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RESPIRATORY TRACT
INFECTIONS
Learning objectives
At the end of the session, the students will be
able to
• Classify and define of respiratory tract
infections
• Describe aetiopathogenesis
• Describe laboratory diagnosis and treatment
of respiratory tract infections
RESPIRATORY TRACT INFECTIONS
• Upper Respiratory Tract Infections
• Infections of airway above glottis or vocal
cords
• Tonsillitis, pharyngitis, laryngitis, sinusitis,
otitis media, and rhinitis
• Symptoms - cough, sore throat, running nose,
nasal congestion, headache, low-grade fever,
facial pressure and sneezing
Rhinitis or common cold
• Mostly caused by viruses:
• Rhinovirus
• Coronavirus
• Adenovirus
• Influenza virus
• Parainfluenza virus
• Human metapneumovirus
• Respiratory syncytial virus
Sinusitis
• Symptoms: Headache/facial pain, nasal mucus, Plugged nose
• Agents of acute sinusitis:
• Viruses (most common cause): Rhinoviruses, Influenza viruses,
Parainfluenza viruses
• Bacterial agents: Streptococcus pneumoniae, Haemophilus influenzae,
Moraxella catarrhalis, Pseudomonas and other gram- neg- ative bacilli
(nosocomial sinusitis)
• Agents of chronic sinusitis: Obligate anaerobes, Staphylococcus aureus
Pharyngitis (sore throat), and
tonsillitis
• Symptoms:
• Pharynx and/or tonsils become inflamed, red,
swollen, and show exudate, and sometimes a
membrane is formed
• Viruses: (most common cause) Influenza virus,
Parainfluenza virus, Coxsackievirus A,
Rhinovirus, Coronavirus, Epstein-Barr virus,
Adenoviruses
Pharyngitis (sore throat), and
tonsillitis
• Bacteria: Streptococcus pyogenes (most
common bacterial cause), Streptococcus
groups C and G, Arcanobacterium species,
Corynebacterium diphtheriae and C. ulcerans,
Mycoplasma pneumoniae
• Vincent angina - Treponema vincentii &
Leptotrichia buccalis
• Fungal: Candida albicans
Laryngitis
• Symptoms: Hoarseness of voice, Lowering and
deepening of voice
• Mostly viral agents: Influenza virus,
Parainfluenza virus, Rhinovirus, Adenovirus,
Coronavirus, Human metapneumovirus
• If membrane or exudate present:
Streptococcus pyogenes, C. diphtheriae,
Epstein-Barr virus
Laryngotracheobronchitis (or croup)
• Age—Children, <3 years age
• Symptoms:
- Inspiratory stridor, Hoarseness, Fever
- Cough (harsh, barking non- productive )
• Agents:
- Parainfluenza virus (most common)
- Influenza virus
- Respiratory syncytial virus
- Adenoviruses
Epiglottis
• Edema and inflammation of epiglottis and soft
tissue above vocal cords
• Age: children 2–6 years
• Symptoms: Fever, Difficulty in swallowing,
Inspiratory stridor
• Most common agent: Haemophilus influenzae
type b
Lower Respiratory Tract Infection
• Pneumonia
• Inflammation of lungs
1. Community acquired—patients acquire the
organisms in the community
2. Hospital acquired— patients acquire the
organisms in the hospital setting.
