Secondary Logo

Journal Logo


Evidence-based diagnosis and management of acute bronchitis

Hart, Ann Marie PhD, FNP

Author Information
doi: 10.1097/01.NPR.0000452978.99676.2b



Acute bronchitis is a common, self-limiting, respiratory tract infection characterized primarily by a cough lasting less than 3 weeks.1 Patients frequently present to nurse practitioners (NPs) with acute cough. Although most acute cough illnesses are benign and self-limited, they are extremely bothersome, and several serious differentials must be excluded. Given the common and potentially serious nature of an acute cough, it is critical for NPs to appropriately diagnose and manage acute bronchitis. This article examines the current research-based evidence for diagnosis and management of acute bronchitis. Recommendations for the diagnosis and management of acute bronchitis in adults who are not immunocompromised and do not have a serious underlying lung disease (for example, chronic obstructive pulmonary disease [COPD] or bronchiectasis) are also explored.

Epidemiology and pathophysiology

Although the exact incidence of acute bronchitis is unknown, it is believed to be an extremely common condition-particularly in the fall and winter months.2 In fact, data from the 2006, 2007, and 2010 National Ambulatory Medical Care Surveys indicate “cough” as the top clinical symptom for which individuals seek care from outpatient healthcare providers.3-5

Over 90% of acute bronchitis cases are viral with etiologies, including influenza A and B, parainfluenza, coronavirus, respiratory syncytial virus, adenovirus, rhinovirus, and human metapneumovirus. Bacterial causes are rare and include Bordetella pertussis, Chlamydia pneumoniae, and Mycoplasma pneumoniae.2

Acute bronchitis stems from inflammation of the bronchial epithelium. This inflammation causes the bronchial and tracheal mucosa to thicken as well as epithelial-cell desquamation and denuding of the basement membrane airway.2,6

One of the most troubling aspects of acute bronchitis is its lengthy nature. A recent meta-analysis of 19 studies found that the mean duration of cough in adults with an acute cough illness was 17.8 days.7 Purulent sputum is also common in acute bronchitis and is the result of sloughing of the tracheobronchial epithelium and inflammatory cells.2,8 Contrary to popular belief, the presence of purulent sputum does not indicate a bacterial infection.9

Clinical presentation and diagnosis

Cough is the primary symptom of acute bronchitis. By definition, adults with acute bronchitis present with a cough illness of less than 3 weeks' duration.1 Although localized symptoms (such as nasal congestion, runny nose, sore throat) associated with nonspecific respiratory infections (colds) may be present with acute bronchitis, systemic symptoms such as fever, myalgia, nausea, malaise, and dyspnea are typically absent. However, it is not uncommon for individuals with acute bronchitis to experience bronchospasm and wheezing, especially if there is an underlying history of asthma.10

In order to accurately diagnose and manage acute bronchitis in adults, the NP should perform a history and physical exam that considers the main differential diagnoses for acute cough illness and primarily focuses on ruling out pneumonia, B. pertussis (commonly referred to as “pertussis”), and influenza. (See Differential diagnoses for acute cough illness.) The history should focus on type and length of symptoms, paying particular attention to worrisome systemic symptoms (such as fevers, myalgia, dyspnea) more commonly seen in pneumonia. The physical exam in acute bronchitis is often normal, although low-grade fever (less than 100.4° F [38°C]) and/or wheezing and rhonchi may be present. However, crackles and other signs of lung consolidation (egophony, increased fremitus, dullness to percussion) should be absent; the presence of these signs warrants further workup.1,2,10 Procalcitonin is currently being evaluated as a potential serum biomarker for distinguishing between bacterial and viral infections (see Role of procalcitonin in the diagnosis of acute bronchitis). Additional diagnostic tests are usually not warranted in the absence of signs and symptoms of pneumonia, pertussis, or influenza.

