Viral lower respiratory tract infection in infants and young children
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
Viruses are the most common cause of lower respiratory tractdisease
in infants and young children and are a major publichealth problem
in this age group. The novel variant of coronavirusthat is
associated with the worldwide outbreak of severe acuterespiratory
syndrome and human metapneumovirus, a recentlyidentified new
respiratory pathogen, have stressed the continuing importance of viral
respiratory infections over the whole agespectrum.
Costs attributable to viral lower respiratory tract infectionsin
both outpatient and inpatient settings are an importantburden on
national healthcare budgets.1 Each year
approximately3% of all children less than 1 year of age need to be
admittedto hospital with moderate or severe viral lower respiratorytract infection.2 This review gives an
update of viral lowerrespiratory tract infection in infants and
young children,with special emphasis on treatment and prevention.
We gathered information from our own experience and by reading
relevant literature on viral respiratory infections in infantsand
children obtained by searching Medline and the Cochranedatabase.
Much literature is available on the topic, so webased our review on
well designed major observational studies,controlled trials, and
systematic reviews. We consulted thewebsites of the World Health
Organization and the Centers forDisease Control for the most recent
information on severe acuterespiratory syndrome.
A great variety of viruses can cause lower respiratory tractdisease
in childrenfor example, respiratory syncytialvirus, influenza
viruses, parainfluenza viruses, rhinovirus,adenovirus, and the
recently identified human metapneumovirus.3,w1,w2
Although most respiratory viral infections occur throughoutthe year,
seasonal variation (in a worldwide comparable pattern)is obvious for
certain viruses, such as respiratory syncytialvirus and influenza
virus (figure).
Epidemiology of
respiratory syncytial virus, influenza A, adenovirus,
and parainfluenza virus in the Netherlands, 1997-2003
Respiratory syncytial virus and influenza viruses
Worldwide, respiratory syncytial virus is by far the most common
cause of viral lower respiratory tract infection in infantsand young
children.4 Virtually all children have developedantibodies to respiratory syncytial virus by the age of 3 years.4In addition, an estimated 75% of all admissions for
bronchiolitisin children under 5 years of age are related to
respiratorysyncytial virus.3
Summary points
Respiratory syncytial virus is still by farthe most common cause of viral lower respiratory
tract infectionin infants and children
Viral lower respiratory tract infections
are self limiting in most cases, and no treatment is
necessary
Passiveimmunisation against respiratory
syncytial virus is effectivein preventing
admission to hospital, although there is doubtabout its economic benefit
Debate is ongoing about whetherinfluenza
vaccination should be broadened to all age groups,including healthy children and adults
Development and implementationof
practical guidelines and educational programmes are
helpfulin the control of viral lower
respiratory tract infections
Influenza viruses also cause the most severe disease in the
youngest age group. A recent study showed that infants andyoung
children have a 12-fold increased risk of admission tohospital for
respiratory tract infection caused by influenzavirus compared with
children aged 5-17 years.5
The concomitant circulation of respiratory syncytial virus and
influenza during outbreaks has compromised the assessment ofthe
relative contribution of each virus to viral lower respiratorytract
infection in population based studies. The similarityin clinical
syndromes caused by respiratory syncytial virusand influenza was
shown in a recent community based observationalstudy in the United
Kingdom. This study showed that respiratorysyncytial virus and
influenza virus occur not only among peopleat the ends of the age
spectrum but also among people aged15-44 years and that in all age
groups more than 20% of influenza-likeillnesses 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 winterseason in
the Netherlands. Further serological studies revealedthat virtually
all children have been exposed to the virusby the age of 5 years.
Studies from several other countrieshave confirmed its role in
respiratory infections in both childrenand adults.89,w3,w4 The exact impact and
epidemiology ofhuman 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 syndromehas
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 morethan
25 countries. A causal association between severe acuterespiratory
syndrome and a newly identified coronavirus, distinctfrom the known
human coronaviruses, has been shown.10 So far,
infants and children do not seem to be a special risk groupfor the
syndrome, and only a few cases have been reported amongchildren
under 15 years of age. Very recently, the clinicalpresentation 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 respiratorytract
infection without systemic symptoms such as chills, rigor,and
myalgia. None of the children died. The clinical courseseemed to be
milder in young children than in teenagers andadults.
