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Anaphylaxis and its Treatment

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Introduction

Anaphylaxis is a sudden onset (or rapidly progressive) severe systemic allergic reaction, affecting multiple organs. Its onset may be heralded by skin and/or mucosal changes (flushing, urticaria, angioedema) and progress to include life-threatening airway, lung and/or circulation problems. Its identification and management is based on the Resuscitation Council UK Guidelines.1

Incidence

The number of people who suffer severe systemic allergic reactions is increasing. The incidence is about 1 - 3 reactions per 10,000 population per annum, although anaphylaxis is not always recognised, so certain UK studies may underestimate the incidence.1

Aetiology

An anaphylactic reaction occurs when an allergen reacts with specific IgE antibodies on mast cells and basophils (type 1 hypersensitivity reaction) triggering the rapid release of stored histamine and the rapid synthesis of newly formed mediators. These cause capillary leakage, mucosal oedema and ultimately shock and asphyxia. Anaphylactic reactions can vary in severity and rate of progression - they may progress rapidly (over a few minutes) or occasionally in a biphasic manner. Rarely manifestations may be delayed by a few hours (adding to diagnostic difficulty), or persist for more than 24 hours.
Anaphylactoid reactions are not IgE mediated but cause similar mast cell activation.

A significant number of cases of anaphylaxis are idiopathic.1
The most common triggers of anaphylaxis:

  • Foods:2
    • Peanuts
    • Pulses
    • Tree nuts (e.g. brazil nut, almond, hazelnut)
    • Fish and shellfish
    • Eggs
    • Milk
    • Sesame
  • Venom, for example:
  • Drugs, including:
    • Antibiotics
    • Opioids
    • NSAI's
    • IV contrast media
    • Muscle relaxants
    • Other anaesthetic drugs
Presentation

There is often (but not always) a history of previous sensitivity to an allergen, or recent history of exposure to a new drug (eg vaccination). Initially patients usually develop skin symptoms include generalised itching, urticaria and erythema, rhinitis, conjunctivitis and angio-oedema.

Signs that the airway is becoming involved include itching of the palate or external auditory meatus, dyspnoea, laryngeal oedema (stridor) and wheezing (bronchospasm). General symptoms include palpitations and tachycardia (as opposed to bradycardia in simple vasovagal at immunisation time), nausea, vomiting and abdominal pain, feeling faint - with a sense of impending doom; and ultimately collapse and loss of consciousness.

Airway swelling, stridor, breathing difficulty, wheeze, cyanosis, hypotension, tachycardia and reduced capillary filling suggest impending severe reaction.1

If no history is available in a collapsed patient use an ABCDE advanced life-support approach to recognise and treat an anaphylactic reaction.Treat life-threatening problems as you find them. The basic principles of treatment are the same for all age groups.

Differential diagnosis1

Life-threatening conditions :

  • Sometimes an anaphylactic reaction can present with symptoms and signs that are very similar to life-threatening asthma – this is commonest in children.
  • A low blood pressure (or normal in children) with a petechial or purpuric rash can be a sign of septic shock.
  • Seek help early if there are any doubts about the diagnosis and treatment.

Non life-threatening conditions
These usually respond to simple measures:

  • Faint (vasovagal episode).
  • Panic attack.
  • Breath-holding episode in child.
  • Idiopathic (non-allergic) urticaria or angioedema.
Emergency treatment1

Treatment in an emergency means following without delay a systematic assessment and treatment plan.

