You are in: eMedicine Specialties > Infectious Diseases > MEDICAL TOPICS Sinusitis, ChronicArticle Last Updated: Feb 20, 2007AUTHOR AND EDITOR INFORMATIONAuthor: Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital Eleftherios Mylonakis is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America Coauthor(s): Himal Bajracharya, MBBS, Assistant Professor, Department of Internal Medicine, Division of Infectious Diseases, Kansas University Medical Center; Daniel Hinthorn, MD, Director, Division of Infectious Diseases, Professor, Departments of Internal Medicine, Pediatrics and Family Medicine, University of Kansas Editors: Kenneth C Earhart, MD, FACP, Deputy Head, Disease Surveillance Program, United States Naval Medical Research Unit #3; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Gordon L Woods, MD, Consulting Staff, Department of Internal Medicine, University Medical Center; Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital; Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital Author and Editor Disclosure Synonyms and related keywords: acute sinusitis, sinus infection, paranasal sinus, postnasal drip, facial pain, hyposmia, rhinitis, fungal sinusitis, cystic fibrosis, CF, asthma, nasal polyps, allergy, allergies, gastroesophageal reflux disease, GERD, brain abscess, meningitis, Streptococcus pneumoniae, S pneumoniae, Haemophilus influenzae, H influenzae, Moraxella catarrhalis, M catarrhalis, functional endoscopic sinus surgery, FESS INTRODUCTIONBackgroundChronic sinusitis is one of the more prevalent chronic illnesses in the United States, affecting persons of all age groups. Generally defined as a sinus infection persisting for more than 3 months, this condition usually manifests differently than acute sinusitis. Symptoms of chronic sinusitis include nasal stuffiness, postnasal drip, facial fullness, and malaise. Most cases are continuations of unresolved acute sinusitis. Allergic and nonallergic rhinitis, anatomic obstruction in the ostiomeatal complex, and immunologic disorders are known risk factors. PathophysiologyAnatomic considerations Knowledge of the anatomy of paranasal sinuses is essential to understand the pathophysiology and management of chronic sinusitis. The 4 pairs of paranasal sinuses are 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 occur in inadequately treated patients and in specific types of sinusitis such as 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 connects 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 by 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. Even though the nasal cavity is usually colonized with bacteria, sinuses are typically sterile. Mechanical obstruction at the ostiomeatal complex secondary to anatomic factors or mucosal edema arising from various etiologies (eg, acute viral or allergic rhinitis) triggers the stasis of secretions inside the sinuses. Mucous stagnation in the sinus forms a rich medium for the growth of various pathogens. Initially, resulting acute sinusitis involves only one type of aerobic bacteria. With persistence of the infection, mixed flora, anaerobic organisms, and, occasionally, fungus contribute to the pathogenesis. Most cases of chronic sinusitis develop in patients with acute sinusitis that does not respond to treatment or in those who have not received treatment. The role of bacteria in the pathogenesis of chronic sinusitis is currently being questioned. Repeated and persistent sinus infections can occur in patients with severe acquired or congenital immunodeficiency states or cystic fibrosis. FrequencyUnited StatesChronic sinusitis affects approximately 32 million persons each year and accounts for 11.6 million visits to physicians' offices. Chronic sinusitis ranks fifth compared to all diseases in frequency of antibiotic use associated with treatment. Incidence of chronic sinusitis in patients with AIDS may be as much as 64%. InternationalChronic sinusitis is a common disease worldwide, particularly in places where atmospheric pollution levels are high. Damp, temperate climates along with higher concentrations of pollens are associated with higher prevalence of this disease in the northern hemisphere. Mortality/MorbidityBecause of its persistent nature, chronic sinusitis can become a significant cause of morbidity. 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. RaceChronic sinusitis is observed in all races. SexBoth sexes are affected equally. AgeAll age groups are affected. CLINICALHistoryChronic sinusitis manifests more subtly than acute sinusitis. Unless an appropriate history is taken, the diagnosis may be missed. The typical symptoms of acute sinusitis, namely fever and facial pain, are usually absent.
PhysicalPhysical examination in patients with chronic sinusitis may reveal a variety of findings.
