Pneumonia and Pleural effusions Flashcards

1
Q

Pneumonia:

A

Inflammation of the lungs with consolidation or interstitial lung infiltrates
Most often categorized according to the causative organism

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2
Q

6th leading cause of death in US:

A

pneumonia

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3
Q

most common S/S of PNA:

A
Cough
Fever
Pleuritic chest pain
Dyspnea
Sputum production 
Rales/crackles on lung exam
Increased tactile fremitus if consolidation
Decreased tactile fremitus if effusion

Causative organisms bacterial, viral, fungal

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4
Q

Bacterial PNA:

A

-mucopurulent sputum

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5
Q

Viral or atypical organism PNA:

A

scant or watery sputum

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6
Q

PNA most common diagnostic tools:

A

-often have leukocytosis with left shift
-History and clinical Exam
CXR
Pulse oximetry
Routine lab testing – CBC, BMP, LFTs
Sputum gram stain and culture
Blood culture
ABG (arterial blood gas)
Thoracentesis if pleural effusion present

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7
Q

Most basic PNA workups:

A

Clinical exam
CXR
(Pulse oximetry)

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8
Q

PNA workup:

A

Patient stable, looks toxic, fever, dyspnea:
Start empiric antibiotic treatment
Obtain labs
Blood culture
Obtain a sputum sample, stain and culture
May add an ABG (hospital setting)
Thoracentesis if effusion found on CXR, ideally in an inpatient setting

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9
Q

Tx of PNA

A
  • bacterial: antibiotics
  • Viral: supportive/anti-virals
  • Fungal: anti-fungals
  • Pleural effusion: thoracentesis
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10
Q

types of PNA

A
Community acquired pneumonia
Hospital acquired pneumonia
Ventilator associated
Aspiration pneumonia
Mycoplasma/atypical
Fungal
PCP
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11
Q

CAP definition:

A

an acute infection of the pulmonary parenchyma in a patient who has acquired the infection in the community, as distinguished from hospital-acquired (nosocomial) pneumonia.

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12
Q

most common cause of CAP:

A

Streptococcus pneumoniae is the most common cause of community-acquired bacterial pneumonia worldwide

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13
Q

CAP general info:

A

The overall rate of community-acquired pneumonia (CAP) in adults is approximately 5.16 to 6.11 cases per 1000 persons per year; the rate of CAP increases with increasing age
There is seasonal variation, with more cases occurring during the winter months
The rates of pneumonia:
Men>Women
African American > Caucasians

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14
Q

Determining whether to tx at home or admit use what score:

A

CURB-65

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15
Q

typical bacterial CAP pathogens:

A

Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis
3 pathogens account for approximately 85% of CAP cases.

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16
Q

antibiotic choice of CAP:

A

Outpatient typically treated for 7-10 days of oral antibiotics with close follow up Culture results?

Most patients with CAP who are admitted to the hospital are treated with intravenous medications initially and then complete a 12-day oral course of therapy for a total of 14 days of combined intravenous and oral therapy.

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17
Q

when to use Pneumovax:

A

Two types of pneumococcal vaccine one that covers 23 serotypes and a new one covering an additional 13 serotypes
All patients ≥65 years: ACIP recommends routine vaccination with both PPSV23 (23-valent pneumococcal polysaccharide vaccine) and PCV13 (13-valent pneumococcal conjugate vaccine)
For those whom an additional dose of PPSV23 is indicated, this subsequent PPSV23 dose should be given 6-12 months after PCV13 and ≥5 yr after the most recent dose of PPSV23

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18
Q

HAP

A

Hospital-acquired (or nosocomial) pneumonia (HAP) is pneumonia that occurs 48 hours or more after admission and did not appear to be incubating at the time of admission.

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19
Q

VAP

A

Ventilator-associated pneumonia (VAP) is a type of HAP that develops more than 48 to 72 hours after endotracheal intubation.

