EAACI guidelines: Anaphylaxis (2021 update)

Allergy. 2022;77:357–377. 
| 
357wileyonlinelibrary.com/journal/all
Received: 12 June 2021 
| 
Accepted: 31 July 2021
DOI: 10.1111/all.15032
G U I D E L I N E S
EAACI guidelines: Anaphylaxis (2021 update)
Antonella Muraro
1 
| Margitta Worm
2 
| Cherry Alviani
3 
| Victoria Cardona 
4 
|
Audrey DunnGalvin
5,6 
| Lene Heise Garvey
7,8 
| Carmen Riggioni
9 
|
Debra de Silva
10 
| Elizabeth Angier
11 
| Stefania Arasi
12 
|
Abdelouahab Bellou
13,14,15 
| Kirsten Beyer
16 
| Diola Bijlhout
17 
|
Maria Beatrice Bilò
18,19 
| Carsten Bindslev-Jensen
20 
| Knut Brockow 
21 
|
Montserrat Fernandez-Rivas
22 
| Susanne Halken
23 
| Britt Jensen
20 
|
Ekaterina Khaleva
3 
| Louise J. Michaelis
24,25 
| Hanneke N. G. Oude Elberink 
26 
|
Lynne Regent 
27 
| Angel Sanchez
28 
| Berber J. Vlieg-Boerstra
29 
|
Graham Roberts 
3,30,31 
| European Academy of Allergy and Clinical Immunology, Food
Allergy, Anaphylaxis Guidelines Group
1
Food Allergy Referral Centre Veneto Region, Department of Women and Child Health, Padua General University Hospital, Padua, Italy
2
Division of Allergy and Immunology, Department of Dermatology, Venerology and Allergy, Charité Universitätsmedizin Berlin, Germany
3
Clinical and Experimental Sciences and Human Development in Health, Faculty of Medicine, University of Southampton, UK
4
Allergy Section, Department of Internal Medicine, Hospital Vall d'Hebron & ARADyAL Research Network, Barcelona, Spain
5
University College Cork, Cork, Ireland
6
Sechnov University Moscow, Moscow, Russia
7
Allergy Clinic, Department of Dermatology and allergy, Copenhagen University Hospital Gentofte, Copenhagen, Denmark
8
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark
9
Allergy, Immunology and Rheumatology Division, Department of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
City, Singapore
10
The Evidence Centre Ltd, London, UK
11
Primary Care, Population Science and Medical Education, Faculty of Medicine, University of Southampton, Southampton, UK
12
Allergy Unit - Area of Translational Research in Pediatric Specialities, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy
13
European Society for Emergency Medicine, Brussels, Belgium
14
Department of Emergency Medicine, Wayne State University School of Medicine, Detroit, Michigan, USA
15
University of Rennes 1, Rennes, France
16
Department of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany
17
Association for Teacher Education in Europe (ATEE, Brussels, Belgium
18
Allergy Unit, Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy
19
Department of Internal Medicine, University Hospital of Ancona, Ancona, Italy
20
Department of Dermatology and Allergy Centre, Odense Research Centre for Anaphylaxis (ORCA), Odense University Hospital, Odense, Denmark
21
Department of Dermatology and Allergy Biederstein, Technical University of Munich, Munich, Germany
22
Allergy Department, Hospital Clinico San Carlos, Facultad Medicina Universidad Complutense, IdISSC, ARADyAL, Madrid, Spain
23
Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense, Denmark
24
Department of Paediatric Immunology, Allergy, and Infectious Diseases, Great North Children's Hospital, Newcastle upon Tyne, UK
25
Faculty of Medical Sciences, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
26
Department of Allergology, University Medical Center Groningen, University of Groningen, and Groningen Research Institute for Asthma and COPD,
Groningen, The Netherlands
© 2021 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.
Antonella Muraro, Margitta Worm and Graham Roberts equally contributed as guideline chairs.

358 
|
MURARO et Al .
1 | I NTRO D U C TI O N
This paper sets out the updated European Academy of Allergy and
Clinical Immunology's (EAACI) guideline regarding the diagnosis,
acute management, and prevention of anaphylaxis. Anaphylaxis is
a clinical emergency and all healthcare professionals need to be fa-
miliar with its recognition and management. Anaphylaxis is a life-
threatening reaction characterized by acute onset of symptoms
involving different organ systems and requiring immediate medical
intervention.
1 
Although the fatality rate due to anaphylaxis remains
low,
2 
the frequency of hospitalization from food and drug-induced
anaphylaxis has been increasing in recent years.
3
The symptoms of anaphylaxis are highly variable. 
4,5 
Data from
patients experiencing anaphylaxis revealed that skin and mucosal
symptoms occur most frequently (>90% of cases) followed by symp-
toms involving the respiratory and cardiovascular systems (>50%).
Food, drug, and Hymenoptera venom are the most common elicitors
of anaphylactic reactions. 
5,6 
The prevalence of the various causes of
anaphylaxis are age- dependent and vary in different geographical
regions. In Europe, typical causes of food-induced anaphylaxis in
children are peanut, hazelnut, milk, and egg and in adults, wheat,
celery, and shellfish; fruits such as peach are also typical causes of
food-induced anaphylaxis in adults in some European countries such
as Spain and Italy.
7,8 
Venom-induced anaphylaxis is typically caused
by wasp and bee venom.
9 
Drug-induced anaphylaxis is typically
caused by antibiotics and non- steroidal anti-inflammatory drugs.
10,11
Among antibiotics, beta-lactam antibiotics are the leading eliciting
allergens.
12 
At times, there is an occupational cause. 
13 
Co-factors
may be aggravating factors in anaphylaxis, examples are exercise,
stress, infection, non- steroidal anti-inflammatory drugs, and alco-
hol.
14–16 
In some cases, the cause is not obvious (idiopathic anaphy -
laxis) and investigations for rarer allergens or differential diagnoses
should be considered.
17–19
This guideline, updated from 2014,
20 
provides evidence- based
guidance to help manage anaphylaxis. The primary audience is clini -
cal allergists (specialists and subspecialists), primary care, paediatri-
cians, emergency physicians, anaesthetists and intensivists, nurses,
dieticians, and other healthcare professionals. The guideline was
27
Anaphylaxis Campaign, Farnborough, UK
28
AEPNAA Spanish Association for People with Food and Latex Allergy, Madrid, Spain
29
Department of Paediatrics, OLVG Hospital, Amsterdam, The Netherlands
30
NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK
31
The David Hide Asthma and Allergy Research Centre, St Mary's Hospital, Isle of Wight, UK
Correspondence
Antonella Muraro, Food Allergy Referral
Centre Veneto Region, Department of
Women and Child Health, Padua General
University Hospital, Padua, Italy.
Email: [email protected]
Funding information
European Academy of Allergy and Clinical
Immunology.
Abstract
Anaphylaxis is a clinical emergency which all healthcare professionals need to be able
to recognize and manage. The European Academy of Allergy and Clinical Immunology
Anaphylaxis multidisciplinary Task Force has updated the 2014 guideline. The guide-
line was developed using the AGREE II framework and the GRADE approach. The
evidence was systematically reviewed and recommendations were created by weigh-
ing up benefits and harms. The guideline was peer-reviewed by external experts and
reviewed in a public consultation. The use of clinical criteria to identify anaphylaxis
is suggested with blood sampling for the later measurement of tryptase. The prompt
use of intramuscular adrenaline as first-line management is recommended with the
availability of adrenaline autoinjectors to patients in the community. Pharmacokinetic
data should be provided for adrenaline autoinjector devices. Structured, comprehen-
sive training for people at risk of anaphylaxis is recommended. Simulation training and
visual prompts for healthcare professionals are suggested to improve the manage-
ment of anaphylaxis. It is suggested that school policies reflect anaphylaxis guidelines.
The evidence for the management of anaphylaxis remains mostly at a very low level.
There is an urgent need to prioritize clinical trials with the potential to improve the
management of patients at risk of anaphylaxis.
K E Y W O R D S
adults, anaphylaxis, children, guidelines
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
359
MURARO et Al .
developed by EAACI's Anaphylaxis Guideline Update task force (TF)
and informed by a systematic review (SR).
21 
Where published evi-
dence was lacking, the findings of the review were supplemented
with expert consensus opinion.
2 | M E TH O D O LO G Y
This guideline was generated using the Appraisal of Guidelines for
Research and Evaluation (AGREE II) approach
22,23 
to ensure appro -
priate representation of the full range of stakeholders, a systematic
search for and critical appraisal of, the relevant literature, and a sys-
tematic approach to formulating and presenting recommendations,
with steps to minimize the risk of bias at each step. The Grading of
Recommendations Assessment, Development and Evaluation (GRADE)
approach provided a structured way to evaluate evidence and poten-
tial recommendations.
24 
The process commenced in September 2019
with a face-to-face discussion to agree the protocol and the key clinical
areas. Regular web conferences took place through to November 2020
with additional email discussion to complete the guideline.
2.1 | Clarifying the scope and
purpose of the guidelines
This guideline provides evidence- based recommendations for the
diagnosis, management and prevention of anaphylaxis in children
and adults. It also highlights gaps where future research is required.
Reactions to allergen immunotherapy are outside the scope of this
guideline.
25
2.2 | Ensuring appropriate stakeholder
involvement
The EAACI TF was drawn from 9 countries and included allergists (spe-
cialist and subspecialists), paediatricians, primary care, immunologists,
emergency physicians, anaesthetists, dieticians, nurses, psychologist,
education and patient organization representatives. Methodologists
took the lead in undertaking the SR, while clinical academics took the
lead in formulating recommendations for clinical care.
2.3 | Systematic review of the evidence
The SR aimed to assess the effectiveness of any approach for the
immediate diagnosis, emergency management and prevention or
long-term management of anaphylaxis in children and adults. 
21,26
It was undertaken by independent methodologists using GRADE
Pro GDT (www.grade pro.org). Comparative studies were eligible
for inclusion plus, in the case of diagnosis and adrenaline only,
prospective case series with at least 20 participants were eligible.
We continued to track evidence published after our SR cut-off date
of 20th April 2020, and studies were considered by the TF chairs
where relevant.
Evidence summaries for each question were prepared by meth-
odologists, including assessments of the risk of bias and certainty
of evidence.
27 
TF members reviewed the summaries and provided
feedback. The certainty of the evidence was assessed as high, mod-
erate, low, or very low based on consideration of risk of bias, direct-
ness of evidence, consistency and precision of the estimates, and
other considerations.
28
2.4 | Formulating recommendations
The TF used the GRADE approach to grade the strength and con-
sistency of key findings from the SR,
21 
which in turn contributed to
formulating evidence-based recommendations for clinical care.
24 
In
generating recommendations, the TF evaluated the importance of
the problem, desirable and undesirable effects, certainty of evidence,
values, balance of effects, resources required, cost-effectiveness, eq-
uity, acceptability and feasibility. All recommendations were agreed
by consensus with a threshold of agreement set at 80%. Table 1
describes the conventions used in this guideline to describe the
strength of recommendations and how this relates to policy and prac-
tice. Recommendations apply to all ages unless otherwise indicated.
TF members identified the resource implications of imple -
menting the recommendations, barriers and facilitators to the im-
plementation of each recommendation, advised on approaches to
implementing the recommendations, and suggested audit criteria
that can help with assessing organizational compliance with each
recommendation.
2.5 | Peer review and public comment
A draft of these guidelines was externally peer-reviewed by invited
experts from a range of organizations, countries and professional
backgrounds. Additionally, the draft guideline was made publicly
available on the EAACI website for a 3-week period in February
2021 to allow a broader array of stakeholders to comment. All feed-
back was considered by the TF members and, where appropriate,
final revisions were made in light of the feedback received. We will
be pleased to continue to receive feedback on this guideline, ad-
dressed to the corresponding author.
2.6 | Identification of evidence gaps
During the development of the guideline, areas where evidence is
lacking were identified and gaps to fill prioritized.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

