Skip to main content
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology logoLink to Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
. 2018 Apr 4;14:12. doi: 10.1186/s13223-018-0234-0

Critical view of anaphylaxis epidemiology: open questions and new perspectives

Luciana Kase Tanno 1,2,3,16,, Ana Luiza Bierrenbach 4,5, F Estelle R Simons 6, Victoria Cardona 7, Bernard Yu-Hor Thong 8, Nicolas Molinari 9, Moises A Calderon 10, Margitta Worm 11, Yoon-Seok Chang 12, Nikolaos G Papadopoulos 13,14, Thomas Casale 15, Pascal Demoly 2,3; on behalf the Joint Allergy Academies
PMCID: PMC5883526  PMID: 29632547

Abstract

In contrast to the majority of allergic or hypersensitivity conditions, worldwide anaphylaxis epidemiological data remain sparse with low accuracy, which hampers comparable morbidity statistics. Data can differ widely depending on a number of variables. In the current document we reviewed the forms on which anaphylaxis has been defined and classified; and how it can affect epidemiological data. With regards to the methods used to capture morbidity statistics, we observed the impact of the anaphylaxis coding utilizing the World Health Organization’s International Classification of Diseases. As an outcome and depending on the anaphylaxis definition, we extracted the cumulative incidence, which may not reflect the real number of new cases. The new ICD-11 anaphylaxis subsection developments and critical view of morbidity statistics data are discussed in order to reach new perspectives on anaphylaxis epidemiology.

Keywords: Anaphylaxis, Classification, Epidemiology, International Classification of Diseases, Rare diseases, World Health Organization

Anaphylaxis epidemiology: open introductory questions

Anaphylaxis has been defined for clinical use by healthcare professionals as a serious, generalized, allergic or hypersensitivity reaction that can be life-threatening and even fatal [13]. In contrast to the majority of allergic or hypersensitivity conditions such as asthma or rhinitis, accurate worldwide anaphylaxis epidemiological data remain lacking for harmonization. Data can differ widely depending on a number of variables. For instance, European data have indicated incidence rates for all-cause anaphylaxis ranging from 1.5 to 7.9 per 100,000 person/year, with an estimate that 0.3% (95% CI 0.1–0.5) of the population will experience anaphylaxis at some point during their lifetime [4]. As well, it is estimated that 1 in every 3000 inpatients in US hospitals suffer from an anaphylactic reaction [5].

Although available data, specifically those collected during the past decade, show an increased frequency of anaphylaxis, there are still challenges in interpreting these informations [6, 7] and its global applicability. The most widely discussed issues in the epidemiology of anaphylaxis filed over the last 10 years are: (I) regional variations in concepts and definitions (Fig. 1) [13, 810], (II) whether prevalence or incidence is the best measure of the frequency of anaphylaxis in the general population, (III) whether the frequency of anaphylaxis is higher than previously thought, and (IV) whether the increasing incidence published is real or reflects different methodologies and definitions used.

Fig. 1.

Fig. 1

Similarities and differences in anaphylaxis definitions worldwide [1, 3, 68]

Over the last several years, an increasing number of clinical databases have been developed to capture reliable anaphylaxis epidemiological data at both national and regional levels (Fig. 2). However, a substantial proportion of the current data on the epidemiology of anaphylaxis has come from registries with limited scope and population source. Different methods have been applied in an attempt to reach reliable epidemiological data, but most of the studies have focused on specific triggers or at-risk populations. Lack of harmonized strategies to record anaphylaxis cases hampers collection of comparable epidemiological data. In general, registries are representative sources to reach epidemiological data, and are applied only if the reporting of the conditions is mandatory and the data are validated.

Fig. 2.

Fig. 2

Annual number of publications retrieved from Pubmed Central® using the search term “anaphylaxis epidemiology”, (accessed November 7, 2016)

On the other hand, broad population-based studies allow descriptive and analytic epidemiological analysis covering the general population and identify all or a known fraction of the cases in a particular community. Generally speaking, population-based studies have adopted the World Health Organization (WHO) International Classification of Diseases (ICD) as the main tool to capture the proposed outcomes. These studies have been especially useful in detailing time-related trends, capturing clinical practice and principal discharge diagnosis coding statistics, and in providing broader morbidity and mortality statistics (MMS). However, anaphylaxis has never been well classified under the ICD context, either for morbidity [11] (Table 1) or for mortality data [12]. This is exemplified by the under-notification of anaphylaxis deaths using the Brazilian national mortality database [12]. An important reason for this is the difficulty of coding anaphylaxis fatalities under the WHO ICD system. In most countries, mortality statistics are routinely compiled according to regulations and recommendations adopted by the World Health Assembly (WHA). Causes of deaths are classified and grouped according to the ICD edition in use at the time and the information on death certificates is collected using the international form recommended by the WHO. However, a limited number of ICD-10 codes are considered to be valid for representing underlying causes of death on the current death certificates, and with regard to anaphylaxis as such, there are simply no valid codes [12].

Table 1.

