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PGY 李翰泓/Supervisor 林詩萍 醫師
The Difference between
the 2016 and 2005 Version
• The use of the Grading of Recommendations Assessment,
Development and Evaluation (GRADE) for all evidence
• Removal of the concept healthcare-associated
pneumonia (HCAP)
• Guide for the optimal choice of antibiotics according to
each specific antibiograms
Why is HCAP removed?
• High risk for MDR organisms?
• Underlying characteristics also as independent
determinants
• Might include into the upcoming community-acquired
pneumonia (CAP)
• Both initially cared for in ER
• Coverage of MDR pathogens depend on validated risk
Definitions
Hospital-Acquired
Pneumonia
• Pneumonia not intubating at the time of admission
• Occurring ≧48 hrs after admission
• Not associated with mechanical ventilation (MV)
HAP
• Most common hospital-acquired infection (HAI): 22%
• HAP: serious complications in 50% of patients
Microbiologic Methods
to Diagnose HAP
Treatment
• Based on _______ sampling with _______ culture results?
A. Invasive; quantitative
B. Noninvasive; quantitative
C. Noninvasive; semiquantitative
• Non-invasive sampling with semi quantitative cultures
• Invasive: bronchoscopic techniques (bronchoalveolar
lavage (BAL), protected specimen brush (PSB), mini-
BAL)
• Noninvasive: endotracheal aspiration
If Invasive Quantitative
Cultures are Performed…
• If results below the diagnostic threshold (PSB <10^3
Colony-Forming Units [CFU]/ml, BAL <10^4 CFU/ml),
should antibiotic treatment…
A. Withheld
B. Continued
• Noninvasive sampling with semiquantitative cultures as
the preference
• Antibiotics withheld rather than continued
• Clinical factors should be considered!
• Avoiding unnecessary harm and cost
If Patients with Suspected
HAP (Non-VAP)…
• Should treatment be guided by…
A. Microbiologic studies of respiratory samples
B. Be empiric
• Results of microbiologic studies of respiratory samples,
which obtained NONINVASIVELY
• deescalate the therapy based upon respiratory and
blood culture results
• Non-invasive methods: spontaneous expectoration, sputum
induction, nasaltracheal suction, endotracheal aspiration
The Use of Biomarkers and the
Clinical Pulmonary Infection
Score to Diagnose HAP
For Patients with
Suspected HAP…
• Should the initiation of antibiotic therapy be based on
_______?
A. Clinical criteria + Procalcitonin (PCT)
B. Clinical criteria alone
• Clinical criteria ALONE
For Patients with
Suspected HAP…
• Should the initiation of antibiotic therapy be based on
_______?
A. Clinical criteria + C-Reactive Protein (CRP)
B. Clinical criteria alone
• Clinical criteria ALONE
For Patients with
Suspected HAP…
• Should the initiation of antibiotic therapy be based on
_______?
A. Clinical criteria + Modified Clinical Pulmonary
Infection Score (CPIS)
B. Clinical criteria alone
Temperature
White blood cell count
Tracheal secretions
Oxygenation, PaO2/FiO2 mmHg
Pulmonary radiography
Culture of tracheal aspirate specimen
• Clinical criteria ALONE
Initial Treatment of
HAP
Selection of the regimen
for HAP…
• Should them be guided by local antibiotic-resistance
data?
A. Yes
B. No
• Generate and disseminate a local antibiogram, specific
to each HAP population ideally
• Treatment informed by local distribution of pathogens
and their susceptibilities
What Antibiotics are
Recommended…
• For clinically suspected HAP (non-VAP)?
