Tanavalee Aree, Thiengwittayaporn Satit
Department of Orthopaedics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
J Med Assoc Thai. 2009 Dec;92 Suppl 6:S11-8.
To report the results of multimodal pain control with the use of parecoxib following minimally invasive total knee arthroplasty (MIS-TKA).
A consecutive series of 103 patients who underwent 122 MIS-TKAs in 120 episodes of admission by a single surgical team was included in the study. A uniform multimodal pain management protocol was used; including 3-dose regimen of parecoxib in patients who had no contraindication. From 12 hours after complete surgery, early ambulation was started according to patient ability. Serial pain scores were recorded, postoperatively. Intravenous tramadol was prescribed for pain rescue as needed.
Mean age was 67.5 +/- 7.8 years and 68% of patients had medical co-morbidities. Twelve patients (10%) did not receive parecoxib. Eighty-nine patients of the studied group (86%) could ambulate within 24 hours after surgery. The mean preoperative and postoperative pain scores of the group at 6 hours, 12 hours, 24 hours and 36 hours were 6.9, 2.5, 2.4, 2.2 and 1.8, respectively. The postoperative pain following TKA was rated as satisfied pain relief (pain score < 3), of which, the parecoxib group had less need of tramadol than that of non-parecoxib group (10.2% vs. 33%). There was no fluctuation of postoperative blood pressure, as well as no complication related to the use of 3-dose intravenous parecoxib. The serum creatinine level after the second dose in the parecoxib group was found 0.1 mg/dL higher than those who did not take parecoxib (delta, 0.3 vs. 0.2 mg/dL). With a variable intravenous fluid rate to maintain adequate hourly urine, the parecoxib group had more volume of 24-hour fluid intake after surgery (3658 vs. 2918 mL).
Multimodal postoperative pain control after MIS-TKA provided satisfied postoperative pain relief and patients receiving parecoxib had less injectable narcotic administration. Although we prevented perioperative inadequate fluid intake, the serum creatinine level was found slightly higher in parecoxib group. Thus, appropriate fluid intake should be considered when parecoxib is prescribed for postoperative pain in TKA.
报告微创全膝关节置换术(MIS-TKA)后使用帕瑞昔布进行多模式疼痛控制的结果。
本研究纳入了由单一手术团队收治的120例次入院患者中连续进行122例MIS-TKA手术的103例患者。采用统一的多模式疼痛管理方案;对无禁忌证的患者采用帕瑞昔布3剂量方案。术后12小时起,根据患者能力开始早期活动。术后记录连续的疼痛评分。根据需要开具静脉注射曲马多用于疼痛解救。
平均年龄为67.5±7.8岁,68%的患者有合并症。12例患者(10%)未接受帕瑞昔布治疗。研究组89例患者(86%)术后24小时内可下地行走。该组术前及术后6小时、12小时、24小时和36小时的平均疼痛评分分别为6.9、2.5、2.4、2.2和1.8。TKA术后疼痛被评为疼痛缓解满意(疼痛评分<3),其中,帕瑞昔布组比非帕瑞昔布组更少需要使用曲马多(10.2%对33%)。术后血压无波动,且未出现与使用3剂量静脉注射帕瑞昔布相关的并发症。发现帕瑞昔布组第二次给药后的血清肌酐水平比未服用帕瑞昔布的组高0.1mg/dL(差值分别为0.3对0.2mg/dL)。在通过可变的静脉输液速率维持足够的每小时尿量的情况下,帕瑞昔布组术后24小时的液体摄入量更多(3658对2918mL)。
MIS-TKA术后多模式疼痛控制提供了满意的术后疼痛缓解,接受帕瑞昔布治疗的患者较少使用注射用麻醉剂。尽管我们预防了围手术期液体摄入不足,但发现帕瑞昔布组的血清肌酐水平略高。因此,在为TKA术后疼痛开具帕瑞昔布处方时应考虑适当的液体摄入量。