Release Date: 2024-03-21

Advanced Cardiac Life Support in Anaphylaxis

Ali Gur (Author)

Release Date: 2024-03-21

Anaphylaxis is a rapid-onset, life-threatening, systemic hypersensitivity reaction that occurs in varying clinical and severities as a result of sudden mediator release from mast cells and basophils. Accurate estimation of the incidence of anaphylaxis is difficult due to difficulties in diagnosis, inadequacies in the recording system or inaccurate reporting. Foods (especially in children), medications and [...]

Media Type
  • PDF

Buy from

Price may vary by retailers

Work TypeBook Chapter
Published inSpecial Circumstances in Resuscitation
First Page1
Last Page26
DOIhttps://doi.org/10.69860/nobel.9786053358923.1
ISBN978-605-335-892-3 (PDF)
LanguageENG
Page Count26
Copyright HolderNobel Tıp Kitabevleri
Licensehttps://nobelpub.com/publish-with-us/copyright-and-licensing
Anaphylaxis is a rapid-onset, life-threatening, systemic hypersensitivity reaction that occurs in varying clinical and severities as a result of sudden mediator release from mast cells and basophils. Accurate estimation of the incidence of anaphylaxis is difficult due to difficulties in diagnosis, inadequacies in the recording system or inaccurate reporting. Foods (especially in children), medications and insect bites have been reported as the most common causes. During anaphylaxis, many different biochemical mediators, chemokines and cytokines are released as a result of the degranulation of mast cells and basophils. Some of these are mediators such as histamine, tryptase, heparin and carboxypeptidase, which are preformed in the granules within the cell; Some of them are newly produced platelet activating factor (PAF), prostaglandin (PG) D2, locotriene (LT) B4 and cysteinyl locotrienes (LTC4, LTD4, LTE4). The diagnosis of anaphylaxis is made with the help of history and physical examination using widely accepted clinical criteria. In anaphylaxis, there is usually involvement of at least two organ systems, but in some cases, involvement of only one organ system (hypotension in CVS) may be considered sufficient for diagnosis. It is vital that the first intervention and treatment be performed, if possible, at the place where the diagnosis was first made. The first drug that should be given in the treatment is adrenaline. Adult dose of adrenaline is 0.2-0.5 mg and the drug should be given intramuscularly (IM) to the front side of the thigh (vastus lateralis muscle). Before discharge, the patient should be evaluated in terms of the risk of recurrence of the reaction, and in addition to explaining other protective measures and recommendations in patients deemed to be at risk, an adrenaline auto-injector should be prescribed, and the patient and, if necessary, his/her relatives should be taught when and how to use it.

Ali Gur (Author)
Associate Professor, Ataturk University
https://orcid.org/0000-0002-7823-0266
3Dr. Ali GÜR is a successful emergency medicine specialist who specializes in emergency medicine and has a 12-year emergency career. He worked in the pre-hospital area, field and management. He has 145 publications to date and many publications in SCI journals. He has given many books on his field and many lectures on anaphylaxis. He has carried out projects, thesis supervision and academic studies related to his field. Provides first aid and advanced cardiac life support training. He has advanced cardiac life support trainer, Hospital Disaster and Emergency Planning Trainer trainer, Automatic External Defibrillator Trainer Trainer and Pediatric advanced cardiac life support trainer certificates. He currently works in the department of emergency medicine at Atatürk University Faculty of Medicine.

  • AAAI Board of Directos. (1994). Position statement: Use of epinephrine in the treatment of anaphylaxis. J Allergy Clin Immunol;94:666-68.

  • Anagnostou K. (2019). Myths, facts and controversies in the diagnosis and management of anaphylaxis. Arch Dis Child;104(1):83-90.

  • Arroabarren E. (2011). Improving anaphylaxis management in a pediatric emergency department. Pediatr Allergy Immunol;22:708-14.

  • Berenguer A. (2013). Anaphylaxis in pregnancy: a rare cause of neonatal mortality. BMJ Case Rep.

  • Bohlke K. (2004). Vaccine Safety Datalink Team. Epidemiology of anaphylaxis among children and adolescents enrolled in a health maintenance organization. J Allergy Clin Immunol; 113:536-42.

  • Brown SG. (2004). Insect sting anaphylaxis; prospective evaluation of treatment with intravenous adrenaline and volume resuscitation. Emerg Med J 2004;21:149-54.

  • Campbell RL. (2014). Members of the Joint Task Force; Practice ParameterWorkgroup. Emergency department diagnosis and treatment of anaphylaxis: a practice parameter. Ann Allergy Asthma Immunol;113:599-608.

