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CLINICAL APPROACH TO PNEUMONIA Dr Izham Cheong, FRCP Professor of Medicine,  UNIVERSITI KEBANGSAAN MALAYSIA “  The most widespread & fatal of all acute diseases,  pneumonia, is now  Captain of the Men of Death” :  Sir William Osler
Facts about pneumonia in USA ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Ten leading causes of hospitalization and death in Malaysia (2000) Hospitalization   (Total=1,559 280) Respiratory diseases 6.58% Deaths (Total=29 447) Heart disease 15.10% Septicaemia 10.98 CVA   9.47 Accident   8.79 Neoplasms   8.75 Perinatal diseases   7.28 GI diseases   4.69 Pneumonia   4.33 Renal disease   3.65 Ill-defined diseases   3.62
CLINICAL APPROACH TO PNEUMONIA Key points to  remember
KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS PNEUMONIA 1. EPIDEMIOLOGY OF RESPIRATORY PATHOGENS NHAP Gram –ve Klebsiella spp. P. aeroginosa Gram +ve S. aureus Anaerobes HAP (VAP) Gram –ve P. aeroginosa Acinetobacter spp. Proteus spp. Klebsiella spp. E. cloacae P. maltophila Legionella spp. Gram +ve S. aureus  (MRSA) S. pneumoniae Other streptococci S. epidermidis Polymicrobial CAP Typical S. pneumoniae H. influenzae M. catarrhalis Atypical L. pneumophila M. pneumoniae C. pneumoniae C. psittacosi C. burnetti
KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS A PNEUMONIA 2. EARLY EMPIRIC TREATMENT IS ESSENTIAL BECAUSE NO SPECIFIC  PATHOGEN CAN BE IDENTIFIED IN 30% to 70% OF PATIENTS. Relationship of  receiving  an antibiotic  within a time frame  and 30-day mortality Meehan TP, 1997 OR of 30-d Survival (95% CI)
KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS A PNEUMONIA 3.THE RISE IN ANTIBIOTIC RESISTANCE Penicillin and macrolide resistant S. pneumoniae ESBL-producing Klebsiella spp. MDR pathogens:  P. aeroginosa   P. maltophila   Enterobacter spp.   Stenotrophomonas spp. MRSA + VRSA VRE
KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS A PNEUMONIA 4. CONTAIN COST WITHOUT NEGATIVELY AFFECTING MORTALITY    Minimize admissions    Oral antibiotics    Shorten hospitalization
CLINICAL APPROACH TO PNEUMONIA What do  I do? mild severe
Clinical Approach to a Patient with CAP History Medicine is learned by the  bedside and not  in the  classroom Sir William Osler (1849-1919)
HISTORY 1. WHICH CATEGORY? CAP NHAP HAP (VAP)
2. CAN THE PATIENT BE IMMUNOCOMPROMISED? HISTORY DON’T TRUST ANY ONE NOWADAYS!!!
HISTORY 3.ANY UNDERLYING LUNG DAMAGE?
HISTORY 4. COMORBIDITY ? “ mimic” pneumonia impact on drug treatment
HISTORY 6. WHAT IS HIS JOB? Any and everything!! Pulmonary TB Q fever Anthrax
HISTORY 7. CONTACT WITH…. Chlamydia pneumoniae Francisella tularensis Yersinia pestis
HISTORY Legionellosis IS IT SAFE TO TRAVEL??
