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Dive into the research topics where Tim Wysocki is active.

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Featured researches published by Tim Wysocki.


The New England Journal of Medicine | 2008

Continuous glucose monitoring and intensive treatment of type 1 diabetes

William V. Tamborlane; Roy W. Beck; Bruce W. Bode; Bruce Buckingham; H. Peter Chase; Robert Clemons; Rosanna Fiallo-Scharer; Larry A. Fox; Lisa K. Gilliam; Irl B. Hirsch; Elbert S. Huang; Craig Kollman; Aaron J. Kowalski; Lori Laffel; Jean M. Lawrence; Joyce M. Lee; Nelly Mauras; Michael J. O'Grady; Katrina J. Ruedy; Michael Tansey; Eva Tsalikian; Stuart A. Weinzimer; Darrell M. Wilson; Howard Wolpert; Tim Wysocki; Dongyuan Xing; Laurel Messer; Victoria Gage; P. Burdick; K. Milaszewski

BACKGROUND The value of continuous glucose monitoring in the management of type 1 diabetes mellitus has not been determined. METHODS In a multicenter clinical trial, we randomly assigned 322 adults and children who were already receiving intensive therapy for type 1 diabetes to a group with continuous glucose monitoring or to a control group performing home monitoring with a blood glucose meter. All the patients were stratified into three groups according to age and had a glycated hemoglobin level of 7.0 to 10.0%. The primary outcome was the change in the glycated hemoglobin level at 26 weeks. RESULTS The changes in glycated hemoglobin levels in the two study groups varied markedly according to age group (P=0.003), with a significant difference among patients 25 years of age or older that favored the continuous-monitoring group (mean difference in change, -0.53%; 95% confidence interval [CI], -0.71 to -0.35; P<0.001). The between-group difference was not significant among those who were 15 to 24 years of age (mean difference, 0.08; 95% CI, -0.17 to 0.33; P=0.52) or among those who were 8 to 14 years of age (mean difference, -0.13; 95% CI, -0.38 to 0.11; P=0.29). Secondary glycated hemoglobin outcomes were better in the continuous-monitoring group than in the control group among the oldest and youngest patients but not among those who were 15 to 24 years of age. The use of continuous glucose monitoring averaged 6.0 or more days per week for 83% of patients 25 years of age or older, 30% of those 15 to 24 years of age, and 50% of those 8 to 14 years of age. The rate of severe hypoglycemia was low and did not differ between the two study groups; however, the trial was not powered to detect such a difference. CONCLUSIONS Continuous glucose monitoring can be associated with improved glycemic control in adults with type 1 diabetes. Further work is needed to identify barriers to effectiveness of continuous monitoring in children and adolescents. (ClinicalTrials.gov number, NCT00406133.)


Diabetes Care | 1996

Deviation from Developmentally Appropriate Self-Care Autonomy: Association with diabetes outcomes

Tim Wysocki; Alexandra Taylor; Brenda S. Hough; Thomas R Linscheid; Keith Owen Yeates; Jack A. Naglieri

OBJECTIVE Treatment of IDDM in youth emphasized balancing childrens self-care autonomy with their psychological maturity. However, few data exist to guide clinicians or parents, and little is known about correlates of deviations from this ideal. RESEARCH DESIGN AND METHODS In this cross-sectional study, IDDM self-care autonomy of 100 youth was assessed using two well-validated measures. Three measures of psychological maturity (cognitive function, social-cognitive development, and academic achievement) were also collected for each child. Composite indexes of self-care autonomy and of psychological maturity were formed, and the ratio of the self-care autonomy index to the psychological maturity index quantified each childs deviation from developmentally appropriate IDDM self-care autonomy. Based on these scores, participants were categorized as exhibiting constrained (lower tertile), appropriate (middle tertile), or excessive (higher tertile) self-care autonomy. Between-group differences in treatment adherence, diabetes knowledge, glycemic control, and hospitalization rates were explored. RESULTS Analysis of covariance controlling for age revealed that the excessive self-care autonomy group demonstrated less favorable treatment adherence, diabetes knowledge, hospitalization rates, and, marginally, glycemic control. Excessive self-care autonomy increased with age and was less common among intact two-parent families but was unrelated to other demographic factors. CONCLUSIONS The findings indicate caution about encouragement of maximal self-care autonomy among youth with IDDM and suggest that families who succeed in maintaining parental involvement in diabetes management may have better outcomes.


