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    <title>Res, J.C.J.</title>
    <link>http://repub.eur.nl/res/aut/3545/</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>
    </image>
    <item>
      <title>Ventricular fibrillation and life-threatening ventricular tachycardia in the setting of outflow tract arrhythmias - The place of ICD therapy (Article)</title>
      <link>http://repub.eur.nl/res/pub/40080/</link>
      <pubDate>2013-05-10T00:00:00Z</pubDate>
      <description></description>
    </item> <item>
      <title>Analysis of 57,148 transmissions by remote monitoring of implantable cardioverter defibrillators (Article)</title>
      <link>http://repub.eur.nl/res/pub/27192/</link>
      <pubDate>2009-03-01T00:00:00Z</pubDate>
      <description>Introduction: Remote monitoring of implantable cardioverter defibrillators (ICD) is designed to decrease the number of ambulatory visits and facilitate the early detection of adverse events. We examined the impact of remote monitoring on clinical workload by a comprehensive analysis of transmitted events. Methods: The study population consisted of 146 recipients of ICD capable of remote monitoring. Data were transmitted daily or in case of pre-specified events (e.g., arrhythmia, out-of-range lead and/or shock impedance). Transmitted events were classified as clinical (disease-related) or system-related. Event rates/patient/month were calculated and compared according to events classification and clinical groups. Results: During a mean follow-up of 22 ± 16 months, a total of 57,148 remote transmissions were recorded. Of these transmissions, 1009 (1.8%) were triggered by a pre-specified event, including induced ventricular fibrillation (VF) episodes during defibrillation threshold testing. The median number of events/patient/month was 0.14. Event rates were similar in patients with primary and secondary prevention indications for ICD (0.15 vs. 0.11). After exclusion of the induced VF episodes, 5.6% of transmitted events were classified as system-related and 94.4% as clinical. The median number of clinical events/patient/month was 0.023. The clinical event-free rates were 62% and 45%, at 1 and 4 years, respectively. Conclusion: Remote monitoring of ICD patients is feasible. Despite the large number of data transmissions, remote monitoring imposed a minimal additional burden on the clinical workload. The rate of triggered data transmissions by critical events was, relatively, very low. </description>
    </item> <item>
      <title>LV lead fixation in a coronary vein may be the cause and result of thrombosis (Article)</title>
      <link>http://repub.eur.nl/res/pub/29389/</link>
      <pubDate>2008-11-01T00:00:00Z</pubDate>
      <description>A recently implanted left ventricular lead was fixated in the coronary sinus due to thrombosis while attempting to reposition the lead because of phrenic nerve stimulation. </description>
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      <title>The BRIGHT study: Bifocal right ventricular resynchronization therapy: A randomized study (Article)</title>
      <link>http://repub.eur.nl/res/pub/36582/</link>
      <pubDate>2007-10-01T00:00:00Z</pubDate>
      <description>Aims: The BRIGHT study evaluated bifocal right ventricular (RV) (apex and outflow tract) pacing in a single, blind, randomized crossover study in patients eligible for cardiac resynchronization therapy (CRT). Forty-two patients were enrolled with the following characteristics: chronic drug refractory heart failure New York Heart Association (NYHA) class III-IV; ejection fraction (EF)&lt;35%; QRS width ≥ 120 ms; and a left bundle branch block. The aim of the study was to assess an improvement in left ventricular (LV) EF, 6 min walk test, Minnesota quality-of-life score, and NYHA classification. Methods and result: Patients were randomized to receive either bifocal pacing or the control mode, each for a period of 3 months. Parameters were measured prior to randomization and after 3 months of control or bifocal pacing. Eight patients failed to make the 7 month follow-up, three patients died (one prior to randomization at the first month), five patients dropped out, and three patients refused further participation. One patient had a persistent lead problem, which was subsequently replaced with an LV lead, and one patient suffered with persistent atrial fibrillation. Compared with baseline, bifocal pacing improved EF from 26 ± 12% to 36 ± 11% (P &lt; 0.0008), NYHA classification decreased from 2.8 ± 0.4 to 2.3 ± 0.7 (P &lt; 0.007). Furthermore, the 6 min walk test improved from 372 ± 129 m to 453 ± 122 m (P &lt; 0.05), and the Minnesota Living with Heart Failure scores decreased from 33 ± 20 to 24 ± 21 (P &lt; 0.006). In the control group, no significant changes in any parameters were observed. Eight patients did not tolerate reprogramming from DDD BRIGHT to control pacing, with symptoms disappearing in all patients after reprogramming to bifocal pacing. Conclusion: Bifocal RV pacing in patients with a classic indication for CRT shows improvement in all parameters. </description>
