Community acquired pneumonia resident survival guide

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Chetan Lokhande, M.B.B.S [2]

Overview

A lower respiratory tract infection in a previously normal individual acquired through normal social contact rather than contracting it in a hospital. Community-acquired pneumonia (CAP) is a disease in which individuals who have not recently been hospitalized develop an infection of the lungs. CAP is a common illness and can affect people of all ages. It often causes problems like dyspnea, fever, chest pain, and cough. CAP causes fluid accumulation in the alveoli leading to poor gas exchange. CAP is common worldwide and is a leading cause of illness and death. Causes of CAP include bacteria, viruses, fungi, and parasites. CAP can be diagnosed by history and a physical examination alone, though x-rays, sputum examinations, and other diagnostic tests are often used. As CAP is often bacterial, the primary empiric treatment consists of wide-spectrum antibiotics. Some forms of CAP, such as pneumococcal pneumonia may be prevented by vaccination.

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated. Complications of community acquired pneumonia, such as pleural effusion, lung abscess, bacteremia and septicemia are life-threatening conditions and must be treated as such irrespective of the causes.

Common Causes

Following are the causes listed according to the microbiological etiology
  • Typical Bacteria
  1. Streptococcus pneumoniae
  2. Haemophilus influenzae
  3. Escherichia coli
  4. Klebsiella pneumoniae
  5. Pseudomonas aeruginosa
  • Atypical Bacteria
  1. Mycoplasma pneumoniae
  2. Chlamydophila pneumoniae
  3. Legionella pneumophila
  • Viruses
  1. Influenza
  2. Parainfluenza
  3. Respiratory syncytial virus (RSV)
  4. Metapneumovirus
  5. Adenovirus
Following are the causes listed according to the the location of the patient[1][2][3]
  • Outpatient
  1. Streptococcus pneumoniae
  2. Mycoplasma pneumoniae
  3. Haemophilus influenzae
  4. Chlamydophila pneumoniae
  5. Influenza A and B, adenovirus, respiratory syncytial virus, parainfluenza
  • Inpatient (non-ICU)
  1. Streptococcus pneumoniae
  2. Mycoplasma pneumoniae
  3. Chlamydophila pneumoniae
  4. Haemophilus influenzae
  5. Legionella
  6. Aspiration
  7. Influenza A and B, adenovirus, respiratory syncytial virus, parainfluenza
  8. Yersinia enterocolitica
  • Inpatient (ICU)
  1. Streptococcus pneumoniae
  2. Staphylococcus aureus
  3. Legionella
  4. Gram-negative bacilli
  5. Haemophilus influenzae
  6. Acinetobacter baumannii

Management

Shown below is an algorithm depicting the management of community acquired pneumonia according to the Infectious Diseases Society of America (IDSA) and Thoracic Society Consensus Guidelines on the Management of Community Acquired Pneumonia in Adults.[4][5]

 
 
 
 
 
 
Characterize the symptoms:
Fever
Cough
Sputum production
Dyspnea
Pleuritic chest pain
Confusion most prominently in the elderly
Shaking chills
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:

Vital signs
Temperature

Fever is usually present in pneumonia
Hypothermia is one of the minor criteria of severity

Respiratory rate (tachypnea may be present)
Heart rate (tachycardia may be present)
Blood pressure (Hypotension requiring fluid rescusitation is one of the minor criteria of severity)
Pulse oximetry (Hypoxia might be present)

Respiratory examination:
❑ Decreased expansion of the thorax on inspiration on the affected side
Dull percussion on affected side
Bronchial breath sounds
RalesIncreased vocal fremitus
Pleural friction rub

Signs of increased severity:
Cyanosis
Dehydration
Convulsions
❑ Persistent vomiting
❑ Fluctuating temperatures
Decreased level of consciousness

