Download Return to play after acute infectious disease in football players

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

West Nile fever wikipedia , lookup

Eradication of infectious diseases wikipedia , lookup

Neonatal infection wikipedia , lookup

Neglected tropical diseases wikipedia , lookup

Marburg virus disease wikipedia , lookup

Chickenpox wikipedia , lookup

Hepatitis B wikipedia , lookup

Chagas disease wikipedia , lookup

Sexually transmitted infection wikipedia , lookup

Hospital-acquired infection wikipedia , lookup

Traveler's diarrhea wikipedia , lookup

Middle East respiratory syndrome wikipedia , lookup

Gastroenteritis wikipedia , lookup

African trypanosomiasis wikipedia , lookup

Schistosomiasis wikipedia , lookup

Pandemic wikipedia , lookup

Leptospirosis wikipedia , lookup

Coccidioidomycosis wikipedia , lookup

Infectious mononucleosis wikipedia , lookup

Transcript
This article was downloaded by: [Universita di Cassino]
On: 16 July 2014, At: 01:14
Publisher: Routledge
Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House,
37-41 Mortimer Street, London W1T 3JH, UK
Journal of Sports Sciences
Publication details, including instructions for authors and subscription information:
http://www.tandfonline.com/loi/rjsp20
Return to play after acute infectious disease in football
players
a
Jürgen Scharhag & Tim Meyer
a
a
Institute of Sports and Preventive Medicine, Saarland University, Saarbrücken, Germany
Published online: 01 May 2014.
To cite this article: Jürgen Scharhag & Tim Meyer (2014) Return to play after acute infectious disease in football players,
Journal of Sports Sciences, 32:13, 1237-1242, DOI: 10.1080/02640414.2014.898861
To link to this article: http://dx.doi.org/10.1080/02640414.2014.898861
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the information (the “Content”) contained
in the publications on our platform. However, Taylor & Francis, our agents, and our licensors make no
representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the
Content. Any opinions and views expressed in this publication are the opinions and views of the authors, and
are not the views of or endorsed by Taylor & Francis. The accuracy of the Content should not be relied upon and
should be independently verified with primary sources of information. Taylor and Francis shall not be liable for
any losses, actions, claims, proceedings, demands, costs, expenses, damages, and other liabilities whatsoever
or howsoever caused arising directly or indirectly in connection with, in relation to or arising out of the use of
the Content.
This article may be used for research, teaching, and private study purposes. Any substantial or systematic
reproduction, redistribution, reselling, loan, sub-licensing, systematic supply, or distribution in any
form to anyone is expressly forbidden. Terms & Conditions of access and use can be found at http://
www.tandfonline.com/page/terms-and-conditions
Journal of Sports Sciences, 2014
Vol. 32, No. 13, 1237–1242, http://dx.doi.org/10.1080/02640414.2014.898861
Return to play after acute infectious disease in football players
JÜRGEN SCHARHAG & TIM MEYER
Institute of Sports and Preventive Medicine, Saarland University, Saarbrücken, Germany
Downloaded by [Universita di Cassino] at 01:14 16 July 2014
(Accepted 24 February 2014)
Abstract
Acute infectious diseases are common in athletes and can impair their ability to train and to compete. Furthermore,
continuing exercise during infectious diseases may lead to prolongation or aggravation of illness with severe acute or chronic
organ manifestations. Therefore, even simple infectious diseases require a sufficient period of convalescence and recovery,
during which exercise may be not allowed. Nowadays, especially in professional football with high pressures on players, staff
and clubs due to broad public interests as well as financial constraints, the return-to-play decision is of utmost significance.
Based on previous suggestions and our own experience within amateur and professional athletes and football players, this
article aims to give a short overview on return-to-play decisions after common acute infectious diseases in football players.
Keywords: football, infections, myocarditis, return to play, team physician, upper respiratory tract infection
Introduction
Acute infectious diseases are very common in athletes