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20
Q

HCAP

A

Healthcare-associated pneumonia (HCAP) is defined as pneumonia that occurs in a non-hospitalized patient with extensive healthcare contact, as defined by one or more of the following:

  • Intravenous therapy, wound care, or intravenous chemotherapy within the prior 30 days
  • Residence in a nursing home or other long-term care facility
  • Hospitalization in an acute care hospital for two or more days within the prior 90 days
  • Attendance at a hospital or hemodialysis clinic within the prior 30 days
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21
Q

QUESTION: Why is it so important to do a good history and find out if a patient has one of these types of pneumonias versus community acquired pneumonia?

A

Multi-drug resistance!!!
For example, the definition of multidrug resistance in gram-negative bacilli, which are an important cause of HAP, VAP, and HCAP, is variably defined as resistance to at least two, three, four, or eight of the antibiotics typically used to treat infections with these organisms
Extensively drug-resistant (XDR) gram-negative bacilli are defined by resistance to all commonly used systemic antibiotics except colistin, tigecycline, and aminoglycosides.
Awareness of local resistance patterns is critical for decisions regarding empiric therapy for HAP, VAP, and HCAP.

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22
Q

HAP epidemiology:

A

Most cases that are diagnosed within 5 days of admission are due to sensitive bacteria, unless the patient was exposed to antibiotics within the last 90 days.

Patients with HAP diagnosed after 5 days typically have pneumonia due to a resistant bacteria.

The crude mortality for HAP may be as high as 30% to 70%, but many patients die of their underlying disease rather than HAP itself.

Attributable mortality is about 10%. (due to PNA bug itself)

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23
Q

HAP is caused most by what?

A

Bacteria cause most cases of HAP and ventilator-associated pneumonia (VAP)
Most are due to aerobic gram-negative bacilli such as Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, and Acinetobacter species
In addition to methicillin-sensitive Staphylococcus aureus (MSSA), both hospital-acquired and community-acquired strains of MRSA are causing an increasing number of HAP cases.

24
Q

most common aerobic gram - bacilli that causes HAP:

A

Psuedomonas aeruginosa

25
Q

HAP Dx testing:

A
Culture the bug!!!!
CXR
CT
Blood culture
CBC, Chem, LFTs
Bronchoalveolar lavage
26
Q

Early onset HAP, VAP, HCAP Tx:

A
Early onset (< 5d since admission) and no MDR risk factors:
Ceftriaxone 2 g IV or IM q24h or
Levofloxacin 750 mg IV or PO q24h or
Ampicillin-sulbactam 3 g IV or IM q6h or
Ertapenem 1 g IV or IM q24h
Duration of therapy: 8d
27
Q

Late onset HAP, VAP, HCAP Tx:

A
Late onset (≥ 5d since admission), MDR risk factors present, or diagnosis of HCAP:
Cefepime 2 g IV q8h or
Ceftazidime 2 g IV q8h or
Imipenem-cilastatin 500 mg IV q6h or 1 g IV q8h or
Meropenem 1 g IV q8h or
Piperacillin-tazobactam 4.5 g IV q8hPLUS
Vancomycin 15 mg/kg IV q12h[5, 6] or
Linezolid 600 mg IV q12h[5] PLUS
Ciprofloxacin 400 mg IV q8h or
Levofloxacin 750 mg IV q24h
28
Q

Duration of HAP, VAP, HCAP tx therapy:

A

If clinical improvement is noted in 48-72h and cultures are negative, consider stopping antibiotics

If clinical improvement is noted in 48-72h and cultures are positive, adjust regimen per susceptibilities and continue antibiotics for 7-8d

If there is no clinical improvement and cultures are negative, look for alternative diagnoses

If there is no clinical improvement and cultures are positive, adjust regimen per susceptibilities

29
Q

Highlights of aspiration PNA

A

Pneumonia caused by the aspiration of oropharygneal or gastric contents

Diagnosis is based on clinical signs or symptoms of pneumonia in a person with a history or risk factors for aspiration.

Sputum or tracheal Gram stain reveals mixed flora.

Infection usually involves the dependent lung lobe.

Complications of disease include lung abscess and empyema.

