Level 2 of 6Must-remember
Community-acquired pneumonia: severity assessment and antibiotics
Assess, manage and stay safe — enough on its own
The card — assess, manage, caution
Assessment— look, ask, measure
- Pneumonia is a clinical and radiographic diagnosis: a compatible history — cough, sputum, fever, dyspnoea — together with a new infiltrate on chest radiography; a febrile cough with a clear film is bronchitis, and an infiltrate without a compatible syndrome is something else. Obtain a film in every patient with suspected pneumonia.
- History to ask for: onset and tempo, fever, chills, rigors or sweats, cough (evolving from non-productive to purulent, sometimes blood-tinged), pleuritic stabbing pain, dyspnoea, fatigue, headache, myalgia and arthralgia — and remember up to 20% have gastrointestinal symptoms (nausea, vomiting or diarrhoea) and may be mistaken for gastroenteritis.
- Ask what antibiotics the patient has had in the last three months — use of a specific antibiotic within the previous three months is the single most important risk factor for resistant pneumococcal infection.
- Ask the exposure history: alcohol excess, COPD or smoking, bronchiectasis or structural lung disease, dementia or stroke or reduced consciousness, hotel or cruise ship within 2 weeks (*Legionella*), local influenza activity, exposure to birds, sheep, goats or parturient cats, travel to South-East Asia, and progressive dyspnoea with oral candidiasis and weight loss (*Pneumocystis* with underlying HIV).
- Gross haemoptysis suggests necrotising pneumonia — think community-associated MRSA.
- Examine for consolidation and fluid: tachypnoea and accessory muscle use; increased tactile fremitus over consolidation, decreased over fluid; a percussion note dull over consolidation and flat or stony dull over an effusion; crackles, bronchial breath sounds and a possible pleural friction rub.
- The sensitivity and specificity of physical examination for pneumonia are only 58% and 67% — a normal-sounding chest excludes nothing.
- Red flags marking severe disease whatever the patient's outward composure: new confusion; respiratory rate at least 30/min; systolic blood pressure at or below 90 mmHg; SpO₂ below 92% on room air; hypothermia; frank haemoptysis; multilobar shadowing; rising lactate; exhaustion. Physiological reserve masks severity in the young — a 25-year-old with a respiratory rate of 34 and multilobar consolidation who is still holding a conversation has severe pneumonia.
- Score CURB-65 to answer "does this patient need a hospital bed?" — one point each for new Confusion (disorientation in person, place or time); Urea above 7 mmol/L (approximately 42 mg/dL, or blood urea nitrogen at least 20 mg/dL); Respiratory rate at least 30/min; Blood pressure systolic at or below 90 or diastolic at or below 60 mmHg; and age 65 years or over.Not available at your setup — Renal function (creatinine/urea).
- Read the CURB-65 score for mortality and disposal: 0 = 0.7% (outpatient); 1 = 3.2% (usually outpatient); 2 = 13.0% (short stay or very close observation); 3 = 17.0% (admit, consider critical care); 4 = 41.5% and 5 = 57.0% (admit and refer for critical care).
- Two findings override any score and mandate admission: room-air SpO₂ below 92%, and inability to maintain oral intake — and admit also if adherence is doubtful because of cognitive impairment or living circumstances.
- Use the IDSA/ATS criteria — not CURB-65 or the PSI — to answer "does this patient need critical care?" Either major criterion (respiratory failure requiring invasive mechanical ventilation, or septic shock requiring vasopressors) mandates critical care; so do any three of the nine minor criteria (respiratory rate at least 30/min; PaO₂/FiO₂ ratio 250 or less; multilobar infiltrates; confusion; blood urea nitrogen at least 20 mg/dL or urea at least approximately 7 mmol/L; white cell count below 4000 cells/µL; platelets below 100,000 cells/µL; core temperature below 36 °C; hypotension requiring aggressive fluid resuscitation).Not available at your setup — Arterial blood gas.
- Measure room-air pulse oximetry in every patient, and take an arterial blood gas where SpO₂ is below 94% on air, respiratory rate is at least 30, or there is confusion, hypotension or chronic lung disease — recording the inspired oxygen concentration and time alongside the result, or the gas is uninterpretable.Not available at your setup — Arterial blood gas.
- In the elderly the presentation is the one most often missed: new or worsening confusion, a fall, or decompensation of a chronic illness, with no fever, no cough and no crackles — a high index of suspicion is essential because delayed treatment leads to rapid evolution of infection with increased severity, morbidity and death.
- In children, count the respiratory rate for a full minute in a quiet child: fast breathing is at least 60/min under 2 months, at least 50/min at 2–11 months, at least 40/min at 1–5 years and at least 30/min over 5 years; children present with fast breathing, chest indrawing, grunting, nasal flaring and feeding difficulty rather than the adult syndrome, and in a young infant it is apnoea, not cough, that kills.
