You are in: eMedicine Specialties > Emergency Medicine > PULMONARY BronchitisArticle Last Updated: May 12, 2008AUTHOR AND EDITOR INFORMATIONAuthor: Samuel Ong, MD, Visiting Assistant Professor, Department of Emergency Medicine, University of California at Los Angeles Medical Center-Olive View Editors: David FM Brown, MD, Assistant Professor, Department of Medicine, Division of Emergency Medicine, Harvard Medical School; Associate-Chief, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Paul Blackburn, DO, FACOEP, FACEP, Program Director, Department of Emergency Medicine, Maricopa Medical Center; Assistant Professor, Department of Surgery, University of Arizona; John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center; Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School Author and Editor Disclosure Synonyms and related keywords: tracheobronchitis, chronic obstructive lung disease, COLD, obstructive airway disease, OAD, chronic obstructive pulmonary disease, COPD, respiratory tract infection, asthma, viral respiratory tract infection, bacterial respiratory tract infection, chronic bronchitis, CB, acute bronchitis, cough, viral infection, adenovirus, influenza, parainfluenza, respiratory syncytial virus, RSV rhinovirus, coxsackievirus, herpes simplex virus, HSV, Streptococcus pneumoniae, Moraxella catarrhalis, Haemophilus influenzae, Chlamydia pneumoniae, Mycoplasma species, air pollution, air pollutants, smoking, INTRODUCTIONBackgroundAcute bronchitis refers simply to inflammation of the tracheobronchial tree. The cause is usually infectious, but allergens and irritants can produce a similar clinical picture. Bronchitis typically occurs in the setting of an upper respiratory illness; thus, it is observed more frequently in the winter months. Asthma can be mistakenly diagnosed as acute bronchitis if the patient has no prior history of asthma. In one study, one third of patients who had been determined to have recurrent bouts of acute bronchitis were eventually identified as having asthma. PathophysiologyAlthough bronchitis refers to inflammation of the trachea and bronchi, other segments of the respiratory tract may also be involved because acute bronchitis usually occurs in relation to the common cold or other respiratory illness. FrequencyUnited StatesAccording to the National Center for Health Statistics, more than 12 million cases of acute bronchitis occurred in 1994, a number roughly equal to 5% of the US population.1 In comparison, 91 million cases of influenza, 66 million cases of the common cold, and 31 million cases of other acute upper respiratory infections occurred during that same year. InternationalAcute bronchitis is common throughout the world and is one of the top 5 reasons for seeking health care in countries that track such data. Mortality/MorbidityBronchitis is nearly always self-limited in the otherwise healthy individual, although it frequently results in absenteeism from work and school. Severe cases occasionally produce deterioration in those with significant underlying cardiopulmonary disease or other comorbid conditions. SexAlthough bronchitis seems to be diagnosed in women more frequently than in men, little difference is observed. AgeAlthough found in all age groups, bronchitis is diagnosed most frequently in children younger than 5 years. In 1994, bronchitis was diagnosed in more than 11 of every 100 children younger than 5 years.1 This compared with only 4 of every 100 individuals in every other age group. CLINICALHistory
Physical
Causes
DIFFERENTIALSAsthma Chronic Obstructive Pulmonary Disease and Emphysema Pediatrics, Bronchiolitis Pediatrics, Croup or Laryngotracheobronchitis Pediatrics, Pertussis Pneumonia, Bacterial Pneumonia, Mycoplasma
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| Drug Name | Erythromycin (EES, E-Mycin, Ery-Tab) |
|---|---|
| Description | Used for prophylaxis in patients with penicillin allergy who are undergoing dental, PO, or respiratory tract procedures. Inhibits RNA-dependent protein synthesis, possibly by stimulating dissociation of peptidyl tRNA from ribosomes, resulting in arrest of bacterial replication. |
| Adult Dose | 250-500 mg PO qid or 333 mg PO tid |
| Pediatric Dose | 30-50 mg/kg/d PO divided qid |
| Contraindications | Documented hypersensitivity; hepatic impairment |
| Interactions | Coadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin or simvastatin increases risk of rhabdomyolysis |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Caution in liver disease; estolate formulation may cause cholestatic jaundice; adverse GI effects are common (administer doses pc); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur |
| Drug Name | Clarithromycin (Biaxin) |
|---|---|
| Description | Reversibly binds to P site of 50S ribosomal subunit of susceptible organisms and may inhibit RNA-dependent protein synthesis by stimulating dissociation of peptidyl tRNA from ribosomes, inhibiting bacterial growth. |
| Adult Dose | 250-500 mg PO bid |
| Pediatric Dose | 7.5 mg/kg PO bid |
| Contraindications | Documented hypersensitivity; concurrent pimozide |
| Interactions | Toxicity increases with coadministration of fluconazole or pimozide; effects decrease and GI adverse 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; coadministration with omeprazole may increase plasma levels of both agents |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Coadministration with ranitidine or bismuth citrate not recommended if 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 | Azithromycin (Zithromax) |
|---|---|
| Description | Used to treat mild-to-moderate infections caused by susceptible strains of microorganisms; indicated for chlamydial and gonorrheal infections of genital tract. |
| Adult Dose | Day 1: 500 mg PO Days 2-5: 250 mg PO |
| Pediatric Dose | 12 mg/kg PO qd; not to exceed 500 mg/dose |
| Contraindications | Documented hypersensitivity; hepatic impairment; concurrent pimozide |
| Interactions | May increase toxicity of theophylline, warfarin, and digoxin; effects reduced with coadministration of aluminum and/or magnesium antacids; nephrotoxicity and neurotoxicity may occur when coadministered with cyclosporine |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| 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 | Cefditoren pivoxil (Spectracef) |
|---|---|
| Description | Semisynthetic cephalosporin administered as prodrug. Hydrolyzed by esterases during absorption and distributed in circulating blood as active cefditoren. Bactericidal activity results from inhibition of cell wall synthesis via affinity for penicillin-binding proteins. No dose adjustment necessary for mild renal impairment (CrCl 50-80 mgL/min/1.73 m2) or mild-to-moderate hepatic impairment. Indicated for the treatment of acute exacerbation of chronic bronchitis caused by susceptible strains of Streptococcus pyogenes. |
| Adult Dose | 400 mg PO with meals bid for 10 d Moderate renal impairment (CrCl 30-49 mL/min/1.73 m2): Not to exceed 200 mg PO bid Severe renal impairment (CrCl <30 mL/min/1.73 m2): 200 mg PO qd |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity to drug, penicillin, related compounds, or milk protein sodium caseinate; carnitine deficiency or inborn errors of metabolism that may result in clinically significant carnitine deficiency |
| Interactions | Absorption reduced with H2 receptor antagonists and antacids of magnesium and aluminum hydroxides; probenecid may increase plasma concentrations of cefditoren |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | May cause diarrhea, nausea, and vaginal moniliasis (yeast infection); pseudomembranous colitis may occur; clinical manifestations of carnitine deficiency may occur with prolonged use; prolonged use may result in emergence and overgrowth of resistant organisms; caution in breastfeeding |
| Drug Name | Tetracycline (Sumycin) |
|---|---|
| Description | For susceptible bacterial infections of both gram-positive and gram-negative organisms as well as infections caused by mycoplasmal, chlamydial, or rickettsial organisms. Inhibits bacterial protein synthesis by binding with 30S and, possibly, 50S ribosomal subunit(s). Provides coverage for mycoplasmal, chlamydial, and B pertussis organisms, but less effective than erythromycin. |
| Adult Dose | 50-500 mg PO qid |
| Pediatric Dose | <8 years: Not recommended >8 years: 10-20 mg/lb (25-50 mg/kg) PO divided qid |
| Contraindications | Documented hypersensitivity; severe hepatic dysfunction |
| Interactions | Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; can decrease effects of PO contraceptives, causing breakthrough bleeding and increased risk of pregnancy; can increase hypoprothrombinemic effects of anticoagulants |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; use during tooth development (ie, last half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines |
| Drug Name | Doxycycline (Bio-Tab, Doryx, Vibramycin) |
|---|---|