360 
|
MURARO et Al .
2.7 | Editorial independence and managing
conflict of interests
The guideline development process was funded by EAACI. The funder
did not have any influence on the guideline contents or on the deci-
sion to publish. TF members' conflicts of interest were declared at the
start of the process and taken into account by the TF chairs, as recom-
mendations were formulated. Specifically, anyone who had a potential
financial conflict of interest was not able to be involved in final deci-
sions about that recommendation (this did not apply to any task force
members). Evidence about effectiveness was compiled independently
by methodologists who had no conflict of interests. Additionally, final
decisions about strength of evidence for recommendations were
checked by the methodologists who had no conflict of interests.
2.8 | Updating the guidelines
European Academy of Allergy and Clinical Immunology plans to
update this guideline in 2026 unless there are important advances
before then.
3 | G U I D E LI N E R ECO M M E N DATI O N S
Table 2 summarizes the guideline recommendations. The follow-
ing sections explore these recommendations in more detail. The
evidence is summarized narratively, with individual studies not de -
scribed as these details can be found in our published SR.
21 
The
online supplement provides a detailed rationale with the relevant
evidence for each recommendation (Tables S1–S4).
4 | D I AG N OS I S O F A N A PH Y L A X I S I N A N
ACU TE CO NTE X T
This section deals with making a diagnosis of anaphylaxis in a situ-
ation where someone has symptoms and signs of an acute allergic
reaction. Further justification about each of the recommendations
about diagnosing anaphylaxis is included in Table S1.
4.1 | Making a diagnosis of anaphylaxis
The EAACI task force suggests using clinical criteria, including rapid
onset of multiple symptoms and signs, for identifying anaphylaxis in an
acute context.
Reason for recommendation: Anaphylaxis is a clinical emergency
so the diagnosis needs to be made rapidly. Research suggests that
National Institute of Allergy and Infectious Disease and Food Allergy
and Anaphylaxis Network clinical criteria has high sensitivity. 
29,30
(Box 1).
Strength of recommendation: This is a conditional recommenda-
tion as the evidence is of very low certainty and derives from case
series or retrospective case-control studies.
Practical implications: Anaphylaxis has variable presentations, oc-
casionally with no cutaneous involvement, and relatively low prev-
alence so it may not be easy to diagnose. Healthcare professionals
TA B L E 1 Conventions used in Guideline wording
Strength and direction Guideline wording Implications for practice Policy implications
Strong recommendation
for an intervention
‘The EAACI Task Force
recommends …’
Most people in this situation should
be offered the intervention
The recommendation can be adopted as a
policy in most situations
Conditional
recommendation for an
intervention
‘The EAACI Task Force
suggests …’
Different choices will be
appropriate for different
people. Clinicians could help
each patient make decisions
consistent with the patient's
preferences
Policies may differ depending on context
and should be developed with the
involvement of a wide range of
stakeholders
Strong recommendation
against an intervention
‘The EAACI Task Force
recommends against …’
Most people in this situation should
not use this intervention
The recommendation can be adopted as a
policy in most situations
Conditional
recommendation
against an intervention
‘The EAACI Task Force
suggests against …’
Different choices will be
appropriate for different
people. Clinicians could help
each patient make decisions
consistent with the patient's
preferences
Policies may differ depending on context
and should be developed with the
involvement of a wide range of
stakeholders
No recommendation ‘There is no recommendation
for or against using …’
Different choices will be
appropriate for different
people. Clinicians could help
each patient make decisions
consistent with the patient's
preferences
Policies may differ depending on context
and should be developed with the
involvement of a wide range of
stakeholders
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
361
MURARO et Al .
require training in how to recognize anaphylaxis
31 
(Box 1) and differ-
entiate it from other diagnoses 
32,33 
(Box 2).
4.2 | Serum tryptase level may help to support the
diagnosis later in the allergy consultation
The EAACI task force suggests measuring serum tryptase half to two
hours after the start of the reaction, and baseline tryptase at least
24 hours after complete resolution of symptoms, to support diagnosing
anaphylaxis respectively.
Reason for recommendation: Although measuring serum tryptase
will not help to make a diagnosis of anaphylaxis in a clinical emer-
gency, an elevated level within two hours of the reaction compared
to a baseline value (measured before or after the reaction) can be
helpful in confirming the diagnosis of anaphylaxis during subsequent
allergy consultation.
Strength of recommendation: This is a conditional recommenda-
tion. Several studies have assessed the diagnostic accuracy of serum
tryptase measurements for anaphylaxis, but the evidence is of very
low certainty, deriving from consecutive case series or case- control
studies.
34–36
Practical implications: Taking the sample should not delay treating
a patient with adrenaline where necessary. A sample taken later than
two hours after the reaction may still demonstrate a raised tryptase
level. A level of serum tryptase half to two hours after the start of
the reaction (1.2 × baseline tryptase) +2 μg/L supports a diagnosis
of anaphylaxis. 
37,38 
A raised serum tryptase level can be associated
with a mast cell disorder or hereditary alpha tryptasaemia,
39–41 
so it
is important to compare with a baseline level at least 24 hours after
complete resolution of a reaction. Also, serum tryptase is not always
elevated in anaphylaxis, especially in children and with food triggers
in all ages.
38 
So failing to find an elevated tryptase level does not rule
out anaphylaxis.
5 | E M E RG E N C Y M A N AG E M E NT O F
A N A PH Y L A X I S
In addition to the early use of adrenaline, the trigger should be
removed where possible, posture should be optimized and assis-
tance should be sought from emergency medical services in the
community or the emergency team in hospital. To ensure adequate
venous return, patients experiencing anaphylaxis should lie flat
with their legs raised. Where respiratory distress is the predomi -
nant presentation, patients may prefer to sit up with elevated legs.
If pregnant, they can be placed on their left side with the bed in a
head-down position.
42 
Where unconscious, patients can be placed
in the recovery position. Avoid any abrupt change to a more up -
right posture.
43
TA B L E 2 EAACI anaphylaxis guideline recommendations
Recommendation
Certainty of
evidence
Diagnosing anaphylaxis in an emergency setting
The EAACI task force suggests using clinical criteria, including rapid onset of multiple symptoms and signs, for identifying anaphylaxis
in an acute context
Very low
The EAACI task force suggests measuring serum tryptase half to two hours after the start of the reaction, and baseline tryptase at
least 24 hours after complete resolution of symptoms, to support diagnosing anaphylaxis retrospectively
Very low
Emergency management of anaphylaxis
The EAACI task force recommends promptly using intramuscular adrenaline in the mid-thigh area as first-line management of
anaphylaxis
Very low
The EAACI task force suggests using adrenaline autoinjectors for the first-line management of anaphylaxis in the community Very low
The EAACI task force recommends that pharmacokinetic data should be provided for each adrenaline autoinjector product as they
cannot be regarded as interchangeable
Very low
The EAACI task force suggests prescribing 0.15mg adrenaline autoinjectors for children from 7.5kg to 25-30kg and 0.3mg adrenaline
autoinjectors for children from 25-30kg, and at least 0.3mg adrenaline autoinjectors for adolescents and adults at risk of
anaphylaxis
Very low
Long-term management of anaphylaxis
The EAACI task force recommends providing structured, comprehensive training to improve recognition of anaphylaxis and use of
adrenaline autoinjectors in people at risk of anaphylaxis. This is in addition to basic instructions about autoinjector use
Low
The EAACI task force makes no recommendation for or against using premedication with antihistamine to prevent anaphylaxis Very low
The EAACI task force suggests using premedication with subcutaneous adrenaline to prevent anaphylaxis when snake bite anti-venom
is given to a patient
Very low
The EAACI task force suggests that school policies reflect anaphylaxis guidelines but more research is needed to understand how
guidelines and legislation in schools are best implemented
Very low
Education and training for healthcare professionals
The EAACI task force suggests using simulation training and visual prompts to improve healthcare professionals' recognition and
management of anaphylaxis in emergency situations
Very low
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

