eMedicine Specialties > Otolaryngology and Facial Plastic Surgery > Nasal & Sinus Diseases
Sinusitis, Acute, Medical Treatment: Treatment & Medication
Updated: Jan 23, 2008
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
Treatment
Medical Care
The primary goals of management of acute sinusitis are to eradicate the infection, decrease the severity and duration of symptoms, and prevent complications. Most patients with acute sinusitis are treated in the primary care setting. Further evaluation by an otolaryngologist is recommended when (1) continued deterioration occurs with appropriate antibiotic therapy, (2) episodes of sinusitis recur, (3) symptoms persist after 2 courses of antibiotic therapy, or (4) comorbid immunodeficiency, nosocomial infection, or complications of sinusitis are present. The goals of management of acute sinusitis are the provision of adequate drainage and appropriate systemic treatment of the likely bacterial pathogens.Drainage of the involved sinus can be achieved both medically and surgically (see the Medication and Surgical Care sections). Aggressively treat patients in intensive care who develop acute sinusitis in order to avoid septic complications. Consider removal of nasotracheal and nasogastric tubes and promote drainage either medically or surgically.
Surgical Care
Sinus puncture and irrigation techniques allow for a surgical means of removal of thick purulent sinus secretions. The purpose of surgical drainage is to enhance mucociliary flow and provide material for culture and sensitivity. A surgical means of sinus drainage should be used when appropriate medical therapy has failed to control the infection and prolonged or slowly resolving symptoms result or when complications of sinusitis occur. Another indication for sinus puncture is to obtain culture material to guide antibiotic selection if empiric therapy has failed or antibiotic choice is limited. This is particularly important in patients who are immunocompromised or in intensive care. Sinusitis can be a prominent source of sepsis in these patients. In adults, sinus puncture can usually be achieved using local anesthesia; however, in children, a general anesthetic is usually necessary.
In today's era of minimally invasive surgical techniques, sinus endoscopy is commonly used to achieve sinus drainage. It offers the advantages of (1) being able to open multiple sinuses or to decompress the orbit in cases of complications and (2) allowing the surgeon to open the natural ostia of the involved sinuses.
The techniques and complications of open and endoscopic sinus surgical approaches are discussed in articles dealing with their individual surgical management.
Consultations
Ophthalmological or neurosurgical consultation should be obtained when either orbital or intracranial complications develop.
Medication
Medical drainage is achieved with topical and systemic vasoconstrictors. Oral alpha-adrenergic vasoconstrictors, including pseudoephedrine and phenylephrine, can be used for 10-14 days to allow for restoration of normal mucociliary function and drainage. Because oral alpha-adrenergic vasoconstrictors may cause hypertension and tachycardia, they may be contraindicated in patients with cardiovascular disease. Oral alpha-adrenergic vasoconstrictors may also be contraindicated in competitive athletes because of rules of competition. Topical vasoconstrictors (eg, oxymetazoline hydrochloride) provide good drainage, but they should be used only for a maximum of 3-5 days, given the increased risk of rebound congestion, vasodilatation, and rhinitis medicamentosa when used for longer periods.
Mucolytic agents (eg, guaifenesin, saline lavage) have the theoretical benefit of thinning mucous secretions and improving drainage. They are not, however, commonly used in clinical practice in the treatment of acute sinusitis. Intranasal steroids have not been conclusively shown to be of benefit in cases of acute sinusitis.
Antihistamines are beneficial for reducing ostiomeatal obstruction in patients with allergies and acute sinusitis; however, they are not recommended for routine use for patients with acute sinusitis. Antihistamines may complicate drainage by thickening and pooling sinonasal secretions.
In cases of suspected or documented bacterial sinusitis, the second principle of treatment is to provide adequate systemic treatment of the likely bacterial pathogens (ie, S pneumoniae, H influenzae, M catarrhalis). The physician should be aware of the probability of bacterial resistance within their community. Approximately 44 % of H influenzae and almost all of M catarrhalis strains have beta-lactamase–mediated resistance to penicillin-based antimicrobials in children. As many as 64% of S pneumoniae strains are penicillin resistant because of altered penicillin-binding proteins. Multiple drug–resistant S pneumoniae strains are also found in substantial numbers of children in daycare settings.5
Initial selection of the appropriate antibiotic therapy should be based on the likely causative organisms given the clinical scenario and the probability of resistant strains within a community. The course of treatment is usually 14 days. First-line therapy at most centers is usually amoxicillin or a macrolide antibiotic in patients allergic to penicillin because of the low cost, ease of administration, and low toxicity of these agents. Amoxicillin should be given at double the usual dose (80-90 mg/kg/d), especially in areas with known S pneumoniae resistance.