  • Cetinkaya F. (2013). Hospital admissions for anaphylaxis in Istanbul, Turkey. Allergy;68:128-30.

  • Campbell RL. (2014). Members of the Joint Task Force; Practice ParameterWorkgroup. Emergency department diagnosis and treatment of anaphylaxis: a practice parameter. Ann Allergy Asthma Immunol;113:599-608

  • Cardona V. (2011). Allergic diseases in the elderly. Clin Transl Allergy;1:11.

  • Choo KJ. (2010). Glucocorticoids for the treatment of anaphylaxis: Cochrane systematic review. Allergy;65:1205-11.

  • Confino-Cohen R. (2010). Allergen immunotherapyinduced biphasic systemic reactions: incidence, characteristics, and outcome: a prospective study. Ann Allergy Asthma Immunol; 104:73-78

  • Dreborg S, et al. (2016). Do epinephrine auto-injectors have an unsuitable needle length in children and adolescents at risk for anaphylaxis from food allergy? Allergy Asthma Clin Immunol; 12:11-18.

  • El-Gamal Y. (2015). Anaphylaxis vulnerable groups. Egypt J Pediatr Allergy Immunol;13:3-6.

  • Fasting S. (2002). Serious intraoperative problems: A five year review of 83,844 anesthetics. Can J Anaesth;49(6):545- 553.

  • Finkelman FD. (2007). Anaphylaxis: lessons from mouse models. J Allergy Clin Immunol; 120:506-15.

  • Gibbs NM. (2013). Survival from perioperative anaphylaxis in Western Australia 2000–2009. Br J Anaesth;111(4):589-593.

  • Greenberger PA. (2007). Fatal anaphylaxis: postmortem findings and associated comorbid diseases. Ann Allergy Asthma Immunol;98:252-57.

  • Hartmann ME. (2016). Pediatric Emergencies and Resuscitation. In: Kliegman R, Stanton B, St. Geme J, Schor N (Eds). Nelson Textbook of Pediatrics. 20th ed. Philadelphia: Elsevier Inc.,:489-506.

  • Hogan AD. (1997). Markers of mast cell degranulation. Methods;13:43-52.

  • Huang F. (2012). Anaphylaxis in a New York City pediatric emergency department: triggers, treatments, and outcomes. J Allergy Clin Immunol;129:162-68.

  • Jarvinen KM. (2008). Use of multiple doses of epinephrine in food-induced anaphylaxis in children. J Allergy Clin Immunol;122:133-38.

  • Kalesnikoff J. (2010). Anaphylaxis: mechanisms of mast cell activation. Chem Immunol Allergy; 95:45-66

  • Kemp SF. (2002). Anaphylaxis: a review of causes and mechanisms. J Allergy Clin Immunol; 110:341-48.

  • Kuhlen JL Jr, et al. (2016). Antibiotics Are the Most Commonly Identified Cause of Perioperative Hypersensitivity Reactions. J Allergy Clin Immunol Pract;4(4):697-704

  • Lee S. (2015). Time of onset and predictors of biphasic anaphylactic reactions: a systematic review and meta-analysis. J Allergy Clin Immunol Pract;3:408-16.

  • Lieberman P. (2005). Biphasic anaphylactic reactions. Ann Allergy Asthma Immunol;95:217-26.

  • Lieberman P, et al. (2010). The diagnosis and management of anaphylaxis practice parameter: 2010 update. J Allergy Clin Immunol;126:477-80.

  • Lieberman P, et al. (2015). Anaphylaxis-a practice parameter update 2015. Ann Allergy Asthma Immunol;115:341-384

  • Ma T, et al. (2004). Correlation of thymidylate synthase, thymidine phosphorylase and dihydropyrimidine dehydrogenase with sensitivity of gastrointestinal cancer cells to 5-fluorouracil and 5-fluoro-2’- deoxyuridine. World J Gastroenterol;10:172-76.

  • MacGinnitie A. (2011). In utero anaphylaxis. Med Hypotheses;76:70-72.

  • Momeni M. (2007). Anaphylactic shock in a beta-blocked child: usefulness of isoproterenol. Paediatr Anaesth;17:897-99.

  • Moneret-Vautrin DA. (2005). Epidemiology of life-threatening and lethal anaphylaxis: A review.Allergy 60(4):443-451.

  • Mueller UR. (2007). Cardiovascular disease and anaphylaxis. Curr Opin Allergy Clin Immunol; 7:337-41.