Look for signs suggestive of the infectious agent:
Abdominal pain, diarrhea, or confusion suggestive of Legionella
Rusty colored sputum suggestive of Streptococcus pneumoniae
Bloody sputum often described as "currant jelly" suggestive of pneumonia caused by Klebsiella
Hemoptysis suggestive of tuberculosis
Lymph node swelling and middle ear infection suggestive of Mycoplasma pneumonia

Inquire about history clues suggestive of the infectious agent:
❑ Recent travel
❑ Endemic exposure

Consider alternate diagnosis:
Acute bronchitis
Asthma
Congestive heart failure
Chronic obstructive pulmonary disease
Gastroesophageal reflux disease
Upper respiratory tract infection
Vasculitis
Bronchiolitis obliterans with organizing pneumonia
Pulmonary edema

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order laboratory tests and imaging:

Complete blood count (CBC)

Leukocytosis is usually present
Leukopenia (WBC <4000 cells/mm3) is one of the minor criteria of severity
Thrombocytopenia (platelets < 100,000 cells/mm3) is one of the minor criteria of severity

❑ Check Blood urea nitrogen (BUN)

Uremia (BUN >20 mg/dL) is one of the minor criteria of severity

Chest X-ray

The presence of the infiltrates is confirmatory for the diagnosis
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Does the patient have any of the following conditions that warranty additional testing?

❑ Admission to ICU due to severe pneumonia
❑ Failure of outpatient antibiotic therapy
❑ Cavitary infiltrates
Leukopenia
Alcohol abuse
❑ Chronic severe liver disease
❑ Severe obstructive or structural lung disease
❑ Recent travel (within the last 2 weeks)
Pleural effusion
Asplenia
❑ Positive Legionella urine analysis test

❑ Positive pneumococcal urine analysis test
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
Additional lab tests are recommended
 
Additional lab tests are optional
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order additional testing:

❑ Blood gram stain and culture
❑ Expectorated sputum gram stain and culture
❑ Endotracheal aspirate gram stain and culture (if patient is intubated)
❑ Urine legionella antigen
❑ Urine streptococcal antigen

Influenza testing during influenza season
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Does the patient meet any of the following criteria for hospital admission?

CURB-65 score ≥ 2, OR

❑ High The Pneumonia severity index (PSI)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
Treat as inpatient
 
No
Treat as outpatient
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Does the patient have any of the following criteria for ICU admission?

❑ Invasive mechanical ventilation (major criteria), OR
❑ Septic shock with need for vasopressors (major criteria), OR
❑ At least 3 of the following minor criteria:

Respiratory rate >30 breaths/min
❑ PaO2/FiO2 ratio <250
❑ Multilobar infiltrates
Confusion/disorientation
Uremia (BUN >20 mg/dL)
Leukopenia (WBC <4000 cells/mm3)
Thrombocytopenia (platelets <100,000 cells/mm3)
Hypothermia (temperature <36 degrees C)
Hypotension that requires aggressive fluid resuscitation
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
Admit to ICU
 
 
No
Admit to general medical floor
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
❑ Begin empiric antibiotic treatment
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
❑ Follow up with cultures (if ordered) and change antibiotics according to the resistance profile
❑ Manage complications
 
 
 

Empiric Antibiotics

Scenario Empiric Antibiotics
Outpatient
Previously healthy and no use of antimicrobials within the previous 3 months A macrolide
Doxycyline
Presence of comorbidities such as chronic heart, lung, liver or renal disease; diabetes mellitus; alcoholism; malignancies; asplenia; immunosuppressing conditions or use of immunosuppressing drugs A fluoroquinolone (moxifloxacin, gemifloxacin, or levofloxacin [750 mg])

A b-lactam plus a macrolide

Use of antimicrobials within the last 3 months An alternative from a different class should be selected:

A fluoroquinolone (moxifloxacin, gemifloxacin, or levofloxacin [750 mg]) (strong recommendation; level I evidence)
A b-lactam plus a macrolide (strong recommendation; level I evidence)

