The natural history of tarsal tunnel syndrome in diabetic subjects

医学 相伴的 跗管综合征 比例危险模型 危险系数 前瞻性队列研究 胫神经 内科学 糖尿病神经病变 糖尿病 自然史 感觉 外科 置信区间 脚踝 神经科学 刺激 内分泌学 生物
作者
Willem D. Rinkel,Manuel Castro Cabezas,Erwin Birnie,J. Henk Coert
出处
期刊:Journal of Plastic Reconstructive and Aesthetic Surgery [Elsevier]
卷期号:73 (8): 1482-1489 被引量:9
标识
DOI:10.1016/j.bjps.2020.02.033
摘要

Introduction Tibial nerve entrapment is highly prevalent in diabetic subjects, resulting in significantly more neuropathic complaints and concomitant sensory disturbances. The study aim was to assess the impact of tarsal tunnel syndrome (TTS) and sensory loss at baseline on incident diabetic foot ulceration (DFU) in diabetic patients, since decompressing the tibial nerve might change the natural history of the disease. Methods In this study, 113 subjects with TTS (69 bilateral, 23 left-sided and 21 right-sided) participating in the prospective Rotterdam Diabetic Foot Study were compared to 303 diabetic controls without TTS, regarding incident DFU. Kaplan–Meier analysis and Cox's regression analysis were used to determine the independent hazard of baseline variables for new DFU. Results The median observation period was 836.5 days (IQR, 459–1077.8). In bilateral TTS, 17.4% (95% CI: 8.4–26.3%) of subjects experienced DFU versus 8.3% (95% CI: 5.1–11.6%) in controls (left or right) during follow-up (p = 0.0036). In left-sided TTS, no subjects versus 6.2% (95% CI: 3.4–9.0%) in controls had DFUs (p = 0.243). Incident ulceration was seen in 14.3% (95% CI: −0.7% to −29.3%) of right-sided TTS subjects versus 4.1% (95% CI: 1.5–6.3%) in controls (p = 0.034). Besides HbA1c, diminished sensation at the hallux independently increased the risk of ulceration, in patients with (HR: 4.692, p = 0.003) and without (HR: 2.307, p = 0.002) prior DFU. Discussion Elevated sensory thresholds in TTS render diabetic patients at a higher risk for DFU. With effective surgery, TTS is likely to be an amenable factor to potentially prevent diabetic foot disease and thereby reduce amputation risk. Level of evidence II.
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