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  <controlfield tag="001">ESSALUD</controlfield>
  <controlfield tag="005">20260902142645.0</controlfield>
  <controlfield tag="007">ta</controlfield>
  <controlfield tag="008">      t        pe ||||| |||| 00| 0 spa d</controlfield>
  <datafield tag="040" ind1=" " ind2=" ">
    <subfield code="a">BMG</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Rosenfield, Kenneth </subfield>
    <subfield code="e">Autor</subfield>
    <subfield code="9">54380</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Ultrasound-Facilitated, Catheter-Directed Fibrinolysis for Acute Pulmonary Embolism</subfield>
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  <datafield tag="300" ind1=" " ind2=" ">
    <subfield code="a">p&#xE1;ginas: 1979-1990</subfield>
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  <datafield tag="520" ind1=" " ind2=" ">
    <subfield code="a">Background: Whether anticoagulation alone is an adequate treatment for acute, intermediate-risk pulmonary embolism is uncertain. Methods: We conducted a multinational, adaptive-design trial with blinded outcome adjudication. Patients with intermediate-risk pulmonary embolism (with a ratio of right ventricular end-diastolic diameter to left ventricular end-diastolic diameter of &#x2265;1.0 and an elevated troponin level) were eligible if they had at least two indicators of cardiorespiratory distress (systolic blood pressure of &#x2264;110 mm Hg, a heart rate of &#x2265;100 beats per minute, or a respiratory rate of &gt;20 breaths per minute). Patients were randomly assigned to undergo ultrasound-facilitated, catheter-directed fibrinolysis with alteplase plus anticoagulation (the intervention group) or anticoagulation alone (the control group) according to prespecified treatment protocols. The primary outcome was a composite of pulmonary embolism&#x2013;related death, cardiorespiratory decompensation or collapse, or symptomatic recurrence of pulmonary embolism within 7 days. Results: The intention-to-treat population comprised 544 patients: 273 in the intervention group and 271 in the control group. The mean (&#xB1;SD) age was 58.2&#xB1;13.5 years, and 42.6% of the patients were women. A primary-outcome event occurred in 11 patients (4.0%; 95% confidence interval [CI], 2.3 to 7.1) in the intervention group and 28 (10.3%; 95% CI, 7.2 to 14.5) in the control group (relative risk, 0.39; 95% CI, 0.20 to 0.77; P=0.005). The effect was driven primarily by a lower risk of cardiorespiratory decompensation or collapse in the intervention group. Major bleeding occurred within 7 days after randomization in 11 patients (4.1%) in the intervention group and 6 (2.2%) in the control group (P=0.32); major bleeding occurred within 30 days in 11 patients (4.1%) and 8 patients (3.0%), respectively (P=0.64). No substantial between-group differences in the incidence of other serious adverse events were observed up to 30 days after randomization; no intracranial hemorrhage occurred. Conclusions: In patients with acute, intermediate-risk pulmonary embolism, ultrasound-facilitated, catheter-directed fibrinolysis plus anticoagulation led to a lower risk of the composite of pulmonary embolism&#x2013;related death, cardiopulmonary decompensation or collapse, or symptomatic recurrence of pulmonary embolism within 7 days than anticoagulation alone.</subfield>
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    <subfield code="a">ANTICOAGULACI&#xD3;N</subfield>
    <subfield code="9">53834</subfield>
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  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">TROMBOEMBOLISMO</subfield>
    <subfield code="9">32218</subfield>
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  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">CARDIOLOG&#xCD;A</subfield>
    <subfield code="9">11301</subfield>
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  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">NEUMOLOG&#xCD;A</subfield>
    <subfield code="9">25628</subfield>
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  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">CUIDADOS INTENSIVOS GENERAL</subfield>
    <subfield code="9">54115</subfield>
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  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">RADIOLOG&#xCD;A GENERAL</subfield>
    <subfield code="9">54381</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Klok, Frederikus A.</subfield>
    <subfield code="9">54382</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Piazza, Gregory </subfield>
    <subfield code="9">54383</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sharp,  Andrew S.P. </subfield>
    <subfield code="9">54384</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">N&#xED; &#xC1;inle, Fionnuala </subfield>
    <subfield code="9">54385</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Jaff, Michael R. </subfield>
    <subfield code="9">54386</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Barco, Stefano </subfield>
    <subfield code="9">54060</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
    <subfield code="0">22717</subfield>
    <subfield code="9">22665</subfield>
    <subfield code="d">Massachusetts NEJM Group</subfield>
    <subfield code="o">NEJM013</subfield>
    <subfield code="t">The New England Journal of Medicine </subfield>
    <subfield code="w">ESSALUD</subfield>
    <subfield code="x">0028-4793</subfield>
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    <subfield code="c">ARTICULOS</subfield>
    <subfield code="e">2026-08-28</subfield>
    <subfield code="z">sqb</subfield>
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  <datafield tag="999" ind1=" " ind2=" ">
    <subfield code="c">22884</subfield>
    <subfield code="d">22884</subfield>
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