用于糖尿病足溃疡的原生 I 型胶原蛋白基质加聚六亚甲基双胍抗菌剂与低温保存的尸体皮肤异体移植的真实世界比较效果评估研究--非劣效性分析。

Eplasty Pub Date : 2024-04-04 eCollection Date: 2024-01-01
Michael L Sabolinski, Tad Archambault
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引用次数: 0

摘要

目的确定原生 I 型胶原基质加聚六亚甲基双胍抗菌剂(PCMP)和低温保存的尸体皮肤异体移植(CCSA)用于糖尿病足溃疡(DFUs)的效果:方法:对 989 例糖尿病足溃疡进行了数字化分析,并进行了一项真实世界数据研究。方法:对 989 个 DFU 进行了数字化分析,其中 325 个和 664 个 DFU 分别接受了 PCMP 和 CCSA 治疗。对 PCMP 和 CCSA 的等效性进行了非劣效性检验,显著性水平为 P <.05:第 4、8、12 和 24 周时,PCMP 和 CCSA 的痊愈率分别为 12% vs 10%、27% vs 24%、39% vs 37% 和 60% vs 64%。差异无统计学意义;P = .95。PCMP 和 CCSA 的中位愈合时间分别为 18 周和 17 周;P = .95。从统计学角度看,PCMP 和 CCSA 的愈合概率相当;危险比 = 0.99;95% CI (0.85, 1.17)。非劣效性统计检验结果显示 P = .01:结论:采用非劣效性假设检验,显著性水平为 P P = .01。PCMP 与 CCSA 在中位时间、痊愈百分比和痊愈概率方面的差异无统计学意义。真实世界数据比较效果评估研究的数据有助于指导临床医生限制无效疗法的过度使用和有效疗法的使用不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-World Comparative Effectiveness Assessment Study of a Native Type I Collagen Matrix Plus Polyhexamethylene Biguanide Antimicrobial and a Cryopreserved Cadaveric Skin Allograft for Use in Diabetic Foot Ulcers - A Non-inferiority Analysis.

Objective: To determine the effectiveness of a native type I collagen matrix plus polyhexamethylene biguanide antimicrobial (PCMP) and a cryopreserved cadaveric skin allograft (CCSA) for use in diabetic foot ulcers (DFUs).

Methods: A real-world data study was conducted on 989 DFUs analyzed digitally. Of these, 325 and 664 DFUs were treated with PCMP and CCSA, respectively. Non-inferiority testing for equivalence of PCMP and CCSA was performed at a level of significance of P < .05.

Results: Cox proportional hazards regression analysis for healing for PCMP and CCSA at weeks 4, 8, 12, and 24 was 12% vs 10%, 27% vs 24%, 39 % vs 37%, and 60% vs. 64%, respectively. No statistically significant differences were shown; P = .95. The median time to healing was 18 and 17 weeks for PCMP and CCSA, respectively; P = .95. The probability of healing was statistically equivalent between PCMP and CCSA; hazard ratio = 0.99; 95% CI (0.85, 1.17). Non-inferiority statistical testing results showed P = .01.

Conclusions: Using non-inferiority hypothesis testing at a level of significance of P <.05, we showed that PCMP was equivalent to CCSA; P = .01. PCMP vs CCSA demonstrated no statistically significant differences in median time, percentage, and probability of healing. Data from real-world data comparative effectiveness assessment studies can help guide clinicians to limit overuse of ineffective therapies and underuse of effective therapies.

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