Diferencia entre revisiones de «COPD exacerbation»

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===Pseudomonas Risk Factors===
===Pseudomonas Risk Factors===
#Recent hospitalization (>2 days within previous 3 months)
*Recent hospitalization (>2 days within previous 3 months)
#Frequent abx tx (>4 courses w/in past year)
*Frequent abx tx (>4 courses w/in past year)
#Severe underlying COPD (FEV1 < 50% predicted)
*Severe underlying COPD (FEV1 < 50% predicted)
#Previous isolation of pseudomonas
*Previous isolation of pseudomonas


==Clinical Presentation==
==Clinical Presentation==
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==Treatment==
==Treatment==
===Oxygen===
===Oxygen===
#Maintain PaO<sub>2</sub> of 60-70 or SpO<sub>2</sub> 90-94%
*Maintain PaO<sub>2</sub> of 60-70 or SpO<sub>2</sub> 90-94%
#If unable to correct hypoxemia with a low FiO2 consider alternative diagnosis
*If unable to correct hypoxemia with a low FiO2 consider alternative diagnosis
#Adequate oxygenation is essential, even if it leads to hypercapnia
*Adequate oxygenation is essential, even if it leads to hypercapnia
#If hypercapnia leads to AMS, dysrhythmias, or acidemia consider [[Intubation]]
*If hypercapnia leads to AMS, dysrhythmias, or acidemia consider [[Intubation]]
===Albuterol/ipratropium===
===Albuterol/ipratropium===
#Improves airflow obstruction and treatment should involve rapid administration upon recognition of COPD exacerbation. <ref>Celli BR. Update on the management of COPD. Chest. Jun 2008;133(6):1451-62.</ref>
*Improves airflow obstruction and treatment should involve rapid administration upon recognition of COPD exacerbation. <ref>Celli BR. Update on the management of COPD. Chest. Jun 2008;133(6):1451-62.</ref>
===Steroids===
===Steroids===
Similar efficacy between oral and intravenous. Treatment options include:
Similar efficacy between oral and intravenous. Treatment options include:
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**[[Levofloxacin]] 500 mg PO BID<ref>Anzueto A, Miravitlles M: Short-course fluoroquinolone therapy in exacerbations of chronic bronchitis and COPD. Respir Med 2010; 104:1396-1403</ref>
**[[Levofloxacin]] 500 mg PO BID<ref>Anzueto A, Miravitlles M: Short-course fluoroquinolone therapy in exacerbations of chronic bronchitis and COPD. Respir Med 2010; 104:1396-1403</ref>


#Outpatient Healthy
*Outpatient Healthy
#*[[Azithromycin]] OR [[Doxycycline]] OR [[TMP/SMX]]
**[[Azithromycin]] OR [[Doxycycline]] OR [[TMP/SMX]]
#Outpatient Unhealthy
*Outpatient Unhealthy
#*Age >65, cardiac disease, >3 exacerbations/per year
**Age >65, cardiac disease, >3 exacerbations/per year
#*[[Levofloxacin]]/[[Moxifloxacin]] OR [[Amoxicillin/Clavulanate]]
**[[Levofloxacin]]/[[Moxifloxacin]] OR [[Amoxicillin/Clavulanate]]
#Inpatient  
*Inpatient  
##If Pseudomonas risk factors the use:
**If Pseudomonas risk factors the use:
##*[[Levofloxacin]] PO or IV OR [[Cefepime]] IV OR [[Ceftazidime]] IV OR [[Piperacillin/Tazobactam]] IV
***[[Levofloxacin]] PO or IV OR [[Cefepime]] IV OR [[Ceftazidime]] IV OR [[Piperacillin/Tazobactam]] IV
##No pseudomonas risk factors:
**No pseudomonas risk factors:
##*[[Levofloxacin]] or [[Moxifloxacin]] PO or IV OR [[Ceftriaxone]] IV OR [[Cefotaxime]] IV  
***[[Levofloxacin]] or [[Moxifloxacin]] PO or IV OR [[Ceftriaxone]] IV OR [[Cefotaxime]] IV  
###Consider oseltamivir during influenza season
***Consider oseltamivir during influenza season


===[[EBQ:NIPPV in COPD|Noninvasive ventilation]] (CPAP or BiPaP)===
===[[EBQ:NIPPV in COPD|Noninvasive ventilation]] (CPAP or BiPaP)===
#CPAP: start at low level and titrate up to max 15
*CPAP: start at low level and titrate up to max 15
#BiPAP: Start IPAP 8 (max 20), EPAP 4 (max 15)
*BiPAP: Start IPAP 8 (max 20), EPAP 4 (max 15)




''Contraindications:''
''Contraindications:''
#Uncooperative or obtunded pt
*Uncooperative or obtunded pt
#Inability to clear secretions
*Inability to clear secretions
#Hemodynamic instability
*Hemodynamic instability


===Mechanical ventilation===
===Mechanical ventilation===
''Indications:''
''Indications:''
#Severe dyspnea w/ use of accessory muscles and paradoxical breathing
*Severe dyspnea w/ use of accessory muscles and paradoxical breathing
#RR>35 bpm with anticipated clinical course for respiratory failure
*RR>35 bpm with anticipated clinical course for respiratory failure
#PaO<sub>2</sub> <50 or PaO2/FiO2 <200
*PaO<sub>2</sub> <50 or PaO2/FiO2 <200
#pH <7.25 and PaCO2 >60
*pH <7.25 and PaCO2 >60
#Altered mental status  
*Altered mental status  
#Cardiovascular complications (hypotension, shock, CHF)
*Cardiovascular complications (hypotension, shock, CHF)