362 
|
MURARO et Al .
Further justification about each of the recommendations
about managing anaphylaxis is included in Table S2. A checklist
for managing anaphylaxis is presented in Box 3 and an algorithm
approach to managing this clinical emergency is presented in
Figure 1.
5.1 | First-line intervention: adrenaline
5.1.1 | Route of administration
The EAACI task force recommends promptly using intramuscular adren-
aline in the mid-thigh area as first-line management of anaphylaxis.
Reason for recommendation: Adrenaline has historically been used
as first-line treatment for anaphylaxis, without evidence of serious
harm. Early use of adrenaline appears to reduce the risk of bipha-
sic reactions.
44–47 
There is evidence that intramuscular adrenaline
gives higher plasma levels than adrenaline via a metered-dose inhal-
er. 
48–51 
The evidence comparing intramuscular with subcutaneous
adrenaline is confounded by injection site but suggests that the for-
mer is associated with higher plasma adrenaline levels. 
52,53 
Injection
mid-thigh gives higher levels than injection into deltoid. 
53 
There is
little evidence of harm when adrenaline is given intramuscularly un-
like with the intravenous dosing.
21
Strength of recommendation: This is a strong recommendation
in favour of adrenaline. The research evidence is of low certainty
due to the challenges of undertaking randomized controlled trials
BOX 1 Clinical criteria for diagnosing anaphylaxis
Anaphylaxis is highly likely when any one of the following
three criteria is fulfilled:
1. Acute onset of an illness (minutes to several hours) with
involvement of the skin, mucosal tissue or both (eg gen -
eralized hives, pruritus or flushing, swollen lips–tongue–
uvula AND AT LEAST ONE OF THE FOLLOWING
a. Respiratory compromise (eg dyspnoea, wheeze–
bronchospasm, stridor, reduced PEF and hypoxemia)
b. Reduced BP or associated symptoms of end-organ
dysfunction (eg hypotonia [collapse], syncope,
incontinence)
2. Two or more of the following that occur rapidly after ex-
posure to a likely allergen for that patient (minutes to
several hours):
a. Involvement of the skin–mucosal tissue (eg general-
ized hives, itch-flush, swollen lips–tongue–uvula
b. Respiratory compromise (eg dyspnoea, wheeze–
bronchospasm, stridor, reduced PEF, hypoxemia)
c. Reduced BP or associated symptoms (eg hypotonia
[collapse], syncope, incontinence)
d. Persistent gastrointestinal symptoms (eg crampy ab-
dominal pain, vomiting)
3. Reduced BP after exposure to known allergen for that
patient (minutes to several hours):
a. Infants and children: low systolic BP (age specific) or
>30% decrease in systolic BP*
b. Adults: systolic BP of <90 mmHg or >30% decrease
from that person's baseline
PEF, peak expiratory flow; BP, blood pressure. *Low sys-
tolic blood pressure for children is defined as <70 mmHg
from 1 month to 1 year, less than (70 mmHg + [2 × age])
from 1 to 10 years and <90 mmHg from 11 to 17 years.
Reproduced from Sampson et al
31 
with permission.
BOX 2 Differential diagnosis of anaphylaxis
Skin or mucosal
• chronic remittent or physical urticaria and angioedema
• pollen food allergy syndrome (just oral symptoms)
Respiratory diseases
• acute laryngotracheitis
• laryngeal, tracheal or bronchial obstruction (eg foreign
substances, intermittent laryngeal obstruction or vocal
cord dysfunction)
• status asthmaticus (without involvement of other
organs)
Cardiovascular diseases
• vasovagal syncope
• pulmonary embolism
• myocardial infarction
• cardiac arrhythmias
• cardiogenic shock
Pharmacological or toxic reactions
• ethanol
• histamine, eg scombroid fish poisoning
• opiates
Neuropsychiatric diseases
• hyperventilation syndrome
• anxiety and panic disorder
• somatoform disorder (eg psychogenic dyspnoea)
• dissociative disorder and conversion (eg globus
hystericus)
• epilepsy
• cerebrovascular event
• psychoses
• factitious disorder
Endocrinological diseases
• hypoglycemia
• thyrotoxic crisis
• carcinoid syndrome
• vasointestinal polypeptide tumours
• pheochromocytoma
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
363
MURARO et Al .
in anaphylaxis. Given the totality of the evidence and clinical expe-
rience over many decades, the task force felt that a strong recom-
mendation for the use of intramuscular adrenaline was appropriate.
Practical implications: Professionals who may need to manage
anaphylaxis should be trained in how to promptly administer in-
tramuscular adrenaline. The task force considers that adrenaline is
best used early especially in patients who have had previous life-
threatening reactions in similar circumstances (eg insect sting) al-
though our literature search did not focus on this and no relevant
good quality evidence was found. Assistance from colleagues should
be sought early when managing a patient with anaphylaxis. In severe
reactions, especially involving the cardiovascular system, intrave-
nous fluids should also be given early with the second dose of intra-
muscular adrenaline.
54 
In some special circumstances, intramuscular
adrenaline may not be effective (eg refractory respiratory distress,
hypotension) so intravenous adrenaline should be used; this is likely
to be more effective at reversing refractory bronchospasm or hypo-
tension. The use of intravenous adrenaline should be restricted to
healthcare professionals who are trained to use it and to monitored
settings such as the emergency room, operating theatres or inten -
sive care unit. Patients on a beta-blocker may also respond poorly
to adrenaline.
5.1.2 | Adrenaline autoinjector or needle-syringe
The EAACI task force suggests using adrenaline autoinjectors for the
first-line management of anaphylaxis in the community.
Reason for recommendation: The benefits of using an autoinjector
outweigh the risks compared with using a (prefilled) needle-syringe
(Table S2). Adrenaline autoinjectors are convenient, relatively safe,
have a low risk of error and are faster to administer compared to a
needle-syringe approach. If autoinjectors are also used to treat ana-
phylaxis in healthcare settings, the patient can practice using it or at
least observe how they are used and experience its effectiveness for
managing anaphylaxis.
Strength of recommendation: This is a conditional recommendation
for using autoinjectors because the certainty of evidence is very low
due to the available trials being at moderate or high risk of bias.
55,56
Practical implications: A number of different adrenaline au-
toinjectors are available, each of which have slightly different
mechanisms. Device- specific training is therefore essential for
each autoinjector and with further training if device is changed.
Adrenaline autoinjectors are designed to be kept at 20–25℃
and have a limited shelf life due to degradation of the adrena -
line. Autoinjectors occasionally fail to deploy and the European
Medicines Agency has stated that patients should have access to
two devices
57 
(see Table 3 for arguments for prescribing one or two
devices). In many countries, adrenaline autoinjectors are not avail-
able or not affordable or there are supply issues with adrenaline
autoinjectors. In these circumstances, a prefilled syringe is an alter-
native. Indications for the prescription of self- injectable adrenaline
are described in Box 4.
5.1.3 | Pharmacokinetic data for adrenaline
autoinjectors and needle-syringe
The EAACI task force recommends that pharmacokinetic data should be
provided for each adrenaline autoinjector product as they cannot be re-
garded as interchangeable.
Reason for recommendation: Pharmacokinetic data are now avail-
able for many of the adrenaline autoinjector products. These data
demonstrate that each type delivers very different plasma adren -
aline levels. It had been thought that the length of the needle was
critical to optimizing the delivery of adrenaline. However, the phar-
macokinetic data indicate that needle length does not dictate adren -
aline plasma levels.
81 
For example, when the same autoinjectors
were used for adults with different skin to muscle depths (associated
with body mass index), some devices have a similar plasma adrena-
line profile in all
82 
whereas there is marked blunting of the height of
the early peak in overweight individuals in others.
83 
(see Table S2).
Plasma adrenaline levels may be more closely related to the force at
which adrenaline is deployed from the device.
82
Strength of recommendation: This is a strong recommendation for
making pharmacokinetic data available. Only some pharmacokinetic
data have been published in peer review journals, and other data
are available via information submitted to European medicine regu-
lators. Given the marked differences in adrenaline profiles between
different products and different patients, they cannot be seen as
interchangeable. The task force considered that these data should
be made available by companies for all adrenaline devices to help
predict their likely clinical effectiveness.
Practical considerations: As we do not know what level of plasma
adrenaline is needed to successfully treat anaphylaxis, the results
of these pharmacokinetic studies need to be interpreted with some
caution. A product that does not achieve similar plasma levels to
other autoinjectors is of concern.
BOX 3 Checklist for managing an acute allergic
reaction
1. Stay with patient
2. Remove the trigger (eg food, drug and venom)
3. Look for signs of anaphylaxis
4. Administer adrenaline if signs of anaphylaxis (eg breath-
ing or circulatory problems)
5. Call for help
6. Lie flat with their legs raised unless in respiratory dis-
tress where patient may prefer to sit up with elevated
legs
7. Repeat adrenaline if no improvement or worsening of
symptoms 5–10 minutes after first administration
8. Do not forget oxygen, beta-2 agonist or i.v. fluids as
indicated
Adrenaline is effective for all symptoms.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

364 
|
MURARO et Al .
5.1.4 | Dose of adrenaline
The EAACI task force suggests prescribing 0.15 mg adrenaline auto-
injectors for children from 7.5 kg to 25–30 kg and 0.3 mg adrenaline
autoinjectors for children from 25–30 kg, and at least 0.3 mg adrenaline
autoinjectors for adolescents and adults at risk of anaphylaxis.
Reason for recommendation: There are no published data for
children weighing under 15 kg although the routinely advised
F I G U R E 1 Schematic illustration of the initial management of anaphylaxis
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
365
MURARO et Al .
intramuscular adrenaline dose is 0.01 mg/kg in healthcare settings.
In the 2014 guideline, we recommended using a 0.15 mg adrenaline
autoinjector for children from 7.5 kg bodyweight on the basis that a
mild overdose does not represent a major risk in otherwise healthy
children.
33 
There have been no reports of any adverse consequences
of this approach and regulators have now licenced some autoinjec-
tors down to 7.5 kg in some European countries (eg Germany).
84
However, there is a danger that the needle will hit the underlying
bone in small children.
85 
We are aware of a 0.1 mg adrenaline auto -
injector product but this only appears to be available in the United
States.
86 
We identified only one study looking at plasma adrenaline
levels with 0.15 and 0.3 mg devices in children.
87 
Similar plasma lev-
els were seen but the 0.3 mg dose was associated with more side
effects in children under 30 kg. Alternatively, children may rapidly
outgrow their dose and adverse effects need to be balanced against
effectiveness. Countries within Europe vary as to whether a switch
happens at 25 or 30 kg for different devices. We therefore sug-
gest using the 0.3 mg dose only in children more than 25–30 kg in
weight. A 0.5 mg dose gives a substantially higher plasma level than
a 0.3 mg dose with one device.
88 
The optimal dose of adrenaline in
anaphylaxis is not known and 0.3 mg devices have been found to be
effective for treating anaphylaxis in most patients,
61 
so the 0.3 mg
adrenaline dose is preferred.
Strength of recommendation: This is a conditional positive recom-
mendation because it is based on small studies enrolling volunteers
who were randomized to different adrenaline autoinjectors. It is un-
certain what plasma adrenaline level is therapeutic in anaphylaxis, so
it is difficult to make definitive recommendations.
Practical considerations: In the relatively rare case of an infant
less than 7.5 kg in bodyweight at risk of anaphylaxis, a prefilled sy -
ringe and adrenaline dose of 0.01 mg/kg can be used instead of an
autoinjector. For adolescents and adult patients, a 0.3 mg device is
recommended although a higher 0.5 mg device can be considered
where a patient is overweight or has experienced a previous episode
of life-threatening anaphylaxis. In a clinical setting, where a patient
presents with severe anaphylaxis, a higher dose (eg 0.5mg or 0.3 mg
repeated for an older adolescent or adult) may be considered.
5.2 | Other interventions
Our systematic review found no eligible randomized controlled tri-
als assessing the effectiveness of other interventions for the acute
management of anaphylaxis. It is recognized that some may be use-
ful as concomitant therapy with adrenaline. These interventions are
briefly described although no robust evidence is available.
5.2.1 | Oxygen
Give high flow oxygen to a patient experiencing anaphylaxis.
5.2.2 | Fluid support
Administer intravenous fluids early with first adrenaline dose to
patients with cardiovascular involvement as adrenaline may not be
effective without restoring the circulatory volume. Crystalloids are
preferred given in boluses of 10 ml/kg (maximum 500 ml per bolus)
for children and 500 ml in adults, repeated as needed. This should
be repeated if lack of response. Fluid support could also be given in
severe anaphylaxis with a respiratory presentation if a second dose
of intramuscular adrenaline is required.
5.2.3 | H1 and H2 antihistamines
Systemic antihistamines have only been demonstrated to relieve cu-
taneous symptoms
89 
and a possible effect on non- cutaneous symp-
toms remains unconfirmed.
90
5.2.4 | Glucocorticoids
Glucocorticoids are commonly used in anaphylaxis as they are
thought to prevent protracted symptoms and possibly biphasic re-
actions but there is limited evidence of their effectiveness and they
may be deleterious in children.
90,91
5.2.5 | Inhaled Beta2-Agonists
In the case of predominant bronchial obstruction, inhaled ß-adrenoreceptor
agonists, (eg salbutamol) can be additionally administered (best using an
oxygen driven nebulizer or via metered-dose inhaler using a ‘spacer’).
5.2.6 | Inhaled adrenaline
In cases with suspected laryngeal/pharyngeal oedema, inhaled ad-
ministration of adrenaline via a nebulizer together with oxygen
TA B L E 3 Reasons for prescribing one or two adrenaline
autoinjectors
Arguments for two autoinjectors Arguments for one autoinjector
• European Medicines Agency
recommends that two
autoinjectors are prescribed
57
• About 10% patients require a
second dose of adrenaline due to
insufficient response to the first
dose
116
• Rarely, an autoinjector will misfire
or be injected in the wrong
place56
• Where there is a likelihood of
delayed medical assistance, for
example remote location or travel
• Only needing to carry
one device may improve
adherence to carriage which
is low
• Most autoinjectors are not
used and have to be replaced
after 12–18 months when
they expire
• Most patients respond to
one dose and second doses
are usually administered by
emergency services 
61,116
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

