Results 41 to 50 of about 25,330,745 (203)

Parents of Youth With Cancer Report on Their Psychosocial Care: iSTEPPP Survey Finds Alignment and Gaps With Standards

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background The Standards for Psychosocial Care for Children with Cancer and Their Families guide the provision of comprehensive psychosocial care. Parallel to research characterizing implementation of the Standards from the perspective of providers, this study examines implementation of the Standards from the perspective of parents of youth ...
Emily M. Pariseau, Kimberly Buff, Michele A. Scialla, Kimberly S. Canter, Lori Wiener, Victoria Sardi‐Brown, Julia B. Tager, Kamyar Arasteh, Anne E. Kazak   +8 more
wiley   +1 more source

Descriptive Statistics, 1980–2002 General Social Survey-National Death Index Linkages with 2008 Mortality Follow-up (N = 23,307).

, 2014
Descriptive Statistics, 1980–2002 General Social Survey-National Death Index Linkages with 2008 Mortality Follow-up (N = 23,307).
Jason Schnittker (512626), Valerio Bacak (512627)   +1 more
core   +1 more source

“We Cannot Talk as a Family”: Complexities of Survivorship Communication Among Hispanic/Latino Young Adult Survivors of Childhood Cancer, Parents, and Clinicians

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Young adult childhood cancer survivors (YA‐CCS) have an increased risk of treatment‐related health complications throughout their lives. Lifelong survivorship care is recommended, yet many YA‐CCS experience disruptions in care during pediatric‐to‐adult transitions and do not receive recommended survivorship care.
Kevin Shanchen Pu, Nicole Fernández‐Viña, Briana C. Martin‐Villa, Daniela Ramirez, Rebecca M. Lewinsohn, Mary Smith, Heidi Boynton, Lidia Schapira, Stephanie M. Smith   +8 more
wiley   +1 more source

Identifying Patterns of Hospitalizations Among Childhood Cancer Survivors: A Population‐Based Study

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Childhood cancer survivors (CCSs) experience more hospitalizations than the general population. We aimed to identify distinct hospitalization patterns among Queensland CCSs and the associated characteristics. Methods Cases (aged ≤14 years) diagnosed between 1995 and 2019 while residents of Queensland were identified through the ...
Hai Pham, Teyl Engstrom, Peter Baade, Natalie Bradford, Sarah Pont, Louise Marquart‐Wilson, Natasha Nassar, Jason D. Pole   +7 more
wiley   +1 more source

Measuring What Matter: A submission to the Australian Treasury by Australian National Development Index (ANDI) Limited

, 2023
ANDI (Australian National Development Index Limited) is a registered Australian not-for-profit and public interest corporation. ANDI’s constitutional mission is to develop a comprehensive framework to measure national progress and wellbeing and promote ...
Salvaris, Mike, Woolcock, Geoffrey, Stanley, Fiona   +2 more
core  

Impact of Initial Treatment Setting on Survival in Relapsed Pediatric and AYA Bone Sarcomas: A Secondary Analysis of a Prospective Clinical Trial

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Outcomes in relapsed or refractory pediatric and AYA bone sarcomas remain poor, and the impact of early referral to specialized sarcoma centers on survival is unclear. Early centralization of care may improve local and systemic treatment quality, but evidence in this population is limited.
Justyna Antoniuk‐Majchrzak, Katarzyna Bilska, Tomasz Koziński, Jadwiga Węcławek‐Tompol, Dorota Sega‐Pondel, Radosław Chaber, Wanda Badowska, Katarzyna Rosłan, Hanna Koseła‐Paterczyk, Anna Raciborska   +9 more
wiley   +1 more source

WELCOME TO THE CAMPUS PRIDE INDEX [PDF]

, 2021
SINCE 2007, THE CAMPUS PRIDE INDEX HAS BEEN THE PREMIER LGBTQ NATIONAL BENCHMARKING TOOL FOR COLLEGES AND UNIVERSITIES TO CREATE SAFER, MORE INCLUSIVE CAMPUS COMMUNITIES.
Campus Pride Index
core  

Representation of Sickle Cell Disease Patients in Pediatric and Adult Care: What We Discovered Using Informatics for Integrating Biology and the Bedside (i2b2) Data

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Transitioning from pediatric to adult care is a high‐risk period for individuals with sickle cell disease (SCD). An initial observation at one academic medical center suggested a sex‐based disparity in clinic populations, prompting a national investigation.
Laurie J. Duckworth, Kholod Alhassan, Ada De La Osa, John Stephen, Yue Yao, Diana J. Wilkie   +5 more
wiley   +1 more source

Measurement invariance of the Death Literacy Index across Flemish Belgium, The Netherlands, and Sweden [PDF]

Death literacy is a construct conceptualizing experience-based knowledge and skills for end-of-life care, which is operationalized as a six-factor model in the 29-item Death Literacy Index (DLI).
Bujacz, Aleksandra, Vanderstichelen, Steven, Johansson, Therese, Eriksson, Lars E., Bujacz, A., Groot, M., Kowalski, L., Groot, Marieke, Nierop-van Baalen, Corine A., Olsson, Å., Cohen, J., Tishelman, C., Goliath, I., Goliath, Ida, Johansson, T., Nierop-van Baalen, C. A., Olsson, Åsa, Cohen, Joachim, Kowalski, Leo, Eriksson, L. E., Tishelman, Carol, Vanderstichelen, S., Olsson, A, Eriksson, LE, Cohen, J, Bujacz, A, Kowalski, L,, Groot, M, Vanderstichelen, S, Johansson, T,, Tishelman, C,, Therese Johansson, Nierop-van, Baalen CA   +32 more
core   +1 more source

Multimorbidity Patterns and Mortality Risk in a National Sample of US Adults Identified Using Latent Class Analysis

Diseases
Background/Objectives: Multimorbidity is increasingly recognized as a major contributor to mortality worldwide, yet its underlying patterns and prognostic implications remain poorly understood in the United States.
Emmanuel U. Azu, Gulzar H. Shah, Toktam Naderimoghaddam, Lili Yu   +3 more
doaj   +1 more source