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应用交联胶原治疗特发性肛痿:一项前瞻性 1 期研究。

Management of idiopathic anal fistula using cross-linked collagen: a prospective phase 1 study.

机构信息

Homerton University Hospital NHS Foundation Trust, London, UK.

出版信息

Colorectal Dis. 2011 Jan;13(1):94-104. doi: 10.1111/j.1463-1318.2009.02087.x.

Abstract

AIM

Fibrin glue and porcine intestinal submucosa are used in novel sphincter-preserving techniques to heal anal fistulae. However, their success is highly variable and decreases with the length of follow up. The aim of this study was to assess the safety, feasibility and potential efficacy of another novel agent, cross-linked collagen, in two different physical formats, to heal anal fistulae.

METHOD

Prospectively recruited patients underwent symptom, continence and anal physiology assessments and magnetic resonance imaging. Patients with secondary tracts or acute sepsis were excluded. At operation, participants were randomized to receiving a solid collagen implant or collagen fibres suspended in fibrin glue. Follow up included repeat symptom, continence and physiological assessments at 3 months, and regular clinical review thereafter.

RESULTS

Twenty-nine of 43 entrants were eligible for inclusion. Thirteen patients received the collagen implant, and 16 collagen-fibrin glue. Three months postoperation, no patient experienced acute sepsis or continence disturbance, and sphincter function and integrity were unchanged. At 29 months, 12 of 15 (one lost to follow up) patients treated with collagen-fibrin glue were healed, compared with seven of 13 who received the implant.

CONCLUSION

In the short-to-medium term, both techniques are safe and equally effective. The results justify continued research into the use of biomaterials to heal anal fistulae.

摘要

目的

纤维蛋白胶和猪肠黏膜被用于新型保留括约肌技术以治疗肛瘘。然而,其成功率高度可变,且随随访时间的延长而降低。本研究旨在评估另一种新型制剂——交联胶原在两种不同物理形式下治疗肛瘘的安全性、可行性和潜在疗效。

方法

前瞻性招募的患者接受症状、控便和肛门生理评估以及磁共振成像检查。排除存在第二瘘管或急性脓毒症的患者。手术时,将参与者随机分配接受固体胶原植入物或纤维蛋白胶中悬浮的胶原纤维。随访包括术后 3 个月重复症状、控便和生理评估,此后定期进行临床复查。

结果

43 名入选者中有 29 名符合条件。13 名患者接受胶原植入物治疗,16 名患者接受胶原纤维-纤维蛋白胶治疗。术后 3 个月,无患者发生急性脓毒症或控便障碍,括约肌功能和完整性无变化。29 个月时,接受胶原纤维-纤维蛋白胶治疗的 15 名患者中有 12 名(1 名失访)治愈,而接受植入物治疗的 13 名患者中只有 7 名治愈。

结论

在短至中期,两种技术均安全且同样有效。结果证明有必要进一步研究生物材料在治疗肛瘘中的应用。

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