and can impair their ability to train and to compete.
Continuing exercise during infectious diseases may
lead to prolongation or aggravation of illness,
combined with the risk of additional acute or chronic
organ manifestations such as bronchitis or pneumonia,
myocarditis, endocarditis or splenic rupture. In
addition, the risk for overload and overtraining can be
increased, and infection-associated fatigue can impair
exercise and predispose to other injuries (Harris,
2011). However, only few data are available for
return-to-play decisions in athletes after acute infectious diseases. Based on previous suggestions
(Karageanes, 2007; Kruse & Cantor, 2007; Metz,
2003; Page & Diehl, 2007) and our own experience
within a wide range of amateur and professional
athletes, this article aims to give a short overview on
return-to-play decisions after common acute infectious
diseases in football players. Of course, many of the
recommendations are not limited to football but have
a similar meaning in other types of sport. Therefore,
some statements are given for athletes in general.
General aspects
Physical examination and blood parameters
After having taken the athlete’s disease history, a
comprehensive physical examination should follow
even if the athlete only presents with minor symptoms
or disease. Especially in high-level players, a trivial
rhinorrhoea may relevantly affect their well-being
and physical performance in training and competition. Besides the physical examination of the heart,
lungs and abdomen, the inspection of the throat (and
if necessary the ears) as well as the palpation of lymph
nodes should be performed. Furthermore, body temperature should be measured and, in addition, it
should be seriously taken into account to record an
electrocardiogram (ECG) at rest (Figure 1).
Particularly in professional athletes, it must
always be considered to obtain a venous blood
sample during the first visit and possibly during
later ones (Figure 1). This will allow to objectively
evaluating the disease and the severity of inflammation, and might simplify the return-to-play
decision. Beyond that, objective measurements
may also gain legal importance in very rare cases.
In athletes, the most helpful routine blood parameters of inflammation are the white blood cell
count (WBCC) and C-reactive protein (CRP),
whereas the blood sedimentation rate is of only
minor relevance. Because procalcitonin only
increases in systemic bacterial inflammation (Lee,
2013), it does not seem useful in athletes with
common infections. Altogether, targeted determination of relevant disease indicators might be of
great help for later return-to-play decisions.
Correspondence: Jürgen Scharhag, Institute of Sports and Preventive Medicine, Campus, Building B8.2, Saarland University, 66123 Saarbrücken, Germany.
E-mail: [email protected]
© 2014 Taylor & Francis
1238
J. Scharhag & T. Meyer
Return to play after
infectious disease?
History
Physical examination
heart, lungs, abdomen
throat, ears
lymph nodes
body temperature
Venous blood sample
inflammatory markers
other blood parameters
Downloaded by [Universita di Cassino] at 01:14 16 July 2014
Follow-up
or
further
examinations
Additional examinations
e.g. ECG, ultrasound imaging
abnormal
abnormal
Follow-up
or
further
examinations
normal & asymptomatic
Return to play
Figure 1. The decision on return to play after acute infectious disease in athletes should be based on the history and symptoms, followed by
a comprehensive physical examination of the heart, lungs and abdomen, the throat (and if necessary the ears) and palpation of lymph nodes.
In addition, the body temperature should be measured. It should also be taken into account to obtain a venous blood sample to determine
inflammatory markers (WBCC, CRP) or further blood parameters (e.g. liver enzymes) as well as additional examinations (e.g. ECG,
ultrasound imaging). If findings are abnormal, return to play should not be allowed and medical follow-ups or further examinations are
necessary. Return to play can be allowed when findings are normal, and the athlete is asymptomatic.
Nevertheless, analysing blood parameters or
recording an ECG may not be possible under certain
conditions (e.g. in training camps or foreign
countries). Therefore, in clinically clearly cured
players, it seems justifiable that the return-to-play