Table 1. Dosage, Route, and Spectrum of Activity of Commonly Used First-Line Antibiotics*
Open table in new window
Table
| Antibiotic | Dosage | Streptococcus pneumoniae | Haemophilus influenzae | Moraxella catarrhalis | Anaerobic bacteria | ||
|---|---|---|---|---|---|---|---|
| Sensitive | Intermediate | Resistant | |||||
| Amoxicillin | 500 mg PO tid | +++ | ++ | + | ++ | + | + |
| Clarithromycin | 250-500 mg PO bid | ++ | ++ | + | ++ | +++ | + |
| Azithromycin | 500 mg PO first day, then 250 mg/d PO for 4 days | ++ | ++ | + | ++ | +++ | + |
| Antibiotic | Dosage | Streptococcus pneumoniae | Haemophilus influenzae | Moraxella catarrhalis | Anaerobic bacteria | ||
|---|---|---|---|---|---|---|---|
| Sensitive | Intermediate | Resistant | |||||
| Amoxicillin | 500 mg PO tid | +++ | ++ | + | ++ | + | + |
| Clarithromycin | 250-500 mg PO bid | ++ | ++ | + | ++ | +++ | + |
| Azithromycin | 500 mg PO first day, then 250 mg/d PO for 4 days | ++ | ++ | + | ++ | +++ | + |
*+, low activity against microorganism; ++, moderate activity against microorganism; +++, good activity against microorganism
Patients who live in communities with a high incidence of resistant organisms, those who fail to respond within 48-72 hours of commencement of therapy, and those with persistence of symptoms beyond 10-14 days should be considered for second-line antibiotic therapy. The most commonly used second-line therapies include amoxicillin clavulanate, second- or third-generation cephalosporins (eg, cefuroxime, cefpodoxime, cefdinir), macrolides (ie, clarithromycin), fluoroquinolones (eg, ciprofloxacin, levofloxacin, moxifloxacin), and clindamycin.
In patients with dental causes of sinusitis or those with foul-smelling discharge, anaerobic coverage using clindamycin or amoxicillin with metronidazole is necessary.
Table 2. Dosage, Route, and Spectrum of Activity of Commonly Used Second-Line Antibiotics*
Open table in new window
Table
| Antibiotic | Dosage | Streptococcus pneumoniae | Haemophilus influenzae | Moraxella catarrhalis | Anaerobic bacteria | ||
|---|---|---|---|---|---|---|---|
| Sensitive | Intermediate | Resistant | |||||
| Amoxicillin/clavulanate | 500 mg PO tid | +++ | ++ | + | +++ | +++ | +++ |
| Cefuroxime | 250-500 mg PO bid | +++ | ++ | + | +++ | ++ | ++ |
| Cefpodoxime + cefixime | 200 mg PO bid 400 mg/d PO | - ++ | +++ - | ++ - | + +++ | +++ +++ | +++ - |
| Ciprofloxacin | 500-750 mg PO bid | ++ | + | + | ++ | +++ | + |
| Levofloxacin | 500 mg/d PO | +++ | +++ | +++ | +++ | +++ | +++ |
| Trovafloxacin | 200 mg/d PO | +++ | +++ | +++ | +++ | +++ | +++ |
| Clindamycin | 300 mg PO tid | +++ | +++ | +++ | - | - | +++ |
| Metronidazole | 500 mg PO tid | - | - | - | - | - | +++ |
| Antibiotic | Dosage | Streptococcus pneumoniae | Haemophilus influenzae | Moraxella catarrhalis | Anaerobic bacteria | ||
|---|---|---|---|---|---|---|---|
| Sensitive | Intermediate | Resistant | |||||
| Amoxicillin/clavulanate | 500 mg PO tid | +++ | ++ | + | +++ | +++ | +++ |
| Cefuroxime | 250-500 mg PO bid | +++ | ++ | + | +++ | ++ | ++ |
| Cefpodoxime + cefixime | 200 mg PO bid 400 mg/d PO | - ++ | +++ - | ++ - | + +++ | +++ +++ | +++ - |
| Ciprofloxacin | 500-750 mg PO bid | ++ | + | + | ++ | +++ | + |
| Levofloxacin | 500 mg/d PO | +++ | +++ | +++ | +++ | +++ | +++ |
| Trovafloxacin | 200 mg/d PO | +++ | +++ | +++ | +++ | +++ | +++ |
| Clindamycin | 300 mg PO tid | +++ | +++ | +++ | - | - | +++ |
| Metronidazole | 500 mg PO tid | - | - | - | - | - | +++ |
*+, low activity against microorganism; ++, moderate activity against microorganism; +++, good activity against microorganism; -, no activity against microorganism
Patients with nosocomial acute sinusitis require adequate intravenous coverage of gram-negative organisms. Aminoglycoside antibiotics are usually the drugs of choice for the treatment of such patients because of their excellent gram-negative coverage and sinus penetration. Selection of an antibiotic is usually based on the culture results of attained maxillary secretion.
