2. Is an infectious disease caused by pathogenic
leptospires.
In its mild form, it may present as an influenza-
like illness with headaches & myalgias.
Severe leptospirosis, characterized by jaundice,
renal dysfunction, & hemorrhagic diathesis, is
referred to as Weil’s syndrome.
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3. Leptospires are spirochetes.
Are coiled, thin, highly motile organisms with
hooked ends & two periplasmic flagella, which
enables it to burrow into tissues.
Organisms are 6-20 µm long and about 0.1 µm
wide.
Stain poorly but can be seen microscopically by
dark-field examination.
Requires special media for growth & may take
weeks for cultures to be positive.
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4. Leptospires may enter host through abrasions in skin or
through intact mucous membranes, especially conjunctiva
& lining of oro- & nasopharynx.
Drinking of contaminated water.
Leptospiremia develops, with subsequent spread to all
organs.
Multiplication takes place in blood & in tissues.
Leptospires can be isolated from blood & CSF during first
4-10 days of illness.
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5. Leptospire-inflicted damage to capillary endothelium
results in vasculitis.
Any organ can be affected but it primarily involves the
kidneys & the liver.
In kidney, leptospires migrate to the interstitium, renal
tubules, & tubular lumen, causing interstitial nephritis &
tubular necrosis.
Hypovolemia due to dehydration or altered capillary
permeability may contribute to the development of renal
failure.
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6. In the liver, centrilobular necrosis with proliferation of Kupffer
cells may be found.
Severe hepatocellular necrosis is not a feature of leptospirosis.
Pulmonary involvement is the result of hemorrhage & not of
inflammation.
Invasion of skeletal muscles by leptospires results in swelling,
vacuolation of the myofibrils, focal necrosis.
In severe leptospirosis, vasculitis may ultimately impair the
microcirculation & increase capillary permeability, resulting in
fluid leakage & hypovolemia.
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7. When antibodies are formed, leptospires are
eliminated from all sites except the eye, the
proximal renal tubules (PCT), & perhaps the brain.
The persistence of leptospires in the aqueous
humor occasionally causes chronic or recurrent
uveitis.
The systemic immune response is effective in
eradicating the organism but may also produce
symptomatic inflammatory reactions.
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8. More than 90% of symptomatic patients have the relatively
mild & usually anicteric form of leptospirosis, with or
without meningitis.
Severe leptospirosis with profound jaundice (Weil’s
syndrome) develops in 5-10% of infected individuals
Incubation period is usually 1-2 weeks but ranges from 2-
26 days.
Typically, an acute leptospiremic phase is followed by an
immune-leptospiruric phase.
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9. Anicteric Leptospirosis:
› May present with influenza-like illness, with fever, chills,
severe headache, N/V, & myalgias.
› Muscle pain, which especially affects the calves, back,
and abdomen, is an important feature of leptospiral
infection.
› Less common features include sore throat & rash.
› Mental confusion may be present.
› Most common finding on P/E is FEVER with conjunctival
suffusion.
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10. Severe Leptospirosis (Weil’s Syndrome):
› Characterized by jaundice, renal dysfunction, hemorrhagic diathesis, &
high mortality.
› Generally develops after 4-9 days.
› Jaundice not associated with severe hepatic necrosis.
› Hepatomegaly & RUQ pain usually detected.
› Splenomegaly is found in 20% of cases.
› Hypovolemia & decreased renal perfusion contribute to the
development of acute tubular necrosis with oliguria or anuria.
› Dialysis sometimes REQUIRED.
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11. Pulmonary involvement occurs frequently, resulting in
cough, dyspnea, chest pain, & blood-stained sputum in
hemoptysis or even respiratory failure.
Hemorrhagic manifestations are seen in Weil’s syndrome:
epistaxis, petechiae, purpura, & ecchymoses.
Rhabdomyolysis, hemolysis, myocarditis, pericarditis,
congestive heart failure, cardiogenic shock, adult
respiratory distress syndrome & multiorgan failure have all
been described during severe leptospirosis.
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12. Kidneys:
› Urinary sediment changes (leukocytes, RBCs, & hyaline/granular
casts)
› Mild/moderate proteinuria
› Renal failure & azotemia (severe)
ESR elevated
Mild thrombocytopenia (associated with renal failure)
PT time may be elevated (Vit. K to correct)
Elevated creatinine phosphokinase
› In first weeks-may help differentiate from viral hepatitis.
Pulmonary radiographic abnormalities (severe):
› Patchy alveolar pattern that corresponds to scattered alveolar
hemorrhage.
› Abnormalities most often affect the lower lobes in the periphery of the
lung fields.
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13. Leptospirosis should be differentiated from other febrile
illnesses associated with headache & muscle pain:
› Malaria
› Enteric fever (typhoid)
› Viral hepatitis
› Dengue
› Hantavirus infections
› Rickettsial diseases
When patients have a flu-like disease with
disproportionately severe myalgia or aseptic meningitis, a
diagnosis of leptospirosis should be considered.
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14. Should be initiated early as possible.
NB: treatment after first 4 days of illness is
effective.
Antimicrobial therapy for mild febrile form of
leptospirosis is controversial, but such
treatment is indicated for more severe forms.
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15. Purpose of drug administration Regimen:
Mild leptospirosis Doxycycline, 100mg PO bid
or
Ampicillin, 500-700mg PO qid
or
Amoxicillin, 500mg PO qid
Moderate/severe leptospirosis Penicillin G, 1.5million units IV qid
or
Ampicillin, 1g IV qid
or
Amoxicillin, 1g IV qid
or
Erythromycin, 500mg IV qid
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16. Purpose of drug administration: Regimen:
Chemoprophylaxis Doxycycline, 200 mg PO once a week
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17. References:
› Emedicine.com
› www.researchgate.com
› Harrison’s Principles of Internal Medicine, 14th
Ed.
› Davidson’s Principles & Practice of Medicine,
22nd Ed.
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