• Not at High Risk of Mortality and no Factors Increasing
the Likelihood of MRSA
ONE OF THE FOLLOWING
Piperacillin-tazobactam 4.5g IV q6h
OR
Cefepime 2g IV q8h
OR
Levofloxacin 750mg IV daily
Imipenem 500mg IV q6h
Meropenem 1g IV q8h
• Not at High Risk of Mortality but with Factors Increasing
the Likelihood of MRSA
ONE OF THE FOLLOWING
Piperacillin-tazobactam 4.5g IV q6h
OR
Cefepime or ceftazidime 2g IV q8h
OR
Levofloxacin 750mg IV daily
Ciprofloxacin 400mg IV q8h
OR
Imipenem 500mg IV q6h
Meropenem 1g IV q8h
OR
Aztreonam 2g IV q8h
PLUS
Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough
level (consider a loading dose of 25-30 mg/kg * 1 for severe illness)
OR
Linezolid 600mg IV q12h
•If patient has severe penicillin allergy and aztreonam is
going to be used insead of any β-lactam-based antibiotic,
include coverage for MSSA
• High Risk of Mortality or Receipt of Intravenous Antibiotics
During the Prior 90 d
TWO OF THE FOLLOWING, AVOID 2 β-LACTAMS
Piperacillin-tazobactam 4.5g IV q6h
OR
Cefepime or ceftazidime 2g IV q8h
OR
Levofloxacin 750mg IV daily
Ciprofloxacin 400mg IV q8h
OR
Imipenem 500mg IV q6h
Meropenem 1g IV q8h
OR
Amikacin 15-20 mg/kg IV daily
Gentamicin 5-7 mg/kg IV daily
Tobramycin 5-7 mg/kg IV daily
OR
Aztreonam 2g IV q8h
PLUS
Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough level (consider a loading dose of
25-30 mg/kg * 1 for severe illness)
OR
Linezolid 600mg IV q12h
•If MRSA coverage is not going to be used, include
coverage for MSSA
•Piperacillin-tazobactam, cefepime, levofloxacin,
imipenam, meropenem
•Oxacillin, nafcillin and cefazolin are preferred for the
treatment of proven MSSA
•Not ordinary used in an empiric regimen for HAP
•If patient has severe penicillin allergy and aztreonam is
going to be used insead of any β-lactam-based antibiotic,
include coverage for MSSA
• Recommend coverage of S.aureus
• Recommend coverage of P.aeruginosa and other G(-)
bacilli
• MRSA: only for
• risky patients
• > 20% S.aureus isolated are methicillin-resistant
• MRSA prevalance unknown
• High risk for mortality (include need for MV due to
HAP and septic shock)
• For MRSA: Vancomycin or Linezolid
• For MSSA: Tazocin, cefepime, levofloxacin, imipenem,
meropenem
• Oxacillin, nafcillin or cefazolin only for proven MSSA
• Antipseudomonal antibiotics: 2 agents from different
classes, only for:
• risky patients
• High risk for mortality
• include need for MV due to HAP and septic shock
• Patients with structural lung disease
• bronchiectasis, cystic fibrosis
• Else: single agent
• Avoid aminoglycosides as the sole antipseudomonal
agent
Pathogen-Specific
Therapy
What Antibiotics should
be used for…
• MRSA HAP?
• Vancomycin or linezolid
• Guided by CBC, serotonin-reuptake inhibitors, renal
function, cost
• SRI+linezolid: serotonin syndrome!!!
What Antibiotics should
be used for…
• P. aeruginosa HAP?
• Based upon the results of antimicrobial susceptibility
testing
• DO NOT USE AMINOGLYCOSIDE MONOTHERAPY
For P.aeruginosa HAP
• Which therapy is applicable?