Box
1: Characteristics of severe acute respiratory syndrome
Most patients have been previously
healthy adults aged 25-70 years
Only a few suspected caseshave
been reported in children
Signs and symptoms
Incubationtime:2-7 days (may be up
to 10 days)
Prodromal signs: fever(> 38°C),
sometimes associated with headache, malaise,and myalgias
Lower respiratory signs: dry cough, dyspnoea
potentiallyprogressing to hypoxaemia,
necessitating artificial ventilationin
10-20% of cases
Case fatality rate: around 9%, but may bemuch higher depending on host and viral
factors
Milder coursein young children
than in teenagers and adults
Chest radiographs
Earlyfocal infiltrates progressing
to more generalised, patchy, interstitial
infiltrates in a substantial proportion of
patients
Abnormalitiesare indistinguishable
from bronchopneumonia due to other causes
Laboratoryabnormalities
Leukopenia with moderate lymphopenia
Elevatedliver enzymes
Treatment
No efficacious treatment is yet
known
Patients have been given a variety of
antibiotics activeagainst known
bacterial agents of atypical pneumonia and
antiviralagents such as oseltamivir or
ribavirin in combination withsteroids
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 toincreased
bacterial adhesion.w6 Despite this evidence for the
important role of preceding viral infections in the aetiologyof
bacterial respiratory infections, the real incidence ofclinically
important bacterial superinfection after viral lowerrespiratory
tract infection remains obscure. The proportionof children with
mixed viral and bacterial respiratory tract infection found in studies using
serology or antigen detectionin serum or urine has been reported to
be as high as 40%.12,w7 However, these methods
are inadequate for assessing the clinicalimportance of the bacterial
infection or the need for antimicrobialtreatment. Other studies,
using clinical methods, have shownthat the risk of serious
concurrent or secondary bacterialinfection in patients with viral
lower respiratory tract infectionis very low.13,w8
Signs and symptoms
Respiratory viruses cause a similar spectrum of respiratoryillness
in children, ranging from pharingitis, otitis media,laryngitis
subglottica, bronchitis, and tracheitis to bronchiolitisand
pneumonia. It is difficult to distinguish clinically betweenthe
causative agents. Infections usually start with rhinorrhoea,cough
and (non-obligate) fever. After one or two days the lowerrespiratory
tract may become involved, with signs of respiratory distress, including
tachypnoea, retractions, and cyanosis insevere cases. Life
threatening apnoea may occur in very younginfants, particularly in
infections with respiratory syncytialvirus. During infections with
influenza virus systemic symptomsmay 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 infantsand
patients with underlying pulmonary disease such as chroniclung
disease or cystic fibrosis; patients with congenital heartdisease,
especially those with pulmonary hypertension, arealso at risk. As
well as these well known risk groups, previouslyhealthy infants may
also deteriorate severely during virallower respiratory tract
infection. Extreme tachypnoea and hypoxaemiaare both associated with
subsequent deterioration. Unfortunately,the sensitivity of these
symptoms in identifying patients whowill deteriorate is very low.w9
Bronchiolitis and pneumonia are the most common manifestationsof
viral lower respiratory tract infection in infants. Differentiation
between these clinical syndromes is difficult as their definitionis
not based on standardised clinical criteria.w10 On the chestradiograph bronchiolitis is associated with air trapping and
hyperinflation with or without focal and patchy atelectasis,whereas
pneumonia lacks signs of hyperinflation and is characterisedby
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 basedon
entangling clinical criteria and so far does not seem tobe relevant
in daily clinical practice. However, increasinginsight into
pathophysiological differences in the clinicalmanifestations of
viral lower respiratory tract infection mayeventually lead to
specific treatment and preventive strategiesin subgroups of
patients, making an early specific diagnosis relevant.14
Additionally, the long term outcome of both groupsmight be
different, eventually needing a differentiated therapeuticapproach
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 causesevere infection in this high
risk population, with considerablemortality. The presence of upper
respiratory tract symptoms,wheezing, and interstitial or lobar
consolidation on the chestradiograph may help in differentiating
viral lower respiratorytract infection from other opportunistic
respiratory pathogens,but definite diagnosis depends on
demonstration of the virusin respiratory secretions by culture or
polymerase chain reactiontechniques. Pre-emptive treatment
strategies are being exploredin stem cell transplant recipients;
these use routine polymerasechain reaction techniques to monitor
viral load.
