- Research article
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Pharmacological primary and secondary cardiovascular prevention among diabetic patients in a multiethnic general practice population: still room for improvements
BMC Health Services Research volume 13, Article number: 182 (2013)
Ethnic minority groups have higher prevalence of cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM). We assessed general practitioners’ (GPs’) performance with respect to the pharmacological prevention of CVD in patients with T2DM from different ethnic backgrounds in Oslo.
Of 1653 T2DM patients cared for by 49 GPs in 2005, 380 had a diagnosis of CVD. Ethnicity was categorized as Norwegian, South Asian and other. Risk factor levels, medication use, achievement of treatment targets (HbA1c ≤ 7.5%, systolic blood pressure (SBP) ≤ 140 mmHg, total cholesterol/HDL-cholesterol < 4) and therapeutic intensity (number of drugs targeting each risk factor) were recorded. Chi-square, Wald tests and multiple linear regression analyses were used.
Of the 1273 patients receiving primary prevention, 1.5% had their Hb1Ac, 4.8% SBP and 12.7% lipids levels above treatment thresholds without relevant prescriptions. Among patients on pharmacological therapy, 66% reached the HbA1c, 62% SBP and 62% lipid target. Proportions not achieving the HbA1c target were 26% in Norwegians, 38% in South Asians and 29% in others (p = 0.008). Proportions not achieving the SBP target were 42% in Norwegians, 22% in South Asians and 25% in others (p ≤ 0.001). Of those not achieving the HbA1c and SBP targets, 43% and 35% respectively, used only one agent.
In secondary prevention, 0.8% of the patients had their HbA1c, 0.5% SBP and 7.4% lipid levels above treatment thresholds without relevant prescriptions. Among patients on pharmacological therapy, 65% reached the HbA1c, 64% SBP and 66% lipid target. Proportions not achieving the HbA1c target were 26% in Norwegians, 47% in South Asians and 40% in others (p = 0.03). Proportions not achieving the SBP target were 36% in Norwegians, 22% in South Asians and 56% in others (p = 0.050). Of those not achieving HbA1c and SBP targets, 49% and 21% respectively, were on mono-therapy.
Norwegian GPs comply reasonably well with guidelines for pharmacological prevention of CVD in T2DM patients across ethnic groups. However, lipid-lowering therapy was generally underused, and the achievement of treatment targets for HbA1c in ethnic minorities and for BP in Norwegians could be improved.
Cardiovascular disease (CVD), in particular coronary heart disease (CHD) and cerebro-vascular disease, are the major causes of morbidity and mortality in patients with diabetes [1, 2]. In Europe, ethnic groups with origin from Asia and Africa have a higher prevalence of type 2 diabetes mellitus (T2DM) [3, 4], higher age-adjusted diabetes mortality rates  and standardised CVD mortality rates  than the majority population.
In several Western countries, improvements in risk factor levels and better treatment for CHD have contributed to reduced CVD mortality in both the general population [7–12] and in individuals with diabetes [13–17]. Data from the UK reveal that these improvements have not to the same extent benefitted ethnic minorities like South Asians .
Because patients with highest risk also gain most from interventions, they should be identified and prioritized by their general practitioners (GPs) . Pharmacological therapy to prevent CVD in individual patients should therefore be based on estimated absolute risk for future CVD [19, 20]. Intensive interventions targeting multiple risk factors to prevent CVD in T2DM patients with ethnic minority backgrounds are needed to reduce ethnic disparities in long term health outcomes [21–23]. To our knowledge, only two diabetes specific risk algorithms, those developed by The United Kingdom Prospective Diabetes Study (UKPDS) Group  and the New Zealand Diabetes Cohort Study Group , include ethnicity as a risk factor. However, guidelines must be tailored to fit the individual. Too intensive glucose-lowering therapy (e.g. aiming at HbA1c < 6%) may increase mortality in patients with previous cardiovascular events  or in elderly patients with a long duration of diabetes . Similarly, intensive anti-hypertensive therapy, aiming at systolic blood pressure (SBP) well below 130 mmHg has also been questioned due to increased risk for hypotension and adverse drug reactions . Moreover, interventions to reduce blood pressure below 120 mmHg have not been shown to reduce cardiovascular risk .
Compared with the majority population, ethnic minority groups in Norway have a higher prevalence of self-reported CVD and diabetes , increased susceptibility for diabetes for a given level of adiposity , and are on average younger at the time of T2DM diagnosis . Despite receiving more intensive glucose-lowering therapy, they also have poorer glycaemic control . Regardless of ethnicity, important processes of care measures are comparable, but only one in four of T2DM patients in all ethnic groups, receiving care in general practice, reach all national treatment targets related to HbA1c, BP and lipid levels .