decision is based on the clinical examination alone
by experienced sports physicians. In unclear cases
with any doubt on the player’s health and no possibility for necessary additional examinations, the
player should not return to play.
Return-to-play
Although the term “return-to-play” has been established over the years, it has to be differentiated between
“return-to-training” and “return-to-competition”.
Because football competition demands can hardly be
controlled and inevitably include high exercise intensities, players should be completely cured before
returning to competition and no doubts on their
proper health should exist.
Before returning to play, football players should
receive a final comprehensive medical check-up. The
athlete should be free of symptoms and the physical
examination without abnormal findings and blood
values for inflammation must be normal (WBCC,
CRP) or almost normal after a significant decrease
over the last days (CRP). If necessary, an ECG at
rest or (less frequently) even during exercise should
be performed.
Before returning to competition, football players
should return to training and exercise with mild
(aerobic) intensities with no or only a mild increase
in blood lactate concentrations on the first day. If
well tolerated, exercise intensity can be increased
stepwise from aerobic (mild) to aerobic–anaerobic
(moderate) on an individual and day-to-day basis.
Depending on the kind and severity of the infectious
disease, after curing most of the common infectious
diseases, maximal exercise intensities can be reached
within a time period from 3–5 days up to 2–3 weeks.
Respiratory tract infections
Upper respiratory tract infection (common cold)
Upper respiratory tract infections (URTIs) represent
the most common acute illnesses in athletes and are
usually caused by viruses. Viral URTI is a benign,
self-limiting syndrome, lasting from 3–5 up to 14
days (Harris, 2011; Page & Diehl, 2007), presenting
with
rhinorrhoea,
sore
throat,
swallowing
problems, cough, and possibly fever and malaise.
Most common viruses are rhinoviruses, coronaviruses and respiratory syncytial virus, but other
viruses can also lead to common cold symptoms
(e.g. influenza, parainfluenza and adenoviruses).
Downloaded by [Universita di Cassino] at 01:14 16 July 2014
Return to play after acute infections
Possible serious complications can be acute bacterial
superinfections, lower respiratory tract infections and
an increase in asthmatic attacks in athletes with this
disease.
Athletes without fever and malaise, general body
aches and pains, without symptoms below the neck
and without elevated blood values for inflammation
may exercise at mild to moderate intensity levels
(e.g. jogging for up to 30 min), as this does not
appear to be harmful for individuals who have common cold symptoms (Page & Diehl, 2007). Intensive
exercise bouts (interval training, sprints and training
matches) should be avoided because the immune
system might be affected negatively (Friman &
Ilbäck, 1998; Gabriel & Kindermann, 1997; Meyer,
Gabriel, Ratz, Müller, & Kindermann, 2001;
Nieman, 2003; Scharhag, Meyer, Gabriel,
Auracher, & Kindermann, 2002). If common cold
symptoms have completely disappeared for about
2–3 days, normal (also intense) training routine can
be resumed. All other athletes should receive medical follow-ups within 2–3 days, and are allowed to
start with mild training when they are free of common cold symptoms and a normalisation of blood
values for inflammation is present.
Acute sinusitis
Acute sinusitis can be caused by viruses or bacteria,
but viral infection is the most common cause.
Whereas viral sinusitis usually resolves within 7–10
days, bacterial sinusitis might last up to 1 month –
without treatment in 75% of all cases (Page & Diehl,
2007). Consequently, acute bacterial sinusitis should
be treated with antibiotics. In unclear cases or in the
presence of worsening courses, additional diagnostic
measures such as sinus aspirate culture or imaging
studies should be considered.
Players with fever, myalgias, symptoms below the
neck (e.g. cough and gastrointestinal [GI] symptoms) or elevated blood values for inflammation
should not be allowed to exercise and receive
continuous medical follow-ups within 2–3 days.
When symptoms worsen within 5–7 days or persist
longer, antibiotic therapy should be initiated for a
10- to 14-day course. Athletes with viral sinusitis
