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http://bmj.com/cgi/content/full/327/7405/36
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BMJ 2003;327:36-40 (5 July)
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J B M van Woensel, pediatric intensivist1, W M C van Aalderen, pediatric pulmonologist1, J L L Kimpen, pediatrician infectiologist2
1 Emma Children's Hospital Academic Medical Centre, Paediatric Intensive Care Unit G8ZW, PO Box 22660, 1100 DD Amsterdam, Netherlands, 2 Wilhelmina Children's Hospital, University Medical Centre, Utrecht, Netherlands
Correspondence to: J B M van Woensel j.b.vanwoensel@amc.uva.nl
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Introduction |
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Viruses are the most common cause of lower respiratory tract disease
in infants and young children and are a major public health problem
in this age group. The novel variant of coronavirus that is
associated with the worldwide outbreak of severe acute respiratory
syndrome and human metapneumovirus, a recently identified new
respiratory pathogen, have stressed the continuing importance of viral
respiratory infections over the whole age spectrum.
Costs attributable to viral lower respiratory tract infections in both outpatient and inpatient settings are an important burden on national healthcare budgets.1 Each year approximately 3% of all children less than 1 year of age need to be admitted to hospital with moderate or severe viral lower respiratory tract infection.2 This review gives an update of viral lower respiratory tract infection in infants and young children, with special emphasis on treatment and prevention.
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Sources and selection criteria |
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We gathered information from our own experience and by reading
relevant literature on viral respiratory infections in infants and
children obtained by searching Medline and the Cochrane database.
Much literature is available on the topic, so we based our review on
well designed major observational studies, controlled trials, and
systematic reviews. We consulted the websites of the World Health
Organization and the Centers for Disease Control for the most recent
information on severe acute respiratory syndrome.
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Epidemiology |
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A great variety of viruses can cause lower respiratory tract disease
in children—for example, respiratory syncytial virus, influenza
viruses, parainfluenza viruses, rhinovirus, adenovirus, and the
recently identified human metapneumovirus.3,w1,w2
Although most respiratory viral infections occur throughout the year,
seasonal variation (in a worldwide comparable pattern) is obvious for
certain viruses, such as respiratory syncytial virus and influenza
virus (figure).
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Respiratory syncytial virus and influenza viruses
Worldwide, respiratory syncytial virus is by far the most common
cause of viral lower respiratory tract infection in infants and young
children.4 Virtually all children have developed
antibodies to respiratory syncytial virus by the age of 3 years.4 In addition, an estimated 75% of all admissions for
bronchiolitis in children under 5 years of age are related to
respiratory syncytial virus.3
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Influenza viruses also cause the most severe disease in the youngest age group. A recent study showed that infants and young children have a 12-fold increased risk of admission to hospital for respiratory tract infection caused by influenza virus compared with children aged 5-17 years.5
The concomitant circulation of respiratory syncytial virus and influenza during outbreaks has compromised the assessment of the relative contribution of each virus to viral lower respiratory tract infection in population based studies. The similarity in clinical syndromes caused by respiratory syncytial virus and influenza was shown in a recent community based observational study in the United Kingdom. This study showed that respiratory syncytial virus and influenza virus occur not only among people at the ends of the age spectrum but also among people aged 15-44 years and that in all age groups more than 20% of influenza-like illnesses are attributable to respiratory syncytial virus.6
Human metapneumovirus
Human metapneumovirus has recently been identified as a new
paramyxovirus causing respiratory tract infections.7
It was isolated from nasopharyngeal aspirates from 28 children with
symptoms of lower respiratory tract infection in the winter season in
the Netherlands. Further serological studies revealed that virtually
all children have been exposed to the virus by the age of 5 years.
Studies from several other countries have confirmed its role in
respiratory infections in both children and adults.8 9,w3,w4 The exact impact and
epidemiology of human metapneumovirus in respiratory infections in
infants and young children needs to be determined in prospective studies.
