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Postoperative Nausea and Vomiting: Validation of the Portuguese Version of the Postoperative Nausea and Vomiting Intensity Score

机译:术后恶心和呕吐:葡萄牙语版本的术后恶心和呕吐强度评分的验证

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Background and objectives The Postoperative Nausea and Vomiting (PONV) Intensity Scale was developed to de?ne clinically important PONV. The aim of this study was to translate, retranslate and validate the PONV Intensity Scale for use in Portuguese Post Anesthetic Care Unit (PACU) settings. Methods The PONV Intensity Scale was translated and back-translated in accordance with available guidelines. The research team conducted an observational and cohort prospective study in a PACU. One-hundred ?fty-seven adult patients admiited after surgery over three weeks were evaluated for PONV. Measurements included nausea visual analogic scale (VAS) at 6 and 24hours, postoperatively. We assessed reliability and observer disagreement using interclass correlation (ICC) and Information-Based Measure of Disagreement (IBMD). We compared VAS scores between patients with clinically signi?cant (≥50) and not signi?cant (<50) PONV. Results Thirty-nine patients (25%) had PONV at 6hours and 54 (34%) had PONV at 24hours. Thirty-six and 54 patients experienced nausea at 6 and 24hours, respectively. Among patients with PONV, 6 patients (15%) and 9 patients (27%) had a clinically signi?cant PONV intensity scale score at 6 and at 24hours, respectively. The reliability was good both for PONV intensity scale score and for VAS and observer disagreement was slightly higher for VAS. The median nausea VAS scores were higher in patients with clinically signi?cant PONV Intensity score. Conclusions The PONV Intensity Scale appears to be an accurate and reliable assessment and monitoring instrument for PONV in the PACU settings.
机译:背景和目的术后恶心和呕吐(PONV)强度量表的开发旨在定义临床上重要的PONV。这项研究的目的是翻译,重新翻译和验证PONV强度量表,以用于葡萄牙麻醉后护理单位(PACU)。方法按照现有指南对PONV强度量表进行翻译和反翻译。研究小组在PACU进行了一项观察性和队列前瞻性研究。对三周后接受手术治疗的147名成年患者进行PONV评估。测量包括术后6小时和24小时的恶心视觉类比量表(VAS)。我们使用类间相关性(ICC)和基于信息的分歧度量(IBMD)评估了可靠性和观察者分歧。我们比较了临床上重要(≥50)和不重要(<50)PONV患者的VAS评分。结果39例患者(25%)在6小时时有PONV,54例患者(34%)在24小时时有PONV。 36名和54名患者分别在6小时和24小时出现恶心。在PONV患者中,有6例(15%)和9例(27%)在6和24小时分别具有临床上显着的PONV强度量表评分。 PONV强度量表评分和VAS的可靠性都很好,VAS的观察者分歧略高。具有临床意义的PONV强度评分的患者中位恶心VAS评分较高。结论PONV强度量表似乎是PACU设置中PONV的准确,可靠的评估和监测工具。

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