BRIEF REPORT
Impact of Changes in Anti-doping Regulations
(WADA Guidelines) on Asthma Care in Athletes
Mariana Couto, MD,*† Luís Horta, MD, PhD,‡ Luís Delgado, MD, PhD,*†
Miguel Capão-Filipe, MD,*§ and André Moreira, MD, PhD*†
Objective: To investigate how changes to the World Anti-Doping
Agency (WADA) guidelines on asthma medication requests have
impacted the management of asthmatic athletes in Portugal.
Design: Retrospective analysis of asthma medication requests
submitted in 2008 to 2010.
Setting: Portuguese Anti-Doping Authority database.
Participants: Athletes requesting the use of inhaled corticosteroids
and/or b
2
-agonists.
Independent Variables: Demographic, therapeutic, and diag-
nostic test data.
Main Outcome Measures: Yearly changes in number of asthma
medication requests and diagnostic procedures.
Results: We analyzed 326 requests: 173 abbreviated Therapeutic
Use Exemptions in 2008 (objective tests not required), 9 Declaration
of Use (DoU) and 76 Therapeutic Use Exemptions (TUEs) in 2009,
and 39 DoU and 29 TUEs in 2010. Spirometry was performed in
87% and 37% of athletes in 2009 and 2010, respectively; the
corresponding figures for bronchoprovocation were 59% and 16%,
almost all positive in both years.
Conclusions: Applications for inhaler use have decreased by app-
roximately half since objective asthma testing became mandatory.
Our findings show that WADA guidelines have an impact on asth-
matic athletes care: In 2009 a more rigorous screening was possible,
leading to withdrawal of unnecessary medication. Constant changes,
however, jeopardize this achievement and nowadays introduce safety
issues stemming from the unsupervised use of inhaled b
2
-agonists.
Key Words: asthma, airway hyperresponsiveness, anti-doping, bron-
choconstriction, exercise, inhaled beta-2 agonists, sports, WADA
(Clin J Sport Med 2012;0:1–3)
INTRODUCTION
Diagnosing asthma in athletes is challenging. Multiple
phenotypes of asthma exist, and different underlying mech-
anisms contribute to etiopathogenesis.
1,2
Also, alternative
diagnoses must be considered,
3
and in athletes, symptoms
are poor predictors of this condition.
4
Objective evidence
(eg, positive bronchodilator or bronchoprovocation test), thus,
is needed to confirm a diagnosis in this setting.
5
The recommendation of the International Olympic
Committee Medical Commission (IOC-MC) for Olympic
athletes to present objective evidence of asthma before
allowing the use of inhaled b
2
-agonists (IBAs), in place since
2002, has facilitated the study of how asthma impacts differ-
ent sports and has benefited athletes by ensuring better care.
In 2009, the World Anti-Doping Agency (WADA) followed
the IOC approach, extending it to all other athletes.
6
The
WADA guidelines on asthma, however, have changed in
recent years. Before 2009, an abbreviated Therapeutic Use
Exemption (aTUE), which did not require objective evidence
of asthma, accompanied by a physician’s report of asthma,
was sufficient for requesting permission to use inhaled corti-
costeroids (ICS) and inhaled formoterol, salbutamol, salme-
terol, and terbutaline. In 2009, although, aTUEs were
withdrawn and replaced by a Declaration of Use (DoU) for
ICS and a full Therapeutic Use Exemption (TUE) requiring
objective evidence for the same 4 IBAs. In 2010, the DoU
was extended to salbutamol and salmeterol, but the other
IBAs still required a TUE.
The aim of this study was to assess the impact of
WADA guideline changes on asthma medication requests by
Portuguese athletes.
METHODS
We retrospectively analyzed asthma medication requests
submitted to the Portuguese Anti-Doping Authority between
2008 and 2010. Athletes older than 16 years who requested
permission to use ICS and/or IBAs for more than 3 months
were included. Data on respiratory symptoms, medication
requested, spirometry, and atopy (at least 1 positive skin prick
test or positive specific IgE) were collected. A diagnosis of
asthma was based on a positive bronchodilator test or broncho-
provocation test.
5
Exhaled nitric oxide results were converted
to personal predicted values using the FeNO Interpretation Aid
tool (http://www.enovis.org) and considered increased if above
150% of predicted. Data were expressed as median and range,
and categorical variables were compared using the x
2
or Fisher
Submitted for publication January 08, 2012; accepted July 05, 2012.
From the *Allergy, Asthma & Sports Unit, Immunoallergology Department,
Centro Hospitalar São João E.P.E., Porto, Portugal; †Immunology Labo-
ratory, Faculty of Medicine, University of Porto, Porto, Portugal; ‡Anti-
Doping Authority of Portugal, Lisbon, Portugal; and §Internal Medicine
Department, Baixo-Vouga Hospital Center, Aveiro, Portugal.
The authors report no financial or conflicts of interest.
Correspondence Author: Mariana Couto, MD, Serviço de Imunoalergologia,
Centro Hospitalar São João, EPE, Alameda Prof. Hernâni Monteiro
4200-319 Porto, Portugal (marianafercouto@gmail.com).
Copyright © 2012 by Lippincott Williams & Wilkins
Clin J Sport Med
Volume 0, Number 0, Month 2012 www.cjsportmed.com
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