HISTORY 8. HIGH RISK BEHAVIOURS ““ Yumm-Seng”” IVDU smoking
HISTORY 9. ASPIRATION ? stroke vomiting unconcious/fits Ryle’s tube
HISTORY 10. WHAT DRUGS ARE YOU TAKING? Amiodarone Nitrofurantoin Bleomycin Chlorambucil Procarbazine Bulsulfan Cyclophosphamide Aziathioprine Methotrexate Sulphonamides Lung infiltrates Heroin Methadone Chlorthiaxide Contrast media Pulmonary oedema
Clinical Presentation Clinical Approach to a Patient with CAP Typical pneumonia acute ill-looking,SOB fever and chills productive cough,  leukocytosis pleurisy Atypical pneumonia as above + extrapulmonary features  CNS involvement:  ENT involvement:  M. pneumoniae  Diarrheas:  M. pneumoniae or L. pneumophila  Abdominal pain:   L. pneumophila  Rash:   C. psittacosis M. pneumoniae
Cutaneous findings Erythema multiforme M. pneumoniae Maculopapular rash Measles Erythema nodosum C. pneumoniae Ecthyma gangrenosum M. tuberculosis P. aeruginosa Oral findings Peridontal disease anaerobic pathogens Foul smelling sputum Clinical Approach to a Patient with CAP Physical examination
Neurologic disease Absent gag Aspiration Altered conciousness Recent seizure Cerebellar ataxia M. pneumoniae L. pneumophila Encephalitis M. pneumoniae C. burnetti Clinical Approach to a Patient with CAP Physical examination
Differential Diagnosis of Common Radiographic Patterns in Patients with Pneumonia Focal opacity Interstitial S. pneumoniae M. pneumoniae L. pneumophila C. pneumoniae M. tuberculosis Aspiration Viral  M. pneumoniae P. carinii C. psittaci
Differential Diagnosis of Common Radiographic Patterns in Patients with Pneumonia Interstitial with lymphadenopathy Cavitation Epstein Barr virus F. tularensis C. psittasi Anaerobic abscess S. aureus Aerobic gram-neg bacilli M. tuberculosis C. neoformans N. asteroides and A. israelii
Differential Diagnosis of Common Radiographic Patterns in Patients with Pneumonia Segmental pneumonia with lymphadenopathy Miliary M. tuberculosis Fungal infection M. tuberculosis H. capsulatum Varicella zooster
COMMUNITY-ACQUIRED PNEUMONIA Which patient require hospitalization?   Respiratory rate > 30/min   Diastolic hypotension   Altered mental status   Renal failure   Age > 65 years   Co-existing disease   Leukopenia   Severe anaemia   Acidosis   Hypoxaemia   Multilobar involvement   Systolic BP < 90mmHg   PaO2/FIO < 250 Niederman, 1993; Barlett, 1995; Fine, 1995; Ewig, 1998
INTERNATIONAL GUIDELINES FOR EMPIRICAL ANTIMICROBIAL THERAPY OF COMMUNITY-ACQUIRED PNEUMONIA Extended spectrum cephalosporin or   –lactam/  -lactamase inhibitor + either IV fluoroquinolone or IV macrolide (if structural lung disease cover  P. aeroginosa )  -lactam with macrolide  OR new fluoroquinolone doxycycline macrolide new floroquinolone Infectious Diseases Society of America (2000) 2 nd  or 3 rd  generation cephalosporin + 2 nd  generation quinolones    rifampicin (2 nd  or 3 rd  generation cephalosporin or   -lactam/  -lactamase inhibitor or IV penicillin)    macrolide or 2 nd  generation quinolones; penicillin or aminopenicillins Alternatives:  macrolodes tetracyclines cephalosporins quinolones European Respiratory Society (1998) ICU General ward Outpatient Guidelines
WHAT DO I USE FOR MY  PATIENTS WITH A COMMUNITY- ACQUIRED PNEUMONIA ?
HOW DO I EMPIRICALLY TREAT MY PATIENT  WITH COMMUNITY-ACQUIRED PNEUMONIA? Izham, 2002 Empiric therapy (pathogen unknown or awaiting cultures)  -lactam/  -lactamase inhibitor alone (ampicillin/sulbactam, pipericillin/tazobactam)) Aspiration pneumonia requiring hospitalization  -lactam (sulperazone or ceftriaxone) + macrolide or antipneumococcal fluoroquinolone Requiring hospitalization Oral   -lactam/  -lactamase inhibitor + macrolide OR Oral antipneumococcal fluoroquinolone Ambulatory, not requiring hospitalization, comorbidity or age over 60 years Oral macrolide (erythromycin or azithromycin) Ambulatory, not requiring hospitalization, age under 60 years THERAPEUTIC OPTIONS SETTING
MY EMPIRICAL THERAPY OF SEVERE CAP  IN COMPROMISED HOST Izham,2002  -lactam/  -lactamase inhibitor OR meropenam S. pneumoniae N. meningitidis H. influenzae Congenital/acquired asplenia or hyposplenia new fluoroquinolone S. pneumoniae Salmonella Legionella HIV Cloxacillin OR vancomycin S. aureus Postviral influenzae 3 rd  or 4 th  generation cephalosporin OR meropenam Oral anaerobes and/or Klebsiella spp . Chronic alcoholics Empiric therapy Usual pathogen Compromised host
Why is pneumonia still a leading  cause of morbidity and mortality ? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
“ Of all the diseases to which man is heir, those  known in   etiology ,  possible of cure ,  capable of prevention , are for the most part caused by  infectious agents” -therefore What shall I do with  my next pneumonia? Choose the right antibiotic. Choose the right physician!!!!!!!!

