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1.
Pediatr Dermatol ; 41(5): 793-799, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-39197846

RESUMO

BACKGROUND/AIMS: Congenital melanocytic nevi (CMN) are often unexpected discoveries at time of childbirth or adoption. Understanding how parents/guardians cope with these visible birthmarks can help clinicians better care for children and their families. Using qualitative methods, we sought to categorize early family responses to CMN and identify approaches to better engage with parents early in their child's life. METHODS: Semi-structured interviews were conducted within a broader study on shared decision making for families with children with CMN. Discussions included information on birth and early life experiences. Data was dual-coded, inductively and deductively, and analyzed with the Parker and Endler framework exploring emotion-, task-, and avoidance-oriented coping. RESULTS: Fifteen parents of 13 children were interviewed. Parents described all three categories of coping. Emotions ranged from guilt, to neutrality, to positive responses seeing their child's CMN. Stress was lower in families with prior knowledge of CMN. Dermatology referral provided an opportunity for learning, but also triggered worry for some families. CONCLUSIONS: Parents process and react to the diagnosis of CMN with a range of emotions and coping styles. Dermatologists can utilize open-ended questions to understand family emotions and provide families with tailored knowledge and resources. Early discussion of the diagnosis and family education are important support tools.


Assuntos
Adaptação Psicológica , Adoção , Nevo Pigmentado , Pais , Período Pós-Parto , Neoplasias Cutâneas , Humanos , Nevo Pigmentado/psicologia , Feminino , Masculino , Pais/psicologia , Neoplasias Cutâneas/psicologia , Adulto , Período Pós-Parto/psicologia , Adoção/psicologia , Pesquisa Qualitativa , Criança , Pré-Escolar , Lactente , Emoções , Gravidez , Entrevistas como Assunto
2.
Curr Opin Pediatr ; 35(4): 445-451, 2023 08 01.
Artigo em Inglês | MEDLINE | ID: mdl-37036282

RESUMO

PURPOSE OF REVIEW: Health literacy influences how children and families participate in their medical care, use health services, and overall health outcomes. Health literacy is underexplored in pediatric dermatology. In this scoping review, we provide examples of how limited health literacy can be a barrier to patient care in pediatric dermatology and how to mitigate its effects. RECENT FINDINGS: Limited health literacy is associated with worse health outcomes, decreased medication adherence, and decreased use of the healthcare system versus those with adequate health literacy. Materials created to help patients understand their medical conditions and treatment options often are written at a reading level far above that of the average patient and caregiver. Given the reading level of patient-facing materials, those with limited health literacy are more susceptible to medication administration errors, with omissions or incorrect dosing being most frequent to occur. There is limited research about how skills related to health literacy, including numeracy and electronic health literacy, can be addressed in pediatric dermatology. SUMMARY: Health literacy impacts patient care, treatment, and adherence in pediatric dermatology. This article gives examples of how to address common challenges in the pediatric dermatology clinic and presents areas for further research and improvement.


Assuntos
Dermatologia , Letramento em Saúde , Criança , Humanos , Adesão à Medicação , Cuidadores
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