Community-Acquired Pneumonia. Lisa G. Winston, MD University of California, San Francisco San Francisco General Hospital. Nothing to disclose.

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Community-Acquired Pneumonia Lisa G. Winston, MD University of California, San Francisco San Francisco General Hospital Nothing to disclose.

Community-Acquired Pneumonia Talk will focus on adults Guideline for healthy infants and children available: www.idsociety.org (Clin Infect Dis 2011;53:617-30) Community-Acquired Pneumonia - Outline Epidemiology Diagnosis Microbiology Risk stratification Treatment Prevention

Community Acquired Pneumonia (CAP): definition At least 2 new symptoms Fever or hypothermia Cough Rigors and/or diaphoresis Chest pain Sputum production or color change Dyspnea New infiltrate on chest x-ray and/or abnormal chest exam No hospitalization or other nursing facility prior to symptom onset CAP: Symptom Frequency Cough 90% Dyspnea 66% Sputum 66% Pleuritic chest pain 50% But, only 4% of all visits for cough turn out to be pneumonia. Halm EA, Teirstein AS. N Engl J Med 2002;347(25):2039.

Epidemiology: Acute Lower Respiratory Tract Infections In U.S., influenza and pneumonia 8 th most common cause of death per the Centers for Disease Control and Prevention (moved up from 9 th in 2010) Ø Most common cause of death from infectious disease Among those 85 and older, at least 1 in 20 hospitalized each year 1. Diseases of heart 2. Malignant neoplasms 3. Chronic lower respiratory diseases 4. Cerebrovascular diseases 5. Accidents (unintentional injuries) 6. Alzheimer s disease 7. Diabetes mellitus 8. Influenza and pneumonia Epidemiology: Acute Lower Respiratory Tract Infections Inpatient mortality rate: may be influenced by coding Ø From 2003 2009, mortality rate for principal diagnosis pneumonia decreased from 5.8% to 4.2% Ø More patients coded with principal diagnosis sepsis or respiratory failure and secondary diagnosis pneumonia v Using all codes, little change in mortality rate Lindenauer et al, JAMA 2012;307:1405-13 Outpatient mortality < 1%; about 80% of CAP treated in outpatient setting More common in winter months

Health Disparities Some data regarding disparities with socioeconomic status and race/ethnicity Study of 4870 adults with community acquired bacteremic pneumonia in 9 states 2003 2004 Annual incidence 24.2 episodes per 100,000 Black adults vs. 10.1 episodes per 100,000 White adults Black residents in most impoverished areas with 4.4 times the incidence of White residents in least impoverished areas Burton et al. AJPH 2010;100(10):1904-11 Host Defenses Mechanical factors Ø Nasal hair Ø Turbinates Ø Mucocilliary apparatus Ø Cough Ø Airway branching Antimicrobial factors Ø IgA (and IgG, IgM) Ø Complement Ø Alveolar lining fluid Ø Cytokines (TNF, IL-1, IL-8, others) Ø Macrophages Ø PMNs Ø Lymphocytes

Diagnosis Chest radiograph needed in all cases? Ø Avoid over-treatment with antibiotics Ø Differentiate from other conditions Ø Specific etiology, e.g. tuberculosis Ø Co-existing conditions, such as lung mass or pleural effusion Ø Evaluate severity, e.g. multilobar Unfortunately, chest physical exam not sensitive or specific and significant variation between observers Arch Intern Med 1999;159:1082-7 Microbiological Investigation Sputum Gram stain and culture Ø Remains somewhat controversial Ø 30-40% patients cannot produce adequate sample Ø Most helpful if single organism in large numbers Ø Usually unnecessary in outpatients Ø Culture (if adequate specimen < 10 squamous cells/ LPF; > 25 PMNs/LPF): antibiotic sensitivities Ø Limited utility after antibiotics for most common organisms

Microbiological Investigation - Inpatients Blood cultures x 2 before antibiotics Ø Blood cultures positive in 5 14% of hospitalized patients Ø Severe disease most important predictor Consider evaluation for Legionella Ø Urinary antigen test for L. pneumophila serogroup 1 (70%) Ø Culture with selective media Pneumococcal urinary antigen test Ø Simple, takes apx. 15 minutes Ø In adults, sensitivity 50-80%, specificity ~90% but specificity poor in children, possibly due to carriage IDSA/ATS Guidelines for CAP in Adults; CID 2007:44(Suppl 2)