Very common in hospitalized patients, patients on a vent, patient with swallowing disorders/post-stroke or some other neurological condition

30
Q

Epidemiology of aspiration PNA:

A

Aspiration can occur regardless of sex, age group, or ethnicity

True incidence of aspiration pneumonia is difficult to assess because many cases of community-acquired pneumonia (CAP) or hospital-acquired pneumonia are likely the result of aspiration that was undiagnosed

Some studies suggest that aspiration pneumonia may be the cause of as many as 5% to 15% of CAP cases

It occurs most commonly in older hospitalized or nursing-home patients

It is the most common cause of death among patients with swallowing dysfunction related to neurologic disease

31
Q

Aspiration PNA presentation and workup:

A

History and PE, history is KEY!!!
Poor dentition, advanced age, swallowing dysfunction, and presence of a feeding tube
Symptoms include cough, dyspnea, and pleuritic chest pain, but may be nonspecific and be present for a week or more after the event
Signs such as fever, rales, tachypnea, and frothy or purulent sputum should raise the suspicion for aspiration pneumonia.
At minimum, CXR, SPO2, CBC
Consider sputum culture/gram stain, not usually blood culture since usually clear and being treated before advances to bacteremia; ABG in hospital

32
Q

Aspiration PNA Tx:

A

Empiric treatment requires coverage for anaerobic organisms
Treatment always tailored to culture and sensitivities if available/useful
Otherwise, empirical antibiotics started as soon as aspiration PNA is diagnosed
In the presence of infection, antibiotics should be continued for at least 7 to 10 days in a patient who responds promptly and for a minimum of 2 weeks if highly resistant pathogens such as Pseudomonas aeruginosa are isolated
Antibiotic choices are slightly different based on where/who you are treating

33
Q

CA aspiration PNA:

A

clindamycin : 300 mg orally every 6 hour; or 600 mg intravenously every 8 hours
levofloxacin : 750 mg orally or intravenously once daily
moxifloxacin : 400 mg orally or intravenously once daily
piperacillin/tazobactam : 3.375 g intravenously every 6 hours ampicillin/sulbactam : 1-2 g intravenously every 6 hours imipenem/cilastatin : 250-500 mg intravenously every 6 hours

34
Q

HA or “toxic” aspiration PNA Tx:

A

cefepime : 1-2 g intravenously every 12 hours or
ampicillin/sulbactam : 1-2 g intravenously every 6 hours or
piperacillin/tazobactam : 4.5 g intravenously every 6 hours
OR
imipenem/cilastatin : consult specialist for guidance on dose or
meropenem : consult specialist for guidance on dose
– AND –
tobramycin : consult specialist for guidance on dose or
gentamicin : consult specialist for guidance on dose
– AND –
linezolid : 600 mg intravenously every 12 hours or
vancomycin : 15 mg/kg intravenously every 12 hours initially, adjust based on vancomycin levels

35
Q

Atypical/ mycoplasma pan is mostly caused by:

A

Mycoplasma pneumoniae, Chlamydophila pneumoniae, or Legionella pneumophila.

36
Q

Atypical PNA highlights:

A

Community-acquired and often seen in young adults living in close proximity.
Atypical bacterial pneumonia is most commonly caused by Mycoplasma pneumoniae, Chlamydophila pneumoniae, or Legionella pneumophila.
Usually presents with a low-grade fever, persistent dry cough, and constitutional symptoms, for example, malaise.
Treatment is often outpatient based with a macrolide or doxycycline.
Extrapulmonary manifestations may occur, especially in Mycoplasma pneumoniae infections.

37
Q

Why is Atypical PNA atypical?

A

Atypical bacterial pneumonia is caused by atypical organisms that are not detectable on Gram stain and cannot be cultured using standard methods.

The most common organisms are Mycoplasma pneumoniae, Chlamydophila pneumoniae, and Legionella pneumophila.

Atypical bacterial pneumonia generally is characterized by a symptom complex that includes headache, low-grade fever, cough and malaise.