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Approach to peumonia

  • 1. CLINICAL APPROACH TO PNEUMONIA Dr Izham Cheong, FRCP Professor of Medicine, UNIVERSITI KEBANGSAAN MALAYSIA “ The most widespread & fatal of all acute diseases, pneumonia, is now Captain of the Men of Death” : Sir William Osler
  • 2.
  • 3. Ten leading causes of hospitalization and death in Malaysia (2000) Hospitalization (Total=1,559 280) Respiratory diseases 6.58% Deaths (Total=29 447) Heart disease 15.10% Septicaemia 10.98 CVA 9.47 Accident 8.79 Neoplasms 8.75 Perinatal diseases 7.28 GI diseases 4.69 Pneumonia 4.33 Renal disease 3.65 Ill-defined diseases 3.62
  • 4. CLINICAL APPROACH TO PNEUMONIA Key points to remember
  • 5. KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS PNEUMONIA 1. EPIDEMIOLOGY OF RESPIRATORY PATHOGENS NHAP Gram –ve Klebsiella spp. P. aeroginosa Gram +ve S. aureus Anaerobes HAP (VAP) Gram –ve P. aeroginosa Acinetobacter spp. Proteus spp. Klebsiella spp. E. cloacae P. maltophila Legionella spp. Gram +ve S. aureus (MRSA) S. pneumoniae Other streptococci S. epidermidis Polymicrobial CAP Typical S. pneumoniae H. influenzae M. catarrhalis Atypical L. pneumophila M. pneumoniae C. pneumoniae C. psittacosi C. burnetti
  • 6. KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS A PNEUMONIA 2. EARLY EMPIRIC TREATMENT IS ESSENTIAL BECAUSE NO SPECIFIC PATHOGEN CAN BE IDENTIFIED IN 30% to 70% OF PATIENTS. Relationship of receiving an antibiotic within a time frame and 30-day mortality Meehan TP, 1997 OR of 30-d Survival (95% CI)
  • 7. KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS A PNEUMONIA 3.THE RISE IN ANTIBIOTIC RESISTANCE Penicillin and macrolide resistant S. pneumoniae ESBL-producing Klebsiella spp. MDR pathogens: P. aeroginosa P. maltophila Enterobacter spp. Stenotrophomonas spp. MRSA + VRSA VRE
  • 8. KEY POINTS TO REMEMBER WHEN YOUR PATIENT HAS A PNEUMONIA 4. CONTAIN COST WITHOUT NEGATIVELY AFFECTING MORTALITY  Minimize admissions  Oral antibiotics  Shorten hospitalization
  • 9. CLINICAL APPROACH TO PNEUMONIA What do I do? mild severe
  • 10. Clinical Approach to a Patient with CAP History Medicine is learned by the bedside and not in the classroom Sir William Osler (1849-1919)
  • 11. HISTORY 1. WHICH CATEGORY? CAP NHAP HAP (VAP)
  • 12. 2. CAN THE PATIENT BE IMMUNOCOMPROMISED? HISTORY DON’T TRUST ANY ONE NOWADAYS!!!
  • 13. HISTORY 3.ANY UNDERLYING LUNG DAMAGE?
  • 14. HISTORY 4. COMORBIDITY ? “ mimic” pneumonia impact on drug treatment
  • 15. HISTORY 6. WHAT IS HIS JOB? Any and everything!! Pulmonary TB Q fever Anthrax
  • 16. HISTORY 7. CONTACT WITH…. Chlamydia pneumoniae Francisella tularensis Yersinia pestis
  • 17. HISTORY Legionellosis IS IT SAFE TO TRAVEL??