Anaphylaxis classification and coding in ICD-10 and in ICD-11

Anaphylaxis ICD-10 codes (2016 version) Anaphylaxis ICD-11 codes (November 2016 version)
Chapter XIX injury, poisoning and certain other consequences of external causes (S00–T98) Chapter 04 disorders of the immune system
Other and unspecified effects of external causes (T66–T78) Section allergic and hypersensitivity conditions
T78 Adverse effects, not elsewhere classified
Note: This category is to be used as the primary code to identify the effects, not elsewhere classifiable, of unknown, undetermined or ill-defined causes. For multiple coding purposes this category may be used as an additional code to identify the effects of conditions classified elsewhere
Subsection anaphylaxis
 T78.0 Anaphylactic shock due to adverse food reaction 4B50 Anaphylaxis due to allergic reaction to food
 T78.1 Other adverse food reactions, not elsewhere classified 4B51 Drug-induced anaphylaxis
 T78.2 Anaphylactic shock, unspecified 4B52 Anaphylaxis due to insect venom
  Allergic shock NOS 4B53 Anaphylaxis provoked by physical factors
  Anaphylactic reaction     4B53.1 Exercise-induced anaphylaxis
  Anaphylaxis     4B53.2 Cold-induced anaphylaxis
 T78.3 Angioneurotic oedema     4B53.Y Anaphylaxis provoked by other specified physical factors
  Giant urticaria     4B53.Z Anaphylaxis provoked by unspecified physical factors
  Quincke oedema 4B54 Anaphylaxis due to inhaled allergens
 T78.4 Allergy, unspecified 4B55 Anaphylaxis due to contact with allergens
4B56 Anaphylaxis secondary to mast cell disorder
  Allergic reaction NOS
  Hypersensitivity NOS 4B5Y Other specified anaphylaxis
  Idiosyncracy NOS
 T78.8 Other adverse effects, not elsewhere classified 4B5Z Anaphylaxis, unspecified
 T78.9 Adverse effect, unspecified

Taking the opportunity presented by the ongoing ICD-11 revision, the under-notification of death data [12] triggered a cascade of strategic international actions supported by the Joint Allergy Academies and the ICD WHO governance [1123] to update the classifications of allergic conditions for the new ICD edition. These efforts have resulted in the construction of the new “Allergic and hypersensitivity conditions” section built under the “Disorders of the Immune system” chapter [17, 24].

In order to better delineate the proposed changes and follow the ICD-11 revision agenda, we reviewed the forms on which anaphylaxis has been defined and classified, and the published anaphylaxis epidemiological data, particularly with regards to the methods used to capture morbidity statistics.

Anaphylaxis: reaching answers based on definition and classification

Anaphylaxis definition impacts in epidemiological data

All anaphylaxis guidelines [13, 810] have consistently defined anaphylaxis as a severe life-threatening generalized or systemic hypersensitivity reaction. Being described as a reaction implies a risk of overestimating the prevalence of anaphylaxis. For some conditions, such as asthma, the number of patients with the condition is different from the number of (asthma) exacerbations (Fig. 3a). However, using the definition of anaphylaxis, the number of exacerbations (reactions) can be wrongly taken as the number of cases (disease) (Fig. 3b), resulting in an overestimated lifetime cumulative incidence.

Fig. 3.

Fig. 3

General model to explain how definitions of allergic conditions can affect prevalence data (a asthma as a model, b anaphylaxis as a model)

Incidence is the measure of the frequency of a new case (or condition) in a population at risk within a period of time. Therefore, given that anaphylaxis is an acute condition with long asymptomatic periods during which the risk of relapse can decrease over time in some patients or when culprit factors such as allergens are avoided or counteracted (e.g. stinging insect venom immunotherapy), knowing the number of new episodes (incidence) over a specific period can not be an adequate measure of frequency. Cumulative incidence, also known as incidence proportion may be not an adequate measure for frequency of anaphylaxis, since the reaction is no longer active once the episode is resolved. For this reason, more detailed data on recurrent episodes are required to overcome this challenge in anaphylaxis epidemiology studies.

Updated anaphylaxis classification and coding in the ICD

The ICD is the broadest classification and coding system used to monitor the incidence and prevalence of diseases and other health problems, reflecting the general health situation in countries and populations [25].

Taking the example of the ICD-10 (2016 version) [26], anaphylaxis has been classified under the “XIX Injury, poisoning and certain other consequences of external causes” chapter, specifically the “T78 Adverse effects, not elsewhere classified” section. Under this section, different hypersensitivity conditions are classified at the same level, such as “Anaphylactic shock due to adverse food reaction”, “Angioneurotic oedema” and “Allergy, unspecified” (Table 1), reflecting a misunderstanding of concepts used by the health care professionals on a daily basis.

The construction of the new ICD-11 section addressing to allergic and hypersensitivity conditions now allows anaphylaxis to be properly classified and attaining greater visibility within ICD (Table 1). Currently, this subsection contains 7 main anaphylaxis headings to be combined with severity and causality classification/specifications. The building process of this framework resulted from combined efforts and constant discussions with the groups of experts and the ICD WHO governance.

The construction of the new subsection addressed to anaphylaxis means that it will now be recognized as a clinical condition requiring specific documentation and management.

Lessons from population-based anaphylaxis morbidity epidemiology publications

From 19th to 26th October 2016, 1896 manuscripts were selected using PubMed Mesh terms “anaphylaxis epidemiology”, “epidemiology of anaphylaxis” or “anaphylaxis epidemiology population-based studies”. After removing those published before 2011 and those not published in English, there were 532 papers published in the last 5 years. We did not include case reports, studies in animal models, quality of life studies, fatality studies, guidelines or reviews (Fig. 4). All publications were independently evaluated by two co-authors and disagreements related to the inclusion into the analysis were resolved through open discussion and consensus.

