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LEPTOSPIROSIS
INTRODUCTION
 Leptospirosis is a zoonotic disease with protean manifestations
 Common synonyms include weils disease , rice field fever
 Mild disease to extremely fatal
 Imperative to suspect and treat early in order to prevent complications
EPIDEMIOLOGY
 Occurs most commonly in tropics and sub tropics
 Around 1 million cases reported yearly worldwide with mean case fatality rate
of about 10%
AGENT
 Leptospira (thin,spiral ) are spirochetes belonging to the order spirochaetales
 Nearly 64 species have been identified ,divided into 2 clades and 4 sub clades
(p1,p2,s1,s2)
 Traditionally classified as pathogenic (l.Interrogans) and free living (l. Biflexa)
 260 serovars
LEPTOSPIROSIS
 1.6- 20 micron long and 0.1 micron
wide
 2. Two polar extrusions
 3.Dark field microscopy / silver
impregnation staining
 4.Special culture media ( fletcher's
, Ellinghausen mccullough – johnson-
harris , or polysorbate 80)
HOST
 Mammals are natural host
 Humans are incidental hosts ( animal or environmental exposure)
 Rodents can persistently shed leptospires in urine throughout their lifespan
HOST – RISK FACTORS
 Men are more commonly infected
 Low socioeconomic status - overcrowding and unhygenic
 Barefoot walking (cuts/abrasions)
 Recreational exposure - rafting , fresh water swimming
 Occupational exposure - farmers , sewage workers
 Domestic animal exposure
 Travel to endemic areas
TRANSMISSION TO
HUMANS
ENVIRONMENT
 Damp soil and water
 Temperature of 28-32 celsius
 Tropical regions
PATHOGENESIS
CLINICAL FEATURES MILD DISEASE
 Majority of cases are mild and go undiagnosed
 Acute febrile illness / flu like syndrome
 Fever,headache,rigors,cough
 Myalgia- calves,backand abdomen
CLINICAL FEATURES
 Conjunctival suffusion
 Pharyngeal congestion
 Muscle tenderness
 Hepatosplenomegaly, lymphadenopathy
 Meningismus
 Transient rash
SEVERE LEPTOSPIROSIS AND
COMPLICATIONS
 Onset similar to mild disease
 May not respect the biphasic course of illness
 Mortality can be as high as 50%
SEVERE LEPTOSPIROSIS
 Hemorrhage
 Acute renal failure
 Acute respiratory failure
 Multiorgan failure
 Weil syndrome – Triad of hemorrhage , jaundice and
acute kidney injury
 SHOCK – common presenting sign (45%) due to
hypovolemia and microvascular dysregulation
CIRCULATORY DYSFUNCTION
 Hypovolemia occurs in sepsis causes vascular leakage or
occur as a consequence of hemorahage
 Shock
 Multiorgan dysfunction
 Hemorrhage manifests due to thrombocytopenia ,
coagulopathy,vascular endothelial damage
RENAL INVOLVEMENT
 Renal impairment attenuated by dehydration from low fluid intake and high fever
 Occurs together with jaundice within first 3-4 days presents as non-oliguric
,oliguric or anuric
 Hyponatremia and hypokalemia due to tubulopathy involving NA-K-2Cl
cotransporter
 Hypokalemia due to impairment of sodium transporter in proximal tubules and
spared distal tubules is more common
 Hypomagnesemia
RENAL INVOLVEMENT
POLYURIC PHASE:
 Develop after 10-18 days
 S.creatinine begins to fall at the end of second
week and normalizes within 3-5 weeks
 In mild cases the only abnormal findings are in
urinary sediment includes albuminuria,
microscopic hematuria,pyuria and granular casts
PULMONARY INVOLVEMENT
Occurs in 20-70% of cases
Most common symptom is cough
Blood tinged sputum or obvious hemoptysis occur
Pulmonary hemorrhage – minimal or severe diffused leading to respiratory
failure
Pulmonary edema with cardiomegaly due to volume overload or congestive
heart failure from myocarditis
Diffuse ground glass opacities without cardiomegaly - ARDS
CARDIAC INVOLVEMENT
 Most commonly non specific st-t changes
 Myocarditis
 Conduction abnormality
 Repolarization abnormalities and arrhthmias
CNS INVOLVEMENT
 Aseptic lymphocytic meningitis
 Leptospira can be isolated from CSF within 5 days
after onset of fever
 Raised CSF opening pressure Raised protein with
normal CSF glucose level
 Lymphocytic pleocytosis
 Encephalomyelitis
 Guillain –Barre syndrome
 Mononeuritis multiplex
 Cranial nerve palsy
 Psychiatric syndrome – Mania
LABORATORY DIAGNOSIS
 Complete Blood Count
 Renal Function Tests
 Liver Function Tests
 CPK
 CSF Analysis
 Urine Analysis
 CXR,ECG
 PT,APTT
 TESTS FOR DIAGNOSIS OF LEPTOSPIROSIS
LABORATORY DIAGNOSIS
 CBC- Leucocytosis( N- 80%)+thrombocytopenia,
anaemia++ Thrombocytopenia is a indicator of
severe disease.
