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  • 1
    Online Resource
    Online Resource
    Elsevier BV ; 2013
    In:  Revista Colombiana de Psiquiatría Vol. 42, No. 2 ( 2013-06), p. 234-235
    In: Revista Colombiana de Psiquiatría, Elsevier BV, Vol. 42, No. 2 ( 2013-06), p. 234-235
    Type of Medium: Online Resource
    ISSN: 0034-7450
    Language: Spanish
    Publisher: Elsevier BV
    Publication Date: 2013
    detail.hit.zdb_id: 2474145-0
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  • 2
    In: Pharmaceutical Biology, Informa UK Limited, Vol. 52, No. 4 ( 2014-04), p. 458-465
    Type of Medium: Online Resource
    ISSN: 1388-0209 , 1744-5116
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2014
    detail.hit.zdb_id: 1483151-X
    SSG: 12
    SSG: 15,3
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  • 3
    In: Diabetes, American Diabetes Association, Vol. 71, No. Supplement_1 ( 2022-06-01)
    Abstract: Objective: Novel Interventions in Children’s Healthcare (NICH) , a program for youth with T1D who experience high rates of avoidable health problems (e.g., DKA) , has been newly implemented in a second region. This study examines how youth with T1D referred for combined health problems and social risk compare to similarly referred youth in another region. Methods: Participants (Oregon=51; Bay Area=24) were referred by medical providers due to avoidable ED visits, hospitalizations and/or chronically elevated A1C values. Caregivers reported on 15 social risks (e.g., housing insecurity, domestic violence) . Results: Social risk prevalence was high at both sites, with an average of 7.6 in Oregon and 5.6 risks endorsed in the Bay Area. Oregon youth and their parents were significantly (p & lt;.05) more likely to have a mental health diagnosis and domestic violence exposure, while Bay Area youth were significantly more likely to identify as Black or Hispanic, and to have experienced parental incarceration. Conclusions: While there are some differences in social risk distribution across sites, the rate of risk is extremely high across sites, highlighting the importance of interventions specifically designed to target social factors for this population. Likewise, rethinking standard diabetes care for this subgroup is warranted given the impact of social factors on diabetes outcomes. Disclosure D.V.Wagner: None. C.Cruz: None. M.A.Harris: None. J.C.Wong: Consultant; Provention Bio, Inc., Research Support; Dexcom, Inc., Tandem Diabetes Care, Inc. A.Reed: None. L.Yglecias: None. A.Bonilla ospina: None. D.Naranjo: None. C.E.Noya: None. J.Viana: None. C.Jenisch: None. Funding The Leona M. and Harry B. Helmsley Charitable Trust
    Type of Medium: Online Resource
    ISSN: 0012-1797
    Language: English
    Publisher: American Diabetes Association
    Publication Date: 2022
    detail.hit.zdb_id: 1501252-9
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  • 4
    In: Diabetes, American Diabetes Association, Vol. 72, No. Supplement_1 ( 2023-06-20)
    Abstract: Discrimination impacts health outcomes but is underexplored in pediatric T1D. In this pilot qualitative study, we evaluate perceived discrimination in provision of diabetes care for parents/guardians (PG) of youth with T1D and public insurance. PG (n=21, 39±8 yrs, youth 8±2 yrs, 67% Hispanic, 48% speak Spanish, 69% make & lt;$50K) completed focus groups/interviews (FGI). FGI were conducted, transcribed, and coded in English (n=11) or Spanish (n=10), per PG preference. FGI transcripts were analyzed inductively by a five member bilingual team. While not always referred to as discrimination, PG reported differences in diabetes care by language, race/ethnicity, and insurance. Reported themes organically organized into the social ecological model (Figure). Systemic inequities via insurers, and institutional inequities via clinicians and schools were reported. Insurers required frequent advocacy from PG to navigate unequal treatment. Community was identified as protective through normalization and education of T1D, familial and communal support, and cultural and linguistic congruency. PG frequently described experiences in diabetes care consistent with the definition of discrimination, but not all readily adopt the terminology “discrimination”. Clinicians and researchers should be aware of this phenomenon to devise meaningful solutions to address diabetes equity. Disclosure R.Medina penaranda: None. K.K.Hood: Consultant; Cecelia Health. A.Addala: None. A.Bonilla ospina: None. H.Ortega: None. D.Pena: None. G.M.Shaw: None. L.Chamberlain: None. D.Naranjo: None. J.Raymond: None. D.M.Maahs: Advisory Panel; Medtronic, LifeScan Diabetes Institute, MannKind Corporation, Consultant; Abbott, Research Support; Dexcom, Inc. Funding Maternal & Child Health Research Institute; National Institute of Diabetes and Digestive and Kidney Diseases (K23DK13134201)
