Case Sinusitis

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CASE DISCUSSION SINUSITIS Supervisor dr. H. Oscar Djauhari, Sp. THT-KL Presentants Marcella Aprilia Lonatrista 2010.061.150 Arga Aditya 200873 0006 Otolaryngology, Head and Neck Department Medical Faculty of Unika Atma Jaya Medical Faculty of Muhammadiyah Jakarta University R. Syamsudin, S.H. Regional General Hospital, Sukabumi 1

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CASE DISCUSSION

SINUSITIS

Supervisordr. H. Oscar Djauhari, Sp. THT-KL

Presentants

Marcella Aprilia Lonatrista 2010.061.150

Arga Aditya 2008730006

Otolaryngology, Head and Neck Department

Medical Faculty of Unika Atma Jaya

Medical Faculty of Muhammadiyah Jakarta University

R. Syamsudin, S.H. Regional General Hospital, Sukabumi

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26th November 2012 – 29th December 2012

CASE DISCUSSION

A. PATIENT’S IDENTITY

 Name : Ms. I

Gender : Female

Age : 28 years old

Occupation : employer  

Address : Sukabumi

B. HISTORY

• Chief Complaint

recurrent common cold since 4 months before admission

• History of Present Illness

A 28-year old woman came to ENT department at Syamsyudin

hospital with a chief complaint of recurrent cold at the morning since 4 month

 before admission. The nose discharge had yellowish geen colour and smelled

odour since 1 month before admission. She also complained had nasal speech.

Fever and cough were denied. She had taken over the counter medication but

she hadn’t feel any improvement. No complainded on eyes.

• Additional Complaints :

headache, located at the base of the nose

• History of Past Illness

o History of right nose trauma with three times nose bleeding since 11 years

ago

o History of hypertension was denied

• History of Family Illness

History of family illness was denied

• Habits

o Recurrent cold

o Does not smoke

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o Does not drink any alcohol substance.

o Does not use any routine medication.

o Does not use any narcotics.

C. PHYSICAL EXAMINATION

General condition : Appear calm

Body weight : 45 kg

Height : 156 cm

Blood pressure : 110/90 mmHg

Pulse : 80 beat per minute

Respiratory rate : 22 times per minutes

Temperature : 36

o

C

ENT Examination

• Ear

Right ear 

- Auricle : normal

-

External auditory canal:

hyperemic (-), edema (-), mass (-), laceration (-) secretion (-) , cerumen (-)

- Tymphanic membrane:

Intact, hyperemic (-), retraction (-), light reflex (+)

 

Left ear 

- Auricle : normal

- External auditory canal:

hyperemic (-), edema (-), mass (-), laceration (-) secretion (-) , cerumen (+)

- Tymphanic membrane:

Intact, bulging (-), light reflex (+)

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Tuning fork test

• Rinne test : air conduction is being louder or louder than bone conduction

on both ear 

• Weber test : no lateralization

• Schwabach test : same with examiner on both ear 

•Nose

Right nose

- Mucous membrane:

hyperemic (+), edema (+), secretion (+), mass (-), laceration (-), crust (-)

- Inferior conchae : eutrophy

- Septum : no deviation

- Air passage : decreased

Left nose

- Mucous membrane:

hyperemic (+), edema (-), secretion (+), mass (-), laceration (-), crust (-)

- Inferior conchae : eutrophy

- Septum : no deviation

- Air passage : normal

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• Oropharynx

- Posterior pharynx : hyperemic (-)

- Palatine tonsils : T1 / T1, hyperemic (-), detritus (-)

- Uvula : symmetrical

- Dental : no abnormatlities

• Maxillofacial : symmetrical

• Neck  : no lymphadenopathy

D. WORKING DIAGNOSIS

Sinusitis

E. DIFFERENTIAL DIAGNOSIS

Allergic sinusitis

F. WORK-UP

Laboratory:

1. Routine blood count

2. Liver function test

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3. Blood glucose test

4. Renal function test

5. Bleeding time- clotting time

Chest X-ray PA position

Paranasal Sinus X-ray Water’s position

ECG

G. TREATMENT

Antral Wash Out dextra

Ceftriaxone 2 x 1 gram vial

Ketorolac 3 x 1 ampul (@30 mg/ml)

Tranexamic acid 3 x 2 ampul (@ 250 mg/ml)

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Laboratory Test Result

Examination Normal value 11/9/2012 25/11/2012

Hemoglobin 12 -16 g/dl 12,9 11,9

Leucocyte count 4000 – 9000 / ul 10.100 7600

Hematrocryte 36,1

Thrombocyte 262.000

SGOT/ASAT < 31 U/L/37 C 22,0

SGPT/ALAT < 36 U/L/37 C 18,3

Ureum 20 -40 mg/dl 24,3

Creatinine < 0.9 mg/dl -1.1 mg/

dl

0,7

Bleeding time 1-3 minutes 2 minutes 1 minute

Clotting time 1-11 minutes 6 minutes 6. 30 minutes

Blood glucose < 180 mg/dl 86 108

Paranasal Sinus X-ray: waters position (1/11/2012)

Interpretation

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• Right antrum wall thickened

• Opaque cloaking seen at right maxillary sinus

• Resume: sinusitis maxillary particularly dextra

Chest X-Ray (11/9/2012)

