首页> 外文期刊>Gastrointestinal Endoscopy >High diagnostic and clinical impact of small-bowel capsule endoscopy in patients with hereditary hemorrhagic telangiectasia with overt digestive bleeding and/or severe anemia.
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High diagnostic and clinical impact of small-bowel capsule endoscopy in patients with hereditary hemorrhagic telangiectasia with overt digestive bleeding and/or severe anemia.

机译:小肠内窥镜检查对遗传性出血性毛细血管扩张伴消化性出血和/或严重贫血的患者具有较高的诊断和临床意义。

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BACKGROUND: Patients with hereditary hemorrhagic telangiectasia (HHT) often present with recurrent anemia because of epistaxis or GI bleeding in relation to telangiectases mostly located in the stomach or small bowel. Capsule endoscopy is considered a major diagnostic tool for small-bowel diseases, but the impact of capsule endoscopy imaging on patient management in HHT is poorly understood. OBJECTIVE: To clarify the contribution of capsule endoscopy in selected patients with HHT. DESIGN: Prospective, descriptive study. SETTING: Multicenter, two university hospital tertiary-care centers, from January 2003 to June 2007. PATIENTS: This study involved 30 patients with HHT and severe anemia (hemoglobin <9 g/dL; normal: 11-15 g/dL) and minimal epistaxis or moderate anemia but overt GI bleeding. INTERVENTION: Capsule endoscopy investigation. MAIN OUTCOME MEASUREMENTS: Clinical characteristics and capsule endoscopy results and their clinical consequences. RESULTS: Capsule endoscopy detected gastric and small-bowel telangiectases in 14 (46.7%) and 26 (86.7%) cases, respectively. Active bleeding was present in 36.7% of cases. Diffuse telangiectases were detected in 42.3% without correlation with age, sex, or type of HHT mutation. Further investigations were carried out as a consequence of the capsule endoscopy results in 67% of cases. Treatment, consisting mostly of endoscopic argon plasma coagulation, was scheduled in 46.7% of patients. LIMITATIONS: Our population was essentially composed of patients with the ALK1 mutation. CONCLUSION: This study shows that there is a high diagnostic yield for capsule endoscopy in selected patients with HHT. Capsule endoscopy makes possible precise mapping of lesions and has a considerable impact on the management of these selected patients by using a predefined algorithm: a limited number of accessible lesions is suitable for endoscopic treatment, whereas innumerable diffuse lesions require a medical approach. We suggest that capsule endoscopy could be a first-line, noninvasive, digestive tract examination in selected patients with HHT.
机译:背景:遗传性出血性毛细血管扩张症(HHT)患者通常由于鼻出血或胃肠道出血而复发性贫血,与主要位于胃或小肠的毛细血管扩张酶有关。胶囊内窥镜被认为是小肠疾病的主要诊断工具,但是对于HHT患者胶囊内镜成像对患者管理的影响知之甚少。目的:阐明胶囊内镜在某些HHT患者中的作用。设计:前瞻性描述性研究。地点:2003年1月至2007年6月,位于多中心,两个大学医院的三级护理中心。患者:这项研究涉及30例HHT和严重贫血(血红蛋白<9 g / dL;正常:11-15 g / dL)且极少的患者鼻出血或中度贫血但明显的胃肠道出血。干预:胶囊内镜检查。主要观察指标:临床特征和胶囊内镜检查结果及其临床后果。结果:胶囊内窥镜检查分别检测到胃和小肠毛细血管扩张酶14例(46.7%)和26例(86.7%)。在36.7%的病例中出现活动性出血。弥漫性毛细血管扩张酶检出率为42.3%,与年龄,性别或HHT突变类型无关。由于胶囊内窥镜检查结果的结果,在67%的病例中进行了进一步的研究。 46.7%的患者计划进行治疗,主要由内窥镜氩气血浆凝结治疗。局限性:我们的人群主要由ALK1突变患者组成。结论:这项研究表明,对于某些HHT患者,胶囊内镜的诊断率很高。胶囊内窥镜检查可以使病变精确定位,并通过使用预定义算法对这些选定患者的治疗产生重大影响:有限数量的可触及病变适用于内窥镜治疗,而无数弥漫性病变则需要医疗方法。我们建议胶囊内窥镜检查可能是某些HHT患者的一线,无创,消化道检查。

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