Constitutional symptoms often predominate over respiratory findings smouldering illness

38
Q

Smoldering illness:

A

exists in a suppressed or concealed state (S/Sx) not as prominent compared to typical PNA

39
Q

atypical PNA epi:

A

Mycoplasma pneumoniae causes up to 15% of cases of community-acquired pneumonia

Infection is common in children and young adults, and is often seen in close community settings such as boarding schools, colleges and military bases

Legionella pneumophila is responsible for a low percentage of community-acquired pneumonia cases, but it is responsible for up to 16% of cases that require hospitalization.

40
Q

atypical prevention /workup:

A

History and PE
normal WBC
Dry cough, that has lasted for a while/not resolving, constitutional symptoms like headache, malaise, with or without overt respiratory symptoms, age <50
A vesicular rash may accompany Mycoplasma
Diarrhea may accompany Legionella infection
CXR, labs like CBC, CMP, sputum culture, usually not toxic appearing enough to warrant a blood culture
The CXR usually confirms infiltrates and may show more extensive abnormalities than PE suggests
A low oxygen saturation indicates a more severe course of disease requiring hospitalization.

41
Q

atypical Tx:

A

Treatment:

Usually treatment is based on clinical diagnosis alone

Atypical bacterial pneumonia pathogens generally do not respond to beta-lactam antibiotics and require treatment with a macrolide, tetracycline, or fluoroquinolone

First-line choices:
Macrolide azithromycin 500 mg orally once daily on the first day, followed by 250 mg once daily for 4 days OR clarithromycin 500 mg orally (immediate-release) twice daily for 14-21 days
Doxycycline100 mg orally twice daily for 14 days

42
Q

common fungi that cause fungal pna

A

Histoplasma capsulatum, Blastomyces dermatitidis, Coccidioides immitis.

43
Q

typical fungal pna s/s

A

Flu like sx’s: Fever, occasional chills, myalgia, cough, dyspnea, chest pain.

44
Q

fungal pna highlights:

A

Uncommon in immunocompetent patients.
Concern in neutropenic patients, organ recipients, chronic steroid use, or other immunocompromised states.
Fungal pneumonia common pathogens include Histoplasma capsulatum, Blastomyces dermatitidis, Coccidioides immitis.
Certain fungi are endemic to certain geographic regions of North America and found in soils contaminated bird/bat droppings, caves, decayed buildings (spores inhaled).
Causes typical respiratory infection symptoms and signs, note it can also spread hematogenously and become disseminated.
Diagnosis is suspected based on clinical and epidemiologic characteristics and confirmed by CXR, culture or specific serum antigen testing.
Treatment is antifungals.
Consultation with Infectious Disease is highly recommended.

45
Q

PCP pneumonia highlights::

A

The organism was known formerly as Pneumocystis carinii (pneumonia, thus PCP), this what defines this infection

Still the most common AIDS-defining opportunistic infection, usually happens with CD4 counts < 200 cells/ul

Suspicion for Pneumocystis pneumonia (PCP) is based on clinical signs or symptoms of pneumonia in a person with immune suppression, especially when due to HIV infection

Diagnosis is made by detection of the organism in either induced sputum or bronchoalveolar lavage (BAL)

The treatment of choice is trimethoprim/sulfamethoxazole (TMP/SMX).

46
Q

PCP pneumonia epi:

A

Pneumocystis pneumonia (PCP) is the most common AIDS-defining illness in the US in children, adolescents, and adults

In HIV-positive adults, the greatest risk factor for developing PCP is a CD4 cell count of <200 cells/microliter, with risk increasing the lower the CD4 cell count falls below this level

In HIV-negative patients, the overall incidence of PCP is low and occurs almost exclusively in patients who have other causes of immunocompromise

47
Q

PCP etiology/pathophys:

A

Pneumocystis pneumonia (PCP) is caused by the fungal organism Pneumocystis jirovecii
Infection in the lung starts with the multiplication of the organism in the alveoli
As infection progresses, alveoli fill with exudates, there is type 2 pneumocyte hyperplasia, and mononuclear cells infiltrate the lung
Desquamation of the alveolar lining cells creates increased permeability of the alveolar capillary membrane and noncardiogenic pulmonary edema.

