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{{Bronchiectasis}}
{{Bronchiectasis}}
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{{CMG}}; {{AE}} {{HQ}}, Saarah T. Alkhairy, M.D.


==Overview==
==Overview==
Treatment of bronchiectasis is aimed at controlling [[infection]]s and bronchial secretions, relieving airway obstruction, and preventing [[Complication (medicine)|complication]]s.
The management of bronchiectasis includes [[Medicine|medical]] therapy and [[Physical therapy|physiotherapy]] strategies. The medical treatment consists of patient [[education]], treatment of the acute exacerbations, prophylactic treatment, [[vaccination]], and other therapies. Antimicrobial therapy is indicated for acute exacerbations of bronchiectasis. The [[Physical therapy|physiotherapy]] strategies focus on airway clearance and [[Lung|pulmonary]] rehabilitation. Supportive therapies include inhaled [[mannitol]], nebulized hypertonic 7% saline, inhaled [[corticosteroids]], and [[oxygen]] therapy. Along with treatment of bronchiectasis, it is important to treat any underlying conditions.


==Medical Therapy==
==Bronchiectasis Medical Therapy==
Common medical therapy for bronchiectasis includes prolonged usage of [[antibiotic|antibiotics]] to prevent detrimental infections<ref>{{cite journal |author=Evans DJ, Bara AI,Greenstone M |title=Prolonged antibiotics for purulent bronchiectasis in children and adults |language=English |journal=The Cochrane Database of Systematic Reviews |volume= |issue=2 |pages= |year=2007 |pmid= |doi=10.1002/14651858.CD001392.pub2}}</ref>, as well as eliminating accumulated fluid with postural drainage and chest physiotherapy. Surgery may also be used to treat localized bronchiectasis, removing obstructions that could cause progression of the disease.<ref>{{cite journal |author=Ötgün B, Karnak B, Tanyel K, Enocak M, Büyükpamukçu N|title=Surgical treatment of bronchiectasis in children. |language=English |journal=Journal of Pediatric Surgery |volume=39 |issue=10 |pages=1532-36 |year=2003 |pmid= |doi=}}</ref>
===Medical Treatment===
====Patient  Education ====
*The patients should understand their [[diagnosis]] clearly.
* [[Smoking]] cessation, regular [[physical exercise|exercise]], and proper [[nutrition]] should be advised.
*The patient should know how to self-manage acute exacerbations with a home supply of [[antibiotic|antibiotics]].


