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Community Acquired Pneumonia
DR. ELLAHI BAKHSH
PGR PULMONOLOGY
FATIMA JINNAH CHEST HOSPITAL QUETTA
References
 Clinical Respiratory Medicine by Stephen G. Spiro
 BTS Guideline for Management of Community Acquired Pneumonia in Adults
updated 2009
 NICE Guideline for Diagnosis and Management of Community Acquired
Pneumonia in Adults ( Published in December 2014 )
 Davidson’s Principles & Practice of Medicine
Objectives
 To Briefly Review of Pneumonia
 Management of Community Acquired Pneumonia in Adults
according to recently published NICE Guideline
Case Scenario
 82 year old male , living in a Nursing Care, presented with Fever,
Breathlessness, purulent sputum with alter level of consciousness for the last 3
days. He has COPD and history of Smoking and Mild Dementia.
 His Chest Xray shows new right lower lobe infiltrates
 CBC shows Raised WBC count 18000/mm3
 Initial Gram Staining report shows Prominent Stains of Gram +ve Organism
Case Scenario
 What is your Diagnosis
 Health Care Associated Pneumonia
 What is most probable Causative Pathogen
 Staphylococcus Aureus
 What should be done next
 Vancomycin 1 gram IV every 12 hours
 Piperacillin and Tazobactam and intravenous levofloxacin incase of MRSA
Community Acquired Pneumonia
 Acc. to BTS Guidelines CAP is defined as
 Acute Lower Respiratory Tract Infection
 Accompanied by New Infiltrates on Chest Radiograph
 Or Ascultatory Findings Consistent with Pneumonia
 in a patient Not Hospitalized or residing in a Long Term Care Facility
 for More than 2 weeks
 before onset of symptoms
What is An Acute Lower Respiratory Tract Infection
 Acc. To NICE Guideline
 An acute Illness (present for 21 days or less)
 usually with Cough as main symptom
 and with at least 1 other Lower respiratory tract symptoms such as
 Fever
 Sputum Production
 Breathlessness
 Wheeze
 Chest Discomfort or Chest Pain
 with No alternative explanation
 Pneumonia, Acute Bronchitis and Exacerbation of COPD
Hospital Acquired Pneumonia
 Pneumonia that develops in a Non-Incubating patient, 48 hours or
more after Hospital Admission
Ventilator Associated Pneumonia
 Pneumonia that develops in a patient receiving Invasive Mechanical
Ventilation for at least 48 hours or more
Health Care Associated Pneumonia
 Pneumonia that develops in a patient with recent contact with the
Health Care System, that include
 Hospitalization for 2 days or more in the preceding 90 days
 Residence in Nursing Care
 Home Infusion Therapy including Antibiotics
 Chronic Dialysis within 30 days
 Home Wound Care
 Family member with MDR Pathogen
Why it is important to differentiate CAP from
other Pneumonia
 Timely Diagnosis and Treatment is the key in Successful
Management of Pneumonia
 Early Pathogen detection and Choice of appropriate Antibiotic
will not only result in better outcome of Pneumonia, But also
reduces problems related to Antibiotic Resistant
Burden of Disease
 Pneumonia remains common cause of Death
 Globally Pneumonia ranked 6th
 CAP is most common cause of Severe Sepsis
 Despite introduction of Antibiotics, Imaging modalities and
Biomarker testing, mortalities related to CAP has not changed
significantly.
Risk Factors
Age
Altered Immunity
Malnutrition
Environmental Factors
Airway Colonization
Alcoholism
Smoking
Risk Factors
 Age
 With the increase in Age , Immunity of body weakens
 Every Year over 65, increases risk for Pneumonia
Risk Factors
 Altered Immunity
 Patients with Immunocompromised state such as
 HIV
 AIDS
 Chemotherapy Treatment
 Lymphopoliferative Diseases
 Cancer
 Diabetes
 CLD
 Heart Failure
are at increased risk for development of CAP
Risk Factors
 Malnutrition
 whatever the cause may be
 Malnutrition leads to alterations in Immunity
 Increasing the chance for Airway colonization and infection with Gram –ve Bacilli
Risk Factors
 Environmental Factors
 Overcrowding
 Occupations associated with exposure to Dust, Fumes, various Chemicals,
Contaminated Water Supply and Cooling Towers of Air-Conditioning Units
 Contact with Animals
Risk Factors
 Airway Colonization
 Results in Impairment of Innate Lung Defense
 Common in Patients with Chronic Obstructive Pulmonary Disease
Risk Factors
 Alcoholism
 Leads to Impaired Level of Consciousness, Cough Reflex and Muco-cilliary Movement
 Also impairs function of Lymphocytes, Monocytes and alveolar Macrophages
Risk Factors
 Smoking
 Smoking, itself is not a Risk Factor for Pneumonia
 But it alters Muco-cilliary Transport
 And increases adhesion of Pathogens to Orophyrangial epithelium
Pathogens
 Virus , Bacteria and Fungi are pathogens of Pneumonia
 Common Pathogens are
 Streptococcus Pneumoniae
 Staphylococcus Aureus
 H. Influenza
 Mycoplasma Pneumoniae
 Ligeonalla Pneumophila
 Pseudomonas
 Clamydia
 Ecoli
 Klebsella Pneumoniae
 MRSA
 Anaerobes
Common Pathogens in CAP
Streptococcus Pneumoniae
Staphylococcus Aureus
H. Influenza
Mycoplasma Pneumoniae
Ligeonalla Pneumophila
Clamydia
Klebsella Pneumoniae
Common Pathogens in HAP
•E. Coli
•Pseudomonas
•Klebsella
Gram –ve are
Most Common
•Staphylococus Aureus
•MRSAGram +ve
Bacteriods
Common Pathogens in VAP
Pseudomonas aeruginosa
E.coli
Klebsiella pneumoniae
Acinetobacter
Staphylococcus Pneumoiae
Common Pathogens in HCAP
Staphylococcus aureus
Pseudomonas aeruginosa
Streptococcus pneumoniae
Haemophilus influenzae.