The aim of this study was to explore GPs’ adherence to the guidelines for pharmacological primary or secondary CVD prevention in T2DM patients [33, 34], achievements of treatment targets, the intensity of treatment, potential overtreatment and to estimate the 10-year risk for CHD in Norwegian and South Asian patients without known CVD.
Design, setting and participants
Cross-sectional data from electronic medical records (EMRs) from 11 practices (49 GPs’ with 58857 listed patients) from multiethnic parts of Eastern Oslo were used . A specially designed data programme was used to identify patients with diabetes and to capture predefined data from the EMR from the years 2003–2005. Data regarding HbA1c, SBP, DBP, microalbuminuria, body weight and foot examinations were from 2005, for eye examinations from 2004 or 2005, and for s-cholesterol and smoking habits from 2003 to 2005. A total of 2064 patients with a diagnosis of diabetes were identified. As our aim was to explore GPs’ adherence to guidelines for T2DM, we excluded T1DM patients (n = 103), T2DM patients with two or more diabetes related hospital visits the previous 12 months (n = 178) as they also had incomplete information of current medication, those with less than six months of follow-up or who had moved or were deceased (n = 128), or who had incomplete information about the country of birth (n = 2), leaving 1653 T2DM patients cared for by their GPs to be included in the present study. The study was approved by the Regional Ethics Committee West, the Directorate for Health and the Data Inspectorate.
Patients who according to the EMR had a diagnosis of angina pectoris, previous myocardial infarction, stroke or transitory ischemic attack, or intermittent claudication, were categorized as having CVD and thus requiring secondary prevention (SP) to reduce their risk of new events. All other patients were considered to require primary prevention (PP) of CVD.
According to the Norwegian national general practice diabetes guidelines from 2005 [33, 34], diabetes patients without CVD should have anti-hypertensive therapy if their BP > 140/90 mmHg, and lipid lowering therapy if their total cholesterol/HDL-cholesterol ratio > 5.0 and they had at least one additional risk factor (current anti-hypertensive therapy, smoking, microalbumiuria or a family history of premature CVD). For diabetes patients with CVD, the corresponding treatment thresholds were BP > 140/90 mmHg and total cholesterol/HDL-cholesterol ratio ≥ 4.0 irrespective of other risk factors. Treatment targets were: HbA1c ≤ 7.5%, SBP ≤ 140 mmHg, diastolic blood pressure (DBP) ≤ 85 mmHg, and total cholesterol/HDL-cholesterol ratio < 4.0 [33, 34].
Age, gender, recorded measurements of CVD risk factors, patient’s age when diabetes was diagnosed, disease duration, and prescription data were captured . For HbA1c, SBP, DBP and lipids, the most recent results were selected.
Prescription of glucose-lowering therapy (anti-diabetic agents, insulin or any combinations), anti-hypertensive (angiotensin converting enzyme inhibitors, calcium channel blockers, alfa blockers, beta blockers, angiotensin II receptor antagonists, diuretics, or any combinations), and lipid-lowering therapy (statins) were dichotomized as “yes” versus “no” for all three therapy groups. The intensity of treatment was categorized by numbers of agents used in combination to target elevated BP, and to lower blood glucose. Because too intensive treatment may put patients at increased risk for side effects like hypoglycaemia and hypotension, we identified patients on glucose-lowering therapy with HbA1c < 6.0% [27, 35] and those on anti-hypertensive therapy with SBP < 130 mmHg or DBP < 65 mmHg .
Ethnicity was based on self-reported country of birth as recorded in the EMR, and categorized as: Norwegians (including about 2% from other Scandinavian countries or Western Europe/North America), South Asians (Pakistanis, Sri Lankans and Indians), others (from other low- and middle income countries).
To estimate individual 10-year absolute risk for CHD for patients without prior CVD in the two largest ethnic groups (Norwegians and South Asians), we used the UKPDS Risk Engine version 2 , which includes age, gender, diabetes duration, HbA1c, SBP, total cholesterol, HDL-cholesterol, smoking status (never, past or current smoker).
Chi- squared, one-way ANOVAs, T-tests and Wald tests were used to test differences between proportions and means in the groups. Because HbA1c values were highly skewed, they were log-transformed and presented as geometric means (estimates with 95% confidence intervals, transformed back to the original scale). Generalized linear models were applied to estimate means for the CVD risk factors, the proportions receiving pharmacological therapy, and the proportions not reaching treatment targets, all adjusted for age and gender. The geometric mean values for HbA1c were also adjusted for diabetes duration.
