Pneumonia Flashcards

1
Q

What are the types of pneumonia based on how it is acquired?

A

CAP (community-acquired pneumonia): not recently hospitalized and without healthcare associated risk factors

Aspiration: from aspiration of GI content

HAP (hospital acquired pneumonia): acquired more than 48 hours after hospitalization

VAP (ventilator associated pneumonia): acquired more than 48-72 hours after endotracheal intubation

HCAP (healthcare associated pneumonia): if was hospitalized for more than 2 days in the last 90 days, lives in nursing home/long-term care, recent IV therapy or wound care in last 30 days, or on hemodialysis

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2
Q

What is the most common pathogen in CAP? Is it different in children?
(what are the possible pathogens)

A

Streptococcus pneumoniae is the most common cause of CAP, Mycoplasma pneumoniae is second

Moraxella catarrhalis is more common cause in young children and elderly
But VIRAL is the common cause of CAP in children (RSV, parainfluenza, influenza A)… while less common in adults (influenza A+B, adenovirus…and even less common rhinovirus, enterovirus, varicella zoster, herpes simplex)

  • H. influenzae colonization risk higher in COPD and cystic fibrosis patients
  • MRSA is associated with necrotizing and more severe forms of CAP
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3
Q

What are the risk factors for obtaining drug resistant S. pneumoniae (DRSP) CAP?

DRSP means strains resistant to 3+ drugs

A

S. pneumoniae is the most common cause

Risk factors: younger than 2 or older than 65, antibiotic therapy in last 3 months, alcoholism, medical comorbidities, immunosuppression

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4
Q

What are the risk factors that the patient might have CA-MRSA?

A

Cavitary pneumonia, lung necrosis, rapidly increasing lung effusion
Gross hemoptysis
Neutropenia, concurrent infection
Erythematous skin rash
Summer season, previously healthy, prior conjugate pneumococcal vaccination (rules out S. pneumo cause)

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5
Q

What are risk factors for aspiration and how might aspirations lead to pneumonia infections?

A

Aspiration risk factors: conditions that cause Dysphagia (stroke, seizure, alcoholism, aging), changed Oropharyngeal colonization (poor hygiene, meds, disease, tube feeding),
Reflux that allows gram-negative bacilli to colonize gastric content
Decreased host defense (impaired mucus or cilia function, decreased immunoglobulin, altered cough reflex)

Oral content has anaerobic variety (Bacteroides spp., Fusobacterium spp, Prevotella etc.)

Gastric content could be overrun by gram-negative bacilli and S. aureus

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6
Q

What is the 2nd most common nosocomial/hospital-acquired infection in the US?

A

HAP, more common with increasing age

Risk factors: intubation and mechanical ventilation, aspiration, oropharyngeal colonization, hyperglycemia (inhibits phagocytosis and feeds bacteria)

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7
Q

When is risk of VAP highest? What species cause the highest rate of death?

A

VAP highest risk in 1st FIVE days of intubation (decreases onward)

Highest mortality due to bacteremia from Pseudomonas and Acinetobacter (both need high coverage treatment, resistant), medical illness rather than surgical, ineffective antibiotic therapy

*Cause is rarely from anaerobes
Causes can be gram-negative aerobic (Ps. aeruginosa, E. coli, K. pneumonia, Acinetobacter sp.) or gram-positive (S.aureus/MRSA)

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8
Q

What are the signs and symptoms of pneumonia? As the patient is admitted, what vitals indicated poor prognosis?

A

Symptoms:
cough, SOB, dyspnea
constitutional (fever, fatigue, myalgia)
neuro (mental status change, confusion, lethargy, disorentation)

Signs: FEVER (sustained or intermittent)
Pulm. (cyanosis, using accessory muscles, diminished breath sounds, rales or rhonchi)

Vitals associated with poor prognosis: RR 30+, BP under 90/60, HR 125+, temp under 35C or over 40C

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9
Q

What diagnostic tests should be performed for suspected pneumonia? What might indicate severity/poor prognosis?

A

O2 sat (should be over 90%)
CBC (shows high or low WBC with neutrophilia)
Sputum gram stain (not done in outpatient setting)
Blood culture REQUIRED in all pneumonia-hospitalized patients (best to get two sets and before treatment)
Chest X-ray supportive of diagnosis if reveals infiltrates…
Can also consider PCR to detect pathogen DNA allowing for more rapid diagnosis/targeted therapy, or urinary antigens (DFA) for diagnosing Legionella pneumophila

*Poor prognosis based on X-ray findings of:
multilobar or rapid progression infiltrates, pleural effusion, necrotizating

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10
Q

How is pneumonia severity determined/classified and how does this impact how the patient receives care?

A

Using Pneumonia Severity Index (5 categories based on 30 day mortality)
or
CURB-65
1 point each given based on confusion, uremia (BUN above 7mmol/L), respiration (30+), blood pressure (below 90/60), age (above 65)

Predicts WHERE patient receives care:
PSI = I-II outpatient, III clinical judgement, IV inpatient, V ICU
or
CURB-65 = 2 points consider hospitalization, 3+ points consider ICU

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11
Q

How can a chest-xray indicate HAP/VAP along with clinical signs?

A

Chest-xray shows NEW infiltrate with at least TWO of the following:
Temp above 38C/100.4F
Leukocytosis or Leukopenia
Purulent secretion
Culture identifies pathogen (definitely should get blood culture, sputum culture should be obtained before Abx)

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12
Q

In general, how is initial treatment for pneumonia guided?

