与钾竞争性胃酸阻滞剂和质子泵抑制剂治疗相关的胃黏膜变化的内窥镜检查结果和疗效。

IF 1.4 Q4 GASTROENTEROLOGY & HEPATOLOGY
DEN open Pub Date : 2024-06-24 DOI:10.1002/deo2.400
Satoshi Shinozaki, Hiroyuki Osawa, Yoshimasa Miura, Hiroaki Nomoto, Hirotsugu Sakamoto, Yoshikazu Hayashi, Tomonori Yano, Edward J. Despott, Hironori Yamamoto
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引用次数: 0

摘要

与长期服用钾竞争性胃酸阻滞剂和质子泵抑制剂(PPI)相关的胃粘膜变化可能会引起人们的关注。与 PPIs 相比,有关长期使用钾竞争性胃酸阻滞剂安全性的证据很少。Vonoprazan(VPZ)是2015年在日本上市的一种代表性钾竞争性酸阻滞剂。为了对长期酸阻滞剂引起的胃黏膜病变的结果进行比较,我们回顾了六种具有代表性的胃黏膜病变:胃底腺息肉、胃增生性息肉、多发性白色扁平隆起病变、鹅卵石样胃黏膜病变、胃黑斑和星尘状胃黏膜病变。对于这些粘膜病变,我们评估了与胃酸阻断类型、患者性别、幽门螺杆菌感染状态、胃萎缩程度和血清胃泌素水平的关联。目前还没有具体证据支持 VPZ/PPI 的使用与神经内分泌肿瘤的发生之间存在显著关系。目前的数据还显示,长期服用 VPZ 和 PPI 发生胃黏膜病变的风险相似。血清高胃泌素血症与某些胃粘膜病变的发生无关。因此,在常规临床实践中,血清胃泌素水平无助于风险评估和与停用这些药物相关的决策。考虑到幽门螺杆菌感染可能带来的肿瘤风险,应在开始 VPZ/PPI 治疗前根除幽门螺杆菌。迄今为止的证据并不支持仅仅因为存在这些相关的胃粘膜病变而停止临床上适当的 VPZ/PPI 治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Endoscopic findings and outcomes of gastric mucosal changes relating to potassium-competitive acid blocker and proton pump inhibitor therapy

Endoscopic findings and outcomes of gastric mucosal changes relating to potassium-competitive acid blocker and proton pump inhibitor therapy

Gastric mucosal changes associated with long-term potassium-competitive acid blocker and proton pump inhibitor (PPI) therapy may raise concern. In contrast to that for PPIs, the evidence concerning the safety of long-term potassium-competitive acid blocker use is scant. Vonoprazan (VPZ) is a representative potassium-competitive acid blocker released in Japan in 2015. In order to shed some comparative light regarding the outcomes of gastric mucosal lesions associated with a long-term acid blockade, we have reviewed six representative gastric mucosal lesions: fundic gland polyps, gastric hyperplastic polyps, multiple white and flat elevated lesions, cobblestone-like gastric mucosal changes, gastric black spots, and stardust gastric mucosal changes. For these mucosal lesions, we have evaluated the association with the type of acid blockade, patient gender, Helicobacter pylori infection status, the degree of gastric atrophy, and serum gastrin levels. There is no concrete evidence to support a significant relationship between VPZ/PPI use and the development of neuroendocrine tumors. Current data also shows that the risk of gastric mucosal changes is similar for long-term VPZ and PPI use. Serum hypergastrinemia is not correlated with the development of some gastric mucosal lesions. Therefore, serum gastrin level is unhelpful for risk estimation and for decision-making relating to the cessation of these drugs in routine clinical practice. Given the confounding potential neoplastic risk relating to H. pylori infection, this should be eradicated before VPZ/PPI therapy is commenced. The evidence to date does not support the cessation of clinically appropriate VPZ/PPI therapy solely because of the presence of these associated gastric mucosal lesions.

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