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    <title>Banga, J.D.</title>
    <link>http://repub.eur.nl/res/aut/34815/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
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    <item>
      <title>Atorvastatin affects low density lipoprotein and non-high density lipoprotein cholesterol relations with apolipoprotein B in type 2 diabetes mellitus: Modification by triglycerides and cholesteryl ester transfer protein (Article)</title>
      <link>http://repub.eur.nl/res/pub/25396/</link>
      <pubDate>2009-07-01T00:00:00Z</pubDate>
      <description>Objectives: Non-HDL-cholesterol (non-HDL-C) and apolipoprotein (apo) B are proposed as treatment targets. The extent to which statin therapy affects relationships of LDL-C and non-HDL-C with apoB was examined in type 2 diabetes. Methods: Analyses were performed in 217 hypertriglyceridaemic type2 diabetic patients (Diabetes Atorvastatin Lipid Intervention (DALI) cohort). 61patients randomized to placebo, 70 to 10mg atorvastatin daily and 65 - 80mg atorvastin daily completed follow-up. Results: Baseline fasting LDL-C of 2.42 mmol/l and non-HDL-C of 3.69 mmol/l corresponded to the apoB guideline target of 0.90 g/l. During atorvastatin (10 and 80 mg daily), the LDL-C target was achieved most frequently, and lower LDL-C (2.38 and 2.29 mmol/l) and non-HDL-C (3.24 and 3.19 mmol/l) concentrations corresponded to this apoB goal. Decreases in LDL-C during atorvastatin treatment were negatively related (p &lt; 0.001), but decreases in non-HDL-C were positively related to changes in triglycerides (p &lt; 0.001), independently from decreases in apoB (p &lt; 0.001 for all). Decreases in LDL-C and non-HDL-C were positively associated with decreases in cholesteryl ester transfer protein mass (p &lt; 0.001). Conclusions: During atorvastatin lower LDL-C and non-HDL-C levels correspond to the apoB guideline target, which would favour its use as treatment target. </description>
    </item> <item>
      <title>Predictors of cardiac events after major vascular surgery: Role of clinical characteristics, dobutamine echocardiography, and beta-blocker therapy (Article)</title>
      <link>http://repub.eur.nl/res/pub/9625/</link>
      <pubDate>2001-01-01T00:00:00Z</pubDate>
      <description>CONTEXT: Patients who undergo major vascular surgery are at increased risk
          of perioperative cardiac complications. High-risk patients can be
          identified by clinical factors and noninvasive cardiac testing, such as
          dobutamine stress echocardiography (DSE); however, such noninvasive
          imaging techniques carry significant disadvantages. A recent study found
          that perioperative beta-blocker therapy reduces complication rates in
          high-risk individuals. OBJECTIVE: To examine the relationship of clinical
          characteristics, DSE results, beta-blocker therapy, and cardiac events in
          patients undergoing major vascular surgery. DESIGN AND SETTING: Cohort
          study conducted in 1996-1999 in the following 8 centers: Erasmus Medical
          Centre and Sint Clara Ziekenhuis, Rotterdam, Twee Steden Ziekenhuis,
          Tilburg, Academisch Ziekenhuis Utrecht, Utrecht, and Medisch Centrum
          Alkmaar, Alkmaar, the Netherlands; Ziekenhuis Middelheim, Antwerp,
          Belgium; and San Gerardo Hospital, Monza, Istituto di Ricovero e Cura a
          Carattere Scientifico, San Giovanni Rotondo, Italy. PATIENTS: A total of
          1351 consecutive patients scheduled for major vascular surgery; DSE was
          performed in 1097 patients (81%), and 360 (27%) received beta-blocker
          therapy. MAIN OUTCOME MEASURE: Cardiac death or nonfatal myocardial
          infarction within 30 days after surgery, compared by clinical
          characteristics, DSE results, and beta-blocker use. RESULTS: Forty-five
          patients (3.3%) had perioperative cardiac death or nonfatal myocardial
          infarction. In multivariable analysis, important clinical determinants of
          adverse outcome were age 70 years or older; current or prior angina
          pectoris; and prior myocardial infarction, heart failure, or
          cerebrovascular accident. Eighty-three percent of patients had less than 3
          clinical risk factors. Among this subgroup, patients receiving
          beta-blockers had a lower risk of cardiac complications (0.8% [2/263])
          than those not receiving beta-blockers (2.3% [20/855]), and DSE had
          minimal additional prognostic value. In patients with 3 or more risk
          factors (17%), DSE provided additional prognostic information, for
          patients without stress-induced ischemia had much lower risk of events
          than those with stress-induced ischemia (among those receiving
          beta-blockers, 2.0% [1/50] vs 10.6% [5/47]). Moreover, patients with
          limited stress-induced ischemia (1-4 segments) experienced fewer cardiac
          events (2.8% [1/36]) than those with more extensive ischemia (&gt;/=5
          segments, 36% [4/11]). CONCLUSION: The additional predictive value of DSE
          is limited in clinically low-risk patients receiving beta-blockers. In
          clinical practice, DSE may be avoided in a large number of patients who
          can proceed safely for surgery without delay. In clinically intermediate-
          and high-risk patients receiving beta-blockers, DSE may help identify
          those in whom surgery can still be performed and those in whom cardiac
          revascularization should be considered.</description>
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