A. Monotherapy
B. Combination therapy
Monotherapy
• Not in septic shock
• Not at high risk for death
• Antibiotic susceptibility testing are known
Combination Therapy
• In septic shock
• High risk for death (mortality > 25%)
• Antibiotic susceptibility testing unknown
• DO NOT CONTINUE COMBINATION THERAPY after shock
subsided but susceptibility unknown
• DO NOT USE AMINOGLYCOSIDE MONOTHERAPY
• DO NOT USE AMINOGLYCOSIDE MONOTHERAPY
• DO NOT USE AMINOGLYCOSIDE MONOTHERAPY
• Not at High Risk of Mortality and no Factors Increasing
the Likelihood of MRSA
ONE OF THE FOLLOWING
Piperacillin-tazobactam 4.5g IV q6h
OR
Cefepime 2g IV q8h
OR
Levofloxacin 750mg IV daily
Imipenem 500mg IV q6h
Meropenem 1g IV q8h
• Not at High Risk of Mortality but with Factors Increasing
the Likelihood of MRSA
ONE OF THE FOLLOWING
Piperacillin-tazobactam 4.5g IV q6h
OR
Cefepime or ceftazidime 2g IV q8h
OR
Levofloxacin 750mg IV daily
Ciprofloxacin 400mg IV q8h
OR
Imipenem 500mg IV q6h
Meropenem 1g IV q8h
OR
Aztreonam 2g IV q8h
PLUS
Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough
level (consider a loading dose of 25-30 mg/kg * 1 for severe illness)
OR
Linezolid 600mg IV q12h
•If patient has severe penicillin allergy and aztreonam is
going to be used insead of any β-lactam-based antibiotic,
include coverage for MSSA
• High Risk of Mortality or Receipt of Intravenous Antibiotics
During the Prior 90 d
TWO OF THE FOLLOWING, AVOID 2 β-LACTAMS
Piperacillin-tazobactam 4.5g IV q6h
OR
Cefepime or ceftazidime 2g IV q8h
OR
Levofloxacin 750mg IV daily
Ciprofloxacin 400mg IV q8h
OR
Imipenem 500mg IV q6h
Meropenem 1g IV q8h
OR
Amikacin 15-20 mg/kg IV daily
Gentamicin 5-7 mg/kg IV daily
Tobramycin 5-7 mg/kg IV daily
OR
Aztreonam 2g IV q8h
PLUS
Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough level (consider a loading dose of
25-30 mg/kg * 1 for severe illness)
OR
Linezolid 600mg IV q12h
•If MRSA coverage is not going to be used, include
coverage for MSSA
•Piperacillin-tazobactam, cefepime, levofloxacin,
imipenam, meropenem
•Oxacillin, nafcillin and cefazolin are preferred for the
treatment of proven MSSA
•Not ordinary used in an empiric regimen for HAP
•If patient has severe penicillin allergy and aztreonam is
going to be used insead of any β-lactam-based antibiotic,
include coverage for MSSA
What Antibiotics should
be used for…
• Acinetobacter species HAP?
• Carbapenem or ampicillin/sulbactam
• If the isolate susceptible
• IV colistin or polymyxin B
• adjunctive inhaled colistin
• If the isolate only sensitive to polymyxins
• For patients with Acinetobacter only sensitive to colistin
• Do not use adjunctive rifampicin
• DO NOT USE TIGECYCLINE
What Antibiotics should
be used for…
• Carbapenem-Resistant pathogens HAP?
• IV colistin or polymyxin B
• adjunctive inhaled colistin
• If the isolate only sensitive to polymyxins
• Inhaled colistin > inhaled polymyxin B
• IV polymyxin B > IV colistin
Length of Therapy
How long should the
duration of treatment be…
• For patients with HAP (non-VAP)?
A. 7 days
B. 8-15 days
• 7 days
• Depending upon the clinical, radiological or laboratory
condition
Should the antibiotics
treatment…
• Be _______ in patients with HAP?
A. Fixed
B. De-escalated
• De-escalated > fixed
• Empiric broad-spectrum antibiotics -> narrower
antibiotic regimen
• Combination therapy -> monotherapy
Should the discontinuation
of antibiotics therapy…
• Be based on _______
A. PCT level + clinical criteria
B. Clinical criteria alone
• PCT level + clinical criteria
Should the discontinuation
of antibiotics therapy…
• Be based on _______
A. CPIS level + clinical criteria
B. Clinical criteria alone
• Clinical criteria ALONE
PPAP

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2016 Hospital Acquired Pneumonia

  • 2. The Difference between the 2016 and 2005 Version
  • 3. • The use of the Grading of Recommendations Assessment, Development and Evaluation (GRADE) for all evidence • Removal of the concept healthcare-associated pneumonia (HCAP) • Guide for the optimal choice of antibiotics according to each specific antibiograms
  • 4.