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      <title>Reversible left bundle branch block induced congestive heart failure. A case report (Article)</title>
      <link>http://repub.eur.nl/res/pub/35360/</link>
      <pubDate>2007-07-01T00:00:00Z</pubDate>
      <description>Intraventricular conduction delay in the form of left bundle branch block plays an important role in the genesis and the progression of congestive hart failure. We report on the clinical course of a patient and the improvement in functional status after the disappearance of left bundle branch block, despite withholding cardiac resynchronization therapy. </description>
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      <title>CRAVT: a prospective, randomized study comparing transvenous cryothermal and radiofrequency ablation in atrioventricular nodal re-entrant tachycardia. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13598/</link>
      <pubDate>2004-12-01T00:00:00Z</pubDate>
      <description>BACKGROUND: Transvenous catheter ablation of atrioventricular nodal
      re-entrant tachycardia (AVNRT) with radiofrequency (RF) is effective and
      safe, but carries a 1-3% incidence of early and potentially late heart
      block. Cryothermy can create transient effects, and identify potentially
      successful ablation sites and decrease the risk for permanent heart block.
      METHODS: In this prospective, randomized trial 102 patients with recurrent
      narrow QRS-complex tachycardia suggestive of AVNRT were randomized to
      either RF or cryoablation before a diagnostic study. RESULTS: In 63
      patients with AVNRT, 33 were randomized to RF and 30 to cryoablation.
      Procedural success was achieved, respectively, in 30 (91%) patients in the
      RF and 28 (93%) in the cryoablation group. The median number of
      cryothermal applications was significantly lower than the number of RF
      applications (2 versus 7, p&lt;0.005). No accelerated junctional rhythm was
      seen with cryothermy, while it was present in 31/33 RF patients. Both
      fluoroscopy and procedural times were comparable. The radiological
      position of the successful site in relation to anatomical landmarks was
      slightly different (p&lt;0.05). No cryothermy related complications were
      observed, and no permanent AV conduction disturbances occurred. During a
      mean follow up of 13+/-7 months long-term clinical success was seen in one
      additional patient in each group. In the same period, 3 patients in both
      groups experienced recurrent AVNRT. CONCLUSION: Cryoablation is as
      effective and safe as RF for AVNRT. Significantly fewer applications are
      necessary, with comparable procedure times. This makes cryothermy useful
      for the treatment of tachyarrhythmias near the compact AV node.</description>
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      <title>Ice mapping during cryothermal ablation of accessory pathways in WPW: the role of the temperature time constant. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13339/</link>
      <pubDate>2004-03-01T00:00:00Z</pubDate>
      <description>AIM: Cryothermal energy has the ability reversibly to demonstrate loss of
      function with cooling, ice mapping, at less deep temperatures. The purpose
      of this study was to investigate the time course of the temperature during
      ice mapping of accessory pathways. METHODS AND RESULTS: Thirteen patients
      with the Wolff-Parkinson-White (WPW) syndrome underwent cryoablation.
      After identification of a prospective ablation site, ice mapping was
      performed by cooling the tip to a minimum of -30 degrees C. Successful ice
      mapping was defined by loss of accessory pathway (AP) conduction. A total
      of 104 ice maps were analyzed. Successful ice mapping was demonstrated in
      17 attempts. There was no significant difference in mapping temperature
      between successful and unsuccessful ice mapping (-29.4+/-3.2 degrees
      Celsius vs -30.4+/-1.7 degrees Celsius). The temperature time constant tau
      during successful ice mapping was significantly shorter compared with
      unsuccessful ice mapping (7.0+/-1.1 s vs 10.1+/-1.3 s; P&lt;0.0001). The
      response time (RT) to mapping temperature of -30 degrees C was
      significantly prolonged in unsuccessful ice mapping attempts (35.8+/-4.5 s
      vs 53.5+/-11.0 s; P&lt;0.0001). Significant correlations were found between
      successful ice mapping and the temperature time constant, and between RT
      and the temperature time constant (P&lt;0.001). CONCLUSION: The ability to
      identify prospective ablation sites by ice mapping was demonstrated.
