Hemolytic uremic syndrome
Hemolytic-uremic syndrome (HUS) is characterized by a triad of symptoms, which are:
HUS is the most common cause of acute renal failure in childhood, with the highest incidence in infancy and toddler age. It can arise from post-infectious causes, where it is either caused by a gastrointestinal infection with enterohemorrhagic E. coli (EHEC) and we classify it as D + HUS (diarrhea associated HUS)  , or a pneumococcal infection.
Under the designation D−HUS ("diarrhea non-associated HUS") is a heterogeneous group of diseases that are not associated with diarrhea. It usually has a severe course. It often leads to kidney failure, which is addressed by a transplant . After transplantation, there is still a risk of recurrence . 
Classification[edit | edit source]
The term hemolytic uremic syndromes includes a set of diseases, which can be divided according to etiology into post-infectious etiology, which includes D + HUS, pneumococcal HUS, or other infections associated with HUS, and D-HUS (diarrhea non-associated HUS).
However, there is also HUS for which we do not know the exact etiology. Risk factors then include HIV infection, malignancies, chemotherapy, radiotherapy, transplantation, pregnancy, HELLP syndrome, SLE and more. 
D + HUS[edit | edit source]
Diarrhea associated HUS is a disease characterized by a specific clinical and laboratory picture, caused by anE. coli toxin.
Incidence and epidemiology[edit | edit source]
It mainly affects infants and toddlers. It is characterized by an endemic occurrence with a high incidence, for example in Argentina, and a low incidence in Europe. The number of new patients per year corresponds to 2,1 cases per 100 000 inhabitants.
Etiology[edit | edit source]
EHEC colonizes the digestive tract of animals, most often cows.
Verotoxigenic enterohemorrhagic E. coli produces a shiga-like toxin and occurs in multiple forms (so-called serotypes). Serotypes O157: H7, O26, O111, O103, and O145 have the ability to cause this disease .
EHEC transmission occurs both between humans and by transmission from an infected animal or by ingesting its contaminated products (unpasteurized cow's or goat's milk, insufficiently heat-treated beef ("hamburger-disease"), home-made juices from EHEC-contaminated vegetables, swimming in a pool with contaminated water, etc...
A small infectious dose is associated with a probability of developing HUS in 15% of cases. The incubation period is 3-8 days.
Pathogenesis[edit | edit source]
Upon entry of EHEC into the digestive system, shiga-like toxin (Stx) is released, which adheres to the intestinal mucosa. It enters the bloodstream transcellularly. It binds to endothelial receptors in the blood. Upon binding, a number of inflammatory changes, induction of apoptosis, and blockade of the synthesis of a number of proteins may occur within the cell.
Stx also binds to glomerular capillary receptors, which it damages and at the same time induces local intravascular coagulation.
Diagnostics[edit | edit source]
Early symptoms include: bloody diarrhea (hemorrhagic enterocolitis), vomiting, and fever. Approximately after a week, pallor (anemia), petechiae (thrombocytopenia), oliguria, dehydration, edema (kidney failure), arterial hypertension, hematuria, and, if CNS is also affected, neurological symptoms (somnolence, impaired consciousness, convulsions, etc.) can be present.
Significant hemolytic anemia with erythrocyte deformity (schistocytes) and thrombocytopenia, which is often very severe, appear in the blood. The result of the Coombs test is negative. Increased levels of urea, creatinine, lactate dehydrogenase and bilirubin are present, while decreased levels of haptoglobin and normal levels of C3 complement are expected.
We observe proteinuria and hematuria in the urine.
One of the possible examinations is a kidney ultrasound . The pathological finding is an enlarged kidney and an echotexture in the cortex. Another method may be, for example, '"serotyping'" of E. coli or Stx detection in stool or blood.
Therapy[edit | edit source]
Therapy is symptomatic. Transfusions, furosemide, antihypertensives, and others are administered. Renal function substitution by peritoneal dialysis or hemodialysis is also possible.
