Abstract
Hemolytic uremic syndrome is a complication in 0.4-0.6% of IPD cases, which is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The symptoms of HUS typically developed 3-13 days (most at 7-9 days) after the onset of the symptoms related to pneumococcal infection. In the circumstance of HUS, the fibrinogen level, prothrombin time, and partial thromboplastin times are usually normal or slightly elevated and active bleeding is rare. Blood transfusion with washed blood product and avoiding the plasma transfusion remains an important concept because these procedures are thought to reduce the exposure to T antigen. Renal placement therapy is indicated for anuria and deteriorated renal function.
Original language | English |
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Title of host publication | Paediatric Infectious Diseases |
Subtitle of host publication | A practical guide and cases |
Publisher | Springer Nature |
Pages | 109-113 |
Number of pages | 5 |
ISBN (Electronic) | 9789811972768 |
ISBN (Print) | 9789811972751 |
DOIs | |
State | Published - 01 01 2023 |
Bibliographical note
Publisher Copyright:© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2023.
Keywords
- Community-acquired pneumonia
- Hemolytic uremic syndrome
- Streptococcus pneumoniae
- Thomsen-Friedenreich antigen