Interpretation

• Cor CTR> 50%, normal Hili, normal costophrenicus sinus

• Increase pulmonary vascular patern

• Resume: Cardiomegaly because of less inspiration, no pulmonary TB

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Follow up

26/11/2012

S: Cold, pain at the forehead especially when she bows

O: Nose

Right nose

- Mucous membrane:

hyperemic (+), edema (+), secretion (+), mass (-), laceration (-), crust (-)

- Inferior conchae : eutrophy

- Septum : no deviation

- Air passage : decreased

Left nose

- Mucous membrane:

hyperemic (+), edema (+), secretion (+), mass (-), laceration (-), crust (-)

- Inferior conchae : eutrophy

- Septum : no deviation

- Air passage : normal

A: Maxillary Sinusitis

26/11/2012

3.15 pm

S: Patient awake 2 hours after AWO. Patient feel sore on the right nose, headache, nausea,

 blood taste inside the mouth, dry lips and thirsty

O: tampon on right nose

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A: post-op sinusitis maxillaris dextra (AWO)

27/11/2012

08.00 am

S: Patient getting better, but still feel sore on the right nose, headache, blood taste inside the

mouth. Patient eat (liquid diet) and drink normally.

O: there’s still tampon plug on right nose

A: post-op sinusitis maxillaris dextra (AWO)

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Chronic Rhinosinusitis

Chronic sinusitis is one of the more prevalent chronic illnesses in the United States,

affecting persons of all age groups. It is an inflammatory process that involves the paranasal

sinuses and persists for 12 weeks or longer. The literature has supported that chronic sinusitis

is almost always accompanied by concurrent nasal airway inflammation and is often preceded

 by rhinitis symptoms; thus, the term chronic rhinosinusitis (CRS) has evolved to more

accurately describe this condition.

Most cases of chronic sinusitis are continuations of unresolved acute sinusitis;

however, chronic sinusitis usually manifests differently from acute sinusitis. Symptoms of 

chronic sinusitis include nasal stuffiness, postnasal drip, facial fullness, and malaise.

Chronic sinusitis may be noninfectious and related to allergy, cystic fibrosis,

gastroesophageal reflux, or exposure to environmental pollutants. Allergic rhinitis,

nonallergic rhinitis, anatomic obstruction in the ostiomeatal complex, and immunologic

disorders are known risk factors for chronic sinusitis.

Medical therapy is directed toward controlling predisposing factors, treating

concomitant infections, reducing edema of sinus tissues, and facilitating the drainage of sinussecretions. The goal in surgical treatment is to reestablish sinus ventilation and to correct

mucosal opposition in order to restore the mucociliary clearance system. Surgery strives to

restore the functional integrity of the inflamed mucosal lining.

Anatomy

Knowledge of the anatomy of paranasal sinuses is essential for understanding the

 pathophysiology and management of chronic sinusitis. The 4 pairs of paranasal sinuses are

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lined with ciliated, pseudostratified columnar epithelium. Goblet cells are interspersed among

the columnar cells. The mucosa is attached directly to the bone. Involvement of the

surrounding bone and further extension of the infection into the orbital and intracranial

compartments can result from inadequate treatment of sinusitis and specific types of sinusitis

(eg, fungal sinusitis).

The maxillary, frontal, and anterior ethmoid sinuses drain through their ostia located

at the ostiomeatal complex lying lateral to the middle turbinate within the middle meatus. The

 posterior ethmoid and sphenoid sinuses open into the superior meatus and sphenoethmoid

recess, respectively. The maxillary ostium is connected to the nasal cavity by a narrow

tubular passage called the infundibulum, located at the highest part of the sinus; hence,

drainage from the maxillary sinus flows against gravity via mucociliary clearance. Because

the floor of the maxillary sinus is the tooth-bearing part of the maxilla, dental infections can

easily extend to the maxillary sinus. Although the nasal cavity is usually colonized with

 bacteria, the sinuses are typically sterile.

Pathophysiology

Stasis of secretions inside the sinuses can be triggered by (1) mechanical obstruction

at the ostiomeatal complex due to anatomic factors or (2) mucosal edema caused by various

etiologies (eg, acute viral or allergic rhinitis).

Mucous stagnation in the sinus forms a rich medium for the growth of various

 pathogens. The early stage of sinusitis is often a viral infection that generally lasts up to 10

days and that completely resolves in 99% of cases. However, a small number of patients may

develop a secondary acute bacterial infection that is generally caused by aerobic bacteria (ie,

Streptococcus pneumoniae,  Haemophilus influenzae,  Moraxella catarrhalis). Initially, theresulting acute sinusitis involves only one type of aerobic bacteria. With persistence of the

infection, mixed flora, anaerobic organisms, and, occasionally, fungus  contributes to the

 pathogenesis, with anaerobic bacteria of oral flora origin often eventually predominating. In

one study, these bacterial changes were demonstrated with repeated endoscopic aspiration in

 patients with maxillary sinusitis. Most cases of chronic sinusitis are due to acute sinusitis that

either is untreated or does not respond to treatment.

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The role of bacteria in the pathogenesis of chronic sinusitis is currently being

reassessed. Repeated and persistent sinus infections can develop in persons with severe

acquired or congenital immunodeficiency states or cystic fibrosis.