without fever, with symptoms only above the neck
(e.g. nasal congestion, runny nose and headaches)
and normal blood values for inflammation and
appropriate symptomatic care (e.g. decongestants
and
non-steroidal
anti-inflammatory
drugs
[NSAIDs]) may exercise at mild intensities, but
medical follow-ups should be performed in intervals
of 2–3 days. Return-to-play should be allowed when
symptoms have completely disappeared and blood
values for inflammation have normalised, usually
starting with mild to moderate exercise intensities
1239
for the first 2–3 days before exercising more intensively again.
Acute pharyngitis
The causes of an acute pharyngitis can be viral or
bacterial, and a large number of pathogens exists
(e.g. rhinovirus, coronavirus, adenovirus, influenza,
herpes simplex virus, Epstein–Barr virus (EBV),
Group A streptococcus, chlamydia and Neisseria).
For most cases, a symptomatic treatment is sufficient. The clinical differentiation between viral and
bacterial infection is difficult, but fever and the
absence of conjunctivitis, cough or rhinorrhoea may
suggest bacterial pharyngitis (Bisno et al., 2002),
which should be treated with antibiotics. NSAIDs
can sufficiently reduce sore throat symptoms.
It has recently been stated by Page and Diehl
(2007) that removal from competition is often unnecessary if the player is under close supervision, has
no fever and systemic symptoms and is treated
appropriately (antibiotic treatment in suspected or
confirmed acute bacterial pharyngitis, improvement
in acute symptoms within 24 h). However, we suggest that athletes with suspected or confirmed acute
bacterial pharyngitis who take antibiotics should not
return to play or training before they are free of fever
as well as of any symptoms, and blood values for
inflammation are normal.
Infectious mononucleosis
Infectious mononucleosis (IM; “kissing disease”) is
caused by the EBV and characterised by lymphadenopathy, tonsillar pharyngitis and fever. Because
symptoms can also be mild (particularly in young
individuals), the disease often remains undiagnosed
(Kinderknecht, 2002). But as splenomegaly occurs
in about half of the patients, and splenic rupture is a
possible complication (Kinderknecht, 2002), all athletes with diagnosed acute IM require close medical
follow-ups including ultrasound imaging of the
spleen. The treatment is symptomatic, usually
including NSAIDs. If an additional antibiotic treatment may be indicated due to pharyngeal bacterial
superinfection, penicillin or ampicillin must be
avoided as these antibiotics can cause severe skin
reactions in patients with IM.
Athletes with acute IM should not participate in
any sport for 3 weeks after the first clinical symptoms, as splenic rupture typically occurs during that
period (Putukian et al., 2008). After 3 weeks, asymptomatic athletes can return to training, starting with
mild intensities (but avoiding contact sports) if (1)
values for inflammatory markers and liver enzymes
are normal; (2) fever is not present; (3) pharyngitis is
resolved; (4) the spleen is not enlarged or painful
Downloaded by [Universita di Cassino] at 01:14 16 July 2014
1240
J. Scharhag & T. Meyer
and (5) there are no signs in the resting ECG for
myocarditis. Fulfilling all these criteria, after 4 weeks
the athlete can return to more intensive exercise as
well as contact sports. However, full recovery usually
takes 2–3 months, but in some cases may even take
longer.
athlete should be completely free of all symptoms,
laboratory inflammatory markers should be normal
(WBC) or almost normal with a significant decrease
within the last days. Training should be started with
mild exercise intensities for 2–3 days, followed by a
moderate increase within the following days.
Influenza
Pneumonia
Caused by influenza viruses, influenza usually
appears seasonally during autumn and winter
months as an acute respiratory disease typically
with a sudden onset which can lead to acute bronchitis. Malaise, myalgias, headache, cough, sore
throat and high fever are typical symptoms.
Complications can be bacterial superinfections,
pneumonia, otitis media, meningitis, encephalitis,
myocarditis,
myositis,
rhabdomyolysis
and
Guillain–Barré syndrome. After an incubation period of 1–5 days, the acute disease persists for about
8–10 days.
Players with influenza should have close medical