==Disposition==
==Disposition==
Consider hospitalization for:
Consider hospitalization for:
#Marked increase in intensity of symptoms (e.g. sudden development of resting dyspnea)
*Marked increase in intensity of symptoms (e.g. sudden development of resting dyspnea)
#Background of severe COPD
*Background of severe COPD
#Onset of new physical signs (e.g., cyanosis, peripheral edema)
*Onset of new physical signs (e.g., cyanosis, peripheral edema)
#Failure of exacerbation to respond to initial medical management
*Failure of exacerbation to respond to initial medical management
#Significant comorbidities
*Significant comorbidities
#Newly occurring arrhythmias
*Newly occurring arrhythmias
#Diagnostic uncertainty
*Diagnostic uncertainty
#Older age
*Older age
#Insufficient home support
*Insufficient home support


==See Also==
==See Also==
[[EBQ:NIPPV in COPD]]
[[EBQ:NIPPV in COPD]]


==Source==
==References==
<references/>
<references/>


[[Category:Pulm]]
[[Category:Pulm]]

Revisión del 02:26 5 may 2015

Background

  • Airflow limitation (FEV1:FVC < 0.70) that is not fully reversible
    • Encompasses chronic bronchitis (85%) and emphysema (15%)
  • Acute exacerbations due to incr V/Q mismatch, not expiratory airflow limitation

Precipitants

  • Infection (75%)
    • 50% viral, 50% bacterial
  • Cold weather
  • B-blockers
  • Narcotics
  • Sedative-hypnotic agents
  • Pneumothorax
  • PE

Pseudomonas Risk Factors

  • Recent hospitalization (>2 days within previous 3 months)
  • Frequent abx tx (>4 courses w/in past year)
  • Severe underlying COPD (FEV1 < 50% predicted)
  • Previous isolation of pseudomonas

Clinical Presentation

Differential Diagnosis

Acute dyspnea

Emergent

Non-Emergent

Diagnosis

  • VBG/ABG
    • Perform if SpO2 <90% or concerned about symptomatic hypercapnia
  • Peak flow
    • <100 indicates severe exacerbation
  • CXR
    • Consider if concerned for PNA or CHF
  • Sputum culture
    • Usually not indicated except for pt w/ recent antibiotic failure

Treatment

Oxygen

  • Maintain PaO2 of 60-70 or SpO2 90-94%
  • If unable to correct hypoxemia with a low FiO2 consider alternative diagnosis
  • Adequate oxygenation is essential, even if it leads to hypercapnia
  • If hypercapnia leads to AMS, dysrhythmias, or acidemia consider Intubation

Albuterol/ipratropium

  • Improves airflow obstruction and treatment should involve rapid administration upon recognition of COPD exacerbation. [1]

Steroids

Similar efficacy between oral and intravenous. Treatment options include:

  • Methylprednisolone 1-2 mg/kg IV daily (usual adult dose 125mg)[2]
  • Prednisone 40 mg PO daily

For outpatients a 5 day dose appears equally effective as longer doses and a taper is not required.[3]

Antibiotics

  • GOLD collaborators recommend antibiotics for patients with purulent sputum or increased sputum production or those who required Non Invasive Positive Pressure Ventilation
  • Antibiotics for COPD exacerbations have an NNT of 3 to prevent 1 conservative treatment failure and 8 to prevent 1 short-term mortality (NNTH of 20 to cause 1 case of diarrhea)[4]
  • Antibiotics should be a 3-5 day course and options include:

Noninvasive ventilation (CPAP or BiPaP)

  • CPAP: start at low level and titrate up to max 15
  • BiPAP: Start IPAP 8 (max 20), EPAP 4 (max 15)


Contraindications:

  • Uncooperative or obtunded pt
  • Inability to clear secretions
  • Hemodynamic instability

Mechanical ventilation

Indications:

  • Severe dyspnea w/ use of accessory muscles and paradoxical breathing
  • RR>35 bpm with anticipated clinical course for respiratory failure
  • PaO2 <50 or PaO2/FiO2 <200
  • pH <7.25 and PaCO2 >60
  • Altered mental status
  • Cardiovascular complications (hypotension, shock, CHF)

Disposition

Consider hospitalization for:

  • Marked increase in intensity of symptoms (e.g. sudden development of resting dyspnea)
  • Background of severe COPD
  • Onset of new physical signs (e.g., cyanosis, peripheral edema)
  • Failure of exacerbation to respond to initial medical management
  • Significant comorbidities
  • Newly occurring arrhythmias
  • Diagnostic uncertainty
  • Older age
  • Insufficient home support

See Also

EBQ:NIPPV in COPD

References

  1. Celli BR. Update on the management of COPD. Chest. Jun 2008;133(6):1451-62.
  2. Eisner MD, et al: An official American Thoracic Society public policy statement: Novel risk factors and the global burden of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2010; 182:693-718
  3. Eisner MD, et al: An official American Thoracic Society public policy statement: Novel risk factors and the global burden of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2010; 182:693-718
  4. Ram FS, et al. Antibiotics for exacerbations of chronic obstructive pulmonary disease. Cochrane Database Syst Rev. 2006.19(2).
  5. Rothberg MB, et al: Antibiotic therapy and treatment failure in patients hospitalized for acute exacerbations of chronic obstructive pulmonary disease. JAMA 2010; 303:2035-2042
  6. Anzueto A, Miravitlles M: Short-course fluoroquinolone therapy in exacerbations of chronic bronchitis and COPD. Respir Med 2010; 104:1396-1403