48
Q

PCP PNA presentation/workup

A

History and PE, history is KEY!!!

Clinicians should suspect PCP when caring for adult or adolescent patients who are HIV-positive

Especially if they are non-adherent with highly active antiretroviral therapy (HAART) or PCP prophylaxis, have had a previous episode of PCP, and/or have a CD4 cell count of <200 cells/microliter.

If NOT HIV positive/AIDs, then have they undergone: bone marrow transplant, solid-organ transplant, a hematologic malignancy or are they under chronic use of corticosteroids ± other immunosuppressive drugs?

In HIV-positive PCP, presentation is often an insidious progression of fatigue, fevers, chills, sweats, nonproductive cough, and dyspnea over several weeks atypical presentation

49
Q

PCP PNA presentation/workup cont:

A

In HIV-negative patients, the presentation is typically more rapid and more severe.

The findings on physical examination are often nonspecific and include the usual fever, tachypnea, and tachycardia

But sometimes pulmonary examination is often normal but occasionally demonstrates mild crackles on auscultation

Other symptoms may include weight loss & oral candidiasis

CXR, LDH (elevated in 90% of HIV patient with active PCP), induced sputum and arterial blood gas (graded as mild or severe depending on results)

Consider bronchoalveolar lavage to get a high quality sputum sample, PFTs and CT of the chest depending on length of course and severity of presentation

50
Q

PCP tx:

A

When PCP is suspected, treatment should be initiated immediately even prior to specific diagnosis

Treatment duration for PCP is 21 days in HIV-positive patients, 14 to 21 days in all other patients

Mild-to-moderate PCP (defined as having both a room air pO2 70 mmHg or greater and an A-a gradient of 35 mmHg or less)
-Trimethoprim/sulfamethoxazole (TMP/SMX), given either intravenously or orally 15-20 mg/kg/day.

Moderate-to-severe PCP (defined by either a room air pO2 <70 mmHg or an A-a gradient of >35 mmHg)
-Admitted to hospital for intravenous TMP/SMX 15-20 mg/kg/day IV) combined with a corticosteroid (prednisone or methylprednisone)
Prophylaxis trimethoprim/sulfamethoxazole : 80/400 mg to 160/800 mg orally once daily

51
Q

Pleural effusions:

A

Accumulation of fluid in pleural cavity between lung and thoracic wall
Etiology (Types):
Transudate
Exudate
Empyema- infection
Hemorrhagic/Hemothorax -blood (trauma)
Neoplastic
Chylous- disruption of thoracic duct

52
Q

most common pleural effusion:

A

Transudative: (Most common)
Caused by increase in pulmonary venous pressure or hypoproteinemia
Clear, yellow/straw colored

Etiologies:
CHF
Cirrhosis
Nephrotic Syndrome

53
Q

Exudative pleural effusion:

A
Caused by inflammation
Higher concentration of protein
Deep color, turbid 
Etiologies: 
Infection: Empyema, TB, Parapneumonic
Neoplastic: Lung CA, Metastatic disease
Trauma: Hemothorax, Chylothorax
54
Q

pleural effusion presentation/ workup

A
Common Symptoms: dyspnea, pleuritic chest pain, dry cough; +/- Fever/Chills
Common Signs: Diminished breath sounds, dullness to percussion, decreased tactile fremitus
Diagnostic Tests: 
Basic Labs (CBC, BMP)
CXR
CT Scan
Thoracentesis
U/S guided vs Bedside
Pleural Fluid Analysis
Cell Count/Cytology
Protein, LDH, Glucose
Gram stain, Fungi, AFB
Cholesterol, Triglycerides
55
Q

pleural effusion tx:

A

Ultimately Goal is treat the underlying cause
Thoracentesis
Pleurodesis (Chronic Effusions)
Serial CXR