Severe acute respiratory syndrome
A worldwide outbreak of a life threatening febrile respiratory
illness that has been named severe acute respiratory syndrome has
recently started (box 1).w5 Hong Kong and the Guangdong
province in China are the epicentres of the syndrome. By the
beginning of May 2003 WHO had reported over 6500 cases in more than
25 countries. A causal association between severe acute respiratory
syndrome and a newly identified coronavirus, distinct from the known
human coronaviruses, has been shown.10 So far,
infants and children do not seem to be a special risk group for the
syndrome, and only a few cases have been reported among children
under 15 years of age. Very recently, the clinical presentation and
outcome in 10 children (aged 1.5-16.4 years) admitted to two
hospitals in Hong Kong has been published.11
Whereas teenagers presented with the same symptoms as adults, young
children presented mainly with signs of an upper respiratory tract
infection without systemic symptoms such as chills, rigor, and
myalgia. None of the children died. The clinical course seemed to be
milder in young children than in teenagers and adults.
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Bacterial co-infections
In addition to having a role as causative agents of respiratory
disease, viral infections can predispose to bacterial superinfection.w6
Indeed, many experimental studies have shown that virus induced
pathological and immunological phenomena may contribute to increased
bacterial adhesion.w6 Despite this evidence for the
important role of preceding viral infections in the aetiology of
bacterial respiratory infections, the real incidence of clinically
important bacterial superinfection after viral lower respiratory
tract infection remains obscure. The proportion of children with
mixed viral and bacterial respiratory tract infection found in studies using
serology or antigen detection in serum or urine has been reported to
be as high as 40%.12,w7 However, these methods
are inadequate for assessing the clinical importance of the bacterial
infection or the need for antimicrobial treatment. Other studies,
using clinical methods, have shown that the risk of serious
concurrent or secondary bacterial infection in patients with viral
lower respiratory tract infection is very low.13,w8
Signs and symptoms
Respiratory viruses cause a similar spectrum of respiratory illness
in children, ranging from pharingitis, otitis media, laryngitis
subglottica, bronchitis, and tracheitis to bronchiolitis and
pneumonia. It is difficult to distinguish clinically between the
causative agents. Infections usually start with rhinorrhoea, cough
and (non-obligate) fever. After one or two days the lower respiratory
tract may become involved, with signs of respiratory distress, including
tachypnoea, retractions, and cyanosis in severe cases. Life
threatening apnoea may occur in very young infants, particularly in
infections with respiratory syncytial virus. During infections with
influenza virus systemic symptoms may be more prominent than signs in
the respiratory tract.
Several patient groups are at high risk of a severe course of viral lower respiratory tract infection, especially in infections with respiratory syncytial virus. Examples are premature infants and patients with underlying pulmonary disease such as chronic lung disease or cystic fibrosis; patients with congenital heart disease, especially those with pulmonary hypertension, are also at risk. As well as these well known risk groups, previously healthy infants may also deteriorate severely during viral lower respiratory tract infection. Extreme tachypnoea and hypoxaemia are both associated with subsequent deterioration. Unfortunately, the sensitivity of these symptoms in identifying patients who will deteriorate is very low.w9
Bronchiolitis and pneumonia are the most common manifestations of viral lower respiratory tract infection in infants. Differentiation between these clinical syndromes is difficult as their definition is not based on standardised clinical criteria.w10 On the chest radiograph bronchiolitis is associated with air trapping and hyperinflation with or without focal and patchy atelectasis, whereas pneumonia lacks signs of hyperinflation and is characterised by interstitial thickening.w11 Overlap exists between the two clinical syndromes and they probably form both ends of a spectrum. The distinction between bronchiolitis and pneumonia is based on entangling clinical criteria and so far does not seem to be relevant in daily clinical practice. However, increasing insight into pathophysiological differences in the clinical manifestations of viral lower respiratory tract infection may eventually lead to specific treatment and preventive strategies in subgroups of patients, making an early specific diagnosis relevant.14 Additionally, the long term outcome of both groups might be different, eventually needing a differentiated therapeutic approach during initial disease.w12
Viral lower respiratory tract infection in immunocompromised patients
Respiratory viruses are a serious threat for immunocompromised patients.w2,w13
All community acquired respiratory viruses, especially adenovirus and
respiratory syncytial virus, can cause severe infection in this high
risk population, with considerable mortality. The presence of upper
respiratory tract symptoms, wheezing, and interstitial or lobar
consolidation on the chest radiograph may help in differentiating
viral lower respiratory tract infection from other opportunistic
respiratory pathogens, but definite diagnosis depends on
demonstration of the virus in respiratory secretions by culture or
polymerase chain reaction techniques. Pre-emptive treatment
strategies are being explored in stem cell transplant recipients;
these use routine polymerase chain reaction techniques to monitor
viral load.
