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Hemolytic-uremic syndrome

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Title: Hemolytic-uremic syndrome  
Author: World Heritage Encyclopedia
Language: English
Subject: Zoonosis, Acquired hemolytic anemia, Verotoxin-producing Escherichia coli, List of MeSH codes (C15), Thrombotic thrombocytopenic purpura
Collection: Acquired Hemolytic Anemia, Blood Disorders, Nephrology, Syndromes
Publisher: World Heritage Encyclopedia

Hemolytic-uremic syndrome

Hemolytic-uremic syndrome
Schistocytes as seen in a person with hemolytic-uremic syndrome
Classification and external resources
Specialty Nephrology
ICD-10 D59.3
ICD-9-CM 283.11
OMIM 235400
DiseasesDB 13052
MedlinePlus 000510
eMedicine ped/960
MeSH D006463

Hemolytic-uremic syndrome (or haemolytic-uraemic syndrome), abbreviated HUS, is a disease characterized by hemolytic anemia (anemia caused by destruction of red blood cells), acute kidney failure (uremia), and a low platelet count (thrombocytopenia). It predominantly, but not exclusively, affects children. Most cases are preceded by an episode of infectious, sometimes bloody, diarrhea acquired as a foodborne illness or from a contaminated water supply and caused by E. coli O157:H7, although Shigella, Campylobacter and a variety of viruses have also been implicated. It is now the most common cause of acquired acute renal failure in childhood. It is a medical emergency and carries a 5–10% mortality; of the remainder, the majority recover without major consequences but a small proportion develop chronic kidney disease and become reliant on renal replacement therapy.The primary target appears to be the vascular endothelial cell. This may explain the pathogenesis of HUS, in which a characteristic renal lesion is capillary microangiopathy.[1]

HUS was first defined as a

  • GeneReviews/NCBI/NIH/UW entry on Atypical hemolytic-uremic syndrome
  • Haemolytic Uraemic Syndrome Help (UK Based Charity for Information and Support)
  • aHUS UK – A Patients and Families Support Group for atypical Haemolytic Uraemic Syndrome
  • Atypical HUS and Complement Deficiencies - Clinical Immunology

External links

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  20. ^ a b c d Zuber, J; Le Quintrec, M; Sberro-Scussan, R; Loirat, C; Fremaux-Bacchi, V; Legendre, C (2011). "New insights into postrenal transplant hemolytic uremic syndrome". Nature Reviews Nephrology 7 (1): 23–35.  
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  22. ^ a b c Neuhaus, TJ; Calonder, S; Leumann, EP (1997). "Heterogeneity of atypical haemolytic uraemis syndromes". Arch Dis Child 76 (6): 518–521.  
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  25. ^ a b c Tsai, H-M (2010). "Pathophysiology of thrombotic thrombocytopenic purpura". Int J Hematol 91 (1): 1–19.  
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  27. ^ Michon, B; et al. (2007). "Complications of apheresis in children". Transfusion 47 (10): 1837–1842.  
  28. ^ Collins, Allan J.; et al. (2010). "Excerpts from the US Renal Data System 2009 Annual Data Report". Am J Kidney Dis 55: S1–S7.  
  29. ^ European Renal Association- European Dialysis and Transplant Association Registry (2011). ERA-EDTA Registry Annual Report 2009. Amsterdam, The Netherlands: Academic Medical Center Department of Medical Informatics. 
  30. ^ "Soliris (eculizumab) prescribing information" (PDF). Cheshire, CT: Alexion Pharmaceuticals. 2011. 
  31. ^ a b Palermo, MS; Exeni, RA; Fernandez, GC (2009). "Hemolytic Uremic Syndrome: pathogenesis and update of interventions". Expert Rev Anti Infect Ther 7 (6): 697–707.  
  32. ^ Robert Koch Institute. "Technical Report: EHEC/HUS O104:H4 Outbreak, Germany, May/June 2011" (PDF). Berlin, Germany: Robert Koch Institute. 
  33. ^ Psotka, MA; et al. (2009). "Shiga toxin 2 targets the murine renal collecting duct epithelium". Infect Immun 77 (3): 959–969.  
  34. ^ Zoja, C; Buelli, S; Morigi, M (2010). "Shoga toxin-associated hemolytic uremic syndrome: pathophysiology of endothelial dysfunction". Pediatr Nephrol 25 (11): 2231–2240.  
  35. ^ Guessous, F; et al. (2005). "Shiga toxin 2 and lipopolysaccharide induce human microvascular endothelial cells to release chemokines and factor that stimulate platelet function". Infect Immun 73 (12): 8306–8316.  
  36. ^ Orth, D; Würzner, R (2010). "Complement in typical hemolytic uremic syndrome". Semin thromb Hemost 36 (3): 620–624.  
  37. ^ Stahl, AL; Startz, L; Karpman, D (2011). "Complement activation on platelet-leukocyte complexes and microparticles in enterohemorrhagic Escherichia coli-induced hemolytic uremic syndrome". Blood 117 (20): 5503–5513.  
  38. ^ Thurman, J.M.; et al. (2009). "Alternative pathway of complement in children with diarrhea-associated hemolytic uremic syndrome". Clin J Am Soc Nephrol 4 (12): 1920–1924.  
  39. ^ a b Mache, C; et al. (June 2010). "Eculizumab in diarrhea-associated hemolytic uremic syndrome". Presented at the 2nd International Conference on HUS-MPGN-PNH (Innsbruck, Austria). 
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  44. ^ Al-Akash, AI; Almond, PS; Savell, VH Jr; Gharaybeth, SI; Hogue, C (2011). "Eculizumab includes long-term remission in recurrent post-transpant HUS associated with C3 gene mutation". Pediatr Nephrol 26 (4): 613–619.  
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  46. ^ Zhen,, XL; et al. (2010). "Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura". Haematologica 95 (9): 1555–1562.  
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See also

