Abid O, Sun Q, Sugimoto K, Mercan D, Vincent J L
Department of Intensive Care, Erasme University Hospital, Free University of Brussels, Belgium.
Chest. 2001 Dec;120(6):1984-8. doi: 10.1378/chest.120.6.1984.
To evaluate the predictive value of microalbuminuria in the development of acute respiratory failure (ARF) and multiple organ failure (MOF) in ICU patients.
Prospective, observational study.
A 31-bed, mixed medicosurgical ICU in a university hospital.
All adult medical patients admitted to the ICU over a 2-month period, except those receiving nephrotoxic drugs, or those with urologic trauma resulting in frank hematuria or urinary infection, or with existing chronic renal disease (serum creatinine level > or 2.0 mg/dL).
None.
Urinary samples for microalbumin measurement were collected at hospital admission and at 8, 24, 48, 72, 96, and 120 h after hospital admission. The severity of illness was assessed by the APACHE (acute physiology and chronic health evaluation) II score calculated on the first ICU day, and the degree of organ dysfunction was assessed using the sequential organ failure assessment (SOFA) score. Acute respiratory failure (ARF) was defined as a SOFA respiratory score > or = 3. Patients were separated into two groups according to the trend in microalbuminuria levels over the first 48 h: patients in group 1 had increasing microalbuminuria levels, and patients in group 2 had decreasing microalbuminuria levels. Group 1 included 14 patients in whom microalbuminuria levels increased from 5.2 +/- 2.0 to 19.0 +/- 3.0 mg/dL. Group 2 included 26 patients in whom microalbuminuria levels decreased from 16.4 +/- 4.0 to 7.8 +/- 3.0 mg/dL. The hospital mortality rate was 43% in group 1 and 15% in group 2 (p < 0.05). The APACHE II score and the SOFA score were higher in group 1 than in group 2. The negative predictive value of increasing microalbuminuria was 100% for the development of ARF and 96% for MOF; the positive predictive value of increasing microalbuminuria was 57% for the development of ARF and 50% for MOF.
Accurate identification of patients destined for ARF and MOF development may enable therapeutic strategies to be applied to limit the disease process. Trend analysis of urinary albumin excretion over the first 48 h of an ICU admission may provide a useful means of identifying such patients. Additional studies need to be performed in larger, mixed patient populations to confirm these findings.
评估微量白蛋白尿对重症监护病房(ICU)患者发生急性呼吸衰竭(ARF)和多器官功能衰竭(MOF)的预测价值。
前瞻性观察性研究。
某大学医院一间有31张床位的内外科混合ICU。
在2个月期间入住该ICU的所有成年内科患者,但接受肾毒性药物治疗的患者、因泌尿系统创伤导致肉眼血尿或尿路感染的患者,或已患有慢性肾病(血清肌酐水平>或2.0mg/dL)的患者除外。
无。
在入院时以及入院后8、24、48、72、96和120小时采集尿样以测定微量白蛋白。在入住ICU的第一天通过计算急性生理与慢性健康状况评估(APACHE)II评分评估疾病严重程度,并使用序贯器官衰竭评估(SOFA)评分评估器官功能障碍程度。急性呼吸衰竭(ARF)定义为SOFA呼吸评分>或=3。根据最初48小时内微量白蛋白尿水平的变化趋势将患者分为两组:第1组患者的微量白蛋白尿水平升高,第2组患者的微量白蛋白尿水平降低。第1组包括14例患者,其微量白蛋白尿水平从5.2±2.0mg/dL升高至19.0±3.0mg/dL。第2组包括26例患者,其微量白蛋白尿水平从16.4±4.0mg/dL降至7.8±3.0mg/dL。第1组的医院死亡率为43%,第2组为15%(p<0.05)。第1组的APACHE II评分和SOFA评分高于第2组。微量白蛋白尿增加对ARF发生的阴性预测值为100%,对MOF发生的阴性预测值为96%;微量白蛋白尿增加对ARF发生的阳性预测值为57%,对MOF发生的阳性预测值为50%。
准确识别有发生ARF和MOF风险的患者可能有助于应用治疗策略来限制疾病进展。对入住ICU最初48小时内尿白蛋白排泄进行趋势分析可能是识别此类患者的有用方法。需要在更大规模的混合患者群体中进行更多研究以证实这些发现。