Multisystem Bacterial Infections

 

  • Typhoid and paratyphoid fever

    Aka enteric fever.

    Pathophysiology and epidemiology

    • Systemic Salmonella infection with S. typhi or S. paratyphoid.
    • After malaria, commonest serious tropical disease in returning travellers from Asia (esp. South and Southeast); also found in Africa and South America.
    • 1-3 weeks incubation.
    • Not to be confused with typhus, an infection by Rickettsia typhi.

    Presentation

    Typhoid fever:

    • Insidious onset of fever, headache, malaise, and constipation. Diarrhoea and vomiting can occur but are less common.
    • Other features: rose spots (macules on chest and abdo), hepatosplenomegaly, lymphadenopathy, dry cough, neurological symptoms, bradycardia.

    Paratyphoid fever:

    • Similar to typhoid fever, but more abrupt onset and milder course.

    Investigations

    • Blood and stool cultures.
    • FBC and LFTs may be deranged.

    Management

    Azithromycin or ceftriaxone.

  • Leptospirosis

    Pathophysiology and epidemiology

    • Infection with the spirochete genus Leptospira.
    • Transmitted to humans in urine of rats, dogs, and other mammals, either directly or in urine-contaminated water.
    • Can be acquired in the UK, but most UK cases are acquired abroad.
    • 1-2 weeks incubation.

    Presentation

    • Biphasic course, with bacteraemic flu-like phase followed 1-3 days later by immune phase.
    • Immune phase may be mild (e.g. fever and myalgia), but severe manifestations include Weil's disease, characterised by haemorrhage, conjunctival suffusion (redness without exudate), jaundice, and hepatorenal failure.
    • Less commonly, there may be GI, respiratory, or CNS manifestations.

    Investigations

    • FBC: ↑neutrophils, and sometimes ↓Hb and ↓PLT.
    • Deranged renal and liver function tests.
    • Diagnosis: IgM serology (>7 days).

    Management

    • Penicillins or tetracyclines.
    • Antibiotics are still given in the immune phase, despite the fact that they may confer little benefit.
  • Whipple's disease

    Pathophysiology and epidemiology

    • Infection by the Gram +ve rod Tropheryma whipplei.
    • Ubiquitous in environment, and often linked to soil or animal exposure e.g. farmer.
    • Minimal immune response by patients suggests specific immunodeficiency as a risk factor.
    • Patients are 90% male, mean age 50, usually white.

    Presentation

    Common:

    • Joints: typically migratory large joins arthralgia, which may precede other symptoms by >5 years. Often misdiagnosed as a seronegative arthritis.
    • GI: chronic intermittent diarrhoea, colicky abdo pain, malabsorption, weight loss.

    Less common:

    • CNS: usually dementia/confusion, less commonly, ophthalmoplegia, nystagmus, seizures, myoclonus.
    • Cardiac: usually endocarditis, less commonly myo/pericarditis.
    • Others: fever, lymphadenopathy, skin hyperpigmentation, cough, uveitis.
    • In rare cases, it can present with one/some of these features alone.

    Investigations

    • Bloods: ↓Hb, ↑WBC, ↑CRP, ↑PT (vit K malabsorption).
    • Diagnosis is by tissue biopsy, usually small bowel from upper GI endoscopy, testing sample with Periodic acid‐Schiff stain (+ve) and PCR.
    • CSF PCR in all, due to potential morbidity of CNS involvement. Other sites only sampled (e.g. joints, lymph nodes) if symptomatic and GI features absent.
    • Very difficult to culture, so even in endocarditis it is only diagnosed from histology of resected valves.

    Management

    Antibiotics IV – e.g. 2 weeks ceftriaxone or penicillin – then 3-12 months co-trimoxazole PO.

    Complications and prognosis

    • Uniformly fatal without treatment.
    • Immune reconstitution inflammatory syndrome (IRIS) in first weeks of treatment.
    • Relapses, often in CNS, if inadequately treated.

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