背景:难治性糖尿病足溃疡(rDFU)和骨髓炎(糖尿病足骨髓炎[DFO])是糖尿病患者的主要问题。通常由多重耐药多重微生物感染引起,这些可能导致截肢或溃疡不愈合。在这项非随机开放标签研究中,我们观察了利福平治疗未愈合的糖尿病足溃疡患者的疗效.
方法:以DFU患者(n=67,n=55,DFO)对常规抗菌治疗无效3个月(rDFU)为研究组。除标准抗生素外,所有患者均接受利福平治疗至少3个月(如果DUF在3个月后未治愈,则最长为6个月),并与组成对照组的类似DFU(n=68,n=55DFO)进行比较。用常规抗菌治疗。随访12个月。6个月时DFU的愈合和截肢是该研究的主要终点。
结果:总计,利福平组中43例患者(64.2%)在3个月时治愈,另外4例患者在利福平持续6个月时治愈(n=47,70.1%)。在对照组中,11例患者在3个月时愈合(16.2%),25例患者在6个月时愈合(36.8%)。总的来说,研究组中的14例患者(20.9%)和对照组中的29例患者(42.6%)必须进行轻微截肢。研究组和对照组3个月和6个月的愈合率和轻微截肢率之间的比较显示有统计学意义的结果(分别为P≤.00001,<.00001和.008)。总的来说,在利福平和对照组中,尽管原发性溃疡已愈合,但仍有6例和8例患者随后复发溃疡。分别。
结论:利福平与其他标准多微生物疗法联合用于对标准抗菌治疗无反应的难治性复杂糖尿病足溃疡,可以显着改善伤口愈合以及减少截肢的需要,除了标准的护理。
BACKGROUND: Refractory diabetic foot ulcer (rDFU) and osteomyelitis (diabetic foot osteomyelitis [DFO]) are a major problem in people with diabetes. Often resulting from multidrug-resistant polymicrobial infection, these may result in amputation or nonhealing ulcers. In this nonrandomized open-label
study, we looked at the outcome of treatment with rifampicin in patients with nonhealing diabetic foot ulcers.
METHODS: Patients with DFUs (n = 67, n = 55 with DFO) unresponsive to conventional antimicrobial therapy for >3 months (rDFU) were taken as the
study group. All patients received rifampicin for a minimum of 3 months (maximum 6 months if DUFs did not heal after 3 months) in addition to standard antibiotics and compared with similar kind of DFUs (n = 68, n = 55 DFO) who formed the control group, treated with conventional antimicrobial therapy. Patients were followed up for 12 months. Healing of DFU at 6 months and amputation were primary endpoints of the
study.
RESULTS: In total, 43 patients (64.2%) in the rifampicin group healed at 3 months and another 4 patients healed when rifampicin was continued for 6 months (n = 47, 70.1%). In the control group, 11 patients healed at 3 months (16.2%) and 25 patients healed at 6 months (36.8%). In total, 14 patients (20.9%) in the
study group and 29 patients (42.6%) in the control group had to undergo minor amputation. Comparison between the rate of healing at 3 and 6 months and minor amputation between the
study group and control group showed statistically significant results (P ≤ .00001, <.00001, and .008, respectively). In total, 6 and 8 patients despite healing of the primary ulcer had a subsequent recurrence of ulcer in the rifampicin and control group, respectively.
CONCLUSIONS: Rifampicin used in conjunction with other standard poly-microbial therapy in refractory complex diabetic foot ulcer unresponsive to standard antimicrobial therapy, can significantly improve wound healing as well as decrease the need for amputation in addition to standard of care.