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多价免疫球蛋白用于预防多发伤患者的细菌感染。一项随机、安慰剂对照研究。

Polyvalent immunoglobulins for prophylaxis of bacterial infections in patients following multiple trauma. A randomized, placebo-controlled study.

作者信息

Glinz W, Grob P J, Nydegger U E, Ricklin T, Stamm F, Stoffel D, Lasance A

出版信息

Intensive Care Med. 1985;11(6):288-94. doi: 10.1007/BF00273538.

Abstract

One hundred and fifty severely injured patients requiring long-term artificial ventilation were evaluated in a prospective, randomized, double blind study comparing the prophylactic effect of an intravenous immunoglobulin (Sandoglobulin; IGIV) against nosocomial infections with a placebo preparation. The groups were comparable in age, sex, injury pattern, and severity of the trauma. Seventy-six patients received 12 g of Sandoglobulin as a 3% solution on day 0, day 5 and day 12, i.e. a total of 36 g. Sandoglobulin significantly reduced the incidence of pneumonia (28 cases in the IGIV group, 43 cases in the placebo group, p = 0.0111). This resulted in a reduced therapeutic use of antibiotics. For the occurrence of sepsis (IGIV: 14 cases; placebo 19 cases) and other infections (IGIV: 11 cases; placebo: 10 cases) no significant differences were found. No side effects of the administration of IGIV were observed. IGIV prophylaxis neither reduced the overall death rate nor those deaths caused by infection. On day 5 after administration of the first 12 g of IGIV, the IgG serum concentrations were significantly higher in the Sandoglobulin group (8.41 +/- 1.96 mg/ml and 7.42 +/- 2.25 mg/ml respectively, p less than 0.001) whereas later serum samples showed no significant differences.

摘要

一项前瞻性、随机、双盲研究对150例需要长期人工通气的重伤患者进行了评估,比较静脉注射免疫球蛋白(Sandoglobulin;IGIV)与安慰剂制剂预防医院感染的效果。两组在年龄、性别、损伤类型和创伤严重程度方面具有可比性。76例患者在第0天、第5天和第12天接受12g 3%溶液的Sandoglobulin,即总共36g。Sandoglobulin显著降低了肺炎的发生率(IGIV组28例,安慰剂组43例,p = 0.0111)。这导致抗生素的治疗性使用减少。对于败血症的发生(IGIV组:14例;安慰剂组:19例)和其他感染(IGIV组:11例;安慰剂组:10例),未发现显著差异。未观察到IGIV给药的副作用。IGIV预防既未降低总体死亡率,也未降低由感染导致的死亡率。在首次给予12g IGIV后第5天,Sandoglobulin组的IgG血清浓度显著更高(分别为8.41±1.96mg/ml和7.42±2.25mg/ml,p<0.001),而随后的血清样本未显示显著差异。

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