Comparative Outcomes of Perioperative Epidural Steroids After Percutaneous Endoscopic Lumbar Discectomy for Lumbar Disc Herniation: A Randomized Placebo-Controlled Trial

被引:3
|
作者
Keorochana, Gun [1 ]
Pairuchvej, Saran [3 ]
Setrkraising, Kittipong [4 ]
Arirachakaran, Alisara [4 ]
Kongtharvonskul, Jatupon [2 ]
机构
[1] Mahidol Univ, Ramathibodi Hosp, Fac Med, Orthoped Dept, Bangkok, Thailand
[2] Mahidol Univ, Ramathibodi Hosp, Fac Med, Sect Clin Epidemiol & Biostat, Bangkok, Thailand
[3] Queen Savang Vadhana Mem Hosp, Orthoped Dept, Chon Buri, Thailand
[4] Police Gen Hosp, Orthoped Dept, Bangkok, Thailand
关键词
MIS; PELD; Percutaneous endoscopic lumbar discectomy; Placebo; RCT; Steroid; LOCAL APPLICATION; BACK-PAIN; BUPIVACAINE; SURGERY; EFFICACY; METHYLPREDNISOLONE; CORTICOSTEROIDS; MANAGEMENT; RECOVERY; DISEASE;
D O I
10.1016/j.wneu.2018.07.122
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: To assess postoperative outcomes and complications after percutaneous endoscopic lumbar discectomy (PELD) with or without epidural steroids (ES) administration in lumbar disc herniation. METHODS: In a double-blind randomized, placebocontrolled trial at Ramathibodi Hospital, Mahidol University, from May 2014 to May 2015, 30 patients were randomly allocated to receive ES or placebo (saline) after PELD. The primary outcome was 24-hour morphine consumption. Secondary outcomes were visual analog scale (VAS) scores for leg and back pain, Oswestry Disability Index score, Roland-Morris Disability Questionnaire score, and complications at 6-month follow-up. RESULTS: Mean patient age was 60.0 years, and 0.57% of patients were male. Mean VAS hack pain, VAS leg pain, Oswestry Disability Index, and Roland-Morris Disability Questionnaire scores at baseline were 4.7, 6.1, 24.9, 17.5 in the ES group and 5.1, 5.5, 24.7, 16.7 in the placebo group, respectively. Mean morphine requirements measured at 8, 16, and 24 hours were 3.47, 2.67, and <0.001 in the ES group and 3.13, 1.67, and 0.40 in the placebo group. The mean VAS scores measured at 4, 8, 12, 16, 20, and 24 hours were 2.99, 2.70, 2.56, 3.30, 3.05, and 2.05 the ES group and 3.13, 1.13, 1.26, 1.65, 1.22, and 1.08 in placebo group. The difference was not statistically significant (P > 0.05 for all). CONCLUSIONS: Administration of ES with PELD for lumbar disc herniation does not improve postoperative pain, morphine requirements, or disability scores in the short-term and midterm periods.
引用
收藏
页码:E244 / E249
页数:6
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