follow-ups to control for possible complications.
Furthermore, a symptomatic athlete should be kept
away from teammates or training rooms to prevent
infections from other athletes and staff. Return to
training and competition can only be allowed when
the disease has resolved completely, meaning that
the athlete is free of all symptoms including a normal
respiratory status, and laboratory inflammatory markers are normal. Training intensities should be mild
for the first 2–3 days, and can be increased moderately within 1–2 weeks. As a preventive measure,
vaccination of players should be considered before
the winter season.
Pneumonia represents an acute infection of the pulmonary parenchyma by viruses and other organisms,
resulting in typical pneumonias (e.g. mostly caused
by Streptococcus pneumoniae in very young and
adults). Frequent symptoms are fever, cough (with
sputum in typical pneumonias), myalgias, headache,
malaise and anorexia. Usually an empiric oral antibiotic therapy can be started with macrolides.
Antibiotic therapy should be initiated in community-acquired pneumonias for 7–10 days and in atypical pneumonias for 10–14 days.
Pneumonia has to be considered a serious illness,
requiring an increased recovery time for the athlete
compared to URTIs. A reactive airway disease,
caused by transient airway hyper-responsiveness
with a temporary decrease in the 1 s forced expiratory volume, is a common complication in athletes
(Kruse & Cantor, 2007). It usually resolves after 3
weeks, but can also persist longer and last up to 2
months (Kruse & Cantor, 2007). Therefore, athletes
with reactive airway disease may have to be treated
temporarily
with
a
short-term
inhaled
bronchodilator.
Players with pneumonia should be informed about
an increased recovery time. They should be allowed
to return to play, when they are completely free of
symptoms and laboratory inflammatory markers are
normal. Training should be started with mild exercise intensities for 2–3 days and can be advanced
with a moderate increase over the following days.
Athletes who have been treated with macrolides
should receive a resting ECG before returning to
exercise, as macrolides are known to prolong the
QT interval and a long QT-syndrome increases the
risk for a sudden cardiac death during exercise.
Acute bronchitis
As an inflammation of the mucous membranes of
the bronchial tree, acute bronchitis is caused by
viruses in about 90% of the cases (e.g. influenza,
parainfluenza, adenovirus, rhinovirus, coronary
virus and respiratory syncytial virus). The most common bacteria involved in acute bronchitis are
Mycoplasma pneumoniae and Chlamydia pneumoniae.
In contrast to URTI, cough with or without sputum
production is the dominant symptom in acute bronchitis, which can persist up to 3 weeks (Kruse &
Cantor, 2007). As fever can be present but is not
typical in acute bronchitis, influenza or pneumonia
should be considered as differential diagnoses.
Symptomatic treatment is sufficient, and antibiotics
are rarely indicated (Gonzales et al., 2001; Snow,
Mottur-Pilson, & Gonzales, 2001).
Players with acute bronchitis should receive close
medical follow-ups and kept away from exercise until
resolution of symptoms. For return to play, the
GI infections
Causes for GI infections can be food borne, viral,
bacterial or parasitic (Karageanes, 2007). Foodborne
illness typically results from toxins in the food due to
bacterial growth as well as from bacterial, viral or
parasitic contamination or toxins of harmful algal
species (Karageanes, 2007). Typical symptoms can
be nausea, vomiting, diarrhoea, abdominal cramping
and fever. Depending on the kind of virus, bacteria
or parasite, illness duration can last from hours to
days, but usually should not last longer than 1 week.
Downloaded by [Universita di Cassino] at 01:14 16 July 2014
Return to play after acute infections
The most common cause of gastroenteritis may be
food contamination by toxins from bacteria, usually
starting suddenly with nausea, abdominal cramping,
vomiting and diarrhoea as a reaction of the GI tract
to the ingested toxin and ending after some hours.
Most GI infections are self-limited, but in bacterial
or parasitic GI infections treatment with antibiotics
can be indicated (Karageanes, 2007). Based on own
experiences, in athletes with GI infections serum
markers of inflammation (especially CRP) are
