Exploring Variation in Glycemic Control Across and Within Eight High-Income Countries: A Cross-sectional Analysis of 64,666 Children and Adolescents With Type 1 Diabetes

被引:92
作者
Charalampopoulos, Dimitrios [1 ]
Hermann, Julia M. [2 ,3 ]
Svensson, Jannet [4 ]
Skrivarhaug, Torild [5 ]
Maahs, David M. [6 ]
Akesson, Karin [7 ]
Warner, Justin T. [8 ]
Holl, Reinhard W. [2 ,3 ]
Birkebaek, Niels H. [9 ]
Drivvoll, Ann K. [5 ]
Miller, Kellee M. [10 ]
Svensson, Ann-Marie [11 ]
Stephenson, Terence
Hofer, Sabine E. [12 ]
Fredheim, Siri
Kummernes, Siv J. [5 ]
Foster, Nicole [10 ]
Hanberger, Lena [13 ]
Amin, Rakesh [1 ]
Rami-Merhar, Birgit [14 ]
Johansen, Anders [15 ]
Dahl-Jorgensen, Knut [16 ,17 ]
Clements, Mark [18 ,19 ,20 ]
Hanas, Ragnar [21 ,22 ]
机构
[1] UCL, UCL Great Ormond St Inst Child Hlth, London, England
[2] Ulm Univ, Inst Epidemiol & Med Biometry, Zent Inst Biomed Tech, Ulm, Germany
[3] German Ctr Diabet Res DZD, Munich, Germany
[4] Herlev Univ Hosp, Dept Pediat, CPH Direct, Herlev, Denmark
[5] Oslo Univ Hosp, Norwegian Childhood Diabet Registry, Div Paediat & Adolescent Med, Oslo, Norway
[6] Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
[7] Linkoping Univ, Dept Clin & Expt Med, Linkoping, Sweden
[8] Childrens Hosp Wales, Dept Paediat Endocrinol & Diabet, Cardiff, S Glam, Wales
[9] Aarhus Univ Hosp, Dept Pediat, Aarhus, Denmark
[10] Jaeb Ctr Hlth Res, Tampa, FL USA
[11] Ctr Registers Reg Vastra Gotaland, Gothenburg, Sweden
[12] Med Univ Innsbruck, Dept Pediat 1, Innsbruck, Austria
[13] Linkoping Univ, Dept Med & Hlth Sci, Div Nursing, Linkoping, Sweden
[14] Med Univ Vienna, Dept Pediat & Adolescent Med, Vienna, Austria
[15] Univ Copenhagen, Rigshosp, Dept Growth & Reprod, Copenhagen, Denmark
[16] Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway
[17] Univ Oslo, Inst Clin Med, Oslo, Norway
[18] Childrens Mercy Hosp, Kansas City, MO 64108 USA
[19] Univ Missouri Kansas City, Kansas City, MO USA
[20] Univ Kansas, Med Ctr, Kansas City, KS 66103 USA
[21] NU Hosp Grp, Dept Pediat, Uddevalla, Sweden
[22] Univ Gothenburg, Sahlgrenska Acad, Inst Clin Sci, Gothenburg, Sweden
关键词
METABOLIC-CONTROL; T1D EXCHANGE; CHILDHOOD; CARE; HVIDOERE; OUTCOMES; REGISTRY; CENTERS; IMPROVEMENT; MANAGEMENT;
D O I
10.2337/dc17-2271
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE International studies on childhood type 1 diabetes (T1D) have focused on whole-country mean HbA(1c) levels, thereby concealing potential variations within countries. We aimed to explore the variations in HbA(1c) across and within eight high-income countries to best inform international benchmarking and policy recommendations. RESEARCH DESIGN AND METHODS Data were collected between 2013 and 2014 from 64,666 children with T1D who were < 18 years of age across 528 centers in Germany, Austria, England, Wales, U.S., Sweden, Denmark, and Norway. We used fixed-and random-effects models adjusted for age, sex, diabetes duration, and minority status to describe differences between center means and to calculate the proportion of total variation in HbA(1c) levels that is attributable to between-center differences (intraclass correlation [ICC]). We also explored the association between within-center variation and children's glycemic control. RESULTS Sweden had the lowest mean HbA(1c) (59mmol/mol [7.6%]) and together with Norway and Denmark showed the lowest between-center variations (ICC <= 4%). Germany and Austria had the next lowest mean HbA(1c) (61-62 mmol/mol [7.7-7.8%]) but showed the largest center variations (ICC similar to 15%). Centers in England, Wales, and the U.S. showed low-to-moderate variation around high mean values. In pooled analysis, differences between counties remained significant after adjustment for children characteristics and center effects (P value < 0.001). Across all countries, children attending centers with more variable glycemic results had higher HbA(1c) levels (5.6mmol/mol [0.5%] per 5mmol/mol [0.5%] increase in center SD of HbA(1c) values of all children attending a specific center). CONCLUSIONS A tsimilar average levels of HbA(1c), countries display different levels of center variation. The distribution of glycemic achievement within countries should be considered in developing informed policies that drive quality improvement.
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页码:1180 / 1187
页数:8
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