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2.
Pediatr Blood Cancer ; 66(1): e27463, 2019 01.
Artículo en Inglés | MEDLINE | ID: mdl-30251318

RESUMEN

BACKGROUND: Sickle cell disease (SCD) is a chronic blood disorder in which mortality has increased for adolescents and young adults (AYA). PROCEDURE: A longitudinal analysis of medical records was conducted to describe the clinical course among AYAs (ages 12-27 years) during transition to adult care. Measures included sociodemographic, complications, SCD severity (modified pediatric SCD severity index), comorbidities, and transfer. Group-based trajectory modeling (GBTM) to identify subgroups with distinct severity trajectories and chi-square and unpaired Student t test to explore subgroup differences were used. RESULTS: Overall, 339 AYAs (97% black, 56% male, 69% hemoglobin SS) had 10 848 clinic, 3840 hospital, and 3152 emergency department visits. Complications included vaso-occlusive crises (80%) and acute chest syndrome (41%). Comorbidities included depression (19%) and anxiety (14%). Most AYAs transferred to adult care (n = 220) at 19 years. Fourteen AYAs died, 10 within seven years from transfer. GBTM identified both stable and increasing severity trajectory groups: stable-low (n = 31, 23%), stable-medium (n = 61, 46%), stable-high (n = 6, 4.5%), low-increasing (n = 13, 10%), and medium-increasing (n = 22, 17%). AYAs with increasing severity (25%) were older, lived closer to the clinic, and had higher risk for SCD complications and comorbidities. They had fewer pediatric clinic visits; however, they were more likely to transfer and remain longer in adult SCD care. CONCLUSIONS: Whereas most AYAs had stable severity, nearly a quarter had increasing severity, over time. AYAs with increasing severity had more complications, were more likely to transfer to adult care, and demonstrated higher and longer adult SCD care utilization compared with AYAs with stable severity.


Asunto(s)
Anemia de Células Falciformes/complicaciones , Anemia de Células Falciformes/epidemiología , Servicio de Urgencia en Hospital/estadística & datos numéricos , Índice de Severidad de la Enfermedad , Transición a la Atención de Adultos/estadística & datos numéricos , Adolescente , Adulto , Anemia de Células Falciformes/terapia , Niño , Comorbilidad , Femenino , Estudios de Seguimiento , Humanos , Estudios Longitudinales , Masculino , Pronóstico , Estudios Retrospectivos , Tasa de Supervivencia , Estados Unidos/epidemiología , Adulto Joven
3.
Acad Pediatr ; 17(4): 450-455, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-27979748

RESUMEN

BACKGROUND: Little is known about how transition readiness relates to other developmental skills of adolescence in youth with chronic illness. Better understanding of how transition readiness relates to these other developmental skills could lead to a broader array of tools to improve transition readiness. Intentional self-regulation (ISR) and hopeful future expectations (HFE) are 2 developmental skills of adolescence that improve with participation in developmental programming and thus are modifiable. METHODS: We explored associations between transition readiness, as measured by the Transition Readiness Assessment Questionnaire 29 (TRAQ-29) and ISR and HFE in youth with chronic illness recruited from a variety of subspecialty clinics from a major southeast medical center. RESULTS: A total of 71 adolescents with chronic illness were included in the analysis. The TRAQ-29 Self-Advocacy domain showed positive associations to both ISR (P = .03) and HFE (P = .009). In addition, the TRAQ-29 overall had positive associations to HFE (P = .04). CONCLUSIONS: The significant associations between TRAQ-29 Self-Advocacy domain scores and ISR and HFE suggest that transition readiness is developing within the context of other developmental areas in adolescence. More work is needed to see if the programming that improves these other developmental skills might also improve transition readiness.


Asunto(s)
Desarrollo del Adolescente , Enfermedad Crónica/psicología , Autocontrol/psicología , Transición a la Atención de Adultos , Adolescente , Anemia de Células Falciformes/psicología , Anemia de Células Falciformes/terapia , Artritis Juvenil/psicología , Artritis Juvenil/terapia , Supervivientes de Cáncer/psicología , Enfermedad Crónica/terapia , Fibrosis Quística/psicología , Fibrosis Quística/terapia , Epilepsia/psicología , Epilepsia/terapia , Femenino , Cardiopatías Congénitas/psicología , Cardiopatías Congénitas/terapia , Esperanza , Humanos , Enfermedades Inflamatorias del Intestino/psicología , Enfermedades Inflamatorias del Intestino/terapia , Intención , Lupus Eritematoso Sistémico/psicología , Lupus Eritematoso Sistémico/terapia , Masculino , Distrofias Musculares/psicología , Distrofias Musculares/terapia , Encuestas y Cuestionarios
4.
Clin Pediatr (Phila) ; 56(5): 451-460, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-27470263

