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One year results of a randomised controlled multi-centre study comparing Prolene and Vypro II-mesh in Lichtenstein hernioplasty

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Abstract

A standard polypropylene mesh used in Lichtenstein’s operation induces a strong foreign tissue reaction with potential harmful effects. A mesh with less polypropylene could possibly be beneficial. Six hundred men with primary unilateral inguinal hernias were randomised to Lichtenstein’s operation using a Prolene- or Vypro II-mesh in six centres. The patients were blinded to which mesh they received. A validated questionnaire assessing recurrence and pain along with SF-36 Health Survey was sent after 1 year to all patients and a selected group was clinically examined. Of the 591 operated patients, 526 (89.0%) returned the questionnaire. 188 patients had some complaints or sensations of which 111 patients were clinically examined. The mean follow-up time was 13.6 (SD. 4.0) months. The incidence of hernia recurrence (four vs. four patients) and neuralgia (three vs. four patients) did not differ between Prolene and Vypro II-groups, respectively. One Vypro II-patient was re-operated due to neuralgia. There was no difference in the SF-36 scores. The results of Lichtenstein’s operation with either Prolene or Vypro II do not seem to differ significantly.

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Acknowledgements

The authors are grateful to RN Cajsa Barthelsson, RN Christina Lindblom, RN Sirpa Jämsä, Secr. Carina Törnkvist. and Secr. Lise-Lotte Lindh, for their skilful work in the study. Financial support: The study was supported by a grant from Ethicon Scandinavia, Ethicon Europe and from the County Council of Stockholm.

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Bringman, S., Wollert, S., Österberg, J. et al. One year results of a randomised controlled multi-centre study comparing Prolene and Vypro II-mesh in Lichtenstein hernioplasty. Hernia 9, 223–227 (2005). https://doi.org/10.1007/s10029-005-0324-z

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  • DOI: https://doi.org/10.1007/s10029-005-0324-z

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