Current thinking supports that chronic rhinosinusitis (CRS) is predominantly a

multifactorial inflammatory disease. Confounding factors that may contribute to

inflammation include the following:

• Persistent infection (including biofilms and osteitis)

• Allergy and other immunologic disorders

• Intrinsic factors of the upper airway

• Superantigens

• Colonizing fungi that induce and sustain eosinophilic inflammation

• Metabolic abnormalities such as aspirin sensitivity

All of these factors can play a role in disruption of the intrinsic mucociliary transport

system. This is because an alteration in sinus ostia patency, ciliary function, or the quality of 

secretions leads to stagnation of secretions, decreased pH levels, and lowered oxygen tension

within the sinus. These changes create a favorable environment for bacterial growth that, in

turn, further contributes to increased mucosal inflammation.

Etiology

Currently, etiologic studies of sinusitis are increasingly focusing on ostiomeatal

obstruction, allergies, polyps, occult and subtle immunodeficiency states, and dental diseases.

Microorganisms are more often recognized as secondary invaders. Any disease process or 

toxin that affects cilia has a negative effect on chronic rhinosinusitis (CRS).

 Bacterial involvement 

The bacteria presumed to be involved in CRS differ from those involved in acute

rhinosinusitis. The following bacteria have been reported in samples obtained through

endoscopy or sinus puncture in patients with chronic sinusitis.

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• Staphylococcus aureus (both methicillin-susceptible S aureus [MSSA] and

methicillin-resistant S aureus [MRSA] strains)

• Coagulase-negative staphylococci

•  H influenzae

•  M catarrhalis

• S pneumoniae

• Streptococcus intermedius

•  Pseudomonas aeruginosa

•  Nocardia species

• Anaerobic bacteria ( Peptostreptococcus, Prevotella, Porphyromonas, Bacteroides ,

 Fusobacterium species

In contrast with the well-established roles of microbes in the etiology of acute

sinusitis, the exact roles of all of these microbes in the etiology of chronic sinusitis are

uncertain. Various researchers disagree on the microbial etiology of chronic sinusitis. Much

of the disagreement may be explained by methodology. Studies that have used adequate

methods for recovery of anaerobes have demonstrated their prominence in chronic sinusitis,

while those that did not use such methods have failed to recover them. When proper 

techniques are used, anaerobic bacteria can be recovered in 50-70% of specimens. The

variable growth of microbes in samples may also be due to prior exposure of various broad-

spectrum antibiotics in patients involved in the studies.

Jyonouchi et al successfully induced chronic sinusitis in rabbits via intrasinus

inoculation of  Bacteroides fragilis. The authors subsequently identified immunoglobulin G

(IgG) antibodies against this organism in the infected animals. In addition, IgG antibodies to

anaerobic organisms have been observed in patients with chronic sinusitis. These findings

further support a role for anaerobes in chronic sinusitis.

Microbiologic studies of chronic sinusitis often show that the infection is

 polymicrobial, with isolation of 1-6 isolates per specimen.

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In some cases, the baseline chronic sinusitis worsens suddenly or causes new

symptoms. This acute exacerbation of chronic sinusitis is often polymicrobial as well, with

anaerobic bacteria predominating. However, aerobic bacteria that are usually associated with

acute sinusitis (eg, S pneumoniae, H influenzae,M catarrhalis) may emerge.

Gram-negative facultative and aerobic bacteria, including  P aeruginosa, are more

often isolated in patients with chronic sinusitis who have undergone endoscopic sinus

surgery. 

Fungal involvement 

The following fungi have been reported in samples obtained with endoscopy or sinus

 puncture in patients with chronic sinusitis:

•  Aspergillus species

• Cryptococcus neoformans

• Candida species

• Sporothrix schenckii

•  Alternaria species

Epidemiology

Chronic sinusitis is one of the more prevalent chronic illnesses in the United States,

affecting persons of all age groups. The overall prevalence of CRS in the United States is 146

 per 1000 population. For unknown reasons, the incidence of this disease appears to be

increasing yearly. This results in a conservative estimate of 18-22 million physician visits inthe United States each year and a direct treatment cost of $3.4-5 billion annually. Chronic

sinusitis is the fifth most common disease treated with antibiotics. Up to 64% of patients with

AIDS develop chronic sinusitis.

 International prevalence

Chronic sinusitis is a common disease worldwide, particularly in places with high

levels of atmospheric pollution. In the Northern Hemisphere, damp temperate climates along

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with higher concentrations of pollens are associated with a higher prevalence of chronic

sinusitis.

 Rhinosinusitis in children

Rhinosinusitis is more common in the pediatric population because this term includes

 both acute and chronic infection and both viral and bacterial disease. This is likely secondary

to an increased frequency of exposure to upper respiratory tract infections in the pediatric

 population.

Risk factors

The following conditions and risk factors predispose patients to the development of 

chronic sinusitis:

• Anatomic abnormalities of the ostiomeatal complex (eg, septal deviation, concha

 bullosa, deviation of uncinate process, Haller cells)

• Allergic rhinitis

•  Nasal polyps

•  Nonallergic rhinitis (eg, vasomotor rhinitis, rhinitis medicamentosa, cocaine abuse)

•  Nasotracheal intubation

•  Nasogastric intubation

• Hormonal (eg, puberty, pregnancy, oral contraception)

• Tumoral obstruction

• Immunologic disorders (eg, common variable immunodeficiency, immunoglobulin A

[IgA] deficiency, IgG subclass deficiency, AIDS)

• Cystic fibrosis

• Primary ciliary dyskinesia, Kartagener syndrome

• Wegener granulomatosis

• Repeated upper respiratory tract infections

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• Smoking

• Environmental pollution

• Periodontitis/significant dental disease

History

Patient history is extremely important in chronic rhinosinusitis (CRS) because of the

 broad overlap between sinus symptoms and other disease processes, as well as poor 

correlation between symptoms and endoscopic and radiographic findings.