In May, 2011 an epidemic of bloody diarrhea caused by E. coli O104:H4-contaminated fenugreek seeds hit Germany. Tracing the epidemic revealed more than 3,800 cases, with HUS developing in more than 800 of the cases, including 36 fatal cases. Nearly 90% of the HUS cases were in adults.[56][57] In response to the crisis, Alexion Pharmaceuticals, Inc., the makers of Soliris (eculizumab), initiated of an open-label clinical trial to investigate eculizumab as a treatment for patients with Shiga-toxin-producing E. coli hemolytic uremic syndrome (STEC-HUS). Alexion also initiated an eculizumab access program whereby the company provided eculizumab free of charge throughout the crisis. The study was designed to include all patients treated with eculizumab during the 2011 STEC-HUS outbreak.[58]

HUS and the E. coli infections that cause it have been the source of much negative publicity for the FDA, meat industries, and fast-food restaurants since the 1990s, especially in the contaminations linked to Jack in the Box restaurants. The disease was also featured in the Robin Cook novel Toxin. In 2006, an epidemic of harmful E. coli emerged in the United States due to contaminated spinach. In June, 2009, Nestle Toll House cookie dough was linked to an outbreak of E. coli 0157:H7 in the United States, which sickened 70 people in 30 states.[1]

In the United States, the overall incidence of HUS is estimated at 2.1 cases per 100,000 persons/year,[42] with a peak incidence between six months and four years of age.[1]

The country with the highest incidence of HUS is Argentina [52][53][54][55] and it performs a key role in the research of this condition.


Acute renal failure occurs in 55-70% of patients with STEC-HUS, although up to 70-85% recover renal function.[50] Patients with aHUS generally have poor outcomes, with up to 50% progressing to ESRD or irreversible brain damage; as many as 25% die during the acute phase.[50] However, with aggressive treatment, more than 90% of patients survive the acute phase of HUS, and only about 9% may develop ESRD. Roughly one-third of persons with HUS have abnormal kidney function many years later, and a few require long-term dialysis. Another 8% of persons with HUS have other lifelong complications, such as high blood pressure, seizures, blindness, paralysis, and the effects of having part of their colon removed. The overall mortality rate from HUS is 5-15%. Children and the elderly have a worse prognosis.[51]


There are case reports of experimental treatments with eculizumab, a monoclonal antibody that blocks part of the complement system, being used to treat congenital atypical hemolytic uremic syndrome,[48] as well as severe shiga-toxin associated hemolytic uremic syndrome.[49] These have shown promising results. Eculizumab was approved by the U.S. Food and Drug Administration (FDA) on March 13, 2007 for the treatment of paroxysmal nocturnal hemoglobinuria (PNH), a rare, progressive, and sometimes life-threatening disease characterized by excessive hemolysis; and on September 23, 2011 for the treatment of atypical hemolytic uremic syndrome (aHUS) It was approved by the European Medicines Agency for the treatment of PNH on June 20, 2007, and on November 29, 2011 for the treatment of aHUS. However, of note is the exceedingly high cost of treatment, with one year of the drug costing over $500,000.

In most children with postdiarrheal HUS, there is a good chance of spontaneous resolution, so observation in a hospital is often all that is necessary, with supportive care such as hemodialysis where indicated. If a diagnosis of STEC-HUS is confirmed, plasmapheresis (plasma exchange) is contraindicated. However, plasmapheresis may be indicated when there is diagnostic uncertainty between HUS and TTP.