In addition to surgical management, complications of acute sinusitis should be managed with a course of intravenous antibiotics. Third-generation cephalosporins (eg, cefotaxime, ceftriaxone) in combination with vancomycin provide adequate intracranial penetration, making them a good first-line choice.
Table 3. Dosage, Route, and Spectrum of Activity of Commonly Used Intravenous Antibiotics*
Open table in new window
Table
| Antibiotic | Dosage | Streptococcus pneumoniae | Haemophilus influenzae | Moraxella catarrhalis | Gram-negative | Anaerobic bacteria |
|---|---|---|---|---|---|---|
| Piperacillin | 3-4 g IV q4-6h | +++ | + | - | +++ | +++ |
| Piperacillin/tazobactam | 3.375 g IV q6h | +++ | +++ | +++ | +++ | ++ |
| Ticarcillin | 3 g IV q4h | +++ | - | - | +++ | ++ |
| Ticarcillin/clavulanate | 3.1 g IV q4h | +++ | +++ | - | +++ | ++ |
| Imipenem | 500 mg IV q6h | +++ | +++ | +++ | +++ | +++ |
| Meropenem | 1 g IV q8h | +++ | +++ | +++ | +++ | ++ |
| Cefuroxime | 1 g IV q8h | +++ | +++ | +++ | ++ | ++ |
| Ceftriaxone | 2 g IV bid | +++ | +++ | +++ | +++ | ++ |
| Cefotaxime | 2 g IV q4-6h | +++ | +++ | +++ | +++ | ++ |
| Ceftazidime | 2 g IV q8h | +++ | +++ | +++ | +++ | ++ |
| Gentamicin | 1.7 mg/kg IV q8h | - | +++ | +++ | ++ | - |
| Tobramycin | 1.7 mg/kg IV q8h | - | +++ | +++ | ++ | - |
| Vancomycin | 1 g IV q6-12h | +++ | - | - | - | ++ |
| Antibiotic | Dosage | Streptococcus pneumoniae | Haemophilus influenzae | Moraxella catarrhalis | Gram-negative | Anaerobic bacteria |
|---|---|---|---|---|---|---|
| Piperacillin | 3-4 g IV q4-6h | +++ | + | - | +++ | +++ |
| Piperacillin/tazobactam | 3.375 g IV q6h | +++ | +++ | +++ | +++ | ++ |
| Ticarcillin | 3 g IV q4h | +++ | - | - | +++ | ++ |
| Ticarcillin/clavulanate | 3.1 g IV q4h | +++ | +++ | - | +++ | ++ |
| Imipenem | 500 mg IV q6h | +++ | +++ | +++ | +++ | +++ |
| Meropenem | 1 g IV q8h | +++ | +++ | +++ | +++ | ++ |
| Cefuroxime | 1 g IV q8h | +++ | +++ | +++ | ++ | ++ |
| Ceftriaxone | 2 g IV bid | +++ | +++ | +++ | +++ | ++ |
| Cefotaxime | 2 g IV q4-6h | +++ | +++ | +++ | +++ | ++ |
| Ceftazidime | 2 g IV q8h | +++ | +++ | +++ | +++ | ++ |
| Gentamicin | 1.7 mg/kg IV q8h | - | +++ | +++ | ++ | - |
| Tobramycin | 1.7 mg/kg IV q8h | - | +++ | +++ | ++ | - |
| Vancomycin | 1 g IV q6-12h | +++ | - | - | - | ++ |
*+, low activity against microorganism; ++, moderate activity against microorganism; +++, good activity against microorganism; -, no activity against microorganism
Described below are recommended antibiotic regimens.
