Weil's disease (leptospirosis)

 

Background

Leptospirosis is an infectious disease of humans and animals that is caused by pathogenic spirochetes of the genus Leptospira. It is considered the most common zoonosis in the world and is associated with rodents in settings of poor sanitation, agricultural occupations, and increasingly "adventure" sports or races involving fresh water, mud, or soil exposure.

 

Leptospirosis ranges in severity from a mild illness suggesting a viral infection to a multi-systemic syndrome with unique features. It is characterised by sudden onset of the following:

- Fever (38-40°C)

- Rigors

- Headache, retro-orbital pain, photophobia

- Conjunctival suffusion

- Dry cough

- Nausea and vomiting, diarrhoea

- Muscle pain localized to the calf and lumbar areas

 

More severe disease manifests as icteric leptospirosis, also known as Weil's disease, with the following features:

- Icterus or frank jaundice

- Renal failure with oliguria

- Hemorrhagic features

- Systemic inflammatory syndrome or shock

 

Leptospirosis is presumed to be the most widespread zoonosis in the world. The source of infection in humans is usually either direct or indirect contact with the urine of an infected animal. The incidence is significantly higher in warm-climate countries than in temperate regions; this is due mainly to longer survival of leptospires in the environment in warm, humid conditions.

 

The great majority of infections caused by leptospires are either subclinical or of very mild severity, and patients will probably not seek medical attention. A smaller proportion of infections, but the overwhelming majority of the recognised cases, present with a febrile illness of sudden onset.

Aseptic meningitis may be found in ≤25% of all leptospirosis cases . Icteric leptospirosis is a much more severe disease in which the clinical course is often very rapidly progressive. Severe cases often present late in the course of the disease, and this contributes to the high mortality rate, which ranges between 5 and 15%. Between 5 and 10% of all patients with leptospirosis have the icteric form of the disease and may account for a significant minority of all causes of aseptic meningitis. The jaundice occurring in leptospirosis is not associated with hepatocellular necrosis, and liver function returns to normal after recovery. The complications of severe leptospirosis emphasise the multi-systemic nature of the disease. Leptospirosis is a common cause of acute renal failure (ARF), which occurs in 16 to 40% of cases. Cardiac, pulmonary, and ocular involvement may occur as well. 

 

Antimicrobial therapy is indicated for the severe form of leptospirosis, but its use is controversial for the mild form of leptospirosis. Mild leptospirosis is treated with doxycycline, ampicillin, or amoxicillin. For severe leptospirosis, intravenous penicillin G has long been the drug of choice, although the third-generation cephalosporins cefotaxime and ceftriaxone have become widely used. Alternative regimens are ampicillin, amoxicillin, or erythromycin. Patients with severe disease should remain hospitalised until adequate resolution of organ failure and clinical infection.