Community-acquired Pneumonia
(CAP)
• Agents: Streptococcus pneumoniae followed
by Mycoplasma pneumoniae
• CURB65 scoring system - To predict prognosis
of CAP
• Score >1 patient should be hospitalized
• Else the treatment can be given on outpatient
basis
Agents of Community-acquired Pneumonia (CAP)
• No co-morbidity:
• Streptococcus pneumoniae (most common)
• Atypical pathogens:
- Chlamydophila pneumoniae and C. psittaci
- Legionella and Mycoplasma
- Coxiella burnetii (Q fever)
- Viral pneumonia (influenza, adenovirus, parainfluenza,
RSV)
Agents of Community-acquired Pneumonia (CAP)
• Associated with Co-morbidity:
• Alcoholism: S. pneumoniae, H. influenzae
• COPD: H. influenzae, M. catarrhalis, S. pneumoniae
• Post-CVA-aspiration: S. pneumoniae
• Post-obstruction of bronchi: pneumoniae, anaerobes
• Post-influenza: S. pneumoniae, S.aureus
Community-acquired Pneumonia
(CAP)
• CURB-65score
- C (Confusion) = 1 point
- U (blood urea nitrogen >19 mg/dL) = 1 point
- R (respiratory rate >30 min) = 1 point
- B (BP <90/60) = 1 point
- 65 (Age ≥65 years) = 1 point
• Higher the score, greater is the mortality
• If the score ≤1, outpatient therapy is indicated If the
score >1, patient should be hospitalized
Hospital-acquired Pneumonia (hAP)
• Hospitalized patients have increased risk of
developing pneumonia; most of which are
ventilator-associated pneumonia
• VAP can be clinically diagnosed by Clinical
Pulmonary Infection (CPIS)
• Likelihood of VAP is higher when total CPIS is
>6
Clinical Pulmonary Infection Score
(CPIS)
Parameter(s) Score 0
Temperature (°C) ≥36.5°C and ≤38.4°C
Leukocytosis ≥4000 and ≤11,000
Tracheal aspirate None
Oxygenation (PaO2/FiO2 mm
Hg)
>250 or ARDS
Chest radiograph No opacity
Progressive radiological
progression
No radiological progression
Culture of tracheal aspirate Pathogenic bacteria
Light or no growth
Clinical Pulmonary Infection Score
(CPIS)
Score 1 Score 2
≥38.5°C and ≤38.9°C ≥390C and ≤36.40C
<4000 and >12000
Non-purulent Purulent
≤250 and no ARDS
Diffuse (patchy) opacity Localized opacity
Radiological progression
Pathogenic bacteria
Moderate or heavy growth
Same morphology as Gram
stain
Hospital-acquired Pneumonia (hAP)
• Bacterial agents:
• Gram-negative bacilli (most common)
– MDR non-fermenters (Pseudomonas and Acinetobacter)
– MDR Enterobacteriaceae (E. coli, Klebsiella and
Enterobacter)
• Staphylococcus aureus (both MRSA and MSSA)
• S. pneumoniae (rarely, in early stage)
• Viral agents:
• Influenza, adenovirus, parainfluenza, RSV
Clinical Manifestations of Pneumonia
• Fever, chills, chest pain and cough
• Based on area of lungs involved, and type of cough
produced
• Lobar pneumonia infecting lung parenchyma (alveoli)
• Consolidation and productive cough with purulent
sputum
- Mostly caused by pyogenic organisms :
– Pneumococcus
– Haemophilus influenzae
– Staphylococcus aureus
– Gram-negative bacilli.
Interstitial or atypical pneumonia
• Infection occurs in interstitial space of lungs
• Cough is characteristically non-productive
• Caused by :
- Chlamydophila pneumoniae
- Mycoplasma pneumoniae
- Viral pneumonia
- Legionella species
Bronchitis
• Inflammation of bronchus, which occurs
either as an extension of upper respiratory
tract infection such as influenza or may be
caused directly by bacterial agents such as
Bordetella.
• Common symptoms - fever, cough, sputum
production, and rarely croup- like features
Bronchitis
• Bacterial agents:
- B. pertussis
- B. parapertussis
- Mycoplasma pneumoniae
- Chlamydophila pneumoniae
• Viral agents:
- Influenza viruses
- Adenoviruses
- Rhinoviruses
- Coronaviruses
Bronchiolitis
• Inflammation of the smaller airways
(bronchioles)
• It presents as an acute viral infection that
primarily occurs in children less than 2 year
• Symptoms: Acute onset of wheeze, dyspnea,
cough, rhinorrhea, and respiratory distress
• Respiratory syncytial viruses account for 40–
80%
Bronchiolitis
• Viral agents:
• Respiratory syncytial viruses
• Parainfluenza viruses
• Rhinoviruses
• Influenza viruses
• Adenoviruses
• Enterovirus
• Human metapneumovirus
Laboratory Diagnosis
• Specimen Collection
• For URTI:
– Throat swab: Two swabs should be collected, one for
direct examination, other one for culture
– A part of the membrane, if present
– Nasopharyngeal aspirate for viral diagnosis or for
B.pertussis
• For LRTI: Sputum, induced sputum, tracheal
aspirate, bronchoalveolar lavage (BAL)
Microscopy
• Albert staining - metachromatic granules in the ends of
the bacilli  of C. diphtheriae
• Gram staining
- Detect the quality of the sputum
- Pus cells >25/low power field and epithelial cells
<5/low power field  good quality sputum
• Acid fast staining - M. tuberculosis
• GMS stain - Pneumocystis jirovecii
• Immunofluorescence microscopy of nasopharyngeal
aspirate
Culture
• For bacteriological culture: Blood agar, chocolate
agar and MacConkey agar
• For isolation of C. diphtheriae: Loeffler’s serum
slope and potassium tellurite agar
• For M. tuberculosis: LJ medium and incubated for
up to 6–8 weeks
• For fungal pathogen isolation: Sabouraud
dextrose agar
• Viral - Appropriate cell lines
Identification of agents of Lobar
Pneumonia
Agents of
pneumonia
Direct
demonstration in
sputum
Culture
identification
Streptococcus
pneumoniae
Pus cells >25/LPF
and epithelial cells
<5/LPF gram-
positive cocci in pair,
lanceolate shaped
Alfa hemolytic,
draughtsman-
shaped colonies on
blood agar
Sensitive to
optochin
Bile soluble,
ferments inulin
Haemophilus
influenzae
Pus cells >25/LPF
and epithelial cells
Satellitism on
blood agar with S.