- Severe paediatric pneumonia is lower chest wall indrawing, grunting, head nodding, nasal flaring, central cyanosis, SpO₂ below 90%, inability to drink or feed, persistent vomiting, convulsions, lethargy, apnoea, and a heart rate that falls as the child tires.
Management— do this, in order
- Give appropriate empirical antibiotics as expeditiously as possible — mortality in hospitalised CAP correlates closely with their timely administration, and no test should delay the first dose: not a biomarker, not a sputum sample, not a radiograph.
- Titrate oxygen to SpO₂ 94–98%, or 88–92% in known or suspected chronic type 2 respiratory failure; in children there is no hypoxic-drive concern, so target 94–98% and never restrict oxygen in a hypoxic child.
- Outpatient, no comorbidity and no resistance risk: amoxicillin 1 g orally three times daily plus a macrolide (azithromycin 500 mg on day 1 then 250 mg daily for 4 days, or clarithromycin 500 mg twice daily) or doxycycline 100 mg orally twice daily; or doxycycline monotherapy; or macrolide monotherapy only where local pneumococcal macrolide resistance is under 25%.
- Outpatient with comorbidity (chronic heart, lung, liver or kidney disease, diabetes, alcohol excess, malignancy, asplenia) or resistance risk: amoxicillin–clavulanate 500/125 mg three times daily or 875/125 mg twice daily, or an oral cephalosporin (cefpodoxime 200 mg twice daily, cefuroxime 500 mg twice daily), plus a macrolide or doxycycline; or a respiratory fluoroquinolone alone (levofloxacin 750 mg daily, moxifloxacin 400 mg daily, gemifloxacin 320 mg daily).
- Inpatient, non-severe, no risk factors: a β-lactam (ampicillin–sulbactam 1.5–3 g IV 6-hourly; ceftriaxone 1–2 g IV daily; cefotaxime 1–2 g IV 8-hourly; ceftaroline 600 mg IV 12-hourly; ertapenem 1 g IV daily) plus a macrolide (azithromycin 500 mg IV or orally daily, or clarithromycin 500 mg IV or orally twice daily), or a respiratory fluoroquinolone alone (levofloxacin 750 mg or moxifloxacin 400 mg IV or orally daily); if both are contraindicated, a β-lactam plus doxycycline 100 mg twice daily.Doctor / Nurse
- Inpatient, severe: a β-lactam alone is not adequate therapy — give a β-lactam (ceftriaxone 2 g IV daily in severe disease) plus a macrolide, or a β-lactam plus a respiratory fluoroquinolone, with observational data favouring the macrolide.Doctor / Nurse
- Add MRSA cover — vancomycin 15 mg/kg IV 12-hourly adjusted to renal function and serum levels, or linezolid 600 mg IV or orally 12-hourly — where MRSA has previously been isolated from the respiratory tract within the past year, or in severe disease with recent hospitalisation and antibiotics.Doctor / Nurse
- Add *Pseudomonas* cover — piperacillin–tazobactam 4.5 g IV 6-hourly, cefepime 2 g IV 8-hourly, ceftazidime 2 g IV 8-hourly, meropenem 1 g IV 8-hourly, imipenem 500 mg IV 6-hourly, or aztreonam 2 g IV 8-hourly in penicillin allergy — where *P. aeruginosa* has previously been isolated from the respiratory tract within the past year.Doctor / Nurse
- Supportive care: adequate hydration is a therapeutic measure, not comfort care, because dehydration suppresses sputum production; give balanced crystalloid to restore perfusion in shock, reassessing after each bolus, with vasopressors for fluid-unresponsive shock; and give thromboprophylaxis unless contraindicated.Doctor / Nurse
- Paracetamol 1 g orally or intravenously 6-hourly (maximum 4 g in 24 hours) matters more than it appears, because a patient splinting against pleuritic pain cannot cough or breathe deeply and will collapse a lower lobe.
- Paediatric antibiotics — weigh every child, never estimate: amoxicillin 45–90 mg/kg/day orally in doses 8 hours apart for non-severe pneumonia; ampicillin 200 mg/kg/day IV in doses 6 hours apart as first-line intravenous therapy in a previously well child; cefotaxime 75–225 mg/kg/day IV in doses 8 hours apart, or ceftriaxone 50–75 mg/kg/day IV 12–24 hourly, for severe illness or where resistance is a concern; benzylpenicillin 250,000–400,000 units/kg/day IV in divided doses 4–6 hours apart as an alternative first-line for pneumococcal disease.Doctor / Nurse
- More paediatric therapy: add vancomycin per local paediatric protocol in the critically ill child, including multilobar pneumonia with hypoxia or hypotension; use clindamycin or vancomycin as first-line alternatives in severe β-lactam hypersensitivity; and give erythromycin 50 mg/kg/day orally in four divided doses for 2 weeks for infant pneumonia due to *Chlamydia trachomatis*.Doctor / Nurse
- Treat for a minimum of 5 days and until clinical stability is achieved, switching to oral therapy when the patient can ingest and absorb the drug, is haemodynamically stable and is improving; hospital-acquired and ventilator-associated pneumonia are treated for 7 days, and anaerobic lung abscess requires a minimum of 3 weeks.