    Type of Medium: Online Resource
    ISSN: 0012-1797
    Language: English
    Publisher: American Diabetes Association
    Publication Date: 2023
    detail.hit.zdb_id: 1501252-9
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  • 5
    In: Children and Youth Services Review, Elsevier BV, Vol. 125 ( 2021-06), p. 106007-
    Type of Medium: Online Resource
    ISSN: 0190-7409
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2021
    detail.hit.zdb_id: 2019862-0
    SSG: 3,4
    SSG: 5,3
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  • 6
    In: JAMA Network Open, American Medical Association (AMA), Vol. 6, No. 4 ( 2023-04-19), p. e238881-
    Abstract: Continuous glucose monitoring (CGM) is associated with improvements in hemoglobin A 1c (HbA 1c ) in youths with type 1 diabetes (T1D); however, youths from minoritized racial and ethnic groups and those with public insurance face greater barriers to CGM access. Early initiation of and access to CGM may reduce disparities in CGM uptake and improve diabetes outcomes. Objective To determine whether HbA 1c decreases differed by ethnicity and insurance status among a cohort of youths newly diagnosed with T1D and provided CGM. Design, Setting, and Participants This cohort study used data from the Teamwork, Targets, Technology, and Tight Control (4T) study, a clinical research program that aims to initiate CGM within 1 month of T1D diagnosis. All youths with new-onset T1D diagnosed between July 25, 2018, and June 15, 2020, at Stanford Children’s Hospital, a single-site, freestanding children’s hospital in California, were approached to enroll in the Pilot-4T study and were followed for 12 months. Data analysis was performed and completed on June 3, 2022. Exposures All eligible participants were offered CGM within 1 month of diabetes diagnosis. Main Outcomes and Measures To assess HbA 1c change over the study period, analyses were stratified by ethnicity (Hispanic vs non-Hispanic) or insurance status (public vs private) to compare the Pilot-4T cohort with a historical cohort of 272 youths diagnosed with T1D between June 1, 2014, and December 28, 2016. Results The Pilot-4T cohort comprised 135 youths, with a median age of 9.7 years (IQR, 6.8-12.7 years) at diagnosis. There were 71 boys (52.6%) and 64 girls (47.4%). Based on self-report, participants’ race was categorized as Asian or Pacific Islander (19 [14.1%]), White (62 [45.9%] ), or other race (39 [28.9%]); race was missing or not reported for 15 participants (11.1%). Participants also self-reported their ethnicity as Hispanic (29 [21.5%] ) or non-Hispanic (92 [68.1%]). A total of 104 participants (77.0%) had private insurance and 31 (23.0%) had public insurance. Compared with the historical cohort, similar reductions in HbA 1c at 6, 9, and 12 months postdiagnosis were observed for Hispanic individuals (estimated difference, −0.26% [95% CI, −1.05% to 0.43%], −0.60% [−1.46% to 0.21%] , and −0.15% [−1.48% to 0.80%]) and non-Hispanic individuals (estimated difference, −0.27% [95% CI, −0.62% to 0.10%] , −0.50% [−0.81% to −0.11%], and −0.47% [−0.91% to 0.06%] ) in the Pilot-4T cohort. Similar reductions in HbA 1c at 6, 9, and 12 months postdiagnosis were also observed for publicly insured individuals (estimated difference, −0.52% [95% CI, −1.22% to 0.15%], −0.38% [−1.26% to 0.33%] , and −0.57% [−2.08% to 0.74%]) and privately insured individuals (estimated difference, −0.34% [95% CI, −0.67% to 0.03%] , −0.57% [−0.85% to −0.26%], and −0.43% [−0.85% to 0.01%] ) in the Pilot-4T cohort. Hispanic youths in the Pilot-4T cohort had higher HbA 1c at 6, 9, and 12 months postdiagnosis than non-Hispanic youths (estimated difference, 0.28% [95% CI, −0.46% to 0.86%], 0.63% [0.02% to 1.20%] , and 1.39% [0.37% to 1.96%]), as did publicly insured youths compared with privately insured youths (estimated difference, 0.39% [95% CI, −0.23% to 0.99%] , 0.95% [0.28% to 1.45%], and 1.16% [−0.09% to 2.13%] ). Conclusions and Relevance The findings of this cohort study suggest that CGM initiation soon after diagnosis is associated with similar improvements in HbA 1c for Hispanic and non-Hispanic youths as well as for publicly and privately insured youths. These results further suggest that equitable access to CGM soon after T1D diagnosis may be a first step to improve HbA 1c for all youths but is unlikely to eliminate disparities entirely. Trial Registration ClinicalTrials.gov Identifier: NCT04336969
