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dc.contributor.authorVenegas, Viviana
dc.contributor.authorManterola, Carla
dc.contributor.authorDe Pablo, Jose
dc.contributor.authorGarcia, Mariano
dc.contributor.authorde León, Sonia Ponce
dc.contributor.authorCavada, Gabriel
dc.date.accessioned2024-04-10T06:37:18Z
dc.date.available2024-04-10T06:37:18Z
dc.date.issued2022
dc.identifier10.1002/epi4.12620
dc.identifier.issn24709239
dc.identifier.urihttps://hdl.handle.net/20.500.12728/11035
dc.description.abstractObjective: This study aimed to describe the characteristics of pediatric neurologists (PNs) in Latin America (LA) who attend to children and adolescents with epilepsy and convey to them the risk of sudden unexpected death in epilepsy (SUDEP). Methods: Personal data and details of discussion of SUDEP with families, including relevance of SUDEP disclosure, frequency of such communication, perceived benefits and risks of disclosure, extent of training received on such disclosure, and professional experience with SUDEP, were collected through an online survey of PNs from LA. Their personal experience in carrying out this conversation was obtained through responses to an open question, further used to identify the main barriers. Results: Of the 442 surveys received, 367 (83%) were analyzed. Most participants (73.8%) responded that the communication of SUDEP risk was relevant or very relevant; however, only 17.9% reported communicating it always or very frequently. Factors that increased the frequency of SUDEP communication included patients with higher levels of complexity (OR = 2.18, P =.003) and the physician's personal experience with SUDEP (OR = 2.305, P <.001). Direct questions from the family and avoiding scaring them about a rare outcome were the main motivations behind discussing and not discussing SUDEP, respectively. In the open question, respondents identified worries about the patient's ability to understand the information and cultural gaps as barriers. “Informing with the intention of improving adherence to treatment” and “establishing an empathic relationship” were significantly related. Further, the concept of “do not scare” was significantly related to “personal difficulties in discussing SUDEP.”. Significance: Although most PNs agree that communication about SUDEP is relevant, only a minority actually engages in it. Participants identified a lack of appropriate training in such communication as a barrier. A better understanding of communication expectations, education of health professionals, and communication techniques have a strong relevance in diminishing the gap between guidelines and practice. © 2022 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.es_ES
dc.description.sponsorshipChilean Society of Psychiatry and Neurology of Childhood and Adolescence; Pediatric Neurology Societies of LA; SOPNIA; Society of Epileptology of Chilees_ES
dc.language.isoenes_ES
dc.publisherJohn Wiley and Sons Inces_ES
dc.subjectcommunicationes_ES
dc.subjectepilepsy mortalityes_ES
dc.subjecthealthcare providerses_ES
dc.subjectpediatric epilepsyes_ES
dc.subjectrisk of deathes_ES
dc.titleHow the characteristics of pediatric neurologists in Latin America influence the communication of sudden unexpected death in epilepsy to patients and caregiverses_ES
dc.typeArticlees_ES


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