Inhaled [[steroid]] therapy that is consistently adhered to can reduce sputum production and decrease airway constriction over a period of time will prevent progression of bronchiectasis. One commonly used therapy is [[Beclometasone dipropionate]], also used in asthma treatment.<ref>{{cite journal |author=Elborn JS, Johnston B, Allen F, Clarke J, McGarry J, Varghese G. |title=Inhaled steroids in patients with bronchiectasis |language=English |journal=Respir Med |volume=86 |issue=2 |pages=121-4 |year=1992 |pmid=1615177 |doi=}}</ref> Use of inhalers such as [[Salbutamol|Albuterol (Salbutamol)]], [[Fluticasone|Fluticasone (Flovent/Flixotide)]] and [[Ipratropium|Ipratropium (Atrovent)]] may help reduce likelihood of infection by clearing the airways and decreasing inflammation.<ref>{{cite web | last = Reports | first = Consumer | authorlink = | coauthors = | title = Ipratropium and Albuterol Inhalation - Drug Review | work = | publisher = Consumer Reports of U.S.| url = http://www.consumerreports.org/mg/drug-reports/ipratropium-and-albuterol-inhalation.htm | format = | doi =}}</ref>
====Treatment of Acute Exacerbations====
*The mainstay of treatment is [[antibiotic]] therapy.
*Once the [[sputum]] specimen is collected and sent for culture, a targeted [[antibiotic]] therapy is recommended.
*It is considered chronic if the same [[microorganism]] is detected in three or more consecutive cultures separated by at least 1 month over a period of 6 months.<ref name="pmid23728208">{{cite journal| author=McDonnell MJ, Ward C, Lordan JL, Rutherford RM| title=Non-cystic fibrosis bronchiectasis. | journal=QJM | year= 2013 | volume= 106 | issue= 8 | pages= 709-15 | pmid=23728208 | doi=10.1093/qjmed/hct109 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23728208  }} </ref>
*[[Intravenous]] (IV) antibiotics may be needed if there has been: no response to oral antibiotics, systemic deterioration, or if the organism is sensitive only to IV agents.<ref name="pmid23728208">{{cite journal| author=McDonnell MJ, Ward C, Lordan JL, Rutherford RM| title=Non-cystic fibrosis bronchiectasis. | journal=QJM | year= 2013 | volume= 106 | issue= 8 | pages= 709-15 | pmid=23728208 | doi=10.1093/qjmed/hct109 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23728208  }} </ref>
*[[Allergic bronchopulmonary aspergillosis]] (ABPA)
**Oral [[prednisone]] 0.5 to 1 mg/kg per day for two weeks followed by alternate day therapy tapered over three to six months.
**A 16 week course of an [[Antifungal drug|antifungal]] agent, such as [[itraconazole]] or [[voriconazole]], may be added in patients who require large doses of [[glucocorticoids]].
===Antibiotic Regimen===
*'''Bronchiectasis'''<ref name="pmid20627931">{{cite journal| author=Pasteur MC, Bilton D, Hill AT, British Thoracic Society Bronchiectasis non-CF Guideline Group| title=British Thoracic Society guideline for non-CF bronchiectasis. | journal=Thorax | year= 2010 | volume= 65 Suppl 1 | issue=  | pages= i1-58 | pmid=20627931 | doi=10.1136/thx.2010.136119 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20627931  }} </ref>
:* 1.'''Acute exacerbations of bronchiectasis'''
::* 1.1 '''Empiric antimicrobial therapy'''
:::* Preferred regimen: [[Amoxicillin]] 0.5-1 g PO/IV q8h for 14 days
:::* Alternative regimen (1): [[Ciprofloxacin]] 500-750 mg PO bid for 14 days
:::* Alternative regimen (2): [[Clarithromycin]] 500 mg PO bid for 14 days
::* 1.2 '''Pathogen-directed antimicrobial therapy'''
:::* 1.2.1 '''Streptococcus pneumoniae'''
::::* Preferred regimen: [[Amoxicillin]] 500 mg PO tid for 14 days
::::* Alternative regimen: [[Clarithromycin]] 500 mg PO bid for 14 days
:::* 1.2.2 '''Haemophilus influenzae (b-lactamase negative)'''
::::* Preferred regimen (1): [[Amoxicillin]] 0.5-1 g PO tid for 14 days
::::* Preferred regimen (2): [[Amoxicillin]] 3 g PO bid for 14 days
::::* Alternative regimen (1): [[Clarithromycin]] 500 mg PO bid for 14 days
::::* Alternative regimen (2): [[Ciprofloxacin]] 500 mg PO bid for 14 days
::::* Alternative regimen (3): [[Ceftriaxone]] 2 g IV q24h for 14 days
:::* 1.2.3 '''Haemophilus influenzae (b-lactamase positive)'''
::::* Preferred regimen: [[Amoxicillin-Clavulanate]] 625 mg PO tid for 14 days
::::* Alternative regimen (1): [[Clarithromycin]] 500 mg PO bid for 14 days
::::* Alternative regimen (2): [[Ciprofloxacin]] 500 mg PO bid for 14 days
::::* Alternative regimen (3): [[Ceftriaxone]] 2 g IV q24h for 14 days
:::* 1.2.4 '''Moraxella catarrhalis'''
::::* Preferred regimen: [[Amoxicillin-Clavulanate]] 625 mg PO tid for 14 days
::::* Alternative regimen: [[Ciprofloxacin]] 500 mg PO bid for 14 days
:::* 1.2.5 '''Staphylococcus aureus (MSSA)'''
::::* Preferred regimen: [[Flucloxacillin]] 500 mg PO qid for 14 days
::::* Alternative regimen: [[Clarithromycin]] 500 mg PO bid 14 days
:::* 1.2.6 '''Staphylococcus aureus (MRSA) (mild-to-moderate)'''
::::* Preferred regimen (weight < 50 kg): [[Rifampicin]] 450 mg PO qd {{and}} [[Trimethoprim]] 200 mg PO bid for 14 days
::::* Preferred regimen (weight > 50 kg): [[Rifampicin]] 600 mg PO qd {{and}} [[Trimethoprim]] 200 mg PO bid for 14 days
::::* Alternative regimen (weight < 50 kg): [[Rifampicin]] 450 mg PO qd {{and}} [[Doxycycline]] 200 mg PO qd for 14 days
::::* Alternative regimen (weight > 50 kg): [[Rifampicin]] 600 mg PO qd {{and}} [[Doxycycline]] 200 mg PO qd for 14 days
::::* Alternative regimen: [[Linezolid]] 600 mg PO bid for 14 days (third-line therapy)
:::* 1.2.7 '''Staphylococcus aureus (MRSA) (severe)'''
::::* Preferred regimen (1): [[Vancomycin]] 1 g IV q12h (trough levels of 10-20 ng/mL)
::::* Preferred regimen (2): [[Teicoplanin]] 400 mg IV q24h for 14 days
::::* Alternative regimen: [[Linezolid]] 600 mg IV q12h for 14 days
:::* 1.2.8 '''Coliforms (eg, Klebsiella, enterobacter)'''
::::* Preferred regimen: [[Ciprofloxacin]] 500 mg PO bid for 14 days
::::* Alternative regimen: [[Ceftriaxone]] 2 g IV od 14 days
:::* 1.2.9 '''Pseudomonas aeruginosa'''
::::* Preferred regimen: [[Ciprofloxacin]] 500-750 mg PO bid for 14 days
::::* Alternative regimen (1): [[Ceftazidime]] 2 g PO tid for 14 days
::::* Alternative regimen (2): [[Piperacillin-Tazobactam]] 4.5 g PO tid for 14 days
::::* Alternative regimen (3): [[Aztreonam]] 2 g PO tid for 14 days
::::* Alternative regimen (4): [[Meropenem]] 2 g PO tid for 14 days
:::* 1.2.10 '''Pediatric Dosing'''
::::* [[Amoxicillin]] 20-50 mg/kg/day PO bid or tid
::::* [[Co-amoxiclav]] 20-45 mg/kg/day PO bid or tid
::::* [[Trimethoprim]] 4-6 mg/kg/day PO bid (Children < 12 yr)
::::* [[Trimethoprim]] 100-200 mg PO bid (Children > 12 yr)
::::* [[Rifampicin]] 450 mg PO qd (weight < 50 kg)
::::* [[Rifampicin]] 600 mg PO qd (weight > 50 kg)
::::* [[Vancomycin]] 45-60 mg/kg/day IV q8-12h
::::* [[Ciprofloxacin]] 15-30 mg/kg/day PO/IV q12h
::::* [[Doxycycline]] 2-5 mg/kg/day PO/IV q12-24h (maximum daily dose: 200 mg)
::::* [[Linezolid]] 10 mg/kg IV/PO q12h
::::* [[Ceftriaxone]] 50-75 mg/kg IV/IM q24h
::::* [[Ceftazidime]] 150 mg/kg/day IV/IM q8h
:* 2. '''Long-term antibiotic prophylaxis'''
:* Patients with ≥3 exacerbations/year requiring [[antibiotic]] therapy or patients with fewer exacerbations that are causing significant morbidity should be considered for long-term [[antibiotic]] prophylaxis
::* 2.1 '''Pathogen-directed antimicrobial therapy'''
:::* 2.1.1 '''Streptococcus pneumoniae'''
::::* Preferred regimen: [[Amoxicillin]] 500 mg PO bid
::::* Alternative regimen: [[Clarithromycin]] 250 mg PO bid
:::* 2.1.2 '''Haemophilus influenzae (b-lactamase negative)'''
::::* Preferred regimen: [[Amoxicillin]] 500 mg PO bid
::::* Alternative regimen: [[Clarithromycin]] 250 mg PO bid
:::* 2.1.3 '''Haemophilus influenzae (b-lactamase positive)'''
::::* Preferred regimen: [[Amoxicillin-Clavulanate]] 375 mg PO tid
::::* Alternative regimen: [[Clarithromycin]] 250 mg PO bid
:::* 2.1.4 '''Moraxella catarrhalis'''
::::* Preferred regimen: [[Amoxicillin-Clavulanate]] 375 mg PO tid
::::* Alternative regimen: [[Clarithromycin]] 250 mg PO bid
:::* 2.1.5 '''Staphylococcus aureus (MSSA)'''
::::* Preferred regimen: [[Flucloxacillin]] 500 mg PO bid
::::* Alternative regimen: [[Clarithromycin]] 250 mg PO bid
:* 3. '''Pseudomonas eradication (colonization)'''
::* 3.1 '''Initial therapy'''
:::* Preferred regimen: [[Ciprofloxacin]] 750 mg PO bid for 14 days
::* 3.2 '''Secondary therapy in case of treatment failure'''
:::* Preferred regimen (1): [[Piperacillin-tazobactam]] 4.5 g PO tid for 14 days
:::* Preferred regimen (2): [[Cefepime]] 1-2 g IV q8-12h
:::* Preferred regimen (3): [[Ciprofloxacin]] 750 mg PO bid for 4 weeks {{and}} [[Colistin]] (Nebulized) 2 MU NEB bid for 3 months
:::* Preferred regimen (3): [[Colistin]] (Nebulized) 2 MU NEB bid for 3 months