A

Initial treatment is EMPIRICAL…so based on history before cultures return
(guide by pneumonia type and severity, onset, specific risk factors and patient factors)
Keep in mind LOCAL resistance patterns

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13
Q

What are the empiric treatment guidelines for CAP (using IDSA guideline)?

A

Healthy Outpatient = Macrolide OR Doxycycline

Outpatient at risk for DRSP or for Inpatient non-ICU = Respiratory Fluoroquinalone OR Beta-Lactam and Macrolide

Inpatient ICU = Beta-lactam and Azithromycin OR Beta-lactam and Respiratory fluoroquinalone

  • Respiratory Fluoroquinalone i.e. Levofloxacin, Moxifloxacin, Gemifloxacin
  • Beta-lactam (inpatient) i.e. Ceftriaxone, Cefotaxime, Ampicillin/Sulbactam
  • For CA-MRSA can use Vancomycin or Linezolid
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14
Q

What are the empiric treatment guidelines for CAP (using JC/CMS guideline)?

A

Distinguishes Non-ICU from ICU patients

Options for Non-ICU = Beta-lactam and Macrolide… or Antipneumococcal Quinalone… or Beta-lactam and doxycycline, Tigecycline monotherapy, Macrolide monotherapy

Options for ICU = Macrolide with beta-lactam or specifically antipneumococcal/antipseudomal Beta-lactam… or Antipneumococcal quinalone, Antipseudomonal quinalone with Beta-lactam or specifically antipneumococcal/antipseudomonal Beta-lactam… or antipneumococcal/antipseudomonal Beta-lactam with aminoglycoside with either antipneumococcal Quinalone or Macrolide

  • Beta-lactam i.e. Ceftriaxone, Cefotaxime, Unasyn
  • Antipneumococcal/Antipseudomonal Beta-lactam i.e. Cefepime, Imipenem, Meropenem, Piperacillin/Tazobactam
  • Antipneumococcal Quinalone i.e. Ciprofloxacin or Levofloxacin
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15
Q

What is the general duration of therapy for pneumonia i.e. when can they be discharged for hospital?

A

Try to identify organism targeted therapy within 24-72 hours after admission

Therapy for 5-7 days, at minimum 5 days until no fever for 48-72 hours

Use oral meds when clinically stable

Discharge patient when vital signs and O2 status is stable and no comorbitidies are unresolved

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16
Q

What antibiotics are used to treat aspiration pneumonia?

A

Depends if the aspiration is from oral contents or oral and gastric contents:

Oral content: full coverage usually with PCN G, Ampicillin/Sulbactam, and Clindamycin

Oral and Gastric: Ampicillin/Sulbactam, Amoxicillin/Clavulanate, Piperacillin/Tazobactam

17
Q

What antibiotics are used to treat HAP and what are general concerns when considering treatment?

A

Treatment is dynamic, utilizes ICU, and broad spectrum antibiotics

Concerns are of prior antibiotic therapy and certain organisms (MRSA, Pseudomonas aeruginosa, Actinobacter spp., Stenotrophomonas maltophilia)

Early onset within 5 days most likely is S. pneumoniae, H. influenzae, MSSA, anaerobes and non-ESBL enteric gram-negative bacilli

So use 3rd generation Cephalosporin with Macrolide… or Respiratory Fluoroquinalone i.e. Moxifloxacin

18
Q

What are risk factors of a patient having MDR (multi-drug resistant pathogen)?

A

Having had antimicrobial therapy in the last 90 day, current hospitalization for 5+ days, high frequency antibiotic resistance in community/hospital

Having risk factors for HCAP: 2+ days hospitalized in last 90 days, living in nursing home/extended care, home infusion therapy, chronic dialysis in last 30 days, family member with MDR pathogen, with immunosuppressive disease/therapy

19
Q

What are the main pathogens of concern for MDR? What is the treatment for MDR?

A

Organisms: Pseudomonas aeruginosa, MRSA, Actinobacter spp., ESBL gram-negative bacilli
*ESBL = extended spectrum beta-lactamase producing

Treatment targets resistance:
Antipseudomonal Cephalosporin i.e. Cefepime or Ceftrazidime
or
Antispseudomonal Carbapenem i.e. Imipenem or Meropenem
or
Beta-/lactamase inhibitor i.e. Piperacillin/Tazobactam
or
Antipseudomonal Fluoroquinalone i.e. Ciprofloxacin or Levofloxacin
or
Aminioglycoside i.e. Amikacin, Gentamycin or Tobramycin… PLUS Aztreonam

AND
Vancomycin or Linezolid to be added for MRSA regimen

20
Q

What is the treatment for VAP (with no MDR risk)? How does treatment duration vary depending on the organism responsible?

A

For early onset VAP:
Choose (IV) either Cefotaxime, Ceftriaxone, Ampicillin/Sulbactam, Antipneumococcal Fluoroquinalone
PLUS
Vancomycin or Linezolid if high rates of MRSA expected
*Usual suspects: S. pneumoniae, H. influenzae, S. aureus, gram-negative Enterobacteriaceae

Treat for 14 days if (tends to be nastier/resistant): MSSA/MRSA, Pseudomonas aeruginosa, Actinobacter baumanii

Treat for 7 days if: S.pneumoniae or other Streptococcus, Staphylococcus epidermis, H.influenzae, E. coli, Enterobacter, Klebsiella spp., ESBL pathogens