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Haemolytic Uraemic Syndrome(HUS) is a serious condition characterised by the combination
of microangiopathic haemolytic anaemia, low platelet levels and
acute kidney injury. It commonly develops after an infection with Shiga
toxin-producing bacteria, particularly certain strains of Escherichia coli,
which may be transmitted through contaminated food, water or contact with
infected individuals. Children are especially susceptible to
infection-associated HUS.
Typical symptoms may begin
with abdominal cramps, vomiting and bloody diarrhoea, followed by reduced urine
production, fatigue, pallor, swelling and weakness as kidney function
deteriorates. Laboratory investigations can reveal anaemia, thrombocytopenia,
elevated markers of red-cell destruction and impaired renal function. A blood
film may show fragmented red blood cells called schistocytes.
Treatment depends on the
underlying cause and severity. Supportive care is central and may include
careful fluid and electrolyte management, blood transfusions when
appropriate, blood pressure control and dialysis for severe kidney failure. Antibiotics
and antimotility medicines may not be appropriate in certain toxin-mediated
infections and should be guided by specialists. Atypical HUS, which may result
from complement abnormalities, may require targeted
complement-inhibiting therapy.
Early recognition and
specialist management are essential because HUS can cause significant kidney
damage and other complications. Most children recover with appropriate
treatment, although some may develop persistent hypertension or chronic kidney disease.