Update on the management of chronic rhinosinusitis
Infection and Drug Resistance
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Update on the management of chronic
rhinosinusitis
This article was published in the following Dove Press journal:
Infection and Drug Resistance
22 January 2013
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Rachel B Cain
Devyani Lal
Department of Otorhinolaryngology,
Mayo Clinic, Phoenix, AZ, USA
Introduction
Correspondence: Devyani Lal
Department of Otorhinolaryngology,
Mayo Clinic, 5777 East Mayo Boulevard,
Phoenix, AZ 85054, USA
Tel +1 480 342 2928
Fax +1 480 342 2626
Email
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http://dx.doi.org/10.2147/IDR.S26134
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Abstract: Chronic rhinosinusitis (CRS) is a common disorder characterized by mucosal
inflammation of the nose and paranasal sinuses with sinonasal symptoms persisting for greater
than 12 weeks. The etiology of CRS is incompletely understood. Current understanding supports
inflammation, rather than infection, as the dominant etiologic factor. CRS significantly impacts
patients’ quality of life and health care expenditure. There is no standard management of CRS.
Treatment strategies differ based on divergent etiologies of the various CRS subclasses. Both
systemic and topical agents are used. These interventions differ in CRS with nasal polyposis
(CRSwNP), CRS without nasal polyposis (CRSsNP) and specific situations such as allergic
fungal rhinosinusitis or aspirin-exacerbated respiratory disease. Antibiotics are the most commonly prescribed medication for CRS, but their role in management is not strongly supported by
high-level studies. This paper provides a succinct review of the evidence supporting or refuting
common therapeutic agents in the management of CRS. Novel and emerging strategies will
also be discussed.
Keywords: review, evidence-based, sinusitis
Chronic rhinosinusitis (CRS) is diagnosed when specific sinonasal symptoms
lasting 12 or more weeks are confirmed by nasal endoscopy or radiographic imaging
(Figure 1).1 CRS is best considered as a group of heterogeneous disorders from a
multitude of causes that result in mild to severe symptomatic inflammation of the
sinonasal mucosa (Figure 2).2 The management of this complex and diverse disease is
therefore a challenge. Much ongoing research is being directed toward the investigation of treatment strategies, as well as developing criteria for diagnosing the various
CRS subsets. The most simplified classification divides CRS into those patients who
have nasal polyps (CRSwNP) and those without (CRSsNP) (Figure 3).3
Medical therapy of CRS is a key strategy, with surgery playing a vital adjunctive
role. Medical therapy is directed toward treatment of the underlying etiology, as well
as the resultant inflammation. A variety of systemic and topical therapeutic agents are
commonly employed. These include corticosteroids, antimicrobials, and immune modulating medications. As CRS is a chronic disease, there are concerns related to the use
of systemic agents over prolonged periods. Long-term use of corticosteroids and antibiotics may lead to adverse effects, drug interactions, and antimicrobial resistance. The
development of topical therapy delivered directly to the sinonasal cavity has created an
alternative treatment strategy to help potentiate these concerns. Many therapeutic agents
Infection and Drug Resistance 2013:6 1–14
© 2013 Cain and Lal, publisher and licensee Dove Medical Press Ltd. This is an Open Access article
which permits unrestricted noncommercial use, provided the original work is properly cited.
1
Dovepress
Cain and Lal
• American Academy of Otolaryngology – Head
and Neck Surgery criteria
≥12 week duration of ≥2 of following:
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• Mucopurulent drainage
• Nasal obstruction
• Facial pain/pressure/fullness
• Decreased sense of smell
AND
Inflammation by one or more objective criteria
• Endoscopy: pus, mucosal edema or polyps
• Imaging showing inflammation of the paranasal sinuses
Figure 1 Diagnosis of CRS.
Note: © 2007 Sage Publications. Reproduced with permission from Rosenfeld RM,
et al. Clinical practice guideline: adult sinusitis. Otolaryngol Head Neck Surg. 2007;
137(3 Suppl)S1–S31.
can now be delivered into the sinonasal cavity by a variety of
delivery methods, such as irrigations, sprays, and aerosols.
This paper will provide a succinct summary of current
and emerging evidence-based strategies to treat CRS.
Epidemiology
CRS is estimated to result in over 18 million physician visits
in the United States each year4 and is self-diagnosed in one
in seven adults.5 It is also the fifth most common diagnosis
for an antibiotic prescription.6 Despite its prevalence, there is
a surprising paucity of accurate epidemiologic data for CRS,
especially CRSsNP. Patient surveys in the United States have
found a 15%–16% prevalence of CRS;7,8 however, a prevalence
of only 2% was found using ICD-9 (International Classification of Diseases, Ninth Revision) codes as an identifier.9 In
studies from Canada, Korea, Scotland, Europe, and Sao Paulo,
prevalence of CRS ranges from 1%–11%.10–14
Population-based studies of CRSwNP from Sweden,
Korea, Finland, and France report the prevalence of CRSwNP
to lie between 0.5% and 4.3%.15–18 Autopsy studies reveal a
higher prevalence between 2% and 42%, with more polyps
found in dissected naso-ethmoidal blocks and endoscopic
sinus surgery (ESS) than with anterior rhinoscopy alone.19,20
Men and women are both affected by CRSwNP, with some
discordance in the literature as to which sex is more frequently affected. In general, nasal polyps occur in all races
and become more common with age, with the average age
of onset being 42 years.18
Etiology
Regarding the etiology of CRS, numerous hypotheses have
been proposed with a great deal of overlap, supporting a
multifactorial basis. One classification method separates
potential contributing entities into host and environmental
factors (Figure 2).2 Although comprehensive, this scheme
fails to illustrate causal relationships and host–environment
interactions. The heterogeneous nature of CRS is important
to understand when planning treatment for this diverse group
of patients whose disease may have arisen from very different
underlying etiologies.
In a broad generalization, CRSwNP in the Caucasian
population is associated more closely with high tissue eosinophilia and increased T helper (Th)-2 cytokine expression
(interleukin [IL]-5 and IL-13) as well as nasal obstruction
and smell loss. Meanwhile, CRSsNP may have more Th-1
polarization and less eosinophilic infiltration (Figure 3).3
However, these characterizations may not hold true for other
ethnic populations. (...truncated)