Pneumonia. Pneumonia should be considered and ruled out when vital signs are abnormal (pulse greater than 100, respirations greater than 24/minute, or temperature greater than 100.4° F [38°C]) and/or when signs of consolidation are present on lung exam. Systemic symptoms should also warrant suspicion for pneumonia. Older individuals may not mount a fever with infections; therefore, pneumonia should also be considered and ruled out in patients over 75 years of age in the presence of respiratory rate greater than 24/minute, decreased oxygen saturation, decreased mental status, and/or a change in behavior.11

According to the most recent consensus guidelines published by the Infectious Diseases Society of America and the American Thoracic Society, the presence of an infiltrate on chest X-ray is considered the gold standard for diagnosing pneumonia.12 However, dehydration may result in a false-negative chest X-ray, and one study found 7% of patients with initial “negative” chest X-rays had findings consistent with pneumonia on repeat chest X-ray.13 Therefore, the absence of infiltrate on chest X-ray should not supersede clinical judgment in ill-appearing patients suspected of having pneumonia.

Pertussis. Pertussis is a highly contagious bacterial respiratory illness with several potentially severe complications, including dehydration, hypoxia, encephalopathy, syncope, seizures, pneumonia, pneumothorax, and rib fractures from severe coughing.14 Although pertussis is more common in children, the incidence in adolescents, adults, and older adults has risen dramatically over the past 2 decades and needs to be considered and ruled out whenever patients present with acute cough illnesses.15-17

Pertussis should be considered when a cough illness lasts for 2 or more weeks without another apparent cause and includes one or more of the following symptoms: paroxysms of cough, inspiratory “whoop” sound, or posttussive vomiting. Pertussis should also be considered during community outbreaks or when an individual has a close contact with an individual with a confirmed case of pertussis.18 The actual diagnosis of pertussis is based upon lab testing. For more information regarding pertussis testing, visit:

Influenza. Influenza is also a highly contagious respiratory virus with potentially severe complications in the older adult and in those with underlying metabolic or cardiopulmonary conditions, such as COPD and diabetes. Annual epidemics of influenza tend to occur during the fall and winter months in the United States; however, the peak of influenza activity can occur as late as April or May. Symptoms of influenza can include fever, myalgia, headache, malaise, cough, sore throat, and runny nose. Fever and body aches usually last for 3 to 5 days, whereas cough and lack of energy may last for 2 or more weeks. The symptoms of influenza are nonspecific; therefore, influenza is often difficult to diagnose based on symptoms alone.19 Rapid diagnostic tests can aid clinicians in diagnosing influenza but should only be obtained if the results of the testing will impact decision making regarding treatments.20 For more information on the diagnosis and treatment of influenza, visit:


Antibiotics. The management of acute bronchitis is primarily supportive and is focused on controlling cough. Antibiotic therapy has a minor role in acute bronchitis, primarily for pertussis. Over the past 30 years, multiple studies have shown little or no improvement when antibiotics are prescribed for adults with acute bronchitis.21-25 More recently, a 2012 Cochrane systematic review of 15 randomized controlled trials (RCTs) with 2,618 patients, including smokers and nonsmokers, found a statistically significant reduction in cough duration by 0.6 days with antibiotic treatment.26 In addition, a recent 12-country RCT of 2,161 adults diagnosed with acute bronchitis found no difference in duration of symptoms between the amoxicillin versus the placebo group.27

Antibiotics are prescribed over 50% of the time for adults with acute bronchitis who present to primary care clinicians.28,29 Although inappropriate antibiotic use for acute bronchitis and other acute viral respiratory infections has decreased over the past decade, recent studies indicate an increase in prescriptions of broad-spectrum antibiotics for acute bronchitis, a phenomenon that goes against the principles of good antibiotic stewardship and promotes antibiotic resistance.30-33

Symptom management. Cough control is the goal of symptom management for acute bronchitis1; however, there is currently no “best” treatment strategy to facilitate this. Although multiple pharmacologic preparations are available for the treatment of cough, there is a dearth of published research literature related to support them. In addition, results from the available studies have been mixed and/or have shown treatments to be minimally effective.

Over-the-counter (OTC) medications. A 2012 Cochrane systematic review of OTC medications for acute cough assessed 18 RCTs with 3,421 adults for the effectiveness of several OTC cough preparations, including antitussives (codeine cough syrup, dextromethorphan, and moguisteine, the latter of which is not available in the United States), an expectorant (guaifenesin), a mucolytic (bromhexine), antihistamines (terfenadine [removed from U.S. market in 1998] and thonzylamine), and antihistamine/decongestant combinations (both loratadine/pseudoephedrine and dexbrompheniramine/pseudoephedrine).34 Study results were mixed across all of these preparations; however, this review was severely limited by the relatively few number of studies for each of these medications.