[[Mannitol]] dry inhalation powder, under the name Bronchitol, has been approved by the FDA for use in Cystic Fibrosis patients with Bronchiectasis. The original [[orphan drug]] indication approved in February 2005 allowed its use for the treatment of bronchiectasis. The original approval was based on the results of phase 2 clinical studies showing the product to be safe, well-tolerated, and effective for stimulating mucus hydration/clearance, thereby improving quality of life in patients with chronic obstructive lung diseases like Bronchiectasis. Long-term studies are currently underway to ensure the safety and effectiveness of the treatment, and it is not yet available on the market for use.
====Other Therapies====
*Inhaled [[mannitol]] and nebulized [[hypertonic]] 7% saline for increased airways clearance and [[sputum]] yield<ref name="pmid23728208">{{cite journal| author=McDonnell MJ, Ward C, Lordan JL, Rutherford RM| title=Non-cystic fibrosis bronchiectasis. | journal=QJM | year= 2013 | volume= 106 | issue= 8 | pages= 709-15 | pmid=23728208 | doi=10.1093/qjmed/hct109 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23728208  }} </ref>
*Inhaled [[corticosteroids]] show a significant decrease in [[sputum]] production and [[cough]]<ref name="pmid23728208">{{cite journal| author=McDonnell MJ, Ward C, Lordan JL, Rutherford RM| title=Non-cystic fibrosis bronchiectasis. | journal=QJM | year= 2013 | volume= 106 | issue= 8 | pages= 709-15 | pmid=23728208 | doi=10.1093/qjmed/hct109 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23728208  }} </ref>
*The combination of a long-acting [[Beta2-adrenergic receptor agonist|beta2-agonists]] ([[LABA]]) with a conventional inhaled [[corticosteroids]] can improve the quality of life
*Oxygen therapy
 
