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Pneumonia

  • Background 

    Definition

    Pathological:

    • Inflammation of lung parenchyma distal to the terminal bronchioles, which includes the respiratory bronchioles, alveolar ducts, and alveoli.

    Clinical:

    • Lower respiratory tract symptoms AND...
    • {Focal chest signs (e.g. crackles) plus systemic signs (e.g. fever)} OR {unexplained CXR shadowing}.

    Chest infection:

    • A non-specific term for lower respiratory tract infections, though tends to be used for milder presentations – i.e. acute bronchitis – rather than pneumonia.
    • Acute bronchitis may or may not feature productive cough and fever, but has no focal chest signs and CXR is clear. Unlike pneumonia, antibiotics are not routinely indicated and only provide minimal symptomatic relief.

    Types

    Community-acquired pneumonia (CAP)

    Causes (% of all cases):

    • Common bacteria: Strep. pneumoniae (50%) and H. influenzae (7%).
    • Other bacteria: Staph. aureus (2%), Moraxella catarrhalis (2%), and the 'atypicals', Chlamydophila pneumoniae (10%), Mycoplasma pneumoniae (5-15%, depending if epidemic), and Legionella pneumophila (3%).
    • Viral: influenza A+B, RSV.
    • Pathogens in the immunosuppressed: Pneumocystis jirovecii (causing Pneumocystis pneumonia, PCP), CMV.

    Hospital-acquired pneumonia (HAP)

    • Develops >48h post-admission.
    • Pathogens are similar to CAP in the first 4 days.
    • Later, Gram -ve enterobacteria (KlebsiellaE. coli), Staph. aureus (inc. MRSA), Legionella, and Pseudomonas become increasingly common.

    Aspiration pneumonia

    • Causes: neuromuscular problem (stroke, myasthenia gravis), ↓consciousness (anaesthesia, alcohol intoxication).
    • Pathogens: similar to HAP, including Klebsiella in alcoholism, and anaerobes like PeptostreptococcusFusobacterium, and Prevotella.
    • Commonly affects right lower lobe.

    Atypical pneumonia

    • Broadly speaking, this refers to any pneumonia not caused by the 'typical' pathogens Strep. pneumoH. influenzae, or Moraxella. Sometimes it more specifically refers to pneumonia caused by bacteria which cannot be easily identified by Gram stain, namely MycoplasmaChlamydophila, and Legionella.
    • Also known as walking pneumonia, as patients are often fairly well. In practice, this mild clinical picture is seen in Mycoplasma and Chlamydophila, the two commonest causes, while Legionella can cause severe disease.
    • Commonly results from close person to person contact, which is the case for Mycoplasma and Chlamydophila. May occur in outbreaks in schools, universities, or workplaces. Mycoplasma tends to occur in 4-yearly epidemics.
    • Legionella occurs in location-specific outbreaks linked to stagnant water e.g. in air-conditioning systems.
  • Signs and symptoms

    Symptoms:

    • SOB
    • Cough with purulent sputum, possibly blood stained.
    • Pleuritic pain.
    • Systemic symptoms: fever, malaise. May be the only symptoms in the old or young.

    Signs:

    • Cyanosis, confusion.
    • ↑RR, ↑HR, AF.
    • Consolidation leads to dull percussion, ↑vocal resonance (VR), and bronchial breathing (i.e. ↑breath sounds, BS). Both pneumonia and effusion cause dull percussion, but pneumonia is noisy (↑VR, ↑BS) while effusion goes shhh (↓VR, ↓BS).