      Successful ice mapping attempts were characterized by a short temperature
      time constant and a short response time to mapping temperature with a
      sudden disappearance of pathway conduction.</description>
    </item> <item>
      <title>Home monitoring in ICD therapy: future perspectives (Article)</title>
      <link>http://repub.eur.nl/res/pub/10111/</link>
      <pubDate>2003-01-01T00:00:00Z</pubDate>
      <description>The expanding indications for ICD therapy and the complexity of current
      devices will have impact on follow-up policy. The application of ICD
      therapy requires elaborate attention to technical aspects, arrhythmias,
      and the clinical course of the underlying disease. Currently, the quality
      of medical supervision is dependent on scheduled regular follow-up visits.
      A disadvantage of long intervals can be a delay in the physician's or
      patient's awareness of changes in the clinical status. Some patients will
      need more intensive follow-up while others will have the device as a
      stand-by and only need technical follow-up. A possibility to address this
      situation, is the transmission of data, already stored in the implanted
      device. This will guarantee continuous patient surveillance and could
      possibly help to avoid unnecessary follow-up visits.</description>
    </item> <item>
      <title>Transseptal left heart catheterisation guided by intracardiac echocardiography (Article)</title>
      <link>http://repub.eur.nl/res/pub/8348/</link>
      <pubDate>2001-01-01T00:00:00Z</pubDate>
      <description>OBJECTIVE: To develop a novel approach of transseptal puncture guided by
      intracardiac echocardiography and to assess its efficacy. METHODS:
      Transcatheter intracardiac echocardiography with a 9 MHz rotating
      transducer was performed to guide transseptal puncture in 12 patients
      (mean age 43.1 years, range 31-68) who underwent radiofrequency catheter
      ablation of left sided accessory pathways. Initially, the echocardiography
      and transseptal catheters were placed adjacent to each other in the
      superior vena cava and were withdrawn to the level of the fossa ovalis.
      RESULTS: The successful puncture site was associated with visualisation of
      the fossa ovalis (12 patients, 100%) and the aorta (12 patients, 100%),
      tenting of the fossa (six patients, 50%), penetration of the needle
      visualised by the ultrasound catheter (12 patients, 100 %), and
      echocardiographic contrast material applied in the left atrium (12
      patients, 100%). The characteristic jump of the needle onto the fossa
      ovalis was observed simultaneously with fluoroscopy and intracardiac
      ultrasound (12 patients, 100%). All procedures were successful. There were
      no complications associated with the transseptal procedure. CONCLUSIONS:
      Intracardiac echocardiography is feasible to guide transseptal puncture.