Streptococus Pneumoniae
Most Common
Pathogen of CAP
If left untreated , it
will eventually result
in Production of Rust
colored Sputum
Pneumonia caused
by Streptococus
Pneumoniae is a
Medical emergency
Because of
•Rapid multiplication
•High Risk for
Secondary
Complications
Staphylococus Pneumoniae
 Most Severe form of CAP
Because of
 Resistant to Multiple Antibiotics
 Leads to formation of Bullae which may repute to Cause Pneumothorax,
Pneumo-Pyothorax and Septicemia
Mycoplasma Pneumoniae
Most Common Pathogen in Atypical
Pneumonia
Usually occurs in small epidemics in
Overcrowded Population
Clinical Presentation CAP
 Classical Symptoms of CAP are
 Fever
 Intense Chills
 Cough
 Sputum Production
 Dyspnea
 Pleuritic Chest Pain
 Generalized Fatigue
 Hemoptysis
Clinical Presentation
 On Chest X ray
Clinical Presentation
 On General Physical Examination
 Hyperthermia
 Tachycardia
 Tachypnea
 Use of Accessory Muscles
 Central Cyanosis
 Altered Mental Status
Clinical Presentation
 On Chest Examination
 Wheezes
 Coarse Crackes
 Tracheal Deviation
 Dull Percussion
 Reduced Breath Sounds
 Decrease Chest Movements on Effected Side
 Bronchial Breathing
Clinical Presentation
 On Arterial Blood Gases
 Decreased PaO2
 Decreased PaCo2
 Type 1 Respiratory Failure with Respiratory Alkalosis
Classification of CAP
 Typical
 Caused by Typical Pathogens
 Streptococus Pneumoniae
 H. Influenze
 Klebsella
 Morexella Cataralis
 Classical Syptoms are Dominant
 Sudden in Onset
 High Grade Fever
 Intense Chills
 Productive Cough
 Pleuritic Chest Pain ( Occasionally)
 CBC Shows Leukocytosis with Neutrophillic
Predominance
 Atypical
 Also Called Walking Pneumonia
 Caused by Atypical Pathogens
 Mycoplasma Pneumoniae
 Clamydia Pneumophila
 Ligionella
 Systemic Menifestations are Dominant
 Generalized Myalgea
 Muscle Ache
 Arthralgia
 Diarhhea
 Nausea
 Vomiting
 Abdominal Pain
 Gradual in Onset
 Low Grade Fever
 Dry Cough
 CBC Shows Absent Leukocytosis
 Do not respond to common Antibiotics
 Do not form Lobar Consolidations rather restricted to Small
Areas
Investigations
 Baseline
 Chest X ray
 Complete Blood Count
 Serum Electrolytes
 Urea Creatinine
 Liver Functioning Test
 Specific
 Arterial Blood Gases
 Gram Staining
 Sputum Culture
 C – reactive Protein
 Pneumococcal and Legionella
Urinary Antigen Test
C – reactive Protein
 C-reactive protein is an acute phase reactant,
 a protein made by the liver and released into the bloodstream
within a few hours
 after tissue injury,
 start of an infection,
 or other cause of inflammation
Abbreviated Mental Test
 Quick and Easy to Use Test to Assess Elderly patients for
 Dementia
 Confusion
 Impaired Cognitive Functions
 10 simple questions are asked from patient
 1 Point is given for every Correct Answer and 0 Point for Incorrect Answers
Abbreviated Mental Test
Name
Time
Give the patient an address and ask for recall at end of test
Year
Name of the place
Identification of any two person ( Doctor, Nurse , Home Help etc)
Date of Birth
Any Historical Event
Name of President/ Prime Minister
Count backward from 20-1
Recall Adress
Differential Diagnosis of CAP
Acute bronchitis
Acute Exacerbation of COPD
Pulmonary T.B
Pulmonary Edema
Pulmonary Infarction
Pulmonary eosinophilia
Pulmonary fibrosis
Bronciolitis Oblitrans Organising Pneumonia
Bronchoalveolar Cell Carcinoma
Drug-induced pulmonary disease
Myocardial infarction
Congestive heart failure and pulmonary edema
Management Of Community
Acquired Pneumonia
Lower Respiratory Tract Infection
 For people presenting with symptoms of Lower Respiratory Tract Infection
in Primary Care,
 Consider C-reactive protein test
 if after clinical assessment a diagnosis of Pneumonia has not been
made
 and it is not clear whether Antibiotics should be prescribed
Lower Respiratory Tract Infection
 Use the results of the C-reactive protein test to guide Antibiotic prescribing
in people without a clinical diagnosis of pneumonia as follows,
 Do not routinely offer antibiotic therapy if the C-reactive protein
concentration is less than 20 mg/litre
 Consider a Delayed Antibiotic Prescription (a prescription for use at a later