    Pathogen-specific features:

    • Strep. pneumo: lobar pneumonia, rusty sputum. Oral herpes may be present, though this is uncommon (10%) and non-specific.
    • H. influenzae and Moraxella: more common in COPD patients.
    • Staph. aureus: may be bilateral, and can occur post-influenza.
    • Mycoplasma pneumo: persistent dry cough, mild fever, malaise, headache, and myalgia. Usually self-resolves over weeks. Peaks in 4-yearly epidemics. Immunological complications include erythema multiforme and haemolytic anaemia.
    • Chlamydophila pneumo: gradual onset, initial pharyngitis/URTI symptoms, and headache. Usually self-resolves, but may take months.
    • Legionella: flu-like prodrome followed by cough (dry then productive or bloody), SOB, and diarrhoea and vomiting. Bilateral in severe cases. Pontiac fever is Legionella infection without lung involvement.
    • PCP: dry cough, bilateral pneumonia, desaturation on exertion.
    • Klebsiella: currant jelly sputum.
    • Coxiella burnetii: acquired from sheep and other farm animals. Part of Q fever, which includes flu-like symptoms, hepatitis, and endocarditis.
    • Chlamydophila psittaci: acquired from birds. Causes fever, dry cough, headache, splenomegaly, and arthritis.
  • Investigations

    CURB-65 to score severity. 1 for each of:

    • Confusion: abbreviated mental test ≤8 or disoriented.
    • Urea >7. In the community, this is optional so use CRB-65 instead.
    • RR ≥30.
    • BP: SBP <90 or DBP ≤60.
    • Age ≥65.
    • 0-1 is mild, 2 may require hospitalisation, and ≥3 is severe and may required ITU.

    Community tests:

    • ~70% of patients have mild CAP and are managed in the community. They require few, if any, investigations beyond basic obs.
    • If the diagnosis is unclear, get a CRP. Diagnose pneumonia and give antibiotics if CRP >100 mg/L. Consider diagnosis if CRP 20-100.

    Inpatient tests:

    • CXR. Also arrange follow up CXR 6 weeks later to check if clear and rule out underlying lung disease.
    • Bloods: FBC, U+E, LFT, CRP, and blood culture.
    • Sputum culture.
    • O2 sats. ABG if <92% or severely unwell.

    Pathogen-specific investigations and results:

    • ↑↑CRP suggests Strep. pneumo.
    • Strep. pneumo and Legionella urine antigen tests. 75% sensitive.
    • High-res CT for PCP may show ground glass opacities.
    • Legionella: ↑urea and ↑creatinine, ↓Na+ due to SIADH, ↑LFTs. While these changes are commoner in Legionella, they are not that specific.
    • Mycoplasma: ↓Na+, +ve cold agglutinin test.
  • Management

    Antibiotics for CAP:

    • Mild-moderate: amoxicillin PO. Clarithromycin or doxycycline if allergic. Clarithromycin if atypical suspected (monotherapy if mild, added to amoxicillin if moderate).
    • Severe: co-amoxiclav, cefuroxime, or cefotaxime IV (or levofloxacin if allergic), plus clarithromycin IV.
    • If hospitalised, start within 4 hours. Monitor response to treatment with CRP.

    Antibiotics in other situations:

    • HAP empirical treatment: piperacillin/tazobactam, 3rd generation cephalosporin, meropenem, or levofloxacin IV. Co-amoxiclav is a PO alternative or stepdown. Add vancomycin or teicoplanin or linezolid if MRSA suspected.
    • Aspiration pneumonia: clindamycin, levofloxacin, or piperacillin/tazobactam.
    • PCP: co-trimoxazole. Add steroids if moderate or severe: prednisolone PO or hydrocortisone IV.

    Antibiotic duration:

    • 5 days total usually sufficient.
    • Longer if remains febrile or unstable, or for certain pathogens e.g. Pseudomonas.
    • If starting IV, review after 48 hours for possible PO stepdown.

    Supportive care:

    • O2
    • Fluids
    • Paracetamol
  • Complications and prognosis

    Recovery:

    • Fever should resolve within 1 week.
    • Cough and SOB may take up to 6 weeks to resolve, and fatigue may persist up to 3 months.

    Complications:

    • Respiratory failure.
    • Sepsis and septic shock.
    • Uncomplicated parapneumonic pleural effusion, empyema (purulent, colonized pleural effusion), or lung abscess.
    • Death: 1% in the community, 10% if admitted.
  • Lung abscess

    Pathophysiology

    • Necrotic tissue leaves pus-filled cavity.
    • May follow pneumonia, aspiration, or lung tissue damage (infarct, tumour, trauma).

