LEPTOSPIROSIS.pptx

28 de May de 2023
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
LEPTOSPIROSIS.pptx
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LEPTOSPIROSIS.pptx

Notas do Editor

  1. Leptospires enter humans through mucous membranes (primarily eyes, nose, and mouth) or abraded skin or by ingestion of contaminated water. After penetration, they circulate in the bloodstream to all body organs, causing endothelial lining damage of small blood vessels with secondary ischemic damage to end organs.
  2. Stages of anicteric and icteric leptospirosis. Correlation between clinical findings and presence of leptospires in body fluids. CSF, cerebrospinal fluid.
  3. The septicemic phase of anicteric leptospirosis has an abrupt onset with flu-like symptoms of fever, shaking chills, lethargy, severe headache, malaise, nausea, vomiting, and severe debilitating myalgia most prominent in the lower extremities, lumbosacral spine, and abdomen. Conjunctival suffusion with photophobia and orbital pain, generalized lymphadenopathy, and hepatosplenomegaly may also be present. A transient (<24 hr) erythematous maculopapular, urticarial, petechial, purpuric, or desquamating rash occurs in 10% of cases. Rarer manifestations include pharyngitis, pneumonitis, arthritis, carditis, cholecystitis, and orchitis. The second or immune phase can follow a brief asymptomatic interlude and is characterized by recurrence of fever and aseptic meningitis. Although 80% of infected children have abnormal CSF profiles, only 50% have clinical meningeal manifestations. CSF abnormalities include a modest elevation in pressure, pleocytosis with early polymorphonuclear leukocytosis followed by mononuclear predominance rarely exceeding 500 cells/μL, normal or slightly elevated protein levels, and normal glucose values. Encephalitis, cranial and peripheral neuropathies, papilledema, and paralysis are uncommon. A selflimited unilateral or bilateral uveitis can occur during this phase, rarely resulting in permanent visual impairment. Central nervous system symptoms usually resolve spontaneously within 1 wk, with almost no mortality.
  4. Weil syndrome is a rare (<10% of cases) severe form of leptospirosis seen more commonly in adults (>30 yr) than in children. The initial manifestations are similar to those described for anicteric leptospirosis. The immune phase, however, is characterized by jaundice, renal failure, thrombocytopenia, and, in fulminant cases, hemorrhage and cardiovascular Collapse. Hepatic involvement leads to right upper quadrant pain, hepatomegaly, direct and indirect hyperbilirubinemia, and modestly elevated serum levels of hepatic enzymes. Liver function usually returns to normal after recovery.
  5. All patients have abnormal findings on urinalysis (hematuria, proteinuria, and casts), and azotemia is common, often associated with oliguria or anuria. Acute kidney failure occurs in 16-40% of cases and is the principal cause of death.
  6. Abnormal electrocardiograms are present in 90% of cases, but congestive heart failure is uncommon.
  7. MAT: taken at least 2 weeks apart and tested in same laboratory
  8. High titre 1:100 Alb:Albuminuria
  9. p