date if symptoms worsen) if the C-reactive protein concentration is
between 20 mg/litre and 100 mg/litre
 Offer Antibiotic Therapy if the C-reactive protein concentration is greater
than 100 mg/litre
Community Acquired Pneumonia
 When a clinical diagnosis of Community Acquired Pneumonia is made in
Primary Care
 Severity is assessed
 To determine whether patients are at Low, Intermediate or High risk of Death
 using the CRB65 Score
CRB65 score
 CRB65 Score is calculated by giving 1 Point for each of the following
prognostic features
 Confusion (abbreviated Mental Test score 8 or less, or new
disorientation in person, place or time)
 Raised Respiratory Rate (30 breaths per minute or more)
 Low Blood Pressure (Diastolic 60 mmHg or less, or Systolic less than 90
mmHg)
 Age 65 Years or more
Mortality Risk
 Patients are stratified for Risk of Death as follows
 0 Low risk (less than 1% mortality)
 1 or 2 Intermediate risk (1-10% mortality risk)
 3 or 4 High risk (more than 10% mortality risk)
Decision For Site Of Care
 Use Clinical Judgment in conjunction with the CRB65 Score to inform
decisions about whether patients need Hospital assessment as
follows
 Consider Home-Based Care for patients with a CRB65 score of 0
 Consider Hospital Assessment for all other patients, particularly those
with a CRB65 Score of 2 or more
Community Acquired Pneumonia
 When a clinical diagnosis of Community Acquired Pneumonia is made in
Hospital
 Severity is assessed
 To determine whether patients are at Low, Intermediate or High risk of
Death
 using the CURB65 Score
CURB65 score
 CURB65 Score is calculated by giving 1 Point for each of the
following prognostic features
 Confusion (abbreviated Mental Test score 8 or less, or new
disorientation in person, place or time)
 Raised Blood Urea Nitrogen (over 7 mmol/litre)
 Raised Respiratory Rate (30 breaths per minute or more)
 Low Blood Pressure (Diastolic 60 mmHg or less, or Systolic less than 90
mmHg)
 Age 65 years or more
Mortality Risk
 Patients are stratified for risk of death as follows
 0 or 1 Low risk (less than 3% mortality risk)
 2 Intermediate Risk (3-15% mortality risk)
 3 to 5 High Risk (more than 15% mortality risk)
Management Of CAP
 Use Clinical Judgment in conjunction with the CURB65 Score to Guide
Management of Community Acquired Pneumonia as follows
 Consider Home-Based Care for patients with a CURB65 Score of 0 -1
 Consider Hospital-Based Care for patients with a CURB65 Score of 2 or more
 Consider Intensive Care assessment for patients with a CURB65 Score of 3 or more
Microbiological Test
 Do not routinely offer Microbiological Tests to patients with Low-severity
Community Acquired Pneumonia
 For patients with Moderate or High-Severity Community Acquired Pneumonia
 take Blood and Sputum Cultures and
 Consider Pneumococcal and Legionella Urinary Antigen Tests.
Timely Diagnosis And Treatment
 Put in place processes to allow diagnosis (including X-rays) and
treatment of Community Acquired Pneumonia within 4 hours of
presentation to Hospital
 Offer Antibiotic Therapy as soon as possible after diagnosis, and certainly
within 4 hours to all patients with Community Acquired Pneumonia who
are admitted to hospital
Antibiotic Therapy
 Low-severity community-acquired pneumonia
 Offer a 5-day course of a Single Antibiotic to patients with Low-Severity
Community Acquired Pneumonia
 Consider Amoxicillin in preference to a Macrolide or a Tetracycline for patients
with Low-Severity Community Acquired Pneumonia
 Consider a Macrolide or a Tetracycline for patients who are Allergic to Penicillin
 Consider Extending the course of the Antibiotic for longer than 5 days as a
possible management strategy for patients with Low-Severity Community
Acquired Pneumonia whose symptoms do not improve as expected after 3
days
Antibiotic Therapy
 Explain to patients with Low-Severity Community Acquired Pneumonia
treated in the community, and when appropriate their families or carer, that
 they should seek further medical advice if their symptoms do not begin to improve
within 3 days of starting the antibiotic, or earlier if their symptoms are worsening.
