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ABSTRACT
New treatment guidelines for acute rhinosinusitis outline
when antibiotic therapy is appropriate, as well as describe
evidence-based treatment to relieve symptoms, prevent
complications, and prevent chronic disease.
Keywords: acute rhinosinusitis, inflammation, IDSA, antibiotics, bacterial
Key points
Clinical diagnosis is the most commonly used and costeffective approach to distinguish between viral and
bacterial rhinosinusitis.
2012 guidelines from the IDSA provide current evidencebased recommendations for treatment of rhinosinusitis.
Empiric antibiotic therapy should be reserved for patients
with symptoms of acute bacterial rhinosinusitis that have
persisted for more than 10 days or been severe for more
than 3 days.
The IDSA guidelines are based on data showing increased
resistance to previously accepted antimicrobial therapy
as well as an increase in the incidence of Haemophilus
influenzae and Moraxella catarrhalis as causative
pathogens of acute bacterial rhinosinusitis.
Copyright 2013 Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited.
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treatment for acute bacterial rhinosinusitis includes antibiotics to eradicate the infection, prevent complications,
and prevent chronic disease.6
Nonpharmacologic therapy Most healthcare providers
will recommend nonpharmacologic treatments such as
increased fluid intake, rest, and good personal hygiene.
Water is the recommended fluid for avoiding dehydration
and keeping mucous membranes moist, with increased
intake requirements for illness. An adequate amount of rest
provides time to fight off infection and is important for a
prompt recovery. Proper hand washing techniques reduce
the spread of virus and bacteria that cause rhinosinusitis
and other illnesses.7
Ancillary therapy Common ancillary therapies include
saline nasal spray, mucolytic agents, antipyretics/analgesics, decongestants, and antihistamines, but not all are
favored by the IDSA guidelines. Saline spray can be used
to irrigate the nasal cavity to soften secretions and improve
mucociliary clearance.8 The IDSA guidelines recommend
the use of nasal saline spray as an adjunctive treatment for
rhinosinusitis in adults with low to moderate symptoms.3
The most common mucolytic agent is guaifenesin, which is
used to thin mucus secretions and improve drainage.6 No
clinical trials validate the use of guaifenesin, so the IDSA
guidelines do not recommend it as adjunctive therapy for
acute rhinosinusitis.3 Analgesics are used to relieve pain, and
help patients to rest. Acetaminophen or an NSAID may be
used for mild to moderate pain.8 Acetaminophen is also an
effective antipyretic. Oral or topical decongestants and/or
antihistamines are not recommended as adjunctive treatment in patients with acute bacterial rhinosinusitis because
of their adverse effects in adults and children.3 Topical
decongestants may induce inflammation and rebound
congestion.6 Oral antihistamines may cause drowsiness
and xerostomia.6 The FDA recommends that these drugs,
found in OTC products, not be given to children younger
than 2 years because of their potentially serious adverse
reactions.3
Antibacterial therapy According to the IDSA guidelines, antibacterial therapy should be initiated as soon as
the diagnosis of acute bacterial rhinosinusitis has been
established. The recommended first-line drug for both
children and adults is amoxicillin-clavulanate.3 Acute
bacterial rhinosinusitis caused by Haemophilus influenzae and Moraxella catarrhalis has increased in children;
and amoxicillin-clavulanate offers greater coverage of
ampicillin-resistant strains of these bacteria. Doxycycline
may be used as an alternative for empiric therapy for
patients who cannot tolerate amoxicillin-clavulanate. In
patients with a penicillin allergy, the recommendations
include doxycycline or a respiratory fluoroquinolone such
as levofloxacin or moxifloxacin. Because of high rates of
resistance among Streptococcus pneumoniae, macrolides,
trimethoprim-sulfamethoxazole, or third-generation
cephalosporins are not recommended for empiric therapy.
Volume 26 Number 7 July 2013
Copyright 2013 Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited.
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