Opioids and tramadol. Codeine has long been considered the “gold standard” for cough suppression. However, there is surprisingly little evidence to support the use of codeine and hydrocodone for the treatment of acute cough. No recent research has been conducted regarding codeine and hydrocodone for cough. A 2007 review explored the effectiveness of codeine in cough; five studies were found, none of which indicated codeine as being more effective than placebo.35 Similarly, the only available published research related to hydrocodone and cough is small and relates to the use of hydrocodone for cough in advanced cancer and during bronchoscopy.36,37 In addition, there is one case report regarding the effectiveness of tramadol in a patient with interstitial pneumopathy.38

Beta-2 agonists. A 2011 Cochrane systematic review assessed the effectiveness of beta (β)-2 agonists (albuterol) for acute bronchitis.39 This study reviewed five RCTs with 418 adults and found no significant benefits from oral (three RCTs) or inhaled (two RCTs) preparations of beta-2 agonists. However, this study was also limited due to the small number of clinical trials. In addition, this review only looked at the use of β-2 agonists in those without pre-existing pulmonary disease, such as asthma, who often experience wheezing and bronchospasm with acute bronchitis and may benefit from an inhaled β-2 agonist.

Nonsteroidal anti-inflammatory drugs (NSAIDs). A 2009 Cochrane systematic review of NSAIDs for the common cold reviewed nine RCTs with 1,064 adult patients.40 Although improvement was observed in noncough symptoms such as sore throat, ear pain, and headache, no improvement was seen for the symptom of cough. However, it is important to note that this review looked at patients experiencing the common cold, not specifically acute bronchitis. There were recent published studies aside from the 2009 systemic review. However, a study is underway comparing ibuprofen, amoxicillin/clavulanic acid, and placebo in adults with acute bronchitis.41

Benzonatate. Benzonatate, a peripherally acting oral antitussive agent, thought to suppress cough by anesthetizing pulmonary stretch receptors, has very little published evidence to support its effectiveness. In fact, a search of the Pubmed database revealed two studies. Most recently, a small RCT was conducted with 30 adult nonsmokers experiencing an acute illness. Each subject received three out of four possible regimens at different times: guaifenesin alone, benzonatate alone, the guaifenesin and benzonatate combined, or placebo. The subjects also inhaled capsaicin until five or more coughs were obtained one hour after ingesting each of these regimens. Results showed that the combination of benzonatate (200 mg) and guaifenesin (600 mg) suppressed cough greater than placebo or either benzonatate alone (p < 0.001) or guaifenesin alone (p = 0.008). However, this study was also limited by both its small sample size and its use of capsaicin to induce cough.42 The second study was a case study of three patients with advanced cancer who experienced cough and responded to benzonatate.43

Nebulized lidocaine. Nebulized lidocaine is frequently used prior to bronchoscopies to suppress the cough reflex and has been proposed as a potential treatment for the cough associated with acute bronchitis. A recent literature review found seven studies where nebulized lidocaine had been successfully and safely used for intractable cough in a variety of conditions.44 However, all of these studies were very small, and further study is warranted with larger samples prior to recommending nebulized lidocaine for routine use.

Herbal remedies

Pelargonium sidoides. P. sidoides is a member of the geranium family, which is native South Africa. It is believed to have mild antibacterial, antiviral, and mucolytic properties and has been available in Germany since 1983.45 A 2009 Cochrane systematic review found three RCTs, including 746 adult patients with acute bronchitis. The review showed inconsistencies in both dosing and results.46 Another RCT was conducted with 406 adults diagnosed with acute bronchitis since this review.47 Participants were assigned to one of four treatment groups: placebo, 30 mg, 60 mg, 90 mg of P. sidoides extract daily. At day 7, there was significant improvement in all three treatment groups compared to placebo with regards to symptoms and quality of life.47 The results from this trial are promising; however, more research is needed regarding the effectiveness and safety of P. sidoides before it can be recommended for acute bronchitis.