 Do not routinely offer patients with Low-Severity Community Acquired
Pneumonia
 a Fluoroquinolone
 Dual Antibiotic Therapy
Antibiotic Therapy
 Moderate- and High-Severity Community Acquired Pneumonia
 Consider a 7 to10 day course of Antibiotic Therapy for patients with Moderate
or High Severity Community Acquired Pneumonia
 Consider Dual Antibiotic Therapy with Amoxicillin and a Macrolide for patients
with Moderate-Severity Community Acquired Pneumonia
 Consider Dual Antibiotic Therapy with a Beta-Lactamase Stable Beta-Lactam
and a Macrolide for patients with High-Severity Community Acquired
Pneumonia
Site
Scoring
System
Severity Management
Antibiotic
Therapy
Antibiotic
Duration
Antibiotics
Primary
Care
CRB-65
Low ( 0 )
Home Based
Treatment
Single 5 Days
Amoxicillin(Preferred)
or
Macrolide
Or
Tetracycline
Moderate
(1-2)
Refer to Hospital
High (2-4)
Do not routinely offer Floroquinolone & Dual Antibiotic Therapy to patients with low-severity CAP
Consider Extending the course of the Antibiotic for longer than 5 days for patients with Low-Severity CAP whose
symptoms do not improve as expected after 3 days
Explain to patients with Low-Severity CAP, their families, that they should seek further Medical advice if their symptoms
do not begin to improve within 3 days of starting the antibiotic, or earlier if their symptoms are worsening
Site
Scoring
System
Severity Management
Antibiotic
Therapy
Antibiotic
Duration
Antibiotics
Hospital CURB-65
Low ( 0-1 )
Home Based
Treatment
Single 5 Days
Amoxicillin(Preferred)
or
Macrolide
Or
Tetracycline
Moderate
(2)
Hospital Based Care
Dual 7-10 Days
Amoxicillin
+
Macrolide
Intensive Care Unit
High (3-5) Dual
7-10 Days
Beta-Lactamase stable
beta-lactam
+
Marcrolide
Macrolides include Erythromycin, Clarithromycin, Azithromycin
Beta-Lactamase stable beta-lactam includes Co-Amoxiclave, Cefotaxime, Ceftroline, Fosamil, Ceftriaxone,
Piperacillin with Tazobactam
Antibiotic Dosage
Amoxicillin
Macrolides
Ceftriaxone
Co-Amoxicalve
Piperacillin with Tazobactam
Cefotaxime
•500mg – 1g 8 Hourly
•500mg 12 Hourly
•2g Once Daily
•1.2g 8 Hourly
•4.5g 8 Hourly
•1g 8 Hourly
Glucocorticoid Treatment
 Do not routinely offer a Glucocorticosteroid to patients with
Community Acquired Pneumonia unless they have other conditions
for which Glucocorticosteroid treatment is indicated
Monitoring in Hospital
 Consider measuring a baseline C-reactive protein concentration in
patients with Community Acquired Pneumonia on admission to Hospital
 Repeat the Test if clinical progress is uncertain after 48 to 72 hours
Safe Discharge from Hospital
 Do not Routinely Discharge patients with Community Acquired Pneumonia
if in the past 24 hours they have had 2 or more of the following findings
 Temperature higher than 37.5°C
 Respiratory Rate 24 breaths per minute or more
 Heart Rate over 100 beats per minute
 Systolic Blood Pressure 90 mmHg or less
 Oxygen Saturation under 90% on room air
 Abnormal Mental Status
 Inability to Eat without Assistance
Consider Delay Discharge
 Consider Delaying Discharge for patients with Community Acquired
Pneumonia if their Temperature is higher than 37.5°C
Patient Counseling
Explain to patients with Community Acquired Pneumonia that after starting treatment their symptoms
should steadily improve, although the rate of improvement will vary with the severity of the pneumonia,
and most people can expect that by
1 week Fever should have resolved
4 weeks Chest Pain and Sputum production should have substantially reduced
6 weeks Cough and Breathlessness should have substantially reduced
3 months most symptoms should have resolved but Fatigue may still be present
6 months most people will feel back to Normal
Patient Counseling
 Advise patients with Community Acquired Pneumonia to consult their Healthcare
Professional if they feel that their Condition is Deteriorating or not Improving as
expected
Hospital Acquired Pneumonia
Antibiotic Therapy
Offer Antibiotic Therapy as soon as possible after diagnosis, and certainly
within 4 hours, to patients with Hospital Acquired Pneumonia
Choose Antibiotic Therapy in accordance with Local Hospital Policy
(which should take into account knowledge of local microbial pathogens)
and clinical circumstances for patients with hospital-acquired pneumonia.
