Pseudomonas aeruginosa
Obligate aerobic, oxidase-positive, non-fermenting Gram-negative bacillus that is a leading cause of nosocomial infections, particularly ventilator-associated pneumonia, burn wound infections, and opportunistic infections in immunocompromised and cystic fibrosis patients.
Organism Card
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| Lab discriminator |
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| Classic traps |
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Exam Intelligence
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GC 102 (Fever after chemotherapy): Pseudomonas aeruginosa is highlighted as a hospital-acquired coloniser that establishes after broad-spectrum antibiotics suppress anaerobic normal flora. It forms biofilm on devices (vascular catheters, ETT, Foley's) that is difficult to eradicate without device removal [2]. This is a key concept for neutropenic fever management questions.
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GC 052 (Fever and purulent sputum): In bronchiectasis exacerbations, Pseudomonas is specifically named as a pathogen in long-standing disease. Anti-pseudomonal antibiotics listed: piperacillin-tazobactam, ceftazidime, carbapenems (meropenem), aminoglycosides (amikacin), fluoroquinolones (levofloxacin) [4].
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Senior notes (Ryan Ho Respiratory): Colonisation in respiratory specimens is common and must be clinically correlated before treating. Ciprofloxacin is better than levofloxacin for Pseudomonas. Ertapenem is the one carbapenem with NO anti-pseudomonal activity. Single agent generally suffices but dual therapy for severe infections. MRPA may need colistin, Zavicefta, Zerbaxa, or cefiderocol [3].
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GC 102: During hospitalisation, Pseudomonas is introduced by hands of medical personnel and various diagnostic/therapeutic procedures — this underpins infection control questions [2].
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HA guidelines (via Adrian Lui / senior notes): For hospitalised patients with chronic lung disease (bronchiectasis), use anti-pseudomonal antibiotics (e.g. piperacillin-tazobactam or cefepime) ± macrolide or doxycycline — this is distinct from standard CAP empirical therapy [6].
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Felix Lai (Medicine/Paeds): Pseudomonas pneumonia is characterised by severe and progressive SOB. Risk factors: bronchiectasis, repeated Abx/steroid courses, structural lung disease including COPD, immunocompromised (neutropenia, HIV, transplant) [7].
- Oxidase test: Pseudomonas is oxidase +ve; Acinetobacter baumannii is oxidase −ve (both are non-fermenters, both cause nosocomial infections — oxidase is the key discriminator).
- Ertapenem trap: Students commonly list "carbapenems" as anti-pseudomonal — but ertapenem specifically lacks Pseudomonas coverage. Exam favourite wrong answer.
- ESBL E. coli vs ceftazidime-resistant Pseudomonas: The 2020 MCQ Q83 tested which is the MOST COMMON MDR organism in HK public hospitals — answer is ESBL-producing E. coli, NOT Pseudomonas [12].
- Colonisation vs infection: Isolating Pseudomonas from sputum in a ventilated patient does NOT automatically mean pneumonia — clinical, radiological, and biochemical correlation required.
- Ecthyma gangrenosum: Black necrotic skin lesion in a febrile neutropenic patient → think Pseudomonas bacteraemia (NOT fungal until later in course).
- Malignant otitis externa: Elderly diabetic with severe ear pain, granulation tissue in ear canal, cranial nerve palsies → Pseudomonas (not typical otitis externa pathogens).
- Anti-pseudomonal cephalosporins: Not all cephalosporins cover Pseudomonas. Ceftriaxone and cefotaxime do NOT. Ceftazidime and cefepime DO.
- Septic arthritis: In IVDU, think Pseudomonas (and S. aureus) rather than typical community pathogens [9].
2020 Fourth Summative MCQ Q83 [12]:
"Which of the following is the MOST COMMON multidrug-resistant organism in Hong Kong's public hospitals? A. Carbapenem-resistant Acinetobacter B. Ceftazidime-resistant Pseudomonas aeruginosa C. Extended-spectrum Beta-lactamases-producing Escherichia coli D. Methicillin-resistant Staphylococcus aureus"
Correct answer: C. ESBL-producing E. coli. Rationale: Despite Pseudomonas and MRSA being well-known MDR organisms, ESBL-producing E. coli is the most common MDR organism in HK public hospitals. This is a direct lecture-derived epidemiological fact. Ceftazidime-resistant Pseudomonas (option B) is a distractor — it is important but less prevalent than ESBL E. coli in HK surveillance data.
2020 Fourth Summative MCQ Q82 [12]:
"What is MORE LIKELY to be the microbial cause of neutropenic fever at day 10 post-chemotherapy? A. Aspergillus fumigatus B. Candida albicans C. Cytomegalovirus D. Streptococcus viridans"
Correct answer: D. Streptococcus viridans (for day 10 = early neutropenia; bacterial causes predominate). Relevance to Pseudomonas: Although Pseudomonas is not an answer option here, it is a key G−ve cause of neutropenic fever alongside E. coli [2][5]. Fungal causes (Aspergillus, Candida) become more important in prolonged neutropenia ( > 7–14 days without response). This question tests the timing concept from GC 102.
No other past paper questions in the indexed context directly name Pseudomonas aeruginosa in their stems.
[1] Lecture slides: GC 101. Diagnosis of infections [Handouts].pdf [2] Lecture slides: GC 102. Fever after chemotherapy infections in immunocompromised hosts [Handout].pdf [3] Senior notes: Ryan Ho Respiratory.pdf [4] Lecture slides: GC 052. Fever and purulent sputum.pdf [5] Senior notes: Block A - High white cell count_ acute and chronic leukaemia; bone marrow transplantation; immunogenetics.pdf [6] Senior notes: Adrian Lui Pediatrics Notes.pdf [7] Senior notes: MBBS Final MB (Medicine) (Felix PY Lai).pdf [8] Senior notes: MBBS Final MB (Surgery) (Felix PY Lai).pdf [9] Senior notes: Ryan Ho Rheumatology.pdf [10] Senior notes: Ryan Ho Cardiology.pdf [11] Senior notes: MBBS Final MB (Surgery) (Felix PY Lai).pdf (sepsis regimen section) [12] Past papers: 2020 Fourth Summative Assessment MCQ paper.pdf
Yersinia enterocolitica
Gram-negative, facultatively anaerobic coccobacillus of the family Yersiniaceae that causes enterocolitis, mesenteric lymphadenitis, and pseudoappendicitis, particularly in children.
Acinetobacter baumannii
Aerobic, non-fermenting Gram-negative coccobacillus that is a leading cause of multidrug-resistant nosocomial infections, particularly ventilator-associated pneumonia, bloodstream infections, and wound infections in critically ill and immunocompromised patients.