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Pneumonia: Anjitha Joseph

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PNEUMONIA

Anjitha Maria Joseph


Definition:
Pneumonia is defined as
inflammation with
exudative solidification of
the lung parenchyma,
generally acute.
Epidemiology
●Each year, 5 million people
die from pneumonia worldwide.
●Pneumonia is the ninth
leading cause of death in the
United States and the leading
cause of infection related
mortality
●Rates are greatest in
children less than five and
adults older than 75 years of
age.
●It occurs about five times
more frequently in the
developing countries versus
developed countries.
CLASSIFICATION
Classification by SITE
Classification by AETIOLOGY
Classification by MODE OF
ACQUIRING PNEUMONIA
1)Classification by Site
ALVEOLARor LOBAR
PNEUMONIA
Lobar pneumonia is a form of
pneumonia characterized by
inflammatory exudate within the intra-
alveolar space resulting in
consolidation that affects a large and
continuous area of the lobe of a lung.
BRONCHOPNEUMONIA
Inflammation is restricted to the
conducting airways,especially
terminal and respiratory
bronchioles.
INTERSTITIAL PNEUMONIA
The inflammation is confined to
interalveolar septa.
There is infiltration of
lymohocytes, macrophages,and
plasma cells into the alveolar
septa.
Radiographically it gives a
reticular pattern
2)Classification by AETIOLOGY
PRIMARY PNEUMONIA
●Caused by a specific
pathogenic organism
●There is no pre-existing
abnormality of the
respiratory system.
COMMON AETIOLOGICAL AGENTS LESS COMMON ATEIOLOGICAL AGENTS

Streptococcus pneumonia Klebsiella pneumonia


(most common)
Haemophilus influenzae Streptococcus pyogenes
Staphylococcus aureus Pseudomonas aerugnosa
Legionella pneumophila Clamidophila pneumoniae
Moraxella catarrhalis VIRUSES:H1N1 Influenza
vIrus,corona virus producing
SARS,Respiratory syncytial virus
Fungi:Histoplasma
capsulatum,Cryptococus
SECONDARY PNEUMONIA
 Characterised by absence of any
specific pathogenic organism in
sputum and presence of some pre-
existing abnormality of respiratory
system.
 ASPIRATION of pus from infected nasal
sinuses.
 Ineffective coughing
 Partial bronchial obstruction(eg:by
tumour)
SUPPURATIVE PNEUMONIA (NECROTISING
PNEUMONIA)
 Main causative organisms are
Staphylococcus aureus ,Klebsiella
pneumonia, and occasionally
H.influenza.
 Prominent features are destruction
of lung tissue by inflammation
,abscess formation and subsequent
development of fibrosis.
3)Classification by mode of
acquiring pneumonia
●Community-Acquired
Pneumonia(CAP)
●Health care-associated
Pneumonia(HCAP)
●Pneumonia in
immunocompromised host
●Hospital Acquired Pneumonia(HAP)
●Ventilated Associated
Pneumonia(VAP)
Community-Acquired
Pneumonia(CAP)
It is defined as acute
pulmonary infection in a
patient who is not hospitalised
or living in a long-term care
facility 14 or more days before
presentation and does not meet
the criteria for HCAP.
Types of CAP:
ACUTE
Acute pneumonia presents with
sudden onset over a few hours to
several days.
The clinical presentation may be
typical or atypical, depending on
the pathogen.
TYPICAL ATYPICAL
Streptococcus Legionella pneumophila
pneumoniae
Haemophilus influenzae Chlamydophila
pneumoniae
Moraxella catarrhalis Mycoplasma
pneumoniae

