Zhao Di, Luo Shaowei, Xu Wencan, Hu Jun, Lin Shaoda, Wang Nasui
Department of Orthopedics, the First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China.
Division of Endocrinology and Metabolism, Department of Medicine, the First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China.
Clin Ther. 2017 Oct;39(10):2088-2094.e2. doi: 10.1016/j.clinthera.2017.08.014. Epub 2017 Sep 19.
The efficacy and safety profile of hyperbaric oxygen therapy (HBOT) in patients with diabetic foot ulcer have been controversial in recent years. Our meta-analysis was undertaken to evaluate the efficacy and safety profile of HBOT in patients with diabetic foot ulcer.
We searched the PubMed, Cochrane Library, EMBASE, and Clinical Trials.gov databases for controlled trials. The efficacy end points included the incidence of healed ulcers, major amputations, minor amputations, and reduction in the ulcer wound area. The tolerability end point was the incidence of adverse events.
Nine randomized clinical trials involving 526 patients met the inclusion criteria. No difference was found in the incidence of healed ulcers (risk ratio [RR] = 2.22; 95% CI, 0.87-5.62; P = 0.32; I = 81%), minor amputations (RR = 0.95; 95% CI, 0.39-2.29; P = 0.91; I = 74%), major amputations (RR = 0.47; 95% CI, 0.17-1.28; P = 0.14; I = 61%), and adverse events (RR = 1.00; 95% CI, 0.64-1.56; P = 0.99; I = 26%) between the HBOT and standard therapy (ST) groups. HBOT was associated with a greater reduction in the ulcer wound area versus ST (standard mean difference = 1.12; 95% CI, 0.20-2.04; P = 0.04; I = 70%).
No differences existed between HBOT and ST with respect to the incidence of healed ulcers, risk of minor or major amputations, and adverse events. HBOT was associated with a greater reduction in the ulcer wound area than ST. HBOT is a clinically meaningful adjuvant therapy for patients with diabetic foot ulcer.
近年来,高压氧疗法(HBOT)治疗糖尿病足溃疡患者的疗效和安全性一直存在争议。我们进行了这项荟萃分析,以评估HBOT治疗糖尿病足溃疡患者的疗效和安全性。
我们在PubMed、Cochrane图书馆、EMBASE和ClinicalTrials.gov数据库中检索对照试验。疗效终点包括溃疡愈合率、大截肢率、小截肢率以及溃疡创面面积缩小情况。耐受性终点是不良事件发生率。
9项涉及526例患者的随机临床试验符合纳入标准。在溃疡愈合率(风险比[RR]=2.22;95%可信区间[CI],0.87-5.62;P=0.32;I²=81%)、小截肢率(RR=0.