阿普匹坦在治疗化疗引起的恶心和呕吐中的作用

Seema Devi
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摘要

导言:与化疗药物相关的恶心和呕吐最为常见,可导致严重的副作用,明显降低生活质量 (1-3)。CINV 的严重程度和发生率取决于催吐抗癌药物的类型。药物的致吐性可分为三类--高、中、低或轻度。阿瑞匹坦是一种神经激肽 1(NK-1),具有不同的作用机制,可控制或预防 CINV。(13).阿瑞匹坦可选择性地阻断物质 P 与中枢神经系统区域 NK2 受体的结合,从而控制急性和延迟性 CINV。(8,9)所有入组患者在化疗前 30 分钟(D1)口服阿瑞匹坦 125 毫克片剂,静脉推注地塞米松 8 毫克或在生理盐水中加入地塞米松,然后在 D2 和 D3 口服阿瑞匹坦 80 毫克。本研究共纳入 270 名患者。结果:男性 116 例,女性 144 例,常见年龄段为 40 至 50 岁。男性最常见的年龄段为 50 至 60 岁。女性中最常见的恶性肿瘤部位是乳腺癌,第二常见的是胆囊癌,第三常见的是宫颈癌。
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ROLE OF APRIPITANT IN TREATMENT OF CHEMOTHERAPY INDUCED NAUSEA AND VOMITING
Introduction: Nausea and vomiting associated with chemotherapy agents are most common and can lead to serious side effects, which can cause marked reduction in quality of life (1 – 3). Severity and incidence of CINV depend on the type of anti-cancer drug emetogenically. Emetogenicity of a drug can be divided into three categories—high, moderate, and low or mild. Aprepitant is a neurokinin 1 (NK-1) which has different action mechanism to control or prevent CINV. (13). Aprepitant can block selectively and binding of substance P at NK2 receptor in central nervous system area causes control of acute and delayed CINV. (8,9) All the enrolled patients received tablet aprepitant 125 Material and Method: mg per oral, dexamethasone 8mg intravenous push or in load normal saline 30 minutes prior to chemotherapy on D1, followed by 80mg per oral on D2 and D3. Total 270 Patients were included in this study. 116 were fe Results: males, 144 were males common age group was 40 to 50 year in females. While 50 to 60 year of age was commonest group among males. Commonest site of malignancy was Carcinoma breast, 2nd commonest was Carcinoma gall bladder and 3rd commonest was carcinoma cervix among females.
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