The peak incidence of bacterial RS occurs between the
ages of 3 and 6 years, similar to the peak years for URIs.[2] Children average 6
to 8 colds a year (more in day care and with multiple siblings), and unless
complicated by bacterial RS, these self-limited infections should resolve within
7 to 10 days.[3]
Allergic rhinitis is an inflammation of the mucous
membranes of the nose, whereas RS is an inflammation of the mucous membranes of
the nasal passages and sinuses. Nasal allergies cause itching and sneezing,
clear rhinorrhea, stuffiness, and postnasal drainage. These symptoms are similar
to those of RS and a common cold. Complete history and physical exam, and often
accompanying imaging help make the correct diagnosis. Allergies also can
contribute to swelling in the sinus and nasal mucous membranes. The swelling can
lead to blockage of the natural openings, trapping bacteria and leading to
infection.
There is controversy surrounding treatment, despite the
fact that RS has a significant adverse effect on health related quality of life.
Many practitioners feel that the disease process is self-limited, rarely needs
antibiotic therapy and almost never requires surgical treatment. Others believe
that these infections require aggressive medical therapy and surgical treatment
when medical therapy fails. The answer is somewhere between these viewpoints,
and it is essential to consider each case individually to avoid serious
complications.
Definitions
Sinusitis is an infection of the mucosa of the
paranasal sinuses. Rhinosinusitis is a better term than sinusitis alone,
since inflammation and infection of the sinuses involves changes in the nasal
epithelium with concurrent nasal airway inflammation. RS is generally divided
into 3 varieties: acute, chronic, and
recurrent.
Acute RS commonly presents as a URI that persists
beyond 10 days with some combination of the following signs and symptoms:
purulent rhinorrhea, persistent cough that is often worse at night, bad breath,
fever, headache, and facial pain. Since most viral URIs resolve within 10 days,
a worsening or persistence of these symptoms beyond this time has been
empirically viewed as RS by practitioners for the purpose of prescribing
antibiotics. Acute bacterial RS that is severe may present with the same
symptoms, but is accompanied by greater toxicity, fever greater than 102.2° F,
and the duration of symptoms observed may be less than 10 days. This is a less
common presentation and can only be objectively differentiated from an acute
viral URI with a CT scan or plain films.
Chronic RS is an infection of greater than 3
months duration, usually with a more benign course. Symptoms include nasal
congestion, cough, bad breath, malaise, decreased energy, headache, behavioral
problems, and nasal discharge. Exacerbation to acute RS is common in children
with chronic RS.
Recurrent acute RS occurs when a child has
complete resolution of an acute infection, but has repeated incidents. Some
element of chronic RS is likely to be present between acute infections, but this
cannot be determined without imaging.
Pathophysiology
Human beings have ethmoid sinuses on either side of the
upper nose, bilateral maxillary sinuses in the
face between the orbital rim and the upper
teeth, and frontal sinuses above the eyes. The sphenoid sinus is in the back of
the nose, at the base of the skull, and is divided by a septum. Because of its
relative isolation, the sphenoid sinus is the least likely sinus to become
infected.
The mucus membrane of each sinus has cilia that move the
mucus to the sinus ostia for clearance through the nose. Maxillary drainage
involves a cilia-dependent upward movement that joins the drainage of the
anterior ethmoid air cells in a functional unit called the ostiomeatal complex.
This area is believed to be the focus of edema during a viral illness, resulting
in obstruction of the maxillary, frontal and anterior ethmoid
drainage.
The failure of normal mucus transport (mucociliary
transport) and decreased sinus ventilation are the major factors contributing to
the development of RS. Obstruction of the sinus ostia occurs with mucosal edema
or anatomic blockage, such as polyps, interfering with sinus drainage. Polyps
are a common product of chronic allergic RS (Figures 1, 2). Noninfectious
inflammation, such as allergic rhinitis can also block the ostia and lead to
RS.

FIGURE 1: Typical nasal polyp seen through a nasal telescope.

FIGURE 2: Sphenochoanal polyp in the nasopharynx visualized with a mirror in
the oral cavity. This is an unusual presentation that can occur with chronic
RS.
