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Randomized controll...
Randomized controlled multicenter international clinical trial of self-gripping Parietex (TM) ProGrip (TM) polyester mesh versus lightweight polypropylene mesh in open inguinal hernia repair: interim results at 3 months
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- Kingsnorth, A (författare)
- Derriford Hospital, England
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- Gingell-Littlejohn, M (författare)
- University of Glasgow, Scotland,University of Ziekenhuizen Leuven, Belgium
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- Nienhuijs, S (författare)
- Catharina Hospital, Netherlands
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- Schuele, S (författare)
- Klinikum Bremen Mitte, Germany
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- Appel, P (författare)
- Herz Jesu Krankenhaus gGmbH, Germany
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- Ziprin, P (författare)
- University of London Imperial College of Science Technology and Med, England
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- Eklund, Arne (författare)
- Uppsala universitet,Centrum för klinisk forskning, Västerås,Central Hospital Vasteras, Sweden
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- Miserez, M (författare)
- University of Ziekenhuizen Leuven, Belgium
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- Smeds, Staffan (författare)
- Östergötlands Läns Landsting,Linköpings universitet,Kirurgi,Hälsouniversitetet,Kirurgiska kliniken i Östergötland
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(creator_code:org_t)
- 2012-03-28
- 2012
- Engelska.
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Ingår i: Hernia. - : Springer Verlag (Germany). - 1265-4906 .- 1248-9204. ; 16:3, s. 287-294
- Relaterad länk:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Ämnesord
Stäng
- To compare clinical outcomes following sutureless Parietex (TM) ProGrip (TM) mesh repair to traditional Lichtenstein repair with lightweight polypropylene mesh secured with sutures. less thanbrgreater than less thanbrgreater thanThis is a 3-month interim report of a 1-year multicenter international study. Three hundred and two patients were randomized; 153 were treated with Lichtenstein repair (L group) and 149 with Parietex (TM) ProGrip (TM) precut mesh (P group) with or without fixation. The primary outcome measure was postoperative pain using the visual analog scale (VAS, 0-150 mm); other outcomes were assessed prior to surgery and up to 3 months postoperatively. less thanbrgreater than less thanbrgreater thanCompared to baseline, pain score was lower in the P group at discharge (-10%) and at 7 days (-13%), while pain increased in the L group at discharge (+39%) and at 7 days (+21%). The difference between groups was significant at both time points (P = 0.007 and P = 0.039, respectively). In the P group, patients without fixation suffered less pain compared to those with single-suture fixation (1 month: -20.9 vs. -6.15%, P = 0.02; 3 months: -24.3 vs. -7.7%, P = 0.01). The infection rate was significantly lower in the P group during the 3-month follow-up (2.0 vs. 7.2%, P = 0.032). Surgery duration was significantly shorter in the P group (32.4 vs. 39.1 min; P andlt; 0.001). No recurrence was observed at 3 months in both groups. less thanbrgreater than less thanbrgreater thanSurgery duration, early postoperative, pain and infection rates were significantly reduced with self-gripping polyester mesh compared to Lichtenstein repair with polypropylene mesh. The use of fixation increased postoperative pain in the P group. The absence of early recurrence highlights the gripping efficiency effect.
Nyckelord
- Parietex (TM) ProGrip (TM)
- Lichtenstein
- Polyester mesh
- Polypropylene mesh
- Lightweight mesh
- Self-gripping mesh
- MEDICINE
- MEDICIN
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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