Long-term outcomes of sacral nerve stimulation for faecal incontinence

Author:

Altomare D F1,Giuratrabocchetta S1,Knowles C H2,Muñoz Duyos A3,Robert-Yap J4,Matzel K E5,De Miguel Velasco M6,Rosen H7,Ganio E8,Ratto C9,Devesa M J10,Cui Z11

Affiliation:

1. Department of Emergency and Organ Transplantation, University Aldo Moro of Bari, Bari, Italy

2. Centre for Digestive Disease, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK

3. Department of Surgery, Hospital Universitari MútuaTerrassa, Barcelona, Spain

4. Department of Surgery, University of Geneva Hospital, Geneva, Switzerland

5. Chirurgische Klinik, Universität Erlangen, Germany

6. Department of Surgery, Hospital Virgen del Camino, Pamplona, Spain

7. Department of Surgery, St Vincent Hospital, Vienna, Austria

8. Gruppo Policlinico di Monza, Divisione di Chirurgia Colorettale, Clinica Santa Rita, Vercelli, Italy

9. Department of Surgical Sciences, Catholic University, Rome, Italy

10. University Hospital Ramón y Cajal, Madrid, Spain

11. Chirurgische Klinik, Universität Erlangen, Erlangen, Germany

Abstract

Abstract Background Sacral nerve stimulation (SNS) has proven short- to medium-term effectiveness for the treatment of faecal incontinence (FI); fewer long-term outcomes have been presented and usually in small series. Here, the long-term effectiveness of SNS was evaluated in a large European cohort of patients with a minimum of 5 years' follow-up. Methods Prospectively registered data from patients with FI who had received SNS for at least 5 years from ten European centres were collated by survey. Daily stool diaries, and Cleveland Clinic and St Mark's incontinence scores were evaluated at baseline, after implantation and at the last follow-up. SNS was considered successful when at least 50 per cent symptom improvement was maintained at last follow-up. Results A total of 407 patients underwent temporary stimulation, of whom 272 (66·8 per cent) had an impulse generator implanted; 228 (56·0 per cent) were available for long-term follow-up at a median of 84 (i.q.r. 70–113) months. Significant reductions in the number of FI episodes per week (from median 7 to 0·25) and summative symptom scores (median Cleveland Clinic score from 16 to 7, St Mark's score from 19 to 6) were recorded after implantation (all P < 0·001) and maintained in long-term follow-up. In per-protocol analysis, long-term success was maintained in 71·3 per cent of patients and full continence was achieved in 50·0 per cent; respective values based on intention-to-treat analysis were 47·7 and 33·4 per cent. Predictive analyses determined no significant association between pretreatment variables and successful outcomes. Risk of long-term failure correlated with minor symptom score improvement during the temporary test phase. Conclusion SNS remains an effective treatment for FI in the long term for approximately half of the patients starting therapy.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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