Your browser doesn't support javascript.
loading
Acceptability, effectiveness and safety of a Renew® anal insert in patients who have undergone restorative proctocolectomy with ileal pouch-anal anastomosis.
Segal, J P; Leo, C A; Hodgkinson, J D; Cavazzoni, E; Bradshaw, E; Lung, P F C; Ilangovan, R; Vaizey, C J; Faiz, O D; Hart, A L; Clark, S K.
Afiliação
  • Segal JP; St Mark's Hospital, Harrow, UK.
  • Leo CA; Department of Surgery and Cancer, Imperial College, London, UK.
  • Hodgkinson JD; St Mark's Hospital, Harrow, UK.
  • Cavazzoni E; Department of Surgery and Cancer, Imperial College, London, UK.
  • Bradshaw E; St Mark's Hospital, Harrow, UK.
  • Lung PFC; Department of Surgery and Cancer, Imperial College, London, UK.
  • Ilangovan R; Department of Surgery, University of Perugia, Perugia, Italy.
  • Vaizey CJ; St Mark's Hospital, Harrow, UK.
  • Faiz OD; St Mark's Hospital, Harrow, UK.
  • Hart AL; Department of Surgery and Cancer, Imperial College, London, UK.
  • Clark SK; St Mark's Hospital, Harrow, UK.
Colorectal Dis ; 21(1): 73-78, 2019 01.
Article em En | MEDLINE | ID: mdl-30218632
ABSTRACT

INTRODUCTION:

Restorative proctocolectomy has gained acceptance in the surgical management of medically refractive ulcerative colitis and cancer prevention in familial adenomatous polyposis. Incontinence following restorative proctocolectomy occurs in up to 25% of patients overnight. The Renew® insert is an inert single-use device which acts as an anal plug. The aim of this study was to assess the acceptability, effectiveness and safety of the Renew® insert in patients who have undergone restorative proctocolectomy. The device has yet to be assessed in patients who have undergone restorative proctocolectomy.

METHOD:

This was a prospective study exploring the acceptability, effectiveness and safety of the Renew® insert in improving incontinence in patients who had undergone restorative proctocolectomy. A total of 15 patients with incontinence were asked to use the Renew® insert for 14 days following their standard care. The Incontinence Questionnaire-Bowels was used pre- and posttreatment to assess response and patients were asked to report the perceived acceptability, effectiveness and safety of the device at the end of the trial.

RESULTS:

The device was acceptable to 8/15 (53%) of patients and was effective in 6/15 (40%). Only 2/15 (13%) of patients raised any safety concerns, and these were minor. The device was associated with a significant reduction in night seepage (P = 0.034).

CONCLUSION:

In a small study, the Renew® insert can be both acceptable and effective and is also associated with few safety concerns. It is also associated with significant reductions in night-time seepage.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações Pós-Operatórias / Aceitação pelo Paciente de Cuidados de Saúde / Colite Ulcerativa / Proctocolectomia Restauradora / Equipamentos e Provisões / Incontinência Fecal Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações Pós-Operatórias / Aceitação pelo Paciente de Cuidados de Saúde / Colite Ulcerativa / Proctocolectomia Restauradora / Equipamentos e Provisões / Incontinência Fecal Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article