usually higher than in athletes with URTIs.
Players with GI infections should receive close
medical follow-ups as diarrhoea can lead to severe
dehydration and electrolyte imbalances. Often
severe malaise over the first few days makes decisions about eligibility for sport easy, and players do
not feel as if they were able to train or compete.
After GI infections, they can return to play when
(1) they are asymptomatic and afebrile; (2) blood
values for inflammatory markers, haematocrit,
electrolytes and liver enzymes are normal (or
clearly decreasing) and (3) body weight is normal
or almost normal after adequate rehydration.
Athletes should start to train with mild exercise
intensities, which can be progressively increased
within a few days.
Cardiac infections
Myocarditis and pericarditis
Myocarditis and pericarditis can be caused by a
variety of infectious and non-infectious agents.
Both diseases can be isolated, but often are combined and named peri-myocarditis. Infections can
be caused by many viruses (e.g. coxsackievirus, adenovirus, cytomegalovirus, echovirus, hepatitis virus,
herpes virus, EBV, influenza and HIV) and bacteria
(e.g. staphylococcus, pneumococcus, streptococcus,
haemophilus and Neisseria). The clinical presentation can be broad, ranging from asymptomatic states
to severe acute heart failure requiring cardiac assist
devices or heart transplantation. Myocarditis and
peri-myocarditis can also induce life-threatening
arrhythmias, chronic heart failure and dilated cardiomyopathy. In addition, pericarditis can progress to
a pericarditis constrictiva. Both diseases may lead to
sudden cardiac death (Htwe & Khardori, 2012).
Recommendations for return-to-play decisions in
athletes with myocarditis/peri-myocarditis have been
given by the 36th Bethesda Conference and the
European Society of Cardiology (Maron & Zipes,
2005; Pelliccia et al., 2005). A re-convalescent period of about 6 months should follow the onset of
clinical manifestation. Athletes may return to
training and competition, when (1) they are asymptomatic; (2) the 12-lead ECG has normalised and
1241
relevant arrhythmias are absent on Holter monitoring; (3) laboratory markers of inflammation,
myocardial necrosis and heart failure are normal
and (4) cardiac function, wall motions and dimensions are normal at rest and during exercise.
Athletes with isolated pericarditis can return to
training and competition when (1) they are asymptomatic; (2) the 12-lead ECG has normalised, and
relevant arrhythmias are absent on Holter monitoring; (3) serum markers of inflammation, myocardial
necrosis and heart failure are normal and (4) a
normal cardiac function and no evidence of effusion
by echocardiography are present (Maron & Zipes,
2005; Pelliccia et al., 2005). Close medical followups should be performed in the first period, after
having returned to training and play in intervals of
3–6 months (Maron & Zipes, 2005; Pelliccia et al.,
2005). If myocarditis progresses to dilated cardiomyopathy or chronic pericardial disease results in
constriction, athletes should be disqualified from all
competitive sports (Maron & Zipes, 2005; Pelliccia
et al., 2005).
Non-medical factors
The influence of public pressure and psychological
factors especially in professional football players
should also be taken into account by the sports or
team physician when the player returns to competition. Perceived expectations from the media and
supporters as well as from teammates may put pressure on football players to return to training and play
prematurely. Additionally, although athletes may be
doubtlessly healthy after an infectious disease, their
transient reduced physical fitness after illness may
not allow a performance at their best. Such reduced
physical fitness leading to underperformance may
also lead to a loss of self-confidence. Under special
circumstances, therefore, it might be wise not to
return to play too early to protect the athlete, and
let him train until he has regained the necessary
physical fitness and self-confidence for competition.
Ideally, the decision to return to play should be
made in agreement between the physician, player
and the coach.
Conclusion
Return-to-play decisions after acute infectious
diseases in football players warrant thorough monitoring of the disease course and it has to include a