      The optimal puncture site can be assessed by simultaneous detection of the
      characteristic downward jump of the transseptal needle onto the fossa
      ovalis by intracardiac ultrasound and fluoroscopy.</description>
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      <title>Immediate PTCA after successful thrombolysis with intracoronary streptokinase, three years follow-up. A matched pair analysis of the effect of PTCA in the randomized multicentre trial of intracoronary streptokinase, conducted by the Interuniversity Cardiology Institute of The Netherlands (Article)</title>
      <link>http://repub.eur.nl/res/pub/4282/</link>
      <pubDate>1988-01-01T00:00:00Z</pubDate>
      <description>Immediate PTCA following thrombolysis with streptokinase was performed in 46 out of 533 patients enrolled in a multicentre randomized trial of early reperfusion in patients with acute myocardial infarction. Additional effects of PTCA in patients with a residual diameter stenosis in the infarct-related coronary artery of 70% or more after thrombolysis were compared with successful thrombolysis alone in a matched pair analysis. Thirty six pairs of patients were formed identical with respect to the infarct related coronary artery, presence or absence of previous myocardial infarction, total ST segment elevation on the ECG at admission to the trial, and delay between onset of symptoms and hospital admission. PTCA after thrombolysis did not lead to additional limitation of infarct size, nor to further preservation of left ventricular function. Infarction rate during the three-year follow-up was 14% after PTCA versus 30% after thrombolysis alone (P = 0.05). Similarly, patients had less angina or heart failure after PTCA, since on average 128 out of 156 weeks follow-up were symptom free, while this was only 102 weeks after thrombolysis alone (P = 0.03). Immediate PTCA after thrombolysis with intracoronary streptokinase seems to prevent recurrent ischemia and reinfarction. Further studies should address the proper indication and timing of PTCA after thrombolysis.</description>
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      <title>Enzyme tests in the evaluation of thrombolysis in acute myocardial infarction (Article)</title>
      <link>http://repub.eur.nl/res/pub/5370/</link>
      <pubDate>1988-01-01T00:00:00Z</pubDate>
      <description>The activity of alpha-hydroxybutyrate dehydrogenase, creatine kinase, creatine kinase MB and aspartate aminotransferase was measured on serial plasma samples from patients with acute myocardial infarction. The study was part of a multicentre randomised trial of the effect of thrombolytic treatment in the acute phase of acute myocardial infarction. The applicability and comparability of enzyme tests for the estimation of myocardial injury were studied in 76 control patients and 74 patients treated with streptokinase. Treatment with streptokinase caused a considerable acceleration of enzyme release after acute myocardial infarction, both in patients with persistent coronary occlusion and in those with successful reperfusion. But this changed pattern of enzyme release did not affect the rate of enzyme elimination from plasma or the released proportions of different enzymes. Thus the assessment of infarct size by measurement of these enzyme activities can also be applied to patients treated with streptokinase. Moreover, the enzymes measured in the present study are all equally valid markers of myocardial injury.</description>
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      <title>Intracoronary thrombolysis in patients with acute myocardial infarction: The Netherlands randomized trial and current status (Article)</title>
      <link>http://repub.eur.nl/res/pub/4240/</link>
      <pubDate>1987-01-01T00:00:00Z</pubDate>
      <description>--</description>
    </item> <item>
      <title>Value of immediate coronary angioplasty following intracoronary thrombolysis in acute myocardial infarction (Article)</title>
      <link>http://repub.eur.nl/res/pub/4249/</link>
      <pubDate>1987-01-01T00:00:00Z</pubDate>
      <description>A total of 533 patients with acute myocardial infarction of less than 4-h duration were enrolled in the multicenter randomized trial of intracoronary thrombolysis compared to conventional treatment. In two of the five participating centers, an additional coronary angioplasty immediately after thrombolysis was attempted in 46 patients. According to the treatment allocation and early and late patency of the infarct related vessel, patients were subdivided into three groups: conventionally treated (group A); successful coronary angioplasty following thrombolysis with persistent patent infarct related vessel (group B); and late patency of the infarct related vessel postthrombolytic therapy without angioplasty (group C). The highest global ejection fractions were observed in group B (54% +/- 10%) and group C (55% +/- 13%), while the lowest ejection fraction was found in group A (47% +/- 14%). The sequential changes in global ejection fraction from the acute to the chronic stage was + 4% (p = 0.05) in group B, while no significant changes could be demonstrated in group C. Furthermore, in the group successfully treated by angioplasty, the improvement in global ejection fraction was more pronounced and persisted up to three months after the intervention. This was supported by analysis of regional myocardial function of the infarct zone (+ 16% improvement, p = 0.01). The long-term clinical follow-up (median 24 months) of the patients successfully treated by combined procedure of thrombolysis and angioplasty (group B) was most favourable with a lower incidence of re-infarction (6%), and late coronary bypass surgery (13%) and/or (re)-percutaneous transluminal coronary angioplasty (3%) was performed less frequently. These results suggest that reperfusion may need to be supplemented by additional revascularization procedures in order to optimize the changes of obtaining full functional recovery and so to improve the prognosis.</description>
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      <title>Verbeterde prognose als gevolg van vroeg thrombolyse bij patienten met een acuut hartinfarct (Article)</title>
      <link>http://repub.eur.nl/res/pub/4179/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>Twee behandelingen werden vergeleken in een gerandomiseerd onderzoek waaraan 533 patiënten met een acuut infarct deelnamen, 264 patiënten werden conventioneel behandeld (groep 1) en 269 kregen een behandeling die gericht was op snelle rekanalisatie van de veelal afgesloten coronairarterie (groep 2). Bij de eerste 152 patiënten in groep 2 werd uitsluitend intracoronair streptokinase gegeven (250.000 eenheden), onmiddellijk na coronariografie. Bij de volgende 117 patiënten werd deze intracoronaire behandeling voorafgegaan door intraveneuze toediening van streptokinase (500.000 eenheden). Bij 198 van de 234 patiënten bij wie angiografie werd verricht in de acute fase van het infarct, was de met het infarct samenhangende coronairarterie doorgankelijk aan het eind van de ingreep (85).