 LFT- Elevated billirubin, elevated liver enzymes
 Markedly Elevated cpk
 PT, APTT- Prolonged.
 RFT- AKI+
 Urine analysis- proteinuria+, rbcs+
 CSF ANALYSIS- ASEPTIC MENINGITIS
SUPPORTIVE TESTS
 Elevated serum amylase
 Elevated creatinine kinase
 Cardiac biomarkers
 Elevated ESR/CRP/Procalcitonin
PULMONARY LEPTOSPIROSIS
HRCT CHEST
• Patchy alveolar infiltration
•Ground glass attenuation
•Interlobular septa thickening
•Mediastinal lymphadenitis
LABORATORY DIAGNOSIS - SPECIFIC
 Direct isolation
 PCR - sensitivity 45-55%
Specificity 99-100%
Can detect even in first five days of illness
Can be done in blood /urine/csf
 Culture - specificity- 100%
Sensitivity - 25%
Requires special media
Time consuming
Blood /csf - first 10 days
Urine - 2nd week to 30 days after resolution of illness
SEROLOGICAL DIAGNOSIS
Microscopic agglutination test (mat)
 Four fold rise in titre or single value of 1:800
 Sensitivity – 16-20%
Igm-elisa
 Simple , sensitive
 Single positive sample adequate for diagnosis becomes positive earlier than mat
 Indicates current infection
 Commonly performed
Antigen detection:
 Using monoclonal anti –lipl32 antibody based antigen capture ellisa- a cost effective alternative to
pcr.
LAB CRITERIA FOR DIAGNOSIS OF CURRENT
LEPTOSPIROSIS
CULTURE –POSITIVE
 MAT-SEROCONVERSION
 ELISA -POSITIVE
MODIFIED
FAINE'S
SCORE
 Presumptive diagnosis of leptospirosis is made of:
 Part A or Part A + B Score : 26 or more
 Part A+B+C (Total) : 25 or more
 A score between 20 and 25 suggests Leptospirosis as a possible
diagnosis.
 Part A+B is useful for diagnosis in the first week as lab tests would be
negative.
 Part A+B+C is valuable in the second week as lab tests would become
positive.
 It is always necessary to confirm the diagnosis with laboratory tests.