  • Muraro A, et al. (2014). Anaphylaxis: guidelines from the European Academy of Allergy and Clinical Immunology. Allergy;69:1026-45

  • Murat I. (1993). Anaphylactic reactions during paediatric anaesthesia; results of the survey of the French Society of Paediatric Anaesthetists (ADARPEF) 1991–1992. Pediatr Anesth;3(6):339- 343.

  • Nieto A, et al. (2017). Clinical Profile of Patients With Severe Anaphylaxis Hospitalized in the Spanish Hospital System: 1997-2011. J Investig Allergol Clin Immunol;27:111-26.

  • Orhan F, et al. (2011). Anaphylaxis in Turkish children: a multi-centre, retrospective,case study. Clin Exp Allergy;41(12):1767-76.

  • Pumphrey RS. (2000). Lessons for management of anaphylaxis from a study of fatal reactions. Clin Exp Allergy;30:1144-50.

  • Pumphrey RS. (2003). Fatal posture in anaphylactic shock. J Allergy Clin Immunol;112:451-52.

  • Sahiner UM, et al. (2014). Serum basal tryptase may be a good marker for predicting the risk of anaphylaxis in children with food allergy. Allergy;69:265-68.

  • Sampson HA, et al. (2006). Second symposium on the definition and management of anaphylaxis: summary report- Second National Institute of Allergy and Infectious Disease/ Food Allergy and Anaphylaxis Network symposium. J Allergy Clin Immunol;117:391-97.

  • Schwartz LB. (1989). Time course of appearance and disappearance of human mast cell tryptase in the circulation after anaphylaxis. J Clin Invest;83:1551-55.

  • Simons FE. (2002). Epinephrine dispensing patterns for an out-of-hospital population: a novel approach to studying the epidemiology of anaphylaxis. J Allergy Clin Immunol; 110:647-51.

  • Simons FE. (2004). First-aid treatment of anaphylaxis to food: focus on epinephrine. J Allergy Clin Immunol;113:837-44.

  • Simons FE. (2010). Anaphylaxis. J Allergy Clin Immunol;125:S161-S181.

  • Simons FE, et al. (2011). World Allergy Organization anaphylaxis guidelines: summary. J Allergy Clin Immunol:127:587- 93.

  • Simons FE. (2012). Anaphylaxis during pregnancy. J Allergy Clin Immunol;130:597-606.

  • Simons FE, et al. (2014). International consensus on (ICON) anaphylaxis. World Allergy Organ J;7:9.

  • Simons et al. (2015). World Allergy Organization Journal;8:32.

  • Sheikh A. (2007). H1- antihistamines for the treatment of anaphylaxis: Cochrane systematic review. Allergy;62:830-37.

  • Steele R. (2012). Anaphylaxis in the community setting: determining risk factors for admission. Ann Allergy Asthma Immunol;109:133-36.

  • Takeda J. (1995). Plasma N-methylhistamine concentration as an indicator of histamine release by intravenous d-tubocurarine in humans: preliminary study in five patients by radioimmunoassay kits. Anesth Analg;80:1015-17.

  • Tejedor Alonso MA. (2015). Epidemiology of anaphylaxis. Clin Exp Allergy;45:1027-39.

  • Thomas M. (2005). Best evidence topic report. Glucagon infusion in refractory anaphylactic shock in patients on betablockers. Emergency Medicine Journal;22:272-73.

  • Truhlar A, et al. (2015). European Resuscitation Council Guidelines for Resuscitation 2015: Section 4. Cardiac arrest in special circumstances. Resuscitation;95:148-201.

  • Turner PJ. (2020). Global trends in anaphylaxis epidemiology and clinical implications. J Allergy Clin Immunol Pract;8(4):1169-1176.

  • Weiss ME, et al. (1989). Association of protamine IgE and IgG antibodies with life-threatening reactions to intravenous protamine. N Engl J Med;320:886-92.

  • Wheeler DW, et al. (2008). The effect of drug concentration expression on epinephrine dosing errors: a randomized trial. Ann Intern Med;148:11-14.

  • Wood RA, et al. (2014). Anaphylaxis in America: the prevalence and characteristics of anaphylaxis in the United States. J Allergy Clin Immunol;133:461-67.

  • Worm M, et al. (2012). Symptom profile and risk factors of anaphylaxis in Central Europe. Allergy; 67:691-98.

  • Vetander M, et al. (2012). Anaphylaxis and reactions to foods in children – a population-based case study of emergency department visits. Clin Exp Allergy;42:568-77.

  • Zwirner J, et al. (1998).The human mast cell line HMC-1 binds and responds to C3a but not C3a(desArg). Scand J Immunol;47:19-24.

Share This Chapter!