Children up to the age of 2 years infected with HIV have an almost fourfold increased risk of severe infection caused by respiratory syncytial virus, parainfluenza virus, influenza virus, and adenovirus than children not infected with HIV.15 In addition, HIV infected children more often present with pneumonia rather than bronchiolitis, more often have secondary bacterial infection, and have a higher mortality than uninfected children.16
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Treatment |
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General considerations
Viral lower respiratory tract infections are usually self limiting. Preservation
of adequate fluid intake and correction of hypoxaemia are mandatory
in mild disease. Although medical treatment is rarely indicated in
immunocompetent patients, great variability exists in the management
of these patients.17,w14 Wilson et al
showed that this variability does not affect clinical outcome but
correlates significantly with costs associated with viral lower
respiratory tract infections.18 No strict
guidelines exist on when to admit or discharge children with a viral
lower respiratory tract infection, but in daily practice physicians'
discretion in decision making and factors associated with socioeconomic
status are important determinants.19
Implementation of educational programmes and practical guidelines
have been shown to be cost saving and may help in standardising
treatment strategies for viral lower respiratory tract infections in children.20
Specific treatment strategies
Box 2 summarises the strategies available for treating viral lower
respiratory tract infections.
Bronchodilator treatment
Despite unproved efficacy, bronchodilators are still often prescribed
in patients with viral lower respiratory tract infection.17,w14
As in asthma, airway obstruction secondary to inflammation,
oedema, and airway smooth muscle contraction are important in the
pathophysiology of viral lower respiratory tract infection,
especially that caused by respiratory syncytial virus. However,
variations between patients in the response to bronchodilators indicate that
differences might exist between patients in the contribution of these
phenomena to airway obstruction. Future studies should focus on the
identification of probable responders and non-responders to this form
of treatment.
Corticosteroids
The efficacy of corticosteroids has been evaluated mainly in infants
and children with respiratory syncytial virus disease, with
disappointing results in mild disease. Very recently our group found
that corticosteroids may be beneficial in artificially ventilated
patients with severe bronchiolitis but had no effect in patients with
pneumonia.14 These findings support the idea
that corticosteroids may be beneficial in certain patients with
a severe course of disease and that distinction between clinical
manifestations of viral lower respiratory tract infection
(bronchiolitis and pneumonia) is important in the evaluation of
certain treatment strategies.
Antiviral treatment
Respiratory syncytial virus—Ribavirin is a synthetic nucleoside analogue
with in vitro activity against respiratory syncytial virus.w31
However, on the basis of the currently available evidence, the
routine use of ribavirin has no place in patients with respiratory
syncytial virus infection.
Influenza virus—Although neuraminidase inhibitors are effective against influenza viruses, infections are relatively mild and self limiting in healthy children. On the other hand, costs attributable to influenza virus infections may be very high, particularly in infants and children.21 The goal of treatment with neuraminidase inhibitors therefore should be epidemiological control of disease rather than reducing the duration of disease in otherwise healthy individuals.