Children up to the age of 2 years infected with HIV have analmost
fourfold increased risk of severe infection caused byrespiratory
syncytial virus, parainfluenza virus, influenzavirus, and adenovirus
than children not infected with HIV.15In
addition, HIV infected children more often present withpneumonia
rather than bronchiolitis, more often have secondarybacterial
infection, and have a higher mortality than uninfected children.16
General considerations
Viral lower respiratory tract infections are usually self limiting. Preservation
of adequate fluid intake and correction of hypoxaemiaare mandatory
in mild disease. Although medical treatment israrely indicated in
immunocompetent patients, great variabilityexists in the management
of these patients.17,w14 Wilson etal
showed that this variability does not affect clinical outcomebut
correlates significantly with costs associated with virallower
respiratory tract infections.18 No strict
guidelinesexist on when to admit or discharge children with a viral
lowerrespiratory tract infection, but in daily practice physicians'
discretion in decision making and factors associated with socioeconomicstatus are important determinants.19
Implementation of educationalprogrammes and practical guidelines
have been shown to be costsaving 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 virallower
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 importantin 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 thecontribution of these
phenomena to airway obstruction. Futurestudies should focus on the
identification of probable respondersand non-responders to this form
of treatment.
Corticosteroids
The efficacy of corticosteroids has been evaluated mainly ininfants
and children with respiratory syncytial virus disease,with
disappointing results in mild disease. Very recently ourgroup found
that corticosteroids may be beneficial in artificiallyventilated
patients with severe bronchiolitis but had no effectin patients with
pneumonia.14 These findings support the ideathat corticosteroids may be beneficial in certain patientswith
a severe course of disease and that distinction betweenclinical
manifestations of viral lower respiratory tract infection
(bronchiolitis and pneumonia) is important in the evaluationof
certain treatment strategies.
Antiviral treatment Respiratory syncytial virusRibavirin is a synthetic nucleoside analogue
with in vitro activity against respiratorysyncytial virus.w31
However, on the basis of the currentlyavailable evidence, the
routine use of ribavirin has no placein patients with respiratory
syncytial virus infection.
Influenza virusAlthough neuraminidase inhibitors are effective
against influenza viruses, infections are relativelymild and self
limiting in healthy children. On the other hand,costs attributable
to influenza virus infections may be veryhigh, particularly in
infants and children.21 The goal of
treatment with neuraminidase inhibitors therefore should be epidemiological
control of disease rather than reducing theduration 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 antimicrobialresistance this overuse should be reduced and future studies
should focus on mechanisms and risk factors for bacterial superinfectionin children with viral lower respiratory tract infection, as
well as on accurate tests to differentiate viral from bacterial disease.
