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Leptospirosis: A Neglected
Infectious Disease In The
Tropics
Fadel Muhammad Garishah, BSc
Department of General Medicine
Faculty of Medicine Diponegoro University
Overview of Leptospirosis
 Zoonotic disease caused by Leptospiral pathogens
 Systemic infection characterized by fever,
thrombocytopathy, liver failure, respiratory failure and
acute tubular necrosis
 An overlooked infectious disease due to poorly
availability of diagnostic tools
 Relatively simple medication
Important to Understand
 Leptospirosis typically presents as a nonspecific,
acute febrile illness characterized by fever, myalgia,
and headache and may be confused with other
entities such as influenza and dengue fever.
 Endemic regions, professions, history of possible
exposures affect Clinical Judgement
Epidemiology
Microbiological Aspects
• Spirochetes
• Length 15-20 um
• Periplasmic flagella
• Unstained with
gram
• Dark
microscopy/silver
impregnation
Reservoir and Transmissions
Transmission
 transmitted to humans by direct contact with
reservoir animals
 by exposure to environmental surface water
or soil that is contaminated with their urine
Risks
Natural History of Leptospirosis
Pathobiology
 Patients progressing to multisystem organ failure have
widespread hematogenous dissemination of pathogens.
 Nonoliguric (high output) renal dysfunction should be
supported with fluids and electrolytes.
 Elevated bilirubin levels are due to hepatocellular damage
and disruption of intercellular junctions between
hepatocytes, resulting in leaking of bilirubin out of bile
caniliculi.
 Hemorrhagic complications are common and are
associated with coagulation abnormalities.
 Severe pulmonary hemorrhage syndrome due to extensive
alveolar hemorrhage has a fatality rate of >50 %.
Clinical Manifestations
Clinical features
Conjunctival Suffusion
Calf Muscle
Tenderness
Leptospiral Rash
Diagnostic Terms
 Suspect case
 Probable case
 Confirmed case
Suspect Case
 Acute fever > 38,5C; with/out severe headache
 Myalgia
 Prostration
 Conjunctival suffusion
 History of exposure!
Probable case
 Calf tenderness
 Cough with/without hemoptysis
 Jaundice
 Hemorrhagic
 Meningism
 Anuria/oliguria/proteinuria
 Breathlessness
 Cardiac arrythmia
 Skin rashes
 With Positive Rapid IgM Test or MAT 200/single sample
Diagnostic Tools
 Dark field microscopy/Ink stain
 Microscopic Agglutination Test
 ELISA
 PCR
 Cultur EMJH/Fletcher’s Medium
Confirmed case
 Suspect/Probable Case
 With isolation of Leptospira spp.
 PCR positive
 Seroconversion of MAT 4 folds
 MAT titre 400/single sample
Chemotherapeutics
Mild
 Doxycyline 2 x 100 mg for 7 days
 Amoxicillin/Ampicillin 2 g/day for 7 days
Severe Case
 Penicillin G 2 MU IV/6hours for 7 days
 Ceftriaxon 1 g/day for 7 days
Supportive managements
 Renal (Dialysis)
 Hepatic
 Pulmonary (Ventilators)
 Hemorrhages (Transfusions)

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Leptospirosis a neglected infectious disease in the tropics

  • 1. Leptospirosis: A Neglected Infectious Disease In The Tropics Fadel Muhammad Garishah, BSc Department of General Medicine Faculty of Medicine Diponegoro University
  • 2. Overview of Leptospirosis  Zoonotic disease caused by Leptospiral pathogens  Systemic infection characterized by fever, thrombocytopathy, liver failure, respiratory failure and acute tubular necrosis  An overlooked infectious disease due to poorly availability of diagnostic tools  Relatively simple medication
  • 3. Important to Understand  Leptospirosis typically presents as a nonspecific, acute febrile illness characterized by fever, myalgia, and headache and may be confused with other entities such as influenza and dengue fever.  Endemic regions, professions, history of possible exposures affect Clinical Judgement
  • 5. Microbiological Aspects • Spirochetes • Length 15-20 um • Periplasmic flagella • Unstained with gram • Dark microscopy/silver impregnation
  • 7. Transmission  transmitted to humans by direct contact with reservoir animals  by exposure to environmental surface water or soil that is contaminated with their urine
  • 9. Natural History of Leptospirosis
  • 10. Pathobiology  Patients progressing to multisystem organ failure have widespread hematogenous dissemination of pathogens.  Nonoliguric (high output) renal dysfunction should be supported with fluids and electrolytes.  Elevated bilirubin levels are due to hepatocellular damage and disruption of intercellular junctions between hepatocytes, resulting in leaking of bilirubin out of bile caniliculi.  Hemorrhagic complications are common and are associated with coagulation abnormalities.  Severe pulmonary hemorrhage syndrome due to extensive alveolar hemorrhage has a fatality rate of >50 %.
  • 12. Clinical features Conjunctival Suffusion Calf Muscle Tenderness Leptospiral Rash
  • 13. Diagnostic Terms  Suspect case  Probable case  Confirmed case
  • 14. Suspect Case  Acute fever > 38,5C; with/out severe headache  Myalgia  Prostration  Conjunctival suffusion  History of exposure!
  • 15. Probable case  Calf tenderness  Cough with/without hemoptysis  Jaundice  Hemorrhagic  Meningism  Anuria/oliguria/proteinuria  Breathlessness  Cardiac arrythmia  Skin rashes  With Positive Rapid IgM Test or MAT 200/single sample
  • 16. Diagnostic Tools  Dark field microscopy/Ink stain  Microscopic Agglutination Test  ELISA  PCR  Cultur EMJH/Fletcher’s Medium
  • 17. Confirmed case  Suspect/Probable Case  With isolation of Leptospira spp.  PCR positive  Seroconversion of MAT 4 folds  MAT titre 400/single sample
  • 18. Chemotherapeutics Mild  Doxycyline 2 x 100 mg for 7 days  Amoxicillin/Ampicillin 2 g/day for 7 days Severe Case  Penicillin G 2 MU IV/6hours for 7 days  Ceftriaxon 1 g/day for 7 days
  • 19. Supportive managements  Renal (Dialysis)  Hepatic  Pulmonary (Ventilators)  Hemorrhages (Transfusions)

Editor's Notes

  1. Mammalian species excrete leptospiral pathogens in their urine and serve as reservoirs for their transmission. The pathogens are maintained in sylvatic and domestic environments by transmission among rodent species. In these reservoirs, infection produces chronic, asymptomatic carriage. Leptospires can then infect livestock and domestic and wild animals and cause a range of disease manifestations and carrier states. Maintenance of leptospirosis in these populations is due to their continued exposure to rodent reservoirs or to transmission within animal herds. Leptospirosis is transmitted to humans by direct contact with reservoir animals or by exposure to environmental surface water or soil that is contaminated with their urine. Leptospires penetrate abraded skin or mucous membranes, enter the bloodstream and disseminate throughout the body tissue. Infection causes an acute febrile illness during the early 'leptospiraemic' phase and progresses during the late 'immune' phase to cause severe multisystem manifestations such as hepatic dysfunction and jaundice, acute renal failure, pulmonary haemorrhage syndrome, myocarditis and meningoencephalitis. Although the immune response eventually eliminates the pathogens, leptospires may persist for prolonged periods in immunoprivileged sites, such as the renal tubules and the anterior chamber and vitreous humor of the eye, where they can produce, respectively, urinary shedding weeks after resolution of the illness and uveitis months after exposure. Humans are an accidental host and do not shed sufficient numbers of leptospires to serve as reservoirs for transmission.