Identification of agents of Lobar
Pneumonia
Agents of
pneumonia
Direct
demonstration in
sputum
Culture
identification
Staphylococcus
aureus
Pus cells >25/LPF
and epithelial cells
<5/LPF gram-
positive cocci in
clusters
BA- golden
yellow
hemolytic
colonies
Catalase
positive,
coagulase
positive
Gram-negative
bacilli
Pus cells >25/LPF
and epithelial cells
Identification is
based on:
Identification of agents of Interstitial Pneumonia
Agents of
pneumonia
Direct demonstration in
sputum
Culture identification
Chlamydop
hila
pneumonia
e
Direct
immunofluorescence test
Antigen detection by
enzyme immunoassay
Nucleic acid amplification
test (NAAT) detecting
specific genes
Serology-antibody
detection by
- CFT using LPS antigen
- ELISA using
recombinant LPS
antigen
- Micro-IF test using
outer membrane
protein antigen
Legionella
pneumophi
Pus cells >25/LPF and
epithelial cells <5/LPF
Growth on BCYE
medium
Identification of agents of Interstitial Pneumonia
Agents of
pneumoni
a
Direct demonstration in
sputum
Culture
identification
Mycoplas
ma
pneumoni
ae
Direct
immunofluorescence test
Capture ELISA-detecting
antigen (P1 adhesin) PCR
targeting P1 adhesin
gene
Culture-fried
egg colonies
on PPLO agar
Antibody
detection
- Non-specific test
(cold agglutination
test)
- Specific test (e.g.
ELISA)
Identification
• Serology:
• Detection of antibodies:
• Mycoplasma: Cold agglutination test,
complement fixation test (CFT) and ELISA
formats are available
• Chlamydial antibodies in serum: Micro-IF and
CFT
• Molecular Test
TREATMENT
• Community-acquired pneumonia (CAP)
• Empiric regimen is determined by presence of co-
morbidity and prediction of prognosis by CURB-
65 scoring system
• CAP, hospitalized (if CURB65 score >1):
- IV ceftriaxone plus azithromycin or
- IV levofloxacin
- Add vancomycin if CA-MRSA suspected
• CAP, outpatient (if CURB-65 score ≤1):
- If no comorbidity present: Oral azithromycin or
azithromycin plus amoxyclav.
- If comorbidity present: Oral levofloxacin
• Hospital-acquired pneumonia (HAP)
• Empirical therapy: comprises of both gram-negative
(e.g. piperacillin-tazobactam or meropenem) plus
gram-positive coverage (e.g. vancomycin).
• Definitive therapy: The empirical treatment should be
tailored based on the organism isolated and its
QUICK ASSESSMENT
MCQs
• CURB65 score is used for:
a) Ventilator-associated
pneumonia
b) Upper respiratory tract
infections
c) Community-associated
pneumonia
d) Tuberculosis
• Clinical-pulmonary
infection score (CPIS) is
used for:
a) Ventilator-associated
pneumonia
b) Upper respiratory tract
infections
c) Community-associated
pneumonia
d) Tuberculosis
• Sputum specimen sent for culture is considered good
quality if it contains:
a. Pus cells <5/low power field and epithelial cells
>25/low power field
b. Pus cells >25/low power field and epithelial cells
<5/low power field
c. Pus cells >25/low power field and epithelial cells
>25/low power field
d. Pus cells <5/low power field and epithelial cells <5/low
power field
THANK YOU...!