CausesThe bacterial pathogens and their roles are well defined in the etiology of acute sinusitis. Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis account for more than 70% of cases of acute sinusitis. The role of viruses in the etiology of acute sinusitis has also been documented. In one study, sinus cavity abnormality occurred in 87% of patients with early common viral rhinitis. Bacterial sinusitis complicated up to 2% of viral rhinitis cases. While the microbiology of acute sinusitis has been well established, various researchers disagree on the microbial etiology of chronic sinusitis. Some studies have documented anaerobes as the prominent pathogens in chronic sinusitis, while others have failed to demonstrate this. The reasons for the variable growth of microbes in the samples obtained from chronic sinusitis may be due to prior exposure of patients with chronic sinusitis to various broad-spectrum antibiotics as well to a difference in sample collection techniques. The exact role of these microbes in the pathogenesis of chronic sinusitis is another unresolved issue. Increasing attention is currently being focused on ostiomeatal obstruction, allergies, polyps, occult and subtle immunodeficiency states, and dental diseases, while the role of bacteria is being reduced to that of opportunistic colonizer.
DIFFERENTIALSFever of Unknown Origin Gastroesophageal Reflux Disease Rhinitis, Allergic Rhinocerebral Mucormycosis Sinusitis, Acute
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| Drug Name | Amoxicillin (Amoxil, Trimox, Biomox) |
|---|---|
| Description | Interferes with synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible bacteria. |
| Adult Dose | 500 mg to 1 g PO q8h |
| Pediatric Dose | 40-45 mg/kg/d PO q8h divided |
| Contraindications | Documented hypersensitivity |
| Interactions | Reduces efficacy of oral contraceptives; increased amoxicillin levels with disulfiram and probenecid |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Skin rash in patients with infectious mononucleosis; potential superinfections with mycotic and bacterial pathogens; adjust dose in renal impairment |
| Drug Name | Amoxicillin and clavulanate (Augmentin) |
|---|---|
| Description | Drug combination treats bacteria resistant to beta-lactam antibiotics. |
| Adult Dose | 500 mg PO q8h or 875 mg PO q12h |
| Pediatric Dose | <3 months: 30 mg/kg/d PO q12h divided ; base dosing protocol on amoxicillin content >3 months: 40-50 mg/kg/d PO divided q8-12h 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 >40 kg |
| Contraindications | Documented hypersensitivity; history of amoxicillin/clavulanate-associated cholestatic jaundice/hepatic dysfunction |
| Interactions | Coadministration with warfarin or heparin increases risk of bleeding |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Skin rash in patients with infectious mononucleosis; potential superinfections with mycotic and bacterial pathogens; adjust dose in renal impairment; periodically monitor renal, hepatic, and hemopoietic functions during prolonged therapy |
| Drug Name | Clarithromycin (Biaxin) |
|---|---|
| Description | Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. |
| Adult Dose | 500 mg PO q12h |
| Pediatric Dose | 7.5 mg/kg PO q12h |
| Contraindications | Documented hypersensitivity; coadministration with cisapride or pimozide |
| Interactions | Toxicity increases with coadministration of fluconazole and pimozide; effects decrease and adverse GI effects may increase with coadministration of rifabutin or rifampin; may increase toxicity of anticoagulants, cyclosporine, tacrolimus, digoxin, omeprazole, carbamazepine, ergot alkaloids, triazolam, and HMG CoA-reductase inhibitors; plasma levels of certain benzodiazepines may increase, prolonging CNS depression; arrhythmias and increase in QTc intervals occur with disopyramide, cisapride, and pimozide; coadministration with omeprazole may increase plasma levels of both agents |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Adjust dose in renal insufficiency; drug interactions and teratogenicity are important considerations; occasionally hepatotoxic; coadministration with ranitidine or bismuth citrate is not recommended with CrCl <25 mL/min; administer 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 |
| Drug Name | Cefuroxime (Ceftin) |
|---|---|
| Description | Second-generation cephalosporin that maintains gram-positive activity of first-generation cephalosporins; adds activity against Proteus mirabilis, H influenzae, Escherichia coli, Klebsiella pneumoniae, and M catarrhalis. Condition of patient, severity of infection, and susceptibility of microorganism determine proper dose and route of administration. |
| Adult Dose | 500 mg PO bid |
| Pediatric Dose | 125-250 mg PO (tab) bid; alternatively, 20-30 mg/kg/d PO (susp) divided 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 (eg, loop diuretics); coadministration with aminoglycosides increases nephrotoxic potential; probenecid increases level of this group of drugs |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Administer one 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; 10% of patients who are allergic to penicillin may show cross-hypersensitivity |