    Type of Medium: Online Resource
    ISSN: 2574-3805
    Language: English
    Publisher: American Medical Association (AMA)
    Publication Date: 2023
    detail.hit.zdb_id: 2931249-8
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  • 7
    In: Diabetes, American Diabetes Association, Vol. 72, No. Supplement_1 ( 2023-06-20)
    Abstract: Background: Adolescents with T1D and elevated A1c are at high risk of acute and chronic complications. While behavioral health interventions have demonstrated promise in optimizing A1c, real-life clinical practice indicates uncertainty regarding which youth will show improvement, extent of improvement, and factors predicting complications over time. Methods: This 5-site longitudinal study enrolled caregivers (n=218) of youth aged 12-17 yrs (M=14.6 ±1.6 yrs) with T1D for & gt;1 year and ≥ one A1c & gt;10% in past year. Data included admissions, ED visits, and A1c one year pre- through 6 months post-enrollment. Family members reported on baseline functioning across multiple domains. Inferential tests (e.g., chi square, nonparametric) examined change over time in A1c and utilization as well as predictors of future ED visits. Results: Acute utilization did not change over time. A1c post enrollment significantly decreased from 11.1% ±1.5% to 10.9% ±2.1% (p=.03), but absolute change was minimal. 40.2% of youth did not have an A1c value available post enrollment. Caregiver reports of higher diabetes distress, higher conflict with healthcare providers, and lower social support were associated with risk of future ED visits (p & lt;.01). Conclusion: Findings indicate strong need for systematic psychosocial screening and more intensive tailored behavioral intervention efforts for this youth with elevated A1c. Disclosure D. V. Wagner: None. A. Bonilla ospina: None. M. E. Hilliard: None. M. A. Harris: None. M. A. Clements: Consultant; Glooko, Inc., Research Support; Dexcom, Inc., Abbott Diabetes. J. Raymond: None. J. C. Wong: Research Support; Dexcom, Inc., Tandem Diabetes Care, Inc. D. Naranjo: None. A. Reed: None. K. A. Torres: None. S. Melnick: None. J. Flores garcia: None. Funding JDRF
    Type of Medium: Online Resource
    ISSN: 0012-1797
    Language: English
    Publisher: American Diabetes Association
    Publication Date: 2023
    detail.hit.zdb_id: 1501252-9
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  • 8
    In: Diabetes, American Diabetes Association, Vol. 71, No. Supplement_1 ( 2022-06-01)
    Abstract: Objective: Health disparities exist in diabetes technology access for those youth with T1D who experience high social risk, despite likely benefits. Novel Interventions in Children’s Healthcare (NICH) , designed to improve health for youth with T1D experiencing such disparities, has previously been associated with improved diabetes technology access. This study compares diabetes technology use prior to and after NICH referral, and is the first such study to include a control group. Methods: Youth with T1D served by NICH (n=65) and referred youth (“controls”: n=73) across 3 sites were included. EHR data included DKAs, hospitalizations, ED visits, and presence of diabetes technology 1 year prior and 2 years after NICH initiation. No significant demographic differences. Results: Compared to the controls, NICH youth were significantly more likely to gain a CGM and experience significantly greater reductions in hospital admits, DKAs, and ED visits. After accounting for prior differences, only DKA event reduction and CGM access continued to be significant. Youth in NICH also averaged more years with tech access. Conclusion: This study demonstrates that while youth referred to NICH experience substantial barriers to accessing diabetes technology, youth in NICH were more likely to gain CGM access and have fewer DKA events than controls - and neither group approached national averages in technology access. Disclosure J.Lely: None. M.A.Harris: None. D.Naranjo: None. C.Jenisch: None. A.F.Manabat: None. C.Cruz: None. R.Bensen: None. A.Bonilla ospina: None. D.V.Wagner: None. Funding The Leona M. and Harry B. Helmsley Charitable Trust
    Type of Medium: Online Resource
    ISSN: 0012-1797
    Language: English
    Publisher: American Diabetes Association
    Publication Date: 2022
    detail.hit.zdb_id: 1501252-9
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  • 9
    In: Diabetes, American Diabetes Association, Vol. 72, No. Supplement_1 ( 2023-06-20)
