| 模型 | 输液导管长度(mm) | 导管数量(pcs) | 输液泵容量(ml) | 流量(毫升/小时) |
| tjps040 - 1 - 100 - 2 | 40 | 1 | One hundred. | 2 |
| tjps060 - 1 - 100 - 2 | 60 | 1 | One hundred. | 2 |
| tjps060 - 1 - 250 - 2 | 60 | 1 | 250 | 2 |
| tjps060 - 1 - 250 - 5 | 60 | 1 | 250 | 5 |
| tjps060 - 2 - 250 - 5 | 60 | 2 | 250 | 5 |
| tjps080 - 1 - 100 - 2 | 80 | 1 | One hundred. | 2 |
| tjps080 - 1 - 250 - 2 | 80 | 1 | 250 | 2 |
| tjps080 - 1 - 250 - 5 | 80 | 1 | 250 | 5 |
| tjps080 - 2 - 250 - 5 | 80 | 2 | 250 | 5 |
| tjps100 - 1 - 100 - 2 | One hundred. | 1 | One hundred. | 2 |
| tjps100 - 1 - 250 - 2 | One hundred. | 1 | 250 | 2 |
| tjps100 - 1 - 250 - 5 | One hundred. | 1 | 250 | 5 |
| tjps100 - 2 - 250 - 5 | One hundred. | 2 | 250 | 5 |
| tjps120 - 1 - 100 - 2 | 120 | 1 | One hundred. | 2 |
| tjps120 - 1 - 250 - 2 | 120 | 1 | 250 | 2 |
| tjps120 - 1 - 250 - 5 | 120 | 1 | 250 | 5 |
| tjps120 - 2 - 250 - 5 | 120 | 2 | 250 | 5 |
| tjps040 - 3 - 250 - 5 | 40 | 3. | 250 | 5 |
| tjps060 - 3 - 250 - 5 | 60 | 3. | 250 | 5 |
| tjps - 2 - 250 - 5 - 120 x040 | 12040 | 2 | 250 | 5 |
| tjps - 2 - 250 - 5 - 120 x060 | 12060 | 2 | 250 | 5 |
| tjps - 2 - 250 - 5 - 100 x060 | 10060 | 2 | 250 | 5 |
| tjps - 2 - 250 - 5 - 100 x040 | 10040 | 2 | 250 | 5 |
| tjps - 2 - 220 - 3.5 - 120 - x040 | 12040 | 2 | 220 | 3．5 |
| tjps - 2 - 220 - 3.5 - 120 - x060 | 12060 | 2 | 220 | 3．5 |
| tjps - 2 - 220 - 3.5 - 060 - x060 | 6060 | 2 | 220 | 3．5 |
| tjps - 2 - 220 - 3.5 - 080 - x080 | 8080 | 2 | 220 | 3．5 |
| tjps - 2 - 220 - 3.5 - 100 x100 | 100100 | 2 | 220 | 3．5 |
| tjps - 2 - 220 - 3.5 - 120 - x120 | 120120 | 2 | 220 | 3．5 |
| tjps - 3 - 250 - 5 - 100 x100x040 | 10010040 | 3. | 250 | 5 |
| tjps - 3 - 250 - 5 - 100 x100x060 | 10010060 | 3. | 250 | 5 |
| tjps - 3 - 250 - 5 - 120 x120x060 | 12012060 | 3. | 250 | 5 |
| tjps - 3 - 250 - 5 - 120 x120x040 | 12012040 | 3. | 250 | 5 |
本品已在北京大学医院和北京大学第三医院对160例患者进行随机检测。测试结果如下:
| 统计数据表 | 对照组(静脉注射吗啡PCA，病例数及百分比) | 实验组(持续局部镇痛，利多卡因，病例数和百分比) | 统计量 | P值 | 结论 | |
| 术后24小时疼痛 | 使用辅助止痛剂 | 10 (12.50) | 14 (17.50) | 0.784 | 0.376 | 无显著差异 |
| 疼痛程度 | 0 N (%) | 32 (40.00) | 27日(33.75) | 0.741 b | 0.459 b | 无显著差异 |
| 1 N (%) | 26日(32.50) | 28日(35.00) | ||||
| 2 N (%) | 21日(26.25) | 25 (31.25) | ||||
| 3 N (%) | 1 (1.25) | 0 (0.00) | ||||
| 术后48小时疼痛 | 使用辅助止痛剂 | 10 (12.50) | 17 (21.25) | 0.784 | 0.376 | 无显著差异 |
| 疼痛程度 | 0 N (%) | 36 (45.00) | 36 (45.00) | 0.173 b | 0.863 b | 无显著差异 |
| 1 N (%) | 42 (52.50) | 44 (55.00) | ||||
| 2 N (%) | 2 (2.50) | 0 (0.00) | ||||
| 3 N (%) | 0 (0.00) | 0 (0.00) | ||||
| 麻醉输注装置患者满意度 | 满意 | 76 (95.00) | 78 (97.50) | 0.681 * | 无显著差异 | |
| 不满意 | 4 (5.00) | 2 (2.50) | ||||
| 安全分析 | 副作用(尿潴留、恶心呕吐等) | 7 | 3. | 1.7067 | 0.191 | 无显著差异 |
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基于“增大化现实”技术
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