Hemolytic-uremic syndrome (HUS), which is characterized by microvascular hemolytic anemia, consumption thrombocytopenia, and acute renal failure, is a complication of the Shiga-toxin-producing Escherichia coli (STEC) infection. We describe the case of a patient who, despite undergoing plasma exchange and renal replacement therapy for STEC-induced HUS, experienced poor improvement in platelet count, serum creatinine level, and serum lactate dehydrogenase level. The patient developed acute encephalopathy but recovered without permanent organ damage after eculizumab therapy. For severe HUS cases involving the central nervous system, early administration of eculizumab, which inhibits the abnormal activation of the complement activation pathway, may be effective.
Published in | American Journal of Clinical and Experimental Medicine (Volume 6, Issue 1) |
DOI | 10.11648/j.ajcem.20180601.15 |
Page(s) | 27-32 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2018. Published by Science Publishing Group |
Hemolytic-Uremic Syndrome, Shiga-Toxin-Producing Escherichia coli Infection, Acute Encephalopathy, Eculizumab
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APA Style
Takahiro Yukawa, Takuto Ishida, Toshinobu Yamagishi, Kazuhiro Sugiyama, Yuichi Hamabe. (2018). Administration of Eculizumab, a C5 Inhibitor, for the Treatment of Shiga-Toxin-Producing Escherichia coli Infection: A Case Report. American Journal of Clinical and Experimental Medicine, 6(1), 27-32. https://doi.org/10.11648/j.ajcem.20180601.15
ACS Style
Takahiro Yukawa; Takuto Ishida; Toshinobu Yamagishi; Kazuhiro Sugiyama; Yuichi Hamabe. Administration of Eculizumab, a C5 Inhibitor, for the Treatment of Shiga-Toxin-Producing Escherichia coli Infection: A Case Report. Am. J. Clin. Exp. Med. 2018, 6(1), 27-32. doi: 10.11648/j.ajcem.20180601.15
AMA Style
Takahiro Yukawa, Takuto Ishida, Toshinobu Yamagishi, Kazuhiro Sugiyama, Yuichi Hamabe. Administration of Eculizumab, a C5 Inhibitor, for the Treatment of Shiga-Toxin-Producing Escherichia coli Infection: A Case Report. Am J Clin Exp Med. 2018;6(1):27-32. doi: 10.11648/j.ajcem.20180601.15
@article{10.11648/j.ajcem.20180601.15, author = {Takahiro Yukawa and Takuto Ishida and Toshinobu Yamagishi and Kazuhiro Sugiyama and Yuichi Hamabe}, title = {Administration of Eculizumab, a C5 Inhibitor, for the Treatment of Shiga-Toxin-Producing Escherichia coli Infection: A Case Report}, journal = {American Journal of Clinical and Experimental Medicine}, volume = {6}, number = {1}, pages = {27-32}, doi = {10.11648/j.ajcem.20180601.15}, url = {https://doi.org/10.11648/j.ajcem.20180601.15}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajcem.20180601.15}, abstract = {Hemolytic-uremic syndrome (HUS), which is characterized by microvascular hemolytic anemia, consumption thrombocytopenia, and acute renal failure, is a complication of the Shiga-toxin-producing Escherichia coli (STEC) infection. We describe the case of a patient who, despite undergoing plasma exchange and renal replacement therapy for STEC-induced HUS, experienced poor improvement in platelet count, serum creatinine level, and serum lactate dehydrogenase level. The patient developed acute encephalopathy but recovered without permanent organ damage after eculizumab therapy. For severe HUS cases involving the central nervous system, early administration of eculizumab, which inhibits the abnormal activation of the complement activation pathway, may be effective.}, year = {2018} }
TY - JOUR T1 - Administration of Eculizumab, a C5 Inhibitor, for the Treatment of Shiga-Toxin-Producing Escherichia coli Infection: A Case Report AU - Takahiro Yukawa AU - Takuto Ishida AU - Toshinobu Yamagishi AU - Kazuhiro Sugiyama AU - Yuichi Hamabe Y1 - 2018/03/08 PY - 2018 N1 - https://doi.org/10.11648/j.ajcem.20180601.15 DO - 10.11648/j.ajcem.20180601.15 T2 - American Journal of Clinical and Experimental Medicine JF - American Journal of Clinical and Experimental Medicine JO - American Journal of Clinical and Experimental Medicine SP - 27 EP - 32 PB - Science Publishing Group SN - 2330-8133 UR - https://doi.org/10.11648/j.ajcem.20180601.15 AB - Hemolytic-uremic syndrome (HUS), which is characterized by microvascular hemolytic anemia, consumption thrombocytopenia, and acute renal failure, is a complication of the Shiga-toxin-producing Escherichia coli (STEC) infection. We describe the case of a patient who, despite undergoing plasma exchange and renal replacement therapy for STEC-induced HUS, experienced poor improvement in platelet count, serum creatinine level, and serum lactate dehydrogenase level. The patient developed acute encephalopathy but recovered without permanent organ damage after eculizumab therapy. For severe HUS cases involving the central nervous system, early administration of eculizumab, which inhibits the abnormal activation of the complement activation pathway, may be effective. VL - 6 IS - 1 ER -