    Abstract: Introduction: A subset of youth with T1D experience avoidable health problems, but it is unclear how specific social factors relate to these problems, particularly during the COVID-19 pandemic. We examined how systemic factors (caregiver, family, medical team) were related to medical outcomes in youth with elevated A1c from five academic medical centers during the pandemic. Methods: Youth 12-17 yrs with 1) T1D for ≥1 yr and 2) A1c≥10% in the past year were enrolled. Caregivers and youth completed measures of family conflict (Diabetes Family Conflict Scale-R); parent practices, stress, and health literacy (Alabama Parenting Questionnaire, Stress Index for Parents of Adolescents, BRIEF Health Literacy Scale); youth strengths and social support (Diabetes Strengths and Resilience, PROMIS); and family-medical team relationship (Quality of Healthcare Relationship) with EHR review including baseline A1c and acute complications (e.g., ED visits). Results: Participants were 157 youth with mean age 14.6 ± 1.6 years and mean A1c 11.0% ± 1.9%. 51% self-identified as Non-Hispanic White. Caregiver, family, and relational factors were significantly (p & lt;.05) related to frequency of complications and A1c, with higher family conflict associated with higher A1c (r=.23) and more ED visits (r=.18). For caregivers, low health literacy (r=.17), inconsistent discipline practices (r=.20), and high parental stress related to low adolescent achievement (r=.26), were significantly (p & lt;.05) associated with acute complications, as was youth report of low social support (r=-.20, p & lt;.01). Positive family-medical team relationship was strongly related to lower A1c (r=-.30, p & lt;.01). Discussion: Given these findings, screening and intervention efforts should emphasize targeting multiple systems and relationships with this population of youth, potentially with increased focus on the family-medical team relationship. Disclosure D.V.Wagner: None. L.Yglecias: None. J.Flores garcia: None. A.Torres sanchez: None. A.Bonilla ospina: None. J.Raymond: None. M.A.Harris: None. M.Perry: None. M.A.Clements: Consultant; Glooko, Inc., Research Support; Dexcom, Inc., Abbott Diabetes. J.C.Wong: Research Support; Dexcom, Inc., Tandem Diabetes Care, Inc. D.Naranjo: None. A.Reed: None. C.Jenisch: None. C.Cruz: None. S.Mitchell: None. Funding JDRF
    Type of Medium: Online Resource
    ISSN: 0012-1797
    Language: English
    Publisher: American Diabetes Association
    Publication Date: 2023
    detail.hit.zdb_id: 1501252-9
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  • 10
    In: Diabetes, American Diabetes Association, Vol. 72, No. Supplement_1 ( 2023-06-20)
    Abstract: Background: Individuals with T1D and elevated A1c may be differentially impacted by the COVID-19 pandemic. We examined the pandemic experiences and psychosocial factors of youth with T1D and their families. Methods: Youth 12-17 years of age with T1D for ≥1 yr and A1c ≥ 10% were enrolled at 5 sites. Caregivers and youth reported pandemic experiences, family functioning, parenting practices, social support, diabetes distress, and family-medical team relationship. Pandemic experiences were compared to benchmark data, and significant associations were examined. Results: Participants (n=157) had mean age of 14.6 ± 1.6 years and mean A1c 11.0 ± 1.9%. Some pandemic experiences (e.g., change of schooling, loss of job) of youth with elevated A1c were similar to reports of other samples of youth with T1D, but youth with elevated A1c endorsed higher frequency of more severe COVID illness (43.9%), less strict social distancing (57.8%) and lower positive diabetes experiences (7.3%). Youth, caregiver, family, and family-medical team relationships were significantly associated with pandemic-related distress and T1D experiences during the pandemic (see Table). Conclusion: Youth with elevated A1c reported more frequent negative pandemic experiences compared to other samples, with related youth, family, caregiver, and family-medical team factors identified as potential targets for screening and intervention. Disclosure D.V. Wagner: None. J. Raymond: None. J.C. Wong: Research Support; Dexcom, Inc., Tandem Diabetes Care, Inc. D. Naranjo: None. A. Reed: None. K.A. Torres: None. S. Melnick: None. S. Mitchell: None. L. Yglecias: None. J. Flores Garcia: None. A. Torres Sanchez: None. A. Bonilla Ospina: None. M.A. Clements: Consultant; Glooko, Inc. Research Support; Dexcom, Inc., Abbott Diabetes. M.A. Harris: None. Funding JDRF
    Type of Medium: Online Resource
    ISSN: 0012-1797
    Language: English
    Publisher: American Diabetes Association
    Publication Date: 2023
    detail.hit.zdb_id: 1501252-9
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