Katrina Erny-Albrecht
IMS Health
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Featured researches published by Katrina Erny-Albrecht.
The Diabetes Educator | 2012
Jacques Tshiananga; Serge Kocher; Christian Weber; Katrina Erny-Albrecht; Karsten Berndt; Kurt Neeser
Purpose The purpose of this meta-analysis was to determine the effect of nurse-led diabetes self-management education (DSME) on blood glucose control and cardiovascular risk factors. Methods The electronic databases PubMed and ISIS Knowledge were searched for relevant randomized controlled studies published between 1999 and 2009. Effect size was calculated for change in A1C, blood pressure, and lipid levels using both fixed- and random-effects models. Subgroup analyses were performed on patient age, gender, diabetes type, baseline A1C, length of follow-up, and study setting. Results A total of 34 randomized controlled trials with a combined cohort size of 5993 patients was identified. Mean patient age was 52.8 years, 47% were male, and mean A1C at baseline was 8.5%. Mean change in A1C was a reduction by −0.70% for nurse-led DSME versus −0.21% with usual care (UC). This corresponded to an effect size of 0.506, using a random-effects model for nurse-led DSME versus UC. Effect size was significantly associated with patient age older than 65 years and with duration of follow-up. Nurse-led DSME was also associated with improvements in cardiovascular risk factors, particularly among male patients, among those with good glycemic control, and in studies conducted in the United States. Conclusions Nurse-led DSME is associated with improved glycemic control, demonstrating that programs are most effective among seniors and with follow-up periods of 1 to 6 months. Future programs tailored to the needs of patients younger than 65 years may improve the impact of DSME on blood glucose.
Advances in Therapy | 2006
Wj Valentine; Andrew J. Palmer; Katrina Erny-Albrecht; Joshua A. Ray; D Cobden; V. Foos; Francisco M. Lurati; S Roze
The purpose of this study was to compare in clinical and economic terms the long-acting insulin analogue detemir with intermediate-acting Neutral Protamine Hagedorn (NPH) insulin and with long-acting insulin glargine. Investigators used the validated Center for Outcomes Research (CORE) Diabetes Model to project clinical and cost outcomes over a 35-year base case time horizon; outcome data were extracted directly from randomized, controlled trials designed to compare detemir with NPH and with insulin glargine. Modeled patient characteristics were derived from corresponding trials, and simulations incorporated published quality-of-life utilities with cost data obtained from a Medicare perspective. Detemir, when compared with NPH, increased quality-adjusted life expectancy by 0.698 quality-adjusted life-years (QALYs). Lifetime direct medical costs were increased by
Advances in Therapy | 2007
Wj Valentine; Katrina Erny-Albrecht; Joshua A. Ray; S Roze; D Cobden; Andrew J. Palmer
10,451 per patient, although indirect costs were reduced by
Advances in Therapy | 2008
Wj Valentine; Gordon Goodall; Mark Aagren; Steffen Nielsen; Andrew J. Palmer; Katrina Erny-Albrecht
4688. On the basis of direct costs, the cost per QALY gained with detemir was
Current Diabetes Reviews | 2011
Richard F. Pollock; Katrina Erny-Albrecht; Anupama Kalsekar; David Bruhn; Wj Valentine
14,974. In comparison with glargine, detemir increased quality-adjusted life expectancy by 0.063 QALYs, reduced direct medical costs by
Cost Effectiveness and Resource Allocation | 2009
W. A. Scherbaum; Gordon Goodall; Katrina Erny-Albrecht; Massimo Massi-Benedetti; Erland Erdmann; Wj Valentine
2072 per patient, and decreased indirect costs by
principles and practice of constraint programming | 2009
Brändle M; Katrina Erny-Albrecht; Gordon Goodall; Spinas Ga; Streit P; Wj Valentine
3103 (dominant). Reductions in diabetes-related comorbidities were also associated with detemir in both instances, most notably in the complications of retinopathy and nephropathy. Relative reductions in rates of complications were greatest in the comparison of detemir with NPH. Results were most sensitive to variation in hemoglobin A1c (HbA1c) levels. However, variation among any of the key assumptions, including HbA1c, did not alter the relative results. Detemir represents an attractive clinical and economic intervention in the US health care setting compared with both NPH insulin and insulin glargine.
Diabetes Care | 2006
Kurt Neeser; Katrina Erny-Albrecht; Christian Weber
The aim of this study was to gain a preliminary indication of the long-term clinical and economic implications of converting treatment for patients with type 2 diabetes to insulin detemir±oral hypoglycemic agents (OHAs) in a routine clinical practice setting in the United States. With the use of outcome data and patient characteristics reported from an ongoing prospective observational trial, a validated computer simulation model of diabetes was used to project the clinical and cost outcomes associated with therapy conversion to insulin detemir over a 35-y period from (1) OHA only, (2) neutral protamine Hagedorn insulin (NPH)±OHA, and (3) insulin glargine±OHA. Cost-effectiveness was assessed from a third-party healthcare payer perspective for the year 2005. Costs and clinical outcomes were discounted at a rate of 3%. Treatment with insulin detemir±OHA was associated with increases in quality-adjusted life expectancy of 0.309, 0.350, and 0.333 quality-adjusted life-years (QALYs) versus treatment with OHA alone, NPH±OHA, and insulin glargine±OHA, respectively. Increases in pharmacy costs were partially offset by reduced complications, particularly renal complications and neuropathy. Projected incremental cost-effectiveness ratios were well within the range considered to represent good value in the United States, at
Swiss Medical Weekly | 2009
Michael Brändle; Gordon Goodall; Katrina Erny-Albrecht; Erland Erdmann; Wj Valentine
7412,
Archive | 2014
Katrina Erny-Albrecht; Lynsey Brown; Melissa Raven; Petra Teresia Bywood
6269, and