Consider a 5 to10 day course of Antibiotic Therapy for patients with
Hospital Acquired Pneumonia
Empirical Coverage for Uncommon Pathogens Causing CAP
Pseudomonas MRSA
Vancomycin
Linezolid
Piperacillin with Tazobactam Or
Cefepime Or Imepenem plus Either
Ciprofloxacin Or Levofloxacin
•Or
Aminoglycoside and Azithromycin
•Or
Beta-Lactam with Aztreonam
Common Causes of Non-Responding Pneumonia
Infective Etiology
Resistant Organism
•Staphylococcus Aureus
•Streptococcus Pneumoniae
Super Infection with Nosocomial
Organism
•Pseudomonas
Rare Organisms
•Fungi
•Mycobacteria
Extra Pulmonary Dissemination
• Endocarditis
• Meningitis
• Arthritis
Empyema or Abscess Formation
Common Causes of Non-Responding Pneumonia
Non-Infective Etiology
Pulmonary Embolism
MI
Heart Failure
Pulmonary Edema
Renal Failure
Vasculitis
Malignancy
Pulmonary Hemorrhage
Bronchiolitis Oblitrans with Organizing Pneumonia
Drug Induced Pulmonary Disease
Complications Of CAP
Lung Abscess
Para-pneumonic Effusion
Empyema
Broncho-pleural Fistula
Organizing Pneumonia
Bronchiectasis
Prevention
 Vaccination against Streptococcus pneumonia and Influenza Virus
 Vaccination status should be assessed at the time of admission
 Vaccination should be performed either at Discharge or during Out Patient follow up
if needed
 Risk Factor Modifications
 Smoking and Alcohol abuse Cessation
Special Thanks
to
Dr. Saeed Ahmed and Dr. Ellahi Bukhsh
Thanks

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Community Acquired Pneumonia Dr Ellahi Bakhsh

  • 1. Community Acquired Pneumonia DR. ELLAHI BAKHSH PGR PULMONOLOGY FATIMA JINNAH CHEST HOSPITAL QUETTA
  • 2. References  Clinical Respiratory Medicine by Stephen G. Spiro  BTS Guideline for Management of Community Acquired Pneumonia in Adults updated 2009  NICE Guideline for Diagnosis and Management of Community Acquired Pneumonia in Adults ( Published in December 2014 )  Davidson’s Principles & Practice of Medicine
  • 3. Objectives  To Briefly Review of Pneumonia  Management of Community Acquired Pneumonia in Adults according to recently published NICE Guideline
  • 4. Case Scenario  82 year old male , living in a Nursing Care, presented with Fever, Breathlessness, purulent sputum with alter level of consciousness for the last 3 days. He has COPD and history of Smoking and Mild Dementia.  His Chest Xray shows new right lower lobe infiltrates  CBC shows Raised WBC count 18000/mm3  Initial Gram Staining report shows Prominent Stains of Gram +ve Organism
  • 5. Case Scenario  What is your Diagnosis  Health Care Associated Pneumonia  What is most probable Causative Pathogen  Staphylococcus Aureus  What should be done next  Vancomycin 1 gram IV every 12 hours  Piperacillin and Tazobactam and intravenous levofloxacin incase of MRSA
  • 6. Community Acquired Pneumonia  Acc. to BTS Guidelines CAP is defined as  Acute Lower Respiratory Tract Infection  Accompanied by New Infiltrates on Chest Radiograph  Or Ascultatory Findings Consistent with Pneumonia  in a patient Not Hospitalized or residing in a Long Term Care Facility  for More than 2 weeks  before onset of symptoms
  • 7. What is An Acute Lower Respiratory Tract Infection  Acc. To NICE Guideline  An acute Illness (present for 21 days or less)  usually with Cough as main symptom  and with at least 1 other Lower respiratory tract symptoms such as  Fever  Sputum Production  Breathlessness  Wheeze  Chest Discomfort or Chest Pain  with No alternative explanation  Pneumonia, Acute Bronchitis and Exacerbation of COPD
  • 8. Hospital Acquired Pneumonia  Pneumonia that develops in a Non-Incubating patient, 48 hours or more after Hospital Admission
  • 9. Ventilator Associated Pneumonia  Pneumonia that develops in a patient receiving Invasive Mechanical Ventilation for at least 48 hours or more
  • 10. Health Care Associated Pneumonia  Pneumonia that develops in a patient with recent contact with the Health Care System, that include  Hospitalization for 2 days or more in the preceding 90 days  Residence in Nursing Care  Home Infusion Therapy including Antibiotics  Chronic Dialysis within 30 days  Home Wound Care  Family member with MDR Pathogen
  • 11. Why it is important to differentiate CAP from other Pneumonia  Timely Diagnosis and Treatment is the key in Successful Management of Pneumonia  Early Pathogen detection and Choice of appropriate Antibiotic will not only result in better outcome of Pneumonia, But also reduces problems related to Antibiotic Resistant
  • 12. Burden of Disease  Pneumonia remains common cause of Death  Globally Pneumonia ranked 6th  CAP is most common cause of Severe Sepsis  Despite introduction of Antibiotics, Imaging modalities and Biomarker testing, mortalities related to CAP has not changed significantly.
  • 13. Risk Factors Age Altered Immunity Malnutrition Environmental Factors Airway Colonization Alcoholism Smoking
  • 14. Risk Factors  Age  With the increase in Age , Immunity of body weakens  Every Year over 65, increases risk for Pneumonia
  • 15. Risk Factors  Altered Immunity  Patients with Immunocompromised state such as  HIV  AIDS  Chemotherapy Treatment  Lymphopoliferative Diseases  Cancer  Diabetes  CLD  Heart Failure are at increased risk for development of CAP
  • 16. Risk Factors  Malnutrition  whatever the cause may be  Malnutrition leads to alterations in Immunity  Increasing the chance for Airway colonization and infection with Gram –ve Bacilli
  • 17. Risk Factors  Environmental Factors  Overcrowding  Occupations associated with exposure to Dust, Fumes, various Chemicals, Contaminated Water Supply and Cooling Towers of Air-Conditioning Units  Contact with Animals
  • 18. Risk Factors  Airway Colonization  Results in Impairment of Innate Lung Defense  Common in Patients with Chronic Obstructive Pulmonary Disease
  • 19. Risk Factors  Alcoholism  Leads to Impaired Level of Consciousness, Cough Reflex and Muco-cilliary Movement  Also impairs function of Lymphocytes, Monocytes and alveolar Macrophages
  • 20. Risk Factors  Smoking  Smoking, itself is not a Risk Factor for Pneumonia  But it alters Muco-cilliary Transport  And increases adhesion of Pathogens to Orophyrangial epithelium
  • 21. Pathogens  Virus , Bacteria and Fungi are pathogens of Pneumonia  Common Pathogens are  Streptococcus Pneumoniae  Staphylococcus Aureus  H. Influenza  Mycoplasma Pneumoniae  Ligeonalla Pneumophila  Pseudomonas  Clamydia  Ecoli  Klebsella Pneumoniae  MRSA  Anaerobes
  • 22. Common Pathogens in CAP Streptococcus Pneumoniae Staphylococcus Aureus H. Influenza Mycoplasma Pneumoniae Ligeonalla Pneumophila Clamydia Klebsella Pneumoniae
  • 23. Common Pathogens in HAP •E. Coli •Pseudomonas •Klebsella Gram –ve are Most Common •Staphylococus Aureus •MRSAGram +ve Bacteriods
  • 24. Common Pathogens in VAP Pseudomonas aeruginosa E.coli Klebsiella pneumoniae Acinetobacter Staphylococcus Pneumoiae
  • 25. Common Pathogens in HCAP Staphylococcus aureus Pseudomonas aeruginosa Streptococcus pneumoniae Haemophilus influenzae.