Cilia can beat only in a fluid medium. Alteration of cilia number, morphology
and function may facilitate secondary bacterial invasion of the nose and
sinuses. In addition to viral URI and allergic inflammation, factors
predisposing the formation of bacterial RS include, adenoid hypertrophy and
infection, cystic fibrosis, immune disorders (especially IgG subclass
deficiency), primary ciliary dyskinesia, trauma, swimming and diving, rhinitis
medicamentosa, choanal atresia, deviated septum, nasal polyps, foreign body,
tumor, dental infections, inhalation of irritants, mechanical ventilation, nasal
dryness, nasotracheal and nasogastric tubes, and gastroesophageal reflux disease
(GERD).
Diagnosis
On physical exam, the patient with acute bacterial RS may
have mucopurulent discharge in the nose or posterior pharynx, with an
erythematous nasal mucosa, but this can occur with acute viral rhinitis as well.
Transillumination may be helpful in adolescents and adults, but does not tell
much in children under 10 years of age, since frontal sinuses are not yet fully
developed. In young children, the physical exam is generally not very helpful
for making a specific diagnosis of acute bacterial RS. Although
otolaryngologists may decongest the nose and use a telescope to view pus coming
directly from the middle meatus, this is not practical for
pediatricians.
One sign that does not predict acute bacterial RS is
rhinorrhea that changes color from clear to cloudy or colored. This event
coincides with migration of polymorphonuclear leukocytes into nasal secretions
and occurs during the natural course of viral URIs.
All children with persistent RS should be evaluated for
allergies to assess the role they play in the etiology. Therapy then can be
directed towards decreasing the allergic response.
Getting culture from nasal discharge, the throat, or the
sinus is not necessary for diagnosis of bacterial RS. Culture of nasal discharge
or the nasopharynx lacks predictive reliability, both for establishing the
diagnosis and for identifying the infective pathogen when acute bacterial RS is
actually present. Organisms recovered from nasopharyngeal washing and throat
culture do not reflect the organisms found in sinus
aspirate.
Needle puncture of the maxillary sinus to get a culture
is impractical and unnecessary in immunocompetent children with uncomplicated
disease, and should be reserved for special circumstances. It is reasonable to
get a culture of the sinus under controlled conditions in the operating room
when a patient is not responding to antibiotics, is immune suppressed, or
beginning to show signs of complications.
The radiographic finding most diagnostic of bacterial RS
is an air-fluid level in, or complete opacification of the sinus cavities.
Standard radiographic projections include anteroposterior, lateral and
occipitomental (Waters projection) views. Complete opacification in a plain
radiograph in a symptomatic patient has a specificity of 85%, and an air-fluid
level has a specificity of 80% in establishing the diagnosis. When clinical
signs and symptoms suggesting acute RS are accompanied by abnormal maxillary
sinus films, bacteria in a sinus aspirate will be present 70% to 75% of the
time.[4]
Computed tomography (CT) scans (Figures 3, 4) are the
best way to view the extent of disease and are reserved for children with
chronic RS, acute RS unresponsive to therapy or for evaluation of complications.
Limited coronal views without contrast will provide information and use the
least amount of radiation, however these studies may not be as sensitive in
identifying the osteomeatal complex.

FIGURE 3: Moderate bilateral maxillary sinus mucosal thickening with
blockage of both osteomeatal complexes in a coronal CT scan.

FIGURE 4: Complete opacification of the right maxillary sinus in a caronal
CT scan.
However, CT scans can overdiagnose RS. In a study of infants and children,
97% of patients who had a cold during the 2 weeks preceding cranial CT performed
for other purposes had mucosal abnormalities suggesting bacterial RS.[5]
Abnormalities of the sinuses also are found frequently on conventional
radiographs and CT scans in children without clinical evidence of sinusitis. MRI
is not the best imaging modality for evaluation the bone/mucus membrane
interface of the sinuses.
The American
College of Radiology has taken the
position that the diagnosis of acute uncomplicated RS in children, especially if
they are less than 6 years of age, should be made on clinical grounds alone,
since the films are technically difficult on young children, and images should
be reserved for worsening clinical circumstance.[6] Similarly, the Subcommittee
on Management of Sinusitis and Committee on Quality Improvement of the
American
Academy of Pediatrics stated that
imaging studies are not necessary to confirm a diagnosis of clinical sinusitis
in children less than 6 years of age.[7] They did not make a recommendation for
older children, leaving open the possibility that imaging may be necessary in
this age group.