    Signs and symptoms

    • Non-specific respiratory and systemic symptoms.
    • Dullness to percussion.
    • Clubbing

    Investigations

    • CXR shows cavitation with fluid level. Consider CT.
    • Bloods: FBC, U+E, LFT, CRP.
    • Blood and sputum cultures.
    • Culture fluid from abscess via bronchoscopy or trans-thoracic aspiration.

    Management

    • 8 weeks antibiotics, initially IV for 2-3 weeks.
    • Chest physio to help drain it.
    • 10% will require CT-guided or open drainage.

Comments

DISEASE CONDITIONS LIST THAT IMPROVED KNOWLEDGE.

Newborn Baby Assessment

Baby check at birth and 6 weeks  Check notes and get equipment ready:   Measuring tape. Ophthalmoscope Sats probe. In notes, look at full details of pregnancy and birth, including Apgar scores at 1 and 5 minutes. Observation: Colour: pink/red, pale, jaundiced. Any rash? Erythema toxicum is a self-limiting rash of red papules and vesicles, surrounded by red blotches which sometimes give a halo appearance. Usually occurs between 2 days and 2 weeks. Behaviour and mood. Movements. Face: dysmorphism? Head: Feel fontanelle (bulging? sunken?) and sutures. Note that posterior fontanelle closes at 1-2 months, and anterior at 7-19 months. Measure circumference at widest point; take the highest of 3 measurements. Looking for hydrocephalus and microcephaly. Eyes: check red reflex with ophthalmoscope. Feel inside top of mouth with little finger for cleft palate. Also gives you the sucking reflex. Inspect ears to see if they are low-set (below eye level), have any tags or lumps, and check behind the

immunization schedule

Infant immunisations  2 months 5-in-1 DTaP/IPV/Hib – diptheria, tetanus, pertussis, polio, Hib – dose 1. Pneumococcal conjugate vaccine (PCV) dose 1. Rotavirus dose 1. Live, oral virus. MenB dose 1. 3 months 5-in-1 dose 2. MenC dose 1. Rotavirus dose 2. 4 months 5-in-1 dose 3. PCV dose 2. MenB dose 2. 12 months MMR dose 1. MenC dose 2 + Hib dose 4 (combined). MenB dose 3. PCV dose 3. Hepatitis B if they have risk factors. Toddler immunisations Flu vaccine Annual, live attenuated nasal spray flu vaccine in September/October at age 2-7. Kids with asthma and other chronic diseases like CF will continue to get this through childhood and beyond. Contraindicated in severe egg allergy, immunosuppression (inc. steroids in past 2 weeks), and severe asthma or active wheeze. Alternative form can be given. Postpone in those with heavy nasal congestion. 3.5 years 4-in-1 DTaP/IPV: dip, tet, pertussis, polio pre-school boost. MMR dose 2. Teenager immunisations 12 years HPV: Girls only. Parental conse

Hypertension (HTN)

Background     Causes Primary causes: Essential HTN (i.e. idiopathic). Commonest cause. Non-pathologically raised during pain or anxiety (including white coat HTN). However, this may suggest underlying problem so consider following up. Kidney diseases (80% of secondary HTN): Chronic kidney disease. Renal artery stenosis: due to atherosclerosis or fibromuscular dysplasia. Latter most commonly occurs in young women, but even then essential HTN is still commoner. Endocrine: Conn's Cushing's Pheochromocytoma Acromegaly Hyperparathyroidism Other: Obstructive sleep apnoea Pregnancy or pre-eclampsia. Coarctation of the aorta. Medication: CE-LESS ('see less'): C yclosporin E strogen (OCP) L iquorice E PO S teroids S ympathomimetics: α-agonists, dopamine agonists, cocaine, amphetamines, and nasal decongestants such as ephedrine. Signs and symptoms Symptoms of HTN itself are rare, and occur only in severe disease. They include heada