Chinese medicinal herbs. Chinese herbs have long been used to treat acute cough illnesses and other respiratory tract infections, and some are believed to have antitussive and antiviral properties. A 2012 Cochrane systematic review found 74 studies with 6,877 patients; however, none of the studies met the inclusion criteria for the review; therefore, no recommendations regarding the use of Chinese medicinal herbs could be made.48

Implications for advanced practice nursing

Acute bronchitis is a common condition treated in primary care settings. Although the diagnosis of acute bronchitis is not difficult to make, it requires careful consideration of the competing differential diagnoses with an eye toward ruling out more serious infections. Unfortunately, there is no “magic bullet” for treating the cough associated with acute bronchitis. Although many cough preparations are available for the treatment of cough associated with acute bronchitis, there is a relative void of research related to these preparations, and most of these studies have been small and/or had inconsistent results (see Summary of diagnostic and treatment recommendations for adults with acute cough illness).

Summary of diagnostic and treatment recommendations for adults with acute cough illness*1,2,10,11,13,18,20-27,30,34-38,41-48,52

Although this review cannot recommend particular pharmacologic or herbal treatments for acute bronchitis, this is not to say that there are no available treatments for the management of acute bronchitis. The NP should consider several points when reviewing this article. First, for the most part, is the fact that high-quality published studies regarding treatments for cough were lacking, and therefore, recommendations could not be made for or against the various treatment recommendations. Second, the various preparations were compared to placebo, which is not the same as “no treatment.” This is important to note because placebos have been shown to have therapeutic value in and of themselves.49 Third, “best research evidence” is only one aspect of the integrated evidence-based practice triad.50 Also included in this triad are patient preferences and experiences as well as clinician expertise. Therefore, in the absence of definitive research evidence, if patient preferences and/or clinician or patient experiences suggest that a particular treatment strategy might work (for example, a treatment with a known safety profile), it is likely worth exploring. Along those lines, NPs should systematically assess and record their patients' experiences with different treatments and publish this work in the form of case studies. This type of research design is known as the single case experimental design, which is both well-suited for busy primary care clinicians and within the purview of doctor of nursing practice (DNP)-prepared NPs.51

There are several supportive strategies that NPs can offer adults who present with acute bronchitis, which might lead to increased satisfaction and decreased inappropriate antibiotic prescribing. A recent study of 655 adults regarding their behaviors and expectations related to acute respiratory infections found that although most of these individuals expected a prescription for antibiotics and/or a prescription for their symptoms, they also desired the following: to have their symptoms listened to; to discuss their worries and concerns; to have their self-knowledge respected; to have the severity, nature, and expected length of their illness explained; to discuss treatment options; to have their concern handled in one visit; and to be able to follow up with the provider after the visit via phone or e-mail.52 These expectations reflect the respectful, relationship-based care that NPs have long been known to provide and should go a long way toward providing high-quality care for adults with acute bronchitis and other acute cough illnesses.

Finally, the reader is encouraged to read a brief summary about the potentially promising role of procalcitonin in the discernment of bacterial from viral etiologies of acute bronchitis.53-62.

Differential diagnoses for acute cough illness1,10

  • ACE inhibitor-induced cough
  • Acute bronchitis
  • Acute exacerbation of COPD
  • Acute sinusitis
  • Asthma
  • Bronchiectasis
  • Gastroesophageal reflux disease
  • Heart failure
  • Influenza
  • Nonspecific upper respiratory tract infection
  • Pertussis
  • Pneumonia
  • Pulmonary embolus
  • Upper airway cough syndrome (previously referred to as postnasal drip syndrome)

Role of procalcitonin in the diagnosis of acute bronchitis53-62

Although acute bronchitis is primarily viral in etiology, a small minority (∼10%) of individuals with acute bronchitis will have a bacterial infection and might benefit from antibiotic therapy. However, distinguishing viral from bacterial etiologies of acute bronchitis on the basis of history and physical exam has been elusive. Procalcitonin is a peptide precursor of calcitonin released in response to bacterial toxins and appears promising in terms of distinguishing bacterial from viral etiologies. Simply put, procalcitonin rises with bacterial infections but appears minimally altered by viral infections. Interestingly, procalcitonin levels do not increase for other inflammatory conditions (such as inflammatory bowel disease or temporal giant cell arteritis). In addition, serum procalcitonin levels are not altered by glucocorticoids or nonsteroidal anti-inflammatory agents. A number of trials have demonstrated the utility of procalcitonin in distinguishing bacterial from viral respiratory infections. Furthermore, a Cochrane review of 14 trials including 4,221 patients found that using a procalcitonin algorithm to guide decision making regarding antibiotics for acute respiratory infections resulted in decreased antibiotic use with no increase in mortality or treatment failure. Procalcitonin appears to be a promising biomarker for helping to distinguish between bacterial and viral etiologies for acute bronchitis and other respiratory tract infections. However, further study is needed, and procalcitonin is not recommended for routine use in primary care at this time.