De sterfte was lager bij patiënten uit groep 2 gedurende de gehele follow-up-periode. De éénjaarsoverleving was 91 bij patiënten in groep 2 en 84 in groep 1. Het voorkomen van ventrikelfibrilleren, pericarditis en cardiogene shock in groep 2 was lager dan in de controlegroep. Daarentegen traden bij patiënten uit groep 2 vaker bloedingen en, in het bijzonder bij patiënten met een onderwandinfarct, vaker recidiefinfarcering op.

Op grond van deze gegevens concluderen wij dat trombolyse een aanwinst is bij de behandeling van patiënten met een acuut hartinfarct.</description>
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      <title>Preservation of global and regional left ventricular function after early thrombolysis in acute myocardial infarction (Article)</title>
      <link>http://repub.eur.nl/res/pub/4184/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>The effect of early myocardial reperfusion (within 4 hours after onset of symptoms) on regional left ventricular function in patients with acute myocardial infarction has been quantitated by analysis of segmental wall motion. Of 533 patients randomized either to conventional coronary care unit therapy or to a reperfusion strategy, in 332 high quality angiograms were obtained 2 to 8 weeks after the onset of myocardial infarction. In those assigned to thrombolytic therapy, angiographic data were also available after acute reperfusion. Analysis on an "intention to treat" basis revealed significant preservation of left ventricular function after thrombolytic therapy (ejection fraction 53%) compared with conventional treatment (ejection fraction 47%). In addition, wall motion analysis showed significant improvement of regional function in the infarct zone in both inferior and anterior infarction. In addition, significant changes occurred in regional function of the remote "noninfarct zone" in the acute as well as the chronic stage. It is concluded that improved regional and global left ventricular function can be achieved with early reperfusion and that this is the likely explanation for the reduction of early and late mortality after thrombolysis observed in this study.</description>
    </item> <item>
      <title>Early thrombolysis in acute myocardial infarction: limitation of infarct size and improved survival (Article)</title>
      <link>http://repub.eur.nl/res/pub/4185/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>The effect of thrombolysis in acute myocardial infarction on infarct size, left ventricular function, clinical course and patient survival was studied in a randomized trial comparing thrombolysis (269 patients) with conventional treatment (264 control patients). All 533 patients were admitted to the coronary care unit within 4 hours after the onset of symptoms related to the infarction. Baseline characteristics were similar in both groups. Informed consent was requested only of patients allocated to thrombolysis; no angiography was performed in 35. The infarct-related artery was patent in 65 patients and occluded in 169. Recanalization was achieved in 133 patients. The median time to angiographic documentation of vessel patency was 200 minutes after the onset of symptoms. The clinical course in the coronary care unit was more favorable after thrombolysis. Infarct size, estimated from myocardial enzyme release, was 30% lower after thrombolysis. In patients admitted within 1 hour after the onset of symptoms the reduction of infarct size was 51%, in those admitted between 1 and 2 hours it was 31% and in those admitted later than 2 hours it was 13%. Left ventricular function measured by radionuclide angiography before hospital discharge was better after thrombolysis (ejection fraction 48 +/- 15%) than in control patients (44 +/- 15%). Similar improvement was observed in patients with a first infarct only (thrombolysis 50 +/- 14%, control subjects 46 +/- 15%), in patients with anterior infarction (thrombolysis 44 +/- 16%, control subjects 35 +/- 14%) and in those with inferior infarction (thrombolysis 52 +/- 12%, control subjects 49 +/- 12%). Similar results were obtained by contrast angiography. Mortality was lower after thrombolysis. After 28 days 16 patients allocated to thrombolysis and 31 control patients had died. One year survival rates were 91 and 84%, respectively. On the other hand, nonfatal reinfarction occurred more frequently after thrombolysis (36 patients) than in control subjects (16 patients). Early thrombolysis by intracoronary streptokinase leads to a smaller infarct size estimated by enzyme release, preserves left ventricular function at the second week and leads to improved 1 year survival.</description>