366 
|
MURARO et Al .
is recommended. The systemic absorption of inhaled adrenaline
is negliable,
49 
and it should only be used as a supplement to i.m.
administration.
5.3 | Monitoring and discharge arrangements
Patients with anaphylaxis are at risk of protracted reactions and
of developing biphasic reactions although the likelihood is low 
90,92
(Table 4). The task force suggests that they are monitored for 6–8 h
with respiratory compromise and at least 12–24 h with hypotension.
Before discharge, assess the risk of future reactions and prescribe
adrenaline autoinjectors to those at risk of recurrence (Box 4).
Provide patients with written advice covering allergen avoidance
measures and instructions for when and how to use the adrenaline
autoinjector. Refer patients to an allergy specialist to investigate
possible triggers. This is particularly important for idiopathic ana -
phylaxis where reactions to hidden allergens, such as alpha- gal or
drug excipients, can be examined. The allergist will also assess the
risk of further reactions, and ensure that patients and caregivers are
BOX 4 Indications for the prescription of self-injectable adrenaline
Recommendation Key references Rationale
Absolute indications for adrenaline autoinjectors
Previous anaphylaxis triggered by food, latex or
aeroallergens
58,59 
High risk of recurrent anaphylaxis
Previous exercise-induced anaphylaxis 
60 
High risk of recurrent anaphylaxis
Previous idiopathic anaphylaxis 
61 
High risk of recurrent anaphylaxis
Co-existing unstable or moderate to severe, persistent
asthma and a food allergy*
62,63 
Asthma is a risk factor for experiencing anaphylaxis in
the context of food allergy
Hymenoptera venom allergy in untreated patients
with more than cutaneous/mucosal systemic
reactions or high risk of re-exposure
During and after VIT, in patients with more than
cutaneous/mucosal systemic reactions if risk
factors for relapse are present
25,64 
High risk of recurrent anaphylaxis
Underlying systemic mastocytosis in adults with any
previous systemic reaction. Children with very
severe skin involvement (>50% body surface) and
increased basal serum tryptase levels (>20 ng/ml)
and with blistering in the first three years of life
65–68 
Systemic mastocytosis is associated with a high risk
of recurrent anaphylaxis and it is not possible to
identify individual at- risk patients
Consider prescribing adrenaline autoinjectors with any of the following additional factors (especially if more than one is present)
Previous mild-to-moderate allergic reaction* to
foods known to be associated with anaphylaxis
in patient's region (eg peanut and/or tree nut,
cow's milk, sea food depending on triggers for
anaphylactic reactions at that location)
69–74 
Relatively high risk of experiencing anaphylaxis in
future with any peanut or tree nut allergy in many
counties. Increasing number of fatal anaphylaxis
with cow's milk in school-age children and young
adults. Seafood is an important hidden allergen in
some countries.
Teenager or young adult with a food allergy with
previous mild-to-moderate reactions*
75,76 
This age group is at higher risk of experiencing
anaphylaxis due to their life style or risk behaviours
Remote from medical help or prolonged travel abroad
in the context of previous mild-to-moderate
allergic reaction to a food, Hymenoptera venom,
latex or aeroallergens
77 
Medical help may not be easily available during travel.
Risks are more difficult to control due to language
barriers and new foods.
Previous mild-to-moderate allergic reaction to traces
of food*
43,77,78 
Contact with a large amount of the food in future may
result in a more severe reaction
Hymenoptera venom or drug allergy in patients with
more than cutaneous/mucosal systemic reactions
and cardiovascular disease
5,79 
Cardiovascular diseases appear to be associated with
a greater risk of severe or fatal anaphylaxis (venom
and drug anaphylaxis)
Oral immunotherapy for food allergy 
80 
Anaphylaxis is a known adverse effect of oral
immunotherapy for food allergy
*Excluding pollen food allergy syndrome unless patient has previously experienced systemic symptoms. VIT: Hymenoptera venom
immunotherapy. Supporting references taken from the anaphylaxis systematic review with additional ones taken from a specific review of
the literature focused on indications.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
367
MURARO et Al .
optimally equipped and trained to manage any further reactions. A
specialist dietitian can provide helpful advice where the trigger is
a food. Also signpost patients to local patient advocacy groups as
sources of further information and ongoing support.
6 | LO N G - TE R M M A N AG E M E NT O F
A N A PH Y L A X I S
The following sections detail the long-term management of patients
at risk of anaphylaxis. Further justification about each of the recom-
mendations about managing anaphylaxis is included in Table S3. A
summary of long-term management in the community is presented
in Box 5. Boxes 6 and 7 provides examples of individualized paediat-
ric emergency action plans.
Instructions as to how to administer a particular autoinjector
can be added to the ‘How to give an adrenaline autoinjector’ box.
Instructions as to how to administer a particular autoinjector can
be added to the ‘How to give an adrenaline autoinjector’ box.
6.1 | Education to improve acute management
6.1.1 | Education and training for patients at risk of
anaphylaxis
The EAACI Task Force recommends providing structured, comprehensive train-
ing to improve knowledge and use of adrenaline autoinjectors in people at risk
of anaphylaxis. This is in addition to basic instructions about autoinjector use.
Reason for recommendation: There is some evidence from research
and clinical experience that repeated information and support helps pa-
tients feel more knowledgeable and confident about managing triggers
and responding in an emergency.
93,94 
(Box 5) (more details in Table S3).
Strength for recommendation: This is a conditional positive recom-
mendation. Although there are randomized controlled trials about
educating patients, the certainty of evidence was low. It is unclear
what types of training and support are most effective.
Practical implications: Education is essential if patients at risk of
anaphylaxis are to successfully recognize and manage future episodes.
Many patient training approaches are available, including the use of
adrenaline autoinjector training devices and online approaches.
75
6.1.2 | Other potential educational interventions
Some studies have also found that supporting patients to practise
using an adrenaline autoinjector or needle and syringe containing 0.9%
saline can reduce anxiety or improve quality of life.
95,96 
This approach
may be helpful in anxious patients but requires adequate resources and
preparation. More research focused on supervised self-injection with
an adrenaline autoinjector with outcomes evaluated using disease-
specific quality-of-life and self-efficacy measures is needed. In the
case of anaphylaxis during an in hospital-based food/ drug challenge,
patients and carers may be encouraged to administer their own adren-
aline autoinjector to improve their confidence in this procedure.
97 
It
is also important for allergists to follow a patient's anaphylaxis man-
agement plan during a provocation challenge (eg giving in adrenaline
with the first sign of anaphylaxis) to re-inforce this self-management
approach.
6.2 | Pharmacological approaches to prevent
anaphylaxis
6.2.1 | Premedication with antihistamine
The EAACI task force makes no recommendation for or against using
premedication with antihistamine to prevent anaphylaxis.
Reason for no recommendation: We found insufficient evi -
dence about the effectiveness of antihistamines in preventing
anaphylaxis. 
98,99 
A recent meta- analysis that included obser -
vational studies and studies where the outcome was hypersen -
sitivity not anaphylaxis concluded that antihistamines and or
glucocorticoids may prevent index reactions to chemotherapy
but not radio- contrast media (very low certainty evidence). 
90
Practical implications: Antihistamines are helpful at reducing re-
actions to allergen immunotherapy but this is outside the scope of
the current guidelines.
100
6.2.2 | Premedication with adrenaline for snake bite
anti-venom
The EAACI task force suggests using premedication with subcutaneous
adrenaline to prevent anaphylaxis when snake bite anti-venom is given
to a patient.
TA B L E 4 Factors leading to need for prolonged observation
following anaphylaxis
Prolonged observation following anaphylaxis: factors to consider
Factors relating to the patient:
• Reactions in individuals with severe asthma
117
• Patients presenting in the evening or at night, or those who may
not be able to respond to any deterioration
117
• Patients in areas where access to emergency care is difficult
117
• Patients with a previous history of biphasic reactions
117
Factors related to the reaction, potentially increasing the risk of a
biphasic reaction:
• With multi-organ involvement
92
• With a severe respiratory component
117
• Needing administration of >1 dose of epinephrine for the
treatment of the initial anaphylaxis
90
• Caused by allergen with continued absorption of the allergen, for
example food
117
• With unknown elicitor
90
Note: Supporting references taken from the anaphylaxis systematic
review with additional ones from a specific review of the literature
focused on prolonged or biphasic reactions.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

368 
|
MURARO et Al .
Reason for recommendation: There is some evidence that low
dose, subcutaneous adrenaline can prevent anaphylaxis caused
when snake anti-venom is given to a patient 
101,102 
(more details in
Table S3).
Practical implications: For this very specific scenario, premedica-
tion with low dose, subcutaneous adrenaline may be useful when
a patient who has suffered a snake bite is treated with snake anti-
venom. The task force found no evidence that antihistamines or hy-
drocortisone could prevent anaphylaxis associated with snake bite
anti-venom (Table S3).
6.3 | Approaches to prevent anaphylaxis in schools
6.3.1 | Use of policy to improve management
in schools
The EAACI task force suggests that school policies should reflect ana-
phylaxis guidelines but more research is needed to understand how
guidelines and legislation in schools are best implemented.
Reason for recommendation: There is emerging evidence to sup -
port the value of school policies in improving the management of
BOX 5 Summary of the long-term management in the community of patients at risk of anaphylaxis
Individualized management plan and emergency kit
• Provision of individualized management plan written clearly in simple, non-medical language; it must include
• personal identification data: name, address, contact number; also consider adding a photograph
• details of the parents, guardian, or next of kin, allergist
• family doctor and the local ambulance service
• clear identification of the source of the allergens to be avoided and allergen avoidance advice
• clear identification of any non-allergen triggers or cofactors (eg exercise) and avoidance advice
• anaphylaxis emergency action plan
• Copy of plan must be kept by the patient, any caregivers, school staff, and family doctor
• Provision of emergency kit with copy of anaphylaxis emergency action plan and medications for self-treatment, for example
• adrenaline autoinjector for treating anaphylaxis, where appropriate (EMA recommends that patients have access to two devices)
• fast-acting, non-sedating, antihistamine for treating cutaneous allergic reactions, where appropriate
• Implementation of the patient's management plan in the community (eg nursery, school university work)
• Advice to carry mobile phone (if appropriate)
• Discuss a form of medic alert notification
• Review of plan including doses with age and weight
Education and training
• Training of patients and caregivers, this must include
• instructions on appropriate allergen avoidance measures, including consultation with an allergy dietitian, where appropriate if
food is the trigger
• instructions on prompt recognition of symptoms of anaphylaxis
• training on when and how to use an adrenaline autoinjector, where appropriate and to carry them at all times
• explanation of expiry of devices, reminders and process for renewal and storage
• Reinforcement with revision at regular intervals, possibly with asthma reviews
• Retraining on device if device switched
• Sign post patient support groups
Specific therapy
• Venom immunotherapy as appropriate
• Desensitization for drug allergy as appropriate
Other considerations
• Psychological support as required to patient and family/carers
• Ensure optimal management of co-morbidities such as rhinitis and asthma
• Support during transition to adulthood with good communication specialist units advice on at-risk behaviour
• Log allergies in hospital and community medical records
• Re-referral or advice and guidance to allergy unit if new symptoms with foods or repeat admissions
EMA: European Medicines Agency.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
369
MURARO et Al .
anaphylaxis in an education setting.
103 
Anaphylaxis due to food
allergy, occurs in schools more than in any other community loca-
tion.
104,105 
It may therefore be helpful to target secondary schools
and community settings with educational support to help raise gen-
eral awareness, empower adolescents to confidently self- manage
food allergy and enable schools to develop protocols to minimize
any adverse events if they occur (more details in Table S3).
Strength recommendation: This is a conditional positive rec-
ommendation because the certainty of the evidence is very low.
Although there was only one study and it was at high risk of bias,
we believe that schools need more support to prioritize systems to
ensure that children at risk of anaphylaxis are protected in schools.
Practical implications: While there is some evidence to sup -
port a policy approach to improving the management of ana -
phylaxis in schools. For example, in a pilot study in two UK
schools,
106 
full stakeholder involvement in toolkit development,
based on EAACI guidelines, was found to raise awareness and
empower pupils with/without allergies to self- manage effec-
tively. However, there are barriers to the implementation of leg -
islation.
107 
Work needs to be done to understand how best to
implement legislation and guidelines in schools, including how
best to train schools staff.
108 
Furthermore, standard allergy pol -
icies, such as those supplied by national or local authorities, may
lack the school- specific practical solutions necessary for effec -
tive implementation. A similar approach may be helpful for pre-
school care settings.
6.3.2 | Other approaches
Other approaches researched to improve the management of
anaphylaxis included nurses checking whether students were
BOX 6 Example of an individualized emergency action plan for a child
Action to take:
• Stay with the child, call or help if necessary
• Locate adrenaline autoinjectors
• Give long-acting, non-sedating antihistamine if required: medication ___________, dose______
• Phone parent/emergency contact: _____________
Watch for signs of ANAPHYLAXIS (life-threatening allergic reaction)
Anaphylaxis may occur without skin symptoms: ALWAYS consider anaphylaxis in someone with known food allergy who has SUDDEN
BREATHING DIFFICULTY
A: AIRWAY
• Persistent cough
• Hoarse voice
• Difficulty swallowing
• Swollen tongue
B: BREATHING
• Difficult or noisy breathing
• Wheeze or persistent cough
C: CIRCULATION
• Persistent dizziness
• Pale or floppy
• Suddenly sleepy
• Collapse/unconscious
IF ANY ONE (OR MORE) OF THESE SIGNS ABOVE ARE PRESENT:
1. Lie child flat with legs raised (if breathing is difficult, sit up with elevated legs)
2. Use Adrenaline autoinjector without delay (Device: ____, dose ____)
3. Dial ____ for ambulance and say ANAPHYLAXIS (“ANA-FIL-AX-IS”)
*** IF IN DOUBT, GIVE ADRENALINE ***
AFTER GIVING ADRENALINE:
1. Stay with child until ambulance arrives, do NOT stand child up
2. Commence CPR if there are no signs of life
3. Phone parent/emergency contact
4. If no improvement after 5–10 min, give a further adrenaline dose using a second autoinjectable device, if available.
You can dial emergency number from any phone, even if there is no credit left on a mobile. Medical observation in hospital is recom-
mended after anaphylaxis.
Adapted from British Society of Allergy and Clinical
Immunology paediatric allergy action plans (https://
www.bsaci.org/professional-resources/resources/
paedi atric-allergy-action-plans/, last accessed 26th
September 2020)
How to give an adrenaline autoinjector:
• Instructions for how to give an adrenaline autoinjector differ between
devices.
• Patients should receive training in how to use the auto-injector they are
prescribed.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