Treatment of HUS is generally supportive, with dialysis as needed. Platelet transfusion may actually worsen the outcome.

The effect of antibiotics in E. coli O157:H7 colitis is controversial. Certain antibiotic may stimulate further verotoxin production and thereby increase the risk of HUS.[40][47] However, there is also tentative evidence that some antibiotics like quinolones may decrease the risk of hemolytic uremic syndrome.[47]


Diagnostic work-up supports the differential diagnosis of TMA-causing diseases. A positive Shiga-toxin/EHEC test confirms an etiological cause for STEC-HUS,[23][31] and severe ADAMTS13 deficiency (i.e., ≤5% of normal ADAMTS13 levels) confirms a diagnosis of TTP.[46]

The similarities between HUS, aHUS, and TTP make differential diagnosis essential.[7][8] All three of these systemic TMA-causing diseases are characterized by thrombocytopenia[14] and microangiopathic hemolysis,[6][14] plus one or more of the following: neurological symptoms (e.g., confusion,[6][22] cerebral convulsions,[22] seizures[19]); renal impairment[14] (e.g., elevated creatinine,[15] decreased estimated glomerular filtration rate [eGFR],[15] abnormal urinalysis[44] ); and gastrointestinal (GI) symptoms (e.g., diarrhea,[17][20] nausea/vomiting,[19] abdominal pain,[19] gastroenteritis[14][17]).The presence of diarrhea does not exclude aHUS as the etiology of TMA, as 28% of patients with aHUS present with diarrhea and/or gastroenteritis.[16][17] First diagnosis of aHUS is often made in the context of an initial, complement-triggering infection, and Shiga-toxin has also been implicated as a trigger that identifies patients with aHUS.[39] Additionally, in one study, mutations of genes encoding several complement regulatory proteins were detected in 8 of 36 (22%) patients diagnosed with STEC-HUS.[45] However, the absence of an identified complement regulatory gene mutation does not preclude aHUS as the etiology of the TMA, as approximately 50% of patients with aHUS lack an identifiable mutation in complement regulatory genes.[17]


[14][8][7], and/or the presence of schistocytes.hemoglobin hemolysis, which is characterized by elevated LDH levels, decreased haptoglobin, decreased microangiopathic and evidence of [14] (platelet count below 150,000 or a decrease from baseline of at least 25%)thrombocytopenia Early signs of systemic complement-mediated TMA include [25][16][7] This leads to [6] Unlike typical HUS, aHUS does not follow STEC infection and is thought to result from one or several genetic mutations that cause chronic, uncontrolled, and excessive activation of complement.

STEC-HUS most often affects infants and young children, but also occurs in adults. The most common form of transmission is ingestion of undercooked meat, unpasteurized fruits and juices, contaminated produce, contact with unchlorinated water, and person-to-person transmission in daycare or long-term care facilities.[23]

HUS occurs after 3-7% of all sporadic E. coli O157:H7 infections and up to approximately 20% or more of epidemic infections.[42] Children and adolescents are commonly affected.[43] Grossly, the kidneys may show patchy or diffuse renal cortical necrosis. Histologically, the glomeruli show thickened and sometimes split capillary walls due largely to endothelial swelling. Large deposits of fibrin-related materials in the capillary lumens, subendothelially, and in the mesangium are also found along with mesangiolysis. Interlobular and afferent arterioles show fibrinoid necrosis and intimal hyperplasia and are often occluded by thrombi.[10]

In contrast with typical disseminated intravascular coagulation seen with other causes of septicemia and occasionally with advanced cancer, coagulation factors are not consumed in HUS (or TTP) and the coagulation screen, fibrinogen level, and assays for fibrin degradation products such as "D-Dimers", are generally normal despite the low platelet count (thrombocytopenia).[41]

[41] As in the related condition TTP, reduced blood flow through the narrowed blood vessels of the [40] The consumption of platelets as they adhere to the thrombi lodged in the small vessels typically leads to mild or moderate thrombocytopenia with a platelet count of less than 60,000 per microliter.