HbA1c was recorded in 95%, BP in 91%, total cholesterol in 94% and smoking habits in 59% of all patients, but the complete set of variables to be used in the UKPDS risk engine was available for only 54% of Norwegian and 43% of South Asian patients. We therefore used multiple imputation techniques for individuals with incomplete data as this is the recommended procedure to limit bias due to missing data when values are missed at random . Age, gender, ethnicity, BMI, glucose-lowering therapy, anti-hypertensive therapy and lipid-lowering therapy were used as predictors for the imputed values and five imputed datasets were created. Multiple regression models were applied to estimate age- and gender adjusted 10-year mean risk for cases with complete data and for all cases after imputation and pooling of the original and imputed data sets.
Two-sided tests were used and p-values ≤ 0.05 were considered statistically significant. The analyses were performed with SPSS 19.0 for Windows and Stata 12.
Of the 1653 included patients with T2DM, 1273 (77%) had no CVD diagnoses (PP group), whereas 380 had one or more CVD diagnoses (SP group). South Asians were youngest both in the PP and SP group, being on average 13 and 18 years younger than Norwegians at the time of diabetes diagnosis (Table 1). In the PP group the prevalence of current smoking was lowest among South Asians (p = 0.001).
Primary prevention of CVD
Among the 1273 T2DM patients without established CVD, 95% had their HbA1c, 90% SBP, 94% total cholesterol and 58% smoking habits recorded. Differences between ethnic groups for these processes of care were minor and significant only for BP-measurements which were less prevalent among South Asians. In total, 950 (75%) received pharmacological glucose-lowering, 700 (55%) anti-hypertensive and 401 (32%) lipid-lowering therapy. Of those on pharmacological therapy 66% reached the HbA1c, 62% SBP and 62% lipid target.
Age- and gender-adjusted mean values for SBP, DBP, HDL-cholesterol and geometric means for HbA1c (also adjusted for diabetes duration), differed significantly between ethnic groups (Table 2). In accordance with risk factor levels, glucose-lowering therapy was prescribed more often and anti-hypertensives less often to ethnic minority patients compared with Norwegians, but the proportion not achieving treatment targets still differed between ethnic groups. Although lipid-lowering therapy was prescribed less often to minority patients, the proportion not reaching the lipid target did not differ between the ethnic groups (Table 2).
Treatment was more intense in those not achieving targets for hyperglycaemia and SBP (Table 3), but 43.4% and 35.3% respectively used only one agent. Among the 82 patients on glucose-lowering therapy despite having HbA1c < 6%, 6 patients were > 75 years, 4 had a diabetes duration > 10 years and 17 received two or three glucose-lowering agents (Table 4). Among the 154 patients on anti-hypertensive therapy having SBP < 130 mmHg, 56 were receiving two or more agents.
Among patients without glucose-lowering therapy, 5% had HbA1c > 7.5% and among those without anti-hypertensive therapy, 11% had SBP > 140 mmHg. Among patients without lipid-lowering therapy, 19% had total cholesterol/HDL-cholesterol ratio > 5. Of the total PP group, 1.5% had hyperglycaemia, 4.8% hypertension and 12.7% dyslipidemia without relevant prescriptions. No ethnic differences were observed for non-prescription of preventive pharmacological treatment.
Risk estimation for CHD by the UKPDS engine based on the 54% of Norwegian and 43% of South Asian patients with complete datasets, revealed comparable age- and gender-adjusted 10-year absolute risk (95% confidence interval) for CHD between the groups (South Asians: 19.0(17.5-20.5)%, Norwegians: 17.2(16.5-17.9)%). Patients with (n = 560) and without (n = 535) complete data for CVD risk estimations were comparable for age at diagnosis, SBP, total cholesterol, and HDL-cholesterol, but differed for age (60 years vs. 62 years, p = 0.027) diabetes duration (5.8 years vs. 6.6 years, p = 0.027), HbA1c (7.0% vs. 7.2%, p = 0.001) and proportions with smoking habits recorded (100% vs. 20%, p<0.001). After imputation and pooling of datasets, the age- and gender 10-year risk estimates for CHD increased for both groups (South Asians: 20.9 (19.7-22.1)%, Norwegians 19.9 (18.7-21.1)%, but ethnic differences remained insignificant.
Secondary prevention of CVD
In the SP group, the proportions of patients with recorded CVD risk factors were comparable between ethnic groups. Pharmacological therapy was more intensive than in the PP group (glucose-lowering drugs: 78%, anti-hypertensives: 89%, lipid-lowering drugs: 64%). Among those on pharmacological therapy, 65% reached the HbA1c, 64% SBP and 66% lipid target, comparable with the PP group.