370 
|
MURARO et Al .
carrying autoinjectors
109 
and availability of a 24- hour hel-
pline.
110 
None of these had sufficient evidence to warrant a
recommendation.
7 | E D U C ATI O N A N D TR A I N I N G FO R
H E A LTH C A R E PRO FE S S I O N A L S
7.1 | Simulation training and visual prompts for
healthcare professionals
The EAACI task force suggests using simulation training and visual
prompts to improve healthcare professionals’ recognition and manage-
ment of anaphylaxis in emergency situations.
Reason for recommendation: Healthcare professionals are
not well prepared to recognize and manage anaphylaxis.
111,112
Simulation-based training is well established across medicine and
there is emerging evidence that it may help professionals recognize
and react to anaphylaxis (more details in Table S4). Similarly, there
is some evidence that visual aids such as wallet sized prompt sheets
or flow diagrams can help healthcare professionals understand and
better manage anaphylaxis.
113–115
Strength of recommendation: This is a conditional positive rec-
ommendation as the quantity and quality of available evidence is
low. It is based on a number of small randomized controlled tri-
als, the majority of which were at high risk of bias and focused on
different endpoints so there was very low overall certainty in the
evidence.
BOX 7 Example of an individualized emergency action plan for a young person or adult
Mild/moderate reaction:
• Swollen lips, face or eyes
• Itchy/tingling mouth
• Hives or itchy skin rash
• Abdominal pain or vomiting
Action to take:
• Let others know, call for help if necessary
• Locate adrenaline autoinjectors
• Take long-acting, non-sedating antihistamine if required: medication ______,
dose______mg
• Watch for development of more severe symptoms
Watch for signs of ANAPHYLAXIS (life-threatening allergic reaction)
Anaphylaxis may occur without skin symptoms. If you have food allergy, ALWAYS consider anaphylaxis if you develop SUDDEN
BREATHING DIFFICULTY
A: AIRWAY
• Persistent cough
• Hoarse voice
• Difficulty swallowing
• Swollen tongue
B: BREATHING
• Difficult or noisy breathing
• Wheeze or persistent cough
C: CIRCULATION
• Persistent dizziness
• Suddenly sleepy
• Collapse/unconsciousness
IF ANY ONE (OR MORE) OF THESE SIGNS ABOVE ARE PRESENT:
1. Lie flat with legs raised (if breathing is difficult, sit up with legs raised.bent)
2. Use Adrenaline autoinjector without delay (Device: ______, dose _____mg)
3. Dial ____ for ambulance and say ANAPHYLAXIS (“ANA-FIL-AX-IS”)
*** IF IN DOUBT, GIVE ADRENALINE ***
AFTER GIVING ADRENALINE:
1. Do NOT stand up
2. CPR should be started if there are no signs of life
3. Phone emergency contact (___________)
4. If no improvement after 5–10 min, give a further adrenaline dose using a second autoinjectable device, if available.
You can dial emergency number from any phone, even if there is no credit left on a mobile. Medical observation in hospital is recom-
mended after anaphylaxis.
Adapted from British Society of Allergy and Clinical
Immunology paediatric allergy action plans (https://
www.bsaci.org/professional-resources/resources/
paedi atric-allergy-action-plans/, last accessed 26th
September 2020)
How to give an adrenaline autoinjector:
• Instructions for how to give an adrenaline autoinjector differ between
devices.
• Patients should receive training in how to use the auto-injector they are
prescribed.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
371
MURARO et Al .
Practical implications: Simulation training is well established
and accepted as a teaching method. Scenarios based on anaphylaxis
could be included in simulation training programmes for healthcare
professionals. With regard to visual aids, these need to be readily
accessible to healthcare professionals who may encounter anaphy-
laxis in their practice. A number of modalities can be considered, for
example wallet size prompt sheets, posters in emergency rooms or
electronic apps.
8 | S U M M A RY, G A P S I N TH E E V I D E N C E
A N D FU T U R E PE R S PEC TI V E S
This guideline is intended to provide the best current evidence on
the appropriate diagnosis and management of anaphylaxis both at
the acute episode and in the long-term management. The diagnosis
of anaphylaxis is still based on the clinical evaluation. In suspected
reactions, measuring serum tryptase within the first 2 hours of
reaction can help the allergist to subsequently make a diagnosis.
Adrenaline is confirmed to be the first-line treatment, to be ad-
ministered intramuscularly and timely. Likewise, the provision of
the adrenaline autoinjector is the cornerstone for the long-term
management. The task force recommends that pharmacokinetic
data should be made available, especially for any new devices. The
European Medicines Agency recommends ‘that two auto-injectors
are prescribed to any patient at-risk who should carry them all times’. 
57
Although this recommendation is valid in all the EU countries, the
task force is aware that there are differences in implementation,
availability of autoinjectors and reimbursement. Patients need an
individualized plan for managing anaphylaxis as well as education.
Health professionals, nursery staff and teachers also need training.
We have considered the facilitators and barriers to implementing
these recommendations (Table 5).
8.1 | Strengths and limitations
A strength of this guideline is that it is informed by a balance of evi -
dence and expert opinion. A comprehensive systematic review was
undertaken evaluating the evidence according to well established
GRADE methods. We focused on randomized controlled trials to
provide the highest quality available evidence. The review was led
by independent methodologists with no conflicts of interest. It is
a strength that the recommendations were also based on expert
clinical and patient opinion, balancing benefits and harms and con -
sidering values and preferences. This included a range of countries,
disciplines and clinical backgrounds, including primary care and pa -
tient organizations. So where the evidence was not clear or suffi-
cient, a broad-based consensus could be achieved.
A limitation of the guideline is that there is heterogeneity and
gaps in existing knowledge, making it difficult to draw firm conclu-
sions. Much of the research does not use robust diagnostic crite-
ria for anaphylaxis and there are other methodological weaknesses
meaning that most recommendations are based on low or moderate
certainty evidence. The heterogeneity in the studies, including dif-
ferent study populations, variations in interventions at different
ages and duration, and varying definitions of anaphylaxis made it
challenging to interpret the evidence. It was not appropriate to un-
dertake meta-analysis to combine such heterogeneous studies.
8.2 | Research gaps
There is much left to learn about diagnosing and managing anaphy-
laxis. Table 6 sets out key priorities. Where possible, evidence ought
to be derived from double- blind, placebo- controlled randomized
trials. Future studies would ideally include a harmonized definition
and robust diagnostic criteria for anaphylaxis. High priority gaps
are the need of biomarkers which can predict the level of risk for
a given patient, the role of monoclonal antibodies in reducing the
risk as well as getting evidence on the most adequate educational
intervention or combination of interventions for prevention of the
acute episode.
8.3 | Conclusions
Implementing these recommendations would result in harmoniza -
tion of the best standards of practice for anaphylaxis. The ultimate
goal would be the development of an evidence- based, multifaceted
and integrated patient-centric approach which may help to alleviate
the burden of anaphylaxis among individuals and families and also
reduce societal healthcare costs.
AC K N OW L E D G E M E N T S
The EAACI Anaphylaxis Guideline Update task force would like to
thank Motohiro Ebisawa, Luciana Kase Tanno, Maximiliano Gomez,
Richard Loh, Paul Turner and Gary Wong for their constructive, ex-
pert review of the draft guidelines; all the EAACI members who com -
mented on the draft guideline via the public web site; to the EAACI
Methodology Committee for their feedback; the EAACI Guideline
Committee for their support; and to funding from EAACI.
CO N FL I C T O F I N T E R E S T
Professor Muraro reports grants and personal fees from Aimmune
and personal fees from DVB, Mylan, ALK and Nestle outside
the submitted work and was past President of EAACI. Professor
Worm reports grants and personal fees from Stallergens, HAL
Allergie, Bencard Allergie, Allergopharma, ALK- Abello, Mylan
Germany, Actelion Pharmaceuticals Deutschland, Biotest, AbbVie
Deutschland, Lilly Deutschland Aimmune, DBV Technologies,
Regeneron Pharmaceuticals, Sanofi Aventis, Leo Pharma, Novartis
and Viatris, outside the submitted work and is past WAO co-chair of
the anaphylaxis committee. Dr. Alviani has nothing to disclose. Dr.
Cardona reports personal fees from Allergopharma and GSK and
a grant from Thermofisher outside the submitted work and SLAAI
chair anaphylaxis committee plus past WAO chair anaphylaxis com -
mittee. Dr. DunnGalvin has nothing to disclose. Dr. Garvey reports
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

372 
|
MURARO et Al .
TA B L E 5
 
Considerations for implementing recommendations made in this guideline
Topic
 
Barriers to implementation
 
Facilitators to implementation
 
Audit criteria
 
Resource implications
Using clinical criteria to identifying
anaphylaxis in an emergencysituation
Various definitions of anaphylaxis
are still in place
Lack of knowledge and experience
Training on validated list of rapid onset of
signs and symptoms with accessiblereminders (eg wallet, phone, Internet)
Proportion of emergency settings
in which the validated criteriais used
Cost of implementing standardized,
validated, universal definition low
Measuring serum tryptase to
support the diagnosis ofanaphylaxis retrospectively
Lack of knowledge regarding
tryptase in emergencydepartment
Tryptase sample should not delay
acute diagnosis and treatment
Lack of infrastructure for taking and
analysing samples
Training about use of tryptase for
emergency department staff
Identification of laboratories with the
relevant equipment
Proportion of anaphylaxis patients
where tryptase is assessed
The cost of measuring tryptase,
although low, needs to be takeninto account
Healthcare professionals
treating anaphylaxis withI.M. adrenaline and using thecorrect dosing
Differences in labelling of adrenaline
(eg ratios 1:1000 or massconcentration 1mg/ml)
Synonym epinephrine used in some
countries
Lack of training
Training healthcare professionalsStandardization of labellingAdd to mandatory annual training
Proportion of cases treated with
I.M. adrenaline using the correctdosage
Resources needed for training and
standardizing adrenaline
Use of adrenaline autoinjectors by
patients
Lack of trainingFear or embarrassment to useNot carrying AAI all timesNeedle phobia
Training patients and caregivers with
simulated scenarios
Identify and treat needle phobiaUse of trainer devicesReminders to carry devicesAccess to training materials including
online videos
Proportion of patients experiencing
anaphylaxis who use anautoinjector
Autoinjectors are relatively expensive,
most of not used and they have arelatively short shelf life
Education and training for patients
and carers in anaphylaxisrecognition and management
Training packages need to be
developed and harmonizedacross regions
Unclear which elements and
structure are most beneficial
Repeated training is likely to be of
greater benefit
Patients and patient groups place great
value on patient training
Multiple different modalities of training
can be developed (face-
to-
face,
virtual)
Online training already provided by
commercial companies and patientorganizations
Proportion of patients/ carers who
have been offered and accesseda comprehensive trainingpackage after diagnosis
Training packages are costly to
develop and implement, bothfinancially and in terms of the timetaken
Use of simulation training and
visual prompts for healthcareprofessionals
Anaphylaxis specific simulation
training packages need to bedeveloped and validated
Visual prompts need to be of a
suitable format and kept updatedand accessible
Simulation training is a well established
training modality Visual prompts areused for other medical emergencies
Standardization of devices where
possible
Proportion of healthcare
professionals who have receivedsimulation training
Proportion of healthcare
professionals with access tovisual management prompts
For simulation training costs can be
high; also time-
 