Shiga-toxin directly activates the alternative complement pathway and also interferes with complement regulation by binding to complement factor H, an inhibitor of the complement cascade. Shiga-toxin causes complement-mediated platelet, leukocyte, and endothelial cell activation, resulting in systemic hemolysis, inflammation and thrombosis.[36][37][38] Severe clinical complications of TMA have been reported in patients from 2 weeks to more than 44 days after presentation with STEC-HUS, with improvements in clinical condition extending beyond this time frame, suggesting that complement activation persists beyond the acute clinical presentation and for at least 4 months.[39]

The typical pathophysiology of HUS involves the binding of Shiga-toxin to the globotriaosylceramide (Gb3; also called ceramide trihexoside which accumulates in Fabry disease) receptor on the surface of the glomerular endothelium.[33] This action includes a cascade of signaling events leading to apoptosis and binding of leukocytes to endothelial cells. The Shiga-toxin-activated endothelial cells then become thrombogenic (clot-producing) by mechanism that is not fully understood,[34] though they have been shown to induce the release of cytokines and chemokines that are implicated in platelet activation.[35] Additionally, the binding action of Shiga-toxin inactivates a metalloproteinase called ADAMTS13, the deficiency of which causes the closely related TTP. Once ADAMTS13 is disabled, multimers of von Willebrand Factor (vWF) form and initiate platelet activation, causing microthrombus formation. The activation of platelets resulting from inhibition of ADAMTS13 is due to the hyperactivity of large multimers of uncleaved vWF. The arterioles and capillaries of the body become obstructed by the resulting complexes of activated platelets, which have adhered to the endothelium via large multimeric vWF. Through a mechanism known as microangiopathic hemolysis, the growing thrombi lodged in smaller vessels destroy red blood cells (RBCs) as they squeeze through the narrowed blood vessels, forming schistocytes, or fragments of sheared RBCs.[25] The presence of schistocytes is a key finding that helps to diagnose HUS. Typically, this hemolysis results in a hemoglobin level of less than 80 g/L.

HUS is one of the thrombotic microangiopathies, a category of disorders that includes STEC-HUS, aHUS, and thrombotic thrombocytopenic purpura (TTP). STEC-HUS is usually preceded by a prodrome of diarrhea, which is often bloody, and is caused by Shiga-like toxin-producing bacteria such as enterohemorrhagic Escherichia coli (EHEC), of which E. coli O157:H7 is the most common serotype.[31] Other serotypes also cause disease and can emerge as new causes of STEC-HUS, as occurred with E. coli O104:H4, which triggered a 2011 epidemic of STEC-HUS in Germany.[32]


Historically, treatment options for aHUS were limited to [26][27] and has not been proven effective in any controlled clinical trials. Patients with aHUS and ESRD have also had to undergo lifelong dialysis, which has a 5-year survival rate of 34-38%.[28][29] In recent years the monoclonal antibody eculizumab (INN and USAN, trade name Soliris), a first-in-class terminal complement inhibitor, has been shown in clinical studies to block terminal complement activity in children and adults with aHUS, and to eliminate the need for PE/PI and new dialysis. In these studies eculizumab was associated with reduced TMA activity, as shown by improvement in platelet counts and kidney function, as well as hematologic normalization, complete TMA response, and TMA event-free status in a majority of patients.[30]

[18][8] Patients who survive the presenting signs and symptoms of aHUS endure a chronic thrombotic and inflammatory state, which puts them at lifelong elevated risk of sudden blood clotting, kidney failure, other severe complications and premature death.[20] and 65% of patients will die, require dialysis, or have permanent renal damage within the first year after diagnosis despite plasma exchange or plasma infusion (PE/PI) therapy.[21][20](ESRD) with the first clinical manifestation of aHUS,end-stage renal disease Despite the use of supportive care, an estimated 33-40% of patients will die or have [14][8][7] and evidence of microangiopathic hemolysis, which is characterized by elevated LDH levels, decreased haptoglobin, decreased hemoglobin (the oxygen-containing component of blood), and/or the presence of schistocytes.[14] (platelet count below 150,000 or a decrease from baseline of at least 25%)thrombocytopenia Early signs of systemic complement-mediated TMA include [25][16][7] This results in platelet activation [6] and is largely due to one or several genetic mutations that cause chronic, uncontrolled, and excessive activation of complement.[6] Atypical HUS (aHUS) represents 5-10% of HUS cases

Atypical HUS

[24][16][13][7][6] elevated [13] low platelet count,[12] Patients with HUS commonly exhibit the signs and symptoms of thrombotic microangiopathy (TMA), which can include abdominal pain,

STEC-HUS occurs after ingestion of a strain of bacteria, usually types of E. coli, that expresses verotoxin (also called Shiga-like toxin). Bloody diarrhea typically follows. HUS develops about 5–10 days after onset of diarrhea, with decreased urine output (oliguria), blood in the urine (hematuria), kidney failure, thrombocytopenia (low levels of platelets) and destruction of red blood cells (microangiopathic hemolytic anemia). Hypertension is common. In some cases, there are prominent neurologic changes.[9][10][11]

Signs and symptoms


  • Signs and symptoms 1
  • Atypical HUS 2
  • Pathogenesis 3
  • Diagnosis 4
  • Treatment 5
  • Prognosis 6
  • Epidemiology 7
  • See also 8
  • References 9
  • External links 10


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