Reason for Modification
 Most cases of leptospirosis are reported in the monsoon and post
monsoon seasons. Therfore factors such as rainfall,and contact with
contaminated environment have been incorporated with appropriate
scores Part (B)
 ELISA and SAT measures IgM antibodies becomes positive by 5th
day ,they are the test of choice for diagnosis of current infection and
more over a single sample is adequate . High titres and rising titres of
MAT have been given appropriate scores Part (C)
MANAGEMENT
 MILD LEPTOSPIROSIS:
 FIRST LINE - Doxycycline 100mg BID PO for 10 days
 ALTERNATIVE –
 Amoxicillin 500mg QID OR 1g q8h
OR
 AMPICILLIN 500MG PO tid
OR
 Azithromycin 1g initially followed by 500 mg OD for 2
more days
SEVERE LEPTOSPIROSIS(WEIL SYNDROME)
PRIMARY :
 Penicillin G 1.5 million units IV q 6 hrs for 7 days
 Ceftriaxone 1gm IV OD for 7 days
ALTERNATIVE :
 Ampicillin 0.5-1 gm q6h
 Azithromycin 500mg OD for 5 days
 Cefotaxime 1gm q6h
 Doxycycline 200mg iv loading dose followed by 100mg iv q12h
ROLE OF STEROIDS
WHY
 To reduce or delay the need for ventillatory support
 To reduce mortality
WHOM
 Patients at high risk of pulmonary hemorrhage
 AKI plus any of the following
Platelet count < 1 lakh
MAP < 65 mm of Hg
Prolonged PT/APTT
Need for ionotropes
When
 Initiate as soon as first sign of pulmonary leptospirosis is detected (
tachypnea, hemoptysis, dyspnea)
STEROID REGIMENS
 Methylprednisolone 500mg IV OD for 3 days with first
dose given as bolus within first 12 hrs of onset of
respiratory involvement
 For those with renal failure – Methylprednisolone 500mg IV
after HD OD for 3 days.
After 3rd MP dose or after any episode of hemoptysis give
Cyclophosphamide 1g IV as single dose
 Bolus Methylprednisolone 1g IV OD for 3 das followed b
1mg/kg/day of oral prednisolone for 7 days
PREVENTION AND CONTROL
 Avoid swimming,bathing ,swallowing or submersing head in potentially
contaminated freshwater especially after periods of heavy rainfall or
flooding
 Rodent control measures
 Chemoprophylaxis with weekly doxycycline 200 mg once weekly
for 6 weeks
 Proper drainage of water bodies
 Vaccination of domestic animals
 General protective measures ( proper footwear,eyewear,bandage of
cuts ,etc)
PROGNOSIS - POOR FACTORS
 AGE>40 YEARS
 CNS/PULMONARY /SEVERE RENAL INVOLVEMENT
 MECHANICAL VENTILATION
 ARRHYTHMIAS AND REPOLARISATION ABNORMALITIES
 SHOCK
 LEUCOCYTOSIS
REFERENCE
 MANSON TROPICAL INFECTION
 HARRISON 21ST EDITION
LEPTOSPIROSIS INFECTION IN CLINICAL ASPECT

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LEPTOSPIROSIS INFECTION IN CLINICAL ASPECT

  • 2. INTRODUCTION  Leptospirosis is a zoonotic disease with protean manifestations  Common synonyms include weils disease , rice field fever  Mild disease to extremely fatal  Imperative to suspect and treat early in order to prevent complications
  • 3. EPIDEMIOLOGY  Occurs most commonly in tropics and sub tropics  Around 1 million cases reported yearly worldwide with mean case fatality rate of about 10%
  • 4. AGENT  Leptospira (thin,spiral ) are spirochetes belonging to the order spirochaetales  Nearly 64 species have been identified ,divided into 2 clades and 4 sub clades (p1,p2,s1,s2)  Traditionally classified as pathogenic (l.Interrogans) and free living (l. Biflexa)  260 serovars
  • 5. LEPTOSPIROSIS  1.6- 20 micron long and 0.1 micron wide  2. Two polar extrusions  3.Dark field microscopy / silver impregnation staining  4.Special culture media ( fletcher's , Ellinghausen mccullough – johnson- harris , or polysorbate 80)
  • 6. HOST  Mammals are natural host  Humans are incidental hosts ( animal or environmental exposure)  Rodents can persistently shed leptospires in urine throughout their lifespan
  • 7. HOST – RISK FACTORS  Men are more commonly infected  Low socioeconomic status - overcrowding and unhygenic  Barefoot walking (cuts/abrasions)  Recreational exposure - rafting , fresh water swimming  Occupational exposure - farmers , sewage workers  Domestic animal exposure  Travel to endemic areas
  • 9. ENVIRONMENT  Damp soil and water  Temperature of 28-32 celsius  Tropical regions
  • 10.