Antibiotics
Therapy must be comprehensive and cover all likely pathogens in the context of this clinical setting.
Amoxicillin (Trimox, Amoxil, Biomox)
First-line antibiotic. Interferes with synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible bacteria.
Adult
250-500 mg PO tid
Pediatric
25-45 mg/kg/d PO divided bid
Reduces efficacy of oral contraceptives
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Gastrointestinal irritation; black hairy tongue, glossitis, stomatitis; hypersensitivity may occur
Rare: pseudomembranous colitis, acute interstitial nephritis, hematologic disorders
Cefdinir (Omnicef)
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
600 mg/d PO for 10 d
Pediatric
14 mg/kg qd or divided bid for 10 d
May increase hypoprothrombinemic effects of anticoagulants; coadministration with potent diuretics and aminoglycosides (eg, loop diuretics) may increase nephrotoxicity
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Reduce dosage by 1/2 if creatinine clearance is 10-30 mL/min, and by 3/4 if <10 mL/min; bacterial or fungal overgrowth of nonsusceptible organisms may occur with prolonged or repeated therapy
Clarithromycin (Biaxin)
First-line antibiotic. Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest.
Adult
250-500 mg PO bid
Pediatric
15 mg/kg/d PO divided bid
Toxicity increases with coadministration of fluconazole and pimozide; effects decrease and GI adverse effects may increase with coadministration of rifabutin or rifampin; may increase toxicity of anticoagulants, cyclosporine, tacrolimus, digoxin, carbamazepine, ergot alkaloids, triazolam, HMG-CoA reductase inhibitors
Plasma levels of certain benzodiazepines may increase, prolonging CNS depression; arrhythmias and increases in QTc intervals occur with disopyramide; coadministration with omeprazole may increase plasma levels of both agents
Documented hypersensitivity; coadministration of pimozide
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Coadministration with ranitidine or bismuth citrate is not recommended with CrCl <25 mL/min; give half dose or increase dosing interval if CrCl <30 mL/min; diarrhea may be sign of pseudomembranous colitis; superinfections may occur with prolonged or repeated antibiotic therapies
Cefuroxime (Ceftin, Kefurox, Zinacef)
Second-line PO and first-line IV antibiotic. Maintains gram-positive activity that first-generation cephalosporins have; adds activity against P mirabilis, H influenzae, E coli, K pneumoniae, and M catarrhalis.
Condition of patient, severity of infection, and susceptibility of microorganism determine proper dose and route of administration.
Adult
250-500 mg PO bid
Alternatively, 1 g IV q8h
Pediatric
Administer as in adults
Disulfiramlike reactions may occur when alcohol is consumed within 72 h after taking cefuroxime; may increase hypoprothrombinemic effects of anticoagulants; may increase nephrotoxicity in patient receiving potent diuretics such as loop diuretics; coadministration with aminoglycosides increases nephrotoxic potential
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Reduce dosage by one half if CrCl is 10-30 mL/min, and by three fourths if <10 mL/min (high doses may cause CNS toxicity); bacterial or fungal overgrowth of nonsusceptible organisms may occur with prolonged or repeated therapy; gastrointestinal irritation
Ceftriaxone (Rocephin)
Third-generation cephalosporin with broad-spectrum, gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms. Arrests bacterial growth by binding to one or more penicillin binding proteins. Has good penetration.
Adult
2 g IV q12h
Pediatric
50-75 mg/kg IM/IV qd or bid
Probenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
Documented hypersensitivity
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity); superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy; caution in breastfeeding women
Vancomycin (Vancocin, Lyphocin, Vancoled)
Potent antibiotic directed against gram-positive organisms and active against Enterococcus species. Useful in the treatment of septicemia and skin structure infections. Indicated for patients who cannot receive or have failed to respond to penicillins and cephalosporins or who have infections with resistant staphylococci. For abdominal penetrating injuries, it is combined with an agent active against enteric flora and/or anaerobes.
