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Therapeutic Agents

Community-Acquired Pneumonia (CAP) in Adults

Annual Impact in the US:

emergency room visits3

1.4M

cause of emergency care & hospitalization1
10
Top

Treatment Considerations

Diagnostic Considerations

Basic Principles

1.4M

Emergency depatment visits annually1

annual deaths2

41,000

cause of infectious mortality2

#1

Antibiotic Duration

Treatment Pathway

Hospitalizations5

740,000

References

Resources

Annually in US

Hospitalizations

740,000

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management practices for CAP across various healthcare settings

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41,000

Annually in US

Deaths

Community-Acquired Pneumonia (CAP) in Adults

Individualized Care

Basic Principles:

Antibiotics

Assess Risk Factors

Identify prior susceptibilities, recent antibiotic use, and comorbidities such as underlying lung disease. Patients who are immunocompromised should be approached differently.

Confirm Diagnosis

Review initial imaging and other diagnostic tests.

Aim to reduce bacterial overgrowth, minimizing disruption to the microbiome.

New Perspective

Pneumonia is comparable with a forest infestation— the overgrowth of pathogens in an active lung ecosystem.

Other Treatments

Focus on modulating the immune response (eg, sepsis management, immunomodulation with steroids, macrolides).

Antibiotics & Beyond

Manage complications like sepsis, respiratory failure, and secretions; add immunomodulation, oxygen/ventilation support, vasopressors, early mobilization, glucose control, and corticosteroids as needed.

Assess Clinical Response

Adaptive Care

Recovery & Prevention

Treatment should be tailored to the individual—what works for most may not work for your patient.

Review diagnostic testing and evaluate patient clinical stability to optimize treatment.

Establish clear follow-up plans, and address modifiable risk factors (eg, smoking, vaccinations, cardiac risks, substance abuse, functional status).

Clinical Stability

Allergy Evaluation

Use evidence-based validated risk strategies for evaluating penicillin allergy and cross-reactivity to other β-lactams.4

Community-Acquired Pneumonia (CAP) in Adults

Diagnostic Considerations:

Diagnosis

Microbiologic Testing

Fungi & Mycobacteria 2%

Bacteria + Viral Codetection 7%

Signs and symptoms of pneumonia

Rapid molecular tests +/- Culture-based confirmation

with chest imaging confirmation5

Pathogen Identification Is Difficult7

Bacteria 29%

Virus 62%

Dx Uncertainty

No Pathogen Detected 62%

Pathogen Identified 38%

1/3rd

of initial pneumonia diagnoses change by discharge6

References

Community-Acquired Pneumonia (CAP) in Adults

Antibiotic Treatment Considerations

Agent selection is impacted by a variety of clinical factors:

Allergies/Adverse Events

Comorbidities

Consider allergies to penicillin or β-lactams. Medication side effects profile.

Different pathogens are linked to specific conditions.Consider bronchiectasis, smoking, chronic obstructive lung disease, etc.

Local Epidemiology

Disease Severity

Antimicrobial resistance rates vary by location.
Ward vs ICU vs outpatient (10% to 20% of patients require ICU Care)

CURB-65

SCAP

PSI

Complications

Resistant Pathogens Assessment

Lung abscess, pleural effusion, cardiovascular events, stroke, or coinfections.
Use rapid diagnostic tests and patient microbiologic history to assess risk for resistant organisms.

Community-Acquired Pneumonia (CAP) in Adults

Empiric Treatment Pathway

β-lactam + macrolide

or

β-lactam

Respiratory fluoroquinolone

or

Nonsevere

Tetracycline

No Comorbidities

Add anti-MRSA if prior infection in past year or validated risk factors & positive PCR

or

Macrolide (if resistance <25%)

Add antipseudomonal if prior P. aeruginosa infection in the past year

Disposition

Outpatient

Inpatient

β-lactam + macrolide

β-lactam with β-lactamase inhibitor AND macrolide or tetracycline

or

Respiratory fluoroquinolone

or

Comorbidities

Severe

Respiratory fluoroquinolone

Add anti-MRSA if prior infection in past year or validated risk factors & positive PCR

Add antipseudomonal if prior P. aeruginosa infection in the past year

Community-Acquired Pneumonia (CAP) in Adults

Excessive Antibiotic Duration

Duration

2/3rds

Whether inpatient or outpatient, the duration of antibiotics should be driven by the patient’s comorbidities, clinical response, and stability.

of hospitalized patients receive excessive antibiotic duration5

Inpatient

3-5

Days

>5

Days

Antibiotics can be stopped in select patients who achieve clinical stability

Longer for patients with complications or risk factors for slow recovery

90%

occur after patients leave the hospital9

Risk Factors

Clinical Stability

Outpatient

3-5

Days

Ensure close communication and follow-up

Excess Antibiotic Duration

Related to higher antibiotic-associated adverse events and antibiotic resistance5