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 theefficacy 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 another10 years before
routine vaccination becomes available.w33
Disappointing results in the development of an active vaccinehave
forced research in the prevention of respiratory syncytialvirus to
focus on other strategies. Passive immunisation withintravenous
hyperimmune globulins against respiratory syncytialvirus has proved
to be beneficial in preventing severe diseasein children at high
risk.23 However, practical problems havelimited its use and further research and have led to the developmentof an intramuscular applicable IgG humanised monoclonal antibodydirected against the F protein of respiratory syncytial virus
(palivizumab). A controlled trial has shown that monthly injections
with palivizumab reduce respiratory syncytial virus relatedhospital
admissions in children at high risk by more than 50%.24
Several reports on experiences in the field have confirmedthe 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 thatguidelines can
not be generalised but should be based on nationalhospital admission
data for respiratory syncytial virus.2526
Inactivated intramuscular influenza vaccine as both cold adapted
and live attenuated intranasal vaccines have been shown tobe safe
and effective in children from 1 year of age onwards,w35 but
immunogenicity is poor in children younger than 6 months.27Although influenza is usually a mild and self limiting disease,
children with underlying chronic medical conditions are atrisk of
severe disease, and vaccination against influenza virushas 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 benefitsin all age groups, debate is
ongoing about whether influenzavaccination should be broadened to
all age groups, includinghealthy children and adults.28
Box
2: Treatment of viral lower respiratory tract infection
Bronchodilatoragents
Studied in viral bronchiolitis irrespective of
the viralcause
Most well designed trials show at best a minor
beneficial effectw15-w17
Two meta-analyses have shown a statisticallysignificant but clinically irrelevant
beneficial effectw18,w19
Corticosteroids
Mainlystudied in patients with
(respiratory syncytial virus) bronchiolitis
Mostwell designed trials showed no
beneficial effect of systemicor
topical corticosteroids in patients with mild to
moderate bronchiolitisw20-w22
A meta-analysis indicated a beneficialclinical effect of systemic corticosteroids
in patients withmoderate or severe
bronchiolitisw23
A recent trial indicateda
beneficial effect in a subgroup of patients with
bronchiolitis14
Antiviraltreatment
Respiratory syncytial virus
Ribavirin aerosol isnot effective in
immune competent patients and is restricted
to immunocompromised patients with severe respiratory
syncytial virus disease, although this practice is not
supported by randomised controlled trials4
Parainfluenza virus and adenovirus
Nospecific treatment is available
Ribavirin has been used in
immunodeficient patients, although this is mainly
based oncase reports and small series
of heterogeneous patient populationsw24
Influenzavirus
Ribavirin aerosol is not effective in
immunocompetent patients,w25 and its
efficacy in immunodeficient patients is unclear
Oral amantadine and rimantadine (M2 protein
inhibitors)have been shown to shorten
disease by one day in adults and
children over 1 year of age with influenza A when
given within48 hours of the start of
symptomsw26
Nasal zanamivir and oral
oseltamivir (neuraminidase inhibitors) are
effective in preventingand treating
influenza A and B in adultsw27
Oseltamivir isalso beneficial in
children aged 1-12 yearsw28
The neuraminidaseinhibitors are
preferred to the M2 inhibitors as they havea broader antiviral activity, have less
tendency for the development of resistance, and
are better toleratedw27
Antibiotics
Antibioticsdo not influence the course of
viral lower respiratory tractinfectionw29,w30
Additional educational resources
Useful articles
Nichol KL,Mallon KP, Mendelman PM. Cost
benefit of influenza vaccination in healthy, working
adults: an economic analysis based on the
results of a clinical trial of trivalent live attenuated
influenzavirus vaccine. Vaccine 2003;21: 2216-26[Medline]
Hall CB. Respiratorysyncytial virus and
parainfluenza virus. N Engl J Med 2001;344: 1917-28[Free Full Text]
Hament JM, Kimpen JL, Fleer A, Wolfs TF. Respiratoryviral infection predisposing for bacterial
disease: a concisereview. FEMS Immunol Med Microbiol
1999;26: 189-95[CrossRef][ISI][Medline]
MeissnerHC. Uncertainty in the management
of viral lower respiratorytract disease.
Pediatrics 2001;108: 1000-3[Free Full Text]
Patel H, PlattR, Lozano JM, Wang EEL.
Glucocorticoids for acute viral bronchiolitisin hospitalized infants and young children
(protocol for aCochrane review). In:
Cochrane Library, Issue 2. Oxford: Update
Software, 2003
Viral lower respiratory tract infections in infants and childrenare
an important medical and socioeconomic problem worldwide.Viral lower
respiratory tract infections are mild and selflimiting in most
cases. Particular patient groups are at riskof a severe course of
disease, although previously healthy infants with a viral lower respiratory
tract infection may alsodevelop severe disease.