To avoid toxicity, current recommendation is to assay vancomycin trough levels after third dose drawn 0.5 h prior to next dosing. Use CrCl to adjust dose in patients diagnosed with renal impairment.
Used in conjunction with gentamicin for prophylaxis in penicillin-allergic patients undergoing gastrointestinal or genitourinary procedures. Effective for resistant S pneumoniae.
Adult
500-1000 mg IV q6-12h
Pediatric
10 mg/kg/dose IV q6h
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
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Caution in renal failure, neutropenia; red man syndrome caused by too rapid IV infusion (dose given over a few min) but rarely happens when dose given IV over 2 h or PO/IP; red man syndrome is not an allergic reaction
Amoxicillin/Clavulanate (Augmentin)
Drug combination treats bacteria resistant to beta-lactam antibiotics.
Adult
250-500 mg PO bid/tid
Pediatric
<3 months: Not established
>3 months: Base dosing protocol on amoxicillin content; because of different amoxicillin/clavulanic acid ratios in 250-mg tab (250/125) vs 250-mg chewable tab (250/62.5), do not use 250-mg tab until child weighs more than 40 kg; 40 mg/kg/d PO divided q8h
Coadministration with warfarin or heparin increases risk of bleeding
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Give for a minimum of 10 d to eliminate organism and prevent sequelae (endocarditis, and rheumatic fever); following treatment, perform cultures to confirm eradication of streptococci
More on Sinusitis, Acute, Medical Treatment |
| Overview: Sinusitis, Acute, Medical Treatment |
| Differential Diagnoses & Workup: Sinusitis, Acute, Medical Treatment |
Treatment & Medication: Sinusitis, Acute, Medical Treatment |
| Follow-up: Sinusitis, Acute, Medical Treatment |
| References |
| « Previous Page | Next Page » |
References
Bishai WR. Issues in the management of bacterial sinusitis. Otolaryngol Head Neck Surg. Dec 2002;127(6 Suppl):S3-9. [Medline].
Ray NF, Baraniuk JN, Thamer M, Rinehart CS, Gergen PJ, Kaliner M. Healthcare expenditures for sinusitis in 1996: contributions of asthma, rhinitis, and other airway disorders. J Allergy Clin Immunol. Mar 1999;103(3 Pt 1):408-14. [Medline].
Rosenfeld RM, Andes D, Bhattacharyya N, Cheung D, Eisenberg S, Ganiats TG, et al. Clinical practice guideline: adult sinusitis. Otolaryngol Head Neck Surg. Sep 2007;137(3 Suppl):S1-31. [Medline].
Savolainen S, Jousimies-Somer H, Karjalainen J. Do simple laboratory tests help in etiologic diagnosis in acute maxillary sinusitis?. Acta Otolaryngol Suppl. 1997;529:144-7. [Medline].
Slack CL, Dahn KA, Abzug MJ, Chan KH. Antibiotic-resistant bacteria in pediatric chronic sinusitis. Pediatr Infect Dis J. Mar 2001;20(3):247-50. [Medline].
Sobol SE, Marchand J, Tewfik TL, Manoukian JJ, Schloss MD. Orbital complications of sinusitis in children. J Otolaryngol. Jun 2002;31(3):131-6. [Medline].
Chandler JR, Langenbrunner DJ, Stevens ER. The pathogenesis of orbital complications in acute sinusitis. Laryngoscope. Sep 1970;80(9):1414-28. [Medline].
AHCPR Evidence Report. Agency for Health Care Policy and Research. In: Diagnosis and treatment of acute bacterial rhinosinusitis. Rockville, MD. 1999.
Brook I, Gooch WM III, Jenkins SG. Medical Management of acute bacterial sinusitis. Recommendations of a clinical advisory committee on pediatric and adult sinusitis. Ann Otol Rhinol Laryngol. 2000;109(Suppl):2-20.
Conrad DA, Jenson HB. Management of acute bacterial rhinosinusitis. Curr Opin Pediatr. 2002;14(1):86-90.