HbA1c, DBP, HDL- cholesterol and total cholesterol/HDL-cholesterol ratio differed between the ethnic groups (Table 5). Compared with the PP group, the ethnic differences for HbA1c were larger in the SP group. For patients on pharmacological therapy not achieving treatment targets, a similar pattern to that found in the PP group was observed for the ethnic groups (Table 5).
Among the 25 patients on glucose-lowering therapy with a HbA1c < 6.0%, 12 were > 75 years, 12 had a diabetes duration > 10 years and 10 received two or three glucose-lowering agents (Table 4). Of the 76 patients on antihypertensive therapy with SBP < 130 mmHg, 21 used two or more anti-hypertensives.
Among patients without glucose-lowering therapy, 4% had HbA1c > 7.5% while 5% of those without anti-hypertensive therapy had SBP > 140 mmHg. Among patients without lipid-lowering therapy, 21% had total cholesterol/HDL-cholesterol ratio ≥ 4. Of the total SP group, 0.8% had hyperglycaemia, 0.5% hypertensjon and 7.4% dyslipidemia without relevant prescriptions. No ethnic differences were observed for these proportions.
Our study adds to a sparse literature on primary and secondary prevention of CVD in T2DM patients of different ethnic origin in general practice. Norwegian GPs comply reasonably well with the guidelines with respect to which patients should be prescribed glucose-lowering and anti-hypertensive therapy across different ethnic groups of patients, but lipid lowering therapy was relatively underused. However, for those on pharmacological treatment, both in the PP and SP group, at least one in three did not reach specified treatment targets, and a significant proportion of these patients used only one drug to lower their HbA1c or BP. There seems to be a potential to safely improve the achievement of treatment targets, especially regarding glucose-lowering therapy in South Asians and anti-hypertensive therapy in Norwegians, as very few seemed to be at risk of potentially adverse effects due to overtreatment of hyperglycemia or hypertension, especially in the PP group.
Strengths and limitations
Our study population is probably representative for the population in suburban areas in Eastern Oslo . Other strengths are the detailed recording of prescriptions, HBA1c, BP and lipid values in EMRs together with physician based diagnosis of diabetes and CVD.
When sampling the data, our focus was on GPs’ adherence to guidelines, and patients receiving specialist care were excluded. This represents a limitation in relation to the total diabetes population. Furthermore, we lack potentially important information regarding side effects of pharmacological therapy, lifestyle intervention and language barriers  or health literacy  which may influence adherence with prescribed medication .
Missing data limit the validity of our results regarding the estimated risk for future CHD. Multiple imputation of missing values may, however, limit this problem if data are missed at random. Estimates after imputation therefore probably reflect the whole study population . The shorter diabetes duration and a better glycaemic control in patients with complete data for risk estimation may explain why the risk estimates increased after imputation. Estimated CHD risks should nevertheless be interpreted with caution due to this limitation.
Adherence to the guidelines
Norwegian GPs performed good quality diabetes care with respect to recommended measurements of HbA1c, SBP and total cholesterol. Our findings here are comparable with those reported from a British general practice study . Although most patients with risk factor levels above treatment thresholds received pharmacological therapy according to guidelines, a significant proportion did not achieve treatment targets despite receiving more intensive treatment compared with those who reached targets for HbA1c and SBP. On the other hand, our results may suggest that patients with higher age, longer diabetes duration and poorer glycaemic control are more likely to miss regular appointments. The GPs should pay particular attention to these patients.
In spite of receiving more intensive glucose-lowering therapy, the ethnic minority groups still had higher HbA1c than the Norwegians, both in PP and SP. This finding is in accordance with previous findings from British general practice [41, 42] and may reflect lower age at diagnosis [42, 43], more pronounced insulin resistance, language barriers or poorer adherence with prescribed therapy [44, 45]. In Norwegian T2DM patients, under-treatment of hypertension or non-adherence with prescribed medication may represent a challenge.
However, a patient’s acceptance of using an intensive and complex pharmacological regimen for CVD prevention must be considered. The patients’ preferences, cultural factors, skepticism towards polypharmacy [37, 39, 46] may all influence GPs’ prescribing practice and patients’ adherence to prescribed therapy and thereby also health outcomes.
Furthermore, the GPs have to take into account additional costs in terms of adverse drug reactions and possible interactions in polypharmacy, without added clinical benefits [28, 47]. This is even more relevant as the latest version of the Norwegian guidelines promote even lower threshold levels for HbA1c (≤ 7.0%) and BP (135/80 mmHg), if not otherwise contraindicated . Hypotension may represent barriers for doctors and patients. However, a recent systematic review and meta-analysis concluded that intensive anti-hypertensive therapy may provide greater protection against CVD events and micro-vascular complications, not least in patients with diabetes . Furthermore, very tight glycaemic control must be individualized and the possible benefit of a reduction of microvascular complications must be weighed against the possibility of hypoglycemia  and increased mortality, especially in elderly patients with CVD and long diabetes duration . In this study we have no information about side effects of therapy and the GPs strategies for shared decision-making with their patients.
