Therapeutic Efficacy of Icatibant in Angioedema Induced by Angiotensin-Converting Enzyme Inhibitors: A Case Series

被引:130
作者
Bas, Murat [1 ]
Greve, Jens [2 ]
Stelter, Klaus [3 ]
Bier, Henning [1 ]
Stark, Thomas [1 ]
Hoffmann, Thomas K. [2 ]
Kojda, Georg [4 ]
机构
[1] Tech Univ Munich, Hals Nasen Ohrenklin & Poliklin, Klinikum Rechts Isar, D-81675 Munich, Germany
[2] Univ Essen Gesamthsch, Dept Otorhinolaryngol, Essen, Germany
[3] Univ Munich, Dept Otorhinolaryngol, Munich, Germany
[4] Univ Duesseldorf, Inst Pharmacol & Clin Pharmacol, Dusseldorf, Germany
关键词
HEREDITARY ANGIOEDEMA; BRADYKININ; RECEPTOR; EDEMA;
D O I
10.1016/j.annemergmed.2010.03.032
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objective: The pathophysiology of angiotensin-converting enzyme inhibitor (ACEi)-induced angioedema most likely resembles that of hereditary angioedema, le, it is mainly mediated by bradykinin-induced activation of vascular bradykinin B2 receptors. We hypothesize that the bradykinin B2 receptor antagonist icatibant might be an effective therapy for ACEi-induced angioedema. Methods: Eight patients with acute ACEi-induced angioedema were treated with a single subcutaneous injection of icatibant. The outcome was assessed by the time to first improvement of symptoms, complete symptom relief, and drug safety. In addition, we retrospectively assessed the clinical course of 47 consecutive patients of our clinic with ACEi-induced angioedema. Results: First symptom improvement after icatibant injection occurred at a mean time of 50.6 minutes (standard deviation [SD] 21 minutes) and complete relief of symptoms at 4.4 hours (SD 0.8 hours). No patient received tracheal intubation, other drug treatment, tracheotomy, or a second icatibant injection. There were no adverse effects except erythema occurring at the injection site. In the historical comparison group treated with methylprednisolone and clemastine, the mean time to complete relief of symptoms was 33 hours (SD 19.4 hours). Some of these patients received a tracheotomy (3/47), were intubated (2/47), or received a second dose of methylprednisolone (12/47). Conclusion: Although sample size limits the external validity of our results, the substantial decrease of time to complete symptom relief suggests that this new treatment is likely effective as a pharmacotherapeutic approach to treat ACEi-induced angioedema. [Ann Emerg Med. 2010;56:278-282.]
引用
收藏
页码:278 / 282
页数:5
相关论文
共 10 条
[1]   Nonallergic angioedema: role of bradykinin [J].
Bas, M. ;
Adams, V. ;
Suvorava, T. ;
Niehues, T. ;
Hoffmann, T. K. ;
Kojda, G. .
ALLERGY, 2007, 62 (08) :842-856
[2]   Increased C-reactive protein in ACE-inhibitor-induced angioedema [J].
Bas, M ;
Hoffmann, TK ;
Bier, H ;
Kojda, G .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 59 (02) :233-238
[3]   Treatment of acute edema attacks in hereditary angioedema with a bradykinin receptor-2 antagonist (Icatibant) [J].
Bork, Konrad ;
Frank, Jorge ;
Grundt, Boris ;
Schlattmann, Peter ;
Nussberger, Juerg ;
Kreuz, Wolfhart .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2007, 119 (06) :1497-1503
[4]   Biological effects of C1 inhibitor [J].
Davis, AE .
DRUG NEWS & PERSPECTIVES, 2004, 17 (07) :439-446
[5]   The pathogenesis of hereditary angioedema [J].
Davis, AE .
TRANSFUSION AND APHERESIS SCIENCE, 2003, 29 (03) :195-203
[6]  
DAVIS AE, 1993, BEHRING I MITT, V93, P313
[7]   Increased vascular permeability in C1 men inhibitor-deficient mice mediated by the bradykinin type 2 receptor [J].
Han, ED ;
MacFarlane, RC ;
Mulligan, AN ;
Scafidi, J ;
Davis, AE .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (08) :1057-1063
[8]   Plasma bradykinin in angio-oedema [J].
Nussberger, J ;
Cugno, M ;
Amstutz, C ;
Cicardi, M ;
Pellacani, A ;
Agostoni, A .
LANCET, 1998, 351 (9117) :1693-1697
[9]   Valsartan, captopril, or both in myocardial infarction complicated by heart failure, left ventricular dysfunction, or both [J].
Pfeffer, MA ;
McMurray, JJV ;
Velazquez, EJ ;
Rouleau, JL ;
Kober, L ;
Maggioni, AP ;
Solomon, SD ;
Swedberg, K ;
Van de Werf, F ;
White, H ;
Leimberger, JD ;
Henis, M ;
Edwards, S ;
Zelenkofske, S ;
Sellers, MA ;
Califf, RM ;
Aylward, P ;
Armstrong, P ;
Barvik, S ;
Belenkov, Y ;
Dalby, A ;
Diaz, R ;
Drexler, H ;
Ertl, G ;
Francis, G ;
Hampton, J ;
Harsanyi, A ;
Kvasnicka, J ;
Mareev, V ;
Marin-Neto, J ;
Murin, J ;
Myers, M ;
Nordlander, R ;
Opolski, G ;
Soler-Soler, J ;
Spac, J ;
Stefenelli, T ;
Sugrue, D ;
Van Gilst, W ;
Varshavsky, S ;
Weaver, D ;
Zannad, F ;
Aguilar, D ;
Alvarez, A ;
Al-Taweel, M ;
Anavekar, N ;
Finn, P ;
Lopez-Jimenez, F ;
Mercier, R ;
Lewis, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (20) :1893-1906
[10]   Effects of the angiotensin-receptor blocker telmisartan on cardiovascular events in high-risk patients intolerant to angiotensin-converting enzyme inhibitors: a randomised controlled trial [J].
Yusuf, S. ;
Teo, K. ;
Anderson, C. ;
Pogue, J. ;
Dyal, L. ;
Copland, I. ;
Schumacher, H. ;
Dagenais, G. ;
Sleight, P. .
LANCET, 2008, 372 (9644) :1174-1183