Fig. 4.

Fig. 4

Anaphylaxis epidemiology publications eligibility selection process

We analyzed methodological aspects, main outcomes and databases used in the remaining 15 publications selected as eligible according to the selection criteria (Fig. 4) from different countries. The methods used and the definitions taken varied among the publications; however, 67% focused on rates of hospitalization or emergency department admissions. National databases were used in 67% of the studies. Overall, 40% were large population-based studies and 100% of these documents used the ICD definition as the starting point of the analysis (Table 2). Based on ICD registries, regardless of the ICD version used, 71% of all the studies had to utilize secondary data in order to capture the anaphylaxis data, meaning that the data have been affected by the misclassification of anaphylaxis in the previous versions of the ICD.

Table 2.

Anaphylaxis morbidity epidemiology publications

References Study location Study design and anaphylaxis definition chosen Epidemiological variables suited and outcomes Number of subjects Study period Study anaphylaxis morbidity database
Beyer et al. [31] Germany Self-reported cases from the general population based on survey questionnaire Incidence of severe anaphylaxis: 4.5 per 100,000 333 2008–2010 Local database
Buka et al. [32] United Kingdom Retrospective observational study based on search terms considering the WAO anaphylaxis definition [7] Incidence of anaphylaxis: 12.0 per 100,000 person-years 426 patient episodes 12 months (2012) National Health Service (NHS) database
Campbell et al. [33] United States of America Historic-prospective observational cohort study with analysis of medical records based on the NIAID/FAAN diagnostic criteria for anaphylaxis [1] Prevalence of anaphylaxis: 582
Patients needing more than 1 dose of epinephrine: 8%
582 2010–2013 National SAS-Display Manager System database
Cetinkaya et al. [34] Turkey Search for ICD-10 anaphylaxis and secondary codes as primary cause of hospitalization Incidence admissions for anaphylaxis: 11.05 per 100,000 person-years 114 patients 12 months (2010–2011) National database: The Health Directorate Network of Istanbul
Gibbison et al. [35] United Kingdom Retrospective analysis of all physician-diagnosed cases in national audit data from critical care units considering NIAID/FAAN anaphylaxis definition [1] as first or secondary cause of admission Paediatric admissions with anaphylaxis: 6–23/year
Adult admissions with anaphylaxis: 183–331/year
1350 admissions for anaphylaxis 2005–2009 National audits of critical care units in the UK: the Intensive Care National Audit and Research
Centre’s (ICNARC) Case Mix Programme (CMP), Scottish
Intensive Care Society Audit Group (SICSAG) and Paediatric Intensive Care Audit Network (PICANet)
Grunau et al. [36] Canada Retrospective cohort study with dichotomized algorithm for “anaphylaxis” considering the WAO definition for anaphylaxis [7] Emergency department visits for anaphylaxis: 23.2 per 100,000 person-years 496 2007–2012 Local electronic medical records database
Harduar-Morano et al. [37] United States of America Population-based epidemiologic study using national database and selected ICD codes Incidence of anaphylaxis: 7.5 per 100,000 person-years 2751 2005–2006 Agency for Health Care Administration
Jeppesen et al. [38] Denmark Population-based cohort study using national database and selected ICD codes Average hospitalization rate for first-time anaphylactic shock was 64.6 per 1,000,000 person-years 6707 1995–2012 Danish National Patient Registry and the Danish Civil Registration System
Kimchi et al. [39] Canada Software program applied to prospectively record characters of anaphylaxis cases taking the WAO definition of anaphylaxis [7] % Anaphylaxis among all calls: 0.31
% Anaphylaxis among calls requiring transport: 0.44
104 12 months (2013–2014) Cross Canada Anaphylaxis Registry database
Lee et al. [40] United States of America Population-based incidence study selected by ICD codes Incidence rate of anaphylaxis was 42 per 100,000 person-years 2386 2001–2010 Rochester Epidemiology Project linked to the list of all Olmsted County residents
Mullins et al. [41] Australia Population-based epidemiologic study using national database and selected ICD codes Increase in overall anaphylaxis admission rates: 1.5-fold/7 years 3.6–17.7 cases/105 population 2005–2006 and 2011–2012 Australian National Hospital morbidity database
Tejedor Alonso et al. [42] Spain Population-based epidemiologic study using national database and selected ICD codes Anaphylaxis admissions in the general population: 1.35–2.38 per 100,000 person-years 11,336 records 1998–2011 Spanish information system for hospital data
Wood et al. [43] United States of America Self-reported cases from the general population based on survey questionnaire considering the main anaphylaxis definitions [1, 3, 6, 7] Prevalence of anaphylaxis in the general population: 1.6% 344 5 months (2011) Local database
Worm et al. [44] European countries (Austria, Bulgaria, France, Germany, Greece, Ireland, Italy, Poland, Spain and Switzerland) Data collection from specialized European countries by online questionnaire considering the EAACI-WAO revised nomenclature [45] Number of anaphylaxis cases: 3333
Recurrence: 34.2%
3333 2011–2014 European anaphylaxis registry
Turner et al. [45] United Kingdom Population-based epidemiologic study using hospital admission data and selected ICD codes Number of hospital admissions for anaphylaxis: 1.0–7.0 cases per 100,000 population per annum Data limited to the number of admissions 1992–2012 Hospital episodes statistics database

Most of the studies (60%) did not address the possibility of recurrence of episodes, and, therefore, of cumulative incidence. This highlights the need to distinguish the number of patients with anaphylaxis per year from the number of episodes per year. Even with the alternative strategy of reaching the mean number of anaphylaxis cases within a started time, data would be influenced by the methodology and definitions applied. In other words, most of epidemiological studies considering incidence as the main variable may be overestimating the number of anaphylactic patients. True frequency of anaphylaxis is also possibly underestimated due to under-recognition by patients and caregivers and under-diagnosis by health care professionals (e.g.: difficulty on diagnosing anaphylaxis in the absence of hypotension or shock).