RESUMEN

We examined vaccination coverage among youth with special health care needs (YSHCN) using data from parents of adolescents (11-17 years) who responded to a statewide survey in 2010-2012 (n = 2156). Using a validated screening tool, we identified 29% of adolescents as YSHCN. Weighted multivariable logistic regression assessed associations between special health care needs and receipt of tetanus booster, meningococcal, and human papillomavirus (HPV) vaccines. Only 12% of youth had received all 3 vaccines, with greater coverage for individual vaccines (tetanus booster, 91%; meningococcal, 32%; HPV, 26%). YSHCN had greater odds of HPV vaccination than other youth (33% vs 23%, OR = 1.70, 95% CI = 1.16-2.50) but vaccination coverage was similar ( P ≥ .05) for other outcomes. In subgroup analyses, HPV vaccination also differed depending on the number and type of special health care needs identified. Findings highlight low levels of vaccination overall and missed opportunities to administer recommended vaccines among all youth, including YSHCN.


Asunto(s)
Vacunación/estadística & datos numéricos , Adolescente , Niño , Niños con Discapacidad , Femenino , Humanos , Inmunización Secundaria , Modelos Logísticos , Masculino , Vacunas Meningococicas/administración & dosificación , Vacunas contra Papillomavirus/administración & dosificación , Encuestas y Cuestionarios , Toxoide Tetánico/administración & dosificación , Vacunación/efectos adversos
5.
World J Clin Pediatr ; 5(2): 206-11, 2016 May 08.
Artículo en Inglés | MEDLINE | ID: mdl-27170931

RESUMEN

AIM: To review empirical evidence on character development among youth with chronic illnesses. METHODS: A systematic literature review was conducted using PubMed and PSYCHINFO from inception until November 2013 to find quantitative studies that measured character strengths among youth with chronic illnesses. Inclusion criteria were limited to English language studies examining constructs of character development among adolescents or young adults aged 13-24 years with a childhood-onset chronic medical condition. A librarian at Duke University Medical Center Library assisted with the development of the mesh search term. Two researchers independently reviewed relevant titles (n = 549), then abstracts (n = 45), and finally manuscripts (n = 3). RESULTS: There is a lack of empirical research on character development and childhood-onset chronic medical conditions. Three studies were identified that used different measures of character based on moral themes. One study examined moral reasoning among deaf adolescents using Kohlberg's Moral Judgement Instrument; another, investigated moral values of adolescent cancer survivors with the Values In Action Classification of Strengths. A third study evaluated moral behavior among young adult survivors of burn injury utilizing the Tennessee Self-Concept, 2(nd) edition. The studies observed that youth with chronic conditions reasoned at less advanced stages and had a lower moral self-concept compared to referent populations, but that they did differ on character virtues and strengths when matched with healthy peers for age, sex, and race/ethnicity. Yet, generalizations could not be drawn regarding character development of youth with chronic medical conditions because the studies were too divergent from each other and biased from study design limitations. CONCLUSION: Future empirical studies should learn from the strengths and weaknesses of the existing literature on character development among youth with chronic medical conditions.

6.
Semin Oncol Nurs ; 31(3): 186-96, 2015 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26210197

RESUMEN

OBJECTIVES: Using a Life Course Health Development framework, this article summarizes what is known about the impact of cancer and its treatment on the biopsychosocial world of the adolescent and young adult. DATA SOURCES: Published peer reviewed literature, web-based resources, and cancer-related professional organizations' resources. CONCLUSION: Adolescents and young adults with cancer, between 15 and 29 years of age, have emerged as a distinct group requiring specialized care. The demands of cancer and its treatment are often directly counter to the developmental needs of this age group and often alter those life course experiences that contribute to resilience, thriving, and flourishing. IMPLICATIONS FOR NURSING PRACTICE: Providing high-quality care to this age group requires a depth of understanding of the complexity of factors that merge to influence the developmental life course.


Asunto(s)
Neoplasias/psicología , Neoplasias/terapia , Calidad de Vida , Transición a la Atención de Adultos/organización & administración , Adaptación Psicológica , Adolescente , Femenino , Humanos , Masculino , Neoplasias/diagnóstico , Neoplasias/mortalidad , Medicina de Precisión/enfermería , Sobrevivientes/psicología , Sobrevivientes/estadística & datos numéricos , Resultado del Tratamiento , Adulto Joven
8.
J Sch Health ; 82(8): 364-70, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22712673

RESUMEN

BACKGROUND: Youth with childhood-onset chronic illness (COCI) are at risk of poor educational attainment. Specific protective factors that promote college graduation in this population have not been studied previously. In this study, we examine the role protective factors during adolescence play in promoting college graduation among young adults with COCI. METHODS: Data were collected from 10,925 participants in the National Longitudinal Study of Adolescent Health (Add Health). Protective factors present before 18 years of age included mentoring, parent relationship quality, school connectedness, and religious attendance. College graduation was the outcome of interest assessed when participants had a mean age of 28 years. Analysis was stratified by presence of COCI. RESULTS: About 2% of participants (N = 230) had 1 of 4 COCIs (cancer, diabetes, epilepsy, or heart disease). All 4 protective factors were associated with college graduation for youth without COCI. In the final multivariate model, only school connectedness was associated with college graduation for youth with COCI. CONCLUSION: School connectedness is of particular importance in promoting educational attainment for youth with COCI.