final medical check-up and, if possible, measurements of venous blood parameters of inflammation
(especially in professional players). Furthermore, it
should be taken into account if the player returns to
training or to competition, because training allows a
stepwise and more careful return to exercise whereas
1242
J. Scharhag & T. Meyer
competition might require higher and less controllable exercise intensities with negative side effects on
health, performance over time and possibly selfconfidence.
Downloaded by [Universita di Cassino] at 01:14 16 July 2014
References
Bisno, A. L., Gerber, M. A., Gwaltney Jr., J. M., Kaplan, E. L.,
Schwartz, R. H., & Infectious Diseases Society of America.
(2002). Practice guidelines for the diagnosis and management
of group A streptococcal pharyngitis. Clinical Infectious Diseases,
35(2), 113–125.
Friman, G., & Ilbäck, N. G. (1998). Acute infection: Metabolic
responses, effects on performance, interaction with exercise,
and myocarditis. International Journal of Sports Medicine, 19
(S3), S172–S182.
Gabriel, H., & Kindermann, W. (1997). The acute immune
response to exercise: What does it mean? International Journal
of Sports Medicine, 18(Suppl 1), S28–S45.
Gonzales, R., Bartlett, J. G., Besser, R. E., Cooper, R. J., Hickner,
J. M., Hoffman, J. R., … Centers for Disease Control and
Prevention. (2001). Principles of appropriate antibiotic use for
treatment of uncomplicated acute bronchitis: Background.
Annals of Emergency Medicine, 37, 720–727.
Harris, M. D. (2011). Infectious disease in athletes. Current Sports
Medicine Reports, 10(2), 84–89.
Htwe, T. H., & Khardori, N. M. (2012). Cardiac emergencies:
Infective endocarditis, pericarditis, and myocarditis. The
Medical Clinics of North America, 96(6), 1149–1169.
Karageanes, S. J. (2007). Gastrointestinal infections in the athlete.
Clinics in Sports Medicine, 26(3), 433–448.
Kinderknecht, J. J. (2002). Infectious mononucleosis and the
spleen. Current Sports Medicine Reports, 1(2), 116–120.
Kruse, R. J., & Cantor, C. L. (2007). Pulmonary and cardiac
infections in Athletes. Clinics in Sports Medicine, 26(3), 361–382.
Lee, H. (2013). Procalcitonin as a biomarker of infectious
diseases. The Korean Journal of Internal Medicine, 28(3), 285.
Maron, B. J., & Zipes, D. P. (2005). Eligibility recommendations
for competitive athletes with cardiovascular abnormalities.
Journal of the American College of Cardiology, 45, 1318–1375.
Metz, J. P. (2003). Upper respiratory tract infections: Who plays,
who sits? Current Sports Medicine Reports, 2(2), 84–90.
Meyer, T., Gabriel, H. H., Ratz, M., Müller, H. J., &
Kindermann, W. (2001). Anaerobic exercise induces moderate
acute phase response. Medicine and Science in Sports and
Exercise, 33(4), 549–555.
Nieman, D. C. (2003). Current perspective on exercise immunology. Current Sports Medicine Reports, 2(5), 239–242.
Page, C. L., & Diehl, J. J. (2007). Upper respiratory tract infections in athletes. Clinics in Sports Medicine, 26(3), 345–359.
Pelliccia, A., Fagard, R., Bjørnstad, H. H., Anastassakis, A.,
Arbustini, E., Assanelli, D., … Working Group of Myocardial
and Pericardial Diseases of the European Society of
Cardiology. (2005). Recommendations for competitive sports
participation in athletes with cardiovascular disease: A consensus document from the Study Group of Sports Cardiology of
the Working Group of Cardiac Rehabilitation and Exercise
Physiology and the Working Group of Myocardial and
Pericardial Diseases of the European Society of Cardiology.
European Heart Journal, 26, 1422–1445.
Putukian, M., OʼConnor, F. G., Stricker, P., McGrew, C., Hosey,
R. G., Gordon, S. M., … Landry, G. (2008). Mononucleosis
and athletic participation: An evidence-based subject review.
Clinical Journal of Sport Medicine, 18(4), 309–315.
Scharhag, J., Meyer, T., Gabriel, H. H. W., Auracher, M., &
Kindermann, W. (2002). Mobilization and oxidative burst of
neutrophils are influenced by carbohydrate supplementation
during prolonged cycling in humans. European Journal of
Applied Physiology, 87(6), 584–587.
Snow, V., Mottur-Pilson, C., Gonzales, R., & American
Academy of Family Physicians, American College of
Physicians-American Society of Internal Medicine, Centers
for Disease Control, Infectious Diseases Society of America.
(2001). Principles of appropriate antibiotic use for treatment of
acute bronchitis in adults. Annals of Internal Medicine, 134,
518–520.