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接受全胃肠外营养的低白蛋白血症患者静脉输注人血白蛋白的随机双盲研究。

Randomized, double-blind study of intravenous human albumin in hypoalbuminemic patients receiving total parenteral nutrition.

作者信息

Rubin H, Carlson S, DeMeo M, Ganger D, Craig R M

机构信息

Department of Medicine, Northwestern University Medical School and Northwestern Memorial Hospital, Chicago, IL 60611, USA.

出版信息

Crit Care Med. 1997 Feb;25(2):249-52. doi: 10.1097/00003246-199702000-00009.

DOI:10.1097/00003246-199702000-00009
PMID:9034259
Abstract

OBJECTIVE

To determine whether replacement of human albumin will improve a patient's prognosis.

DESIGN

A randomized, double-blind, controlled study in which 25 g of human albumin vs. placebo was administered intravenously daily.

SETTING

A university-affiliated hospital.

PATIENTS

Thirty-six patients with hypoalbuminemia (serum albumin of <2.5 g/dL), receiving total parenteral nutrition. None of the patients had known cancer, cirrhosis, or nephrotic syndrome.

INTERVENTIONS

Each patient received at least 6 days of therapy (6 to 24 days of albumin; 7 to 32 days of placebo). Four subjects were excluded from the study since they received therapy for <6 days. One patient was excluded from the study after nephrotic syndrome was identified. Albumin metabolic rates for those patients receiving albumin were estimated using the formula: Metabolism of albumin = 25 g/day + (albumin 1 - albumin 2)(Vd)/days, where albumin 1 and 2 are the serum albumin concentrations (g/L) at the beginning and end of the serum sampling intervals, respectively; Vd is the volume of distribution (L); and days relates to the number of days of the sampling interval.

MEASUREMENTS AND MAIN RESULTS

Sixteen patients received albumin; 15 patients received placebo. One patient receiving placebo and two patients receiving albumin died within 30 days. One patient who received placebo and three patients who received albumin developed sepsis or bacteremia; four patients who received placebo and seven patients who received albumin developed pneumonia during the study (NS). The serum albumin increased in all patients receiving intravenous albumin, but one patient received intravenous albumin for only 6 days. The mean serum albumin concentration increased by 1.42 g/dL in the albumin patients, and increased by 0.29 in the placebo patients (p < .0001 by unpaired t-test). Mean initial albumin metabolism was 17.4 g/day (0.3 g/kg/day). At the end of therapy, albumin metabolism was 20.5 g/day (0.36 g/kg/day) (paired t-test, p = .4, NS).

CONCLUSIONS

a) The administration of intravenous albumin to hypoalbuminemic patients receiving total parenteral nutrition does not improve morbidity or mortality. b) Albumin metabolic rates, initially related to the catabolic state, are high; later, these rates are high related to filling of the albumin space and gluconeogenesis. c) On the basis of the high albumin catabolic rates at the end of the infusion, doses of albumin of <25 g/day might be sufficient to replace albumin stores.

摘要

目的

确定输注人血白蛋白是否会改善患者的预后。

设计

一项随机、双盲、对照研究,每天静脉注射25 g人血白蛋白或安慰剂。

地点

一家大学附属医院。

患者

36例低白蛋白血症患者(血清白蛋白<2.5 g/dL),接受全胃肠外营养。所有患者均无已知癌症、肝硬化或肾病综合征。

干预措施

每位患者接受至少6天的治疗(白蛋白治疗6至24天;安慰剂治疗7至32天)。4名患者因治疗时间不足6天被排除在研究之外。1例患者在确诊为肾病综合征后被排除在研究之外。使用以下公式估算接受白蛋白治疗患者的白蛋白代谢率:白蛋白代谢量=25 g/天 +(白蛋白1 - 白蛋白2)(分布容积)/天数,其中白蛋白1和2分别是血清采样间隔开始和结束时的血清白蛋白浓度(g/L);分布容积(L);天数为采样间隔的天数。

测量指标及主要结果

16例患者接受白蛋白治疗;15例患者接受安慰剂治疗。1例接受安慰剂治疗的患者和2例接受白蛋白治疗的患者在30天内死亡。1例接受安慰剂治疗的患者和3例接受白蛋白治疗的患者发生败血症或菌血症;4例接受安慰剂治疗的患者和7例接受白蛋白治疗的患者在研究期间发生肺炎(无显著性差异)。所有接受静脉白蛋白治疗的患者血清白蛋白均升高,但1例患者仅接受了6天静脉白蛋白治疗。白蛋白治疗组患者的平均血清白蛋白浓度升高了1.42 g/dL,安慰剂组患者升高了0.29 g/dL(非配对t检验,p < .0001)。平均初始白蛋白代谢量为17.4 g/天(0.3 g/kg/天)。治疗结束时,白蛋白代谢量为20.5 g/天(0.36 g/kg/天)(配对t检验,p = .4,无显著性差异)。

结论

a)对接受全胃肠外营养的低白蛋白血症患者静脉输注白蛋白并不能改善发病率或死亡率。b)白蛋白代谢率最初与分解代谢状态有关,较高;之后,这些速率与白蛋白空间填充和糖异生有关,也较高。c)基于输注结束时较高的白蛋白分解代谢率,每天<25 g的白蛋白剂量可能足以补充白蛋白储备。

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