Reaching new perspectives for anaphylaxis epidemiology

In this manuscript, we provide arguments for the need of reviewing the current definitions in use for anaphylaxis. The definitions are able to directly impact in the epidemiology of anaphylaxis as a disease. Incorporating refined strategies to achieve accuracy and comparable MMS can support public health changes to reach better patients’ care and prevention worldwide.

Due to recent achievements at the international level on enhancing terminology, classification, definitions and coding of allergic and hypersensitivity conditions through the ongoing WHO ICD revision process, anaphylaxis is now considered a condition. Importantly the new classification system for anaphylaxis will surely enable the collection of more accurate epidemiological data to support quality management of patients with allergies, better health care planning and decision-making and public health measures to reduce the morbidity and mortality attributable to anaphylaxis.

Based on current developments, reviewing the definition of anaphylaxis and epidemiology strategies by clarifying differences between anaphylaxis episodes (reactions) from anaphylaxis as a condition itself will lead to more precision on MMS. Cumulative incidence is an inadequate measure here, since the reaction is no longer active once the episode is resolved and one patient can present different episodes of anaphylactic reactions in his/her life. Most of the publications have so far considered the episodes (illness), regardless to the subject suffering of this condition (patient). A possible strategy in order to avoid cumulative incidence of anaphylaxis would be reaching recurrence of anaphylactic episodes. Consistent scientific, economical and political changes may follow this move, which will likely be reflected in better management of patients with anaphylaxis worldwide. For instance, precise and broader anaphylaxis MMS will support the global availability of auto-injectable adrenaline, currently available in less than 35% of all countries [23]. Specific focus in the patients’ care, and not just in the episodes, would also support primary and secondary prevention actions.

As demonstrated, anaphylaxis regional epidemiological data differ considerably according to many variables and it is still unclear whether the increasing incidence published is real or the results reflect different methods used to define and characterize anaphylaxis. However, based on current statistics [4, 5], severe anaphylaxis fits well the definition of a rare disease. Conceptually, rare diseases can be defined as life-threatening or chronic debilitating disorders, which are of low prevalence and typically require a multi-disciplinary approach to address prevention and treatment. The Orphanet, lead by the French National Institution of Health and Medical Research (INSERM) and the French Ministry of Health, is responsible for developing an inventory of rare diseases and a classification system which could serve as a template to update International terminologies. When the WHO launched the revision process of the ICD, a rare diseases Topic Advisory Group was established. So far 5400 rare diseases listed in the Orphanet database have an endorsed representation in the foundation layer of ICD-11 [27, 28], but severe anaphylaxis is not yet included on the list. In addition to all the benefits expected by the actions to update terminology, definitions and classification of allergic and hypersensitivity conditions through the ICD-11 revision, we strongly believe that anaphylaxis is a public health priority, therefore in order to strengthen awareness and quality clinical management of patients it should therefore be formally added to the list of rare diseases. Including severe anaphylaxis into the list of rare diseases may allow, in first instance, the allocation of resources to better understand the national and global epidemiology of anaphylaxis as a disease; monitor the patterns of this disorder to follow hospitalizations, mortality, avoidable deaths and costs. Having more precise epidemiological data may support the global availability of adrenaline auto-injectors worldwide at affordable price addressed to the patients’ care through argumentation with national bodies and stakeholders. For instance, the French Ministry of Health, in coordination with the State Secretariat for Higher Education and Research, implements a proactive policy based on the mobilization of health/research professionals and patients’ associations in order to improve quality diagnosis, management and prevention of the 3 million patients affected by rare diseases in France. This health intervention/policy model can be took as an example in different countries in order to implement essential actions according to individual national needs, such as the availability of adrenaline auto-injectors in low incoming countries [23].

Anaphylaxis epidemiological publications are also hampered by the inclusion of all severity degrees of anaphylaxis. Mild reactions in which manifestations are generally limited to one organ or system, such as the skin, usually do not incur any risk of death. The inclusion of these cases in the epidemiological studies provides mistaken perception of high and increasing incidence of severe anaphylaxis. Our focus would be addressing severe reactions in which the risk of mortality is strong and requires additional prevention measures and a coordinated management such as the one provided by the rare disease network in our country. To date, there is no available data regarding severe cases of anaphylaxis in Europe. French data suggests that less than 30,000 people are affected by severe anaphylaxis and, 9.2 per 100,000 person-years based on the University Hospital of Montpellier data [29]. Australian data demonstrated the increasing number of patients at risk of anaphylaxis, from 0.98% in 2009 reaching 1.38% in 2014 in school aged children. In contrast, the number of adrenaline auto-injectors activated (severe cases) per year per 1000 students at risk of anaphylaxis was 6 and 8 in 2010 and 2014 respectively [30]. If taken as isolated data of patients at risk, it can drive readers to think that anaphylaxis is increasing in this country. However, the administration of the treatment as objective data indicates that severe anaphylaxis can be considered as rare disease.

