An update for atypical haemolytic uraemic syndrome: Diagnosis and treatment. A consensus document

被引:140
|
作者
Campistol, Josep M. [1 ]
Arias, Manuel [2 ]
Ariceta, Gema [3 ]
Blasco, Miguel [1 ]
Espinosa, Laura [4 ]
Espinosa, Mario [5 ]
Grinyo, Josep M. [6 ]
Macia, Manuel [7 ]
Mendizabal, Santiago [8 ]
Praga, Manuel [9 ]
Roman, Elena [8 ]
Torra, Roser [10 ]
Valdes, Francisco [11 ]
Vilalta, Ramon [3 ]
Rodriguez de Cordoba, Santiago [12 ]
机构
[1] Hosp Clin Barcelona, Serv Nefrol, E-08036 Barcelona, Spain
[2] Hosp Univ Marques De Valdecilla, Serv Nefrol, Santander, Spain
[3] Univ Autonoma Barcelona, Hosp Univ Maternoinfantil Vall Hebron, Serv Nefrol Pediat, E-08193 Barcelona, Spain
[4] Hosp La Paz, Serv Nefrol Pediat, Madrid, Spain
[5] Hosp Univ Reina Sofia, Serv Nefrol, Cordoba, Spain
[6] Hosp Univ Bellvitge, Serv Nefrol, Barcelona, Spain
[7] Hosp Virgen Candelaria, Serv Nefrol, Santa Cruz De Tenerife, Spain
[8] Hosp La Fe, Serv Nefrol Pediat, E-46009 Valencia, Spain
[9] Hosp Univ 12 Octubre, Serv Nefrol, Madrid, Spain
[10] Fdn Puigvert, Enfermedades Renales Hereditarias, Barcelona, Spain
[11] Complejo Hosp A Coruna, Serv Nefrol, La Coruna, Spain
[12] CSIC, Ctr Invest Biol, Dept Med Celular & Mol, Madrid, Spain
来源
NEFROLOGIA | 2015年 / 35卷 / 05期
关键词
Atypical haemolytic uraemic; syndrome; Eculizumab; Complement; Thrombotic microangiopathy; COMPLEMENT-FACTOR-H; THROMBOTIC THROMBOCYTOPENIC PURPURA; LIVER-KIDNEY TRANSPLANTATION; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; COFACTOR PROTEIN CD46; RENAL-TRANSPLANTATION; INHIBITOR ECULIZUMAB; FACTOR-I; PROPHYLACTIC ECULIZUMAB; PERIPHERAL GANGRENE;
D O I
10.1016/j.nefro.2015.07.005
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Haemolytic uraemic syndrome (HUS) is a clinical entity defined as the triad of nonimmune haemolytic anaemia, thrombocytopenia, and acute renal failure, in which the underlying lesions are mediated by systemic thrombotic microangiopathy (TMA). Different causes can induce the TMA process that characterizes HUS. In this document we consider atypical HUS (aHUS) a sub-type of HUS in which the TMA phenomena are the consequence of the endotelial damage in the microvasculature of the kidneys and other organs due to a disregulation of the activity of the complement system. In recent years, a variety of aHUs-related mutations have been identified in genes of the the complement system, which can explain approximately 60% of the aHUS cases, and a number of mutations and polymorphisms have been functionally characterized. These findings have stablished that aHUS is a consequence of the insufficient regulation of the activiation of the complement on cell surfaces, leading to endotelial damage mediated by C5 and the complement terminal pathway. Eculizumab is a monoclonal antibody that inhibits the activation of C5 and blocks the generation of the pro-inflammatory molecule C5a and the formation of the cell membrane attack complex. In prospective studies in patients with aHUS, the use of Eculizumab has shown a fast and sustained interruption of the TMA process and it has been associated with significative long-term improvements in renal function, the interruption of plasma therapy and important reductions in the need of dialysis. According to the existing literature and the accumulated clinical experience, the Spanish aHUS Group published a consensus document with recommendations for the treatment of aHUs (Nefrologia 2013;33[1]:27-45). In the current online version of this document, we update the aetiological classification of TMAs, the pathophysiology of aHUS, its differential diagnosis and its therapeutic management. (C) 2015 Sociedad Espanola de Nefrologia. Published by Elsevier Espana, S.L.U.
引用
收藏
页码:421 / 447
页数:27
相关论文
共 50 条
  • [1] An update for atypical haemolytic uraemic syndrome: diagnosis and treatment. A consensus document
    Campistol, Josep M.
    Arias, Manuel
    Ariceta, Gema
    Blasco, Miguel
    Espinosa, Mario
    Grinyo, Josep M.
    Praga, Manuel
    Torra, Roser
    Vilalta, Ramon
    Rodriguez de Cordoba, Santiago
    NEFROLOGIA, 2013, 33 (01): : 27 - 45
  • [2] A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome
    Westra, D.
    Wetzels, J. F. M.
    Volokhina, E. B.
    van den Heuvel, L. P.
    van de Kar, N. C. A. J.
    NETHERLANDS JOURNAL OF MEDICINE, 2012, 70 (03): : 121 - 129
  • [3] The Spanish atypical haemolytic uraemic syndrome registry: A genetic update
    de Jorge, Elena Goicoechea
    Barricarte, Ruben Martinez
    Tortajada, Agustin
    Montes, Tamara
    Pinto, Sheila
    Garrido, Cyn-Thia Aberrategui
    Lopez-Trascasa, Margarita
    Sanchez-Corral, Pilar
    de Cordoba, Santiago Rodriguez
    MOLECULAR IMMUNOLOGY, 2007, 44 (16) : 3923 - 3923
  • [4] Atypical haemolytic uraemic syndrome
    Kavanagh, David
    Goodship, Timothy H. J.
    Richards, Anna
    BRITISH MEDICAL BULLETIN, 2006, 77-78 : 5 - 22
  • [5] Early treatment with eculizumab in atypical haemolytic uraemic syndrome
    Garjau, Maria
    Azancot, Maria
    Ramos, Rosa
    Sanchez-Corral, Pilar
    Angeles Montero, Maria
    Seron, Daniel
    CLINICAL KIDNEY JOURNAL, 2012, 5 (01) : 31 - 33
  • [6] Interventions for atypical haemolytic uraemic syndrome
    Pugh, Dan
    O'Sullivan, Eoin D.
    Duthie, Fiona Ai
    Masson, Philip
    Kavanagh, David
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2021, (03):
  • [7] Atypical haemolytic uraemic syndrome and its treatment: A case report
    Khan, Azhar Ali
    Ahraf, Muhammad Usman
    Javaid, Usman
    JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION, 2021, 71 (05) : 1496 - 1498
  • [8] Atypical haemolytic uraemic syndrome in a postpartum patient
    Hierholzer, Ashton
    Majdinasab, Elleana
    Young, Madeline
    Kauffman, Robert P.
    BMJ CASE REPORTS, 2023, 16 (11)
  • [9] Cardiovascular complications in atypical haemolytic uraemic syndrome
    Noris, Marina
    Remuzzi, Giuseppe
    NATURE REVIEWS NEPHROLOGY, 2014, 10 (03) : 174 - 180
  • [10] Cardiovascular complications in atypical haemolytic uraemic syndrome
    Marina Noris
    Giuseppe Remuzzi
    Nature Reviews Nephrology, 2014, 10 : 174 - 180