Microbiological Investigation - Inpatients Other studies as clinically indicated, e.g. influenza M. pneumoniae serologic studies can be considered but are uncommon in routine practice (mostly IgM-specific assays) Serologic studies of Chlamydophila largely for epidemiology Ø For C. pneumoniae, IgM is available, titer > 1:16 considered positive Bronchoscopy perhaps for fulminant course, unresponsive to conventional therapy, or for specific pathogens (e.g. Pneumocystis) Biomarkers - procalcitonin Other diagnostics? Ø Procalcitonin is produced in response to endotoxin and endogenous mediators released in the setting of bacterial infections Ø Rises in bacterial infections much more than, e.g., viral infections or inflammatory states Ø Rises and falls quickly Unfortunately, probably not sensitive / specific enough to rule out / rule in bacterial CAP in individual cases in most settings Ø May help limit duration of antibiotic exposure BMC Medicine 2011;9:107

Etiology Clinical syndrome and CXR not reliably predictive Ø Streptococcus pneumoniae 20-60% Ø Haemophilus influenzae 3-10% Ø Mycoplasma pneumoniae up to 10% Ø Chlamydophila pneumoniae up to 10% Ø Legionella up to 10% Ø Enteric Gram negative rods up to 10% Ø Staphylococcus aureus up to 10% Ø Viruses up to 10% Ø No etiologic agent 20-70% Typical vs. Atypical Typical Ø Visible on Gram stain, grows in routine culture Ø Susceptible to beta lactams Ø S. pneumoniae, H. influenzae Atypical Ø Not visible on Gram stain, special culture techniques Ø Not treated with beta lactams Ø M. pneumoniae, C. pneumoniae, Legionella X X

S. pneumoniae 2/3 of CAP cases where etiology known 2/3 lethal pneumonia 2/3 bacteremic pneumonia Ø Apx. 20% of cases with pneumococcal pneumonia are bacteremic (variable) Risk factors include Extremes of age Alcoholism COPD and/or smoking Nursing home residence Influenza Injection drug use Airway obstruction *HIV infection S. pneumoniae drug resistance Clinical and Laboratory Standards Institute (CLSI) minimum inhibitory standards for penicillin in µg/ml Sensitive Intermediate Resistant Parenteral (penicillin G) Non-meningitis Parenteral (penicillin G) 2 = 4 > 8 0.06 0.12 Meningitis Oral (penicillin V) 0.06 0.12-1 > 2

S. pneumoniae drug resistance ~ 25-35% penicillin non-susceptible by old standard nationwide, but most < 2 µg/ml Using the new breakpoints for patients without meningitis, 93% would be considered susceptible to IV penicillin Other beta-lactams are more active than pencillin, especially Ø Ceftriaxone, cefotaxime, cefepime, amoxicillin, amoxicillin-clavulanate MMWR, 2008;57(50)1353-1355

S. pneumoniae drug resistance Other drug resistance more common with increasing penicillin minimum inhibitory concentration (MIC) Ø Macrolides and doxycycline more reliable for PCN susceptible pneumococcus, less for penicillin nonsusceptible Trimethoprim-sulfamethoxazole not reliable Fluoroquinolones most S. pneumoniae are susceptible Ø Clinical failures have been reported No resistance with vancomycin, linezolid Legionella Geographic differences in rates Perhaps suggested by high fever, hyponatremia, markedly elevated LDH, CNS abnormalities, severe disease Severe disease: fluoroquinolone or azithromycin likely drug of choice; usual rx 14-21 days Risk factors: Age Smoking Immune compromise, cell mediated Travel Renal disease Liver disease Diabetes Malignancy

Haemophilus influenzae Increased risk with smoking and COPD Beta-lactamase production ~30% Ø With beta-lactamase production, resistant to ampicillin and amoxicillin Active oral antibiotics include amoxicillinclavulanate, fluoroquinolones, azithromycin, clarithromycin, doxycycline Mycoplasma pnuemoniae Common cause respiratory infections in children/ young adults Ø Pneumonia relatively uncommon Epidemics in close quarters May have sore throat, nausea, vomiting, hemolytic anemia, rash Treatment with doxycycline, macrolide, or fluoroquinolone Pediatr Infect Dis J 2012;31:409-11 Ø Rising rate of macrolide resistance U.S. 8.2%; China 90%

