Multicentric observational study of pain after the use of a self-gripping lightweight mesh

Introduction Investigation in the field of inguinal hernia surgery is now focused on postoperative pain. The extended use of lightweight meshes and alternative methods of fixation may play a relevant role in the reduction of pain. In this study, a new self-gripping lightweight polypropylene mesh is...

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Published inHernia : the journal of hernias and abdominal wall surgery Vol. 15; no. 5; pp. 511 - 515
Main Authors García Ureña, M. Á., Hidalgo, M., Feliu, X., Velasco, M. Á., Revuelta, S., Gutiérrez, R., Utrera, A., Porrero, J. L., Marín, M., Zaragoza, C.
Format Journal Article
LanguageEnglish
Published Paris Springer-Verlag 01.10.2011
Springer Nature B.V
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Summary:Introduction Investigation in the field of inguinal hernia surgery is now focused on postoperative pain. The extended use of lightweight meshes and alternative methods of fixation may play a relevant role in the reduction of pain. In this study, a new self-gripping lightweight polypropylene mesh is tested. Methods A multicentric, observational study was scheduled to prospectively evaluate this new mesh. Ten centers agreed to participate. Only primary, type 1 or 2 uncomplicated hernias in adults were included. The mesh was placed as a Lichtenstein procedure without any fixation. A complete pain questionnaire was followed at 1 week, and at 1, 3 and 6 months postoperatively. The principal goal of the study was to evaluate maximum pain score at 6 months. Pain was assessed by a visual analog scale. A total of 256 patients were operated. Mean operative time was 35.6 min; 76.2% of patients were operated in an ambulatory setting. Results There were a few postoperative complications: 2 wound infections, 17 seromas, 21 hematomas, 6 orchitis. The incidence of acute pain was 27.3% at week 1 and 7.5% at month 1. The incidence of chronic pain was 3.6% at month 3 and 2.8% at month 6. No recurrences or long-term complications were observed. Conclusion This self-gripping mesh can be used safely in type 1 and 2 primary, uncomplicated inguinal hernia with minimal morbidity and most patients under ambulatory setting. The registered incidence of chronic pain is lower than 3%.
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ISSN:1265-4906
1248-9204
DOI:10.1007/s10029-011-0811-3