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The development of a protocol for the use of 5-HT3 antagonists in chemotherapy-induced nausea and vomiting.

机译:在化学疗法诱发的恶心和呕吐中使用5-HT3拮抗剂的方案的开发。

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The purpose of this study was to evaluate the effectiveness of three 5-HT3 antagonists in routine clinical practice. The ultimate aim was to develop an antiemetic protocol, selecting a single 5-HT3 antagonist. Each of the drugs was studied for a 4-month period and data was collected from patients on nausea, vomiting (both acute and delayed) and side-effects by means of a diary card. A total of 274 patients were enrolled into the study. Success rates for acute emesis seen over the study period were in excess of 90%. There were no statistically significant differences between any of the three drugs investigated with respect to both acute and delayed nausea and vomiting. Similarly, there was no difference between the three groups for the incidence of constipation, diarrhoea and headache. Granisetron demonstrated a lesser deviation from the protocol in respect of the number of intravenous doses given to patients. The study allowed an effective 5-HT3 antagonist protocol to be developed for use in the management of nausea and vomiting in cancer patients.
机译:本研究的目的是评估三种5-HT3拮抗剂在常规临床实践中的有效性。最终目的是开发止吐方案,选择单个5-HT3拮抗剂。对每种药物进行了为期4个月的研究,并通过日记卡从患者收集了有关恶心,呕吐(急性和延迟性呕吐)和副作用的数据。总共274名患者被纳入研究。在研究期间发现的急性呕吐成功率超过90%。在所研究的三种药物中,就急性和延迟性恶心和呕吐而言,没有统计学上的显着差异。同样,三组之间便秘,腹泻和头痛的发生率也没有差异。 Granisetron在向患者提供静脉注射剂量方面显示出与方案的偏差较小。该研究允许开发有效的5-HT3拮抗剂方案,用于治疗癌症患者的恶心和呕吐。

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