Antibiotics
Despite their lack of beneficial effects, antibiotics are often
prescribed for patients with viral lower respiratory tract infection.17w14,w29,w32 In this era of increasing antimicrobial
resistance this overuse should be reduced and future studies
should focus on mechanisms and risk factors for bacterial superinfection
in children with viral lower respiratory tract infection, as
well as on accurate tests to differentiate viral from bacterial disease.
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Prevention |
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Research into vaccination for viral lower respiratory tract
infections in infants and children has mainly focused on respiratory
syncytial virus and influenza virus. A recently published systematic
review found no significant effect of vaccines against respiratory
syncytial virus on preventing respiratory syncytial virus. The review
included five controlled trials that evaluated the efficacy of
subunit vaccines in children and adults mainly seropositive for respiratory
syncytial virus.22 Although progress
has been made during the past decade, particularly with live attenuated
vaccines, it will take probably at least another 10 years before
routine vaccination becomes available.w33
Disappointing results in the development of an active vaccine have forced research in the prevention of respiratory syncytial virus to focus on other strategies. Passive immunisation with intravenous hyperimmune globulins against respiratory syncytial virus has proved to be beneficial in preventing severe disease in children at high risk.23 However, practical problems have limited its use and further research and have led to the development of an intramuscular applicable IgG humanised monoclonal antibody directed against the F protein of respiratory syncytial virus (palivizumab). A controlled trial has shown that monthly injections with palivizumab reduce respiratory syncytial virus related hospital admissions in children at high risk by more than 50%.24 Several reports on experiences in the field have confirmed the trial results as well as the good safety profile of palivizumab. Although guidelines have been developed for use of palivizumab,w34 cost effectiveness studies in Europe have recommended that guidelines can not be generalised but should be based on national hospital admission data for respiratory syncytial virus.25 26
Inactivated intramuscular influenza vaccine as both cold adapted and live attenuated intranasal vaccines have been shown to be safe and effective in children from 1 year of age onwards,w35 but immunogenicity is poor in children younger than 6 months.27 Although influenza is usually a mild and self limiting disease, children with underlying chronic medical conditions are at risk of severe disease, and vaccination against influenza virus has mainly been focused on this patient group. In addition, although studies from the United States and western Europe have shown that vaccination is associated with economic benefits in all age groups, debate is ongoing about whether influenza vaccination should be broadened to all age groups, including healthy children and adults.28
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Progress has been made in the development of a parainfluenza virus vaccine. However, no effective human vaccine is yet available.w2
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Conclusion |
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Viral lower respiratory tract infections in infants and children are
an important medical and socioeconomic problem worldwide. Viral lower
respiratory tract infections are mild and self limiting in most
cases. Particular patient groups are at risk of a severe course of
disease, although previously healthy infants with a viral lower respiratory
tract infection may also develop severe disease.
Treatment for moderate viral lower respiratory tract infection is mainly supportive. Lack of means to control viral lower respiratory tract infection has led to great variation in management worldwide.17,w14 Development of practical guidelines and educational programmes in both clinical and outpatient settings may be helpful and cost saving in the control of viral lower respiratory tract infection in infants and children.
Additional
references (w1-w35) are on bmj.com
Contributors: JBMvW drafted the original manuscript. All three authors jointly wrote the final paper.
Competing interests: JBMvW and JLLK have received fees for giving presentations at symposia organised by Abbot Laboratories, manufacturer of palivizumab.
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References |
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© 2003 BMJ Publishing Group Ltd
Return to Vaccination News Home Page __» Right-click to "open in new window"
DISCLAIMER: All information, data, and material contained, presented, or provided here is for general information purposes only and is not to be construed as reflecting the knowledge or opinions of the publisher, and is not to be construed or intended as providing medical or legal advice. The decision whether or not to vaccinate is an important and complex issue and should be made by you, and you alone, in consultation with your health care provider.