  • 12. CLINICAL FEATURES MILD DISEASE  Majority of cases are mild and go undiagnosed  Acute febrile illness / flu like syndrome  Fever,headache,rigors,cough  Myalgia- calves,backand abdomen
  • 13. CLINICAL FEATURES  Conjunctival suffusion  Pharyngeal congestion  Muscle tenderness  Hepatosplenomegaly, lymphadenopathy  Meningismus  Transient rash
  • 14. SEVERE LEPTOSPIROSIS AND COMPLICATIONS  Onset similar to mild disease  May not respect the biphasic course of illness  Mortality can be as high as 50%
  • 15. SEVERE LEPTOSPIROSIS  Hemorrhage  Acute renal failure  Acute respiratory failure  Multiorgan failure  Weil syndrome – Triad of hemorrhage , jaundice and acute kidney injury  SHOCK – common presenting sign (45%) due to hypovolemia and microvascular dysregulation
  • 16. CIRCULATORY DYSFUNCTION  Hypovolemia occurs in sepsis causes vascular leakage or occur as a consequence of hemorahage  Shock  Multiorgan dysfunction  Hemorrhage manifests due to thrombocytopenia , coagulopathy,vascular endothelial damage
  • 17. RENAL INVOLVEMENT  Renal impairment attenuated by dehydration from low fluid intake and high fever  Occurs together with jaundice within first 3-4 days presents as non-oliguric ,oliguric or anuric  Hyponatremia and hypokalemia due to tubulopathy involving NA-K-2Cl cotransporter  Hypokalemia due to impairment of sodium transporter in proximal tubules and spared distal tubules is more common  Hypomagnesemia
  • 18. RENAL INVOLVEMENT POLYURIC PHASE:  Develop after 10-18 days  S.creatinine begins to fall at the end of second week and normalizes within 3-5 weeks  In mild cases the only abnormal findings are in urinary sediment includes albuminuria, microscopic hematuria,pyuria and granular casts
  • 19. PULMONARY INVOLVEMENT Occurs in 20-70% of cases Most common symptom is cough Blood tinged sputum or obvious hemoptysis occur Pulmonary hemorrhage – minimal or severe diffused leading to respiratory failure Pulmonary edema with cardiomegaly due to volume overload or congestive heart failure from myocarditis Diffuse ground glass opacities without cardiomegaly - ARDS
  • 20. CARDIAC INVOLVEMENT  Most commonly non specific st-t changes  Myocarditis  Conduction abnormality  Repolarization abnormalities and arrhthmias
  • 21. CNS INVOLVEMENT  Aseptic lymphocytic meningitis  Leptospira can be isolated from CSF within 5 days after onset of fever  Raised CSF opening pressure Raised protein with normal CSF glucose level  Lymphocytic pleocytosis  Encephalomyelitis  Guillain –Barre syndrome  Mononeuritis multiplex  Cranial nerve palsy  Psychiatric syndrome – Mania
  • 22. LABORATORY DIAGNOSIS  Complete Blood Count  Renal Function Tests  Liver Function Tests  CPK  CSF Analysis  Urine Analysis  CXR,ECG  PT,APTT  TESTS FOR DIAGNOSIS OF LEPTOSPIROSIS
  • 23. LABORATORY DIAGNOSIS  CBC- Leucocytosis( N- 80%)+thrombocytopenia, anaemia++ Thrombocytopenia is a indicator of severe disease.  LFT- Elevated billirubin, elevated liver enzymes  Markedly Elevated cpk  PT, APTT- Prolonged.  RFT- AKI+  Urine analysis- proteinuria+, rbcs+  CSF ANALYSIS- ASEPTIC MENINGITIS
  • 24. SUPPORTIVE TESTS  Elevated serum amylase  Elevated creatinine kinase  Cardiac biomarkers  Elevated ESR/CRP/Procalcitonin
  • 25. PULMONARY LEPTOSPIROSIS HRCT CHEST • Patchy alveolar infiltration •Ground glass attenuation •Interlobular septa thickening •Mediastinal lymphadenitis
  • 26. LABORATORY DIAGNOSIS - SPECIFIC  Direct isolation  PCR - sensitivity 45-55% Specificity 99-100% Can detect even in first five days of illness Can be done in blood /urine/csf  Culture - specificity- 100% Sensitivity - 25% Requires special media Time consuming Blood /csf - first 10 days Urine - 2nd week to 30 days after resolution of illness
  • 27. SEROLOGICAL DIAGNOSIS Microscopic agglutination test (mat)  Four fold rise in titre or single value of 1:800  Sensitivity – 16-20% Igm-elisa  Simple , sensitive  Single positive sample adequate for diagnosis becomes positive earlier than mat  Indicates current infection  Commonly performed Antigen detection:  Using monoclonal anti –lipl32 antibody based antigen capture ellisa- a cost effective alternative to pcr.
