Everything about Leptospirosis totally explained
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ICD9
OMIM = 607948 |
MedlinePlus = 001376 |
eMedicineSubj = med |
eMedicineTopic = 1283 |
eMedicine_mult = |
MeshName = Leptospirosis |
MeshNumber = C01.252.400.511 |
}}
Leptospirosis (also known as
Weil's disease,
canicola fever,
canefield fever,
nanukayami fever,
7-day fever and many more) is a
bacterial zoonotic disease caused by
spirochaetes of the
genus Leptospira that affects
humans and a wide range of animals, including mammals, birds, amphibians, and reptiles. It was first described by
Adolf Weil in
1886 when he reported an "acute infectious disease with
enlargement of spleen,
jaundice and
nephritis".
Leptospira was first observed in
1907 from a
post mortem renal tissue slice.
Though being recognised among the world's most common
zoonoses, leptospirosis is a relatively rare bacterial
infection in humans. The infection is commonly transmitted to humans by allowing
fresh water that has been contaminated by animal
urine to come in contact with unhealed breaks in the
skin,
eyes or with the
mucous membranes. Outside of
tropical areas, leptospirosis cases have a relatively distinct seasonality with most of them occurring August-September/February-March.
Causes
Leptospirosis is caused by a spirochaete bacterium called
Leptospira spp. that has at 5 different
serovars of importance in the
United States causing disease (icterohaemorrhagiae, canicola, pomona, grippotyphosa, and bratislava). There are other (less common) infectious strains. It should however be noted that genetically different leptospira organisms may be identical serologically and vice versa. Hence, an argument exists on the basis of strain identification. The traditional serologic system is seemingly more useful from diagnostic and epidemiologic standpoint at the moment (which may change with further development and spread of technologies like
PCR).
Leptospirosis is transmitted by the urine of an infected animal, and is contagious as long as it's still moist. Although rats, mice and voles are important primary hosts, a wide range of other mammals including dogs, deer, rabbits, hedgehogs, cows, sheep, raccoons, possums, skunks, and even certain marine mammals are also able to carry and transmit the disease as secondary hosts. Dogs may lick the urine of an infected animal off the grass or soil, or drink from an infected puddle. There have been reports of "house dogs" contracting leptospirosis apparently from licking the urine of infected mice that entered the house. The type of habitats most likely to carry infective bacteria are muddy riverbanks, ditches, gulleys and muddy livestock rearing areas where there's regular passage of either wild or farm mammals. There is a direct correlation between the amount of rainfall and the incidence of leptospirosis, making it seasonal in temperate climates and year-round in tropical climates.
Leptospirosis is also transmitted by the semen of infected animals. Abattoir workers can contract the disease through contact with infected blood or body fluids.
Humans become infected through contact with water, food, or soil containing urine from these infected animals. This may happen by swallowing contaminated food or water or through skin contact. The disease isn't known to be spread from person to person and cases of bacterial dissemination in convalescence are extremely rare in humans. Leptospirosis is common among watersport enthusiasts in specific areas as prolonged immersion in water is known to promote the entry of the bacteria. Occupational risk factors include
veterinarians, slaughter house workers, farmers, and sewer workers. An outbreak in an inner city environment has been linked to contact with rat urine.
Symptoms
In animals, the
incubation period (time of exposure to first
symptoms) is anywhere from 2 to 20 days. In dogs, the liver and kidney are most commonly damaged by leptospirosis.
Vasculitis can occur, causing
edema and potentially
disseminated intravascular coagulation (DIC).
Myocarditis,
pericarditis,
meningitis, and
uveitis are also possible sequelae. One should strongly suspect leptospirosis and include it as part of a
differential diagnosis if the sclerae of the dog's eyes appear
jaundiced (even slightly yellow), though the absence of jaundice doesn't eliminate the possibility of leptospirosis, and its presence could indicate
hepatitis or other liver pathology rather than leptospirosis.
Vomiting, fever, failure to eat, reduced urine output, unusually dark or brown urine, and
lethargy are also indications of the disease.
In humans, leptospiral infection causes a wide range of
symptoms, and some infected persons may have no symptoms at all. Leptospirosis is a
biphasic disease that begins with flu-like symptoms (fever, chills,
myalgias, intense headache). The first phase resolves and the patient is asymptomatic briefly before the second phase begins that's characterized by meningitis, liver damage (causing jaundice), and renal failure. Because of the wide range of symptoms the infection is often
wrongly diagnosed. This leads to a lower registered number of cases than there really are. Symptoms of leptospirosis include high
fever, severe
headache, chills, muscle aches, and
vomiting, and may include
jaundice, red eyes,
abdominal pain,
diarrhea, and/or a
rash. The symptoms in humans appear after a 4-14 day incubation period.
Complications
Complications include
meningitis, respiratory distress and renal interstitial tubular necrosis, which results in
renal failure and often
liver failure (the severe form of this disease is known as
Weil's disease, though it's sometimes named
Weil Syndrome). Cardiovascular problems are also possible. Approximately 5-50% of severe leptospirosis cases are fatal, however, such cases only constitute about 10% of all registered incidents.