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ppt on respiratory infections.pptx

  • 2. Learning objectives At the end of the session, the students will be able to • Classify and define of respiratory tract infections • Describe aetiopathogenesis • Describe laboratory diagnosis and treatment of respiratory tract infections
  • 3. RESPIRATORY TRACT INFECTIONS • Upper Respiratory Tract Infections • Infections of airway above glottis or vocal cords • Tonsillitis, pharyngitis, laryngitis, sinusitis, otitis media, and rhinitis • Symptoms - cough, sore throat, running nose, nasal congestion, headache, low-grade fever, facial pressure and sneezing
  • 4. Rhinitis or common cold • Mostly caused by viruses: • Rhinovirus • Coronavirus • Adenovirus • Influenza virus • Parainfluenza virus • Human metapneumovirus • Respiratory syncytial virus
  • 5. Sinusitis • Symptoms: Headache/facial pain, nasal mucus, Plugged nose • Agents of acute sinusitis: • Viruses (most common cause): Rhinoviruses, Influenza viruses, Parainfluenza viruses • Bacterial agents: Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, Pseudomonas and other gram- neg- ative bacilli (nosocomial sinusitis) • Agents of chronic sinusitis: Obligate anaerobes, Staphylococcus aureus
  • 6. Pharyngitis (sore throat), and tonsillitis • Symptoms: • Pharynx and/or tonsils become inflamed, red, swollen, and show exudate, and sometimes a membrane is formed • Viruses: (most common cause) Influenza virus, Parainfluenza virus, Coxsackievirus A, Rhinovirus, Coronavirus, Epstein-Barr virus, Adenoviruses
  • 7. Pharyngitis (sore throat), and tonsillitis • Bacteria: Streptococcus pyogenes (most common bacterial cause), Streptococcus groups C and G, Arcanobacterium species, Corynebacterium diphtheriae and C. ulcerans, Mycoplasma pneumoniae • Vincent angina - Treponema vincentii & Leptotrichia buccalis • Fungal: Candida albicans
  • 8. Laryngitis • Symptoms: Hoarseness of voice, Lowering and deepening of voice • Mostly viral agents: Influenza virus, Parainfluenza virus, Rhinovirus, Adenovirus, Coronavirus, Human metapneumovirus • If membrane or exudate present: Streptococcus pyogenes, C. diphtheriae, Epstein-Barr virus
  • 9. Laryngotracheobronchitis (or croup) • Age—Children, <3 years age • Symptoms: - Inspiratory stridor, Hoarseness, Fever - Cough (harsh, barking non- productive ) • Agents: - Parainfluenza virus (most common) - Influenza virus - Respiratory syncytial virus - Adenoviruses
  • 10. Epiglottis • Edema and inflammation of epiglottis and soft tissue above vocal cords • Age: children 2–6 years • Symptoms: Fever, Difficulty in swallowing, Inspiratory stridor • Most common agent: Haemophilus influenzae type b
  • 11. Lower Respiratory Tract Infection • Pneumonia • Inflammation of lungs 1. Community acquired—patients acquire the organisms in the community 2. Hospital acquired— patients acquire the organisms in the hospital setting.