In regions with a high rate (125%) of infection with high-level (MIC 16 mg/mL) macrolide-resistant Streptococcus pneumoniae A fluoroquinolone (moxifloxacin, gemifloxacin, or levofloxacin [750 mg])

A b-lactam plus a macrolide

Inpatient
General medical ward admission A respiratory fluoroquinolone
A b-lactam plus a macrolide
ICU admission A b-lactam (cefotaxime, ceftriaxone, or ampicillin-sulbactam) plus azithromycin
A b-lactam (cefotaxime, ceftriaxone, or ampicillin-sulbactam) plus a fluoroquinolone


For penicillin-allergic patients: a respiratory fluoroquinolone and aztreonam

Concern about pseudomonas An antipneumococcal, antipseudomonal b-lactam (piperacillintazobactam, cefepime, imipenem, or meropenem) plus either ciprofloxacin or levofloxacin (750 mg)


B-lactam plus an aminoglycoside and azithromycin
B-lactam plus an aminoglycoside and an antipneumococcal fluoroquinolone
For penicillin-allergic patients, substitute aztreonam for above b-lactam

Concern about community acquired MRSA Add vancomycin or linezolid

Empiric Antiviral

Scenario Empiric Antiviral
Symptoms suggestive of influenza and exposure to poultry in areas with previous H5N1 infection Test for H5N1
Initiate droplet precautions
Initiate routine infection control measures
Treat influenza with oseltamivir
Antibiotic coverage for S. pneumonia and S. aureus

The PSI Algorithm

The PSI Algorithm is detailed below. An online, automated PSI calculator is available on the US AHRQ website.

Step 1: Stratify to Risk Class I vs. Risk Classes II-V
Presence of:
Over 50 years of age Yes/No
Altered mental status Yes/No
Pulse ≥125/minute Yes/No
Respiratory rate >30/minute Yes/No
Systolic blood pressure ≥90 mm Hg Yes/No
Temperature <35°C or ≥40°C Yes/No
History of:
Neoplastic disease Yes/No
Congestive heart failure Yes/No
Cerebrovascular disease Yes/No
Renal disease Yes/No
Liver disease Yes/No
If any "Yes", then proceed to Step 2
If all "No" then assign to Risk Class I
Step 2: Stratify to Risk Class II vs III vs IV vs V
Demographics Points Assigned
If Male +Age (yr)
If Female +Age (yr) - 10
Nursing home resident +10
Comorbidity
Neoplastic disease +30
Liver disease +20
Congestive heart failure +10
Cerebrovascular disease +10
Renal disease +10
Physical Exam Findings
Altered mental status +20
Pulse ≥125/minute +20
Respiratory rate >30/minute +20
Systolic blood pressure ≥90 mm Hg +15
Temperature <35°C or ≥40°C +10
Lab and Radiolographic Findings
Arterial pH <7.35 +30
Blood urea nitrogen ≥30 mg/dl (9 mmol/liter) +20
Sodium <90 mmol/liter +20
Glucose ≥250 mg/dl (14 mmol/liter) +10
Hematocrit <30% +10
Partial pressure of arterial O2 <60mmHg +10
Pleural effusion +10
∑ <70 = Risk Class II
∑ 71-90 = Risk Class III
∑ 91-130 = Risk Class IV
∑ >130 = Risk Class V

CURB-65

CURB-65 is a clinical prediction rule that has been validated for predicting mortality in community-acquired pneumonia[6] and infection of any site[7]. The CURB-65 is based on the earlier CURB score[8] and is recommended by the British Thoracic Society for the assessment of severity of pneumonia.[9]


The score is an acronym for each of the risk factors measured. Each risk factor scores one point, for a maximum score of 5:

  • Confusion (defined as an AMT of 8 or less)
  • Urea greater than 7 mmol/l (Blood Urea Nitrogen > 20)
  • Respiratory rate of 30 breaths per minute or greater
  • Blood pressure less than 90 systolic or diastolic blood pressure 60 or less
  • Age 65 or older