Short courses generally safe

References

References:
  1. Cairns C, Kang K. National Hospital Ambulatory Medical Care Survey: 2021 Emergency Department Summary Tables. Centers for Disease Control and Prevention, National Center for Health Statistics. 2021. https://ftp.cdc.gov/pub/Health_Statistics/NCHS/Dataset_Documentation/NHAMCS/doc21-ed-508.pdf
  2. Dequin PF, Meziani F, Quenot JP, et al. Hydrocortisone in severe community-acquired pneumonia. N Engl J Med. 2023;388(21):1931-1941. doi:10.1056/NEJMoa2215145
  3. Jain S, Self WH, Wunderink RG, et al. Community-acquired pneumonia requiring hospitalization among U.S. adults. N Engl J Med. 2015;373(5):415-427. Preprint. Posted online July 14, 2015. doi: 10.1056/NEJMoa1500245
  4. Jones BE, Chapman AB, Ying J, et al. Diagnostic discordance, uncertainty, and treatment ambiguity in community-acquired pneumonia : a national cohort study of 115 U.S. Veterans Affairs hospitals. Ann Intern Med. 2024;177(9):1179-1189. Preprint. Posted online August 6, 2024. doi:10.7326/M23-2505
  5. Metlay JP, Waterer GW, Long AC, et al. Diagnosis and treatment of adults with community-acquired pneumonia. An official clinical practice guideline of the American Thoracic Society and Infectious Diseases Society of America. Am J Respir Crit Care Med. 2019;200(7):e45-e67. doi:10.1164/rccm.201908-1581ST
  6. Mortality Data on CDC WONDER. Centers for Disease Control and Prevention, National Center for Health Statistics. 2018-2022. Accessed November 4, 2024. http://wonder.cdc.gov/ucd-icd10-expanded.html
  7. Vaughn VM, Flanders SA, Snyder A, et al. Excess antibiotic treatment duration and adverse events in patients hospitalized with pneumonia: a multihospital cohort study. Ann Intern Med. 2019;171(3):153-163. doi:10.7326/M18-3640
Inpatient

Severe

Diagnostic tests:

  • Viral tests according to clinical suspicion, local prevalence, and availability
  • Blood & respiratory cultures
  • Legionella urinary antigen & respiratory culture/nucleic acid assay
  • Strep urinary antigen
  • MRSA PCR if initiating anti-MRSA therapy or risk factors for MRSA
  • Chronic heart, lung, liver, or renal disease
  • Diabetes mellitus
  • Alcoholism
  • Malignancy
  • Asplenia

Clinical Stability

  • Resolution of vital sign abnormalities:
    • Heart rate
    • Respiratory rate
    • Blood pressure
    • Oxygen saturation
    • Temperature
  • Ability to eat
  • Normal mentation

*Utilized in combination with β-lactamic agents for hospitalized patients and as monotherapy if patients do not have comorbidities

Outpatient

No Comorbidities

Diagnostic tests: Viral tests according to clinical suspicion, local prevalence, and availability

Inpatient

Severe Risk Factors
  • Prior history of positive cultures for MRSA/pseudomonas
  • IV antibiotics
  • Less strongly recent hospitalization

Inpatient

Severe Risk Factors
  • Prior history of positive cultures for MRSA/pseudomonas
  • IV antibiotics
  • Less strongly recent hospitalization

Virus

  • Human rhinovirus
  • Influenza A or B
  • Human metapneumovirus
  • Respiratory syncytial virus
  • Parainfluenza virus
  • Coronavirus (**SARS-CoV-2)
  • Adenovirus

Clinical Stability

  • Resolution of vital sign abnormalities:
    • Heart rate
    • Respiratory rate
    • Blood pressure
    • Oxygen saturation
    • Temperature
  • Ability to eat
  • Normal mentation

Inpatient

Severe Risk Factors
  • Prior history of positive cultures for MRSA/pseudomonas
  • IV antibiotics
  • Less strongly recent hospitalization

*Used in combination for atypical coverage.

Inpatient

Severe Risk Factors
  • Prior history of positive cultures for MRSA/pseudomonas
  • IV antibiotics
  • Less strongly recent hospitalization
Outpatient

Comorbidities

  • Chronic heart, lung, liver, or renal disease
  • Diabetes mellitus
  • Alcoholism
  • Malignancy
  • Asplenia

Diagnostic tests: Viral tests according to clinical suspicion, local prevalence, and availability

Inpatient

Not Severe

Diagnostic tests:

  • Viral tests according to clinical suspicion, local prevalence, and availability
  • Blood & respiratory culture if risk of MRSA or P. aeruginosa
  • Legionella urinary antigen if local outbreak
  • MRSA PCR if initiating anti-MRSA therapy or risk factors for MRSA
  • Chronic heart, lung, liver, or renal disease
  • Diabetes mellitus
  • Alcoholism
  • Malignancy
  • Asplenia