1. Irwin RS, Baumann MH, Bolser DC, et al. Diagnosis and management of cough executive summary: ACCP evidence-based clinical practice guidelines. Chest. 2006;129(suppl 1):1S-23S.
2. Wenzel RP, Fowler AA 3rd. Clinical practice. Acute bronchitis. N Engl J Med. 2006;355(20):2125–2130.
3. Cherry DK, Hing E, Woodwell DA, Rechtsteiner EA. National Ambulatory Medical Care Survey: 2006 summary. Natl Health Stat Report. 2008;(3):1–39.
4. Hsiao CJ, Cherry DK, Beatty PC, Rechtsteiner EA. National Ambulatory Medical Care Survey: 2007 summary. Natl Health Stat Report. 2010;(27):1–32.
    5. National Ambulatory Medical Care Survey: 2010 Summary Tables. 2013.
    6. Walsh JJ, Dietlein LF, Low FN, Burch GE, Mogabgab WJ. Bronchotracheal response in human influenza. Type A, Asian strain, as studied by light and electron microscopic examination of bronchoscopic biopsies. Arch Intern Med. 1961;108:376–388.
    7. Ebell MH, Lundgren J, Youngpairoj S. How long does a cough last? Comparing patients' expectations with data from a systematic review of the literature. Ann Fam Med. 2013;11(1):5–13.
    8. Robertson AJ. Green sputum. Lancet. 1952;1(6697):12–15.
    9. Altiner A, Wilm S, Däubener W, et al. Sputum colour for diagnosis of a bacterial infection in patients with acute cough. Scand J Prim Health Care. 2009;27(2):70–73.
    10. File TM. Acute bronchitis in adults. In: Sexton DJ, Lin FH, eds. UpToDate; 2013.
    11. Bartlett JG. Diagnostic approach to community-acquired pneumonia in adults. In: Calderwood SB, Thorner AR, eds. UpToDate; 2012.
    12. Mandell LA, Wunderink RG, Anzueto A, et al. Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007;44(suppl 2):S27–S72.
    13. Basi SK, Marrie TJ, Huang JQ, Majumdar SR. Patients admitted to hospital with suspected pneumonia and normal chest radiographs: epidemiology, microbiology, and outcomes. Am J Med. 2004;117(5):305–311.
    14. Centers for Disease Control and Prevention. Pertussis: clinical complications. 2013.
    15. Centers for Disease Control and Prevention: National Notifiable Diseases Surveillance System and Supplemental Pertussis Surveillance System. Reported pertussis incidence by age group: 1990–2012. 2013.
    16. Halperin SA. The control of pertussis—2007 and beyond. N Engl J Med. 2007;356(2):110–113.
      17. McGuiness CB, Hill J, Fonseca E, Hess G, Hitchcock W, Krishnarajah G. The disease burden of pertussis in adults 50 years old and older in the United States: a retrospective study. BMC Infect Dis. 2013;13:32.
      18. Centers for Disease Control and Prevention. Epidemiology and Prevention of Vaccine-Preventable Diseases. 12th ed. Annapolois Junction, MD: Public Health Foundation; 2012:215–232.
      19. Centers for Disease Control and Prevention. Clinical Signs and Symptoms of Influenza: Influenza Prevention & Control Recommendations. 2013.
      20. Centers for Disease Control and Prevention. Clinical Description & Lab Diagnosis of Influenza. 2013.
      21. Stott NC, West RR. Randomised controlled trial of antibiotics in patients with cough and purulent sputum. Br Med J. 1976;2(6035):556–559.
      22. Williamson HA Jr. A randomized, controlled trial of doxycycline in the treatment of acute bronchitis. J Fam Pract. 1984;19(4):481–486.
        23. King DE, Williams WC, Bishop L, Shechter A. Effectiveness of erythromycin in the treatment of acute bronchitis. J Fam Pract. 1996;42(6):601–605.
          24. Dowell J, Pitkethly M, Bain J, Martin S. A randomised controlled trial of delayed antibiotic prescribing as a strategy for managing uncomplicated respiratory tract infection in primary care. Br J Gen Pract. 2001;51(464):200–205.