The ICD-11 intends will be presented to the WHA in 2018. A known issue regarding accurate epidemiological data and miscoding is the lack of training regarding how disorders should be classified and coded in administrative and institutional databases. For this reason, the core ALLERGY in ICD-11 operational team (LKT, PD) in collaboration with the WHO and with the support of our international academies network, intends to implement education tools to support the allergy community in the transition process, preparing health professionals and stakeholders for the new logic of the ICD-11, when it is launched. Educational efforts will also help to decrease the under-recognition of anaphylaxis by patients, caregivers, and health professionals, health authorities and governments and have been the main aim of allergy academies by promoting education programs and publications in the field.

The construction of the new section dealing with anaphylaxis means that the latter will now be recognized as a clinical condition requiring specific documentation and management. Besides increasing the accuracy and sensitivity of clinical diagnosis data, unifying the allergic and hypersensitivity conditions into a single section of the ICD, endorsed by the WHO ICD governance bodies can be considered a strong epidemiological, economical and political move that advocates to optimal diagnosis and management of allergic patients worldwide. By allowing all the relevant diagnostic terms for anaphylaxis to be included into the ICD-11 framework, WHO has recognized their importance not only to clinicians but also to epidemiologists, statisticians, health care planners and other stakeholders. In the current manuscript we raise awareness of the outcomes of the ongoing ICD revision process as an instrument that has been developed to provide more precise anaphylaxis MMS to ensure comparability in monitoring, decision-making and achieving quality clinical practice. Meanwhile we propose strategies to improve anaphylactic patients’ care through reviewing definitions and epidemiological data. This document and critical view intend to support national and international health interventions and health policy changes.

Authors’ contributions

LKT and PD contributed to the construction of the document (designed the study, analyzed and interpreted the data, and wrote the manuscript). ALB and NM supported the discussion of concepts and reviewed the manuscript. FERS, TC, VC, BY-HT, NGP, MAC, MW and Y-SC contributed to tuning the document and revision of the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We are extremely grateful to all the representatives of the ICD-11 Revision Project with whom we have been carrying on fruitful discussions, helping us to refine the classification presented here: Robert Jakob, Linda Best, Nenad Kostanjsek, Robert J. G. Chalmers, Jeffrey Linzer, Linda Edwards, Ségolène Ayme, Bertrand Bellet, Rodney Franklin, Matthew Helbert, August Colenbrander, Satoshi Kashii, Paulo E. C. Dantas, Christine Graham, Ashley Behrens, Julie Rust, Megan Cumerlato, Tsutomu Suzuki, Mitsuko Kondo, Hajime Takizawa, Nobuoki Kohno, Soichiro Miura, Nan Tajima and Toshio Ogawa.

Joint Allergy Academies: American Academy of Allergy Asthma and Immunology (AAAAI), European Academy of Allergy and Clinical Immunology (EAACI), World Allergy Organization (WAO), American College of Allergy Asthma and Immunology (ACAAI), Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI), Latin American Society of Allergy, Asthma and Immunology (SLAAI).

Competing interests

The authors declare that they have no competing interests.

Ana Luiza Bierrenbach, Bernard Y. Thong, Nicolas Molinari, Yoon-Seok Chang, Thomas Casale: have no competing interests. Luciana Kase Tanno and Pascal Demoly received an unrestricted AstraZeneca ERS-16-11927 Grant and from MEDA Pharma through CHRUM administration. Luciana Kase Tanno is the allergy representative of the WHO Medical and Scientific Advisory Committee for International Classification of Diseases (ICD)-11 and other WHO classifications. Pascal Demoly: has received honoraria for consultation and lectures from ALK, Circassia, Stallergèns Greer, Allergopharma, ThermofisherScientific, Meda, Ménarini and is president of the French Allergy Federation. F. Estelle R. Simons: member, Medical Advisory Boards of ALK, Mylan, and Sanofi. Victoria Cardona: has received fees as an advisor and speaker for ALK. M. Calderon: has received honorarium in Advisory Boards for ALK and Hal-Allergy, as speaker for ALK, Merck and Stallergenes-Greer. Margitta Worm: has received honoraria for consultation and lectures from Meda, ALK, and Allergopharma.

Availability of data and materials

Data sharing not applicable to this article as no datasets were generated or analysed during the current study. The ICD-11 beta draft and Pubmed platforms are open to the public.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

Funding

This research was conducted with support from AstraZeneca, as an unrestricted AstraZeneca ERS-16-11927 Grant and from MEDA Pharma through CHRUM administration.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Abbreviations

AAAAI

American Academy of Allergy Asthma and Immunology

ACAAI

American College of Allergy Asthma and Immunology

ASCIA

Australian Society of Clinical Immunology and Allergy

EAACI

European Academy of Allergy and Clinical Immunology

ICD

International Classification of Diseases

MMS

morbidity and mortality statistics

NIAID/FAAN

National Institute of Allergy and Infectious Disease/Food Allergy and Anaphylaxis Network

WAO

World Allergy Organization

WHO

World Health Organization

Contributor Information

Luciana Kase Tanno, Phone: +33 467336107, Email: luciana.tanno@gmail.com.