consuming
For visual prompts, costs are low as
these are inexpensive to produce
Use of policy to improve
management in schools
Inaccessible clinically focussed
documents
Impractical standard allergy policies
Identification of specific needs and
concerns in order to develop practicalapplications for schools that can beimplemented in real-
world context
Implementation of policy in schoolProportion of students who
experience anaphylaxis
Initially relatively high, but
subsequently low once protocolsare in effect
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
373
MURARO et Al .
personal fees from Novo Nordisk, Merck, Lundbeck, Biomarin and
Thermofisher Scientific outside the submitted work. Dr. Riggioni
has nothing to disclose. Professor de Silva has no conflict to dis -
close in relation to the guideline. Her organization received a grant
from EAACI to conduct a systematic review, which was one of the
tools the task force drew on tool when developing recommenda-
tions. Dr. Angier reports BSACI member and Anaphylaxis Campaign
scientific board member. Dr. Arasi has nothing to disclose.
Professor Bellou has nothing to disclose. Dr. Beyer reports grants
and personal fees from Aimmune, grants and personal fees from
ALK, grants and personal fees from Danone, grants and personal
fees from DBV, grants and personal fees from Infectopharm, grants
and personal fees from ThermoFisher, grants and personal fees
from Hycor, grants from DST Diagnostic, Good Mills, Hipp, VDI,
EU, German Research Foundation, BMBF and personal fees from
Allergopharma, Bausch & Lomb, Bencard, Jenpharma, Mabylon,
Mylan, Nestle, Novartis, and Nutricia outside the submitted work.
Dr. Bijlhout has nothing to disclose. Dr Bilo reports personal fees
from ALK, Allergy Therapeutics, Astra, GSK and Sanofi outside the
submitted work. Prof Dr Bindslev-Jensen reports research grants
from Novartis outside the submitted work. Dr Brockow reports
personal fees from ThermoFisher and Mylan outside the submit -
ted work. Dr Fernandez- Rivas reports grants from ISCIII (Ministry
of Science, Spanish Government), grants and personal fees from
Aimmune and personal fees from Ga2len, DBV, Novartis, SPRIM,
Diater, GSK, HAL Allergy and Thermofisher Scientific outside
the submitted work. Professor Halken has nothing to disclose.
Dr Jensen has nothing to disclose. Dr. Khaleva has nothing to dis -
close. Dr Michaelis has nothing to disclose. Dr Oude Elberink re -
ports grants from Pure IMS and Blueprint, support from Novartis,
TA B L E 6 Gaps in the evidence for managing anaphylaxis
Gaps Suggestion to address Priority
Data comparing the pharmacokinetics of different
adrenaline auto-injector devices
Clinical randomized controlled trial High (1st)
Optimal dose and dosing intervals of intramuscular
adrenaline in patients experiencing anaphylaxis
Clinical randomized controlled trial High (2nd)
Clinical definition and diagnostic criteria for
anaphylaxis that are easy to use in emergency
situations.
Large community-based studies to develop, validate and assess ease
of use of criteria
High (3rd)
Identification of biomarkers to predict severity of
anaphylaxis
Follow up of clinical cohorts at varying risks of anaphylaxis Medium (4th)
Biomarkers for bedside testing to support diagnosis Clinical cohorts experiencing anaphylaxis and similar presentations Medium (5th)
Standardized severity grading for anaphylaxis Clinical cohorts experiencing acute allergic reactions and consensus
discussion
Medium (5th)
Role antihistamines, corticosteroids or adrenaline
to prevent anaphylactic reactions in high-risk
situations
Large randomized controlled trials in high-risk situations (ie re-
administration of contrast media after a previous reaction)
Medium (7th)
Value of practising self-injection (using functioning
adrenaline autoinjector devices) to a sub-group of
patients that may be too anxious otherwise to use
their autoinjector in real life.
Randomized controlled studies with outcomes focused on allergy
specific quality of life, self-efficacy and anxiety
Medium (8th)
Role of second- and third-line drugs in the treatment of
anaphylaxis
Clinical randomized controlled trial Medium (9th)
Identification of different endotypes of anaphylaxis
which may benefit from different management
Analysis of large data sets considering different elicitors Medium (10th)
More convenient routes of administration of
adrenaline, for example intranasal, inhalational,
sublingual
Clinical randomized controlled trial, initially pharmacokinetic studies
in well individuals, then randomized controlled trials in high-risk
patients or situations
Low (11th)
Effectiveness of smartphone- based applications
to improve recognition and management of
anaphylaxis for patients
Community randomized controlled studies, with a focus on patient
involvement in app development and patient engagement
Low (12th)
Best approach to implementing guidelines and
legislation in schools
Qualitative methods (eg Interviews/focus groups) with students and
staff to identify specific needs and concerns in order to develop
practical applications
Then large school-based randomized controlled trial to assess the
effectiveness of implementation
Low (13th)
Standardized questionnaires for quality of life for
patients at risk of anaphylaxis from any elicitor
Analysis of large data sets from patients considering different
elicitors
Low (14th)
Note: Prioritization was agreed by consensus within the guideline task force.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