| Description | Provides coverage for mycoplasmal and chlamydial organisms but not active against B pertussis; inhibits protein synthesis and bacterial growth by binding with 30S and, possibly, 50S ribosomal subunits of susceptible bacteria. |
| Adult Dose | 100 mg PO bid |
| Pediatric Dose | <8 years: Not recommended >8 years: 2-5 mg/kg/d PO qd or divided q12h; not to exceed 200 mg/d |
| Contraindications | Documented hypersensitivity; severe hepatic dysfunction |
| Interactions | Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; can increase hypoprothrombinemic effects of anticoagulants; can decrease effects of PO contraceptives, causing breakthrough bleeding and increased risk of pregnancy |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; use during tooth development (ie, last half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines |
| Drug Name | Trimethoprim-sulfamethoxazole (Bactrim) |
|---|---|
| Description | Inhibits bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid, inhibiting bacterial growth. Antibacterial activity of TMP-SMZ includes common urinary tract pathogens except Pseudomonas aeruginosa. Like tetracycline, has in vitro activity against B pertussis; not useful in mycoplasmal infections. |
| Adult Dose | 160 mg TMP/800 mg SMZ PO q12h for 10-14 d |
| Pediatric Dose | <2 months: Contraindicated >2 months: 15-20 mg/kg/d (TMP) PO divided tid/qid for 14 d |
| Contraindications | Documented hypersensitivity; megaloblastic anemia due to folate deficiency; age <2 mo |
| 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 thrombocytopenic purpura in elderly people; may increase phenytoin levels; may potentiate effects of methotrexate in bone marrow depression; may increase hypoglycemic response to sulfonylureas; may increase levels of zidovudine |
| 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 | Discontinue at first appearance of 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, chronic alcoholism, elderly persons, those receiving anticonvulsant therapy, those with malabsorption syndrome); hemolysis may occur in G-6-PD deficiency; patients with AIDS may not tolerate or respond to TMP-SMZ; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); administer fluids to prevent crystalluria and stone formation |
These agents are used to control fever as well as myalgias and arthralgias.
| Drug Name | Ibuprofen (Ibuprin, Advil, Motrin) |
|---|---|
| Description | Usually DOC for treatment of mild to moderate pain if no contraindications are recognized. Inhibits inflammatory reactions and pain, probably by decreasing activity of enzyme cyclooxygenase, which results in inhibition of prostaglandin synthesis. |
| Adult Dose | 400-800 mg PO q4-6h |
| Pediatric Dose | 10 mg/kg PO q6-8h |
| Contraindications | Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding |
| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effects of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase risk of methotrexate toxicity; may increase phenytoin levels |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Caution in CHF, hypertension, and decreased renal or hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy, monitor PT closely and instruct patients to watch for signs of bleeding |
| Drug Name | Acetaminophen (Tylenol, Panadol, Aspirin-free Anacin) |
|---|---|
| Description | DOC for treatment of pain in those with documented hypersensitivity to aspirin or NSAIDs, with upper GI disease, or taking PO anticoagulants |
| Adult Dose | 625-1000 mg PO q4h; not to exceed 4 g/d |
| Pediatric Dose | <12 years: 10-15 mg/kg/dose PO q4-6h prn; not to exceed 2.6 g/d >12 years: 325-650 mg PO q4h; not to exceed 5 doses in 24 h |
| Contraindications | Documented hypersensitivity; G-6-PD deficiency |
| Interactions | Rifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, or isoniazid may increase hepatotoxicity |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Hepatotoxicity possible in chronic alcoholism following various dose levels; severe or recurrent pain or high or continued fever may indicate serious illness; acetaminophen is contained in many OTC products and combined use with these products may result in cumulative acetaminophen doses exceeding recommended maximum dose |
Little data on the efficacy of expectorants outside the test tube are available. The prototype antitussive, codeine, has been used successfully in some chronic cough and induced cough models;7 however, little clinical data on upper respiratory infections are available. Existing data indicate that codeine is slightly better or equal in efficacy to guaifenesin, dextromethorphan, or even placebo.
