DRKS00025079已完成不适用
Pilot study on the use of albumin function test by ESR method in ICU patients for the detection of sepsis/septic shock and its follow-up.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 26
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Sepsis Group
- •- At least 18 years
- •- Patients diagnosed with sepsis as defined by Sepsis-3 (life-threatening organ dysfunction caused by a dysregulated immune response to infection.
- •Clinical Criteria: SOFA score =2, screening tool: qSOFA at least 2 of 3 (AF=22/min; RR syst. =100mmHg; impaired mental status: GCS<15).
- •Septic shock
- •- At least 18 yrs.
- •- Septic shock = sepsis + cardiovascular collapse unresponsive to hydration and vasopressors necessary to maintain MAP > 65mmHg, lactate = 2 mmol/L
- •Control group
- •- At least 18 yrs.
- •- Patient -of the intensive care unit of the Internal Medicine of the University Medical Center Rostock without sepsis / septic shock.
- •- If sepsis / septic shock occurs within 7 days, the patient will be kept as control group 2, but an additional control patient without sepsis / septic shock will be included in the study
- •Translated with www.DeepL.com/Translator (free version)
排除标准
- •Extracorporeal treatment with citrate anticoagulation ongoing at the time of blood collection;
- •Albumin substitution;
- •More than 500ml of FFP or red cell concentrate 12 hours prior to blood collection;
- •Patients with liver cirrhosis;
研究者
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