Stimulated graciloplasty is used to treat refractory faecal incontinence (for example, anorectal atresia) as an alternative to colostomy. Other approaches aimed at establishing continence are insertion of an artificial anal sphincter and sacral nerve stimulation.
Stimulated graciloplasty involves creating a new anal sphincter using transposed gracilis muscle. Electrodes are implanted in the transposed muscle and connected to an electric pulse generator implanted in the abdominal wall. A continuous current from the pulse generator gradually alters the character of the gracilis muscle fibres.
The procedure can be performed in one or two stages. In the latter case, the muscle wrapping precedes the electrode implantation stage by a few weeks.
A systematic review of 37 studies of graciloplasty found that between 42% and 85% of patients became continent after the procedure (different definitions of continence were used and continence was assessed at different time points in the studies). A controlled study found that at 24 months, frequency of incontinence had significantly improved from baseline in 48 patients who had undergone graciloplasty (p<0.0001); there was no improvement during this period in patients who were not offered surgery. A case series reported successful outcomes in 72% (144 out of 200) of patients, with 5-year follow-up.
A controlled trial found that quality of life improved more in patients treated with graciloplasty (n=46) than in those not offered surgery who were being medically managed (n=40). The following scales were used to assess quality of life: the Cleveland Clinic Faecal Incontinence Scale (p=0.001); the Hospital Anxiety and Depression Scale for anxiety (p=0.03) and depression (p=0.05); and a validated study-specific scale for psychological wellbeing (p<0.0001) and lifestyle characteristics (p<0.0001). In a case series of 129 patients who had graciloplasty, patients' quality of life was significantly improved on the SF-36 scale for physical and social functioning at 12 months' follow-up. For more details, refer to the overview.
The Specialist Advisors suggested that this procedure has been largely superseded by sacral nerve stimulation.
The most common complication of stimulated graciloplasty is wound infection. In a systematic review that included 403 patients assessed for safety outcomes, the overall rate of infection was 28%. In a case series of 121 patients, serious infection needing hospitalisation and/or surgery was reported in 15% of patients, and in another series, it occurred in 14% (17 out of 123) of patients.
Electrical or technical problems with the pulse generator leading to hospitalisation occurred in 48% (23 out of 48) of patients who had undergone graciloplasty in a controlled trial at 42 months' follow-up. In a case series of 123 patients, 3 patients (2%) had a deep vein thrombosis, and one patient died following a pulmonary embolism 3 weeks after surgery.
In a comparative study 69% (33 out of 48) of patients had evacuation difficulties or pain requiring hospitalisation following graciloplasty. Disturbed evacuation was reported in 16% (32 out of 200) of patients in a prospective case series. For more details, refer to the overview.
The Specialist Advisors noted that the main reported adverse events were related to the pulse generator, particularly the risk of infection (both in the short and the long term).