| Drug Name | Cefixime (Suprax) |
|---|---|
| Description | Arrests bacterial cell wall synthesis and inhibits bacterial growth by binding to one or more of the penicillin-binding proteins. |
| Adult Dose | 400 mg/d PO or divided q12h |
| Pediatric Dose | <12 years: 8 mg/kg/d PO or 4 mg/kg/d PO bid >12 years or >50 kg: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Coadministration of aminoglycosides increases nephrotoxicity; probenecid may increase effects; carbamazepine levels may be increased |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Superinfections possible during prolonged therapy; adjust dose in renal insufficiency |
| Drug Name | Doxycycline (Vibramycin) |
|---|---|
| Description | Antibiotic with wide antimicrobialactivity against gram-positive and gram-negative organisms. |
| Adult Dose | 100 mg PO q12h |
| Pediatric Dose | >8 years and >100 lb: Administer as in adults; not for use in children younger than 8 y (can cause permanent dental staining and bone development abnormality) |
| Contraindications | Hypersensitivity to tetracyclines |
| Interactions | Tetracyclines decrease prothrombin activity; hence, exercise caution in patients on anticoagulants; may interfere with oral contraceptives; barbiturates, phenytoin, and carbamazepine decrease the level of tetracyclines; absorption of tetracyclines is affected by calcium, iron, aluminium, and magnesium |
| Pregnancy | C - Safety during pregnancy has not been established |
| Precautions | Not for administration in children <8 y or in pregnant or lactating women |
| Drug Name | Levofloxacin (Levaquin) |
|---|---|
| Description | Inhibits bacterial topoisomeraseIV and DNA gyrase, which are required for bacterial DNA replication and transcription. |
| Adult Dose | 500 mg PO qd |
| Pediatric Dose | Not recommended for children <18 y |
| Contraindications | Documented hypersensitivity to fluoroquinolones |
| Interactions | Enhances effects of warfarin; increased levels of theophylline may occur; increased risk of CNS stimulation when used with NSAIDs |
| Pregnancy | C - Safety during pregnancy has not been established |
| Precautions | Avoid if allergic to other quinolones |
| Drug Name | Gatifloxacin (Tequin) |
|---|---|
| Description | Inhibits bacterial topoisomeraseIV and DNA gyrase, which are required for bacterial DNA replication and transcription. |
| Adult Dose | 400 mg PO qd |
| Pediatric Dose | Not recommended for children <18 y |
| Contraindications | Documented hypersensitivity to fluoroquinolones |
| Interactions | May enhance effects of warfarin; may increase levels of digoxin; exacerbates adverse CNS effects of NSAIDs |
| Pregnancy | C - Safety during pregnancy has not been established |
| Precautions | May increase QTc; should be avoided in patients receiving class 1A (eg, quinidine, procainamide) or class III (eg, amiodarone, sotalol) antiarrhythmic agents; should be used with caution in patients taking drugs that may affect QTc such as cisapride, erythromycin, antipsychotics, and TCAs |
| Drug Name | Trimethoprim and sulfamethoxazole (Bactrim DS, Septra DS) |
|---|---|
| Description | Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid. One double-strength tab contains trimethoprim (TMP) 160 mg and sulfamethoxazole (SMX) 800 mg |
| Adult Dose | 1 DS tab PO q12h |
| Pediatric Dose | 8 mg/kg/d TMP and 40 mg/kg/d SMX PO q12h divided |
| Contraindications | Documented hypersensitivity; megaloblastic anemia due to folate deficiency; term pregnancy; breastfeeding women and infants <2 mo because of possibility of development of kernicterus |
| Interactions | May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly patients; phenytoin levels may increase with coadministration; may potentiate effects of MTX in bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Discontinue at first appearance of skin rash or sign of adverse reaction; obtain CBC counts frequently; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; prolonged IV infusions or high doses may cause bone marrow depression (if signs occur, administer 5-15 mg/d leucovorin); caution in folate deficiency (eg, patients with chronic alcoholism, elderly patients, those receiving anticonvulsant therapy, or those with malabsorption syndrome); hemolysis may occur in individuals who are G-6-PD deficient; patients with AIDS may not tolerate or respond to TMP-SMX; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); administer fluids to prevent crystalluria and stone formation |
Alpha-adrenergic agonists that act by constricting dilated mucosal vessels. Topical preparations of oxymetazoline, naphazoline, tetrahydrozoline, and xylometazoline are available. Use all adrenergic topical preparations with caution in young patients and the elderly population. Topical agents can produce rebound vasodilation on discontinuation and rhinitis medicamentosa on prolonged use. Both of these adverse effects respond well to topical steroids.
