÁLÍČKOVÁ, Tomáš FREIBERGER (203 Czech Republic, belonging to the institution), Petr JANKŮ (203 Czech Republic), Marcela VLKOVÁ (203 Czech Republic, belonging to the institution) and Jiří LITZMAN (203 Czech Republic, belonging to the institution)
Edition
Journal of Clinical Immunology, New York, Springer, 2018, 0271-9142
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30102 Immunology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 4.128
RIV identification code
RIV/00216224:14110/18:00104428
Organization unit
Faculty of Medicine
UT WoS
000447514500016
Keywords in English
Hereditary angioedema; pregnancy; therapy; icatibant; recombinant C1 inhibitor
Tags
International impact, Reviewed
Změněno: 11/2/2019 15:41, Soňa Böhmová
Abstract
V originále
PurposeHereditary angioedema (HAE) is a rare disease caused by a C1 inhibitor (C1-INH) deficit. Clinically, HAE is manifested by repeated episodes of localized subcutaneous or submucosal oedema attacks. Managing HAE patients in pregnancy is challenging, since there are only limited data on the safety and efficacy of various therapeutic approaches.MethodsWe present our clinical experience treating acute HAE attacks during pregnancy in six consecutive patients.ResultsDuring the pregnancies, 79 HAE attacks occurred. The most frequent were abdominal 53 (67.1%) followed by peripheral 21 (26.6%), facial 10 (12.7%), and laryngeal 10 (12.7%) oedemas; 13 (16.5%) attacks were combined. Fifty (63.3%) attacks were treated with recombinant human C1-INH (rhC1-INH); 17 (21.5%) with plasma-derived, pasteurized, nanofiltered C1-INH (pnfC1-INH); 13 (16.5%) with icatibant; and 1 (1.3%) with plasma-derived, nanofiltered C1-INH (nfC1-INH). Treatment had to be repeated in 5 attacks (6.3%). All six deliveries (one caesarean section and five spontaneous vaginal deliveries) were complication free. All pregnancies went to the full term and the patients delivered healthy babies with a birth weight ranging from 2850 to 3690g. No congenital abnormalities were detected in the neonates. No abortions occurred.ConclusionsOur results show good C1-INH or icatibant treatment efficacy for HAE attacks in pregnancy. The treatment by the first drug used was effective in 93.7% of all attacks. In 6.3% of attacks, a second treatment had to be used. No adverse effects were observed.
Links
MUNI/A/0925/2017, interní kód MU |
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NV15-28732A, research and development project |
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NV16-34414A, research and development project |
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NV18-05-00330, research and development project |
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