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首页> 外文期刊>JPEN. Journal of parenteral and enteral nutrition. >Comment on: probiotic prophylaxis in predicted severe acute pancreatitis: a randomized, double-blind, placebo-controlled trial.
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Comment on: probiotic prophylaxis in predicted severe acute pancreatitis: a randomized, double-blind, placebo-controlled trial.

机译:评论:预测严重急性胰腺炎中的益生菌预防:一项随机,双盲,安慰剂对照试验。

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BACKGROUND: Infectious complications and associated mortality are a major concern in acute pancreatitis. Enteral administration of probiotics could prevent infectious complications, but convincing evidence is scarce. Our aim was to assess the effects of probiotic prophylaxis in patients with predicted severe acute pancreatitis. METHODS: In this multicentre randomised, double-blind, placebo-controlled trial, 298 patients with predicted severe acute pancreatitis (Acute Physiology and Chronic health Evaluation [APACHE II] score > or =8, Imrie score > or =3, or C-reactive protein >150 mg/L) were randomly assigned within 72 h of onset of symptoms to receive a multispecies probiotic preparation (n = 153) or placebo (n = 145), administered enterally twice daily for 28 days. The primary endpoint was the composite of infectious complications-ie, infected pancreatic necrosis, bacteraemia, pneumonia, urosepsis, or infected ascites-during admission and 90-day follow-up. Analyses were by intention to treat. This study is registered, number ISRCTN38327949. FINDINGS: One person in each group was excluded from analyses because of incorrect diagnoses of pancreatitis; thus, 152 individuals in the probiotics group and 144 in the placebo group were analysed. Groups were much the same at baseline in terms of patients' characteristics and disease severity. Infectious complications occurred in 46 (30%) patients in the probiotics group and 41 (28%) of those in the placebo group (relative risk 1.06, 95% CI 0.75-1.51). 24 (16%) patients in the probiotics group died, compared with nine (6%) in the placebo group (relative risk 2.53, 95% CI 1.22-5.25). Nine patients in the probiotics group developed bowel ischaemia (eight with fatal outcome), compared with none in the placebo group (p = 0.004). INTERPRETATION: In patients with predicted severe acute pancreatitis, probiotic prophylaxis with this combination of probiotic strains did not reduce the risk of infectious complications and was associated with an increased risk of mortality. Probiotic prophylaxis should therefore not be administered in this category of patients. (Lancet. 2008;371:651-659) Besselink MG, van Santvoort HC, Buskens E, et al; Dutch Acute Pancreatitis Study Group.
机译:背景:传染性并发​​症和相关的死亡率是急性胰腺炎的主要关注点。肠内施用益生菌可以预防感染并发症,但缺乏令人信服的证据。我们的目的是评估预防性益生菌在预计患有严重急性胰腺炎的患者中的作用。方法:在这项多中心,随机,双盲,安慰剂对照试验中,有298位预计患有严重急性胰腺炎的患者(急性生理和慢性健康评估[APACHE II]评分>或= 8,Imrie评分>或= 3或C-症状发作后72小时内将活性蛋白> 150 mg / L)随机分配,以接受多种益生菌制剂(n = 153)或安慰剂(n = 145),每天两次肠内给药,持续28天。主要终点是感染并发症的综合,即在入院和90天随访期间感染的胰腺坏死,菌血症,肺炎,尿毒症或腹水感染。分析是按意向进行的。该研究已注册,编号ISRCTN38327949。结果:由于对胰腺炎的诊断不正确,每组中的一个人被排除在分析之外。因此,分析了益生菌组中的152个人和安慰剂组中的144个人。就患者的特征和疾病严重程度而言,各组在基线时基本相同。益生菌组46例(30%)和安慰剂组41例(28%)发生感染性并发症(相对风险1.06,95%CI 0.75-1.51)。益生菌组中有24名(16%)患者死亡,而安慰剂组中有9名(6%)(相对风险2.53,95%CI 1.22-5.25)。与安慰剂组相比,益生菌组中有9名患者出现肠缺血(八名具有致命结局)(p = 0.004)。解释:在预计患有严重急性胰腺炎的患者中,结合使用益生菌菌株预防益生菌并不能降低感染并发症的风险,并且与死亡风险增加相关。因此,不应在此类患者中进行预防性益生菌的治疗。 (Lancet.2008; 371:651-659)Besselink MG,van Santvoort HC,Buskens E等,等。荷兰急性胰腺炎研究组。

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