Treatment for moderate viral lower respiratory tract infectionis
mainly supportive. Lack of means to control viral lowerrespiratory
tract infection has led to great variation in management worldwide.17,w14 Development of practical guidelines and
educationalprogrammes in both clinical and outpatient settings may
behelpful and cost saving in the control of viral lower respiratorytract infection in infants and children.
Contributors: JBMvW drafted the original manuscript. All threeauthors jointly wrote the final paper.
Competing interests: JBMvW and JLLK have received fees for
giving presentations at symposia organised by Abbot Laboratories, manufacturerof palivizumab.
Miedema CJ, Kors AW, Tjon a Ten WE, Kimpen JLL. Medical
consumption and socioeconomic effects of infection with respiratory
syncytial virus in the Netherlands. Pediatr Infect Dis J 2001;20:
160-3.[CrossRef][ISI][Medline]
Shay DK, Holman RC, Newman RD, Liu LL, Stout JW, Anderson
LJ. Bronchiolitis-associated hospitalizations among US children,
1980-1996. JAMA 1999;282: 1440-6.[Abstract/Free Full Text]
Muller-Pebody B, Edmunds WJ, Zambon MC, Gay NJ, Crowcroft
NS. Contribution of respiratory syncytial virus to bronchiolitis and
pneumonia-associated hospitalizations in English children, April
1995-March 1998. Epidemiol Infect 2002;129: 99-106.[ISI][Medline]
Izurieta HS, Thompson WW, Kramarz P, Shay DK, Davis RL,
DeStefano F, et al. Influenza and the rates of hospitalization for
respiratory disease among infants and young children. N Engl J Med
2000;342: 232-9.[Abstract/Free Full Text]
Zambon MC, Stockton JD, Clewley JP, Fleming DM. Contribution
of influenza and respiratory syncytial virus to community cases of
influenza-like illness: an observational study. Lancet 2001;358:
1410-6.[CrossRef][ISI][Medline]
Van den Hoogen BG, de Jong JC, Groen J, Kuiken T, de Groot
R, Fouchier RA, et al. A newly discovered human pneumovirus isolated from
young children with respiratory tract disease. Nat Med 2001;7:
719-24.[CrossRef][ISI][Medline]
Peret TC, Boivin G, Li Y, Couillard M, Humphrey C, Osterhaus
AD, et al. Characterization of human metapneumoviruses isolated from
patients in North America. J Infect Dis 2002;185: 1660-3.[CrossRef][ISI][Medline]
Greensill J, McNamara PS, Dove W, Flanagan B, Smyth RL, Hart
CA. Human metapneumovirus in severe respiratory syncytial virus
bronchiolitis. Emerg Infect Dis 2003;9: 372-5.[ISI][Medline]
Ksiazek TG, Erdman D, Goldsmith CS, Zaki SR, Peret T, Emery
S, et al. A novel coronavirus associated with severe acute respiratory
syndrome. N Engl J Med 2003;348: 1953-66.[Abstract/Free Full Text]
Hon K, Leung CW, Cheng W, Chan P, Chu W, Kwan YW, et al.
Clinical presentations and outcome of severe acute respiratory syndrome in
children. Lancet 2003;361: 1701-3.[CrossRef][ISI][Medline]
Korppi M, Leinonen M, Koskela M, Makela PH, Launiala K.
Bacterial coinfection in children hospitalized with respiratory syncytial
virus infections. Pediatr Infect Dis J 1989;8: 687-92.[ISI][Medline]
Hall CB, Powell KR, Schnabel KC, Gala CL, Pincus PH. Risk
of secondary bacterial infection in infants hospitalised with respiratory
syncytial viral infection. J Pediatr 1988;113: 266-71.[ISI][Medline]
Van Woensel JBM, van Aalderen WMC, de Weerd W, Jansen NJG,
van Gestel JPJ, Markhorst DG, et al. The efficacy of dexamethasone in the
treatment of patients mechanically ventilated for lower respiratory tract
infection caused by respiratory syncytial virus: a randomized controlled
trial. Thorax 2003;58: 383-7.[Abstract/Free Full Text]
Madhi SA, Schoub B, Simmank K, Blackburn N, Klugman KP.