Risk Factors

  • Pneumonia complications (e.g., empyema/parapneumonic effusion, abscess/necrotizing process, bacteremia, extrapulmonary infection)
  • Organism requiring longer duration (e.g., Staphylococcus aureus, Pseudomonas aeruginosa, suspected Legionella pneumophila or other intracellular microorganisms)
  • Radiographic findings (high burden of disease, necrotizing process, dense consolidations)
  • Underlying lung disease (e.g., bronchiectasis, post-obstructive pneumonia, chronic hypoxemia)
  • Barriers to self assessment, follow-up, or communication to ensure recovery
References:
  1. McDermott KW, Roemer M. Most Frequent Principal Diagnoses for Inpatient Stays in U.S. Hospitals, 2018. HCUP Statistical Brief #277. Agency for Healthcare Research and Quality. July 2021. https://www.hcup-us.ahrq.gov/reports/statbriefs/sb277-TopReasons-Hospital-Stays-2018.pdf
  2. Mortality Data on CDC WONDER. Centers for Disease Control and Prevention, National Center for Health Statistics. 2018-2022. Accessed November 4, 2024. http://wonder.cdc.gov/ucd-icd10-expanded.html
  3. Cairns C, Kang K. National Hospital Ambulatory Medical Care Survey: 2021 Emergency Department Summary Tables. Centers for Disease Control and Prevention, National Center for Health Statistics. 2021. https://ftp.cdc.gov/pub/Health_Statistics/NCHS/Dataset_Documentation/NHAMCS/doc21-ed-508.pdf
  4. Khan DA, Banerji A, Blumenthal KG, et al. Drug allergy: a 2022 practice parameter update. J Allergy Clin Immunol. 2022;150(6):1333-1393. doi: 10.1016/j.jaci.2022.08.028
  5. Metlay JP, Waterer GW, Long AC, et al. Diagnosis and treatment of adults with community-acquired pneumonia. An official clinical practice guideline of the American Thoracic Society and Infectious Diseases Society of America. Am J Respir Crit Care Med. 2019;200(7):e45-e67. doi:10.1164/rccm.201908-1581ST
  6. Jones BE, Chapman AB, Ying J, et al. Diagnostic discordance, uncertainty, and treatment ambiguity in community-acquired pneumonia : a national cohort study of 115 U.S. Veterans Affairs hospitals. Ann Intern Med. 2024;177(9):1179-1189. Preprint. Posted online August 6, 2024. doi:10.7326/M23-2505
  7. Jain S, Self WH, Wunderink RG, et al. Community-acquired pneumonia requiring hospitalization among U.S. adults. N Engl J Med. 2015;373(5):415-427. Preprint. Posted online July 14, 2015. doi: 10.1056/NEJMoa1500245
  8. Dequin PF, Meziani F, Quenot JP, et al. Hydrocortisone in severe community-acquired pneumonia. N Engl J Med. 2023;388(21):1931-1941. doi:10.1056/NEJMoa2215145
  9. Vaughn VM, Flanders SA, Snyder A, et al. Excess antibiotic treatment duration and adverse events in patients hospitalized with pneumonia: a multihospital cohort study. Ann Intern Med. 2019;171(3):153-163. doi:10.7326/M18-3640
References:
  1. Cairns C, Kang K. National Hospital Ambulatory Medical Care Survey: 2021 Emergency Department Summary Tables. Centers for Disease Control and Prevention, National Center for Health Statistics. 2021. https://ftp.cdc.gov/pub/Health_Statistics/NCHS/Dataset_Documentation/NHAMCS/doc21-ed-508.pdf
  2. Dequin PF, Meziani F, Quenot JP, et al. Hydrocortisone in severe community-acquired pneumonia. N Engl J Med. 2023;388(21):1931-1941. doi:10.1056/NEJMoa2215145
  3. Jain S, Self WH, Wunderink RG, et al. Community-acquired pneumonia requiring hospitalization among U.S. adults. N Engl J Med. 2015;373(5):415-427. Preprint. Posted online July 14, 2015. doi: 10.1056/NEJMoa1500245
  4. Jones BE, Chapman AB, Ying J, et al. Diagnostic discordance, uncertainty, and treatment ambiguity in community-acquired pneumonia : a national cohort study of 115 U.S. Veterans Affairs hospitals. Ann Intern Med. 2024;177(9):1179-1189. Preprint. Posted online August 6, 2024. doi:10.7326/M23-2505
  5. Metlay JP, Waterer GW, Long AC, et al. Diagnosis and treatment of adults with community-acquired pneumonia. An official clinical practice guideline of the American Thoracic Society and Infectious Diseases Society of America. Am J Respir Crit Care Med. 2019;200(7):e45-e67. doi:10.1164/rccm.201908-1581ST
  6. Mortality Data on CDC WONDER. Centers for Disease Control and Prevention, National Center for Health Statistics. 2018-2022. Accessed November 4, 2024. http://wonder.cdc.gov/ucd-icd10-expanded.html
  7. Vaughn VM, Flanders SA, Snyder A, et al. Excess antibiotic treatment duration and adverse events in patients hospitalized with pneumonia: a multihospital cohort study. Ann Intern Med. 2019;171(3):153-163. doi:10.7326/M18-3640

Bacteria

  • Streptococcus pneumoniae
  • Mycoplasma pneumoniae
  • Staphylococcus aureus
  • Legionella pneumophila
  • Enterobacteriaceae
  • Other

Inpatient

Severe Risk Factors
  • Prior history of positive cultures for MRSA/pseudomonas
  • IV antibiotics
  • Less strongly recent hospitalization