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Impact of sphincter lesions and delayed sphincter repair on sacral neuromodulation treatment outcomes for faecal incontinence: results from a Finnish national cohort study

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Abstract

Purpose

The aim of this multicentre study was to analyse the effects of patent sphincter lesions and previous sphincter repair on the results of sacral neuromodulation (SNM) treatment on patients with faecal incontinence (FI).

Methods

Patients examined by endoanal ultrasound (EAUS) with FI as the indication for SNM treatment were included in the study. Data was collected from all the centres providing SNM treatment in Finland and analysed for differences in treatment outcomes.

Results

A total of 237 patients treated for incontinence with SNM had been examined by EAUS. Of these patients, 33 had a history of previous delayed sphincter repair. A patent sphincter lesion was detected by EAUS in 128 patients. The EAUS finding did not influence the SNM test phase outcome (p = 0.129) or the final treatment outcome (p = 0.233). Patient’s history of prior sphincter repair did not have a significant effect on the SNM test (p = 0.425) or final treatment outcome (p = 0.442).

Conclusions

Results of our study indicate that a sphincter lesion or previous sphincter repair has no significant effect on the outcome of SNM treatment. Our data suggests that delayed sphincter repair prior to SNM treatment initiation for FI is not necessary.

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Acknowledgments

We would like to thank Ms. Elizabeth Prouty, for her revision of the English language.

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Ethics declarations

This study was conducted in accordance with Finnish Medical Research Act 488/199, 295/2004 and approved by the Ethics Committee of the Hospital District of Southwest Finland (ETMK: 163/1801/2015).

Appendices

Appendix 1

The EAUS imaging devices were all supplied by BK Medical. The models varied over the period of 1999–2017, with models Cheetah and Leopard being in use from 1999 to 2002, Falcon from 1999 to 2009, Hawk from 2000 to 2009, Pro Focus Yellow and Green from 2005 to 2010, Pro Focus Blue from 2005 to 2012, Pro Focus Ultraview and Flex Focus 400 from 2009 to 2017, Flex Focus 500 from 2011 to 2017, Flex Focus 800 from 2012 to 2017 and bk3000 and bk5000 from 2014 to 2017. Transducers used with these scanners have varied over the period from 1999 to 2017, with model 1850 being in use from 1999 to 2012, model 2050 from 1999 to 2012, model 2052 from 2005 to 2017 and model 20R3 from 2015 to 2017

Appendix 2

All of the implanted devices were supplied by Medtronic® Inc. (Minneapolis, Minnesota, USA). Until 2002, a non-tined lead was used. Model 3057 PNE (Medtronic® Inc. Minneapolis, USA) was used for temporary evaluation of therapeutic success. A Quadripolar lead model 3093 tined lead was used from 2003 and changed to model 3889 in 2014

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Kirss, J., Pinta, T., Rautio, T. et al. Impact of sphincter lesions and delayed sphincter repair on sacral neuromodulation treatment outcomes for faecal incontinence: results from a Finnish national cohort study. Int J Colorectal Dis 33, 1709–1714 (2018). https://doi.org/10.1007/s00384-018-3161-0

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