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危重症患者的连续性血液滤过与血小板功能

Continuous hemofiltration and platelet function in critically ill patients.

作者信息

Boldt J, Menges T, Wollbrück M, Sonneborn S, Hempelmann G

机构信息

Department of Anesthesiology and Intensive Care Medicine, Justus-Liebig-University Giessen, FRG.

出版信息

Crit Care Med. 1994 Jul;22(7):1155-60. doi: 10.1097/00003246-199407000-00018.

Abstract

OBJECTIVE

To evaluate platelet function in patients undergoing continuous pump-driven veno-venous hemofiltration.

DESIGN

Prospective study.

SETTING

Surgical intensive care unit of a university hospital.

PATIENTS

Twenty consecutive, critically ill patients with acute renal failure (serum creatinine concentration > 3.0 mg/dL (> 265 mumol/L), serum urea > 200 mg/dL (> 33 mmol/L), urine output < 20 mL/hr) secondary to sepsis or trauma. A comparable group (n = 20) without renal failure and not undergoing hemofiltration served as a control group.

INTERVENTIONS

Continuous pump-driven veno-venous hemofiltration was used in patients with renal insufficiency. Pump flow ranged from 60 to 100 mL/hr.

MEASUREMENTS AND MAIN RESULTS

Platelet function was assessed by a turbidimetric technique using a double-channel aggregometer. Aggregation was induced by adenosine diphosphate (ADP) (2.0 mumol/L), collagen (4 micrograms/mL), epinephrine (25 mumol/L), and saline solution (control). Maximum aggregation was considered to be the maximum increase in light transmission after the addition of the aggregating agents. The maximum gradient of aggregation was considered to be the maximum increase per minute. Measurements were carried out before hemofiltration (baseline values) and during the following 5 days. In the control group, blood samples were taken at corresponding data points. Eight patients undergoing continuous hemofiltration survived during the investigation period; 16 patients in the control group survived. There were no significant differences among the two groups with respect to standard coagulation variables. Maximum platelet aggregation was lower than in normal patients after the addition of all three inductors (ADP, collagen, and epinephrine). In control patients, all aggregation variables remained almost stable during the entire investigation period. In the hemofiltered patients, maximum platelet aggregation was significantly reduced (ADP, decrease of 62 relative % from baseline values; collagen, decrease of 86 relative % from baseline values; epinephrine, decrease of 77 relative % from baseline values). Maximum platelet aggregation was also depressed in these patients (ADP, decrease of 40 relative % from baseline values; collagen, decrease of 88 relative % from baseline values; epinephrine, decrease of 85 relative % from baseline values). When platelet aggregation variables were reduced greater than a decrease of 60 relative % from baseline values (in all induction groups), the mortality rate was 100%.

CONCLUSIONS

Continuous pump-driven veno-venous hemofiltration significantly changed platelet aggregability, which became obvious 2 to 3 days after the start of hemofiltration.

摘要

目的

评估接受持续泵驱动静脉 - 静脉血液滤过的患者的血小板功能。

设计

前瞻性研究。

地点

大学医院的外科重症监护病房。

患者

20例因败血症或创伤继发急性肾衰竭(血清肌酐浓度>3.0mg/dL(>265μmol/L),血清尿素>200mg/dL(>33mmol/L),尿量<20mL/小时)的连续危重症患者。一个无肾衰竭且未接受血液滤过的可比组(n = 20)作为对照组。

干预措施

肾功能不全患者采用持续泵驱动静脉 - 静脉血液滤过。泵流量范围为60至100mL/小时。

测量和主要结果

采用双通道凝集仪的比浊技术评估血小板功能。通过二磷酸腺苷(ADP)(2.0μmol/L)、胶原(4μg/mL)、肾上腺素(25μmol/L)和盐溶液(对照)诱导聚集。最大聚集被认为是加入聚集剂后透光率的最大增加。聚集的最大梯度被认为是每分钟的最大增加。在血液滤过前(基线值)和随后5天内进行测量。在对照组中,在相应数据点采集血样。8例接受持续血液滤过的患者在研究期间存活;对照组16例患者存活。两组在标准凝血变量方面无显著差异。加入所有三种诱导剂(ADP、胶原和肾上腺素)后,最大血小板聚集低于正常患者。在对照患者中,所有聚集变量在整个研究期间几乎保持稳定。在接受血液滤过的患者中,最大血小板聚集显著降低(ADP,相对于基线值降低62%;胶原,相对于基线值降低86%;肾上腺素,相对于基线值降低77%)。这些患者的最大血小板聚集也受到抑制(ADP,相对于基线值降低40%;胶原,相对于基线值降低88%;肾上腺素,相对于基线值降低85%)。当血小板聚集变量相对于基线值降低大于60%(在所有诱导组中)时,死亡率为100%。

结论

持续泵驱动静脉 - 静脉血液滤过显著改变血小板聚集性,在血液滤过开始后2至3天变得明显。

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