Chinese Journal of Tissue Engineering Research ›› 2014, Vol. 18 ›› Issue (9): 1325-1330.doi: 10.3969/j.issn.2095-4344.2014.09.003
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Du Xue-ping1, Lu Jian-quan1, Xu Ping1, Zhu Yu-chang2, Dong Da-yong1
Online:
2014-02-26
Published:
2014-02-26
Contact:
Lu Jian-quan, Associate chief physician, Qidong Hospital of Traditional Chinese Medicine (Qidong Branch, Tenth People’s Hospital, School of Medicine, Tongji University), Qidong 226200, Jiangsu Province, China
About author:
Du Xue-ping, Studying for master’s degree, Attending physician, Qidong Hospital of Traditional Chinese Medicine (Qidong Branch, Tenth People’s Hospital, School of Medicine, Tongji University), Qidong 226200, Jiangsu Province, China
CLC Number:
Du Xue-ping, Lu Jian-quan, Xu Ping, Zhu Yu-chang, Dong Da-yong. Analgesic effects of intraarticular cocktail versus intravenous parecoxib injection after total hip arthroplasty[J]. Chinese Journal of Tissue Engineering Research, 2014, 18(9): 1325-1330.
2.4 置换后疼痛目测类比评分 置换前关节内鸡尾酒注射治疗组与帕瑞昔布静脉注射对照组的目测类比评分分别为2.5±0.8及2.8±1.2,两者之间差异无显著性意义 (P > 0.05)。静息状态下关节内鸡尾酒注射治疗组患者置换后12,24,48 h及置换后3,7,14 d的目测类比评分依次为3.0±0.9,2.5±0.7,2.1±0.9,2.5±0.7,2.4±1.1及2.1±1.2分,而帕瑞昔布静脉注射对照组其置换后12,24,48 h及置换后3,7,14 d的目测类比评分则依 次为4.4±1.8,3.8±2.1,3.6±1.5,2.6±0.9,2.3±1.3及2.5±1.1分,关节内鸡尾酒注射治疗组患者置换后12,24,48 h疼痛较帕瑞昔布静脉注射对照组有明显缓解 (P < 0.05),而帕瑞昔布静脉注射对照组在置换后3,7,14 d疼痛程度虽较关节内鸡尾酒注射治疗组患者高,但二者之间差异无显著性意义(P > 0.05,表2)。 置换前关节内鸡尾酒注射治疗组患者置换后12,24,48 h及置换后3,7,14 d活动时疼痛目测类比评分依次为4.6±1.6,3.6±1.5,3.0±1.2,3.2±0.9,3.1±1.2及3.0±1.6,而帕瑞昔布静脉注射对照组患者置换后12,24,48 h及置换后3,7,14 d活动时疼痛目测类比评分依次为5.9±2.1,4.2±0.7,4.0±1.2,3.6±1.5,3.4±1.6及2.9±1.9分,治疗组患者置换后12,48 h活动疼痛较对照组有明显优势(P < 0.05,表2)。 2.5 手术时间和住院时间比较 关节内鸡尾酒注射治疗组和帕瑞昔布静脉注射对照组患者全髋置换从切皮到缝合结束的平均用时依次为(60.2±5.2) min及(55.2± 6.2) min,关节周围及关节腔内注射延长了手术时间,差异有显著性意义(P=0.001)。关节内鸡尾酒注射治疗组的住院时间为(10.4±2.1) d,帕瑞昔布静脉注射对照组的住院时间为(11.0±2.5) d,两组比较差异无显著性意义(P=0.318)。"
2.6 置换后髋关节功能评分比较 置换前髋关节活动度(主要指伸屈髋运动)两组间差异无显著性意义(P > 0.05),置换后48 h关节内鸡尾酒注射治疗组髋关节活动度大于帕瑞昔布静脉注射对照组,置换后3,7,14 d两组间髋关节活动度比较差异无显著性意义(P > 0.05,表3)。 2.7 置换后止痛药的用量及相关并发症的比较 置换后24 h到置换后第3天,治疗组的平均盐酸曲马多的用量为(650.0±50.2) mg,而对照组患者则为(700.0±85.8) mg,对照组需要消耗明显多的止痛药来维持患者的功能锻炼(P < 0.05)。 所有60例患者中,未出现术中或者术后栓塞,无肺部感染,无死亡患者。治疗组有1例患者出现髋关节深部血肿,后经引流后症状改善痊愈,1例注射部位的组织坏死,经局部切开引流后痊愈。治疗组及对照组分别有9及12例患者出现药物相关的恶心、呕吐反应,停药或者减量后症状改善,两组并发症发生率差异无显著性意义。"
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