2012
DOI: 10.1007/s00268-012-1810-y
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Trans‐cutaneous Closure of Central Defects (TCCD) in Laparoscopic Ventral Hernia Repairs (LVHR)

Abstract: The incidence of seroma, mesh and tissue eventration, and hernia recurrence was significantly lower following LVHR-TCCD when compared to sLVHR. Subjective improvement in overall patient satisfaction, cosmetic satisfaction, and functional status was reported with closing the central defect. The LVHR-TCCD technique may be superior for treating ventral hernias due to lower complication rates and higher patient satisfaction and functional status.

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Cited by 85 publications
(44 citation statements)
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“…A randomized clinical trial involving laparoscopic ventral repair demonstrated increased pain from transfascial fixation sutures for mesh placement [20]. Contrarily, pain rates did not increase in another study describing laparoscopic repair with transcutaneous closure of the defects [10]. Pain assessment in this current study reported no significant difference in patients who underwent primary closure with barbed sutures compared to the mesh-only technique.…”
Section: Discussionmentioning
confidence: 42%
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“…A randomized clinical trial involving laparoscopic ventral repair demonstrated increased pain from transfascial fixation sutures for mesh placement [20]. Contrarily, pain rates did not increase in another study describing laparoscopic repair with transcutaneous closure of the defects [10]. Pain assessment in this current study reported no significant difference in patients who underwent primary closure with barbed sutures compared to the mesh-only technique.…”
Section: Discussionmentioning
confidence: 42%
“…Several approaches in laparoscopic ventral hernia repair have been described in literature in the last few decades [9,10]. The forms of suture, mesh, fixation device, and surgical techniques depend on the experience of the surgeon and postoperative factors such as pain, seroma formation, and adhesions.…”
Section: Discussionmentioning
confidence: 99%
“…A skin, B left rectus abdominis muscle, C right rectus abdominis muscle, D peritoneum (hernia sac), E EndoClose™ a median follow-up period of 10.5-50.4 months. To date, three reports [27,30,31] have indicated that IPOM-Plus was associated with a lower recurrence rate compared with that of sIPOM based on their data: 0 and 16.7, 3.0 and 4.8, and 5.7 and 15.1 %, respectively. However, two studies [32,33] reported that IPOM-Plus did not contribute to a reduction in the recurrence rate.…”
Section: Recurrencementioning
confidence: 94%
“…Out of these articles, four [30,31,33,34] compared sIPOM with IPOM-Plus, and only one report was a randomized controlled study (RCT) [34]. (Table 1) The publication year, number of patients, and the size (surface area and width) of the hernial orifice in the previous literature are shown in Table 1.…”
Section: Introductionmentioning
confidence: 98%
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