    </item> <item>
      <title>Which patients benefit most from early thrombolytic therapy with intracoronary streptokinase? (Article)</title>
      <link>http://repub.eur.nl/res/pub/4213/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>The effect of thrombolysis in acute myocardial infarction on enzymatic infarct size, left ventricular function, and early mortality was studied in subsets of patients in a randomized trial. Early thrombolytic therapy with intracoronary streptokinase (152 patients) or with intracoronary streptokinase preceded by intravenous streptokinase (117 patients) was compared with conventional treatment (264 patients). All 533 patients were admitted to the coronary care unit within 4 hr after onset of symptoms indicative of acute myocardial infarction. Four hundred eighty-eight patients were eligible for this detailed analysis, and 245 of these were allocated to thrombolytic therapy and 243 to conventional treatment. Early angiographic examinations were performed in 212 patients allocated to thrombolytic therapy. Patency of the infarct-related artery was achieved in 181 patients (85%). Enzymatic infarct size, as measured from cumulative alpha-hydroxybutyrate dehydrogenase release, was smaller in patients allocated to thrombolytic therapy (median 760 vs 1170 U/liter in control patients, p = .0001). Left ventricular ejection fraction measured by radionuclide angiography before discharge from the hospital was higher after thrombolytic therapy (median 50% vs 43% in control patients, p = .0001). Three month mortality was lower in patients allocated to thrombolytic therapy (6% vs 14% in the control group, p = .006). With the use of multivariate regression analysis, infarct size limitation, improvement in left ventricular ejection fraction, and three month mortality were predicted by sum of the ST segment elevation, time from onset of symptoms to admission, and Killip class at admission. Thrombolysis was most effective in patients admitted within 2 hr after onset of symptoms and in patients with a sum of ST segment elevation of 1.2 mV or more. On the other hand, no beneficial effects of streptokinase on enzymatic infarct size, left ventricular function, or mortality were observed in the subset of patients with a sum of ST segment elevation of less than 1.2 mV who were admitted between 2 and 4 hr after onset of symptoms.</description>
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      <title>Effects of early intracoronary streptokinase on infarct size estimated from cumulative enzyme release and on enzyme release rate: A randomized trial of 533 patients with acute myocardial infarction (Article)</title>
      <link>http://repub.eur.nl/res/pub/4214/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>The effects of early intracoronary streptokinase (SK) on enzymatic infarct size and rate of enzyme release were studied in a randomized multicenter trial. A total of 533 patients with acute myocardial infarction (AMI) were allocated to either the SK treatment group (n = 269) or the conventional (control) treatment group (n = 264). Enzymatic infarct size was represented by the cumulative quantity of alpha-hydroxybutyrate dehydrogenase (HBDH) released by the heart per liter of plasma in the first 72 hours. Rate of enzyme release was represented by the ratio of HBDH quantities released in 24 hours and 72 hours. On an "intention to treat" basis, the SK group had a smaller (by 30%; p = 0.0001) median enzymatic infarct size and a higher (by 35%; p = 0.0001) median rate of enzyme release than the control group. Limitation of infarct size was less apparent in patients treated with intracoronary SK only (25%) than in patients treated with intravenous plus intracoronary SK (34%). Compared to the control group, the enzyme release rate in patients treated with intracoronary SK only was slightly less (34%) than that in patients treated with intravenous plus intracoronary SK (38%). Patients with a patent infarct-related coronary artery at acute angiography had a median infarct size which was 55% (p = 0.0001) smaller than the median infarct size of the control group, and the median rate of enzyme release was 38% (p = 0.001) higher than the median release rate of the control group. Patients with successful recanalization during intracoronary SK infusion had a median infarct size which was 31% (p = 0.002) smaller than the median infarct size of the control group and a median rate of enzyme release which was 42% (p = 0.0001) higher than the median release rate of the control group. Patients with persistent coronary occlusion in spite of thrombolytic therapy had a median infarct size which was 11% (NS) higher than the median infarct size of the control group, although the median rate of enzyme release was still 23% (p = 0.02) higher than the median release rate of the control group. It is concluded that thrombolysis in the early phase of AMI limits infarct size and that intracoronary SK treatment itself accelerates the process of enzyme release from infarcted myocardium, independent of the angiographic result.</description>
