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1.
J Clin Ethics ; 35(2): 85-92, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38728697

RESUMO

AbstractDespite broad ethical consensus supporting developmentally appropriate disclosure of health information to older children and adolescents, cases in which parents and caregivers request nondisclosure continue to pose moral dilemmas for clinicians. State laws vary considerably regarding adolescents' rights to autonomy, privacy, and confidentiality, with many states not specifically addressing adolescents' right to their own healthcare information. The requirements of the 21st Century Cures Act have raised important ethical concerns for pediatricians and adolescent healthcare professionals regarding the protection of adolescent privacy and confidentiality, given requirements that chart notes and results be made readily available to patients via electronic portals. Less addressed have been the implications of the act for adolescents' access to their health information, since many healthcare systems' electronic portals are available to patients beginning at age 12, sometimes requiring that the patients themselves authorize their parents' access to the same information. In this article, we present a challenging case of protracted disagreement about an adolescent's right to honest information regarding his devastating prognosis. We then review the legal framework governing adolescents' rights to their own healthcare information, the limitations of ethics consultation to resolve such disputes, and the potential for the Cures Act's impact on electronic medical record systems to provide one form of resolution. We conclude that although parents in cases like the one presented here have the legal right to consent to medical treatment on their children's behalf, they do not have a corresponding right to direct the withholding of medical information from the patient.


Assuntos
Confidencialidade , Pais , Humanos , Adolescente , Confidencialidade/legislação & jurisprudência , Confidencialidade/ética , Masculino , Estados Unidos , Revelação/legislação & jurisprudência , Revelação/ética , Autonomia Pessoal , Consentimento dos Pais/legislação & jurisprudência , Consentimento dos Pais/ética , Direitos do Paciente/legislação & jurisprudência , Criança , Privacidade/legislação & jurisprudência , Registros Eletrônicos de Saúde/ética , Registros Eletrônicos de Saúde/legislação & jurisprudência , Acesso à Informação/legislação & jurisprudência , Acesso à Informação/ética
2.
J Pediatr Health Care ; 38(4): 480-485, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38260925

RESUMO

INTRODUCTION: To address healthcare disparities among transgender and gender diverse (TGD) adolescents, we examined vaccination coverage in those receiving gender-affirming care. METHOD: Our study analyzed de-identified data (2013-2022) from a tertiary care clinic. Comparing vaccination rates of 203 TGD adolescent patients to age-matched peers in New York State using CDC National Immunization Survey-Teen data. RESULTS: We found TGD patients had similar vaccination coverage to the general adolescent population. Notably, TGD patients had significantly higher up-to-date human papillomavirus vaccination coverage (76.4%, CI=69.9, 82.0) than the NYS adolescent population (60.5%, CI=53.0, 67.5). DISCUSSION: This suggests TGD adolescents at gender-affirming clinics maintain or exceed vaccination rates of their cisgender counterparts. Future research should explore vaccination rates for TGD individuals without access to gender-affirming care.


Assuntos
Centros de Atenção Terciária , Pessoas Transgênero , Cobertura Vacinal , Humanos , Adolescente , Pessoas Transgênero/estatística & dados numéricos , Masculino , Feminino , Cobertura Vacinal/estatística & dados numéricos , Estados Unidos/epidemiologia , New York/epidemiologia , Vacinas contra Papillomavirus/administração & dosagem , Vacinação/estatística & dados numéricos , Disparidades em Assistência à Saúde/estatística & dados numéricos
3.
J Pediatr ; 240: 272-279, 2022 01.
Artigo em Inglês | MEDLINE | ID: mdl-34547338

RESUMO

Within pediatric graduate medical education, the care of transgender youth presents opportunities for deepening learners' understanding of equity, access, the role of the physician as an advocate, and health disparities caused by stigma and minority stress. However, when a pediatric resident objects to providing health care to this uniquely vulnerable population owing to their personal beliefs and values, how should pediatrician-educators respond? Important reasons to respect healthcare professionals' conscience have been described in the scholarly literature; however, equally important concerns have also been raised about the extent to which conscientious objection should be permitted in a pluralistic society, particularly given power differentials that favor healthcare professionals and grants them a monopoly over certain services. In the context of medical education, however, residents are in a unique position: they are simultaneously learners and employees, and although privileged relative to their patients, they are also vulnerable in relation to the hierarchy of healthcare and of institutions. We must find a compassionate balance between nurturing the evolving conscience of students and trainees and protecting the health and well-being of our most vulnerable patients. Educators have an obligation to foster empathy, mitigate bias, and mentor their learners, regardless of beliefs, but in some cases, they may recognize that there are limits: patients' welfare ultimately takes precedence and trainees should be guided toward alternative career paths. We explore the limits of conscientious objection in medical training and propose a framework for pediatrician-educators to support learners and patients in challenging circumstances.