Risk Stratification Cost differential in CAP: Colice et al, Chest 2004 Inpatient: $10,227 / case Outpatient: $466 / case Who can be safely managed as an outpatient??? Risk Stratification Outpatient vs. inpatient? Ø Pneumonia Patient Outcomes Research Team (PORT) study (Fine et al, NEJM 1997;336:243-250) v Prediction rule to identify low risk patients with CAP v Stratify into one of 5 classes Class I: age < 50, none of 5 co-morbid conditions, apx. normal VS, normal mental status Class II-V: assigned via a point system

Risk Stratification Mortality < 1% for classes I, II Low risk patients hospitalized more than necessary Caveats: Ø Does not take into account social factors Pneumonia Severity Index Calculator http://www.mdcalc.com/psi-port-score -pneumonia-severity-index-adult-cap/ Age and sex; resident of nursing home {yes/no} Comorbid diseases {yes/no}: renal disease, liver disease, CHF, cerebrovascular disease, neoplasia Physical exam {yes/no}: altered mental status, SBP < 90, temp < 35 or >=40, RR>=30, HR>=125 Labs/studies {yes/no}: ph<7.35, PO2<60 or Sat<90, Na<130, HCT<30, gluc>250, BUN>30, pleural eff

Hypothetical Patient #1 60 year-old man with diabetes presents with fever and dyspnea. Positive PORT items include HR=130, Na=129, glucose=300. Should this patient be hospitalized? Please vote: 1. Yes 2. No Pneumonia Severity Index Results Class: IV Score: 100 Risk Class Score Mortality Low I < 51 0.1% Low II 51-70 0.6% Low III 71-90 0.9% Medium IV 90-130 9.5% High V > 130 26.7% Hospitalization is recommended for class IV and V. Class III should be based on clinical judgment.

Hospitalization for other patients 55 year-old woman with no other risk factors? Hospitalization? Please vote: 1. Yes 2. No Class : II Score : 45 Mortality : 0.1% Hospitalization for other patients 92 year-old man with no other risk factors? Hospitalization? Please vote: 1. Yes 2. No Class : IV Score : 92 Mortality : 9.5%

Hospitalization for other patients 20 year-old woman with SBP < 90 and a pleural effusion? Hospitalization? Please vote: 1. Yes 2. No Class : II Score : 40 Mortality : 0.6% Other Scoring Systems CURB-65 (British Thoracic Society) Ø Has only 5 variables, compared with 20 for Pneumonia Severity Index Severe Community Acquired Pneumonia (SCAP) Ø Has 8 variables SMART-COP Ø Used for predicting need for mechanical ventilation or vasopressors

Guidelines, guidelines, guidelines. Previously, at least 4 major sets: Ø American Thoracic Society (ATS) Ø Infectious Diseases Society of America (IDSA) Ø Canadian Infectious Diseases Society and Canadian Thoracic Society Ø British Thoracic Society Clinical Infectious Diseases; March 1, 2007 Supplement 2

Do guidelines improve outcomes? Maybe results vary Studies generally not randomized Trend toward decreased length of hospital stay Possible decrease in mortality Is coverage of atypical organisms important? In Europe, amoxicillin commonly used as a single drug with data supporting a short course (3 days in responding patients) el Moussaoui et al, BMJ 2006;332:1355-62 One review shows no benefit of empirical atypical coverage on survival or clinical efficacy in hospitalized patients Shefet et al, Arch Intern Med 2005;165:1992-2000

JAMA 2014;311(21):2199-2208 V.A. retrospective, cohort study of patients 65 and older hospitalized with pneumonia 2002-2012 31,863 patients treated with azithromycin compared with 31,863 propensity matched patients with no exposure 90 day mortality significantly lower 17.4% vs. 22.3%, O.R. 0.73 Myocardial infarct significantly higher 5.1% vs. 4.4%, O.R. 1.17 Empirical Treatment: IDSA/ATS Consensus Guidelines Outpatient treatment Previously healthy, no antibiotics in 3 months Ø Macrolide (1 st choice) or Ø Doxycycline Co-morbid conditions or antibiotics within 3 months (select a different class) Ø Respiratory fluoroquinolone: moxifloxacin, gemifloxacin, or levofloxacin (750 mg) Ø Beta-lactam (especially high dose amoxicillin) plus a macrolide (1 st choice) or doxycycline