  • 5. Why is HCAP removed? • High risk for MDR organisms? • Underlying characteristics also as independent determinants • Might include into the upcoming community-acquired pneumonia (CAP) • Both initially cared for in ER • Coverage of MDR pathogens depend on validated risk
  • 7. Hospital-Acquired Pneumonia • Pneumonia not intubating at the time of admission • Occurring ≧48 hrs after admission • Not associated with mechanical ventilation (MV)
  • 8. HAP • Most common hospital-acquired infection (HAI): 22% • HAP: serious complications in 50% of patients
  • 10. Treatment • Based on _______ sampling with _______ culture results? A. Invasive; quantitative B. Noninvasive; quantitative C. Noninvasive; semiquantitative
  • 11. • Non-invasive sampling with semi quantitative cultures • Invasive: bronchoscopic techniques (bronchoalveolar lavage (BAL), protected specimen brush (PSB), mini- BAL) • Noninvasive: endotracheal aspiration
  • 12. If Invasive Quantitative Cultures are Performed… • If results below the diagnostic threshold (PSB <10^3 Colony-Forming Units [CFU]/ml, BAL <10^4 CFU/ml), should antibiotic treatment… A. Withheld B. Continued
  • 13. • Noninvasive sampling with semiquantitative cultures as the preference • Antibiotics withheld rather than continued • Clinical factors should be considered! • Avoiding unnecessary harm and cost
  • 14. If Patients with Suspected HAP (Non-VAP)… • Should treatment be guided by… A. Microbiologic studies of respiratory samples B. Be empiric
  • 15. • Results of microbiologic studies of respiratory samples, which obtained NONINVASIVELY • deescalate the therapy based upon respiratory and blood culture results • Non-invasive methods: spontaneous expectoration, sputum induction, nasaltracheal suction, endotracheal aspiration
  • 16. The Use of Biomarkers and the Clinical Pulmonary Infection Score to Diagnose HAP
  • 17. For Patients with Suspected HAP… • Should the initiation of antibiotic therapy be based on _______? A. Clinical criteria + Procalcitonin (PCT) B. Clinical criteria alone
  • 19. For Patients with Suspected HAP… • Should the initiation of antibiotic therapy be based on _______? A. Clinical criteria + C-Reactive Protein (CRP) B. Clinical criteria alone
  • 21. For Patients with Suspected HAP… • Should the initiation of antibiotic therapy be based on _______? A. Clinical criteria + Modified Clinical Pulmonary Infection Score (CPIS) B. Clinical criteria alone
  • 22. Temperature White blood cell count Tracheal secretions Oxygenation, PaO2/FiO2 mmHg Pulmonary radiography Culture of tracheal aspirate specimen
  • 25. Selection of the regimen for HAP… • Should them be guided by local antibiotic-resistance data? A. Yes B. No
  • 26. • Generate and disseminate a local antibiogram, specific to each HAP population ideally • Treatment informed by local distribution of pathogens and their susceptibilities
  • 27. What Antibiotics are Recommended… • For clinically suspected HAP (non-VAP)?