Chronic sinusitis manifests more subtly than acute sinusitis. Unless an appropriate

history is taken, the diagnosis may be missed. The typical symptoms of acute sinusitis—fever 

and facial pain—are usually absent in chronic sinusitis. Fever, when present, may be low

grade.

Patients with chronic sinusitis may present with the following symptoms:

•  Nasal stuffiness

 Nasal discharge (of any character from thin to thick and from clear to purulent)

• Postnasal drip

• Facial fullness, discomfort, and headache

• Chronic unproductive cough

• Hyposmia

• Sore throat

• Fetid breath

• Malaise

• Easy fatigability

• Anorexia

• Exacerbation of asthma

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• Dental pain

• Visual disturbances

• Sneezing

• Stuffy ears

• Unpleasant taste

• Fever of unknown origin

In pediatric settings, halitosis is reported more commonly by parents of younger 

children. Nasal obstruction with mouth breathing and associated sore throat may be present.In some individuals with chronic sinusitis, parents may note occasional and painless morning

eye swelling. Older children may complain of loss of taste due to associated nasal obstruction

and anosmia. Nocturnal symptoms may include snoring and coughing due to associated

 postnasal drip.

The patient history should focus on the following key factors, beginning with

consideration of major and minor diagnostic criteria:

• The presence of major symptoms (including purulent anterior nasal drainage,

 purulent-discolored posterior nasal drainage, nasal obstruction or blockage, facial

congestion or fullness, facial pain or pressure, and hyposmia or anosmia)

• The presence of minor symptoms (including headache, ear pain or fullness, halitosis,

dental pain, cough, fever, fatigue)

• Duration of symptoms

• Exacerbating and relieving factors

• History of previous nasal or paranasal sinus surgery

• Current medications

• Previous treatments and their duration

• Other confounding health problems (including asthma, allergy, and

immunocompromising disorders)

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• Active or passive tobacco smoke

Physical Examination

Physical examination in patients with chronic sinusitis may reveal various findings. It

should include a complete head and neck examination (lymphadenopathy) to confirm the

diagnosis and to rule out more serious disorders.

Sinus palpation is performed to evaluate tenderness or swelling. Pain or tenderness on

 palpation over frontal or maxillary sinuses may be noted. Transillumination of maxillary or 

frontal sinuses may be useful; it lacks sensitivity but may have value in experienced hands.

An oral cavity and oropharynx examination is used to evaluate the integrity of the

 palate and the condition of dentition and to look for evidence of postnasal drip.

Oropharyngeal erythema and purulent secretions may be noted. Dental caries may be present.

Anterior rhinoscopy, with the use of a nasal speculum, is used to evaluate the

condition of the nasal mucosa and to look for purulent drainage or evidence of polyps or 

other nasal masses. Other contributing factors to CRS that can be evaluated are nasal septal

deviation and turbinate hypertrophy. The nasal examination should be carried out both beforeand after the use of a topical decongestant.

The nasal examination can be supplemented with the use of nasal endoscopy (if 

available). Endoscopic (rhinoscopic) examination findings include the following:

•  Nasal mucosal erythema, edema

• Purulent secretions

•  Nasal obstruction due to deviated nasal septum or hypertrophied turbinates

•  Nasal polyps

Ear examination for the presence of middle ear fluid that may be the sign of a mass in

the nasopharynx is indicated.

Ocular examination for spread of disease to the orbit and function of ocular 

musculature is indicated. Ophthalmic manifestations include the following:

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• Conjunctival congestion

• Lacrimation

• Proptosis, extraocular muscle palsies, and visual disturbances (when complicated by

orbital extension)

Laryngeal examination is used to look for other confounding upper airway pathology

including laryngeal-pharyngeal reflux (LPR). Lung examination is performed to determine if 

coexisting lower airway disease is present.

Cranial nerve examination is performed to look for underlying sinus malignancy or 

neurological disorder.

 Manifestations of fungal sinusitis

Fungal sinusitis can manifest in different ways. Unlike acute invasive fungal sinusitis,

which is observed in patients who are immunosuppressed or who have diabetes, chronic

fungal sinusitis is usually observed in immunocompetent patients. Mycetomas or fungus balls

may be asymptomatic or may manifest as chronic sinusitis. Allergic fungal sinusitis usually

manifests as nasal polyps and allergic sinusitis. Fungal elements in the sinuses are the inciting

allergens.

Diagnostic Criteria

In 1996, the American Academy of Otolaryngology-Head & Neck Surgery convened

a multidisciplinary Rhinosinusitis Task Force (RTF). This group defined adult rhinosinusitis

diagnostic criteria. These 1996 diagnostic criteria required 2 or more major factors or 1 major 

factor and 2 minor factors for the diagnosis of rhinosinusitis.