Staphylococcus aureus
CHRONIC
The onset of chronic pneumonia
is more insidious, often with
gradually escalating symptoms
over days, weeks, or months.
Causetive organisms:
Mycobacterium tuberculosis
Histoplasma capsulatum
Blastomycosis dermatitidis
Health care-associated
Pneumonia(HCAP)
 Defined as infections occurring within 90
days of a 2 day or longer hospitalisation,
stay in a nursing home or long term care
residence in last 30 days; within 30 days of
receiving intravenous antibacterial therapy,
chemotherapy or wound care or after a
hospital or haemodialysis clinic visit;or in
any patient in contact with any multidrug
resistant pathogen
Hospital Acquired
Pneumonia(HAP)
HAP is defined as an LRTI that
develops in hospitalized patients
more than 48 hours after
admission and excludes
community-acquired infections
that are incubating at the time of
admission.
 HAP is a common clinical problem and
represents the second most common
nosocomial infection in the United States,
accounting for 15% to 22% of all such
infections.
 Current estimates suggest that more than
150,000 individuals develop HAP each year.
HAP increases hospital length of stay 7 to 9
days at an average incremental per-patient
cost of $40,000.
Ventilated Associated
Pneumonia(VAP)
VAP is defined as an LRTI
that develops more than
48 to 72 hours after
endotracheal intubation
Pneumonia in
immunocompromised host
●Neutropenic patients
●HIV patients
●Malignancies
●Patients on
mimmunouppressives
PATHOGENESIS
Six pathogenetic mechanisms may contribute to
the developmentof pneumonia.
Mechanism of Disease:
1)Inhalation of aerosolized
infectious particles
Examples of Specific Infections:
Tuberculosis
Histoplasmosis
Cryptococcosis
Blastomycosis
2) Aspiration of organisms
colonizing the oropharynx
Examples of Specific Infections:
 Community-acquired bacterial pneumonia
 Aspiration pneumonia
 Hospital-acquired pneumonia
 Ventilator-associated pneumonia
3)Direct inoculation of organisms
into the lower airway
 Hospital-acquired pneumonia
 Ventilator-associated pneumonia
4)Spread of infection to the
lungs from adjacent
structures
 Amebicpneumonia from rupture of
amebic liver abscess into the lung.
5)Spread of infection to the lung
through the blood
 Staphylococcus aureus pneumonia
arising from right-sided bacterial
endocarditis
6) Reactivation of latent infection,
usually resulting from
immunosuppression
●Reactivation tuberculosis
●Cytomegalovirus
Pathological Stages in development of
Pneumonia
 1)STAGE OF CONGESTION
Just congestion of vessels without alveolar
exudation
 2)STAGE OF RED HEPATISATION
Intra alveolar exudation especially with RBCs
 3)STAGE OF GREY HEPATISATION
The exudation is of mainly WBCs with minimal
RBCs
 4)STAGE OF RESOLUTION
The exudate is removed or absorbed by
macrophages and proteolytic enzymes
CLINICAL FEATURES
SUDDEN ONSET OF RIGORS
FEVER
PLEURITICCHEST PAIN
COUGH PRODUCTIVE OF
PURULENT SPUTUM
HAEMOPTYSIS
Extrapulmonary features:
MYALGIA
ARTHRALGIA
HEADACHE
MENTAL CONFUSION
ABDOMINAL PAIN
DIARRHOEA
EXAMINATION:
 TACHYPNEA
 TACHYCARDIA
 INCREASED TACTILE AND VOCAL
FERMITUS
 DULL PERCUSSION NOTE OVER THE
AREA OF INFECTION
 CREPITATIONS
INVESTIGATIONS
●Total and differential leucocyte count
●Blood culture
●Sputum stain and culture
●Serological and antigen detection tests
●ABG analysis
●Radiological studies
●PCR
Lobar pneumonia caused by Streptococcus
pneumoniae.
A 36-year-old previously healthy woman presents
with abrupt onset of fevers and shaking chills, cough
productive of yellow sputum, and right-sided
pleuritic chest pain. Chest
radiograph reveals lobar consolidation. Sputum
culture yields S. pneumoniae.
DIFFERENTIAL DIAGNOSIS
 Pulmonary edema
• Pulmonary infarction
• Acute respiratory distress syndrome
• Pulmonary hemorrhage
• Lung cancer or metastatic cancer
• Atelectasis
• Drug reactions involving the lung
• Pulmonary eosinophilia
MANAGEMENT AND
TREATMENT
Criteria for risk stratification (CURB‐65)
 • Confusion
 • Urea >40mg/dl
 • Respiratory rate ≥30/min
 • Low blood pressure (diastolic blood pressure
≤60 mm Hg or systolic blood pressure <90
mmHg)
 • Age ≥65 years
MANAGEMENT
● General Measures:
Check the AIRWAY BREATHING ana CIRCULATION
● OXYGEN THERAPY
Correct Hypoxia
●maintain FLUID BALANCE
Give IV fluids
●Treatment of Pleuritic chest pain
using mild analgesics
●ANTIBIOTIC TREATMENT
Major Classes of Antibiotics Used in
the Treatment of Pneumonia
Antibiotic Class REPRESENTATIVE DRUG

PENCILLINS PENCILLIN G, AMPICILLIN

UREIDOPENCILLINS PIPERACILLIN

2nd generation cephalosporins CEFUROXIME

3rd generation cephalosporins CEFTRIAXONE ,CEFOTAXIME

QUNILONES LEVOFLOXACIN ,MOXIFLOXACIN

MACROLIDES AZITHROMYCIN, ERYTHROMYCIN

TETRACYCLINES DOXYCYCLINE

Beta-lactam/beta-lactamase piperacillin/
inhibitor combinations tazobactum
COMPLICATIONS OF PNEUMONIA
 PLEURAL EFFUSION
 LUNG ABSCESS
 ARDS
 SEPSIS
 PNEUMOTHORAX
 EMPYEMA
PREVENTION STRATEGIES OF
NOSOCOMIAL PNEUMONIA
 Handwashing
 Isolation of patients with resistant organisms
 Infection control and surveillance
 Subglottic secretion aspiration
 Selective digestive decontamination
 Topical tracheobronchial antibiotics
VAP BUNDLE
The Ventilator Bundle contains four
components:
 elevation of the head of the bed to 30-45
degrees
 daily 'sedation vacation’ and daily
assessment of readiness to extubate
 peptic ulcer disease prophylaxis
 and deep venous thrombosis prophylaxis

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