| Drug Name | Oxymetazoline (Afrin) |
|---|---|
| Description | Applied directly to mucous membranes, where it stimulates alpha-adrenergic receptors and causes vasoconstriction. Decongestion occurs without drastic changes in blood pressure, vascular redistribution, or cardiac stimulation. |
| Adult Dose | Available in 0.05% nasal solution; 2-3 gtt each nostril q12h; generally, use for no longer than 5 d |
| Pediatric Dose | <6 years: Not recommended >6 years: 1-2 gtt q12h for 3-5 d |
| Contraindications | Documented hypersensitivity; MAOIs |
| Interactions | Hypotensive action of guanethidine may be reversed; concurrent administration with methyldopa may result in increased vasopressor response; concurrent use of MAOIs and ephedrine may result in hypertensive crisis; pressor sensitivity to mixed-acting agents such as ephedrine may be increased; guanethidine potentiates effects of epinephrine and inhibits effects of ephedrine; phenothiazines may reverse action of nasal decongestants such as oxymetazoline; TCAs potentiate vasopressor response and may result in dysrhythmias |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in patients with hyperthyroidism, coronary artery and ischemic heart disease, diabetes mellitus, increased intraocular pressure, or prostatic hypertrophy; because of increase in vasoconstriction, patients who are hypertensive may experience change in blood pressure; do not use topical decongestants for longer than 3-5 d |
| Drug Name | Naphazoline (Privine) |
|---|---|
| Description | Alpha-adrenergic effects on arterioles of conjunctiva and nasal mucosa produce vasoconstriction. |
| Adult Dose | 2 gtt of 0.05% nasal solution in each nostril q3-6h; generally, not to exceed 3-5 d |
| Pediatric Dose | <6 years: Not recommended 6-12 years: Administer 1-2 gtt of 0.025% solution; do not use for more than 3-5 d |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma; do not use before a peripheral iridectomy is performed |
| Interactions | Risk of hypertensive reactions increases when used concurrently with TCAs or MAOIs; toxicity increases when used concurrently with anesthetics |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Prolonged use may cause rebound congestion; caution in patients with diabetes, hypertension, heart disease, cerebral arteriosclerosis, hyperthyroidism, and asthma |
| Drug Name | Tetrahydrozoline (Tyzine, Visine) |
|---|---|
| Description | Alpha-adrenergic effects on nasal mucosa produce vasoconstriction. |
| Adult Dose | 2-4 gtt of 0.1% nasal solution in each nostril q4-6h; do not use longer than 3-5 d |
| Pediatric Dose | <2 years: Not recommended 2-6 years: May administer 2-3 gtt of 0.05% nasal solution in each nostril q4-6h, not to exceed 3-5 d |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma |
| Interactions | Risk of hypertensive reactions increases when used concurrently with TCAs or MAOIs |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Prolonged use may cause rebound congestion; caution in patients with diabetes, hypertension, heart disease, cerebral arteriosclerosis, hyperthyroidism, and asthma |
| Drug Name | Xylometazoline (Otrivin) |
|---|---|
| Description | Applied directly to mucous membranes, where it stimulates alpha-adrenergic receptors and causes vasoconstriction. |
| Adult Dose | 2-3 gtt of 0.1% nasal solution in each nostril q8-10h; generally, do not use for longer than 3-5 d |
| Pediatric Dose | <2 years: Use only under direct supervision of physician 2-12 years: 2-3 gtt of 0.05% nasal solution q8-10h >12 years: Administer as in adults; duration of treatment generally not to exceed 5 d |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma |
| Interactions | Risk of hypertensive reactions increases when used concurrently with TCAs or MAOIs; toxicity increases when used concurrently with anesthetics |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Prolonged use may cause rebound congestion; caution in patients with diabetes, hypertension, heart disease, cerebral arteriosclerosis, hyperthyroidism, and asthma |
Particularly effective for chronic sinusitis associated with allergic rhinitis, nasal polyps, and rhinitis medicamentosa. Topical steroids along with systemic antibiotics are now the key components of the medical armamentarium in the management of chronic sinusitis.