Diagnostics
On infection the
microorganism can be found in
blood for the first 7 to 10 days (invoking serologically identifiable reactions) and then moving to the kidneys. After 7 to 10 days the microorganism can be found in fresh urine. Hence, early diagnostic efforts include testing a serum or blood sample serologically with a panel of different strains. It is also possible to
culture the microorganism from blood, serum, fresh urine and possibly fresh kidney biopsy. Kidney function tests (
Blood Urea Nitrogen and
creatinine) as well as blood tests for liver functions are performed. The later reveal a moderate elevation of transaminases. Brief elevations of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma-glutamyltransferase (GGT) levels are relatively mild. These levels may be normal, even in children with jaundice.
Diagnosis of leptospirosis is confirmed with tests such as
Enzyme-Linked Immunosorbent Assay (ELISA) and
PCR. Serological testing, the MAT (microscopic agglutination test), is considered the
gold standard in diagnosing leptospirosis. As a large panel of different leptospira need to be subcultured frequently, which is both laborious and expensive, it's underused, mainly in developing countries.
Differential diagnosis list for leptospirosis is very large due to diverse symptomatics. For forms with middle to high severity, the list includes
dengue fever and other hemorrhagic
fevers,
hepatitis of various
etiologies, viral
meningitis,
malaria and
typhoid fever. Light forms should be distinguished from
influenza and other related viral diseases. Specific tests are a must for proper diagnosis of leptospirosis. Under circumstances of limited access (for example, developing countries) to specific diagnostic means, close attention must be paid to
anamnesis of the patient. Factors like certain dwelling areas, seasonality, contact with
stagnant water (swimming, working on flooded meadows, etc) and/or rodents in the medical history support the leptospirosis hypothesis and serve as indications for specific tests (if available).
Leptospira can be cultured in
Ellinghausen-McCullough-Johnson-Harris medium, which is incubated at 28 to 30ºC. The median time to positivity is three weeks with a maximum of 3 months. This makes culture techniques useless for diagnostic purposes, but is commonly used in research.
Treatment
Leptospirosis treatment is a relatively complicated process comprising two main components - suppressing the causative agent and fighting possible complications.
Aetiotropic drugs are
antibiotics, such as
doxycycline,
penicillin,
ampicillin, and
amoxicillin (doxycycline can also be used as a
prophylaxis). There are no human
vaccines; animal vaccines are only for a few strains, and are only effective for a few months. Human therapeutic dosage of drugs is as follows: doxycycline 100 mg orally every 12 hours for 1 week or penicillin 1-1.5 MU every 4 hours for 1 week. Doxycycline 200-250 mg once a week is administered as a
prophylaxis. In dogs, penicillin is most commonly used to end the leptospiremic phase (infection of the blood), and doxycycline is used to eliminate the
carrier state.
Supportive therapy measures (esp. in severe cases) include
detoxication and normalization of the
hydro-electrolytic balance. Glucose and salt solution infusions may be administered;
dialysis is used in serious cases. Elevations of serum potassium are common and if the potassium level gets too high special measures must be taken. Serum phosphorus levels may likewise increase to unacceptable levels due to renal failure. Treatment for hyperphosphatemia consists of treating the underlying disease,
dialysis where appropriate, or oral administration of
calcium carbonate, but not without first checking the serum calcium levels (these two levels are related).
Corticosteroids administration in gradually reduced doses (for example,
prednisolone starting from 30-60 mg) during 7-10 days is recommended by some specialists in cases of severe haemorrhagic effects.
Research
Leptospirosis: a zoonotic disease of global importance. Lancet Infect Dis. 2003 Dec;3(12):757-71
Bharti AR, Nally JE, Ricaldi JN, Matthias MA, Diaz MM, Lovett MA, Levett PN, Gilman RH, Willig MR, Gotuzzo E, Vinetz JM; Peru-United States Leptospirosis Consortium.
In the past decade, leptospirosis has emerged as a globally important infectious disease. It occurs in urban environments of industrialised and developing countries, as well as in rural regions worldwide. Mortality remains significant, related both to delays in diagnosis due to lack of infrastructure and adequate clinical suspicion, and to other poorly understood reasons that may include inherent pathogenicity of some leptospiral strains or genetically determined host immunopathological responses. Pulmonary haemorrhage is recognised increasingly as a major, often lethal, manifestation of leptospirosis, the pathogenesis of which remains unclear. The completion of the genome sequence of Leptospira interrogans serovar lai, and other continuing leptospiral genome sequencing projects, promise to guide future work on the disease. Mainstays of treatment are still tetracyclines and beta-lactam/cephalosporins. No vaccine is available. Prevention is largely dependent on sanitation measures that may be difficult to implement, especially in developing countries.
In a study of 38 dogs diagnosed and properly treated for leptospirosis published in the February 2000 issue of the
Journal of the American Veterinary Association, the survival rate for the dialysis patients was slightly higher than the ones not put on dialysis, but both were in the 85% range (plus or minus). Of the dogs in this study that didn't die, most recovered adequate kidney function, although one had chronic renal problems.
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