Is Hyaluronic Acid or Corticosteroid Superior to Lactated Ringer Solution in the Short-Term Reduction of Temporomandibular Joint Pain After Arthrocentesis? Part 1

被引:37
作者
Bouloux, Gary F. [1 ]
Chou, Jolie [2 ,3 ]
Krishnan, Deepak [4 ]
Aghaloo, Tara [5 ]
Kahenasa, Nora [5 ]
Smith, Julie Ann [6 ]
Giannakopoulos, Helen [7 ]
机构
[1] Emory Univ, Sch Med, Dept Oral & Maxillofacial Surg, 1365B Clifton Rd NE,Suite 2300, Atlanta, GA 30322 USA
[2] SUNY Buffalo, Dept Oral & Maxillofacial Surg, Buffalo, NY USA
[3] Univ Penn, Philadelphia, PA 19104 USA
[4] Univ Cincinnati, Dept Oral & Maxillofacial Surg, Cincinnati, OH USA
[5] Univ Calif Los Angeles, Dept Oral & Maxillofacial Surg, Los Angeles, CA USA
[6] Oregon Hlth & Sci Univ, Dept Oral & Maxillofacial Surg, Portland, OR 97201 USA
[7] Univ Penn, Dept Oral & Maxillofacial Surg, Philadelphia, PA 19104 USA
关键词
RANDOMIZED CONTROLLED-TRIAL; OF-THE-LITERATURE; SODIUM HYALURONATE; SYNOVIAL-FLUID; CLOSED LOCK; DISC DISPLACEMENT; INTERNAL DERANGEMENT; HYDRAULIC DISTENSION; TREATMENT OUTCOMES; PROGNOSTIC-FACTORS;
D O I
10.1016/j.joms.2016.08.006
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: Arthrocentesis has been used for the management of patients with temporomandibular joint (TMJ) pain, with good success. The additional use of hyaluronic acid (HA) or corticosteroid (CS) remains controversial. The purpose of this study was to compare HA, CS, and lactated Ringer solution (LR; placebo) after arthrocentesis. Materials and Methods: This was a prospective multicenter double-blinded randomized clinical trial. Consecutive patients presenting to the oral and maxillofacial departments at Emory University, the University of Pennsylvania, the University of California-Los Angeles, the University of Cincinnati, and the Oregon Health Sciences University were enrolled in the study. Patients were randomized to HA, CS, or LR. All patients underwent arthrocentesis and then the instillation of HA, CS, or LR. Patients were evaluated clinically at 1 and 3 months. The primary outcome variable was pain at 1 month (by visual analog scale). Secondary outcome variables were pain at 3 months and analgesic consumption. Univariate, bivariate, and multivariate statistics were computed, with a P value less than .05 considered significant. Results: One hundred two patients were enrolled in the study. Four were lost to follow-up, leaving 98 patients for the final analysis. The mean age of patients in the HA, CS, and LR groups was 39.6, 44.3, and 51.8 years, respectively (P = .02). There was no difference among groups in time to follow-up at 1 month (P = .11). The mean decrease in pain in the CS group was 19% for right-side procedures (P = .12) and 36% for left-side procedures (P = .02). The mean decrease in pain in the HA group was 31% for right-side procedures (P = .01) and 34% for left-side procedures (P = .01). The mean decrease in pain in the LR group was 43% for right-side procedures (P < .01) and 37% for left-side procedures (P < .01). There was no differencein pain decrease among groups (P = .55). There was no difference in the use of narcotic (P = .52) or nonsteroidal anti-inflammatory drugs (P = .71) among groups. Conclusion: Arthrocentesis alone is as efficacious as arthrocentesis with HA or CS in decreasing TMJ pain. (C) 2016 American Association of Oral and Maxillofacial Surgeons
引用
收藏
页码:52 / 62
页数:11
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