  • 28. • Not at High Risk of Mortality and no Factors Increasing the Likelihood of MRSA ONE OF THE FOLLOWING Piperacillin-tazobactam 4.5g IV q6h OR Cefepime 2g IV q8h OR Levofloxacin 750mg IV daily Imipenem 500mg IV q6h Meropenem 1g IV q8h
  • 29. • Not at High Risk of Mortality but with Factors Increasing the Likelihood of MRSA ONE OF THE FOLLOWING Piperacillin-tazobactam 4.5g IV q6h OR Cefepime or ceftazidime 2g IV q8h OR Levofloxacin 750mg IV daily Ciprofloxacin 400mg IV q8h OR Imipenem 500mg IV q6h Meropenem 1g IV q8h OR Aztreonam 2g IV q8h PLUS Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough level (consider a loading dose of 25-30 mg/kg * 1 for severe illness) OR Linezolid 600mg IV q12h
  • 30. •If patient has severe penicillin allergy and aztreonam is going to be used insead of any β-lactam-based antibiotic, include coverage for MSSA
  • 31. • High Risk of Mortality or Receipt of Intravenous Antibiotics During the Prior 90 d TWO OF THE FOLLOWING, AVOID 2 β-LACTAMS Piperacillin-tazobactam 4.5g IV q6h OR Cefepime or ceftazidime 2g IV q8h OR Levofloxacin 750mg IV daily Ciprofloxacin 400mg IV q8h OR Imipenem 500mg IV q6h Meropenem 1g IV q8h OR Amikacin 15-20 mg/kg IV daily Gentamicin 5-7 mg/kg IV daily Tobramycin 5-7 mg/kg IV daily OR Aztreonam 2g IV q8h PLUS Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough level (consider a loading dose of 25-30 mg/kg * 1 for severe illness) OR Linezolid 600mg IV q12h
  • 32. •If MRSA coverage is not going to be used, include coverage for MSSA •Piperacillin-tazobactam, cefepime, levofloxacin, imipenam, meropenem •Oxacillin, nafcillin and cefazolin are preferred for the treatment of proven MSSA •Not ordinary used in an empiric regimen for HAP
  • 33. •If patient has severe penicillin allergy and aztreonam is going to be used insead of any β-lactam-based antibiotic, include coverage for MSSA
  • 34. • Recommend coverage of S.aureus • Recommend coverage of P.aeruginosa and other G(-) bacilli
  • 35. • MRSA: only for • risky patients • > 20% S.aureus isolated are methicillin-resistant • MRSA prevalance unknown • High risk for mortality (include need for MV due to HAP and septic shock)
  • 36. • For MRSA: Vancomycin or Linezolid • For MSSA: Tazocin, cefepime, levofloxacin, imipenem, meropenem • Oxacillin, nafcillin or cefazolin only for proven MSSA
  • 37. • Antipseudomonal antibiotics: 2 agents from different classes, only for: • risky patients • High risk for mortality • include need for MV due to HAP and septic shock • Patients with structural lung disease • bronchiectasis, cystic fibrosis • Else: single agent
  • 38. • Avoid aminoglycosides as the sole antipseudomonal agent
  • 39.
  • 41. What Antibiotics should be used for… • MRSA HAP?
  • 42. • Vancomycin or linezolid • Guided by CBC, serotonin-reuptake inhibitors, renal function, cost • SRI+linezolid: serotonin syndrome!!!
  • 43. What Antibiotics should be used for… • P. aeruginosa HAP?