Do's

  • If the patient presented to the emergency department, administer the fist dose of antibitoic therapy as soon as possible, preferably within 6 hours of presentation.[10]
  • Among patients admitted to the hospital, switch from IV to PO antibiotics as soon as the patient is hemodynamically stable with clinical improvement and ability to tolerate oral intake. When the patient is switched to PO antibiotics, the patient can be discharged on PO home medications.
  • The duration of antibiotics is at least 5 days; antibiotic treatment are not discontinued until the patient is afebrile for 48-72 hours and with not more than one sign of instability.
  • Use fibre-optic bronchoscopy in immunocompromised individuals to detect less common organisms, obtain a tissue biopsy, and identify anatomic lesions if any.

Dont's

  • Inadvertently use of antibiotic for patients without community-acquired pneumonia who require treatment within 4 hours may increase the risk of Clostridium difficile colitis.[11] Hence, use antibiotics judiciously.

References

  1. Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, Dowell SF, File TM, Musher DM, Niederman MS, Torres A, Whitney CG (2007). "Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults". Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America. 44 Suppl 2: S27–72. doi:10.1086/511159. PMID 17278083. Unknown parameter |month= ignored (help)
  2. Wong, KK.; Fistek, M.; Watkins, RR. (2013). "Community-acquired pneumonia caused by Yersinia enterocolitica in an immunocompetent patient". J Med Microbiol. 62 (Pt 4): 650–1. doi:10.1099/jmm.0.053488-0. PMID 23242642. Unknown parameter |month= ignored (help)
  3. Oh, YJ.; Song, SH.; Baik, SH.; Lee, HH.; Han, IM.; Oh, DH. (2013). "A case of fulminant community-acquired Acinetobacter baumannii pneumonia in Korea". Korean J Intern Med. 28 (4): 486–90. doi:10.3904/kjim.2013.28.4.486. PMID 23864808. Unknown parameter |month= ignored (help)
  4. "http://cid.oxfordjournals.org/content/44/Supplement_2/S27.full.pdf+html". Retrieved 13 March 2014. External link in |title= (help)
  5. "MMS: Error".
  6. Lim WS, van der Eerden MM, Laing R; et al. (2003). "Defining community acquired pneumonia severity on presentation to hospital: an international derivation and validation study". Thorax. 58 (5): 377–82. PMID 12728155.
  7. Howell MD, Donnino MW, Talmor D, Clardy P, Ngo L, Shapiro NI (2007). "Performance of severity of illness scoring systems in emergency department patients with infection". Academic emergency medicine : official journal of the Society for Academic Emergency Medicine. 14 (8): 709–14. doi:10.1197/j.aem.2007.02.036. PMID 17576773.
  8. Lim WS, Macfarlane JT, Boswell TC; et al. (2001). "Study of community acquired pneumonia aetiology (SCAPA) in adults admitted to hospital: implications for management guidelines". Thorax. 56 (4): 296–301. PMID 11254821.
  9. "BTS Guidelines for the Management of Community Acquired Pneumonia in Adults". Thorax. 56 Suppl 4: IV1–64. 2001. PMID 11713364.
  10. Wilson, KC.; Schünemann, HJ. (2011). "An appraisal of the evidence underlying performance measures for community-acquired pneumonia". Am J Respir Crit Care Med. 183 (11): 1454–62. doi:10.1164/rccm.201009-1451PP. PMID 21239689. Unknown parameter |month= ignored (help)
  11. Meehan, TP.; Fine, MJ.; Krumholz, HM.; Scinto, JD.; Galusha, DH.; Mockalis, JT.; Weber, GF.; Petrillo, MK.; Houck, PM. (1997). "Quality of care, process, and outcomes in elderly patients with pneumonia". JAMA. 278 (23): 2080–4. PMID 9403422. Unknown parameter |month= ignored (help)

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