Antibiotics are not recommended due to the breakdown of bacteria, which would lead to further release of Stx.
Prognosis[edit | edit source]
The decisive factor is the duration of the oligo / anuria. Spontaneous remission should occur in 1-3 weeks. If it does not occur, there is a risk of progression of glomerular filtration disorders and chronic renal failure.
D + HUS is lethal in approximately 5% of cases. Risk factors include late diagnosis, severe hyperhydration, sepsis, and extrarenal symptoms (CNS).
HUS associated with pneumococcal infection[edit | edit source]
This type of HUS arises as a complication of primary pneumococcal infection, most often in children under two years of age. It is associated with a difficult course with a mortality of around 30%. Pneumococcus produces the enzyme neuraminidase, which cleaves N-acetylmuramic acid from glycoproteins on the cell membrane of erythrocytes, platelets, and endothelial cells of glomeruli. This in turn leads to the detection of Thomsen-Friedenreich antigen (T antigen), which can then react with anti-T IgM antibodies present in the plasma.
A characteristic presentation is a positive direct Coombs' test.
Therapeutically, it is appropriate to use antibiotics or plasmapheresis. Conversely, the use of frozen plasma is contraindicated due to cold hemolysis (IgM has an ideal erythrocyte binding temperature of about 4 degrees). 
HUS induced by a complement regulation disorder[edit | edit source]
In this disorder, pathological activation of the complement system occurs. The mechanism is based on the formation of a membranolytic complex with cytotoxic activity. It arises either from a genetic mutation, or by autoantibodies, which lead to the activation of the alternative complement pathway. It can often end in spontaneous remission,  and is treated therapeutically by symptomatic adjustment of the internal environment or dialysis. Another treatment option is the use of plasmapheresis or fresh frozen plasma.
HUS with a genetic basis is usually associated with a poor prognosis. It often leads to the development of chronic renal failure with a transition to end-stage chronic renal failure. In extreme cases, it is necessary to replace kidney function. In some mutations a very high incidence of recurrence after kidney transplantation is described.
HUS arising from ADAMTS 13 protease deficiency[edit | edit source]
- HUS / TTP (thrombotic thrombocytopenic purpura)
- congenital and acquired form
- ADAMTS 13 is a metalloproteinase that cleaves multimers of von Willebrand factor, which binds platelets
- with ADAMTS 13 deficiency, thrombi form in many organs (brain, heart, kidneys)
- The clinical picture is similar to HUS, but is also accompanied by fever and more pronounced neurological and hematological symptoms.
- acute renal failure requiring dialysis is rather rare; frequent relapses, transition to chronicity;
- treatment: frozen plasma, alternatively plasmapheresis, sometimes immunosuppression, and if needed: splenectomy. 
HUS from other causes[edit | edit source]
- HUS is associated with some congenital defects of vitamin B12 metabolism - manifestation in neonatal or early infant age
- after quinine administration (drug-induced HUS)
- In case of malignancies, HUS incidence is very likely due to therapy
- in patients after organ transplants and bone marrow transplants treated with calcineurin inhibitors
- secondary forms after administration of antiaggregants (ticlodipine, clopidogrel)
- during pregnancy, most often during the 3rd trimester
- in HIV patients and in patients with systemic lupus erythematosus, antiphospholipid syndrome, and in individuals with chronic glomerulonephritis.
References[edit | edit source]
Related articles[edit | edit source]
Citations[edit | edit source]
- ZIEG, J, K BLÁHOVÁ a J DUŠEK, et al. Hemolyticko-uremický syndrom. Pediatrie pro praxi [online]. 2011, roč. 12, vol. 2, s. 102-104, dostupné
- MUNTAU, Ania Carolina. Pediatrics. 4. edition. Prague : Grada, 2009. pp. 417-419. ISBN 978-80-247-2525-3.
- LEBL, J, J JANDA a P POHUNEK, et al. Klinická pediatrie. 1. vydání. Galén, 2012. 698 s. s. 610-611. ISBN 978-80-7262-772-1.