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Proof of concept of an experimental prototype for the prevention of parastomal hernia

dc.contributor.authorGarcía Manzanares, María Elena
dc.contributor.authorZaragoza García, Ignacio
dc.contributor.authorAvilés Escudero, Mercedes
dc.contributor.authorAlonso-Cortés Fradejas, Beatriz
dc.date.accessioned2024-07-12T06:55:30Z
dc.date.available2024-07-12T06:55:30Z
dc.date.issued2024-05-27
dc.description.abstractPurpose: The aim of this study was to analyse the complications and problems associated with the use of an experimental prototype designed for the prevention of parastomal hernia (PSH), one of the most frequent complications in ostomates. Methods: A single-centre, non-comparative, proof-of-concept interventional pilot study of an experimental prototype designed to be used in conjunction with an abdominal compression binder to prevent PSH was conducted. The "Ostomy Fixation Device for Hernia Prevention" (patent P201531826) is a semi-rigid ostomy protector, to be used in conjunction with a compression binder. It is designed to adapt to the dimensions of standard ostomy bags from different brands and serves to transmit, in a localised manner, the support coming from the compression binder in the peristomal area without putting pressure on the collection bag. The main outcome measures were efficacy, safety, and patient-users' opinion/perception. Results: Ten patients were studied for 12 months. Mean age was 61 years (± 11.59), 70% (7) were male, 80% (8) ostomised for colorectal cancer, 90% (9) underwent planned surgery and 80% (8) had a colostomy. Efficacy: the incidence of HPE was 10% (1). Safety: no participant experienced pain, discomfort, itching, stinging, leakage, pouch detachment, allergy to components, or injury to the stoma or peristomal skin due to rubbing or pressure. 90% (n = 9) were considered "very satisfied" or "satisfied" with the device. Conclusions: An innovative device designed in collaboration between healthcare professionals and end-users has been shown to be safe and effective in reducing PSH in the group of ostomates studied.
dc.description.departmentDepto. de Enfermería
dc.description.facultyFac. de Enfermería, Fisioterapia y Podología
dc.description.fundingtypeAPC financiada por la UCM
dc.description.refereedTRUE
dc.description.sponsorshipUniversidad Complutense de Madrid. Instituto de Salud Carlos III (ISCIII) in its 2017 call for proposals under the “Technological Development Projects” modality (DTS17/00179); Research Institute of the Hospital Universitario 12 de Octubre (i+12) (Ref. i12-AY2002241)
dc.description.statuspub
dc.identifier.citationGarcía-Manzanares, M.E., Zaragoza-García, I., Avilés-Escudero, M. et al. Proof of concept of an experimental prototype for the prevention of parastomal hernia. Updates Surg (2024). https://doi.org/10.1007/s13304-024-01898-0
dc.identifier.doi10.1007/s13304-024-01898-0
dc.identifier.issn2038-131X
dc.identifier.issn2038-3312
dc.identifier.officialurlhttps://doi.org/10.1007/s13304-024-01898-0
dc.identifier.urihttps://hdl.handle.net/20.500.14352/106002
dc.journal.titleupdates in surgery
dc.language.isoeng
dc.publisherspringer
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu61
dc.subject.keywordOstomy
dc.subject.keywordParastomal hernia
dc.subject.keywordPrevention
dc.subject.keywordStoma support garments
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco32 Ciencias Médicas
dc.titleProof of concept of an experimental prototype for the prevention of parastomal hernia
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication84b8824f-1624-447b-9ede-b85f21a7d3c3
relation.isAuthorOfPublication61989576-46c1-456c-bca0-73cd8e2581a3
relation.isAuthorOfPublication.latestForDiscovery84b8824f-1624-447b-9ede-b85f21a7d3c3

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Purpose: The aim of this study was to analyse the complications and problems associated with the use of an experimental prototype designed for the prevention of parastomal hernia (PSH), one of the most frequent complications in ostomates. Methods: A single-centre, non-comparative, proof-of-concept interventional pilot study of an experimental prototype designed to be used in conjunction with an abdominal compression binder to prevent PSH was conducted. The "Ostomy Fixation Device for Hernia Prevention" (patent P201531826) is a semi-rigid ostomy protector, to be used in conjunction with a compression binder. It is designed to adapt to the dimensions of standard ostomy bags from different brands and serves to transmit, in a localised manner, the support coming from the compression binder in the peristomal area without putting pressure on the collection bag. The main outcome measures were efficacy, safety, and patient-users' opinion/perception. Results: Ten patients were studied for 12 months. Mean age was 61 years (± 11.59), 70% (7) were male, 80% (8) ostomised for colorectal cancer, 90% (9) underwent planned surgery and 80% (8) had a colostomy. Efficacy: the incidence of HPE was 10% (1). Safety: no participant experienced pain, discomfort, itching, stinging, leakage, pouch detachment, allergy to components, or injury to the stoma or peristomal skin due to rubbing or pressure. 90% (n = 9) were considered "very satisfied" or "satisfied" with the device. Conclusions: An innovative device designed in collaboration between healthcare professionals and end-users has been shown to be safe and effective in reducing PSH in the group of ostomates studied.

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