Eibling DE. Maxillary Sinus: Irrigation Techniques. In: Myers EN, ed. Operative Otolaryngology-Head and Neck Surgery. Philadelphia, Pa: WB Saunders; 1997:81-85.
Frenkiel S. Embryology of the Nose and Sinuses. In: Tewfik TL, Der Kaloustian VM, eds. Congenital Anomalies of the Ear, Nose, and Throat. New York: Oxford University Press; 1997:183-187.
Graney DO, Rice DH. Anatomy. In: Cummings CW, Frederickson JM, Harker LA, Krause CJ, Richardson MA, Schuller DE, eds. Otolaryngology-Head & Neck Surgery. 3rd ed. St. Louis: Mosby; 1998:1059-1064.
International Rhinosinusitis Advisory Board. Infectious rhinosinusitis in adults: classification, etiology and management. International Rhinosinusitis Advisory Board. Ear Nose Throat J. Dec 1997;76(12 Suppl):1-22. [Medline].
Johnson JT, Ferguson BJ. Infection. In: Cummings CW, Frederickson JM, Harker LA, Krause CJ, Richardson MA, Schuller DE, eds. Otolaryngology-Head & Neck Surgery. 3rd ed. St. Louis: Mosby; 1998:1107-1118.
Josephson GD, Gross CW. Diagnosis & management of acute & chronic sinusitis. Compr Ther. Nov 1997;23(11):708-14. [Medline].
Kaliner MA, Osguthorpe JD, Fireman P. Sinusitis: bench to bedside. Current findings, future directions. Otolaryngol Head Neck Surg. Jun 1997;116(6 Pt 2):S1-20. [Medline].
Laine K, Maatta T, Varonen H. Diagnosing acute maxillary sinusitis in primary care: a comparison of ultrasound, clinical examination and radiography. Rhinology. Mar 1998;36(1):2-6. [Medline].
Low DE, Desrosiers M, McSherry J. A practical guide for the diagnosis and treatment of acute sinusitis. CMAJ. Mar 15 1997;156 Suppl 6:S1-14. [Medline].
Manning SC. Medical Management of Infectious and Inflammatory Disease. In: Cummings CW, Frederickson JM, Harker LA, Krause CJ, Richardson MA, Schuller DE, eds. Otolaryngology-Head & Neck Surgery. 3rd ed. St. Louis: Mosby; 1998:1135-1144.
McCaig LF, Hughes JM. Trends in antimicrobial drug prescribing among office-based physicians in the United States. JAMA. Jan 18 1995;273(3):214-9. [Medline].
Poole MD. A focus on acute sinusitis in adults: changes in disease management. Am J Med. May 3 1999;106(5A):38S-47S; discussion 48S-52S. [Medline].
Rhys-Evans PH. Anatomy of the Nose and Paranasal Sinuses. In: Kerr AG, Groves J, eds. Scott-Brown's Otolaryngology. 5th ed. London: Butterworths; 1987:138-161.
Talmor M, Li P, Barie PS. Acute paranasal sinusitis in critically ill patients: guidelines for prevention, diagnosis, and treatment. Clin Infect Dis. Dec 1997;25(6):1441-6. [Medline].
Taylor JA, Weber W, Standish L, et al. Efficacy and safety of echinacea in treating upper respiratory tract infections in children: a randomized controlled trial. JAMA. Dec 3 2003;290(21):2824-30. [Medline].
Wald ER. Expanded role of group A streptococci in children with upper respiratory infections. Pediatr Infect Dis J. Aug 1999;18(8):663-5. [Medline].
Wald ER. Microbiology of acute and chronic sinusitis in children and adults. Am J Med Sci. Jul 1998;316(1):13-20. [Medline].
Wald ER. Sinusitis. Pediatr Ann. Dec 1998;27(12):811-8. [Medline].
Westergren V. Artificial ventilation-acquired sinopathy in the critically ill - the maxillary sinuses revisited. Clin Exp Allergy. Mar 1999;29(3):298-305. [Medline].
Further Reading
Keywords
medical treatment for acute sinusitis, sinus infection, cold, runny nose, sinus headache, acute sinusitis, infection of the sinuses, recurrent acute sinusitis, subacute sinusitis, paranasal sinuses, chronic sinusitis
Treatment & Medication: Sinusitis, Acute, Medical Treatment