  • 26. Streptococus Pneumoniae Most Common Pathogen of CAP If left untreated , it will eventually result in Production of Rust colored Sputum Pneumonia caused by Streptococus Pneumoniae is a Medical emergency Because of •Rapid multiplication •High Risk for Secondary Complications
  • 27. Staphylococus Pneumoniae  Most Severe form of CAP Because of  Resistant to Multiple Antibiotics  Leads to formation of Bullae which may repute to Cause Pneumothorax, Pneumo-Pyothorax and Septicemia
  • 28. Mycoplasma Pneumoniae Most Common Pathogen in Atypical Pneumonia Usually occurs in small epidemics in Overcrowded Population
  • 29. Clinical Presentation CAP  Classical Symptoms of CAP are  Fever  Intense Chills  Cough  Sputum Production  Dyspnea  Pleuritic Chest Pain  Generalized Fatigue  Hemoptysis
  • 31.
  • 32.
  • 33. Clinical Presentation  On General Physical Examination  Hyperthermia  Tachycardia  Tachypnea  Use of Accessory Muscles  Central Cyanosis  Altered Mental Status
  • 34. Clinical Presentation  On Chest Examination  Wheezes  Coarse Crackes  Tracheal Deviation  Dull Percussion  Reduced Breath Sounds  Decrease Chest Movements on Effected Side  Bronchial Breathing
  • 35. Clinical Presentation  On Arterial Blood Gases  Decreased PaO2  Decreased PaCo2  Type 1 Respiratory Failure with Respiratory Alkalosis
  • 37.  Typical  Caused by Typical Pathogens  Streptococus Pneumoniae  H. Influenze  Klebsella  Morexella Cataralis  Classical Syptoms are Dominant  Sudden in Onset  High Grade Fever  Intense Chills  Productive Cough  Pleuritic Chest Pain ( Occasionally)  CBC Shows Leukocytosis with Neutrophillic Predominance  Atypical  Also Called Walking Pneumonia  Caused by Atypical Pathogens  Mycoplasma Pneumoniae  Clamydia Pneumophila  Ligionella  Systemic Menifestations are Dominant  Generalized Myalgea  Muscle Ache  Arthralgia  Diarhhea  Nausea  Vomiting  Abdominal Pain  Gradual in Onset  Low Grade Fever  Dry Cough  CBC Shows Absent Leukocytosis  Do not respond to common Antibiotics  Do not form Lobar Consolidations rather restricted to Small Areas
  • 38. Investigations  Baseline  Chest X ray  Complete Blood Count  Serum Electrolytes  Urea Creatinine  Liver Functioning Test  Specific  Arterial Blood Gases  Gram Staining  Sputum Culture  C – reactive Protein  Pneumococcal and Legionella Urinary Antigen Test
  • 39. C – reactive Protein  C-reactive protein is an acute phase reactant,  a protein made by the liver and released into the bloodstream within a few hours  after tissue injury,  start of an infection,  or other cause of inflammation
  • 40. Abbreviated Mental Test  Quick and Easy to Use Test to Assess Elderly patients for  Dementia  Confusion  Impaired Cognitive Functions  10 simple questions are asked from patient  1 Point is given for every Correct Answer and 0 Point for Incorrect Answers
  • 41. Abbreviated Mental Test Name Time Give the patient an address and ask for recall at end of test Year Name of the place Identification of any two person ( Doctor, Nurse , Home Help etc) Date of Birth Any Historical Event Name of President/ Prime Minister Count backward from 20-1 Recall Adress
  • 42. Differential Diagnosis of CAP Acute bronchitis Acute Exacerbation of COPD Pulmonary T.B Pulmonary Edema Pulmonary Infarction Pulmonary eosinophilia Pulmonary fibrosis Bronciolitis Oblitrans Organising Pneumonia Bronchoalveolar Cell Carcinoma Drug-induced pulmonary disease Myocardial infarction Congestive heart failure and pulmonary edema
  • 44. Lower Respiratory Tract Infection  For people presenting with symptoms of Lower Respiratory Tract Infection in Primary Care,  Consider C-reactive protein test  if after clinical assessment a diagnosis of Pneumonia has not been made  and it is not clear whether Antibiotics should be prescribed
  • 45. Lower Respiratory Tract Infection  Use the results of the C-reactive protein test to guide Antibiotic prescribing in people without a clinical diagnosis of pneumonia as follows,  Do not routinely offer antibiotic therapy if the C-reactive protein concentration is less than 20 mg/litre  Consider a Delayed Antibiotic Prescription (a prescription for use at a later date if symptoms worsen) if the C-reactive protein concentration is between 20 mg/litre and 100 mg/litre  Offer Antibiotic Therapy if the C-reactive protein concentration is greater than 100 mg/litre
  • 46. Community Acquired Pneumonia  When a clinical diagnosis of Community Acquired Pneumonia is made in Primary Care  Severity is assessed  To determine whether patients are at Low, Intermediate or High risk of Death  using the CRB65 Score