Assuntos
Atitude do Pessoal de Saúde , Pediatria/educação , Recusa em Tratar , Pessoas Transgênero , Consciência , Humanos , Internato e Residência , Populações Vulneráveis
4.
J Pediatr Adolesc Gynecol ; 34(3): 291-296, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-33810968

RESUMO

Exposure to pediatric and adolescent gynecology (PAG) varies across residency programs in obstetrics and gynecology, family medicine, and pediatrics, as well as fellowship programs in adolescent medicine. Nevertheless, these programs are responsible for training residents and fellows and providing opportunities within their programs to fulfill PAG learning objectives. To that end, the North American Society for Pediatric and Adolescent Gynecology has taken a leadership role in PAG education by creating and systematically updating the Short Curriculum. This curriculum outlines specific learning objectives that are central to PAG education and lists essential resources for learners' reference. This updated curriculum replaces the previous 2018 publication with added content, resources, and updated references.


Assuntos
Medicina do Adolescente/educação , Currículo , Ginecologia/educação , Internato e Residência/métodos , Pediatria/educação , Adolescente , Criança , Feminino , Humanos , Estados Unidos
5.
J Pediatr Adolesc Gynecol ; 32(5): 469-480, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31301359

RESUMO

In 2015 the Resident Education Committee published the Long Curriculum in Resident Education to provide educators with a comprehensive document to be used in post-graduate medical education. The original curriculum was designed to meet the resident learning objectives for CREOG, RCPSC and ABP and to provide a more intensive, broader learning experience. This Committee Document is an updated version of the 2015 Long Curriculum.


Assuntos
Currículo , Ginecologia/educação , Internato e Residência/métodos , Obstetrícia/educação , Pediatria/educação , Adolescente , Medicina do Adolescente/educação , Criança , Feminino , Humanos , Gravidez
6.
J Pediatr Adolesc Gynecol ; 32(5): 520-524, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31121320

RESUMO

STUDY OBJECTIVE: In this study, we aimed to determine the frequency of menstrual history and sexual history documentation in the inpatient setting. DESIGN, SETTING, AND PARTICIPANTS: A retrospective chart review was conducted for 307 female patients ages 11-18 years admitted from the emergency department at a single institution within a 7-month period. These charts were reviewed for documentation of menstrual and sexual history. INTERVENTIONS AND MAIN OUTCOME MEASURES: Rates of menstrual and sexual history documentation were compared according to patient age, chief complaint, admitting specialty, and medical complexity. RESULTS: Sexual history documentation was noted in 158 (45.9%) of the 344 reviewed charts. Sexual history documentation rates were higher for patients with mental health symptoms (62.9%; 61 of 98 charts; P = .02) and lower for patients admitted to surgical services (30.6%; 19 of 62 charts; P = .04). At least 1 aspect of menses was documented in 113 (32.8%) of the 344 reviewed charts. Last menstrual period was the most commonly documented aspect of menstrual history, appearing in 100 (29.1%) of the 344 reviewed charts. Menarche (4.4%; 15/344), menses frequency (7.0%; 24/344), menses duration (2.6%; 9/344), flow quantity (4.9%; 17/344), and dysmenorrhea (4.4%; 15/344) were rarely documented, regardless of chief complaint or admitting service. Menstrual history documentation rates were significantly higher for patients requiring a gynecology consultation (73.3%; 11 of 15 charts; P < .01). CONCLUSION: Menstrual and sexual history documentation rates for adolescent patients requiring inpatient admission were low, with fewer than half of patients having a documented menstrual or sexual history.


Assuntos
Anamnese/métodos , Menstruação , Comportamento Sexual , Adolescente , Criança , Serviço Hospitalar de Emergência/estatística & dados numéricos , Feminino , Hospitalização/estatística & dados numéricos , Humanos , Anamnese/estatística & dados numéricos , Estudos Retrospectivos
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