Microbiology
Children and adults have similar RS bacteriology. The
predominant organisms include Streptococcus pneumoniae, Moraxella catarrhalis, and Hemophilus influenzae, found in
approximately 75% of maxillary sinus aspirates. Both H influenzae and M catarrhalis may produce
beta-lactamase and are amoxicillin resistant.
The role of bacteria in chronic RS is controversial,
since there may be disease in the absence of bacterial growth, as described
below. Group A streptococci, Staphylococcus aureus, and enteric
bacilli have been cultured in children with chronic RS, but 20% to 35% of sinus
aspirates are sterile. Treatment with antibiotics in such cases most likely will
not be effective. These patients are candidates for surgery to create better
drainage, if medicines fail.
Fungi are normal flora of the
upper airway, but can cause acute RS in
immunocompromised and diabetic patients, with invasion that leads to life
threatening disease. The noninvasive forms of fungal RS, mycetoma (fungus ball)
and allergic fungal sinusitis, are likely caused by an IgE-mediated
hypersensitivity to a fungus, and are not life threatening. Aspergillus is the most common
organism cultured, but several other fungal species have been identified.
Bacterial RS and noninvasive fungal infection can look alike and are difficult
to distinguish radiographically, except when there is a distinct fungal ball or
mycetoma. Noninvasive disease has an indolent, often asymptomatic and benign
course. Invasive disease is accompanied by severe toxicity, and inflammation and
necrosis in the nose, sinuses, and surrounding
tissues.
Treatment
The treatment of acute RS is directed at the predominant
organisms. Physicians should consider use of the most narrow spectrum antibiotic
for the initial treatment. Risk factors to consider for penicillin-resistant
S pneumoniae include day care,
recent antimicrobial therapy (less than 30 days), age less than 2 years, and
exposure to environmental tobacco smoke. In a child without these risk factors,
standard dose amoxicillin or amoxicillin/ clavulanate may be considered as
initial therapy. In children with the above risk factors, high dosage
amoxicillin (80-90mg/kg/day) or amoxicillin/clavulanate with a high dosage
amoxicillin component may be used as first-line
therapy.
Cefprozil, cefdinir, cefuroxime, and cefpodoxime are
reasonable choices as secondline agents. Third-line agents with failure of above
include clindamycin and cefixime. In penicillin allergic patients, second- or
third-line agents, in addition to the macrolides and azilides may be considered.
The efficacy of macrolides (erythromycin, clarithromycin), azilides
(azithromycin) and sulfa containing agents has not been
established.
The duration of therapy should be a minimum of 10 to 14
days and is often continued for several weeks depending on the clinical
response. If no improvement occurs or there is worsening after 72 hours, a
change in antibiotics should be considered. Optimum duration of therapy in acute
disease has never been proven in scientific trials, although recommendations
typically include 10 to 21 days, or until symptoms resolve, plus an additional 7
days.[8] In patients with persistent or recurrent RS, it is important to
consider an otolaryngology consultation after antibiotic therapy of at least 6
weeks duration or 3 separate courses of unsuccessful
treatment.
Patients with severe acute RS who cannot take oral
therapy may require initial parenteral therapy. Therapy by intravenous injection
has not been shown to be superior to oral therapy for acute RS in the absence of
complications.
Successful treatment of chronic RS with antibiotics is
critical because failure will usually lead to surgical therapy. There are many
conflicting studies regarding adjuvant therapy, and the efficacy of nasal
steroids, saline spray, oxymetazolone, mucolytics, and antihistamines has not
been established. Saline spray may help clear nasal secretions, and
antihistamines may be beneficial in children with RS where allergy is suspected
as a causative factor. Control of causative factors, including allergy and GERD,
is important in the prevention and treatment of recurrent or chronic
infections.
Surgical therapy is indicated for children with chronic
RS or recurrent acute RS who have failed maximum medical therapy, including
treatment of any underlying disease. Occasionally, it is necessary to drain an
acute infection unresponsive to antibiotic therapy for relief of severe
symptoms.
Adenoid tissue serves as a reservoir of bacterial
pathogens. Adenoidectomy for enlarged adenoids is almost always the first-line
intervention for preschoolers, with a 70% to 80% expected rate of improvement.