Diabetes Care | 2007

Randomized Trial of Behavioral Family Systems Therapy for Diabetes Maintenance of effects on diabetes outcomes in adolescents

Tim Wysocki; Michael A. Harris; Lisa M. Buckloh; Debbie Mertlich; Amanda S. Lochrie; Nelly Mauras; Neil H. White

OBJECTIVE—Studies showing that family communication and conflict resolution are critical to effective management of type 1 diabetes in adolescents have stimulated interest in evaluating psychological treatments targeting these processes. Previous trials have shown that Behavioral Family Systems Therapy (BFST) improved parent-adolescent relationships but not treatment adherence or glycemic control. This study evaluates a revised intervention, BFST for Diabetes (BFST-D), modified to achieve greater impact on diabetes-related family conflict, treatment adherence, and metabolic control. RESEARCH DESIGN AND METHODS—A sample of 104 families of adolescents with inadequate control of type 1 diabetes was randomized to either remain in standard care (SC) or to augmentation of that regimen by 12 sessions of either a multifamily educational support (ES) group or 12 sessions of BFST-D over 6 months. Pertinent measures were collected at baseline and at follow-up evaluations at 6, 12, and 18 months. RESULTS—BFST-D was significantly superior to both SC and ES in effects on A1C, while effects on treatment adherence and family conflict were equivocal. Improvement in A1C appeared to be mediated by improvement in treatment adherence. A significantly higher percentage of BFST-D youth achieved moderate or greater improvement (>0.5 SD) in treatment adherence compared with the SC group at each follow-up and the ES group at 6 and 18 months. Change in treatment adherence correlated significantly with change in A1C at each follow-up. CONCLUSIONS—These results support the efficacy of BFST-D in improving A1C, but further research is needed to identify the mechanisms of this effect and to achieve cost-effective dissemination of the intervention.


Behavior Therapy | 2008

Randomized, Controlled Trial of Behavioral Family Systems Therapy for Diabetes: Maintenance and Generalization of Effects on Parent-Adolescent Communication

Tim Wysocki; Michael A. Harris; Lisa M. Buckloh; Deborah Mertlich; Amanda S. Lochrie; Alexandra Taylor; Michelle Sadler; Neil H. White

We report a randomized trial of a revised Behavioral Family Systems Therapy for Diabetes (BFST-D) intervention. Families of 104 adolescents with diabetes were randomized to standard care (SC) or to 6 months of an educational support group (ES) or BFST-D. Family communication and problem-solving skills were assessed at 0, 6, 12, and 18 months by independent rating of videotaped family problem-solving discussions. BFST-D improved individual communication of adolescents and mothers, but not fathers. BFST-D significantly improved quality of family interaction compared to SC (10 of 12 comparisons) and ES (6 of 12 comparisons). Changes in family communication were differentially associated with changes in glycemic control, adherence, and family conflict. BFST-D improved family communication and problem solving relative to SC and modestly relative to ES.


Pediatric Diabetes | 2005

Comparison of fingerstick hemoglobin A1c levels assayed by DCA 2000 with the DCCT/EDIC central laboratory assay: results of a Diabetes Research in Children Network (DirecNet) Study.

H. Peter Chase; Rosanna Fiallo-Scharer; Jennifer Fisher; Barbara Tallant; Eva Tsalikian; Michael Tansey; Linda F. Larson; Julie Coffey; Tim Wysocki; Nelly Mauras; Larry A. Fox; Keisha Bird; Kelly L. Lofton; Bruce Buckingham; Darrell M. Wilson; Jennifer M. Block; Paula Clinton; Stuart A. Weinzimer; William V. Tamborlane; Elizabeth A. Doyle; Kristin A. Sikes; Roy W. Beck; Katrina J. Ruedy; Craig Kollman; Dongyuan Xing; Cynthia R. Silvester; Dorothy M. Becker; Christopher Cox; Christopher M. Ryan; Neil H. White

Abstract:  Background:  The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) high‐performance liquid chromatography (HPLC) method for measuring hemoglobin A1c (HbA1c) serves as a reference standard against which other assays are compared. The DCA 2000® + Analyzer (Bayer Inc., Tarrytown, NY, USA), which uses an immunoassay, is a very popular device for measuring HbA1c levels in pediatric diabetes practices.