Empirical Treatment: IDSA/ATS Consensus Guidelines Inpatient treatment, non-icu Respiratory fluoroquinolone or Beta-lactam (cefotaxime, ceftriaxone, ampicillin; consider ertapenem) plus a macrolide (1 st choice) or doxycycline Empirical Treatment: IDSA/ATS Consensus Guidelines Inpatient treatment, ICU Beta-lactam (cefotaxime, ceftriaxone, or ampicillin-sulbactam) plus Azithromycin or a respiratory fluoroquinolone Ø For penicillin allergy: respiratory fluoroquinolone + aztreonam

Empirical Treatment: IDSA/ATS Consensus Guidelines For suspected Pseudomonas aeruginosa: Antipneumococcal, antipseudomonal beta-lactam (piperacillin-tazobactam, cefepime, imipenem, or meropenem) plus either ciprofloxacin or levofloxacin (750 mg) Or The above beta-lactam plus an aminoglycoside and either azithromycin or a respiratory fluoroquinolone Ø For penicillin allergy: substitute aztreonam for the betalactam Suspect with structural lung disease (e.g. bronchietasis), frequent steroid use, prior antibiotic therapy Empirical Treatment: IDSA/ATS Consensus Guidelines Inpatient therapy, concern for community methicillin-resistant Staphylococcus aureus (MRSA): Ø Add vancomycin or linezolid to regimen you would select otherwise *Strongly consider for patients admitted to the ICU Gram strain of respiratory specimen (sputum or tracheal aspirate) can be helpful

What about steroids? Lancet 2015: http://dx.doi.org/10.1016/s0140-6736(14)62447-8 Randomized, double blind trial in Switzerland 785 adult inpatients received 50 mg prednisone daily x 7 days or placebo Primary outcome clinical stability: 3.0 days prednisone vs. 4.4 days placebo, p<.0001 Time to hospital discharge 6 days prednisone vs. 7 days placebo, p=.01 No difference complications except slightly higher in-hospital hyperglycemia with prednisone Questions re study 2911 patients assessed to randomize 802 Why was length of stay so long? Ø 4% prednisone and 6% placebo admitted to ICU Ø Death from any cause 4% prednisone and 3% placebo Last follow up 30 days post discharge Ø Telephone interview

Treatment Empirical therapy is usually required, at least initially Timing of antibiotics Ø Better outcomes if given within 8 hrs of admission?; 4 hrs even better? Meehan et al, JAMA, 1997;278:2080-4 Houck et al, Arch Intern Med, 2004;164:637-44 Ø Centers for Medicare & Medicaid Services (CMS): core measure of 6-hours; now retired Ø Very controversial: delays mostly with atypical presentations; antibiotic overuse Joint Commission and CMS Performance Measures 2013 2014: PN-3a and PN-3b are retired - reporting optional

Length of Therapy 7 10 days has been standard for most patients but may not be necessary Ø Shorter course with azithromycin or high dose levofloxacin Ø Meta-analysis that patients with mild to moderate disease can be treated with 7 days or less Li et al. Am J Med. 2007;120(9):783-90 Switch to Oral Therapy Reduces costs, shortens length of stay, may reduce complications As soon as improving clinically, able to take POs, GI tract functioning Ø Usually within 3 days; no need to observe in hospital Narrow spectrum agent if organism identified (usually S. pneumoniae) Empirical therapy: macrolide, doxycycline, antipneumococcal fluoroquinolone, or combination therapy

Prevention There are steps patients and providers can take. Influenza vaccine Prevention Pneumococcal vaccines

Prevention Smoking, with or without COPD, is a significant risk factor Do gastric acid-suppressive drugs, especially proton pump inhibitors, increase risk for CAP? Ø Risk may only be associated with drugs that are recently started, not with long-term use; may not be causal Sarkar et al, Ann Intern Med, 2008;149(6):391-98 Ø Association seen in some studies may be due to confounding Filion et al, Gut, 2014;63(4):552-8 We love doxycycline Adult inpatients June 2005 December 2010 Compared those who received ceftriaxone + doxycycline to those who received ceftriaxone alone 2734 hospitalizations: 1668 no doxy, 1066 with doxy Outcome: CDI within 30 days of doxycycline receipt CDI incidence 8.11 / 10,000 patient days in those receiving ceftriaxone alone; 1.67 / 10,000 patient days in those who received ceftriaxone and doxycycline Doernberg et al, Clin Infect Dis 2012;55:615-20