At the time of our study, GPs seemed to focus more on glucose-lowering and anti-hypertensive than on lipid-lowering therapy. Since we collected our data, prescription of newer glucose-lowering agents and statins in the general population has increased . Statins have a modest effect on HDL-cholesterol levels, other strategies for lipid therapy may be considered, especially for South Asians where HDL-cholesterol seems to be particularly important .
CHD risk estimation
The age- and gender adjusted 10-year risk for CHD were lower than corresponding estimates from the US (22.5%)  and in Australian general practice (20.3%) . This may relate to our exclusion of patients receiving specialist care, who may be at higher risk for CVD. The UKPDS Risk Engine is considered to be a useful tool to identify individuals with T2DM at high risk for CVD in order to target preventive therapy, but may not provide equally valid absolute risk estimates in different populations [55, 56]. We do not have cause-specific mortality statistics for different ethnic minority groups in Norway. However, lower rates of hypertension and smoking in South Asians may balance out the effect of higher HBA1c compared with Norwegians .
GPs adhered to guidelines and prescribed pharmacological therapy for the primary and secondary prevention of CVD in most T2DM patients with risk factor levels above treatment thresholds in all ethnic groups. However, more intensive pharmacological therapy may be justified for the relatively large proportion of patients on pharmacological therapy that does not reach treatment targets. This relates in particular to lipid-lowering therapy for all ethnic groups, antihypertensive therapy for Norwegians and glucose-lowering therapy in ethnic minorities. Reaching treatment targets for HbA1c in South Asians is challenging both in primary and secondary prevention. Future clinical guidelines for the primary and secondary prevention of CVD in patients with T2DM should take into account the role of ethnicity. Updated risk estimates based on observed CVD morbidity- and mortality rates for the major ethnic groups are warranted.
Nathan DM, Meigs J, Singer DE: The epidemiology of cardiovascular disease in type 2 diabetes mellitus: how sweet it is … or is it?. Lancet. 1997, 350 (Suppl 1): SI4-SI9.
Seshasai SR, Kaptoge S, Thompson A, Di AE, Gao P, Sarwar N, Whinncup PH, Mukamal KJ, Gillum RF, Holm I, Njølstad I, Fletcher A, Nilsson P, Lewington S, Collins R, Gudnason V, Thompsom SG, Sattar N, Selvin E, Hu FB, Danesh J: Diabetes mellitus, fasting glucose, and risk of cause-specific death. N Engl J Med. 2011, 364: 829-841.
Mather HM, Keen H: The Southall diabetes survey: prevalence of known diabetes in Asians and Europeans. Br Med J (Clin Res Ed). 1985, 291: 1081-1084. 10.1136/bmj.291.6502.1081.
Wandell PE, Carlsson A, Steiner KH: Prevalence of diabetes among immigrants in the Nordic countries. Curr Diabetes Rev. 2010, 6: 126-133. 10.2174/157339910790909404.
Vandenheede H, Deboosere P, Stirbu I, Agyemang CO, Harding S, Juel K, Rafnsson SB, Regidor E, Rey G, Rosato M, Mackenbach JP, Kunst AE: Migrant mortality from diabetes mellitus across Europe: the importance of socio-economic change. Eur J Epidemiol. 2012, 27: 109-117. 10.1007/s10654-011-9638-6.
Chaturvedi N, Fuller JH: Ethnic differences in mortality from cardiovascular disease in the UK: do they persist in people with diabetes?. J Epidemiol Community Health. 1996, 50: 137-139. 10.1136/jech.50.2.137.
Bertuccio P, Levi F, Lucchini F, Chatenoud L, Bosetti C, Negri E, La Wecchia C: Coronary heart disease and cerebrovascular disease mortality in young adults: recent trends in Europe. Eur J Cardiovasc Prev Rehabil. 2011, 18: 627-634. 10.1177/1741826710389393.
Ford ES, Capewell S: Proportion of the decline in cardiovascular mortality disease due to prevention versus treatment: public health versus clinical care. Annu Rev Public Health. 2011, 32: 5-22. 10.1146/annurev-publhealth-031210-101211.
Vaartjes I, O’Flaherty M, Grobbee DE, Bots ML, Capewell S: Coronary heart disease mortality trends in the Netherlands 1972–2007. Heart. 2011, 97: 569-573. 10.1136/hrt.2010.206565.