Ana Luiza Bierrenbach, Email: albierrenbach@yahoo.com.br.

F. Estelle R. Simons, Email: simons@ms.umanitoba.ca

Victoria Cardona, Email: carvicky@gmail.com.

Bernard Yu-Hor Thong, Email: bernard_thong@ttsh.com.sg.

Nicolas Molinari, Email: nicolas.molinari@inserm.fr.

Moises A. Calderon, Email: m.calderon@imperial.ac.uk

Margitta Worm, Email: margitta.worm@charite.de.

Yoon-Seok Chang, dr.changys@googlemail.com.

Nikolaos G. Papadopoulos, Email: ngpallergy@gmail.com

Thomas Casale, Email: tbcasale@health.usf.edu.

Pascal Demoly, Email: pascal.demoly@inserm.fr.

References

  • 1.Sampson HA, Munoz-Furlong A, Campbell RL, Adkinson NF, Jr, Bock SA, Branum A, et al. Second symposium on the definition and management of anaphylaxis: summary report—Second National Institute of Allergy and Infectious Disease/Food Allergy and Anaphylaxis Network Symposium. J Allergy Clin Immunol. 2006;117:391–397. doi: 10.1016/j.jaci.2005.12.1303. [DOI] [PubMed] [Google Scholar]
  • 2.Simons FER, Ardusso LR, Bilò MB, Cardona V, Ebisawa M, El-Gamal YM, et al. International consensus on (ICON) anaphylaxis. World Allergy Organ J. 2014;30(7):9. doi: 10.1186/1939-4551-7-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Muraro A, Roberts G, Worm M, Bilo MB, Brockow K, Fernandez-Rivas M, Santos AF, Zolkipli ZQ, Bellou A, Bindslev-Jensen C, Cardona V, Clark AT, Demoly P, Dubois AEJ, Dunn Galvin A, Eigenmann P, Halken S, Harada L, Lack G, Jutel M, Niggemann B, Rueff F, Timmermans F, Vlieg-Boerstra BJ, Werfel T, Dhami S, Panesar S, Sheikh A, on behalf of EAACI Food Allergy and Anaphylaxis Guidelines Group Anaphylaxis: guidelines from the European Academy of Allergy and Clinical Immunology. Allergy. 2014 doi: 10.1111/all.12437. [DOI] [PubMed] [Google Scholar]
  • 4.Panesar SS, Javad S, de Silva D, Nwaru BI, Hickstein L, Muraro A, Roberts G, Worm M, Bilò MB, Cardona V, Dubois AEJ, DunnGalvin A, Eigenmann P, Fernandez-Rivas M, Halken S, Lack G, Niggemann B, Santos AF, Vlieg-Boerstra BJ, Zolkipli ZQ, Sheikh A, on behalf of the EAACI Food Allergy and Anaphylaxis Group The epidemiology of anaphylaxis in Europe: a systematic review. Allergy. 2013;68:1353–1361. doi: 10.1111/all.12272. [DOI] [PubMed] [Google Scholar]
  • 5.Neugut AI, Ghatak AT, Miller RL. Anaphylaxis in United States: an investigation into its epidemiology. Arch Intern Med. 2001;161(1):15–21. doi: 10.1001/archinte.161.1.15. [DOI] [PubMed] [Google Scholar]
  • 6.Ansotegui IJ, Sánchez-Borges M, Cardona V. Current trends in prevalence and mortality of anaphylaxis. Curr Treat Options Allergy. 2016;3:205. doi: 10.1007/s40521-016-0094-0. [DOI] [Google Scholar]
  • 7.Tejedor Alonso MA, Moro Moro M, Múgica García MV. Epidemiology of anaphylaxis. Clin Exp Allergy. 2015;45(6):1027–1039. doi: 10.1111/cea.12418. [DOI] [PubMed] [Google Scholar]
  • 8.Lieberman P, Nicklas RA, Oppenheimer J, et al. The diagnosis and management of anaphylaxis practice parameter: 2010 update. J Allergy Clin Immunol. 2010;126:477–480. doi: 10.1016/j.jaci.2010.06.022. [DOI] [PubMed] [Google Scholar]
  • 9.Simons FER, Ardusso LRF, Bilo MB, et al. World Allergy Organization guidelines for the assessment and management of anaphylaxis. World Allergy Organ J. 2011;4:13–37. doi: 10.1097/WOX.0b013e318211496c. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Brown SG, Mullins RJ, Gold MS. Anaphylaxis: diagnosis and management. Med J Aust. 2006;185:283–289. doi: 10.5694/j.1326-5377.2006.tb00619.x. [DOI] [PubMed] [Google Scholar]
  • 11.Tanno LK, Calderon MA, Goldberg BJ, Akdis CA, Papadopoulos NG, Demoly P. Categorization of allergic disorders in the new World Health Organization International Classification of Diseases. Clin Transl Allergy. 2014;4:42. doi: 10.1186/2045-7022-4-42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Tanno LK, Ganem F, Demoly P, Toscano CM, Bierrenbach AL. Undernotification of anaphylaxis deaths in Brazil due to difficult coding under the ICD-10. Allergy. 2012;67:783–789. doi: 10.1111/j.1398-9995.2012.02829.x. [DOI] [PubMed] [Google Scholar]
  • 13.Demoly P, Tanno LK, Akdis CA, Lau S, Calderon MA, Santos AF, et al. Global classification and coding of hypersensitivity diseases—an EAACI—WAO survey, strategic paper and review. Allergy. 2014;69:559–570. doi: 10.1111/all.12386. [DOI] [PubMed] [Google Scholar]
