DeWitt Daughtry Family Department of Surgery and.
Division of Nephrology and Hypertension, Leonard M. Miller School of Medicine, University of Miami, Miami, Florida.
J Am Soc Nephrol. 2018 Mar;29(3):1030-1040. doi: 10.1681/ASN.2017050559. Epub 2018 Jan 2.
The frequency of primary failure in arteriovenous fistulas (AVFs) remains unacceptably high. This lack of improvement is due in part to a poor understanding of the pathobiology underlying AVF nonmaturation. This observational study quantified the progression of three vascular features, medial fibrosis, intimal hyperplasia (IH), and collagen fiber organization, during early AVF remodeling and evaluated the associations thereof with AVF nonmaturation. We obtained venous samples from patients undergoing two-stage upper-arm AVF surgeries at a single center, including intraoperative veins at the first-stage access creation surgery and AVFs at the second-stage transposition procedure. Paired venous samples from both stages were used to evaluate change in these vascular features after anastomosis. Anatomic nonmaturation (AVF diameter never ≥6 mm) occurred in 39 of 161 (24%) patients. Neither preexisting fibrosis nor IH predicted AVF outcomes. Postoperative medial fibrosis associated with nonmaturation (odds ratio [OR], 1.55; 95% confidence interval [95% CI], 1.05 to 2.30; =0.03, per 10% absolute increase in fibrosis), whereas postoperative IH only associated with failure in those individuals with medial fibrosis over the population's median value (OR, 2.63; 95% CI, 1.07 to 6.46; =0.04, per increase of 1 in the intima/media ratio). Analysis of postoperative medial collagen organization revealed that circumferential alignment of fibers around the lumen associated with AVF nonmaturation (OR, 1.38; 95% CI, 1.03 to 1.84; =0.03, per 10° increase in angle). This study demonstrates that excessive fibrotic remodeling of the vein after AVF creation is an important risk factor for nonmaturation and that high medial fibrosis determines the stenotic potential of IH.
动静脉瘘(AVF)的初次失败频率仍然高得令人无法接受。这种改善不佳的部分原因是对 AVF 不成熟的基础病理生理学的理解不足。这项观察性研究量化了在早期 AVF 重塑过程中三种血管特征(中膜纤维化、内膜增生(IH)和胶原纤维组织)的进展,并评估了它们与 AVF 不成熟的关系。我们从一家中心的 2 期上臂 AVF 手术患者中获得了静脉样本,包括一期通路创建手术时的术中静脉和二期转位手术时的 AVF。使用两个阶段的配对静脉样本来评估吻合后这些血管特征的变化。在 161 例患者中,39 例(24%)发生了解剖学上的不成熟(AVF 直径从未≥6mm)。预先存在的纤维化或 IH 均不能预测 AVF 结果。与非成熟相关的术后中膜纤维化(比值比 [OR],1.55;95%置信区间 [95%CI],1.05 至 2.30;=0.03,每增加 10%绝对纤维化),而仅在中膜纤维化高于人群中位数的个体中,术后 IH 与失败相关(OR,2.63;95%CI,1.07 至 6.46;=0.04,内膜/中膜比值每增加 1)。对术后中膜胶原组织的分析表明,纤维围绕管腔的周向排列与 AVF 不成熟相关(OR,1.38;95%CI,1.03 至 1.84;=0.03,角度每增加 10°)。这项研究表明,AVF 形成后静脉过度纤维化重塑是不成熟的重要危险因素,而中膜纤维化程度高决定了 IH 的狭窄潜能。