Skip to main content

Bradykinin-Mediated Angioedema

  • Chapter
  • First Online:
  • 1681 Accesses

Abstract

Bradykinin-mediated angioedema (AE) is a clinical syndrome characterised by episodes of subcutaneous or mucosal oedema (extremities, throat, respiratory and digestive tracts) referred to as attacks. Any ICU physician could encounter patient during an attack. The diagnosis of AE must be evoked in cases of transient and recurrent oedema and/or abdominal pain. All attacks localised over the shoulders (face, neck, throat and respiratory tract) and all abdominal attacks with pain rated >5 on the VAS must be considered severe. Severe ENT attacks may be life-threatening. In the absence of specific treatment, the mortality rate reaches 25–30 % due to asphyxia. In emergency situations, a step-by-step approach is necessary to establish a diagnosis and evaluate the severity. This is not an allergic reaction. Antihistamines are not effective because bradykinin is the key mediator. There are hereditary and acquired forms, notably associated with the use of ACE inhibitors. All severe attacks should benefit from early specific treatment. The availability of these treatments varies by country and there is currently no consensus as to the correct choice of a specific treatment. Even in the absence of previous attack, short-term prophylaxis is necessary during the perioperatory period. The rarity of this disease and the characteristics of the specific drugs (i.e., their retention periods, modes of delivery, prices and methods for reimbursement) should encourage hospitals to make strategic choices regarding the creation of an emergency supply of drugs or an institute-wide protocol for the rapid transfer of patients to specialised centres for treatment.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   119.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   159.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   159.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

References

  1. Bowen T, Cicardi M, Farkas H, Bork K, Longhurst HJ, Zuraw B et al (2010) 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol 6(1):24

    Article  PubMed Central  PubMed  Google Scholar 

  2. Bowen T (2011) Hereditary angioedema: beyond international consensus—circa December 2010—the Canadian society of allergy and clinical immunology Dr. David McCourtie lecture. Allergy Asthma Clin Immunol 7(1):1

    Article  PubMed Central  PubMed  Google Scholar 

  3. Caballero T, Baeza ML, Cabanas R, Campos A, Cimbollek S, Gomez-Traseira C et al (2011) Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis. J Investig Allergol Clin Immunol 21(5):333–347

    CAS  PubMed  Google Scholar 

  4. Caballero T, Baeza ML, Cabanas R, Campos A, Cimbollek S, Gomez-Traseira C et al (2011) Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part II. Treatment, follow-up, and special situations. J Investig Allergol Clin Immunol 21(6):422–441

    CAS  PubMed  Google Scholar 

  5. Cicardi M, Bork K, Caballero T, Craig T, Li HH, Longhurst H et al (2011) Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: consensus report of an International Working Group. Allergy 67(2):147–157

    Article  PubMed  Google Scholar 

  6. Zuraw BL (2008) Clinical practice. Hereditary angioedema. N Engl J Med 359(10):1027–1036

    Article  CAS  PubMed  Google Scholar 

  7. Cicardi M, Zanichelli A (2010) Acquired angioedema. Allergy Asthma Clin Immunol 6(1):14

    Article  PubMed Central  PubMed  Google Scholar 

  8. Agostoni A, Aygoren-Pursun E, Binkley KE, Blanch A, Bork K, Bouillet L et al (2004) Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol 114(3 Suppl):S51–S131

    Article  PubMed  Google Scholar 

  9. Bork K, Siedlecki K, Bosch S, Schopf RE, Kreuz W (2000) Asphyxiation by laryngeal edema in patients with hereditary angioedema. Mayo Clin Proc 75(4):349–354

    Article  CAS  PubMed  Google Scholar 

  10. Bork K, Hardt J, Schicketanz KH, Ressel N (2003) Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency. Arch Intern Med 163(10):1229–1235

    Article  PubMed  Google Scholar 

  11. Bork K, Staubach P, Eckardt AJ, Hardt J (2006) Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency. Am J Gastroenterol 101(3):619–627

    Article  CAS  PubMed  Google Scholar 

  12. Nzeako UC (2010) Diagnosis and management of angioedema with abdominal involvement: a gastroenterology perspective. World J Gastroenterol 16(39):4913–4921

    Article  PubMed Central  PubMed  Google Scholar 

  13. Guichon C, Floccard B, Coppere B, Hautin E, Bages-Limoges F, Rouviere O et al (2011) One hypovolaemic shock…two kinin pathway abnormalities. Intensive Care Med 37(7):1227–1228

    Article  PubMed  Google Scholar 

  14. Bork K, Hardt J, Staubach-Renz P, Witzke G (2011) Risk of laryngeal edema and facial swellings after tooth extraction in patients with hereditary angioedema with and without prophylaxis with C1 inhibitor concentrate: a retrospective study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 112(1):58–64

    Article  PubMed  Google Scholar 

  15. Bork K, Hardt J, Witzke G (2012) Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency. J Allergy Clin Immunol 130(3):692–697

    Article  PubMed  Google Scholar 

  16. Maurer M, Bader M, Bas M, Bossi F, Cicardi M, Cugno M, et al (2011) New topics in bradykinin research. Allergy 66(11):1397–1406

    Google Scholar 

  17. Davis AE 3rd (2005) The pathophysiology of hereditary angioedema. Clin Immunol 114(1):3–9

    Article  CAS  PubMed  Google Scholar 

  18. Bas M, Adams V, Suvorava T, Niehues T, Hoffmann TK, Kojda G (2007) Nonallergic angioedema: role of bradykinin. Allergy 62(8):842–856