Quick reference anaphylaxis algorithm

  • Rapid assessment
    • Airway: Look for and relieve airway obstruction, call for help early if signs of obstruction.
    • Breathing: Look for and treat bronchospasm and signs of respiratory distress.
    • Circulation: Colour, pulse and blood pressure.
    • Disability: Assess whether responding or unconscious.
    • Exposure: Assess skin with adequate exposure, but avoid excess heat loss.
  • Consider anaphylaxis when compatible history of rapid onset severe allergic-type reaction with respiratory difficulty and/or hypotension especially if skin changes present.
  • Give high flow oxygen - using a mask with an oxygen reservoir (greater than 10 litres min-1 to prevent reservoir collapse).
  • Lie patient flat:
    • Raise the legs (care as may worsen any breathing problems).
    • In pregnant patients use a left lateral tilt of at least 15 degrees (to avoid caval compression).
  • ADRENALINE IM in anterolateral aspect of the middle third of the thigh (safe, easy, effective):
    • Adult intramuscular (IM) dose 0.5 mg IM (= 500 micrograms = 0.5 mL of 1:1000) adrenaline
    • Child IM dose (The equivalent volume of 1:1000 adrenaline is shown in brackets):
      • > 12 years: 500 micrograms IM (0.5 mL) i.e. same as adult dose
        300 micrograms (0.3 mL) if child is small or prepubertal
      • > 6 – 12 years: 300 micrograms IM (0.3 mL)
      • < 6 years: 150 micrograms IM (0.15 mL)
    • Note: Half doses of adrenaline (epinephrine) may be safer for patients on amitriptyline, imipramine, MAOI or betablocker.
  • When skills and equipment available:
    • Establish airway (in anaphylaxis airway obstruction from tissue swelling difficult to overcome and early expert intubation often needed)
    • IV fluid challenge:
      • Insert one or more large-bore intravenous cannulae (enable the highest flow).
      • Use intraosseous access (if trained to do so) in children when intravenous access is difficult.
      • Give a rapid fluid challenge:
        • Adults - 500 mL of warmed crystalloid solution (e.g., Hartmann’s or 0.9% saline) in 5-10 minutes if the patient is normotensive or one litre if the patient is hypotensive.
        • Use smaller volumes (e.g., 250 mL) for adult patients with known cardiac failure and use closer monitoring (listen to the chest for crepitations after each bolus).
        • The use of invasive monitoring, e.g., central venous pressure (CVP), can help to assess fluid resuscitation.
        • For children give 20 mL/kg of warmed crystalloid.
    • Chlorphenamine (after initial resuscitation). Dose depends on age:
      • >12 years and adults: 10 mg IM or IV slowly
      • >6 – 12 years: 5 mg IM or IV slowly
      • >6 months – 6 years: 2.5 mg IM or IV slowly
      • <6 months: 250 micrograms/kg IM or IV slowly
    • Hydrocortisone (after initial resuscitation). Dose depends on age:
      • >12 years and adults: 200 mg IM or IV slowly
      • >6 – 12 years: 100 mg IM or IV slowly
      • >6 months – 6 years: 50 mg IM or IV slowly
      • <6 months: 25 mg IM or IV slowly
    • Monitor:

Monitoring

  • All critically ill patients should be given oxygen.
  • Maintain the PaO2 as close to normal as possible (approximately 13 kPa or 100 mm Hg).
  • When/if pulse oximeter available:
    • Titrate the oxygen to maintain an oxygen saturation of 94-98%.
    • In the sickest patients this is not always possible so you may have to accept a lower value, i.e., above 8 kPa (60 mm Hg), or 90-92% oxygen saturation on a pulse oximeter.
  • A normal SpO2 on oxygen does not necessarily mean ventilation is adequate (because the pulse oximeter detects oxygenation and not hypercapnoea). The patient may be breathing inadequately (with a high PaCO2).
  • Use bag-mask ventilation while calling urgently for expert help. In an anaphylactic reaction upper airway obstruction or bronchospasm can make bag mask ventilation difficult or impossible.
  • Consider early tracheal intubation (if equipment and expertise available). If the patient is intubated, give high concentration oxygen with a self-inflating bag.

Blood pressure
Reassess the pulse rate and BP regularly (every 5 min). Aim for:

  • In adults normal BP (or a systolic BP greater than 100 mmHg).
  • In children:
    • 0 to1 month: minimum 50-60 mmHg.
    • >1 to12 months: minimum 70 mmHg.
    • >1 to 10 years 70 + (age in years x 2) mmHg.
    • >10 years: minimum 90 mmHg.
  • If the patient does not improve, repeat the fluid challenge.
  • If there are symptoms and signs of cardiac failure (shortness of breath, increased heart rate, raised JVP, a third heart sound, and inspiratory crackles in the lungs on auscultation):
    • Decrease or stop the fluid infusion.
    • Seek expert help (inotropes or vasopressors may be needed).
Follow up

When time allows.

  • Immediate:
    • Take a full history from the patient (relatives, friends, and other staff).
    • Review the patient’s notes and charts. Study both absolute and trends of values relating to vital signs.
    • Check that important routine medications are prescribed and being
      given.
    • Review the results of laboratory or radiological investigations.
    • Consider what level of care is required by the patient, e.g., transport to hospital if
      in the community.
    • Make complete entries in the patient’s notes of your findings, assessment and
      treatment. Record the patient’s response to therapy.
    • Consider definitive treatment of the patient’s underlying condition.
  • Long term:
    • Refer to an allergist or allergy clinic to try and identify allergen so that it may be avoided in future.
    • Organise self-use of pre-loaded pen injections for future attacks (e.g. EpiPen ®; containing 0.3 mL of 1 in 1000 strength (that is 300 μg) for adults; and for children 0.3 mL of 1 in 2000 (150 μg)). This again may be best done in allergy clinics.
    • Give a written self-management plan and arrange to teach patient and relatives how to use syringes.1
    • Encourage patient to wear a Medic alert bracelet/necklace endorsed by doctor.



Document references
  1. Emergency treatment of anaphylactic reactions - guidelines for healthcare providers, Resuscitation Council (January 2008)
  2. Bindslev-Jensen C; ABC of allergies: Food allergy. BMJ 1998 316:1299-1302.

Internet and further reading Acknowledgements EMIS is grateful to Dr Huw Thomas for writing this article and to Dr Richard Draper for earlier versions. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
DocID: 1802
Document Version: 20
DocRef: bgp570
Last Updated: 20 Jan 2009
Review Date: 20 Jan 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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