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1.
J Pediatr Gastroenterol Nutr ; 67(2): 169-172, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-29620594

RESUMO

OBJECTIVES: Coping with patient death among pediatric liver transplant teams has received little attention despite general recognition of the potentially negative emotional consequences associated with such loss. The purpose of this study was to investigate the ways in which members of pediatric liver transplant teams cope with the death of patients on the waitlist and post-transplant and the institutional resources available to facilitate this coping. METHODS: Participants included 120 physicians, nurses, and mental health professionals from multiple transplant centers across the United States. Participants completed an online questionnaire that assessed the availability of formal coping resources at their institutions, informal sources of support used to cope with patient death, and as indices of coping, bereavement, and emotional exhaustion symptoms experienced. RESULTS: Debriefing, the most commonly offered support, was available to about half (55.8%) of the sample; yet, nearly all respondents (98.3%) indicated that debriefing would be useful. On average, bereavement and emotional exhaustion levels were comparable to normative data, but patterns of coping varied based on participants' position within the transplant team. For participants who reported that debriefing was available at their institutions, emotional exhaustion was lower. CONCLUSIONS: Overall, formal supports were inconsistently offered to pediatric transplant team members. Team members expressed high acceptability for debriefing, which has been associated with benefits in other populations, and findings indicated better coping in the transplant setting when it was offered.


Assuntos
Adaptação Psicológica , Luto , Transplante de Fígado , Equipe de Assistência ao Paciente , Sistemas de Apoio Psicossocial , Criança , Serviços de Saúde da Criança , Humanos , Inquéritos e Questionários , Estados Unidos
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J Am Coll Health ; 66(5): 331-339, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-29405879

RESUMO

OBJECTIVE: This study examined barriers to engagement in self-management behaviors among food-allergic college students (1) within the frameworks of the health belief model (HBM) and common sense self-regulation model (CS-SRM) and (2) in the context of overall risky behaviors. PARTICIPANTS: Undergraduate college students who reported having a physician-diagnosed food allergy (N = 141). Research was conducted from February 2015 through May 2016. METHODS: Participants were recruited from college campuses through email and social media. The frequency of adherence to self-management behaviors was measured along with HBM, CS-SRM, and risk-taking behaviors through a self-report survey. RESULTS: Among all participants, HBM and CS-SRM constructs and Tobacco Use explained 30.6% of the variance in adherence. CS-SRM constructs and Tobacco Use explained 44.8% of the variance for participants with self-injectable epinephrine (SIE). CONCLUSIONS: Food-allergic college students demonstrate inconsistent adherence, and interventions designed to improve adherence should take both SIE prescription status and contextual factors into consideration.


Assuntos
Anafilaxia/dietoterapia , Anafilaxia/prevenção & controle , Comportamento Alimentar/psicologia , Hipersensibilidade Alimentar/dietoterapia , Autogestão/métodos , Autogestão/psicologia , Estudantes/psicologia , Adolescente , Adulto , Feminino , Fidelidade a Diretrizes , Humanos , Masculino , Autorrelato , Estudantes/estatística & dados numéricos , Inquéritos e Questionários , Universidades/estatística & dados numéricos , Adulto Jovem
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