Major factors included facial pain or pressure, nasal obstruction or blockage, nasal

discharge or purulence or discolored postnasal discharge, hyposmia or anosmia, purulence in

nasal cavity, and fever (for acute rhinosinusitis only).

Minor factors were defined as headache, fever (for CRS), halitosis, fatigue, dental

 pain, cough, and ear pain, pressure, or fullness. Of note, facial pain requires another major 

factor associated with it for diagnosis (facial pain plus 2 minor factors is not deemed

sufficient for diagnosis of rhinosinusitis).

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In 2003, the RTF’s definition was amended to require confirmatory radiographic or 

nasal endoscopic or physical examination findings in addition to suggestive history.The 2003

diagnostic criteria for CRS require the above criteria for longer than 12 weeks or more than

12 weeks of physical findings. In addition, one of the following signs of inflammation must

 be present:

• Discolored nasal drainage from the nasal passages, nasal polyps, or polypoid swelling

as identified on physical examination with anterior rhinoscopy after decongestion or 

nasal endoscopy

• Edema or erythema of the middle meatus or ethmoid bulla on nasal endoscopy

• Generalized or localized erythema, edema, or granulation tissue (If the middle meatus

or ethmoid bulla is not involved, radiologic imaging is required to confirm a

diagnosis.)

Imaging modalities confirming the diagnosis include the following:

• Computed tomography (CT) scanning demonstrating isolated or diffuse mucosal

thickening, bone changes, or air-fluid levels

OR

• Plain sinus radiography revealing air-fluid levels or greater than 5 mm of 

opacification of one or more sinuses

• Magnetic resonance imaging (MRI) not recommended for routine diagnosis because

of its excessive sensitivity and lack of specificity

In general, plain radiography has low sensitivity and specificity. CT scanning isconsidered the imaging standard for evaluation of chronic sinusitis.

The latest executive summary on adult sinusitis has altered the definition for CRS to

read 12 weeks or longer of 2 or more of the following symptoms:

• Anterior or posterior mucopurulent drainage

•  Nasal obstruction

• Facial-pain-pressure-fullness

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• Decreased sense of smell

In addition, inflammation must be documented by demonstrating one of the

following:

• Purulent mucus or edema in the middle meatus or ethmoid region

• Polyps in the nasal cavity or middle meatus

• Imaging showing inflammation of the paranasal sinuses

This is in contrast to recurrent acute sinusitis, which is present when 4 or more

episodes per year of acute bacterial rhinosinusitis without signs and symptoms of 

rhinosinusitis between episodes.

Imaging Studies

Plain radiography may show mucosal thickenings or sinus opacities. Air fluid levels

are uncommon in chronic sinusitis. Ethmoid sinuses and the ostiomeatal complex are not

visualized well on plain sinus radiography.

Contrast-enhanced CT scanning is the current radiologic criterion standard for the

evaluation of sinus diseases, although performing CT scanning in all patients with chronic

sinus disease may be prohibitively expensive or medically unnecessary. CT scans are usually

indicated after failure of maximal medical therapy, before surgical planning for evaluation of 

suspected complications, and when a neoplasm is a possibility. CT scan combined with

endoscopic examination helps the surgeon to make operative decisions.

Coronal CT scan of the sinus correlates best with the surgical approach, permitting

visualization of the anatomy of the nasal cavity, ostiomeatal complex, sinus cavities, and

surrounding structures such as the orbit, cribriform plate, and optic canal. Anatomic

obstructions at the ostiomeatal complex and dental pathologies are visualized well. Specific

entities in the sinus cavity, such as aspergilloma, are also visualized well.

Most centers now offer limited sinus CT scans that consist of 5-12 coronal cuts. These

limited or screening CT scans cost about the same as a plain radiography but provide more

information.

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Magnetic resonance imaging (MRI) is generally reserved only for complex cases.

Soft-tissue contrast is better with MRI. Neoplasms, orbital and intracranial complications,

and fungal sinusitis can be better evaluated with MRI.

Biopsy

Biopsy samples from the maxillary sinus mucosa of patients with chronic sinusitis

show basement membrane thickening, atypical gland formation, goblet cell hyperplasia,

mononuclear cell infiltration, and subepithelial edema. The mononuclear cell infiltrate often

 predominantly demonstrates neutrophils in acute disease and eosinophils in chronic disease.

Rarely, squamous cell metaplasia may be seen.

 Brush biopsy or turbinate biopsy

Evaluation of cilia function with a brush biopsy or turbinate biopsy can be considered

in cases of presumed cilia dysfunction.

 Endoscopic biopsy

Specimens obtained from sinus openings via endoscopy correlate well with those

obtained with endoscopic surgery or sinus puncture. These should be processed for 

cultivation of aerobic and anaerobic bacteria, as well as fungi. Specimens evaluated for 

anaerobic bacteria should be sent in proper transport media. Liquid specimens are preferred

to swab specimens.

Cultures

Calcium-alginate tipped applicators are a readily available device that can be used to

obtain a culture. Studies of chronic sinusitis have demonstrated no correlation between nasal

flora and culture from the sinuses. Nasal swab cultures have no diagnostic value.

Occasionally, an abundance of eosinophils in the nasal smear suggests an allergic etiology. In

severe cases, blood cultures, including fungal blood cultures, may be helpful.

