Difference between revisions of "Atypical hemolytic uremic syndrome"
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# Cofiell R, Kukreja A, Bedard K, Yan Y, Mickle AP, Ogawa M, Bedrosian CL, Faas SJ. Eculizumab reduces complement activation, inflammation, endothelial damage, thrombosis, and renal injury markers in aHUS. Blood. 2015 May 21;125(21):3253-62. Epub 2015 Apr 1. [http://www.bloodjournal.org/content/125/21/3253.long link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449039/ link to PMC article] '''contains verified protocol''' [https://www.ncbi.nlm.nih.gov/pubmed/25833956 PubMed] | # Cofiell R, Kukreja A, Bedard K, Yan Y, Mickle AP, Ogawa M, Bedrosian CL, Faas SJ. Eculizumab reduces complement activation, inflammation, endothelial damage, thrombosis, and renal injury markers in aHUS. Blood. 2015 May 21;125(21):3253-62. Epub 2015 Apr 1. [http://www.bloodjournal.org/content/125/21/3253.long link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449039/ link to PMC article] '''contains verified protocol''' [https://www.ncbi.nlm.nih.gov/pubmed/25833956 PubMed] | ||
− | [[Category:Atypical hemolytic-uremic syndrome | + | [[Category:Atypical hemolytic-uremic syndrome regimens]] |
[[Category:Disease-specific pages]] | [[Category:Disease-specific pages]] | ||
[[Category:Complementopathies]] | [[Category:Complementopathies]] | ||
[[Category:Hemolytic disorders]] | [[Category:Hemolytic disorders]] |
Revision as of 19:21, 27 February 2019
Section editors | |||
---|---|---|---|
Shruti Chaturvedi, MBBS, MSCI Johns Hopkins University Baltimore, MD |
Benjamin Tillman, MD Vanderbilt University Nashville, TN |
2 regimens on this page
2 variants on this page
|
All lines of therapy
Eculizumab monotherapy
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Regimen
Study | Evidence |
---|---|
Legendre et al. 2013 (C08-002) | Phase II |
Legendre et al. 2013 (C08-003) | Phase II |
Cofiell et al. 2015 | Non-randomized |
Eligible patients enrolled in Cofiell et al. 2015 had platelet counts less than 150 × 109/L, hemoglobin levels less than or equal to the lower limit of normal, LDH levels greater than or equal to 1.5x upper limit of normal, serum creatinine levels greater than or equal to the upper limit of normal, ADAMTS13 activity greater than or equal to 5%, and no positive Shiga toxin-producing Escherichia coli test.
Immunosuppressive therapy
- Eculizumab (Soliris) 900 mg IV once per week for 4 weeks, then 1200 mg IV once on week 5, then 1200 mg IV every 2 weeks
Supportive medications
- Patients were vaccinated against Neisseria meningitidis or received "appropriate antibiotics" if vaccination occurred within 14 days of the first dose
Indefinite course
References
- C08-002/C08-003: Legendre CM, Licht C, Muus P, Greenbaum LA, Babu S, Bedrosian C, Bingham C, Cohen DJ, Delmas Y, Douglas K, Eitner F, Feldkamp T, Fouque D, Furman RR, Gaber O, Herthelius M, Hourmant M, Karpman D, Lebranchu Y, Mariat C, Menne J, Moulin B, Nürnberger J, Ogawa M, Remuzzi G, Richard T, Sberro-Soussan R, Severino B, Sheerin NS, Trivelli A, Zimmerhackl LB, Goodship T, Loirat C. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med. 2013 Jun 6;368(23):2169-81. link to original article PubMed
- Cofiell R, Kukreja A, Bedard K, Yan Y, Mickle AP, Ogawa M, Bedrosian CL, Faas SJ. Eculizumab reduces complement activation, inflammation, endothelial damage, thrombosis, and renal injury markers in aHUS. Blood. 2015 May 21;125(21):3253-62. Epub 2015 Apr 1. link to original article link to PMC article contains verified protocol PubMed