- Proven influenza warrants oseltamivir 75 mg orally or by nasogastric tube twice daily for 5 days in addition to antibacterials, with vigilance for MRSA superinfection.
- Sample a significant effusion in a septic patient for pH, glucose, protein, lactate dehydrogenase, Gram stain, culture, cytology and acid-fast bacilli — drainage is required if pH is below 7.2, glucose below 2.2 mmol/L or LDH above 1000 U/L, if bacteria are seen or cultured, or if the fluid is frank pus.DoctorNot available at your setup — Chest drain / tube thoracostomy.
- Offer an HIV test to every patient with pneumonia, since pneumonia is a common initial presenting illness in previously undiagnosed HIV infection.
- Reassess formally at about day 3, or sooner if deteriorating, working through five possibilities: is this pneumonia at all; is there a sequestered focus the antibiotic cannot reach (lung abscess or empyema); is the pathogen resistant or unexpected; is the drug, dose or frequency wrong and was it actually given; and is there a nosocomial superinfection.
Caution— what harms
- Daptomycin must never be used for pneumonia of any kind — pulmonary surfactant inactivates it. This is a classic, lethal error extrapolated from MRSA bacteraemia.
- Never withhold the first antibiotic dose pending a biomarker, a sputum sample or a radiograph: procalcitonin is insufficiently accurate for diagnosing bacterial CAP, and an initial procalcitonin must not be grounds for withholding initial antibiotic treatment; CRP is even less sensitive.
- A β-lactam alone is not adequate therapy for severe CAP — β-lactam plus macrolide, or a fluoroquinolone alone in non-severe disease, gives lower mortality than β-lactam monotherapy.
- Carbapenems should not be the sole primary agent for *P. aeruginosa* pneumonia because resistance emerges during therapy; and guidelines recommend against continuing combination therapy once susceptibility is known.
- Do not use macrolide monotherapy empirically where local pneumococcal macrolide resistance exceeds 25% — resistance exceeds 25% in several countries (about 40% in the United States) and is often high-level.
- Neither CURB-65 nor the Pneumonia Severity Index is accurate for the intensive care decision — use the IDSA/ATS severe-CAP criteria, and remember that mortality was higher among less ill patients admitted to a general ward who subsequently deteriorated than among equally ill patients monitored in intensive care from the outset.
- Do not be reassured by a score of 0 or 1 if room-air SpO₂ is below 92%, oral intake cannot be maintained, or adherence is doubtful; conversely, if the score is generated entirely by age 65 or over in an otherwise well patient, admission may not be needed.
- Leucopenia in pneumonia marks overwhelming infection, not mild disease — a white cell count below 4000 cells/µL is a minor severity criterion.
- Do not repeat the film daily or change antibiotics because the shadow persists on day 3: radiographic abnormalities take 4–12 weeks to clear, and the film clears far more slowly than the patient.
- Do not miss the effusion — look for it on every film, deliberately. It complicates over 40% (up to 50%) of CAP, about 15% become secondarily infected, and unrecognised empyema is the commonest reason an apparent treatment failure is not one; suspect it when pleural fluid is accompanied by fever and a leucocytosis, even low-grade, after 4–5 days of appropriate antibiotic treatment.
- Avoid corticosteroids in influenza pneumonia, where they may be associated with higher mortality.
- A positive viral PCR does not establish causation — PCR detects respiratory viruses in 20–30% of healthy adults and the same proportion of pneumonia patients; and if a virus is identified with no apparent bacterial pathogen, antibacterials may be stopped except in severe illness, where bacterial–viral co-infection must be assumed.
- Do not accept a sputum sample that is saliva: it is suitable only if there are more than 25 neutrophils and fewer than 10 squamous epithelial cells per low-power field.
- Pneumonia is a setting in which non-invasive ventilation frequently fails, and a failed trial that delays intubation is dangerous.Not available at your setup — Mechanical ventilator.
Refer / escalate
Admit anyone with a CURB-65 of 2 or more, or with room-air SpO₂ below 92% or inability to maintain oral intake whatever the score, and refer immediately for critical care where either IDSA/ATS major criterion is present (invasive mechanical ventilation, or septic shock requiring vasopressors) or any three minor criteria are met — monitoring the borderline patient in critical care from the outset rather than waiting for deterioration on the ward.
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