            25. Nduba VN, Mwachari CW, Magaret AS, et al. Placebo found equivalent to amoxicillin for treatment of acute bronchitis in Nairobi, Kenya: a triple blind, randomised, equivalence trial. Thorax. 2008;63(11):999–1005.
            26. Smith SM, Fahey T, Smucny J, Becker LA. Antibiotics for acute bronchitis. Cochrane Database Syst Rev. 2014;3:CD000245.
            27. Little P, Stuart B, Moore M, et al. Amoxicillin for acute lower-respiratory-tract infection in primary care when pneumonia is not suspected: a 12-country, randomised, placebo-controlled trial. Lancet Infect Dis. 2013;13(2):123–129.
            28. Gonzales R, Camargo CA Jr,, MacKenzie T, et al. Antibiotic treatment of acute respiratory infections in acute care settings. Acad Emerg Med. 2006;13(3):288–294.
            29. Aspinall SL, Good CB, Metlay JP, Mor MK, Fine MJ. Antibiotic prescribing for presumed nonbacterial acute respiratory tract infections. Am J Emerg Med. 2009;27(5):544–551.
            30. Gill JM, Fleischut P, Haas S, Pellini B, Crawford A, Nash DB. Use of antibiotics for adult upper respiratory infections in outpatient settings: a national ambulatory network study. Fam Med. 2006;38(5):349–354.
            31. Grijalva CG, Nuorti JP, Griffin MR. Antibiotic prescription rates for acute respiratory tract infections in US ambulatory settings. JAMA. 2009;302(7):758–766.
              32. Vergidis P, Hamer DH, Meydani SN, Dallal GE, Barlam TF. Patterns of antimicrobial use for respiratory tract infections in older residents of long-term care facilities. J Am Geriatr Soc. 2011;59(6):1093–1098.
                33. Hart AM. Antibiotic stewardship to preserve benefits. The Clinical Advisor. 2011;14(11):46–55.
                34. Smith SM, Schroeder K, Fahey T. Over-the-counter (OTC) medications for acute cough in children and adults in ambulatory settings. Cochrane Database Syst Rev. 2012;8:CD001831.
                35. Bolser DC, Davenport PW. Codeine and cough: an ineffective gold standard. Curr Opin Allergy Clin Immunol. 2007;7(1):32–36.
                36. Homsi J, Walsh D, Nelson KA, et al. A phase II study of hydrocodone for cough in advanced cancer. Am J Hosp Palliat Care. 2002;19(1):49–56.
                37. Stolz D, Chhajed PN, Leuppi JD, Brutsche M, Pflimlin E, Tamm M. Cough suppression during flexible bronchoscopy using combined sedation with midazolam and hydrocodone: a randomised, double blind, placebo controlled trial. Thorax. 2004;59(9):773–776.
                38. Louly PG, Medeiros-Souza P, Santos-Neto L. N-of-1 double-blind, randomized controlled trial of tramadol to treat chronic cough. Clin Ther. 2009;31(5):1007–1013.
                39. Becker LA, Hom J, Villasis-Keever M, van der Wouden JC. Beta2-agonists for acute bronchitis. Cochrane Database Syst Rev. 2011;(7):CD001726.
                40. Kim SY, Chang YJ, Cho HM, Hwang YW, Moon YS. Non-steroidal anti-inflammatory drugs for the common cold. Cochrane Database Syst Rev. 2013;6:CD006362.
                41. Llor C, Moragas A, Bayona C, et al. Effectiveness of anti-inflammatory treatment versus antibiotic therapy and placebo for patients with non-complicated acute bronchitis with purulent sputum. The BAAP Study protocol. BMC Pulm Med. 2011;11:38.
                42. Dicpinigaitis PV, Gayle YE, Solomon G, Gilbert RD. Inhibition of cough-reflex sensitivity by benzonatate and guaifenesin in acute viral cough. Respir Med. 2009;103(6):902–906.
                43. Doona M, Walsh D. Benzonatate for opioid-resistant cough in advanced cancer. Palliat Med. 1998;12(1):55–58.
