Inclusion criteria | |
• SAH confirmed by CT and aneurysm by CTA or DSA | |
• Admission to the UMC Utrecht < 12 h after ictus | |
• Age 18 years and older | |
Exclusion criteria | |
• Life expectancy < 10 days | |
• Pregnant or breastfeeding women | |
• Participation in another clinical therapeutic study | |
• History of splenectomy or asplenia | |
• Haematologic malignancy | |
• Patients receiving chemotherapy | |
• Patients who will undergo or underwent an organ transplantation | |
• Patients with myasthenia gravis, glucose-6-phosphate dehydrogenase (G6PD) deficiency, or tuberculosis | |
• Patients who are or will be treated by plasmapheresis or haemodialysis | |
• Patient with a creatinine clearance of < 30 or serum creatinine levels of > 169 μmol/l | |
• Patients with a known hereditary complement deficiency | |
• Patients allergic to eculizumab, proteins derived from mouse products, or other monoclonal antibodies | |
• Patients allergic to (prophylactic) antibiotic treatment for Neisseria meningitidis (quinolones or ceftriaxone) | |
• If on admission, it is likely that the aneurysm can only be treated with extracranial-intracranial bypass surgery | |
• If based on head imaging, it will be unlikely that CSF can be obtained at day 3 after ictus | |
• Patients with an ongoing infection on admission which is not appropriately treated | |
• Patients who were treated > 4 times with antibiotics during the last year | |
• Patients on immunosuppressive therapy |