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      <title>Long term improvement in global left ventricular function after early thrombolytic treatment in acute myocardial infarction (Article)</title>
      <link>http://repub.eur.nl/res/pub/4225/</link>
      <pubDate>1986-01-01T00:00:00Z</pubDate>
      <description>The effect of reperfusion achieved by early intracoronary streptokinase in acute myocardial infarction on left ventricular function was studied in 533 patients enrolled in a prospective randomised multicentre study. Two hundred and sixty four patients were allocated to conventional treatment and 269 patients to thrombolysis. At the end of the procedure patency of the infarct related vessel was achieved in 198 (85%) of 234 patients in whom coronary angiography was performed. The median interval from onset of symptoms till the angiographic documentation of patency was 200 minutes. Data were analysed according to the original treatment allocation. Global left ventricular ejection fraction was determined by radionuclide angiography in 418 patients within two days of admission, in 361 patients after two weeks, and in 307 patients after three months. Global left ventricular function remained unchanged throughout the observation period in the control group, whereas it improved during the first two weeks in patients allocated to thrombolytic treatment. Improved function in these patients persisted up to three months after the infarction. Global left ventricular ejection fraction was significantly better in the thrombolysis group than in the control group at two days, two weeks, and at three months. In patients with anterior myocardial infarction the left ventricular ejection fraction was 9% better than in the control group at two weeks and at three months. In the patients with inferior myocardial infarction differences between the two treatment groups were smaller because of photon attenuation within the body. Angiographic evidence suggested that the improvement in function seen after thrombolysis is indeed associated with the patency of the infarct related artery.</description>
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      <title>Bleeding complications of intracoronary fibrinolytic therapy in acute myocardial infarction. Assessment of risk in a randomised trial (Article)</title>
      <link>http://repub.eur.nl/res/pub/4152/</link>
      <pubDate>1985-01-01T00:00:00Z</pubDate>
      <description>The risk of bleeding associated with intracoronary infusion of streptokinase in acute myocardial infarction was determined in a randomised controlled trial containing 302 patients under the age of 70. Intracoronary streptokinase infusion was given to 152 patients and 150 patients were treated conventionally. Bleeding was seen in 24 (16%) patients in the streptokinase group and in two of the conventionally treated patients. Bleeding was most common (28%) in patients over the age of 60 years. The groin was the site of bleeding in all patients except one. In the first 48 hours after admission the haematocrit in streptokinase treated patients with manifest bleeding fell by 0.07 (0.04) (mean (SD)). The fall in haematocrit in the streptokinase treated patients without manifest bleeding was 0.05 (0.04) and in the conventionally treated patients it fell by 0.03 (0.04). Sixty six units of packed cells were transfused in the streptokinase group (50 units to those who bled); the control group required only 17 units. There were no deaths due to bleeding. The occurrence of bleeding and the fall in haematocrit in the streptokinase group correlated with the occurrence of systemic fibrinolysis but not with the dose of streptokinase given. Thus, in about 15% of patients treatment with intracoronary streptokinase resulted in significant non-fatal bleeding from the femoral puncture site that required substantial transfusion support. Furthermore, there was a significant drop in haematocrit in patients without manifest bleeding. These results emphasise the need for more specific fibrinolytic agents.</description>
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