| Drug Name | Guaifenesin and codeine (Robitussin A-C, Guiatuss AC, Mytussin AC) |
|---|---|
| Description | Treats minor cough resulting from bronchial and throat irritation. |
| Adult Dose | 5-10 mL PO q4-8h; not to exceed 60 mL/d |
| Pediatric Dose | 1-1.5 mg/kg/d codeine PO divided qid |
| Contraindications | Documented hypersensitivity |
| Interactions | Increases toxicity of CNS depressant drugs |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Do not administer for productive cough or persistent chronic cough from emphysema; caution in renal impairment |
| Drug Name | Guaifenesin with dextromethorphan (Humibid DM, Mytussin, Robitussin DM) |
|---|---|
| Description | Treats minor cough resulting from bronchial and throat irritation. |
| Adult Dose | 10 mL PO q4h |
| Pediatric Dose | <2 years: Not recommended 2-6 years: 2.5 mL PO q4h 6-12 years: 5 mL PO q4h >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| 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 | Do not use to treat productive cough or persistent chronic cough resulting from emphysema |
Studies have shown that bronchodilators are advantageous and may even be superior to antibiotics for bronchitis symptoms. However, patient numbers in trials are disappointingly few given how commonly acute bronchitis is diagnosed.
| Drug Name | Albuterol sulfate (Proventil, Ventolin) |
|---|---|
| Description | Beta-agonist used in treatment of bronchospasm refractory to epinephrine. Relaxes bronchial smooth muscle by action on beta2-receptors and shows little effect on cardiac muscle contractility. |
| Adult Dose | 2 puffs q4-6h or 2-4 mg PO tid/qid |
| Pediatric Dose | 0.1-2 mg/kg PO tid |
| Contraindications | Documented hypersensitivity |
| Interactions | Beta-adrenergic blockers antagonize effects; inhaled ipratropium may increase duration of bronchodilatation by albuterol; cardiovascular effects may increase with MAOIs, inhaled anesthetics, tricyclic antidepressants, or sympathomimetic agents |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in hyperthyroidism, diabetes mellitus, and cardiovascular disorders |
Influenza vaccinations offer greater protection for the appropriate populations because they offer coverage for influenza A and B. Amantadine and rimantadine have been demonstrated to be useful during epidemics of influenza A. Zanamivir and oseltamivir are the neuraminidase inhibitors that are now preferred for chemoprophylaxis during outbreaks of influenza A and B, although data from institutional outbreaks are limited.
| Drug Name | Oseltamivir (Tamiflu) |
|---|---|
| Description | Inhibits neuraminidase, which is a glycoprotein on the surface of influenza virus that destroys an infected cell's receptor for viral hemagglutinin. By inhibiting viral neuraminidase, decreases release of viruses from infected cells and thus viral spread. Effective to treat influenza A or B. Start within 40 h of symptom onset. Available as cap and PO susp. |
| Adult Dose | Acute illness: 75 mg PO bid for 5 d Prophylaxis: 75 mg PO qd for 10 d |
| Pediatric Dose | Acute illness: <1 year: Not indicated >1 year: <15 kg: 30 mg PO bid for 5 d >15-23 kg: 45 mg PO bid for 5 d >23-40 kg: 60 mg PO bid for 5 d >40 kg: Administer as in adults Prophylaxis: <1 year: Not established >1 year: <15 kg: 30 mg PO qd for 10 d >15-23 kg: 45 mg PO qd for 10 d 24-40 kg: 60 mg PO qd for 10 d >40 kg: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| 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 impairment, chronic cardiac or respiratory disease, and breastfeeding; do not use in children <1 y (preclinical trials have demonstrated death in young animals, possibly related to immature blood-brain barriers) |
| Drug Name | Zanamivir (Relenza) |
|---|---|
| Description | Inhibitor of neuraminidase, which is a glycoprotein on the surface of the influenza virus that destroys the infected cell's receptor for viral hemagglutinin. By inhibiting viral neuraminidase, release of viruses from infected cells and viral spread are decreased. Effective against both influenza A and B. To be inhaled through Diskhaler PO inhalation device. Circular foil discs containing 5-mg blisters of drug are inserted into supplied inhalation device. |
| Adult Dose | Treatment: 10 mg (2 inhalations, 5 mg/inhalation) inhaled PO q12h for 5 d; initiate within 2 d of symptom onset Prophylaxis: 10 mg (2 inhalations, 5 mg/inhalation) inhaled PO qd for 10 d; initiate within 36 h of exposure |
| Pediatric Dose | Treatment: <7 years: Not established >7 years: Administer as in adults Prophylaxis: <5 years: Not established >5 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; obstructive airway disease |
| Interactions | None reported |
| 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 | Monitor respiratory status; may cause bronchospasm; caution in breastfeeding |
Article Last Updated: May 12, 2008