Increased burden of respiratory viral associated severe lower respiratory
tract infections in children infected with human immunodeficiency virus
type-1. J Pediatr 2000;137: 78-84.[CrossRef][ISI][Medline]
Graham SM, Gibb DM. HIV disease and respiratory infection
in children. Br Med Bull 2002;61: 133-50.[Abstract/Free Full Text]
Kimpen JLL, Schaad UB. Treatment of respiratory syncytial
virus bronchiolitis: 1995 poll of members of the European Society for
Paediatric Infectious Diseases. Pediatr Infect Dis J 1997;16:
479-81.[CrossRef][ISI][Medline]
Wilson DF, Horn SD, Hendley JO, Smout R, Gassaway J. Effect
of practice variation on resource utilization in infants hospitalized for
viral lower respiratory illness. Pediatrics 2001;108: 851-5.[Abstract/Free Full Text]
McConnochie KM, Roghmann KJ, Liptak GS. Hospitalization for
lower respiratory tract illness in infants: variation in rates among
counties in New York State and areas within Monroe County. J Pediatr
1995; 126: 220-9.[ISI][Medline]
Adcock PM, Sanders CL, Marshall GS. Standardizing the care
of bronchiolitis. Arch Pediatr Adolesc Med 1998;152: 739-44.[Abstract/Free Full Text]
Neuzil KM, Mellen BG, Wright PF, Mitchel EF Jr, Griffin MR.
The effect of influenza on hospitalizations, outpatient visits, and
courses of antibiotics in children. N Engl J Med 2000;342: 225-31.[Abstract/Free Full Text]
Simoes EA, Tan DH, Ohlsson A, Sales V, Wang EE. Respiratory
syncytial virus vaccine: a systematic overview with emphasis on
respiratory syncytial virus subunit vaccines. Vaccine 2001;20:
954-60.[CrossRef][ISI][Medline]
Groothuis JR, Simoes EAE, Levin MJ, Hall CB, Long CE,
Rodriguez WJ. Prophylactic administration of respiratory syncytial virus
immune globulin to high-risk infants and young children. N Engl J Med
1993;329: 1524-30.[Abstract/Free Full Text]
The Impact-RSV Study Group. Palivizumab, a humanized
respiratory syncytial virus monoclonal antibody, reduces hospitalization
from respiratory syncytial virus infection in high-risk infants.
Pediatrics 1998;102: 531-7.[Abstract/Free Full Text]
Clark SJ, Beresford MW, Subhedar NV, Shaw NJ. Respiratory
syncytial virus infection in high risk infants and the potential impact of
prophylaxis in a United Kingdom cohort. Arch Dis Child 2000;83:
313-6.[Abstract/Free Full Text]
Roeckl-Wiedmann I, Liese JG, Grill E, Fischer B, Carr D,
Belohradsky BG. Economic evaluation of possible prevention of respiratory
syncytial virus-related hospitalizations in premature infants in Germany.
Eur J Pediatr 2003;162: 237-44.[ISI][Medline]
Clements ML, Makhene MK, Karron RA, Murphy BR, Steinhoff
MC, Subbarao K, et al. Effective immunization with live attenuated
influenza A virus can be achieved in early infancy. J Infect Dis
1996;173: 44-51.[ISI][Medline]
Nichol KL, Mallon KP, Mendelman PM. Cost benefit of
influenza vaccination in healthy, working adults: an economic analysis
based on the results of a clinical trial of trivalent live attenuated
influenza virus vaccine. Vaccine 2003;21: 2216-26.[Medline]
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.
"A foolish faith in authority is the worst enemy of truth."
-- Albert Einstein, letter to a friend, 1901
"I know of no safe depository of the ultimate powers of the society but the people themselves, and if we think them not enlightened enough to exercise control with a wholesome discretion, the remedy is not to take it from them, but to inform their discretion by education."
-- Thomas Jefferson, letter to William C. Jarvis, September 28, 1820
"What's the point of vaccination if it doesn't protect you from the unvaccinated?"
-- Sandy Gottstein
"Who gets to decide what the greater good is and how many will be sacrificed to it?"