Asunto(s)
Enfermedad Crónica , Escolaridad , Apoyo Social , Adolescente , Adulto , Enfermedad Crónica/psicología , Femenino , Humanos , Estudios Longitudinales , Masculino , Mentores , Relaciones Padres-Hijo , Espiritualidad , Estudiantes/psicología , Encuestas y Cuestionarios , Estados Unidos , Adulto Joven
9.
J Adolesc Health ; 49(2): 206-12, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21783055

RESUMEN

OBJECTIVES: We compared adult educational, vocational, and social outcomes among young adults with and without childhood-onset chronic illness in a nationally representative U.S. sample. METHODS: We used data from Wave IV (2008) of the National Longitudinal Study of Adolescent Health. We compared respondents who reported childhood-onset cancer, heart disease, diabetes, or epilepsy with young adults without these chronic illnesses in terms of marriage, having children, living with parents, romantic relationship quality, educational attainment, income, and employment. Multivariate models controlled for sociodemographic factors and adult-onset chronic illness. RESULTS: As compared with those without childhood chronic illness, respondents with childhood chronic illness had similar odds of marriage (odds ratios [OR] = .89, 95% CI: .65-1.24), having children (OR = .99, 95% CI: .70-1.42), and living with parents (OR = 1.49, 95% CI .94-2.33), and similar reports of romantic relationship quality. However, the chronic illness group had lower odds of graduating college (OR = .49, 95% CI: .31-.78) and being employed (OR = .56, 95% CI: .39-.80), and higher odds of receiving public assistance (OR = 2.13, 95% CI: 1.39-3.25), and lower mean income. CONCLUSIONS: Young adults growing up with chronic illness succeed socially, but are at increased risk of poorer educational and vocational outcomes.


Asunto(s)
Enfermedad Crónica , Escolaridad , Empleo/estadística & datos numéricos , Relaciones Interpersonales , Adolescente , Adulto , Edad de Inicio , Enfermedad Crónica/epidemiología , Enfermedad Crónica/psicología , Femenino , Humanos , Renta/estadística & datos numéricos , Masculino , Matrimonio , Análisis Multivariante , Padres , Adulto Joven
10.
Arch Pediatr Adolesc Med ; 165(3): 256-61, 2011 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21383274

RESUMEN

OBJECTIVE: To examine young adult outcomes in a nationally representative US cohort of young adults growing up with a chronic illness. DESIGN: Secondary analysis of nationally representative data from wave III (in 2001) of the National Longitudinal Study of Adolescent Health. SETTING: United States. PARTICIPANTS: The analytic sample comprised 13 236 young adults aged 18 to 28 years at wave III. MAIN EXPOSURE: Self-report of a chronic physical illness (asthma, cancer, diabetes mellitus, or epilepsy) in adolescence. Respondents with asthma or nonasthmatic chronic illness (cancer, diabetes mellitus, or epilepsy) were compared with individuals without these conditions. MAIN OUTCOME MEASURES: Self-report of high school graduation, ever having employment, currently having employment, living with a parent/guardian, and ever receiving public assistance. RESULTS: Three percent of young adults had nonasthmatic chronic illness (cancer, diabetes, or epilepsy), and 16.0% had asthma. Most young adults with chronic illness graduated high school (81.3%) and currently had employment (60.4%). However, compared with healthy young adults, those with nonasthmatic chronic illness were significantly less likely to graduate high school, ever have had employment, or currently have employment and were more likely to receive public assistance. Compared with young adults with asthma, those with nonasthmatic chronic illness again had significantly worse young adult outcomes on all measures. CONCLUSIONS: Most young adults growing up with a chronic illness graduate high school and have employment. However, these young adults are significantly less likely than their healthy peers to achieve these important educational and vocational milestones.


Asunto(s)
Enfermedad Crónica/epidemiología , Escolaridad , Empleo/estadística & datos numéricos , Seguro por Discapacidad/estadística & datos numéricos , Asistencia Pública/estadística & datos numéricos , Adolescente , Adulto , Asma/epidemiología , Femenino , Humanos , Estudios Longitudinales , Masculino , Análisis Multivariante , Características de la Residencia , Estados Unidos/epidemiología , Adulto Joven
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