The procedure is safe, has minimal morbidity, and no effect on long-term immune
function.
For treatment of chronic disease, functional endoscopic
sinus surgery (FESS) has replaced the creation of nasal antral windows in
children. The technique is designed to alleviate the cause of RS, which is
mechanical obstruction to drainage at the ostiomeatal complex, with a net effect
of widening the outflow tract. The natural ostia are enlarged while preserving
most or all of the sinus mucosa. Surgical outcome is dependent on the degree of
mucosal disease present before the operation. With careful patient selection,
the published results indicate 80% to 100% improvement with surgery.[9] FESS
should only be performed in children by an otolaryngologist experienced in
pediatric sinus surgery. The incidence of major complications in experienced
surgeons is less than 1%.[10]
Complications
In the era of antibiotic therapy and adequate access to
primary care, major complications are uncommon. Complications of RS can be
divided into orbital, intracranial, and local.
Orbital complications are the most common category, and
include orbital cellulitis, orbital abscess, optic neuritis or retrobulbar
neuritis, superior orbital fissure syndrome, and cavernous sinus thrombosis.
Seventy five percent of orbital infections are a direct result of
RS.
Intracranial complications are the second most common
category, and include intracranial mucocoele, meningitis, epidural abscess, and
subdural abscess. Finally, brain abscess, which has a high mortality rate, also
is a possible complication of RS.
Local complications include the formation of mucocoeles
and pyoceles, which may enlarge and cause bone erosion, pain, and swelling over
the sinus. Other local manifestations include osteitis, especially of the
maxillary sinus, with swelling and erythema of the cheek and osteomyelitis of
the frontal or maxillary sinus, and rarely, the sphenoid
bone.
What's new?
RS is complex and we are far from completely
understanding all aspects of this disease. Clinical trials that target its
various causes will help clinicians understand better how to prevent and treat
RS.[11] Some of the more promising research directions are listed
below:
• Aerosolized antimicrobials and steroids are widely
prescribed now, but evidence of their effectiveness has not been established and
is being evaluated.
• No studies have established the role of vaccines in
prevention of acute RS and chronic RS, but it is reasonable to expect that
severely affected children would benefit from the conjugated pneumococcal
vaccine.
• Biofilms can develop in patients with chronic disease.
A film of glycocalyx may protect bacteria from contact with antimicrobials,
explaining the poor response to medical therapy in some
patients.
Summary
RS is a common pediatric infection that usually responds
well to medical therapy. The goal for clinicians is to prevent complications and
improve quality of life for children with this disease. Treatment depends on
accurate diagnosis, identification and correction of underlying contributing
factors, as well as adequate antimicrobial therapy. Surgery, including
adenoidectomy and functional endoscopic sinus surgery, is effective in selected
patients who are refractory to more conservative measures, and in patients with
complications of RS.
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Jenson HB. Management of acute bacterial rhinosinusitis. Current Opinion in
Pediatrics 2002;14:86-90.
[3.] Aitken M,
Taylor JA. Prevalence of clinical sinusitis in
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[4.] Wald ER,
Milmoe GJ. Bowen A, et al. Acute maxillary sinusitis in children. N Engl J Med
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[5.] Glasier
CM, Ascher DP, Williams KD. Incidental paranasal sinus abnormalities on CT of
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[6.] AAP
Subcommittee on Management of Sinusitis and Committee on Quality Improvement.
Clinical practice guideline: Management of sinusitis. Pediatrics
2001;108:798-808.
[7.] American College of Radiology Expert Panel on Pediatric
Imaging. Sinusitis in the pediatric population. ACR Appropriateness Criteria,TM
1999. Available at: http://www.acr.org/ac_pda. Accessed July
21, 2005.
[8.] Morris P,
Leach A. Antibiotics for persistent nasal discharge (rhinosinusitis) in
children. Cochrane Database of Systematic Reviews 2;
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[9.] Goldsmith
AJ, Rosenfeld RM. Treatment of pediatric sinusitis. Pediatric Clin N Am
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[10.] Hebert
RL, Bent JP. Meta-analysis of outcomes of pediatric functional endoscopic sinus
surgery. Laryngoscope 1998;108:796-799.
[11.] Meltzer
EO, et al. Rhinosinusitis: Establishing definitions for clinical research and
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