Landi B, Cellier C, Gaudric M, Demont H, Guimbaud R, Cuillerier E, Couturier D, Barbier J-P, Marteau P
Department of Hepatogastroenterology, Georges Pompidou European Hospital, Paris, France.
Endoscopy. 2002 May;34(5):355-9. doi: 10.1055/s-2002-25276.
Little is known of the long-term outcome in patients with gastrointestinal bleeding of obscure origin, who undergo investigation by means of push enteroscopy. The aim of this study was to assess the rate of recurrent bleeding and its predictive factors in patients with gastrointestinal bleeding of obscure origin, after exploration by push enteroscopy.
105 patients with gastrointestinal bleeding of obscure origin (iron-deficiency anemia: n = 56; overt bleeding: n = 49) underwent exploration by push enteroscopy from December 1994 to December 1998. They were classified into three groups according to enteroscopy findings: no lesion found (group A; 56 patients), arteriovenous malformations (group B; 18 patients), and other gastrointestinal lesions (group C; 31 patients). Actuarial rates of rebleeding during follow-up were calculated and factors associated with rebleeding were assessed by means of univariate and multivariate analysis.
Follow-up data were obtained for 101 patients (96 %). The mean follow-up was 29 months (6 - 54 months). The 2-year actuarial rate of rebleeding was 31 % in the overall population, and 27.6 %, 56 % and 24 % in groups A, B, and C, respectively (P = 0.13). The number of previous bleeding episodes and the number of packed red cell units transfused were two independent factors predictive of recurrent bleeding. The modality of recurrent bleeding (anemia or overt bleeding) was similar to that of the initial episode in 94 % of cases. In group A, a gastrointestinal lesion was found after rebleeding in one of the 12 patients with iron-deficiency anemia, and in four of the five patients with overt bleeding.
Recurrent bleeding occurs in about one-third of patients who undergo investigation by push enteroscopy for gastrointestinal bleeding of obscure origin, with a trend towards more frequent rebleeding in patients with arteriovenous malformations. Frequent previous bleeding episodes and transfusion requirements are predictive of recurrent bleeding.
对于不明原因胃肠道出血患者接受推进式小肠镜检查后的长期预后情况,人们了解甚少。本研究旨在评估不明原因胃肠道出血患者在接受推进式小肠镜检查后再出血的发生率及其预测因素。
1994年12月至1998年12月期间,105例不明原因胃肠道出血患者(缺铁性贫血:56例;显性出血:49例)接受了推进式小肠镜检查。根据小肠镜检查结果,他们被分为三组:未发现病变(A组;56例患者)、动静脉畸形(B组;18例患者)和其他胃肠道病变(C组;31例患者)。计算随访期间再出血的精算发生率,并通过单因素和多因素分析评估与再出血相关的因素。
101例患者(96%)获得了随访数据。平均随访时间为29个月(6 - 54个月)。总体人群中2年再出血精算发生率为31%,A组、B组和C组分别为27.6%、56%和24%(P = 0.13)。既往出血发作次数和输注的红细胞悬液单位数是预测再出血的两个独立因素。94%的病例中,再出血的方式(贫血或显性出血)与初始发作相似。在A组中,12例缺铁性贫血患者中有1例在再出血后发现了胃肠道病变,5例显性出血患者中有4例发现了胃肠道病变。
接受推进式小肠镜检查的不明原因胃肠道出血患者中,约三分之一会发生再出血,动静脉畸形患者的再出血频率有更高的趋势。既往频繁出血发作和输血需求可预测再出血。