 Endoscopically directed middle meatal culture

Recent literature has supported the use of endoscopically directed culture of themiddle meatus (the primary drainage system of the anterior ethmoid, maxillary, and frontal

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sinuses) with the use of either a suction trap or a swab. Endoscopically directed middle

meatal cultures had a sensitivity of 80.9% and a specificity of 90.5% in a recent meta-

analysis.

 Maxillary sinus tap

Traditionally, maxillary sinus tap via inferior meatal puncture was performed for 

sinus culture. Many otolaryngologists have moved away from maxillary sinus tap because of 

the discomfort of the procedure and the understanding that a culture of an organism from the

middle meatus may be more accurate to determine the bacteria involved in the disease

 process.

Symptomatic Treatment

Symptoms may be relieved with topical decongestants, topical steroids, antibiotics,

nasal saline, topical cromolyn, or mucolytics.

Steam inhalation and nasal saline irrigation may help by moistening dry secretions,

reducing mucosal edema, and reducing mucous viscosity.

Initial oral steroid therapy followed by topical steroid therapy was found to be more

effective than topical steroid therapy alone in decreasing polyp size and improving olfaction

in patients with chronic rhinosinusitis (CRS) with at least moderate nasal polyposis.

Catalano et al evaluated balloon dilation for the treatment of chronic frontal sinusitis

in 20 patients with advanced sinus disease in whom medical therapy had failed and therefore

required operative intervention. Preoperative and postoperative CT scans were compared.

There were no significant complications from balloon dilation, and there was significantimprovement in patients with certain subsets of CRS.

Antimicrobial Therapy

An adequate antibiotic trial in CRS usually consists of a minimum of 3-4 weeks of 

treatment, preferably culture directed. Oral antibiotic regimens are generally used to treat

chronic sinusitis, since this condition is primarily treated in an outpatient setting. For resistant

cases, there may be a role for intravenous antibiotic therapy.

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Initial choice of the appropriate antimicrobial(s) is usually empiric. Sinus cultures are

not generally obtained for community-acquired infections unless empiric therapy fails to

elicit a response. The agent(s) chosen should be effective against the most likely bacterial

etiologies, including both aerobic and anaerobic pathogens. The likelihood of involvement by

 beta-lactamase–producing organisms should be considered. If methicillin-resistant

Staphylococcus aureus (MRSA) is a possible pathogen, coverage for this should be included.

History of drug allergies (if any) and cost of therapy should be taken into account as well. In

addition, if the patient has received antibiotics during the preceding 3 months, a different

class of antibiotics should be used.

Therapeutic regimens include the combination of a penicillin (eg, amoxicillin) plus a

 beta-lactamase inhibitor (eg, clavulanic acid), clindamycin, a combination of metronidazole

 plus a macrolide or a second- or third-generation cephalosporin, and the newer quinolones

(eg, moxifloxacin). All of these agents (or similar ones) are available in oral and parenteral

forms. Other effective antimicrobials are available only in parenteral form (eg, cefoxitin,

cefotetan). If aerobic gram-negative organisms (eg,  Pseudomonas aeruginosa) are involved,

 parenteral therapy with an aminoglycoside, a fourth-generation cephalosporin (cefepime or 

ceftazidime), or oral or parenteral treatment with a fluoroquinolone (only in postpubertal

 patients) is added. Parenteral therapy with a carbapenem (ie, imipenem, meropenem) is more

expensive but provides coverage for most potential pathogens, both anaerobes and aerobes.

Clindamycin as initial therapy provides coverage for MRSA and is effective against

anaerobes. Alternatives include trimethoprim-sulfamethoxazole or linezolid, which are added

to other regimens that cover anaerobes. Parenteral antimicrobials effective against MRSA

include vancomycin, linezolid, and daptomycin.

Ferguson et al performed a prospective observational study of 125 adults with classic

symptoms of chronic rhinosinusitis who underwent nasal endoscopy and sinus CT. Severe

symptoms occurred more often in younger patients with normal CT scans of the sinus than in

those with positive CT findings. Improvement in response to antibiotics was similar for 

 patients with positive CT findings and those with normal CT scans. The authors concluded

that most symptoms considered to be typical for chronic rhinosinusitis proved to be

nonspecific, and they suggest that objective evidence of mucopurulence assessed by

endoscopy or CT should be obtained if a prolonged course of antibiotics is being considered.

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Surgical Care

Presurgical

A preoperative antibiotic course may be administered in the weeks prior to surgery if 

an active infection is present. A preoperative steroid course may be administered if 

significant edema or polyps are observed on examination.

In the preoperative holding area, nasal decongestion is begun with the patient

receiving sprays of oxymetazoline. Following the commencement of general endotracheal

anesthesia, the eyes are protected with eye ointment and thin strips of tape. The nasal

 passages are decongested with appropriate vasoconstrictors such as topical cocaine if not

medically contraindicated.

If septoplasty is to be performed, the septum should be infiltrated with 1% lidocaine

with 1:100,000 epinephrine in the submucochondrial plane. Then, the patient is draped and

 prepared for surgery. A 4-mm 0- or 30-degree endoscope may be used, depending on the

surgeon's preference. If septoplasty is to be performed, it may be done either before or after 

sinus surgery. Place the septoplasty incision in the unobstructed nasal passage to allow better 

visualization of the more obstructed side.

Management of Chronic Maxillary Sinusitis

Three main surgical options are available: (1) endoscopic uncinectomy with or 

without maxillary antrostomy, (2) the Caldwell-Luc procedure, and (3) inferior antrostomy

(nasoantral window).

Today, endoscopic maxillary antrostomy and uncinectomy are the standard for 

treatment for refractory chronic maxillary sinusitis. The Caldwell-Luc and inferior 

antrostomy approaches are reserved for rare circumstances, such as a case of severe allergic

fungal sinusitis in which standard antrostomy alone does not allow complete extirpation of 

fungal concretions or complete drainage.

Additionally, further FESS with mucosal-sparing techniques may be performed if 

additional disease is present within the ethmoid, sphenoid, and frontal sinuses.

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Endoscopic Maxillary Antrostomy

Under endoscopic guidance, the middle turbinate may gently be moved medially, with

care to avoid fracturing the turbinate–skull base junction. At this point, the uncinate process

should be within view, and it is injected with 1% lidocaine with 1:100,000 epinephrine. Local

injections can be made using a 10-mL control syringe with a Luer lock 27-gauge needle

attached.

First, the root of the uncinate process is injected. Next, the inferior portion of the

uncinate process is injected. The root of the middle turbinate is infiltrated as well. Finally, an

injection is placed at the inferior junction of the basal lamella with the lateral nasal wall. This

serves to vasoconstrict the sphenopalatine artery. Approximately 1-2 mL of local anesthetic isused at each injection site, with the bevel down (toward mucosa). An appreciable blanch of 

the mucosa should be observed with each injection.

If using an image-guided system, it can be calibrated at this time (thereby giving time

for vasoconstriction from the injections to take effect). Alternatively, the system may be

calibrated prior to beginning the case. When using an image-guided system, checking the

 position of the guidance tracking in a few different known points and confirming the

accuracy in 3 dimensions is important. Typically, for isolated chronic maxillary sinus disease,

image-guided surgery is not necessary.

After decongestion, uncinectomy is the next step. Uncinectomy can be performed in

numerous ways. The following is the authors' preference. Under endoscopic guidance, a

maxillary ostium seeker is insinuated just behind the uncinate process and used carefully to

displace the free edge of the uncinate outwardly and anteriorly. To prevent lamina papyracea

injury, care is taken to very gently manipulate only the uncinate process and not to penetratedeeply.

 Next, 90-degree upbiting forceps are used to grasp the free edge of the uncinate

 process. In a controlled push-and-pull fashion, staying parallel to the lacrimal duct, the

uncinate process is then removed. Care is taken to engage the uncinate process parallel to the

lateral nasal wall to prevent injury to the lamina papyracea. Any remaining uncinate process

may be removed using a combination of microdebrider powered instrumentation and

 pediatric forceps. All portions of the uncinate should be taken down completely to permit

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visualization of the natural maxillary sinus ostium, roughly parallel to the inferior portion of 

the middle turbinate.

Once the natural ostium is identified, an ostium seeker can be placed through the

ostium and then carefully pushed posteriorly to widen the ostium. Using a through-cutting

forceps, the ostium is enlarged, thereby completing a maxillary antrostomy. The maxillary

sinus should be inspected with a 30- or 70-degree scope to ensure that no further disease is

 present within the sinus and that the natural ostium was included in the antrostomy.

If either a microlith or a polyp is present, it may be removed using curved giraffe

forceps or a curved suction. Further endoscopic work can be performed if disease is present

in other sinuses.

If lateralization of the middle turbinate is a concern and to allow easier postoperative

examination of the maxillary antrostomy in the office, the controlled synechiae technique, as

described by Bolger et al, may be used. Briefly, this involves abrading the opposing areas of 

mucosa from the medial middle turbinate and septum. With healing, the two roughened areas

appose, thus medializing the turbinate for improved postoperative visualization of the

maxillary sinus antrostomy.

The middle meatus may be packed with various products if either postoperative

 bleeding or lateralization of the middle turbinate is a concern. Many packing materials have

 been described, ranging from rolled Gelfilm to Merocel packing. The authors' preference is

for a latex-free, glove-covered, trimmed Merocel in the middle meatus. This should be

removed at the first postoperative visit (3-5 d).

 Balloon catheters in endoscopic sinus surgery

Balloon catheter technology has been used to dilate the maxillary sinus natural ostia

without bone or soft-tissue removal. Early reports show sustained patient symptom

improvement and sinus ostia patency. Further study and long-term outcomes with this

technology will determine its role in endoscopic sinus surgery.

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Caldwell-Luc Procedure

For patient comfort, this procedure typically is performed under general anesthesia.

However, if medical comorbidities preclude general anesthesia, the procedure may be

 performed with local anesthetic and sedation. It may be performed in conjunction with

nasoantral window (inferior antrostomy) to facilitate postoperative surveillance.

Lidocaine, 1% with 1:100,000 epinephrine, is injected in the incision site, and time is

allowed for vasoconstriction. Make a 3-cm incision centered over the canine tooth and first

 premolar while leaving about 0.5-1 cm of gingiva intact above the dentition to facilitate

closure.

Using electrocautery, dissection is carried down through the soft tissue and

 periosteum to bone. Next, a periosteal elevator is used to widely elevate periosteum from the

anterior wall of the maxilla. Care is taken to identify and avoid injury to the infraorbital

nerve, which is vertical and inferior to the midpupillary line. In the canine fossa, with mallet

and osteotome, the maxillary sinus is entered through its anterior thin bone. Thereafter,

rongeurs are used to enlarge the opening. Any pus from the maxillary cavity may be sent for 

culture. The disease within the sinus can be addressed appropriately. Next, the sinus is

irrigated. The incision is then closed using 3-0 or 4-0 absorbable suture.