== Physiotherapy  Strategies==
====Airway Clearance====
*Postural drainage
*Autogenic drainage
* ActiveCycle of [[breathing]] techniques
*Positive expiratory pressure (PEP)
*Oscillatory PEP devices
*High-frequency chest wall [[percussion]]
 
====Pulmonary Rehabilitation====
*[[Physical exercise|Exercise]] training
*[[Nutrition|Nutritional]] counseling
*Education of the patient's disease and how to manage it
*Techniques on how to conserve energy
*Strategies on breathing
*[[Psychology|Psychological]] counseling


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


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Latest revision as of 20:43, 29 July 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2], Saarah T. Alkhairy, M.D.

Overview

The management of bronchiectasis includes medical therapy and physiotherapy strategies. The medical treatment consists of patient education, treatment of the acute exacerbations, prophylactic treatment, vaccination, and other therapies. Antimicrobial therapy is indicated for acute exacerbations of bronchiectasis. The physiotherapy strategies focus on airway clearance and pulmonary rehabilitation. Supportive therapies include inhaled mannitol, nebulized hypertonic 7% saline, inhaled corticosteroids, and oxygen therapy. Along with treatment of bronchiectasis, it is important to treat any underlying conditions.

Bronchiectasis Medical Therapy

Medical Treatment

Patient Education

  • The patients should understand their diagnosis clearly.
  • Smoking cessation, regular exercise, and proper nutrition should be advised.
  • The patient should know how to self-manage acute exacerbations with a home supply of antibiotics.

Treatment of Acute Exacerbations

  • The mainstay of treatment is antibiotic therapy.
  • Once the sputum specimen is collected and sent for culture, a targeted antibiotic therapy is recommended.
  • It is considered chronic if the same microorganism is detected in three or more consecutive cultures separated by at least 1 month over a period of 6 months.[1]
  • Intravenous (IV) antibiotics may be needed if there has been: no response to oral antibiotics, systemic deterioration, or if the organism is sensitive only to IV agents.[1]
  • Allergic bronchopulmonary aspergillosis (ABPA)