  • 12. Community-acquired Pneumonia (CAP) • Agents: Streptococcus pneumoniae followed by Mycoplasma pneumoniae • CURB65 scoring system - To predict prognosis of CAP • Score >1 patient should be hospitalized • Else the treatment can be given on outpatient basis
  • 13. Agents of Community-acquired Pneumonia (CAP) • No co-morbidity: • Streptococcus pneumoniae (most common) • Atypical pathogens: - Chlamydophila pneumoniae and C. psittaci - Legionella and Mycoplasma - Coxiella burnetii (Q fever) - Viral pneumonia (influenza, adenovirus, parainfluenza, RSV)
  • 14. Agents of Community-acquired Pneumonia (CAP) • Associated with Co-morbidity: • Alcoholism: S. pneumoniae, H. influenzae • COPD: H. influenzae, M. catarrhalis, S. pneumoniae • Post-CVA-aspiration: S. pneumoniae • Post-obstruction of bronchi: pneumoniae, anaerobes • Post-influenza: S. pneumoniae, S.aureus
  • 15. Community-acquired Pneumonia (CAP) • CURB-65score - C (Confusion) = 1 point - U (blood urea nitrogen >19 mg/dL) = 1 point - R (respiratory rate >30 min) = 1 point - B (BP <90/60) = 1 point - 65 (Age ≥65 years) = 1 point • Higher the score, greater is the mortality • If the score ≤1, outpatient therapy is indicated If the score >1, patient should be hospitalized
  • 16. Hospital-acquired Pneumonia (hAP) • Hospitalized patients have increased risk of developing pneumonia; most of which are ventilator-associated pneumonia • VAP can be clinically diagnosed by Clinical Pulmonary Infection (CPIS) • Likelihood of VAP is higher when total CPIS is >6
  • 17. Clinical Pulmonary Infection Score (CPIS) Parameter(s) Score 0 Temperature (°C) ≥36.5°C and ≤38.4°C Leukocytosis ≥4000 and ≤11,000 Tracheal aspirate None Oxygenation (PaO2/FiO2 mm Hg) >250 or ARDS Chest radiograph No opacity Progressive radiological progression No radiological progression Culture of tracheal aspirate Pathogenic bacteria Light or no growth
  • 18. Clinical Pulmonary Infection Score (CPIS) Score 1 Score 2 ≥38.5°C and ≤38.9°C ≥390C and ≤36.40C <4000 and >12000 Non-purulent Purulent ≤250 and no ARDS Diffuse (patchy) opacity Localized opacity Radiological progression Pathogenic bacteria Moderate or heavy growth Same morphology as Gram stain
  • 19. Hospital-acquired Pneumonia (hAP) • Bacterial agents: • Gram-negative bacilli (most common) – MDR non-fermenters (Pseudomonas and Acinetobacter) – MDR Enterobacteriaceae (E. coli, Klebsiella and Enterobacter) • Staphylococcus aureus (both MRSA and MSSA) • S. pneumoniae (rarely, in early stage) • Viral agents: • Influenza, adenovirus, parainfluenza, RSV
  • 20. Clinical Manifestations of Pneumonia • Fever, chills, chest pain and cough • Based on area of lungs involved, and type of cough produced • Lobar pneumonia infecting lung parenchyma (alveoli) • Consolidation and productive cough with purulent sputum - Mostly caused by pyogenic organisms : – Pneumococcus – Haemophilus influenzae – Staphylococcus aureus – Gram-negative bacilli.
  • 21. Interstitial or atypical pneumonia • Infection occurs in interstitial space of lungs • Cough is characteristically non-productive • Caused by : - Chlamydophila pneumoniae - Mycoplasma pneumoniae - Viral pneumonia - Legionella species
  • 22. Bronchitis • Inflammation of bronchus, which occurs either as an extension of upper respiratory tract infection such as influenza or may be caused directly by bacterial agents such as Bordetella. • Common symptoms - fever, cough, sputum production, and rarely croup- like features
  • 23. Bronchitis • Bacterial agents: - B. pertussis - B. parapertussis - Mycoplasma pneumoniae - Chlamydophila pneumoniae • Viral agents: - Influenza viruses - Adenoviruses - Rhinoviruses - Coronaviruses
  • 24. Bronchiolitis • Inflammation of the smaller airways (bronchioles) • It presents as an acute viral infection that primarily occurs in children less than 2 year • Symptoms: Acute onset of wheeze, dyspnea, cough, rhinorrhea, and respiratory distress • Respiratory syncytial viruses account for 40– 80%
  • 25. Bronchiolitis • Viral agents: • Respiratory syncytial viruses • Parainfluenza viruses • Rhinoviruses • Influenza viruses • Adenoviruses • Enterovirus • Human metapneumovirus
  • 26. Laboratory Diagnosis • Specimen Collection • For URTI: – Throat swab: Two swabs should be collected, one for direct examination, other one for culture – A part of the membrane, if present – Nasopharyngeal aspirate for viral diagnosis or for B.pertussis • For LRTI: Sputum, induced sputum, tracheal aspirate, bronchoalveolar lavage (BAL)
  • 27. Microscopy • Albert staining - metachromatic granules in the ends of the bacilli  of C. diphtheriae • Gram staining - Detect the quality of the sputum - Pus cells >25/low power field and epithelial cells <5/low power field  good quality sputum • Acid fast staining - M. tuberculosis • GMS stain - Pneumocystis jirovecii • Immunofluorescence microscopy of nasopharyngeal aspirate
  • 28. Culture • For bacteriological culture: Blood agar, chocolate agar and MacConkey agar • For isolation of C. diphtheriae: Loeffler’s serum slope and potassium tellurite agar • For M. tuberculosis: LJ medium and incubated for up to 6–8 weeks • For fungal pathogen isolation: Sabouraud dextrose agar • Viral - Appropriate cell lines
  • 29. Identification of agents of Lobar Pneumonia Agents of pneumonia Direct demonstration in sputum Culture identification Streptococcus pneumoniae Pus cells >25/LPF and epithelial cells <5/LPF gram- positive cocci in pair, lanceolate shaped Alfa hemolytic, draughtsman- shaped colonies on blood agar Sensitive to optochin Bile soluble, ferments inulin Haemophilus influenzae Pus cells >25/LPF and epithelial cells Satellitism on blood agar with S.