Davidsen M, Bronnum-Hansen H, Jorgensen T, Madsen M, Gerdes LU, Osler M, Schroll M: Trends in incidence, case-fatality and recurrence of myocardial infarction in the Danish MONICA population 1982–1991. Eur J Epidemiol. 2001, 17: 1139-1145. 10.1023/A:1021229016230.
Mannsverk J, Wilsgaard T, Njolstad I, Hopstock LA, Lochen ML, Mathiesen EB, Thelle DS, Rasmussen K, Bonaa KH: Age and gender differences in incidence and case fatality trends for myocardial infarction: a 30-year follow-up. The Tromso Study. Eur J Cardiovasc Prev Rehabil. 2012, 19: 927-934.
Lundblad D, Holmgren L, Jansson JH, Naslund U, Eliasson M: Gender differences in trends of acute myocardial infarction events: the Northern Sweden MONICA study 1. BMC Cardiovasc Disord. 2008, 8: 17-10.1186/1471-2261-8-17.
Gregg EW, Cheng YJ, Saydah S, Cowie C, Garfield S, Geiss L, Barker L: Trends in death rates among u.s. Adults with and without diabetes between 1997 and 2006: findings from the national health interview survey. Diabetes Care. 2012, 35: 1252-1257. 10.2337/dc11-1162.
Thomas RJ, Palumbo PJ, Melton LJ, Roger VL, Ransom J, O’Brien PC, Leibson CL: Trends in the mortality burden associated with diabetes mellitus: a population-based study in Rochester, Minn, 1970–1994. Arch Intern Med. 2003, 163: 445-451. 10.1001/archinte.163.4.445.
Lipscombe LL, Hux JE: Trends in diabetes prevalence, incidence, and mortality in Ontario, Canada 1995–2005: a population-based study. Lancet. 2007, 369: 750-756. 10.1016/S0140-6736(07)60361-4.
Dale AC, Midthjell K, Nilsen TI, Wiseth R, Vatten LJ: Glycaemic control in newly diagnosed diabetes patients and mortality from ischaemic heart disease: 20-year follow-up of the HUNT Study in Norway. Eur Heart J. 2009, 30: 1372-1377. 10.1093/eurheartj/ehp039.
Nauta ST, Deckers JW, Akkerhuis KM, van Domburg RT: Short- and long-term mortality after myocardial infarction in patients with and without diabetes: changes from 1985 to 2008. Diabetes Care. 2012, 35: 2043-2047. 10.2337/dc11-2462.
Harding S, Rosato M, Teyhan A: Trends for coronary heart disease and stroke mortality among migrants in England and Wales, 1979–2003: slow declines notable for some groups. Heart. 2008, 94: 463-470.
The national guidelines for individual primary prevention of cardiovascular diseases: [http://helsedirektoratet.no/publikasjoner/nasjonal-faglig-retningslinje-for-individuell-primerforebygging-av-hjerte-og-karsykdommer/Sider/default.aspx]
Graham I, Atar D, Borch-Johnsen K, Boysen G, Burell G, Cifkova R, Dallongeville J, De Backer G, Ebrahim S, Gjelsvik B, Herrmann-Lingen C, Hoes A, Humphries S, Knapton M, Perk J, Priori SG, Pyorala K, Reiner Z, Ruilope L, Sans-Menendez S, Op Reimer WS, Weissberg P, Wood D, Yarnell J, Zamorano JL, Walma E, Fitzgerald T, Cooney MT, Dudina A, Vahanian A: European guidelines on cardiovascular disease prevention in clinical practice: full text. Fourth Joint Task Force of the European Society of Cardiology and other societies on cardiovascular disease prevention in clinical practice (constituted by representatives of nine societies and by invited experts). Eur J Cardiovasc Prev Rehabil. 2007, 14 (Suppl 2): 1-113.
Lanting LC, Joung IM, Mackenbach JP, Lamberts SW, Bootsma AH: Ethnic differences in mortality, end-stage complications, and quality of care among diabetic patients: a review. Diabetes Care. 2005, 28: 2280-2288. 10.2337/diacare.28.9.2280.
Millett C, Netuveli G, Saxena S, Majeed A: Impact of pay for performance on ethnic disparities in intermediate outcomes for diabetes: longitudinal study. Diabetes Care. 2008, 32: 404-409.
Trivedi AN, Zaslavsky AM, Schneider EC, Ayanian JZ: Trends in the quality of care and racial disparities in Medicare managed care. N Engl J Med. 2005, 353: 692-700. 10.1056/NEJMsa051207.
Stevens RJ, Kothari V, Adler AI, Stratton IM: The UKPDS risk engine: a model for the risk of coronary heart disease in Type II diabetes (UKPDS 56). Clin Sci (Lond). 2001, 101: 671-679. 10.1042/CS20000335.