  • 28.
  • 29. LAB CRITERIA FOR DIAGNOSIS OF CURRENT LEPTOSPIROSIS CULTURE –POSITIVE  MAT-SEROCONVERSION  ELISA -POSITIVE
  • 31.  Presumptive diagnosis of leptospirosis is made of:  Part A or Part A + B Score : 26 or more  Part A+B+C (Total) : 25 or more  A score between 20 and 25 suggests Leptospirosis as a possible diagnosis.  Part A+B is useful for diagnosis in the first week as lab tests would be negative.  Part A+B+C is valuable in the second week as lab tests would become positive.  It is always necessary to confirm the diagnosis with laboratory tests.
  • 32. Reason for Modification  Most cases of leptospirosis are reported in the monsoon and post monsoon seasons. Therfore factors such as rainfall,and contact with contaminated environment have been incorporated with appropriate scores Part (B)  ELISA and SAT measures IgM antibodies becomes positive by 5th day ,they are the test of choice for diagnosis of current infection and more over a single sample is adequate . High titres and rising titres of MAT have been given appropriate scores Part (C)
  • 33. MANAGEMENT  MILD LEPTOSPIROSIS:  FIRST LINE - Doxycycline 100mg BID PO for 10 days  ALTERNATIVE –  Amoxicillin 500mg QID OR 1g q8h OR  AMPICILLIN 500MG PO tid OR  Azithromycin 1g initially followed by 500 mg OD for 2 more days
  • 34. SEVERE LEPTOSPIROSIS(WEIL SYNDROME) PRIMARY :  Penicillin G 1.5 million units IV q 6 hrs for 7 days  Ceftriaxone 1gm IV OD for 7 days ALTERNATIVE :  Ampicillin 0.5-1 gm q6h  Azithromycin 500mg OD for 5 days  Cefotaxime 1gm q6h  Doxycycline 200mg iv loading dose followed by 100mg iv q12h
  • 35. ROLE OF STEROIDS WHY  To reduce or delay the need for ventillatory support  To reduce mortality WHOM  Patients at high risk of pulmonary hemorrhage  AKI plus any of the following Platelet count < 1 lakh MAP < 65 mm of Hg Prolonged PT/APTT Need for ionotropes When  Initiate as soon as first sign of pulmonary leptospirosis is detected ( tachypnea, hemoptysis, dyspnea)
  • 36. STEROID REGIMENS  Methylprednisolone 500mg IV OD for 3 days with first dose given as bolus within first 12 hrs of onset of respiratory involvement  For those with renal failure – Methylprednisolone 500mg IV after HD OD for 3 days. After 3rd MP dose or after any episode of hemoptysis give Cyclophosphamide 1g IV as single dose  Bolus Methylprednisolone 1g IV OD for 3 das followed b 1mg/kg/day of oral prednisolone for 7 days
  • 37. PREVENTION AND CONTROL  Avoid swimming,bathing ,swallowing or submersing head in potentially contaminated freshwater especially after periods of heavy rainfall or flooding  Rodent control measures  Chemoprophylaxis with weekly doxycycline 200 mg once weekly for 6 weeks  Proper drainage of water bodies  Vaccination of domestic animals  General protective measures ( proper footwear,eyewear,bandage of cuts ,etc)
  • 38. PROGNOSIS - POOR FACTORS  AGE>40 YEARS  CNS/PULMONARY /SEVERE RENAL INVOLVEMENT  MECHANICAL VENTILATION  ARRHYTHMIAS AND REPOLARISATION ABNORMALITIES  SHOCK  LEUCOCYTOSIS
  • 39. REFERENCE  MANSON TROPICAL INFECTION  HARRISON 21ST EDITION