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Parietex™ Composite mesh versus DynaMesh(®)-IPOM for laparoscopic incisional and ventral hernia repair: a retrospective cohort study.

机译:parietex™复合网与Dynamesh(®)-IpOm用于腹腔镜切口和腹疝修复:一项回顾性队列研究。

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摘要

INTRODUCTION Laparoscopic incisional and ventral hernia repair (LIVHR) is widely accepted and safe but the type of mesh used is still debated. We retrospectively compared postoperative outcomes with two different meshes commonly used in LIVHR. METHODS This is a retrospective study of patients who underwent incisional hernia repair between January 2008 and December 2010. Two meshes were used: Parietex™ Composite (Covidien, New Haven, CT, USA) and the DynaMesh(®)-IPOM (FEG Textiltechnik mbH, Aachen, Germany). The two groups were compared with respect to recurrence rates, incidence of seroma and intestinal obstruction. RESULTS Among the 88 patients who underwent LIVHR, 75 patients (85.2%) presented with primary incisional hernia, 10 (11.4%) presented with a first recurrence and 3 (3.4%) presented with a second recurrence. Median follow-up was 53.6 months (range 40-61 months). 12.9% of patients had recurrence in the Parietex™ Composite mesh group (n=62) in comparison to 3.8% in the DynaMesh(®)-IPOM mesh group (n=26; P=0.20). DynaMesh(®)-IPOM was associated with a significantly higher incidence of intestinal obstruction secondary to adhesions (11.5% vs. 0%, P=0.006) and lower incidence of seroma and haematoma formation compared to Parietex™ composite mesh group (0% vs. 6.4% of patients; P=0.185). CONCLUSIONS LIVHR is a safe and feasible technique. Dynamesh(®)-IPOM is associated with a significantly higher incidence of adhesion related bowel obstruction, albeit with a lower incidence of recurrence, seroma and haematoma formation compared with Parietex™ Composite mesh. However, there is a need for further well-designed, multicentre randomised controlled studies to investigate the use of these meshes.
机译:引言腹腔镜切开和腹侧疝修补术(LIVHR)已被广泛接受并且安全,但是仍在争论使用的网片类型。我们回顾性比较了LIVHR中常用的两种不同网片的术后结局。方法这是一项对2008年1月至2010年12月进行切口疝修补术的患者的回顾性研究。使用了两种网片:Parietex™复合材料(美国康涅狄格州纽黑文的Covidien)和DynaMesh®-IPOM(FEG Textiltechnik mbH)。 (德国亚琛)。比较两组的复发率,血清肿发生率和肠梗阻。结果在88例行LIVHR的患者中,有75例(85.2%)出现原发性切开疝,其中10例(11.4%)首次复发,3例(3.4%)再次复发。中位随访时间为53.6个月(范围40-61个月)。在Parietex™复合材料网片组(n = 62)中有12.9%的患者复发,而DynaMesh®-IPOM网片组(n = 26; P = 0.20)则为3.8%。与Parietex™复合网状组相比,DynaMesh(®)-IPOM与继发于肠粘连的肠梗阻发生率显着较高(11.5%vs. 0%,P = 0.006)以及血清肿和血肿形成的发生率较低(0%vs 6.4%的患者; P = 0.185)。结论LIVHR是一种安全可行的技术。与Parietex™复合材料网相比,Dynamesh(®)-IPOM与粘连相关的肠梗阻发生率显着较高,尽管复发,血清肿和血肿形成的发生率较低。但是,需要进一步设计完善的多中心随机对照研究来研究这些网格的使用。

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