Elley CR, Robinson E, Kenealy T, Bramley D, Drury PL: Derivation and validation of a new cardiovascular risk score for people with type 2 diabetes: the new zealand diabetes cohort study. Diabetes Care. 2010, 33: 1347-1352. 10.2337/dc09-1444.
Gerstein HC, Miller ME, Byington RP, Goff DC, Bigger JT, Buse JB, Cushmann WC, Genuth S, Ismail-Beigi F, Grimm RH, Simons-Morton DG: Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med. 2008, 358: 2545-2559.
Cheng AY, Leiter LA: Diabetes and cardiovascular disease: the role of glycemic control. Curr Diab Rep. 2009, 9: 65-72. 10.1007/s11892-009-0012-y.
Kerr EA, Lucatorto MA, Holleman R, Hogan MM, Klamerus ML, Hofer TP, Va Diabetes Quality Enhancement Reasearch Initiative (QUERI) Workgroup on Clinical Action Measures: Monitoring performance for blood pressure management among patients with diabetes mellitus: too much of a good thing?Monitoring performance for BP management in diabetes. Arch Intern Med. 2012, 172: 938-945.
Cushman WC, Evans GW, Byington RP, Goff DC, Grimm RH, Cutler JA, Simons-Morton DG, Basile JN, Corson MA, Probstifield JL, Peterson KA, Friedewald WT, Buse JB, Bigger JT, Gerstein HC, Ismail-Beigi F: Effects of intensive blood-pressure control in type 2 diabetes mellitus. N Engl J Med. 2010, 362: 1575-1585.
Tran AT, Straand J, Diep LM, Meyer HE, Birkeland KI, Jenum AK: Cardiovascular disease by diabetes status in five ethnic minority groups compared to ethnic Norwegians. BMC Publ Health. 2011, 11: 554-10.1186/1471-2458-11-554.
Jenum AK, Holme I, Graff-Iversen S, Birkeland KI: Ethnicity and sex are strong determinants of diabetes in an urban Western society: implications for prevention. Diabetologia. 2005, 48: 435-439. 10.1007/s00125-005-1668-8.
Tran AT, Diep LM, Cooper JG, Claudi T, Straand J, Birkeland K, Ingskog W, Jenum AK: Quality of care for patients with type 2 diabetes in general practice according to patients’ ethnic background: a cross-sectional study from Oslo, Norway. BMC Health Serv Res. 2010, 10: 145-10.1186/1472-6963-10-145.
Claudi T, Ingskog W, Cooper JG, Jenum AK, Hausken MF: [Quality of diabetes care in Norwegian general practice]. Tidsskr Nor Laegeforen. 2008, 128: 2570-2574.
Cooper JG, Claudi T, Jenum AK, Thue G, Hausken MF, Ingskog W, Sanberg S: Quality of care for patients with type 2 diabetes in primary care in Norway is improving. Results of cross-sectional surveys of 33 general practices in 1995 and 2005. Diabetes Care. 2008, 32: 81-83.
Zoungas S, Chalmers J, Ninomiya T, Li Q, Cooper ME, Colagiuri S, Fulcher G, de Galan BE, Harrap S, Hamet P, Heller S, MacMahon S, Marre M, Poulter N, Travert F, Patel A, Neal B, Woodward M: Association of HbA1c levels with vascular complications and death in patients with type 2 diabetes: evidence of glycaemic thresholds. Diabetologia. 2012, 55: 636-643. 10.1007/s00125-011-2404-1.
Sterne JA, White IR, Carlin JB, Spratt M, Royston P, Kenward MG, Wood AM, Carpenter JR: Multiple imputation for missing data in epidemiological and clinical research: potential and pitfalls. BMJ. 2009, 338: b2393-10.1136/bmj.b2393.
Hakonsen H, Toverud EL: Cultural influences on medicine use among first-generation Pakistani immigrants in Norway. Eur J Clin Pharmacol. 2012, 68: 171-178. 10.1007/s00228-011-1111-7.
Safeer RS, Keenan J: Health literacy: the gap between physicians and patients. Am Fam Physician. 2005, 72: 463-468.
Cramer JA, Benedict A, Muszbek N, Keskinaslan A, Khan ZM: The significance of compliance and persistence in the treatment of diabetes, hypertension and dyslipidaemia: a review. Int J Clin Pract. 2008, 62: 76-87.
Gray J, Millett C, Saxena S, Netuveli G, Khunti K, Majeed A: Ethnicity and quality of diabetes care in a health system with universal coverage: population-based cross-sectional survey in primary care. J Gen Intern Med. 2007, 22: 1317-1320. 10.1007/s11606-007-0267-4.