                44. Slaton RM, Thomas RH, Mbathi JW. Evidence for therapeutic uses of nebulized lidocaine in the treatment of intractable cough and asthma. Ann Pharmacother. 2013;47(4):578–585.
                45. Umckaloabo (Pelargonium sidoides). Natural Standard. 2013.
                46. Timmer A, Günther J, Rücker G, Motschall E, Antes G, Kern WV. Pelargonium sidoides extract for acute respiratory tract infections. Cochrane Database Syst Rev. 2008;(3):CD006323.
                47. Matthys H, Lizogub VG, Funk P, Malek FA. Pelargonium sidoides in acute bronchitis—health-related quality of life and patient-reported outcome in adults receiving EPs 7630 treatment. Wien Med Wochenschr. 2010;160(21-22):564–570.
                48. Jiang L, Li K, Wu T. Chinese medicinal herbs for acute bronchitis. Cochrane Database Syst Rev. 2012;2:CD004560.
                49. Hróbjartsson A, Gøtzsche PC. Placebo interventions for all clinical conditions. Cochrane Database Syst Rev. 2010;(1):CD003974.
                50. Straus WE, Richardson WS, Glasziou P, Haynes RB. Evidence-based Medicine: How to Practice and Teach EBM. 4th ed. Edinburgh: Elsevier; 2005.
                51. Janosky JE. Use of the single subject design for practice based primary care research. Postgrad Med J. 2005;81(959):549–551.
                52. Hart AM, Morgan KM. Acute respiratory infection-related patient behaviors and expectations in Wyoming. J Nurse Pract. 2013;9(4):202–207.
                53. Schuetz P, Amin DN, Greenwald JL. Role of procalcitonin in managing adult patients with respiratory tract infections. Chest. 2012;141(4):1063–1073.
                54. Gilbert DN. Procalcitonin as a biomarker in respiratory tract infection. Clin Infect Dis. 2011;52(suppl 4):S346–S350.
                  55. Thia KT, Chan ES, Ling KL, Ng WY, Jacob E, Ooi CJ. Role of procalcitonin in infectious gastroenteritis and inflammatory bowel disease. Dig Dis Sci. 2008;53(11):2960–2968.
                  56. Scirè CA, Cavagna L, Perotti C, Bruschi E, Caporali R, Montecucco C. Diagnostic value of procalcitonin measurement in febrile patients with systemic autoimmune diseases. Clin Exp Rheumatol. 2006;24(2):123–128.
                    57. Preas HL 2nd,, Nylen ES, Snider RH, et al. Effects of anti-inflammatory agents on serum levels of calcitonin precursors during human experimental endotoxemia. J Infect Dis. 2001;184(3):373–376.
                      58. Perren A, Cerutti B, Lepori M, et al.. Influence of steroids on procalcitonin and C-reactive protein in patients with COPD and community-acquired pneumonia. Infection. 2008;36(2):163–166.
                        59. Briel M, Schuetz P, Mueller B, et al. Procalcitonin-guided antibiotic use vs a standard approach for acute respiratory tract infections in primary care. Arch Intern Med. 2008;168(18):2000–2007.
                        60. Schuetz P, Christ-Crain M, Thomann R, et al. Effect of procalcitonin-based guidelines vs standard guidelines on antibiotic use in lower respiratory tract infections: the ProHOSP randomized controlled trial. JAMA. 2009;302(10):1059–1066.
                          61. Burkhardt O, Ewig S, Haagen U, et al.Procalcitonin guidance and reduction of antibiotic use in acute respiratory tract infection. Eur Respir J. 2010;36(3):601–607.
                            62. Schuetz P, Müller B, Christ-Crain M, et al. Procalcitonin to initiate or discontinue antibiotics in acute respiratory tract infections. Cochrane Database Syst Rev. 2012;9:CD007498.

                            acute bronchitis; acute cough illness; respiratory tract infection

                            Copyright © 2014 Wolters Kluwer Health, Inc. All rights reserved.