374 
|
MURARO et Al .
Behring, Viatric, Takeda and Sanofi outside the submitted work and
is on the Advisory Board of PIMS Epinephrine. Ms Regent reports
she is employed by the Anaphylaxis Campaign, UK; the organization
received support from ALK- Abello and Mylan. Dr Sanchez reports
a personal fees from Aimmune Therapeutics outside the submit -
ted work. Dr Vlieg- Boerstra reports grants and personal fees from
Nutricia and personal fees from Mead Johnson, Abbott and Marfo
Food Groups outside the submitted work. Professor Roberts re-
ports he was Editor in Chief Clinical & Experimental Allergy until
December 2020.
AU T H O R CO N T R I B U T I O N S
Antonella Muraro, Graham Robert and Margitta Worm chaired the
EAACI Anaphylaxis Guideline Task Force. Cherry Alviani, Victoria
Cardona, Audrey DunnGalvin, Lene H. Garvey, Carmen Riggioni,
Graham Roberts and Margitta Worm led the discussions for in-
dividual sections drafting the evidence table, recommendations
and gaps for specific sections based on the underpinning system-
atic review and task force discussions which involved the authors.
Graham Roberts, Antonella Muraro and Margitta Worm wrote the
initial draft of the guideline. All authors participated in the discus-
sion of the draft guideline, its revision and approved the final version.
Antonella Muraro chaired the EAACI Food Allergy and Anaphylaxis
Guidelines Update. Graham Roberts coordinated the update of the
guidelines supported by Ekaterina Khaleva. Debra de Siva provided
methodological support and advice as well as contributing to draft-
ing sections.
O R C I D
Margitta Worm https://orcid.org/0000-0002-3449-1245
Cherry Alviani https://orcid.org/0000-0003-1527-0495
Victoria Cardona https://orcid.org/0000-0003-2197-9767
Audrey DunnGalvin https://orcid.org/0000-0002-1540-3959
Lene Heise Garvey https://orcid.org/0000-0002-7777-4501
Carmen Riggioni https://orcid.org/0000-0002-8745-0228
Debra de Silva https://orcid.org/0000-0001-8413-5487
Stefania Arasi https://orcid.org/0000-0002-8135-0568
Abdelouahab Bellou https://orcid.org/0000-0003-3457-5585
Maria Beatrice Bilò https://orcid.org/0000-0002-9324-6039
Knut Brockow https://orcid.org/0000-0002-2775-3681
Montserrat Fernandez-Rivas https://orcid.
org/0000-0003-1748-2328
Ekaterina Khaleva https://orcid.org/0000-0002-2220-7745
Berber J. Vlieg-Boerstra https://orcid.org/0000-0001-7962-5406
Graham Roberts https://orcid.org/0000-0003-2252-1248
R E F E R E N C E S
1. Simons FE, Ardusso LR, Bilo MB, et al. International consensus on
(ICON) anaphylaxis. World Allergy Organ J. 2014;7(1):9.
2. Bilo MB, Corsi A, Martini M, Penza E, Grippo F, Bignardi D. Fatal
anaphylaxis in Italy: analysis of cause- of-death national data,
2004–2016. Allergy. 2020;75(10):2644-2652.
3. Turner PJ, Gowland MH, Sharma V, et al. Increase in anaphylaxis-
related hospitalizations but no increase in fatalities: an analysis of
United Kingdom national anaphylaxis data, 1992-2012. J Allergy
Clin Immunol. 2015;135(4):956-963.e1.
4. Greenhawt M, Gupta RS, Meadows JA, et al. Guiding principles for
the recognition, diagnosis, and management of infants with ana-
phylaxis: an expert panel consensus. J Allergy Clin Immunol Pract
2019;7(4):1148-1156 e1145.
5. Francuzik W, Ruëff F, Bauer A, et al. Phenotype and risk factors of
venom-induced anaphylaxis: a case- control study of the European
Anaphylaxis Registry. J Allergy Clin Immunol. 2021;147(2):653-662.
e9. https://doi.org/10.1016/j.jaci.2020.06.008. Epub 2020 Jun 22.
6. Aurich S, Dölle-Bierke S, Francuzik W, et al. Anaphylaxis in elderly
patients—data from the European Anaphylaxis Registry. Front
Immunol. 2019;24(10):750.
7. Grabenhenrich LB, Dolle S, Moneret-Vautrin A, et al. Anaphylaxis
in children and adolescents: the European Anaphylaxis Registry.
J Allergy Clin Immunol. 2016;137(4):1128-1137 e1121.
8. Worm M, Eckermann O, Dolle S, et al. Triggers and treatment of
anaphylaxis: an analysis of 4,000 cases from Germany, Austria and
Switzerland. Dtsch Arztebl Int. 2014;111(21):367-375.
9. Worm M, Moneret-Vautrin A, Scherer K, et al. First European data
from the network of severe allergic reactions (NORA). Allergy.
2014;69(10):1397-1404.
10. Gomes ER, Demoly P. Epidemiology of hypersensitivity drug reac-
tions. Curr Opin Allergy Clin Immunol. 2005;5(4):309-316.
11. Joint Task Force on Practice Parameters; American Academy of
Allergy, Asthma and Immunology; American College of Allergy,
Asthma and Immunology; Joint Council of Allergy, Asthma and
Immunology. Drug allergy: an updated practice parameter. Ann
Allergy Asthma Immunol. 2010;105(4):259-273.
12. Romano A, Atanaskovic-Markovic M, Barbaud A, et al. Towards
a more precise diagnosis of hypersensitivity to beta-lactams - an
EAACI position paper. Allergy. 2020;75(6):1300-1315.
13. Siracusa A, Folletti I, Gerth van Wijk R, et al. Occupational anaphylaxis–an
EAACI task force consensus statement. Allergy. 2015;70(2):141-152.
14. Brockow K, Kneissl D, Valentini L, et al. Using a gluten oral food chal-
lenge protocol to improve diagnosis of wheat- dependent exercise-
induced anaphylaxis. J Allergy Clin Immunol. 2015;135(4):977-984
e974.
15. Christensen MJ, Eller E, Mortz CG, Brockow K, Bindslev-Jensen
C. Wheat- dependent cofactor-augmented anaphylaxis: a prospec-
tive study of exercise, aspirin, and alcohol efficacy as cofactors.
J Allergy Clin Immunol Pract. 2019;7(1):114-121.
16. Cardona V, Luengo O, Garriga T, et al. Co-factor-enhanced food
allergy. Allergy. 2012;67(10):1316-1318.
17. Akin C. Mast cell activation syndromes presenting as anaphylaxis.
Immunol Allergy Clin North Am. 2015;35(2):277-285.
18. Bilo MB, Martini M, Tontini C, Mohamed OE, Krishna MT.
Idiopathic anaphylaxis. Clin Exp Allergy. 2019;49(7):942-952.
19. Carter MC, Akin C, Castells MC, Scott EP, Lieberman P. Idiopathic
anaphylaxis yardstick: practical recommendations for clinical
practice. Ann Allergy Asthma Immunol. 2020;124(1):16-27.
20. Muraro A, Roberts G, Worm M, et al. Anaphylaxis: guidelines
from the European Academy of Allergy and Clinical Immunology.
Allergy. 2014;69(8):1026-1045.
21. de Silva D, Singh C, Muraro A, et al. Diagnosing, manag-
ing and preventing anaphylaxis: systematic review. Allergy.
2021;76:1493–1506.
22. Brouwers MC, Kho ME, Browman GP, et al. AGREE II: advancing
guideline development, reporting and evaluation in health care.
CMAJ. 2010;182(18):E839-E842.
23. AGREE Collaboration. Development and validation of an inter-
national appraisal instrument for assessing the quality of clini-
cal practice guidelines: the AGREE project. Qual Saf Health Care.
2003;12(1):18-23.
24. Andrews J, Guyatt G, Oxman AD, et al. GRADE guide-
lines: 14. Going from evidence to recommendations: the
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
375
MURARO et Al .
significance and presentation of recommendations. J Clin
Epidemiol. 2013;66(7):719-725.
25. Sturm GJ, Varga EM, Roberts G, et al. EAACI guidelines on al-
lergen immunotherapy: hymenoptera venom allergy. Allergy.
2018;73(4):744-764.
26. de Silva D, Roberts G, Worm M, Muraro A, Allergy EF, Anaphylaxis GG.
EAACI anaphylaxis guidelines: systematic review protocol. Clin Transl
Allergy. 2020;10:14. https://doi.org/10.1186/s13601-020-00320-3
27. Zhang Y, Akl EA, Schunemann HJ. Using systematic reviews in
guideline development: the GRADE approach. Res Synth Methods.
2019;10(3):312-329.
28. Guyatt G, Oxman AD, Akl EA, et al. GRADE guidelines: 1.
Introduction-GRADE evidence profiles and summary of findings
tables. J Clin Epidemiol. 2011;64(4):383-394.
29. Erlewyn-Lajeunesse M, Dymond S, Slade I, et al. Diagnostic utility
of two case definitions for anaphylaxis: a comparison using a retro-
spective case notes analysis in the UK. Drug Saf. 2010;33(1):57-64.
30. Loprinzi Brauer CE, Motosue MS, Li JT, et al. Prospective validation
of the NIAID/FAAN criteria for emergency department diagnosis
of anaphylaxis. J Allergy Clin Immunol Pract. 2016;4(6):1220-1226.
31. Sampson HA, Munoz-Furlong A, Campbell RL, et al. Second sym-
posium on the definition and management of anaphylaxis: sum-
mary report–Second National Institute of Allergy and Infectious
Disease/Food Allergy and Anaphylaxis Network symposium. J
Allergy Clin Immunol. 2006;117(2):391-397.
32. Simons FE, Ardusso LR, Dimov V, et al. World Allergy Organization
Anaphylaxis Guidelines: 2013 update of the evidence base. Int
Arch Allergy Immunol. 2013;162(3):193-204.
33. Muraro A, Roberts G, Clark A, et al. The management of anaphy-
laxis in childhood: position paper of the European academy of al-
lergology and clinical immunology. Allergy. 2007;62(8):857-871.
34. Brown SG, Blackman KE, Heddle RJ. Can serum mast cell
tryptase help diagnose anaphylaxis? Emerg Med Australas.
2004;16(2):120-124.
35. Sala-Cunill A, Cardona V, Labrador-Horrillo M, et al. Usefulness
and limitations of sequential serum tryptase for the diagno-
sis of anaphylaxis in 102 patients. Int Arch Allergy Immunol.
2013;160(2):192-199.
36. Francis A, Fatovich DM, Arendts G, et al. Serum mast cell tryptase
measurements: sensitivity and specificity for a diagnosis of ana -
phylaxis in emergency department patients with shock or hypox -
aemia. Emerg Med Australas. 2018;30(3):366-374.
37. Valent P, Akin C, Arock M, et al. Definitions, criteria and global
classification of mast cell disorders with special reference to mast
cell activation syndromes: a consensus proposal. Int Arch Allergy
Immunol. 2012;157(3):215-225.
38. Vitte J, Amadei L, Gouitaa M, et al. Paired acute-baseline serum
tryptase levels in perioperative anaphylaxis: an observational
study. Allergy. 2019;74(6):1157-1165.
39. Lyons JJ, Yu X, Hughes JD, et al. Elevated basal serum trypt-
ase identifies a multisystem disorder associated with increased
TPSAB1 copy number. Nat Genet. 2016;48(12):1564-1569.
40. Lyons JJ, Chovanec J, O'Connell MP, et al. Heritable risk for se-
vere anaphylaxis associated with increased alpha- tryptase-
encoding germline copy number at TPSAB1. J Allergy Clin Immunol.
2020;147:622–632.
41. Valent P, Akin C. Doctor, I think i am suffering from MCAS: dif-
ferential diagnosis and separating facts from fiction. J Allergy Clin
Immunol Pract. 2019;7(4):1109-1114.
42. Simons FE, Ardusso LR, Bilo MB, et al. 2012 Update: World Allergy
Organization Guidelines for the assessment and management of
anaphylaxis. Curr Opin Allergy Clin Immunol. 2012;12(4):389-399.
43. Pumphrey RS, Gowland MH. Further fatal allergic reactions to
food in the United Kingdom, 1999–2006. J Allergy Clin Immunol.
2007;119(4):1018-1019.
44. Mehr S, Liew WK, Tey D, Tang ML. Clinical predictors for biphasic
reactions in children presenting with anaphylaxis. Clin Exp Allergy.
2009;39(9):1390-1396.
45. Manuyakorn W, Benjaponpitak S, Kamchaisatian W, Vilaiyuk S,
Sasisakulporn C, Jotikasthira W. Pediatric anaphylaxis: triggers,
clinical features, and treatment in a tertiary-care hospital. Asian
Pac J Allergy Immunol. 2015;33(4):281-288.
46. Liu X, Lee S, Lohse CM, Hardy CT, Campbell RL. Biphasic reac -
tions in emergency department anaphylaxis patients: a pro -
spective cohort study. J Allergy Clin Immunol Pract. 2020;8(4):
1230- 1238.
47. Pumphrey RS. Lessons for management of anaphylaxis from a
study of fatal reactions. Clin Exp Allergy. 2000;30(8):1144-1150.
48. Breuer C, Wachall B, Gerbeth K, Abdel-Tawab M, Fuhr U.
Pharmacokinetics and pharmacodynamics of moist inhala-
tion epinephrine using a mobile inhaler. Eur J Clin Pharmacol.
2013;69(6):1303-1310.
49. Simons FE, Gu X, Johnston LM, Simons KJ. Can epinephrine inha -
lations be substituted for epinephrine injection in children at risk
for systemic anaphylaxis? Pediatrics. 2000;106(5):1040-1044.
50. Heilborn H, Hjemdahl P, Daleskog M, Adamsson U. Comparison of
subcutaneous injection and high- dose inhalation of epinephrine–
implications for self-treatment to prevent anaphylaxis. J Allergy
Clin Immunol. 1986;78(6):1174-1179.
51. Foucard T, Cederblad F, Dannaeus A, Swenne I, Niklasson F.
Anaphylaxis in severe food allergy. Adrenaline injection is safer
than inhalation. Läkartidningen. 1997;94(16):1478-1483.
52. Simons FE, Roberts JR, Gu X, Simons KJ. Epinephrine absorption
in children with a history of anaphylaxis. J Allergy Clin Immunol.
1998;101(1 Pt 1):33-37.
53. Simons FE, Gu X, Simons KJ. Epinephrine absorption in adults: in -
tramuscular versus subcutaneous injection. J Allergy Clin Immunol.
2001;108(5):871-873.
54. Turner PJ, Ruiz-Garcia M, Durham SR, Boyle RJ. Limited effect of
intramuscular epinephrine on cardiovascular parameters during
peanut-induced anaphylaxis: an observational cohort study. J
Allergy Clin Immunol Pract. 2021;9(1):527-530 e521.
55. Asch D, Pfeifer KE, Arango J, et al. JOURNAL CLUB: benefit of
epinephrine autoinjector for treatment of contrast reactions: com -
parison of errors, administration times, and provider preferences.
AJR Am J Roentgenol. 2017;209(2):W363-W369.
56. Suwan P, Praphaiphin P, Chatchatee P. Randomized compari-
son of caregivers' ability to use epinephrine autoinjectors and
prefilled syringes for anaphylaxis. Asian Pac J Allergy Immunol.
2018;36(4):248-256.
57. European Medicines Agency. Adrenaline Auto-injectors. European
Medicines Agency. https://www.ema.europa.eu/en/medic ines/
human/referrals/adrenaline-auto-injectors. Accessed 31st January
2021.
58. Anagnostou K, Harrison B, Iles R, Nasser S. Risk factors for child-
hood asthma deaths from the UK Eastern Region Confidential
Enquiry 2001–2006. Prim Care Respir J. 2012;21(1):71-77.
59. Hourihane JO, Kilburn SA, Dean P, Warner JO. Clinical character-
istics of peanut allergy. Clin Exp Allergy. 1997;27(6):634-639.
60. Shadick NA, Liang MH, Partridge AJ, et al. The natural history of
exercise-induced anaphylaxis: survey results from a 10-year fol-
low-up study. J Allergy Clin Immunol. 1999;104(1):123-127.
61. Noimark L, Wales J, Du Toit G, et al. The use of adrenaline autoinjec-
tors by children and teenagers. Clin Exp Allergy. 2012;42(2):284-292.
62. Simons FE, Clark S, Camargo CA Jr. Anaphylaxis in the com-
munity: learning from the survivors. J Allergy Clin Immunol.
2009;124(2):301-306.
63. Rudders SA, Banerji A, Corel B, Clark S, Camargo CA Jr. Multicenter
study of repeat epinephrine treatments for food-related anaphy-
laxis. Pediatrics. 2010;125(4):e711-e718.
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