  • 47. CRB65 score  CRB65 Score is calculated by giving 1 Point for each of the following prognostic features  Confusion (abbreviated Mental Test score 8 or less, or new disorientation in person, place or time)  Raised Respiratory Rate (30 breaths per minute or more)  Low Blood Pressure (Diastolic 60 mmHg or less, or Systolic less than 90 mmHg)  Age 65 Years or more
  • 48. Mortality Risk  Patients are stratified for Risk of Death as follows  0 Low risk (less than 1% mortality)  1 or 2 Intermediate risk (1-10% mortality risk)  3 or 4 High risk (more than 10% mortality risk)
  • 49. Decision For Site Of Care  Use Clinical Judgment in conjunction with the CRB65 Score to inform decisions about whether patients need Hospital assessment as follows  Consider Home-Based Care for patients with a CRB65 score of 0  Consider Hospital Assessment for all other patients, particularly those with a CRB65 Score of 2 or more
  • 50. Community Acquired Pneumonia  When a clinical diagnosis of Community Acquired Pneumonia is made in Hospital  Severity is assessed  To determine whether patients are at Low, Intermediate or High risk of Death  using the CURB65 Score
  • 51. CURB65 score  CURB65 Score is calculated by giving 1 Point for each of the following prognostic features  Confusion (abbreviated Mental Test score 8 or less, or new disorientation in person, place or time)  Raised Blood Urea Nitrogen (over 7 mmol/litre)  Raised Respiratory Rate (30 breaths per minute or more)  Low Blood Pressure (Diastolic 60 mmHg or less, or Systolic less than 90 mmHg)  Age 65 years or more
  • 52. Mortality Risk  Patients are stratified for risk of death as follows  0 or 1 Low risk (less than 3% mortality risk)  2 Intermediate Risk (3-15% mortality risk)  3 to 5 High Risk (more than 15% mortality risk)
  • 53. Management Of CAP  Use Clinical Judgment in conjunction with the CURB65 Score to Guide Management of Community Acquired Pneumonia as follows  Consider Home-Based Care for patients with a CURB65 Score of 0 -1  Consider Hospital-Based Care for patients with a CURB65 Score of 2 or more  Consider Intensive Care assessment for patients with a CURB65 Score of 3 or more
  • 54. Microbiological Test  Do not routinely offer Microbiological Tests to patients with Low-severity Community Acquired Pneumonia  For patients with Moderate or High-Severity Community Acquired Pneumonia  take Blood and Sputum Cultures and  Consider Pneumococcal and Legionella Urinary Antigen Tests.
  • 55. Timely Diagnosis And Treatment  Put in place processes to allow diagnosis (including X-rays) and treatment of Community Acquired Pneumonia within 4 hours of presentation to Hospital  Offer Antibiotic Therapy as soon as possible after diagnosis, and certainly within 4 hours to all patients with Community Acquired Pneumonia who are admitted to hospital
  • 56. Antibiotic Therapy  Low-severity community-acquired pneumonia  Offer a 5-day course of a Single Antibiotic to patients with Low-Severity Community Acquired Pneumonia  Consider Amoxicillin in preference to a Macrolide or a Tetracycline for patients with Low-Severity Community Acquired Pneumonia  Consider a Macrolide or a Tetracycline for patients who are Allergic to Penicillin  Consider Extending the course of the Antibiotic for longer than 5 days as a possible management strategy for patients with Low-Severity Community Acquired Pneumonia whose symptoms do not improve as expected after 3 days
  • 57. Antibiotic Therapy  Explain to patients with Low-Severity Community Acquired Pneumonia treated in the community, and when appropriate their families or carer, that  they should seek further medical advice if their symptoms do not begin to improve within 3 days of starting the antibiotic, or earlier if their symptoms are worsening.  Do not routinely offer patients with Low-Severity Community Acquired Pneumonia  a Fluoroquinolone  Dual Antibiotic Therapy
  • 58. Antibiotic Therapy  Moderate- and High-Severity Community Acquired Pneumonia  Consider a 7 to10 day course of Antibiotic Therapy for patients with Moderate or High Severity Community Acquired Pneumonia  Consider Dual Antibiotic Therapy with Amoxicillin and a Macrolide for patients with Moderate-Severity Community Acquired Pneumonia  Consider Dual Antibiotic Therapy with a Beta-Lactamase Stable Beta-Lactam and a Macrolide for patients with High-Severity Community Acquired Pneumonia
  • 59. Site Scoring System Severity Management Antibiotic Therapy Antibiotic Duration Antibiotics Primary Care CRB-65 Low ( 0 ) Home Based Treatment Single 5 Days Amoxicillin(Preferred) or Macrolide Or Tetracycline Moderate (1-2) Refer to Hospital High (2-4) Do not routinely offer Floroquinolone & Dual Antibiotic Therapy to patients with low-severity CAP Consider Extending the course of the Antibiotic for longer than 5 days for patients with Low-Severity CAP whose symptoms do not improve as expected after 3 days Explain to patients with Low-Severity CAP, their families, that they should seek further Medical advice if their symptoms do not begin to improve within 3 days of starting the antibiotic, or earlier if their symptoms are worsening