  • 14.Tanno LK, Calderon MA, Goldberg BJ, Gayraud J, Bircher AJ, Casale T, et al. Constructing a classification of hypersensitivity/allergic diseases for ICD-11 by crowdsourcing the allergist community. Allergy. 2015;70:609–615. doi: 10.1111/all.12604. [DOI] [PubMed] [Google Scholar]
  • 15.Tanno LK, Calderon M, Papadopoulos NG, Demoly P. Mapping hypersensitivity/allergic diseases in the International Classification of Diseases (ICD)-11: cross-linking terms and unmet needs. Clin Transl Allergy. 2015;5:20. doi: 10.1186/s13601-015-0063-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Tanno LK, Calderon MA, Demoly P, on behalf the Joint Allergy Academies Optimization and simplification of the allergic and hypersensitivity conditions classification for the ICD-11. Allergy. 2016;71(5):671–676. doi: 10.1111/all.12834. [DOI] [PubMed] [Google Scholar]
  • 17.Tanno LK, Calderon MA, Demoly P, on behalf the Joint Allergy Academies New allergic and hypersensitivity conditions section in the International Classification of Diseases-11. Allergy Asthma Immunol Res. 2016;8(4):383–388. doi: 10.4168/aair.2016.8.4.383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Tanno LK, Calderon MA, Papadopoulos NG, Sanchez-Borges M, Moon HB, Sisul JC, Jares EJ, Sublett JL, Casale T, Demoly P, Joint Allergy Academies Surveying the new allergic and hypersensitivity conditions chapter of the International Classification of Diseases (ICD)-11. Allergy. 2016 doi: 10.1111/all.12945. [DOI] [PubMed] [Google Scholar]
  • 19.Tanno LK, Calderon M, Demoly P, Joint Allergy Academies Supporting the validation of the new allergic and hypersensitivity conditions section of the World Health Organization International Classification of Diseases-11. Asia Pac Allergy. 2016;6(3):149–156. doi: 10.5415/apallergy.2016.6.3.149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Tanno LK, Bierrenbach AL, Calderon MA, Sheikh A, Simons FE, Demoly P, Joint Allergy Academies Decreasing the under notification of anaphylaxis deaths in Brazil through the International Classification of Diseases (ICD)-11 revision. Allergy. 2016 doi: 10.1111/all.13006. [DOI] [PubMed] [Google Scholar]
  • 21.Tanno LK, Calderon M, Sublett JL, Casale T, Demoly P, Joint Allergy Academies Smoothing the transition from International Classification of Diseases, tenth revision, clinical modification to International Classification of Diseases, eleventh revision. J Allergy Clin Immunol Pract. 2016 doi: 10.1016/j.jaip.2016.06.024. [DOI] [PubMed] [Google Scholar]
  • 22.Tanno LK, Simons FE, Annesi-Maesano I, Calderon MA, Aymé S, Demoly P, Joint Allergy Academies Fatal anaphylaxis registries data support changes in the who anaphylaxis mortality coding rules. Orphanet J Rare Dis. 2017;12(1):8. doi: 10.1186/s13023-016-0554-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Tanno LK, Simons FER, Cardona V, Calderon M, Sanchez-Borges M, Sisul JC, Moon HB, Sublett JL, Casale T, Demoly P, Joint Allergy Academies Applying prevention concepts to anaphylaxis: a call for worldwide availability of adrenaline auto-injectors. Clin Exp Allergy. 2017;47:1108–1114. doi: 10.1111/cea.12973. [DOI] [PubMed] [Google Scholar]
  • 24.World Health Organization. ICD-11 beta draft website. http://apps.who.int/classifications/icd11/browse/l-m/en. Accessed Oct 2016.
  • 25.World Health Organization. International Classification of Diseases website http://www.who.int/classifications/icd/en/. Accessed Nov 2016.
  • 26.World Health Organization. ICD-10 version 2016 website. http://apps.who.int/classifications/icd10/browse/2016/en. Accessed Nov 2016.
  • 27.Orphanet website, rare diseases page. http://www.orpha.net/consor/cgi-bin/Disease.php?lng=EN. Accessed July 2016.
  • 28.Aymé S, Bellet B, Rath A. Rare diseases in ICD11: making rare diseases visible in health information systems through appropriate coding. Orphanet J Rare Dis. 2015;26(10):35. doi: 10.1186/s13023-015-0251-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Tanno LK, Molinari N, Bruel S, Bourrain JL, Calderon MA, Aubas P, Demoly P, Joint Allergy Academies Field-testing the new anaphylaxis’ classification for the WHO International Classification of Diseases-11 revision. Allergy. 2017;72(5):820–826. doi: 10.1111/all.13093. [DOI] [PubMed] [Google Scholar]
  • 30.Loke P, Koplin J, Beck C, Field M, Dharmage SC, Tang ML, Allen KJ. Statewide prevalence of school children at risk of anaphylaxis and rate of adrenaline autoinjector activation in Victorian government schools, Australia. J Allergy Clin Immunol. 2016;138(2):529–535. doi: 10.1016/j.jaci.2016.02.014. [DOI] [PubMed] [Google Scholar]