Diabetes Care | 2010

The Cost-Effectiveness of Continuous Glucose Monitoring in Type 1 Diabetes

Elbert S. Huang; Michael J. O'Grady; Anirban Basu; Aaron N. Winn; Priya M. John; Joyce M. Lee; David O. Meltzer; Craig Kollman; Lori Laffel; William V. Tamborlane; Stuart A. Weinzimer; Tim Wysocki

OBJECTIVE Continuous glucose monitoring (CGM) has been found to improve glucose control in type 1 diabetic patients. We estimated the cost-effectiveness of CGM versus standard glucose monitoring in type 1 diabetes. RESEARCH DESIGN AND METHODS This societal cost-effectiveness analysis (CEA) was conducted in trial populations in which CGM has produced a significant glycemic benefit (A1C ≥7.0% in a cohort of adults aged ≥25 years and A1C <7.0% in a cohort of all ages). Trial data were integrated into a simulation model of type 1 diabetes complications. The main outcome was the cost per quality-adjusted life-year (QALY) gained. RESULTS During the trials, CGM patients experienced an immediate quality-of-life benefit (A1C ≥7.0% cohort: 0.70 quality-adjusted life-weeks [QALWs], P = 0.49; A1C <7.0% cohort: 1.39 QALWs, P = 0.04) and improved glucose control. In the long-term, CEA for the A1C ≥7.0% cohort, CGM was projected to reduce the lifetime probability of microvascular complications; the average gain in QALYs was 0.60. The incremental cost-effectiveness ratio (ICER) was


BMJ open diabetes research & care | 2014

Closing the loop overnight at home setting: psychosocial impact for adolescents with type 1 diabetes and their parents

Katharine Barnard; Tim Wysocki; Janet M. Allen; Daniela Elleri; Hood Thabit; Lalantha Leelarathna; Arti Gulati; Marianna Nodale; David B. Dunger; Tannaze Tinati; Roman Hovorka

98,679/QALY (95% CI −60,000 [fourth quadrant] to −87,000 [second quadrant]). For the A1C <7.0% cohort, the average gain in QALYs was 1.11. The ICER was


Diabetes Care | 2010

Quality-of-life measures in children and adults with type 1 diabetes: Juvenile Diabetes Research Foundation Continuous Glucose Monitoring randomized trial.

Jean M. Lawrence; Lori Laffel; Tim Wysocki; Dongyuan Xing; Roy W. Beck; Elbert S. Huang; Brett Ives; Craig Kollman; Joyce M. Lee; Katrina J. Ruedy; William V. Tamborlane

78,943/QALY (15,000 [first quadrant] to −291,000 [second quadrant]). If the benefit of CGM had been limited to the long-term effects of improved glucose control, the ICER would exceed


Journal of Pediatric Psychology | 2009

Generic and Diabetes-specific Parent–Child Behaviors and Quality of Life Among Youth with Type 1 Diabetes

Jill Weissberg-Benchell; Tonja R. Nansel; Grayson N. Holmbeck; Rusan Chen; Barbara J. Anderson; Tim Wysocki; Lori Laffel

700,000/QALY. If test strip use had been two per day with CGM long term the ICER for CGM would improve significantly. CONCLUSIONS Long-term projections indicate that CGM is cost-effective among type 1 diabetic patients at the


Behavior Modification | 2006

Behavioral Assessment and Intervention in Pediatric Diabetes

Tim Wysocki

100,000/QALY threshold, although considerable uncertainty surrounds these estimates.

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Neil H. White

Washington University in St. Louis

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Craig Kollman

National Marrow Donor Program

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Katrina J. Ruedy

Washington University in St. Louis

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