    Article  CAS  PubMed  Google Scholar 

  19. Kaplan A (2011) Bradykinin and the pathogenesis of hereditary angiodema. WAO J 4:73–75

    Google Scholar 

  20. Bossi F, Fischetti F, Regoli D, Durigutto P, Frossi B, Gobeil F Jr et al (2009) Novel pathogenic mechanism and therapeutic approaches to angioedema associated with C1 inhibitor deficiency. J Allergy Clin Immunol 124(6):1303–1310

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  21. Bouillet L (2010) Hereditary angioedema in women. Allergy Asthma Clin Immunol 6(1):17

    Article  PubMed Central  PubMed  Google Scholar 

  22. Brown NJ, Byiers S, Carr D, Maldonado M, Warner BA (2009) Dipeptidyl peptidase-IV inhibitor use associated with increased risk of ACE inhibitor-associated angioedema. Hypertension 54(3):516–523

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  23. Hoover T, Lippmann M, Grouzmann E, Marceau F, Herscu P (2010) Angiotensin converting enzyme inhibitor induced angio-oedema: a review of the pathophysiology and risk factors. Clin Exp Allergy 40(1):50–61

    CAS  PubMed  Google Scholar 

  24. Miller DR, Oliveria SA, Berlowitz DR, Fincke BG, Stang P, Lillienfeld DE (2008) Angioedema incidence in US veterans initiating angiotensin-converting enzyme inhibitors. Hypertension 51(6):1624–1630

    Article  CAS  PubMed  Google Scholar 

  25. Tai S, Mascaro M, Goldstein NA (2010) Angioedema: a review of 367 episodes presenting to three tertiary care hospitals. Ann Otol Rhinol Laryngol 119(12):836–841

    PubMed  Google Scholar 

  26. Morgan BP (2010) Hereditary angioedema-therapies old and new. N Engl J Med 363:581–583

    Article  CAS  PubMed  Google Scholar 

  27. De Serres J, Groner A, Lindner J (2003) Safety and efficacy of pasteurized C1 inhibitor concentrate (Berinert P) in hereditary angioedema: a review. Transfus Apher Sci 29(3):247–254

    Article  PubMed  Google Scholar 

  28. Longhurst HJ (2005) Emergency treatment of acute attacks in hereditary angioedema due to C1 inhibitor deficiency: what is the evidence? Int J Clin Pract 59(5):594–599

    Article  CAS  PubMed  Google Scholar 

  29. Craig TJ, Levy RJ, Wasserman RL, Bewtra AK, Hurewitz D, Obtulowicz K et al (2009) Efficacy of human C1 esterase inhibitor concentrate compared with placebo in acute hereditary angioedema attacks. J Allergy Clin Immunol 124(4):801–808

    Article  CAS  PubMed  Google Scholar 

  30. Craig TJ, Bewtra AK, Bahna SL, Hurewitz D, Schneider LC, Levy RJ, et al (2011) C1 esterase inhibitor concentrate in 1085 hereditary angioedema attacks—final results of the I.M.P.A.C.T.2 study. Allergy 66(12):1604–1611

    Google Scholar 

  31. Cicardi M, Banerji A, Bracho F, Malbran A, Rosenkranz B, Riedl M et al (2010) Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema. N Engl J Med 363(6):532–541

    Article  CAS  PubMed  Google Scholar 

  32. Longhurst H (2008) Rhucin, a recombinant C1 inhibitor for the treatment of hereditary angioedema and cerebral ischemia. Curr Opin Investig Drugs 9(3):310–323

    CAS  PubMed  Google Scholar 

  33. Zuraw BL, Busse PJ, White M, Jacobs J, Lumry W, Baker J et al (2010) Nanofiltered c1 inhibitor concentrate for treatment of hereditary angioedema. N Engl J Med 363(6):513–522

    Article  CAS  PubMed  Google Scholar 

  34. Cicardi M, Levy RJ, McNeil DL, Li HH, Sheffer AL, Campion M et al (2010) Ecallantide for the treatment of acute attacks in hereditary angioedema. N Engl J Med 363(6):523–531

    Article  CAS  PubMed  Google Scholar 

  35. Craig TJ, Wasserman RL, Levy RJ, Bewtra AK, Schneider L, Packer F, et al (2010) Prospective study of rapid relief provided by c1 esterase inhibitor in emergency treatment of acute laryngeal attacks in hereditary angioedema. J Clin Immunol 126(4):821–827

    Google Scholar 

  36. Floccard B, Crozon J, Rimmele T, Vulliez A, Coppere B, Chamouard V, et al (2011) Management of bradykinin-mediated angioedema. Ann F Anesth Reanim 30(7–8):578–588

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bernard Floccard .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2014 Springer International Publishing Switzerland

About this chapter

Cite this chapter

Floccard, B., Crozon, J., Coppere, B., Bouillet, L., Allaouchiche, B. (2014). Bradykinin-Mediated Angioedema. In: Leone, M., Martin, C., Vincent, JL. (eds) Uncommon Diseases in the ICU. Springer, Cham. https://doi.org/10.1007/978-3-319-04576-4_16

Download citation

  • DOI: https://doi.org/10.1007/978-3-319-04576-4_16

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-04575-7

  • Online ISBN: 978-3-319-04576-4

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics