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Otolaryngology and Facial Plastic Surgery > PEDIATRIC OTOLARYNGOLOGY
Pediatric Sinusitis, Medical Treatment
Article Last Updated: Aug 25, 2006
AUTHOR AND EDITOR INFORMATION
Section 1 of 12
Author: Hassan H Ramadan, MD, MSc, Professor and Vice-Chair, Department of Otolaryngology-Head and Neck Surgery, Professor, Department of Pediatrics, West Virginia University
Hassan H Ramadan is a member of the following medical societies: American Academy of Otolaryngic Allergy, American Academy of Otolaryngology-Head and Neck Surgery, American College of Surgeons, and American Rhinologic Society
Coauthor(s):
Lincoln Lippincott, MD, Consulting Staff, Department of Otolaryngology, Statesboro ENT
Editors: Ted L Tewfik, MD, FRCS(C), Professor, Department of Otolaryngology, Director of Continuing Medical Education of Otolaryngology, McGill University Medical School; Director, Director of Professional Affairs of Otolaryngology, Department of Otolaryngology, Montreal Children's Hospital; Senior Staff, Montreal General Hospital and Royal Victoria Hospital; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Gregory C Allen, MD, Assistant Professor, Department of Otolaryngology-Head and Neck Surgery, University of Colorado School of Medicine; Christopher L Slack, MD, Otolaryngology-Facial Plastic Surgery, Private Practice, Associated Coastal ENT; Medical Director, Treasure Coast Sleep Disorders; Arlen D Meyers, MD, MBA, Professor, Department of Otolaryngology-Head and Neck Surgery, University of Colorado School of Medicine
Author and Editor Disclosure
Synonyms and related keywords:
rhinosinusitis, sinus infection, ostiomeatal complex, OMC, sinusitis, uncinate process, infundibulum ethmoidalis, hiatus semilunaris, ethmoid bulla, frontal recess, chronic maxillary sinusitis, frontal sinusitis, mucosal inflammation, upper respiratory tract infection, URTI, nasal allergy, allergic rhinitis, chronic rhinosinusitis, chronic sinusitis, recurrent sinusitis, adenoiditis, immune deficiency
Background
Pediatric sinusitis is a common problem treated by primary care physicians and otolaryngologists. Although this disorder has been addressed for many centuries, full appreciation for its scope, pathophysiology, diagnosis, treatment, and complications has been realized only relatively recently. Children with occasional episodes of acute sinusitis following a routine cold are treated with short courses of antibiotic therapy with good results. However, treatment of chronic and recurrent sinusitis can be more challenging for physicians and frustrating for families. In these cases, the physician must not only treat with an appropriate antibiotic but must also address the associated conditions contributing to the problem.
The goal in treating these children is to combine antibiotic therapy with treatment of associated conditions for a time sufficient to allow resolution of symptoms with return of normal sinus physiology and mucociliary clearance. This article addresses the medical management of pediatric sinusitis.
Pathophysiology
The ostiomeatal complex (OMC) is believed to be the critical anatomic structure in sinusitis and is entirely present, though not at full size, in newborns. Present within the middle meatus, the OMC is composed of the uncinate process, infundibulum ethmoidalis, hiatus semilunaris, ethmoid bulla, and frontal recess. Although obstruction of the OMC has not been proven to be the primary source for pediatric sinusitis, changes occurring in the anterior ethmoids are known to impair drainage through the OMC, resulting in chronic maxillary sinusitis and, occasionally, frontal sinusitis.
The normal metachronous movement of mucous toward the natural ostia of the sinuses and eventually to the nasopharynx can be disrupted by mucosal inflammation. This most commonly occurs secondary to routine viral upper respiratory tract infections (URTIs) or nasal allergies and the host response to these insults. In addition, many other predisposing factors to chronic disease exist, including allergic rhinitis, anatomical abnormalities, gastroesophageal reflux (GER), immune deficiency, and disorders of ciliary function.
Frequency
United States
Although the exact incidence of sinusitis in the pediatric population is unclear, it is diagnosed commonly, most often following a viral URTI. The number of URTIs that an individual has per year may be as high as 25 (children will have on average 6-8 per year); the number depends on a several factors, including age, day care attendance, and number of siblings. Approximately 5-13% of URTIs are complicated by bacterial sinusitis. Many viral URTIs are mislabeled early in their course as acute sinusitis and are inappropriately treated with antibiotics.
International
International incidence is similar to that in the United States.
Mortality/Morbidity
Recent health-related quality of life measures showed a poor result in children with chronic rhinosinusitis. Because quantifying the morbidity caused by pediatric conditions is difficult, it must also be viewed in other terms. A child with an acute episode of sinusitis may lead the caregiver to experience emotional distress and lack of sleep and miss days from work. Chronic illness may have a negative impact on a child's quality of life in many ways, including complications of chronic antibiotic therapy, school absences, poor sleep patterns, impaired school performance, and irritability. Children are also susceptible to more serious sequelae from a complication of sinusitis such as orbital cellulites (in about 9.3% of the cases) and intracranial complications (in 3.7-11% of patients). With close follow-up care, counseling of the family, and proper medical treatment, morbidity from this disease should be very low.
Race
No race predilection exists.
Sex
No sex predilection exists.
Age
The ethmoid and maxillary sinuses are present at birth. The sphenoid sinuses are pneumatized by age 5 years, and the frontal sinuses appear by age 7 years but are not completely developed until adolescence. Thus, children are predisposed to sinus infection at an early age. In young children, the most common sinuses involved are the ethmoid and maxillary sinuses. Acute sinusitis is much less common in young children than routine URTI or adenoiditis.
In an older child, the sphenoid and frontal sinuses are more likely to be involved with disease. Allergic rhinitis is also more common in older children. It affects only 1% of infants and 5% of children aged 5-9 years, while 15% of the adolescent population is affected. Allergic rhinitis is one of the most common predisposing factors for sinusitis, second only to viral URTIs.
History
Any condition that alters mucociliary clearance, decreases ventilation through a patent sinus ostium, or interferes with local or systemic defense mechanisms can lead to a cycle of sinus infection that can be very difficult to clear without concurrently addressing the associated condition.
- Acute sinusitis
- Signs and symptoms normally clear within 30 days.
- URTI symptoms persisting longer than 7-10 days suggest acute sinusitis.
- Daytime cough and rhinorrhea are the 2 most common symptoms.
- Other common signs and symptoms include the following:
- Nasal congestion
- Infrequent low-grade fever
- Otitis media (50-60% of patients)
- Irritability
- Headache
- Signs and symptoms of severe infection include the following:
- Purulent rhinorrhea
- High fever (ie, >39°C)
- Periorbital edema
- Uncomplicated sinusitis spontaneously resolves in 40% of patients.
- Recurrent acute sinusitis: This condition is defined as episodes each lasting fewer than 30 days and separated by intervals of at least 10 days during which the patient is asymptomatic.
- Subacute sinusitis: This condition is defined as signs and symptoms lasting between 30-90 days.
- Chronic sinusitis
- Chronic sinusitis is defined as low-grade persistence of signs and/or symptoms lasting longer than 90 days without improvement.
- The patient may have 6 or more recurrent episodes per year.
- The patient may have a history of acute exacerbations without ever being completely well between episodes.
- Nighttime cough is more prevalent.
Physical
Perform a thorough head and neck examination on patients with sinusitis, with emphasis on otoscopy, anterior rhinoscopy, and nasal endoscopy to examine the middle meatus, nasopharynx, and adenoids.
- Anterior rhinoscopy
- This study can be difficult to perform in young children.
- Examine the middle turbinate and middle meatus for evidence of purulence or sinus discharge.
- Using a nasal spray mixture of a vasoconstrictive agent, such as oxymetazoline and lidocaine, is helpful.
- Polyps, if present, should prompt an evaluation for cystic fibrosis.
- Nasal endoscopy
- This study provides an excellent look at the middle meatus and provides the most accurate examination results outside the operating room.
- Nasal endoscopy can be difficult to perform in young and uncooperative children.
- Transillumination of the sinuses: This study is not usually helpful.
Causes
Causes of rhinosinusitis are best organized according to microbiological agents and associated conditions.
Allergic Fungal Sinusitis
Cystic Fibrosis
Malignant Tumors of the Nasal Cavity
Malignant Tumors of the Sinuses
Sinonasal Papillomas, Treatment
Sinusitis, Acute, Medical Treatment
Sinusitis, Chronic, Medical Treatment
Sinusitis, Ethmoid, Acute, Surgical Treatment
Sinusitis, Frontal, Acute, Surgical Treatment
Sinusitis, Fungal
Sinusitis, Maxillary, Acute, Surgical Treatment
Sinusitis, Maxillary, Chronic, Surgical Treatment
Sinusitis, Sphenoid, Acute, Surgical Treatment
Other Problems to be Considered
Adenoid hypertrophy
Adenoiditis
Benign tumors of the nasal cavity
Benign tumors of the sinuses
Ciliary dyskinesia
Congenital malformations of the sinuses
Immune deficiency
Upper respiratory infection
Lab Studies
- Laboratory tests are normally not particularly helpful in making the diagnosis of sinusitis. However, they can be essential in determining whether associated conditions such as allergic rhinitis, cystic fibrosis, or immunodeficiency are present. In addition, in patients with suppurative complications or in a very toxic-appearing child, some blood work and cultures may be helpful for determining treatment.
Imaging Studies
- CT scanning
- CT scanning is the criterion standard for evaluation of both mucosal inflammation and anatomical abnormalities in the paranasal sinuses. CT scanning provides a reliable picture of the ostiomeatal complex in a noninvasive fashion.
- CT scanning demonstrates exceptional diagnostic accuracy for the diagnosis of pediatric sinusitis with excellent sensitivity and specificity. However, its predictive value depends on prevalence of chronic rhinosinusitis in the population being evaluated.
- CT scanning is mandatory before endoscopic sinus surgery and very valuable when an impending complication of sinusitis such as periorbital or intracranial involvement exists.
- Thin-cut axial and coronal images of the paranasal sinuses are optimal. A limited number of coronal images alone are used by some as a screening method.
- Contrast is not necessary for routine sinus evaluation, but it is necessary when a complication such as orbital or intracranial abscess is suspected.
- The best images for chronic sinusitis are taken at the point of maximal wellness, usually during the last week of a 4-week course of maximal medical therapy. Maximal medical therapy includes appropriate antibiotics and possibly nasal saline irrigations, topical nasal steroids, or decongestants.
- A 45% occurrence of incidental sinusitis/opacification has been found on pediatric facial CT scans taken for other reasons. In an asymptomatic patient, no treatment or further workup is necessary. In children younger than 12 years, mucosal thickening or sinus opacification are associated with only a 50% chance of actual sinusitis. During an acute viral URTI, the sinuses are routinely opacified on CT scan. In the early stages, URTIs do not require treatment with antibiotics.
- Note anatomic abnormalities, hypoplastic maxillary sinuses, concha bullosa, and changes consistent with cystic fibrosis (eg, medial displacement of the lateral nasal wall) on review of CT scans.
- A thinning of the surrounding bone with wispy areas of calcium density may be observed in patients with allergic fungal sinusitis.
- Plain radiography/sinus series
- These studies have a poor correlation with CT scanning; as many as 75% of them either underestimate or overestimate disease.
- Plain radiography is a fairly inaccurate screening method even for maxillary sinus disease.
- Inaccuracies are compounded by mucosal tears, asymmetric facial or sinus development, overlying soft tissue, multiple septal walls, sinus overlap, improper exposure, and head rotation.
- MRI: MRI is useful when intracranial complications are suggested or when allergic fungal sinusitis (nonenhancing on T1, bright on T2, central signal void) is suggested.
- Ultrasonography
- Ultrasonography can be used to evaluate the maxillary sinuses, but results have been somewhat inconsistent.
- It has not yet gained widespread acceptance in the United States.
Procedures
- Rigid or flexible nasal endoscopy
- Nasal endoscopy provides an excellent view of the OMC.
- It is helpful for evaluation of the adenoid pad.
- This procedure requires patient cooperation.
- Maxillary sinus puncture
- This test is the criterion standard for obtaining maxillary sinus cultures.
- Aerobic and anaerobic culture and sensitivity and Gram staining may enable pathogen-directed antibiotic therapy.
- Indications for maxillary sinus puncture include the following:
- Severe toxic illness
- Acute illness unresponsive to antibiotics within 72 hours
- Immunocompromised patients
- Suppurative complications
- Workup for fever of unknown origin
- Contents of the maxillary sinus may be aspirated safely through the canine fossa or inferior meatus, but in the pediatric population this often requires a brief general anesthetic. In this instance, the physician may also consider obtaining a culture via the natural maxillary sinus ostia.
- Middle meatal swab
- Cultures taken from the middle meatus or anterior middle turbinate have good (>80%) correlation with cultures taken from ipsilateral maxillary or ethmoid sinuses.
- Having a carefully guided endoscopic sample of purulence from the middle meatus is important. Random nasal swabs show little correlation with maxillary cultures.
- This procedure requires a cooperative child but is definitely less invasive than sinus puncture.
Histologic Findings
A submucosal inflammatory infiltrate is observed in acute and chronic sinusitis. Only allergic fungal sinusitis has a characteristic finding on histopathologic examination, with Charcot-Leyden crystals and eosinophilia. An abundance of eosinophils may also be seen in the submucosa of any patient with allergic rhinitis.
Medical Care
- Antibiotic therapy for acute sinusitis
- Indications are as follows:
- Toxic child with suspected complications
- Severe acute sinusitis
- Persistent acute sinusitis
- Because of the growing problem of bacterial resistance, do not administer antibiotics indiscriminately or without confirmation of history by physical examination.
- Treat for 10-14 days or for 1 week beyond symptom resolution.
- Adjunctive medical therapy for acute sinusitis
- Saline sinus irrigation has demonstrated efficacy in the treatment of acute and chronic sinusitis. It increases mucociliary flow rates and aids in vasoconstriction. It mechanically clears secretions, decreases bacterial counts, and clears allergens and environmental irritants from the nose.
- Nasal steroids are essential for patients with concurrent allergic rhinitis. Of patients with allergic rhinitis, 90% report improvement in symptoms, including nasal congestion.
- Absorption through the nasal mucosa to the systemic system is minimal with most steroid preparations.
- Adverse effects, including suppression of the pituitary axis and glaucoma, have been reported in adults.
- Severe varicella infections have been reported in the pediatric population.
- Few nasal steroids have been studied for their safety in young patients.
- Carefully consider all choices.
- Short bursts of systemic steroids can be helpful for patients with allergies. Many otolaryngologists also give patients with nasal polyposis a short burst before surgical intervention to decrease intraoperative blood loss.
- Nasal decongestants are variably effective. Topical decongestants may improve patients' level of comfort. Restricting use to the first 4-5 days of medical treatment is best in order to avoid rebound vasodilatation.
- Mucolytics are variably effective. No controlled studies have demonstrated efficacy.
- Antihistamines are most useful in patients with atopy.
- Immunotherapy is effective for patients with known specific allergies who have symptoms not responsive to other forms of traditional medical therapy.
- Optimization of associated medical conditions
- Allergic rhinitis: Measures include allergen avoidance, optimal environment, nasal steroids, a second-generation antihistamine, and possible immunotherapy.
- Gastroesophageal reflux: Treat in consultation with a pediatrician or GI specialist. Conservative measures include elevating the head of the bed, not feeding immediately before bedtime, and thickening feeds. Medical therapy includes H-2 blockers, prokinetic agents, and hydrogen ion pump inhibitors.
- Immune deficiency: Treat in consultation with an immunologist and possibly an infectious-disease specialist. Treatment involves aggressive routine medical therapy and possibly intravenous gamma-globulin injections. This is an expensive type of therapy with many possible associated complications.
- Asthma: Measures include avoidance of exacerbating factors and use of bronchodilators and inhaled steroids.
- Cystic fibrosis: Aggressive nasal toilet with saline irrigations, nasal steroids, and antibiotic irrigations for pseudomonad colonization may help optimize this condition, although antibiotic irrigations have never been prospectively studied effectively.
- Immotile cilia syndromes: Mechanical clearance of secretions with daily irrigations is helpful in reducing the number of infections.
- Chronic sinusitis
- For patients with chronic rhinosinusitis, administer at least 4 weeks of a broad-spectrum beta-lactamase–resistant second-line antibiotic therapy.
- Consider changing antibiotics if no significant response has occurred within 1 week. A culture may be required at that point to more appropriately adjust antibiotic coverage.
- All of the above medical adjuncts may play a role, especially nasal steroids and saline irrigations.
- Excluding or maximally treating all associated conditions is essential.
Surgical Care
Consultations
- Ophthalmologist for orbital complications
- Neurosurgeon for intracranial complications
- Allergist for allergic rhinitis
- Gastroenterologist for unmanageable GER
- Immunologist for immune deficiencies
- Pulmonologist for asthma or cystic fibrosis
Diet
Patients with GER should eliminate caffeine, chocolate, and acidic beverages from their diets. Also, patients should not lie supine after meals, and no food should be consumed for 2 hours before bedtime. With food allergies, which are common in the pediatric population, appropriate restrictions are necessary.
Activity
Tailor activity guidelines to the individual patient. Restrictions depend on the severity of illness and the patient's age. Patients with environmental allergies may require restrictions to avoid exposure to allergens. All patients with chronic sinusitis should be restricted from exposure to environmental irritants such as tobacco smoke.
Antibiotic therapy is the mainstay of medical treatment for pediatric rhinosinusitis. Because of increasing prevalence of beta-lactam–resistant bacteria in the community, administer antibiotics only for suspected infection as based on a careful history and physical examination. Direct the therapeutic regimen against the prevalent pathogens in the community and carefully consider suspicion for highly resistant bacteria. Typically, uncomplicated cases of acute sinusitis are responsive to amoxicillin. Most patients respond to this initial regimen. For children allergic to penicillin, a second- or third-generation cephalosporin can be used (only if the allergic reaction is not a type 1 hypersensitivity reaction). In cases of serious allergic reaction, a macrolide or clindamycin can be used.
Second-line antibiotics should account for bacterial resistance and should be safe in the pediatric population. For chronic sinusitis, a 4-week course of a broad-spectrum beta-lactam–stable antibiotic should be administered. This should allow treatment for more than a week beyond symptom resolution and ensure restoration of mucociliary function and resolution of mucosal edema. Antibiotic prophylaxis as a strategy to prevent infection in patients who experience recurrent episodes of acute bacterial rhinosinusitis has not been systemically evaluated and is controversial. There is little enthusiasm for this approach in light of the current concern with antibiotic resistance. Antibiotics for treatment of chronic sinusitis are best chosen based on culture results and sensitivities. Listed below are excellent choices for second-line antibiotics.
Drug Category: Antibiotics
Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.
| Drug Name | Amoxicillin (Trimox, Biomox) |
| Description | First-line therapy; may be administered at mealtime; has a pleasant taste. Interferes with synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible bacteria. |
| Adult Dose | 250-500 mg PO tid or 500-875 mg PO bid |
| Pediatric Dose | 45 mg/kg/d PO divided bid Pediatric high dose: 90 mg/kg/d PO divided bid; consider in children in large day care settings |
| Contraindications | Documented hypersensitivity; infectious mononucleosis (eg, Epstein-Barr virus) |
| Interactions | Reduces efficacy of oral contraceptives |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | More likely than other penicillins to produce a rash; adjust dose in renal impairment; may enhance chance of candidiasis |
| Drug Name | Amoxicillin-clavulanate (Augmentin) |
| Description | First-line choice for chronic sinusitis; clavulanate gives beta-lactamase resistance (H influenzae, M catarrhalis, S aureus, anaerobes); may be administered at mealtime; IV form available. |
| Adult Dose | 250-500 mg PO tid or 500-875 mg PO bid |
| Pediatric Dose | <3 months: 125 mg/5mL PO susp based on amoxicillin; 30 mg/kg/d divided bid for 7-10 d >3 months: If using 200 mg/5 mL or 400 mg/5 mL susp, 45 mg/kg/d PO divided q12h; if using 125 mg/5 mL or 250 mg/5 mL suspension, 40 mg/kg/d PO divided q8h for 7-10 d, or high dose 80-90 mg/kg/d PO divided bid >40 kg: Administer as in adults |
| Contraindications | Documented hypersensitivity; infectious mononucleosis |
| Interactions | Coadministration with warfarin or heparin increases risk of bleeding |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | GI adverse effects; still subject to pneumococcal resistance, but amoxicillin is active against intermediate-grade resistance; give for a minimum of 10 d to eliminate organism and prevent sequelae (eg, endocarditis, rheumatic fever); following treatment, perform cultures to confirm eradication of streptococci; adjust dose in renal impairment; cross allergy may occur with other beta-lactams and cephalosporins |
| Drug Name | Cefuroxime (Ceftin, Kefurox) |
| Description | Highly active against all common sinusitis-causing pathogens; useful with resistance to amoxicillin; good coverage of Haemophilus and Moraxella species; IV form available; good CSF penetration makes it appropriate in cases of suspected orbital or intracranial extension. Administer with meals; follow with yogurt. |
| Adult Dose | 250-500 mg PO bid |
| Pediatric Dose | 20-30 mg/kg/d PO divided bid; not to exceed 250 mg PO bid |
| Contraindications | Documented hypersensitivity |
| Interactions | Disulfiramlike reactions may occur when alcohol is consumed within 72 h after taking cefuroxime; may increase hypoprothrombinemic effects of anticoagulants; may increase nephrotoxicity in patients receiving potent diuretics such as loop diuretics; coadministration with aminoglycosides increases nephrotoxic potential |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | Administer half dose if CrCl is 10-30 mL/min and one-quarter dose if <10 mL/min; fungal and microorganism overgrowth may occur with prolonged therapy |
| Drug Name | Cefpodoxime (Vantin) |
| Description | Highly active against all common sinusitis-causing pathogens; useful with resistance to amoxicillin. Administer with meals; follow with yogurt. |
| Adult Dose | 100-400 mg PO bid |
| Pediatric Dose | 10 mg/kg/d PO divided bid; not to exceed 800 mg/d |
| Contraindications | Documented hypersensitivity |
| Interactions | May increase nephrotoxicity in patient receiving potent diuretics such as loop diuretics; coadministration with aminoglycosides increases nephrotoxic potential; antacids and H2-receptor blockers may decrease absorption; probenecid may increase serum levels |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | Administer half dose if CrCl is 10-30 mL/min and one-quarter dose if <10 mL/min; fungal and microorganism overgrowth may occur with prolonged therapy |
| Drug Name | Cefdinir (Omnicef) |
| Description | Used to treat acute maxillary sinusitis. Classified as a third-generation cephalosporin and inhibits mucopeptide synthesis in the bacterial cell wall. Typically bactericidal, depending on organism susceptibility, dose, and serum or tissue concentrations. |
| Adult Dose | 600 mg PO qd or divided bid |
| Pediatric Dose | 14 mg/kg/d PO qd or bid; not to exceed 600 mg/d |
| Contraindications | Documented hypersensitivity |
| Interactions | May increase hypoprothrombinemic effects of anticoagulants; coadministration with potent diuretics and aminoglycosides (eg, loop diuretics) may increase nephrotoxicity |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | Administer half dose if CrCl is 10-30 mL/min and one-quarter dose if <10 mL/min; fungal and microorganism overgrowth may occur with prolonged therapy |
| Drug Name | Azithromycin (Zithromax) |
| Description | Has better coverage against Haemophilus species than erythromycin. |
| Adult Dose | 500 mg PO first day, 250 mg/d next 4 d Alternatively, 500 mg/d IV |
| Pediatric Dose | 10 mg/kg PO first d, 5 mg/kg/d PO next 4 d; not to exceed adult dose |
| Contraindications | Documented hypersensitivity; hepatic impairment; do not administer with pimozide |
| Interactions | May increase toxicity of theophylline, warfarin, and digoxin; effects are reduced with coadministration of aluminum and/or magnesium antacids; nephrotoxicity and neurotoxicity may occur when coadministered with cyclosporine |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | Site reactions can occur with IV route; bacterial or fungal overgrowth may result with prolonged antibiotic use; may increase hepatic enzymes and cholestatic jaundice; caution in patients with impaired hepatic function, prolonged QT intervals, or pneumonia; caution in hospitalized, geriatric, or debilitated patients |
| Drug Name | Vancomycin (Vancocin, Lyphocin) |
| Description | Provides good coverage for resistant S pneumoniae. |
| Adult Dose | 1 g IV q12h |
| Pediatric Dose | 10 mg/kg IV q6h; not to exceed adult dose |
| Contraindications | Documented hypersensitivity |
| Interactions | Erythema, histaminelike flushing, and anaphylactic reactions may occur when administered with anesthetic agents; taken concurrently with aminoglycosides, risk of nephrotoxicity may increase above that with aminoglycoside monotherapy; effects in neuromuscular blockade may be enhanced when coadministered with nondepolarizing muscle relaxants |
| Pregnancy | C - Safety for use during pregnancy has not been established.
|
| Precautions | Caution in renal failure and neutropenia; red man syndrome is caused by too rapid IV infusion (dose given over a few min) but rarely happens when dose given as 2-h administration or as PO or IP administration; red man syndrome is not an allergic reaction |
| Drug Name | Clindamycin (Cleocin) |
| Description | Good for polymicrobial infections and in cases of S pneumoniae resistance shown to be sensitive by culture; poor activity against Haemophilus species. |
| Adult Dose | 150-450 mg PO qid 600-900 mg IV q8h |
| Pediatric Dose | 8-20 mg/kg/d PO divided tid/qid 20-40 mg IV divided q6-8h |
| Contraindications | Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis |
| Interactions | Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects; antidiarrheals may delay absorption |
| Pregnancy | B - Usually safe but benefits must outweigh the risks.
|
| Precautions | Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis by allowing overgrowth of Clostridium difficile |
Further Inpatient Care
- In general, sinusitis can be managed on an outpatient basis. In cases of resistant organisms or for patients with orbital or intracranial complications, inpatient treatment with intravenous antibiotics may be necessary.
Further Outpatient Care
- Family support is essential in treating this disorder.
- Just giving medication to a child can be taxing on all involved, so the less frequent dosing the better.
- Management of chronic sinusitis or an associated condition may be very labor intensive.
- Children in day care settings are often sent home when they have URTI symptoms. This results in missed days of work for family members and additional financial stressors. Still, most patients with sinusitis are treated as outpatients.
In/Out Patient Meds
Transfer
- If a pediatric intensive care unit or skill in dealing with acutely ill children is unavailable, transfer children with sinusitis complications to the nearest appropriate facility.
Deterrence/Prevention
- Good nasal hygiene and use of saline irrigations may be critical for the prevention of exacerbations of acute or chronic sinusitis. Maximize control of associated conditions and warn patients to avoid exposure to environmental irritants such as cigarette smoke.
Complications
- Orbital involvement
- Orbital involvement usually occurs subsequent to direct spread from disease in the ethmoid sinuses.
- Obtain a CT scan with contrast study to determine the full extent of orbital involvement and to identify ring-enhancing fluid collections typical of a subperiosteal abscess.
- Chandler classification is as follows:
- Preseptal cellulitis - Eyelid edema, erythema, normal globe movement
- Orbital cellulitis - Proptosis, chemosis
- Periorbital abscess - Proptosis with globe displaced inferolaterally, decreased extraocular muscle movement
- Orbital abscess - Severe proptosis, impaired visual acuity, fixed globe, toxic patient
- Cavernous sinus thrombosis - High fever, bilateral symptoms
- Sinusitis involving the orbit is potentially life threatening and has a high risk of rapid visual loss. Manage orbital involvement closely, even in early cases, because visual changes may be permanent.
- Orbital involvement requires intravenous antibiotics and possible endoscopic or open surgical management by physicians with expertise in treating these patients.
- Strongly consider consulting an ophthalmologist early in the course of sinusitis to document and monitor the visual examination.
- Intracranial involvement
- Intracranial involvement usually occurs subsequent to direct spread from sphenoid or frontal sinus disease.
- Subdural and frontal lobe abscesses are most common.
- Meningitis may occur.
- Administer intravenous antibiotics with good cerebrospinal fluid (CSF) penetration, such as third-generation cephalosporins. Obtain empiric broad-spectrum intravenous antibiotic coverage while awaiting more specific culture and sensitivity results.
- Obtain a CT scan with contrast to detect ring-enhancing fluid collections.
- Consulting a neurosurgeon is necessary.
Prognosis
- Prognosis is excellent for acute rhinosinusitis. Chronic sinusitis can be much more difficult to manage, but with optimal treatment of associated conditions and full medical treatment, high cure rates are probable. Only rarely is surgery required.
Patient Education
- Patient and family education is important. Understanding the mechanism underlying development of rhinosinusitis gives the caregiver much more incentive for the often-arduous task of compliance with medical treatment for a child.
- With the rising rate of resistant pathogens, educating the public about the proper uses of antibiotics is mandatory. Dispensing antibiotics over the phone or prophylactically is strongly discouraged. Long courses of antibiotics should be based on culture results.
Medical/Legal Pitfalls
- The only likely pitfall is a failure to recognize a life- or vision-threatening complication in its early stages. Physicians should have a low threshold for starting intravenous antibiotics and ordering a CT scan if orbital or intracranial spread is suspected.
Special Concerns
- One current concern in the United States is the rising number of children in day care. In addition to the potential social and psychological effects, a well-documented increase in the number of illnesses exists. Groups of more than 5 children have dramatically higher rates of URTIs because of the easy spread of viruses. Not only is the number of URTIs increased, but these viral infections are much more likely to progress to bacterial rhinosinusitis. In addition, this population of children is much more likely to be infected with resistant strains of bacteria. Inquire about day care attendance in every pediatric interview, and treat children who attend day care more aggressively than other patients.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author, Karla R Brown, MD, to the development and writing of this article.
| Media file 1:
Preseptal cellulitis of the left eye. Courtesy of Dwight Jones, MD. |
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| Media file 2:
Axial CT scan of subperiosteal abscess of the left eye. |
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| Media file 3:
Coronal CT scan of subperiosteal abscess of the left eye. |
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| Media file 4:
Coronal CT scan of superior subperiosteal abscess of the left eye. |
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| Media file 5:
Axial CT scan of orbital cellulitis of the right eye. |
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Pediatric Sinusitis, Medical Treatment excerpt Article Last Updated: Aug 25, 2006
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