376 
|
MURARO et Al .
64. Bilo MB, Cichocka-Jarosz E, Pumphrey R, et al. Self-medication of
anaphylactic reactions due to Hymenoptera stings- an EAACI Task
Force Consensus Statement. Allergy. 2016;71(7):931-943.
65. Brockow K, Jofer C, Behrendt H, Ring J. Anaphylaxis in patients
with mastocytosis: a study on history, clinical features and risk fac-
tors in 120 patients. Allergy. 2008;63(2):226-232.
66. Gulen T, Hagglund H, Dahlen B, Nilsson G. High prevalence of ana-
phylaxis in patients with systemic mastocytosis - a single-centre
experience. Clin Exp Allergy. 2014;44(1):121-129.
67. Gorska A, Niedoszytko M, Lange M, et al. Risk factors for ana-
phylaxis in patients with mastocytosis. Pol Arch Med Wewn.
2015;125(1– 2):46-53.
68. Schuch A, Brockow K. Mastocytosis and anaphylaxis. Immunol
Allergy Clin North Am. 2017;37(1):153-164.
69. Vander Leek TK, Liu AH, Stefanski K, Blacker B, Bock SA. The nat-
ural history of peanut allergy in young children and its association
with serum peanut-specific IgE. J Pediatr. 2000;137(6):749-755.
70. Ewan PW, Clark AT. Efficacy of a management plan based on se-
verity assessment in longitudinal and case- controlled studies of
747 children with nut allergy: proposal for good practice. Clin Exp
Allergy. 2005;35(6):751-756.
71. Pouessel G, Beaudouin E, Tanno LK, et al. Food-related anaphy-
laxis fatalities: analysis of the Allergy Vigilance Network
® 
data-
base. Allergy. 2019;74(6):1193-1196.
72. Turner PJ, Gowland MH, Sharma V, et al. Increase in anaphylaxis-
related hospitalizations but no increase in fatalities: an analysis of
United Kingdom national anaphylaxis data, 1992–2012. J Allergy
Clin Immunol. 2015;135(4):956-963.
73. Conrado AB, Ierodiakonou D, Gowland MH, Boyle RJ, Turner
PJ. Food anaphylaxis in the United Kingdom: analysis of national
data, 1998-2018. BMJ. 2021:372. https://doi.org/10.1136/bmj.
n251
74. Mullins RJ, Wainstein BK, Barnes EH, Liew WK, Campbell DE.
Increases in anaphylaxis fatalities in Australia from 1997 to 2013.
Clin Exp Allergy. 2016;46(8):1099-1110.
75. Roberts G, Vazquez-Ortiz M, Knibb R, et al. EAACI Guidelines on
the effective transition of adolescents and young adults with al-
lergy and asthma. Allergy. 2020;75(11):2734-2752.
76. Vazquez-Ortiz M, Angier E, Blumchen K, et al. Understanding the
challenges faced by adolescents and young adults with allergic
conditions: a systematic review. Allergy. 2020;75(8):1850-1880.
77. Sicherer SH, Simons FE. Quandaries in prescribing an emergency
action plan and self- injectable epinephrine for first- aid manage-
ment of anaphylaxis in the community. J Allergy Clin Immunol.
2005;115(3):575-583.
78. Bock SA, Munoz-Furlong A, Sampson HA. Further fatalities
caused by anaphylactic reactions to food, 2001–2006. J Allergy
Clin Immunol. 2007;119(4):1016-1018.
79. Turner PJ, Jerschow E, Umasunthar T, Lin R, Campbell DE, Boyle
RJ. Fatal anaphylaxis: mortality rate and risk factors. J Allergy Clin
Immunol Pract. 2017;5(5):1169-1178.
80. Pajno GB, Fernandez-Rivas M, Arasi S, et al. EAACI Guidelines
on allergen immunotherapy: IgE-mediated food allergy. Allergy.
2018;73(4):799-815.
81. Duvauchelle T, Robert P, Donazzolo Y, et al. Bioavailability and
cardiovascular effects of adrenaline administered by Anapen 
®
autoinjector in healthy volunteers. J Allergy Clin Immunol Pract.
2018;6(4):1257-1263.
82. Worm M, Nguyen D, Rackley R, et al. Epinephrine delivery via
EpiPen
®
((R)) Auto- Injector or manual syringe across participants
with a wide range of skin-to-muscle distances. Clin Transl Allergy.
2020;10:21.
83. Jext® 0.3mg SmPC. https://www.medicines.org.uk/emc/produ
ct/5748/smpc. Accessed 24th December 2020.
84. https://www.mein-fastj ekt.de/filea dmin/user_uploa d/EpiPe n®_
de/pdf/0719_GI_Fastj ekt2_Jun_56DE2065203- 08.pdf. Accessed
31st January 2021.
85. Kim L, Nevis IF, Tsai G, et al. Children under 15 kg with food allergy
may be at risk of having epinephrine auto-injectors administered
into bone. Allergy Asthma Clin Immunol. 2014;10(1):40.
86. Auvi-Q website. https://www.auvi-q.com/about-auvi-q. Accessed
14th April 2021.
87. Simons FE, Gu X, Silver NA, Simons KJ. EpiPen
® 
Jr versus EpiPen
®
in young children weighing 15 to 30 kg at risk for anaphylaxis. J
Allergy Clin Immunol. 2002;109(1):171-175.
88. Patel N, Isaacs E, Duca B, et al. What dose of epinephrine? Safety
and pharmacokinetics of 0.5mg versus 0.3mg epinephrine by au-
toinjector in food-allergic teenagers: a randomized cross-over trial.
J Allergy Clin Immunol. 2020;145(2):AB6.
89. Nurmatov UB, Rhatigan E, Simons FE, Sheikh A. H2-antihistamines
for the treatment of anaphylaxis with and without shock: a sys-
tematic review. Ann Allergy Asthma Immunol. 2014;112(2):126-131.
90. Shaker MS, Wallace DV, Golden DBK, et al. Anaphylaxis-a 2020
practice parameter update, systematic review, and Grading of
Recommendations, Assessment, Development and Evaluation
(GRADE) analysis. J Allergy Clin Immunol. 2020;145(4):1082-1123.
91. Gabrielli S, Clarke A, Morris J, et al. Evaluation of prehospital
management in a Canadian Emergency Department Anaphylaxis
Cohort. J Allergy Clin Immunol Pract. 2019;7(7):2232-2238 e2233.
92. Kraft M, Dölle-Bierke S, Hofmeier KS, Worm M. Features and
predictors of biphasic anaphylaxis: data from the European
Anaphylaxis Registry. J Allergy Clin Immunol. 2020;145(2):AB335.
93. Brockow K, Schallmayer S, Beyer K, et al. Effects of a structured ed-
ucational intervention on knowledge and emergency management
in patients at risk for anaphylaxis. Allergy. 2015;70(2):227-235.
94. Fernandez-Mendez F, Saez-Gallego NM, Barcala-Furelos R, et al.
Learning and treatment of anaphylaxis by laypeople: a simulation
study using Pupilar technology. Biomed Res Int. 2017;2017:9837508.
95. Shemesh E, D'Urso C, Knight C, et al. Food-allergic adolescents
at risk for anaphylaxis: a randomized controlled study of super-
vised injection to improve comfort with epinephrine self- injection.
J Allergy Clin Immunol Pract. 2017;5(2):391-397 e394.
96. Hellstrom A, Eriksson K, Efraimsson EO, Svedmyr J, Borres MP.
Assessment of self-administered epinephrine during a training
session. Acta Paediatr. 2011;100(7):e34-e35.
97. Burrell S, Patel N, Vazquez-Ortiz M, Campbell DE, DunnGalvin A,
Turner PJ. Self-administration of adrenaline for anaphylaxis during
in-hospital food challenges improves health- related quality of life.
Arch Dis Child. 2021;106:558–563.
98. Lorenz W, Doenicke A, Dittmann I, Hug P, Schwarz B. Anaphylactoid
reactions following administration of plasma substitutes in man.
Prevention of this side-effect of haemaccel by premedication with
H1- and H2-receptor antagonists (author's transl). Anaesthesist.
1977;26(12):644-648.
99. Tryba M, Zevounou F, Zenz M. Prevention of anaphylactoid reac-
tions using intramuscular promethazine and cimetidine. Studies of
a histamine infusion model. Anaesthesist. 1984;33(5):218-223.
100. Roberts G, Pfaar O, Akdis CA, et al. EAACI Guidelines on
Allergen Immunotherapy: allergic rhinoconjunctivitis. Allergy.
2018;73(4):765-798.
101. Premawardhena AP, de Silva CE, Fonseka MM, Gunatilake
SB, de Silva HJ. Low dose subcutaneous adrenaline to pre-
vent acute adverse reactions to antivenom serum in people
bitten by snakes: randomised, placebo controlled trial. BMJ.
1999;318(7190):1041-1043.
102. de Silva HA, Pathmeswaran A, Ranasinha CD, et al. Low-dose
adrenaline, promethazine, and hydrocortisone in the prevention
of acute adverse reactions to antivenom following snakebite: a
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License

| 
377
MURARO et Al .
randomised, double-blind, placebo- controlled trial. PLoS Med.
2011;8(5):e1000435.
103. Cicutto L, Julien B, Li NY, et al. Comparing school environments
with and without legislation for the prevention and management
of anaphylaxis. Allergy. 2012;67(1):131-137.
104. Greenhawt M. Environmental exposure to peanut and the risk of
an allergic reaction. Ann Allergy Asthma Immunol. 2018;120(5):476-
481 e473.
105. Muraro A, Agache I, Clark A, et al. EAACI food allergy and anaphy-
laxis guidelines: managing patients with food allergy in the com-
munity. Allergy. 2014;69(8):1046-1057.
106. Higgs J, Styles K, Bowyer S, Warner A & Dunn Galvin A.
Dissemination of EAACI food allergy guidelines using a flexible,
practical, whole school allergy awareness toolkit. Allergy. 2021;76:
3479-3488. https://doi.org/10.1111/all.14871
107. Portnoy JM, Shroba J. Managing food allergies in schools. Curr
Allergy Asthma Rep. 2014;14(10):467.
108. Moneret-Vautrin DA, Kanny G, Morisset M, et al. Food anaphylaxis
in schools: evaluation of the management plan and the efficiency
of the emergency kit. Allergy. 2001;56(11):1071-1076.
109. Spina JL, McIntyre CL, Pulcini JA. An intervention to increase high
school students' compliance with carrying auto- injectable epi-
nephrine: a MASNRN study. J Sch Nurs. 2012;28(3):230-237.
110. Kelleher MM, Dunngalvin A, Sheikh A, Cullinane C, Fitzsimons J,
Hourihane JO. Twenty four-hour helpline access to expert man-
agement advice for food-allergy-triggered anaphylaxis in infants,
children and young people: a pragmatic, randomized controlled
trial. Allergy. 2013;68(12):1598-1604.
111. Kastner M, Harada L, Waserman S. Gaps in anaphylaxis manage-
ment at the level of physicians, patients, and the community: a sys-
tematic review of the literature. Allergy. 2010;65(4):435- 444.
112. Plumb B, Bright P, Gompels MM, Unsworth DJ. Correct recogni-
tion and management of anaphylaxis: not much change over a de -
cade. Postgrad Med J. 2015;91(1071):3-7.
113. Hernandez-Trujillo V, Simons FE. Prospective evaluation of an ana-
phylaxis education mini-handout: the AAAAI Anaphylaxis Wallet
Card. J Allergy Clin Immunol Pract. 2013;1(2):181-185.
114. Joshi D, Alsentzer E, Edwards K, Norton A, Williams SE. An algo-
rithm developed using the Brighton Collaboration case definitions
is more efficient for determining diagnostic certainty. Vaccine.
2014;32(28):3469-3472.
115. Gardner JB, Rashid S, Staib L, et al. Benefit of a visual aid in the
management of moderate- severity contrast media reactions. AJR
Am J Roentgenol. 2018;211(4):717-723.
116. Patel N, Chong KW, Yip AYG, Ierodiakonou D, Bartra J, Boyle RJ,
Turner PJ. Use of multiple epinephrine doses in anaphylaxis: a sys-
tematic review and meta-analysis. JACI. 2021. ISSN 0091-6749.
https://doi.org/10.1016/j.jaci.2021.03.042
117. Resuscitation Council UK. Guidance: Anaphylaxis. Resuscitation
Council UK. https://www.resus.org.uk/libra ry/additional-guida
nce/guidance-anaphylaxis/emergency-treatment. Accessed 2nd
June 2021.
S U P P O R T I N G I N FO R M AT I O N
Additional supporting information may be found online in the
Supporting Information section.
How to cite this article: Muraro A, Worm M, Alviani C, et al;
European Academy of Allergy, Clinical Immunology Food
Allergy, Anaphylaxis Guidelines Group. EAACI guideline:
Anaphylaxis (2021 update). Allergy. 2022;77:357–377. https://
doi.org/10.1111/all.15032
13989995, 2022, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/all.15032, Wiley Online Library on [14/04/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License