  • 30. Identification of agents of Lobar Pneumonia Agents of pneumonia Direct demonstration in sputum Culture identification Staphylococcus aureus Pus cells >25/LPF and epithelial cells <5/LPF gram- positive cocci in clusters BA- golden yellow hemolytic colonies Catalase positive, coagulase positive Gram-negative bacilli Pus cells >25/LPF and epithelial cells Identification is based on:
  • 31. Identification of agents of Interstitial Pneumonia Agents of pneumonia Direct demonstration in sputum Culture identification Chlamydop hila pneumonia e Direct immunofluorescence test Antigen detection by enzyme immunoassay Nucleic acid amplification test (NAAT) detecting specific genes Serology-antibody detection by - CFT using LPS antigen - ELISA using recombinant LPS antigen - Micro-IF test using outer membrane protein antigen Legionella pneumophi Pus cells >25/LPF and epithelial cells <5/LPF Growth on BCYE medium
  • 32. Identification of agents of Interstitial Pneumonia Agents of pneumoni a Direct demonstration in sputum Culture identification Mycoplas ma pneumoni ae Direct immunofluorescence test Capture ELISA-detecting antigen (P1 adhesin) PCR targeting P1 adhesin gene Culture-fried egg colonies on PPLO agar Antibody detection - Non-specific test (cold agglutination test) - Specific test (e.g. ELISA)
  • 33. Identification • Serology: • Detection of antibodies: • Mycoplasma: Cold agglutination test, complement fixation test (CFT) and ELISA formats are available • Chlamydial antibodies in serum: Micro-IF and CFT • Molecular Test
  • 34. TREATMENT • Community-acquired pneumonia (CAP) • Empiric regimen is determined by presence of co- morbidity and prediction of prognosis by CURB- 65 scoring system • CAP, hospitalized (if CURB65 score >1): - IV ceftriaxone plus azithromycin or - IV levofloxacin - Add vancomycin if CA-MRSA suspected
  • 35. • CAP, outpatient (if CURB-65 score ≤1): - If no comorbidity present: Oral azithromycin or azithromycin plus amoxyclav. - If comorbidity present: Oral levofloxacin • Hospital-acquired pneumonia (HAP) • Empirical therapy: comprises of both gram-negative (e.g. piperacillin-tazobactam or meropenem) plus gram-positive coverage (e.g. vancomycin). • Definitive therapy: The empirical treatment should be tailored based on the organism isolated and its
  • 37. MCQs • CURB65 score is used for: a) Ventilator-associated pneumonia b) Upper respiratory tract infections c) Community-associated pneumonia d) Tuberculosis • Clinical-pulmonary infection score (CPIS) is used for: a) Ventilator-associated pneumonia b) Upper respiratory tract infections c) Community-associated pneumonia d) Tuberculosis
  • 38. • Sputum specimen sent for culture is considered good quality if it contains: a. Pus cells <5/low power field and epithelial cells >25/low power field b. Pus cells >25/low power field and epithelial cells <5/low power field c. Pus cells >25/low power field and epithelial cells >25/low power field d. Pus cells <5/low power field and epithelial cells <5/low power field