  • 60. Site Scoring System Severity Management Antibiotic Therapy Antibiotic Duration Antibiotics Hospital CURB-65 Low ( 0-1 ) Home Based Treatment Single 5 Days Amoxicillin(Preferred) or Macrolide Or Tetracycline Moderate (2) Hospital Based Care Dual 7-10 Days Amoxicillin + Macrolide Intensive Care Unit High (3-5) Dual 7-10 Days Beta-Lactamase stable beta-lactam + Marcrolide Macrolides include Erythromycin, Clarithromycin, Azithromycin Beta-Lactamase stable beta-lactam includes Co-Amoxiclave, Cefotaxime, Ceftroline, Fosamil, Ceftriaxone, Piperacillin with Tazobactam
  • 61. Antibiotic Dosage Amoxicillin Macrolides Ceftriaxone Co-Amoxicalve Piperacillin with Tazobactam Cefotaxime •500mg – 1g 8 Hourly •500mg 12 Hourly •2g Once Daily •1.2g 8 Hourly •4.5g 8 Hourly •1g 8 Hourly
  • 62. Glucocorticoid Treatment  Do not routinely offer a Glucocorticosteroid to patients with Community Acquired Pneumonia unless they have other conditions for which Glucocorticosteroid treatment is indicated
  • 63. Monitoring in Hospital  Consider measuring a baseline C-reactive protein concentration in patients with Community Acquired Pneumonia on admission to Hospital  Repeat the Test if clinical progress is uncertain after 48 to 72 hours
  • 64. Safe Discharge from Hospital  Do not Routinely Discharge patients with Community Acquired Pneumonia if in the past 24 hours they have had 2 or more of the following findings  Temperature higher than 37.5°C  Respiratory Rate 24 breaths per minute or more  Heart Rate over 100 beats per minute  Systolic Blood Pressure 90 mmHg or less  Oxygen Saturation under 90% on room air  Abnormal Mental Status  Inability to Eat without Assistance
  • 65. Consider Delay Discharge  Consider Delaying Discharge for patients with Community Acquired Pneumonia if their Temperature is higher than 37.5°C
  • 66. Patient Counseling Explain to patients with Community Acquired Pneumonia that after starting treatment their symptoms should steadily improve, although the rate of improvement will vary with the severity of the pneumonia, and most people can expect that by 1 week Fever should have resolved 4 weeks Chest Pain and Sputum production should have substantially reduced 6 weeks Cough and Breathlessness should have substantially reduced 3 months most symptoms should have resolved but Fatigue may still be present 6 months most people will feel back to Normal
  • 67. Patient Counseling  Advise patients with Community Acquired Pneumonia to consult their Healthcare Professional if they feel that their Condition is Deteriorating or not Improving as expected
  • 68. Hospital Acquired Pneumonia Antibiotic Therapy Offer Antibiotic Therapy as soon as possible after diagnosis, and certainly within 4 hours, to patients with Hospital Acquired Pneumonia Choose Antibiotic Therapy in accordance with Local Hospital Policy (which should take into account knowledge of local microbial pathogens) and clinical circumstances for patients with hospital-acquired pneumonia. Consider a 5 to10 day course of Antibiotic Therapy for patients with Hospital Acquired Pneumonia
  • 69. Empirical Coverage for Uncommon Pathogens Causing CAP Pseudomonas MRSA Vancomycin Linezolid Piperacillin with Tazobactam Or Cefepime Or Imepenem plus Either Ciprofloxacin Or Levofloxacin •Or Aminoglycoside and Azithromycin •Or Beta-Lactam with Aztreonam
  • 70. Common Causes of Non-Responding Pneumonia Infective Etiology Resistant Organism •Staphylococcus Aureus •Streptococcus Pneumoniae Super Infection with Nosocomial Organism •Pseudomonas Rare Organisms •Fungi •Mycobacteria Extra Pulmonary Dissemination • Endocarditis • Meningitis • Arthritis Empyema or Abscess Formation
  • 71. Common Causes of Non-Responding Pneumonia Non-Infective Etiology Pulmonary Embolism MI Heart Failure Pulmonary Edema Renal Failure Vasculitis Malignancy Pulmonary Hemorrhage Bronchiolitis Oblitrans with Organizing Pneumonia Drug Induced Pulmonary Disease
  • 72. Complications Of CAP Lung Abscess Para-pneumonic Effusion Empyema Broncho-pleural Fistula Organizing Pneumonia Bronchiectasis
  • 73. Prevention  Vaccination against Streptococcus pneumonia and Influenza Virus  Vaccination status should be assessed at the time of admission  Vaccination should be performed either at Discharge or during Out Patient follow up if needed  Risk Factor Modifications  Smoking and Alcohol abuse Cessation
  • 74. Special Thanks to Dr. Saeed Ahmed and Dr. Ellahi Bukhsh