  • 31.Beyer K, Eckermann O, Hompes S, Grabenhenrich L, Worm M. Anaphylaxis in an emergency setting elicitors, therapy and incidence of severe allergic reactions. Allergy. 2012;67:1451–1456. doi: 10.1111/all.12012. [DOI] [PubMed] [Google Scholar]
  • 32.Buka RJ, Crossman RJ, Melchior CL, Huissoon AP, Hackett S, Dorrian S, Cooke MW, Krishna MT. Anaphylaxis and ethnicity: higher incidence in British South Asians. Allergy. 2015;70:1580–1587. doi: 10.1111/all.12702. [DOI] [PubMed] [Google Scholar]
  • 33.Campbell RL, Bashore CJ, Lee S, Bellamkonda VR, Li JT, Hagan JB, et al. Predictors of repeat epinephrine administration for emergency department patients with anaphylaxis. J Allergy Clin Immunol Pract. 2015;3(4):576–584. doi: 10.1016/j.jaip.2015.04.009. [DOI] [PubMed] [Google Scholar]
  • 34.Cetinkaya F, Incioglu A, Birinci S, Karaman BE, Dokucu AI, Sheikh A. Hospital admissions for anaphylaxis in Istanbul, Turkey. Allergy. 2013;68:128–130. doi: 10.1111/all.12069. [DOI] [PubMed] [Google Scholar]
  • 35.Gibbison B, Sheikh A, McShane P, Haddow C, Soar J. Anaphylaxis admissions to UK critical care units between 2005 and 2009. Anaesthesia. 2012;67(8):833–839. doi: 10.1111/j.1365-2044.2012.07159.x. [DOI] [PubMed] [Google Scholar]
  • 36.Grunau BE, Li J, Yi TW, Stenstrom R, Grafstein E, Wiens MO, et al. Incidence of clinically important biphasic reactions in emergency department patients with allergic reactions or anaphylaxis. Ann Emerg Med. 2014;63(6):736–744. doi: 10.1016/j.annemergmed.2013.10.017. [DOI] [PubMed] [Google Scholar]
  • 37.Harduar-Morano L, Simon MR, Watkins S, Blackmore C. A population-based epidemiologic study of emergency department visits for anaphylaxis in Florida. J Allergy Clin Immunol. 2011;128(3):594–600. doi: 10.1016/j.jaci.2011.04.049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Jeppesen AN, Christiansen CF, Frøslev T, Sørensen HT. Hospitalization rates and prognosis of patients with anaphylactic shock in Denmark from 1995 through 2012. J Allergy Clin Immunol. 2016;137(4):1143–1147. doi: 10.1016/j.jaci.2015.10.027. [DOI] [PubMed] [Google Scholar]
  • 39.Kimchi N, Clarke A, Moisan J, Lachaine C, La Vieille S, Asai Y, et al. Anaphylaxis cases presenting to primary care paramedics in Quebec. Immun Inflamm Dis. 2015;3(4):406–410. doi: 10.1002/iid3.78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Lee S, Hess EP, Lohse C, Gilani W, Chamberlain AM, Campbell RL. Trends, characteristics, and incidence of anaphylaxis in 2001–2010: a population-based study. J Allergy Clin Immunol. 2016 doi: 10.1016/j.jaci.2016.04.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Mullins RJ, Dear KB, Tang ML. Time trends in Australian hospital anaphylaxis admissions in 1998–1999 to 2011–2012. J Allergy Clin Immunol. 2015;136(2):367–375. doi: 10.1016/j.jaci.2015.05.009. [DOI] [PubMed] [Google Scholar]
  • 42.Alonso MA, García MV, Hernández JE, Moro MM, Ezquerra PE, Ingelmo AR, et al. Recurrence of anaphylaxis in a Spanish series. J Investig Allergol Clin Immunol. 2013;23(6):383–391. [PubMed] [Google Scholar]
  • 43.Wood RA, Camargo CA, Jr, Lieberman P, Sampson HA, Schwartz LB, Zitt M, et al. Anaphylaxis in America: the prevalence and characteristics of anaphylaxis in the United States. J Allergy Clin Immunol. 2014;133(2):461–467. doi: 10.1016/j.jaci.2013.08.016. [DOI] [PubMed] [Google Scholar]
  • 44.Worm M, Moneret-Vautrin A, Scherer K, Lang R, Fernandez-Rivas M, Cardona V, Kowalski ML, Jutel M, Poziomkowska-Gesicka I, Papadopoulos NG, Beyer K, Mustakov T, Christoff G, Bilo MB, Muraro A, Hourihane JOB, Grabenhenrich LB. First European data from the network of severe allergic reactions (NORA) Allergy. 2014;69:1397–1404. doi: 10.1111/all.12475. [DOI] [PubMed] [Google Scholar]
  • 45.Turner PJ, Gowland MH, Sharma V, Ierodiakonou D, Harper N, Garcez T, 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. doi: 10.1016/j.jaci.2014.10.021. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data sharing not applicable to this article as no datasets were generated or analysed during the current study. The ICD-11 beta draft and Pubmed platforms are open to the public.


Articles from Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology are provided here courtesy of BMC

RESOURCES