Soljak MA, Majeed A, Eliahoo J, Dornhorst A: Ethnic inequalities in the treatment and outcome of diabetes in three English Primary Care Trusts. Int J Equity Health. 2007, 6: 8-10.1186/1475-9276-6-8.
McElduff P, Edwards R, Burns JA, Young RJ, Heller R, Long B, Jones G, New JP: Comparison of processes and intermediate outcomes between South Asian and European patients with diabetes in Blackburn, north-west England. Diabet Med. 2005, 22: 1226-1233. 10.1111/j.1464-5491.2005.01614.x.
Mukhopadhyay B, Forouhi NG, Fisher BM, Kesson CM, Sattar N: A comparison of glycaemic and metabolic control over time among South Asian and European patients with Type 2 diabetes: results from follow-up in a routine diabetes clinic. Diabet Med. 2006, 23: 94-98. 10.1111/j.1464-5491.2005.01735.x.
Gafvels C, Wandell PE: Coping strategies in immigrant men and women with type 2 diabetes. Diabetes Res Clin Pract. 2007, 76: 269-278. 10.1016/j.diabres.2006.09.011.
Palaniappan LP, Carnethon MR, Fortmann SP: Heterogeneity in the relationship between ethnicity, BMI, and fasting insulin. Diabetes Care. 2002, 25: 1351-1357. 10.2337/diacare.25.8.1351.
Goldenberg N, Glueck C: Efficacy, effectiveness and real life goal attainment of statins in managing cardiovascular risk. Vasc Health Risk Manag. 2009, 5: 369-376.
Timbie JW, Hayward RA, Vijan S: Variation in the net benefit of aggressive cardiovascular risk factor control across the US population of patients with diabetes mellitus. Arch Intern Med. 2010, 170: 1037-1044.
The national guidelines for prevention, diagnosis and treatment of diabetes: [http://helsedirektoratet.no/publikasjoner/nasjonal-faglig-retningslinje-diabetes/Sider/default.aspx]
Lv J, Neal B, Ehteshami P, Ninomiya T, Woodward M, Rodgers A, Wang H, MacMahon S, Turnbull F, Hillis G, Chalmers J, Perkovic V: Effects of intensive blood pressure lowering on cardiovascular and renal outcomes: a systematic review and meta-analysis. PLoS Med. 2012, 9: e1001293-10.1371/journal.pmed.1001293.
Hemmingsen B, Lund SS, Gluud C, Vaag A, Almdal T, Hemmingsen C, Wetterslev J: Intensive glycaemic control for patients with type 2 diabetes: systematic review with meta-analysis and trial sequential analysis of randomised clinical trials. BMJ. 2011, 343: d6898-10.1136/bmj.d6898.
Norwegian Prescription Database: [http://www.norpd.no]
Cziraky MJ, Watson KE, Talbert RL: Targeting low HDL-cholesterol to decrease residual cardiovascular risk in the managed care setting. J Manag Care Pharm. 2008, 14 (8 Suppl): 3-28.
Kirk JK, Bertoni AG, Case D, Bell RA, Goff DC, Narayan KM: Predicted risk of coronary heart disease among persons with type 2 diabetes. Coron Artery Dis. 2007, 18: 595-600. 10.1097/MCA.0b013e3282f0902b.
Wan Q, Harris MF, Jayasinghe UW, Flack J, Georgiou A, Penn DL, Burns JR: Quality of diabetes care and coronary heart disease absolute risk in patients with type 2 diabetes mellitus in Australian general practice. Qual Saf Health Care. 2006, 15: 131-135. 10.1136/qshc.2005.014845.
Van der Heijden AA, Ortegon MM, Niessen LW, Nijpels G, Dekker JM: Prediction of coronary heart disease risk in a general, pre-diabetic, and diabetic population during 10 years of follow-up: accuracy of the Framingham, SCORE, and UKPDS risk functions: The Hoorn Study. Diabetes Care. 2009, 32: 2094-2098. 10.2337/dc09-0745.
Guzder RN, Gatling W, Mullee MA, Mehta RL, Byrne CD: Prognostic value of the Framingham cardiovascular risk equation and the UKPDS risk engine for coronary heart disease in newly diagnosed Type 2 diabetes: results from a United Kingdom study. Diabet Med. 2005, 22: 554-562. 10.1111/j.1464-5491.2005.01494.x.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6963/13/182/prepub
The authors would like to thank The Norwegian Medical Association, The Norwegian Diabetes Association and South-Eastern Norway Regional Health Authority for funding this project.
The authors declare that they have no competing interests.
The data collection was conceived and designed by AKJ, TC, and JGC. ATT and ID performed the analysis. All authors participated in discussing the results. ATT wrote the first draft of the manuscript and all authors commented on the drafts and approved the final version.