Antibiotic Regimen

  • Bronchiectasis[2]
  • 1.Acute exacerbations of bronchiectasis
  • 1.1 Empiric antimicrobial therapy
  • Preferred regimen: Amoxicillin 0.5-1 g PO/IV q8h for 14 days
  • Alternative regimen (1): Ciprofloxacin 500-750 mg PO bid for 14 days
  • Alternative regimen (2): Clarithromycin 500 mg PO bid for 14 days
  • 1.2 Pathogen-directed antimicrobial therapy
  • 1.2.1 Streptococcus pneumoniae
  • 1.2.2 Haemophilus influenzae (b-lactamase negative)
  • Preferred regimen (1): Amoxicillin 0.5-1 g PO tid for 14 days
  • Preferred regimen (2): Amoxicillin 3 g PO bid for 14 days
  • Alternative regimen (1): Clarithromycin 500 mg PO bid for 14 days
  • Alternative regimen (2): Ciprofloxacin 500 mg PO bid for 14 days
  • Alternative regimen (3): Ceftriaxone 2 g IV q24h for 14 days
  • 1.2.3 Haemophilus influenzae (b-lactamase positive)
  • 1.2.4 Moraxella catarrhalis
  • 1.2.5 Staphylococcus aureus (MSSA)
  • 1.2.6 Staphylococcus aureus (MRSA) (mild-to-moderate)
  • Preferred regimen (weight < 50 kg): Rifampicin 450 mg PO qd AND Trimethoprim 200 mg PO bid for 14 days
  • Preferred regimen (weight > 50 kg): Rifampicin 600 mg PO qd AND Trimethoprim 200 mg PO bid for 14 days
  • Alternative regimen (weight < 50 kg): Rifampicin 450 mg PO qd AND Doxycycline 200 mg PO qd for 14 days
  • Alternative regimen (weight > 50 kg): Rifampicin 600 mg PO qd AND Doxycycline 200 mg PO qd for 14 days
  • Alternative regimen: Linezolid 600 mg PO bid for 14 days (third-line therapy)
  • 1.2.7 Staphylococcus aureus (MRSA) (severe)
  • Preferred regimen (1): Vancomycin 1 g IV q12h (trough levels of 10-20 ng/mL)
  • Preferred regimen (2): Teicoplanin 400 mg IV q24h for 14 days
  • Alternative regimen: Linezolid 600 mg IV q12h for 14 days
  • 1.2.8 Coliforms (eg, Klebsiella, enterobacter)
  • 1.2.9 Pseudomonas aeruginosa
  • 1.2.10 Pediatric Dosing
  • 2. Long-term antibiotic prophylaxis
  • Patients with ≥3 exacerbations/year requiring antibiotic therapy or patients with fewer exacerbations that are causing significant morbidity should be considered for long-term antibiotic prophylaxis
  • 2.1 Pathogen-directed antimicrobial therapy
  • 2.1.1 Streptococcus pneumoniae
  • 2.1.2 Haemophilus influenzae (b-lactamase negative)
  • 2.1.3 Haemophilus influenzae (b-lactamase positive)
  • 2.1.4 Moraxella catarrhalis
  • 2.1.5 Staphylococcus aureus (MSSA)
  • 3. Pseudomonas eradication (colonization)
  • 3.1 Initial therapy
  • 3.2 Secondary therapy in case of treatment failure
  • Preferred regimen (1): Piperacillin-tazobactam 4.5 g PO tid for 14 days
  • Preferred regimen (2): Cefepime 1-2 g IV q8-12h
  • Preferred regimen (3): Ciprofloxacin 750 mg PO bid for 4 weeks AND Colistin (Nebulized) 2 MU NEB bid for 3 months
  • Preferred regimen (3): Colistin (Nebulized) 2 MU NEB bid for 3 months

Other Therapies

Physiotherapy Strategies

Airway Clearance

  • Postural drainage
  • Autogenic drainage
  • ActiveCycle of breathing techniques
  • Positive expiratory pressure (PEP)
  • Oscillatory PEP devices
  • High-frequency chest wall percussion

Pulmonary Rehabilitation

  • Exercise training
  • Nutritional counseling
  • Education of the patient's disease and how to manage it
  • Techniques on how to conserve energy
  • Strategies on breathing
  • Psychological counseling

References

  1. 1.0 1.1 1.2 1.3 McDonnell MJ, Ward C, Lordan JL, Rutherford RM (2013). "Non-cystic fibrosis bronchiectasis". QJM. 106 (8): 709–15. doi:10.1093/qjmed/hct109. PMID 23728208.
  2. Pasteur MC, Bilton D, Hill AT, British Thoracic Society Bronchiectasis non-CF Guideline Group (2010). "British Thoracic Society guideline for non-CF bronchiectasis". Thorax. 65 Suppl 1: i1–58. doi:10.1136/thx.2010.136119. PMID 20627931.

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