| Drug Name | Fluticasone propionate (Flonase) |
|---|---|
| Description | Applied as nasal spray. Particularly effective in allergic and vasomotor rhinosinusitis and rhinosinusitis medicamentosa. Used as prophylaxis for nasal polyps. Plasma concentrations very low following intranasal administration in recommended doses. |
| Adult Dose | 50 mcg/spray; 2 sprays in each nostril qd or 1 spray in each nostril bid; not to exceed total dose of 200 mcg/d |
| Pediatric Dose | <12 years: Not recommended >12 years: 1 spray (50 mcg) in each nostril qd |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported; concomitant use with other inhaled and/or systemically absorbed corticosteroids can increase risk of hypercorticism and/or suppression of HPA |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Epistaxis or sensations of nasal burnings may occur; local candidal infections of nasopharynx have been reported with topical steroid use; always consider potential risk of suppression of HPA when using large dose for prolonged periods; rare cases of cataract, glaucoma, and increased intraocular pressure have been reported following intranasal use of corticosteroids; concomitant use of intranasal corticosteroids and other inhaled and/or systemically absorbed corticosteroids may cause hypercorticism and/or HPA suppression; if exposed to measles or chickenpox, consider prophylactic therapy |
| Drug Name | Beclomethasone dipropionate (Beconase AQ) |
|---|---|
| Description | Topical steroid nasal spray. Acts locally as anti-inflammatory and vasoconstrictor. Readily absorbed through nasopharyngeal mucosa and GI tract. Useful in allergic and vasomotor rhinosinusitis and sinusitis medicamentosa. |
| Adult Dose | 42 mcg/spray; 1 spray in each nostril bid/tid/qid |
| Pediatric Dose | <6 years: Not recommended 6-12 years: 1 spray in each nostril tid >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported; concomitant use with other inhaled and/or systemically absorbed corticosteroids can increase risk of hypercorticism and/or suppression of HPA |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Always consider potential risk of suppression of HPA when using large dose for prolonged periods; rare cases of cataract, glaucoma, and increased intraocular pressure have been reported following intranasal use of corticosteroids; concomitant use of intranasal corticosteroids and other inhaled and/or systemically absorbed corticosteroids may cause hypercorticism and/or HPA suppression; if exposed to measles or chickenpox, consider prophylactic therapy |
Nasal saline spray and steam inhalation help by moistening dry secretions, reducing mucosal edema, and reducing mucous viscosity. Symptomatic relief gained in some patients can be substantial; moreover, these are benign modalities of therapy.
| Drug Name | Saline nasal spray (Ayr, Ocean) |
|---|---|
| Description | Loosens mucous secretions to help remove mucus from nose and sinuses. |
| Adult Dose | 0.65% buffered isotonic sodium chloride nasal solution, 1-2 sprays or gtt in each nostril |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | A - Safe in pregnancy |
| Precautions | None reported |
May be helpful in chronic sinusitis associated with allergic rhinitis.
| Drug Name | Cromolyn sodium (Nasalcrom) |
|---|---|
| Description | Inhibits degranulation of sensitized mast cells following their exposure to specific antigens. |
| Adult Dose | 5.2 mg/spray; 1 spray in each nostril q4-6h; begin 1-2 wk before exposure to known allergen |
| Pediatric Dose | <6 years: Not recommended >6 years: 1 spray of 5.2 mg q6h |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in renal or hepatic impairment; symptoms may reoccur when withdrawing drug |
Although no controlled studies on the efficacy of mucolytics in chronic sinusitis are available, guaifenesin (mucolytic agent) may be helpful in ameliorating some symptoms.
| Drug Name | Guaifenesin (Humibid-LA) |
|---|---|
| Description | Increases respiratory tract fluid secretions and helps to loosen phlegm and bronchial secretions. Indicated for patients with bronchiectasis complicated by tenacious mucous and/or mucous plugs. |
| Adult Dose | 600-mg sustained-release tab 1-2 tab PO q12h |
| Pediatric Dose | <2 years: Not recommended 2-6 years: One-half tab PO q12h 6-12 years: 1 tab PO q12h |
| Contraindications | Documented hypersensitivity |
| Interactions | May increase renal clearance of urate and lower serum uric acid levels; may interfere with urine laboratory tests for 5-hydroxyindoleacetic acid and urine testing for catecholamines |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | When prescribing medication that may suppress cough, important to identify cause of cough so that suppression does not increase risk of clinical or physiologic complications |
Article Last Updated: Feb 20, 2007