  • 44. • Based upon the results of antimicrobial susceptibility testing • DO NOT USE AMINOGLYCOSIDE MONOTHERAPY
  • 45. For P.aeruginosa HAP • Which therapy is applicable? A. Monotherapy B. Combination therapy
  • 46. Monotherapy • Not in septic shock • Not at high risk for death • Antibiotic susceptibility testing are known
  • 47. Combination Therapy • In septic shock • High risk for death (mortality > 25%) • Antibiotic susceptibility testing unknown • DO NOT CONTINUE COMBINATION THERAPY after shock subsided but susceptibility unknown
  • 48. • DO NOT USE AMINOGLYCOSIDE MONOTHERAPY • DO NOT USE AMINOGLYCOSIDE MONOTHERAPY • DO NOT USE AMINOGLYCOSIDE MONOTHERAPY
  • 49. • Not at High Risk of Mortality and no Factors Increasing the Likelihood of MRSA ONE OF THE FOLLOWING Piperacillin-tazobactam 4.5g IV q6h OR Cefepime 2g IV q8h OR Levofloxacin 750mg IV daily Imipenem 500mg IV q6h Meropenem 1g IV q8h
  • 50. • Not at High Risk of Mortality but with Factors Increasing the Likelihood of MRSA ONE OF THE FOLLOWING Piperacillin-tazobactam 4.5g IV q6h OR Cefepime or ceftazidime 2g IV q8h OR Levofloxacin 750mg IV daily Ciprofloxacin 400mg IV q8h OR Imipenem 500mg IV q6h Meropenem 1g IV q8h OR Aztreonam 2g IV q8h PLUS Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough level (consider a loading dose of 25-30 mg/kg * 1 for severe illness) OR Linezolid 600mg IV q12h
  • 51. •If patient has severe penicillin allergy and aztreonam is going to be used insead of any β-lactam-based antibiotic, include coverage for MSSA
  • 52. • High Risk of Mortality or Receipt of Intravenous Antibiotics During the Prior 90 d TWO OF THE FOLLOWING, AVOID 2 β-LACTAMS Piperacillin-tazobactam 4.5g IV q6h OR Cefepime or ceftazidime 2g IV q8h OR Levofloxacin 750mg IV daily Ciprofloxacin 400mg IV q8h OR Imipenem 500mg IV q6h Meropenem 1g IV q8h OR Amikacin 15-20 mg/kg IV daily Gentamicin 5-7 mg/kg IV daily Tobramycin 5-7 mg/kg IV daily OR Aztreonam 2g IV q8h PLUS Vancomycin 15 mg/kg IV q8-12h with goal to target 15-20 mg/ml trough level (consider a loading dose of 25-30 mg/kg * 1 for severe illness) OR Linezolid 600mg IV q12h
  • 53. •If MRSA coverage is not going to be used, include coverage for MSSA •Piperacillin-tazobactam, cefepime, levofloxacin, imipenam, meropenem •Oxacillin, nafcillin and cefazolin are preferred for the treatment of proven MSSA •Not ordinary used in an empiric regimen for HAP
  • 54. •If patient has severe penicillin allergy and aztreonam is going to be used insead of any β-lactam-based antibiotic, include coverage for MSSA
  • 55. What Antibiotics should be used for… • Acinetobacter species HAP?
  • 56. • Carbapenem or ampicillin/sulbactam • If the isolate susceptible • IV colistin or polymyxin B • adjunctive inhaled colistin • If the isolate only sensitive to polymyxins
  • 57. • For patients with Acinetobacter only sensitive to colistin • Do not use adjunctive rifampicin • DO NOT USE TIGECYCLINE
  • 58. What Antibiotics should be used for… • Carbapenem-Resistant pathogens HAP?
  • 59. • IV colistin or polymyxin B • adjunctive inhaled colistin • If the isolate only sensitive to polymyxins • Inhaled colistin > inhaled polymyxin B • IV polymyxin B > IV colistin
  • 61. How long should the duration of treatment be… • For patients with HAP (non-VAP)? A. 7 days B. 8-15 days
  • 62. • 7 days • Depending upon the clinical, radiological or laboratory condition
  • 63. Should the antibiotics treatment… • Be _______ in patients with HAP? A. Fixed B. De-escalated
  • 64. • De-escalated > fixed • Empiric broad-spectrum antibiotics -> narrower antibiotic regimen • Combination therapy -> monotherapy
  • 65. Should the discontinuation of antibiotics therapy… • Be based on _______ A. PCT level + clinical criteria B. Clinical criteria alone
  • 66. • PCT level + clinical criteria
  • 67. Should the discontinuation of antibiotics therapy… • Be based on _______ A. CPIS level + clinical criteria B. Clinical criteria alone
  • 69. PPAP