  • 18. HISTORY 8. HIGH RISK BEHAVIOURS ““ Yumm-Seng”” IVDU smoking
  • 19. HISTORY 9. ASPIRATION ? stroke vomiting unconcious/fits Ryle’s tube
  • 20. HISTORY 10. WHAT DRUGS ARE YOU TAKING? Amiodarone Nitrofurantoin Bleomycin Chlorambucil Procarbazine Bulsulfan Cyclophosphamide Aziathioprine Methotrexate Sulphonamides Lung infiltrates Heroin Methadone Chlorthiaxide Contrast media Pulmonary oedema
  • 21. Clinical Presentation Clinical Approach to a Patient with CAP Typical pneumonia acute ill-looking,SOB fever and chills productive cough, leukocytosis pleurisy Atypical pneumonia as above + extrapulmonary features  CNS involvement:  ENT involvement: M. pneumoniae  Diarrheas: M. pneumoniae or L. pneumophila  Abdominal pain: L. pneumophila  Rash: C. psittacosis M. pneumoniae
  • 22. Cutaneous findings Erythema multiforme M. pneumoniae Maculopapular rash Measles Erythema nodosum C. pneumoniae Ecthyma gangrenosum M. tuberculosis P. aeruginosa Oral findings Peridontal disease anaerobic pathogens Foul smelling sputum Clinical Approach to a Patient with CAP Physical examination
  • 23. Neurologic disease Absent gag Aspiration Altered conciousness Recent seizure Cerebellar ataxia M. pneumoniae L. pneumophila Encephalitis M. pneumoniae C. burnetti Clinical Approach to a Patient with CAP Physical examination
  • 24. Differential Diagnosis of Common Radiographic Patterns in Patients with Pneumonia Focal opacity Interstitial S. pneumoniae M. pneumoniae L. pneumophila C. pneumoniae M. tuberculosis Aspiration Viral M. pneumoniae P. carinii C. psittaci
  • 25. Differential Diagnosis of Common Radiographic Patterns in Patients with Pneumonia Interstitial with lymphadenopathy Cavitation Epstein Barr virus F. tularensis C. psittasi Anaerobic abscess S. aureus Aerobic gram-neg bacilli M. tuberculosis C. neoformans N. asteroides and A. israelii
  • 26. Differential Diagnosis of Common Radiographic Patterns in Patients with Pneumonia Segmental pneumonia with lymphadenopathy Miliary M. tuberculosis Fungal infection M. tuberculosis H. capsulatum Varicella zooster
  • 27. COMMUNITY-ACQUIRED PNEUMONIA Which patient require hospitalization?  Respiratory rate > 30/min  Diastolic hypotension  Altered mental status  Renal failure  Age > 65 years  Co-existing disease  Leukopenia  Severe anaemia  Acidosis  Hypoxaemia  Multilobar involvement  Systolic BP < 90mmHg  PaO2/FIO < 250 Niederman, 1993; Barlett, 1995; Fine, 1995; Ewig, 1998
  • 28. INTERNATIONAL GUIDELINES FOR EMPIRICAL ANTIMICROBIAL THERAPY OF COMMUNITY-ACQUIRED PNEUMONIA Extended spectrum cephalosporin or  –lactam/  -lactamase inhibitor + either IV fluoroquinolone or IV macrolide (if structural lung disease cover P. aeroginosa )  -lactam with macrolide OR new fluoroquinolone doxycycline macrolide new floroquinolone Infectious Diseases Society of America (2000) 2 nd or 3 rd generation cephalosporin + 2 nd generation quinolones  rifampicin (2 nd or 3 rd generation cephalosporin or  -lactam/  -lactamase inhibitor or IV penicillin)  macrolide or 2 nd generation quinolones; penicillin or aminopenicillins Alternatives: macrolodes tetracyclines cephalosporins quinolones European Respiratory Society (1998) ICU General ward Outpatient Guidelines
  • 29. WHAT DO I USE FOR MY PATIENTS WITH A COMMUNITY- ACQUIRED PNEUMONIA ?
  • 30. HOW DO I EMPIRICALLY TREAT MY PATIENT WITH COMMUNITY-ACQUIRED PNEUMONIA? Izham, 2002 Empiric therapy (pathogen unknown or awaiting cultures)  -lactam/  -lactamase inhibitor alone (ampicillin/sulbactam, pipericillin/tazobactam)) Aspiration pneumonia requiring hospitalization  -lactam (sulperazone or ceftriaxone) + macrolide or antipneumococcal fluoroquinolone Requiring hospitalization Oral  -lactam/  -lactamase inhibitor + macrolide OR Oral antipneumococcal fluoroquinolone Ambulatory, not requiring hospitalization, comorbidity or age over 60 years Oral macrolide (erythromycin or azithromycin) Ambulatory, not requiring hospitalization, age under 60 years THERAPEUTIC OPTIONS SETTING
  • 31. MY EMPIRICAL THERAPY OF SEVERE CAP IN COMPROMISED HOST Izham,2002  -lactam/  -lactamase inhibitor OR meropenam S. pneumoniae N. meningitidis H. influenzae Congenital/acquired asplenia or hyposplenia new fluoroquinolone S. pneumoniae Salmonella Legionella HIV Cloxacillin OR vancomycin S. aureus Postviral influenzae 3 rd or 4 th generation cephalosporin OR meropenam Oral anaerobes and/or Klebsiella spp . Chronic alcoholics Empiric therapy Usual pathogen Compromised host
  • 32.
  • 33. “ Of all the diseases to which man is heir, those known in etiology , possible of cure , capable of prevention , are for the most part caused by infectious agents” -therefore What shall I do with my next pneumonia? Choose the right antibiotic. Choose the right physician!!!!!!!!