疗效评价采用视觉模拟评分法(VAS)。
Visual Analogue Scale (VAS) was used to evaluate therapeutic effect.
采用视觉模拟评分(VAS)评估镇痛效果。
Postoperative pain score was recorded by visual analogue scale (VAS).
镇痛效果评价采用视觉模拟评分（VAS）。
The efficacy of pain relief was assessed using a visual analogue scale (VAS).
术后疼痛由视觉模拟评分和言语反应形式评定。
Postoperative pain was evaluated with use of a visual analogue scale and a verbal response form.
主要结果测量：人口统计学数据和视觉模拟评分。
Main Outcome Measurements: Demographics and visual analog scale appropriateness scores were collected on each patient.
采用视觉模拟评分法(VAS)测评产妇镇痛程度。
Assessed the degree of the pain by using visual analog scale (VAS).
分组治疗中采用视觉模拟评分法观察止痛时间和止痛效果。
Visual analogue scale(VAS) was used to observe analgesic time and effect during treatment in each group.
疼痛评估使用视觉模拟评分(管)在0没有痛苦和10疼痛难忍。
Pain was evaluated using a visual analogue scale (VAS) where 0 was no pain and 10 was unbearable pain.
采用视觉模拟评分法(VAS)评定病人的疼痛程度及治疗结果。
Degree of pain and results of treatment were scored by visual analogue scale (VAS).
主要的结果评测采用术后24小时理疗时进行疼痛视觉模拟评分。
Scores on a visual analog pain scale administered during physiotherapy twenty-four hours postoperatively were used as the primary outcome measured.
以视觉模拟评分（VAS）和睡眠质量评分（QS）综合评定治疗效果。
The curative effect was evaluated by visual analogue scale (VAS) and quality of sleep (QS).
使用疼痛缓解视觉模拟评分法(vas)和睡眠质量评估疼痛缓解程度。
Visual analogy score (VAS) and the sleep quality were used for the evaluation of pain releasing.
采用疼痛视觉模拟评分法(VAS)评分对两组患者的疼痛程度进行效果评价。
Visual analogue scale (VAS) scores were used to assess the pain degree of patients in the two groups.
所有患者视觉模拟评分(VAS)疼痛与情绪评分明显降低，无严重并发症发生。
Pain and mood scores of visual analogue scale (VAS) reduced significantly in all patients and no severe complications occurred.
记录静息及被动运动时视觉模拟评分(VAS)、肌力分级、镇静程度及副作用发生情况。
Visual analogue score (VAS) during rest and movement, muscle strength grades, sedation level and complications were recorded.
方法动物实验采用兔齿髓刺激法和小鼠福尔·马林实验，临床疼痛评定采用视觉模拟评分法。
METHODS Formalin test in mice, tooth pulp stimulation procedure in rabbits and human oral pain were used.
选择60例结肠镜检查病人，用视觉模拟评分法（VAS）和状态焦虑问卷（SAI）评估疼痛程度和焦虑水平。
Method: A total of 60 patients underwent coloscopy were evaluated on their pain degree and anxiety by filling out both visual analogue scales (VAS) and state anxiety inventory(SAI).
分别记录术前和最后随访时的日本骨科学会评分（JOA评分及下肢根性痛的视觉模拟评分（VAS），并比较；
The respective scales of Japanese Orthopedics Association (JOA) and sciatica View analog scales(VAS) before and at final follow-up were recorded and compared.
按照WHO推荐视觉模拟评分方法评估，采用0～10数字进行镇痛强度分级，完全无痛为0分，难以忍受疼痛为10分；
Visual analogous scale (VAS) suggested by WHO was used to assess. Analgesia intensity expressed with 0-10, 0 point as without pain completely, 10 points as unbearable pain;
Oswestry功能障碍指数(ODI)、视觉模拟疼痛评分(VAS)用来评估术前、术后1和2年情况。
Oswestry Disability Index (ODI), visual analog pain scores (VAS) were evaluated preoperative, 1 and 2 years postoperative.
镜检术后立即将患者术中痛感记录在视觉模拟疼痛评分(VAS)量表上(0 ~10分)，同时记录呼吸频率及脉率。
Patients' pain feeling were recorded on an VAS (visual analog pain scale) ranging from 0 to 10 after flexible cystoscopy. The pulse and respiratory rate were also recorded.
镜检术后立即将患者术中痛感记录在视觉模拟疼痛评分(VAS)量表上(0 ~10分)，同时记录呼吸频率及脉率。
Patients' pain feeling were recorded on an VAS (visual analog pain scale) ranging from 0 to 10 after flexible cystoscopy. The pulse and respiratory rate were also recorded.
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