Inferior Antrostomy

Vasoconstriction is begun with topical oxymetazoline on pledgets. Next, 1% lidocaine

with 1:100,000 epinephrine is injected under endoscopic guidance along the lateral nasal wall

underneath the inferior turbinate. A 3-mL syringe with a 27-gauge needle facilitates the

injection. Because the nasolacrimal duct lies approximately 1 cm anterior to the natural

maxillary ostium, the injection and surgical antrostomy site is about one to two thirds of the

distance back along the inferior turbinate.

 Next, the maxillary sinus is punctured in this region using a curved suction or trocar.

This antrostomy should then be enlarged with through-cutting forceps. The maxillary sinus

disease should then be extirpated as appropriate.

Functional Endoscopic Sinus Surgery

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Surgical care is used as an adjunct to medical treatment in some cases. Surgical care is

usually reserved for cases that are refractory to medical treatment and for patients with

anatomic obstruction. Recent studies suggest that preoperative CT findings prior to sinus

surgery may be poor predictors of surgical outcomes.

The goal in surgical treatment is to reestablish sinus ventilation and to correct

mucosal opposition in order to restore the mucociliary clearance system. Surgery strives to

restore the functional integrity of the inflamed mucosal lining.

Recent advances in endoscopic technology and a better understanding of the

importance of the ostiomeatal complex in the pathophysiology of sinusitis have led to the

establishment of functional endoscopic sinus surgery (FESS) as the surgical procedure of 

choice for the treatment of chronic sinusitis.

FESS facilitates the removal of disease in key areas, restores adequate aeration and

drainage of the sinuses by establishing patency of the ostiomeatal complex, and causes less

damage to normal nasal functioning. FESS is successful in restoring sinus health, with

complete or at least moderate relief of symptoms in 80-90% of patients. Supportive medical

treatment is instituted preoperatively and postoperatively. In children, surgical management is

not as well established and should be reserved for complicated cases.

Occupational exposure may affect FESS outcomes. Symptoms may persist with work-

related exposure to inhaled agents, and revision surgery may be required.

Management of Fungal Sinusitis

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The preferred treatment for chronic fungal sinusitis is surgical debridement.

Mycetomas or fungus balls are best treated by means of surgical removal. Allergic fungal

sinusitis, which usually manifests as nasal polyps and allergic sinusitis, is treated by means of 

systemic steroids and surgical removal of polyps and mucinous secretions.

Prognosis

Because of its persistent nature, chronic sinusitis can become a significant cause of 

morbidity. If left untreated, it can reduce the quality of life and the productivity of the

affected person.

Chronic sinusitis is associated with exacerbation of asthma and serious complications

such as brain abscess and meningitis, which can produce significant morbidity and mortality.

Early and aggressive medical treatment for chronic sinusitis typically results in

satisfactory outcomes. Functional endoscopic sinus surgery (FESS) restores sinus health with

complete or moderate relief of symptoms in 80-90% of patients with recurrent or medically

unresponsive chronic sinusitis.

Chronic sinusitis is rarely life threatening, although serious complications can occur 

 because of the proximity to the orbit and cranial cavity. Approximately 75% of all orbital

infections are directly related to sinusitis. Intracranial complications remain comparatively

rare, with 3.7-10% of intracranial infections related to sinusitis.

Complications

The most common complication of chronic sinusitis is superimposed acute sinusitis.

In children, the presence of pus in the nasopharynx may cause adenoiditis, and a high percentage of such patients develop secondary serous or purulent otitis media. Dacryocystitis

and laryngitis may also occur as complications of chronic sinusitis in children.

Orbital complications include preseptal cellulitis, subperiosteal abscess, orbital cellulitis,

orbital abscess, and cavernous sinus thrombosis. Intracranial complications include

meningitis, epidural abscess, subdural abscess, and brain abscess.

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Some studies have suggested a higher incidence of complications associated with

fungal sinusitis. Untreated chronic sinusitis can lead to life-threatening complications, as in

 patients with cystic fibrosis. Other complications include osteomyelitis and mucocele

formation.

Reference

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Adams L George, Boies L, et al. Boies Buku Ajar Penyakit THT edisi 6 . Penerbit buku

kedokteran EGC. Jakarta 1997

Brook, Itzhakm, et al. Chronic Sinusitis. Updated: Feb 15, 2012. Medscape.

http://emedicine.medscape.com/article/232791-overview  

Patel, Ankit, et al. Surgical Treatment of Chronic Maxillary Sinusitis Surgical Overview .

Updated: Mar 29, 2011. Medscape. http://emedicine.medscape.com/article/861886-

overview#aw2aab6b4

Soepardi, Efiaty Arsyad dan Nurbaiti Iskandar (ed.). 2003.  Buku Ajar Telinga Tenggorok 

 Kepala Leher . Jakarta : Fakultas Kedokteran Universitas Indonesia.

Singh, Ameet, et al.  Paranasal Sinus Anatomy. Updated: Jun 28, 2011. Medscape.

http://emedicine.medscape.com/article/1899145-overview#showall