Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Comparison of Low-Molecular-Weight Heparin (LMWH) and Unfractionated Heparin (UFH) in Combination With Thrombolytic Treatment of Acute Massive Pulmonary Thromboembolism

7 de octubre de 2013 actualizado por: Elif Yilmazel Ucar, Ataturk University

Purpose and rationale: Acute pulmonary embolism (PE) is a common and often fatal disease, with an approximately 30% mortality rate without treatment. Treatment is important to reduce mortality and recurrence in acute PE. Therapeutic options for PE include subcutaneous low molecular weight heparin (SC LMWH), intravenous unfractionated heparin (IV UFH), subcutaneous unfractionated heparin and subcutaneous fondaparinux with or without thrombolysis. In the treatment of acute PE, SC LMWH has been shown, at least, as effective and safe as IV UFH [4]. Compared to IV UFH, SC LMWH associated with lower mortality, fewer recurrent thrombotic events and less major bleeding. Current guidelines recommend use of SC LMWH for most hemodynamically stable patients with PE and they say that SC LMWH have not been tested in the setting of acute massive PE.

The purpose of this study is to demonstrate that SC LMWH is as safe as IV UFH in the treatment of acute PE in combination with thrombolytic treatment.

Descripción general del estudio

Descripción detallada

  1. Introduction 1.1. Background Acute pulmonary embolism (PE) is a common and often fatal disease, with an approximately 30% mortality rate without treatment [1]. Treatment is important to reduce mortality and recurrence in acute pulmonary embolism. Anticoagulation is the mainstay of the therapy for acute PE. It decreases the mortality rate to 3 to 8 percent, when effective therapy is instituted as quickly as possible [2, 3]. In those cases, therapeutic options include subcutaneous low molecular weight heparin (SC LMWH), intravenous unfractionated heparin (IV UFH), subcutaneous unfractionated heparin and subcutaneous fondaparinux with or without thrombolysis [3].

    In the treatment of acute PE, SC LMWH is at least as effective and safe as IV UFH [4]. In general, compared to IV UFH, SC LMWH associated with lower mortality, fewer recurrent thrombotic events and less major bleeding [5]. Current guidelines recommend the use of SC LMWH for most haemodynamically stable patients with PE and they say that SC LMWH have not been tested in the setting of hypotension and shock [3, 6]. However, it seems to be more feasible to use it because of its advantages such as easy administration route, i.e. SC. We have been using SC LMWHs in the cases with acute PE with or without requirement of thrombolysis in our clinical practice since they were available, because of their advantages for practical use and their use in primary or secondary care settings in the patients with because of PE suspicion just before their admission to our hospital. In our 10 years' clinical experience, we observed comparable hemorrhage risk (3.7% vs 0.7% and 12.1% vs 3.8%, for major and minor hemorrhage risk, respectively) with the use of LMWH plus thrombolysis in the cases with massive PE, even compared the cases treated with LMWH alone without massive PE (7). Yet, there is no head to head study comparing LMWH with UFH in the treatment of massive PE.

    The study will evaluate safety of LMWH use with thrombolytic treatment in the management of acute PE.

    1.2. Purpose The purpose of this study, because of its practical use such as no need for monitoring, is to demonstrate that SC LMWH, enoxaparin, is to be a safe alternative to IV UFH in the management of acute PE cases, who require thrombolytic treatment, in combination with thrombolytic treatment.

  2. Study Objectives 2.1. Primary aim The primary aim of the study is to compare the major hemorrhage risk between the use of LMWH plus thrombolytic treatment and UFH plus thrombolytic in the treatment of acute massive PE.

    2.2. Secondary Aim The secondary aim of the study is to compare the minor hemorrhage risk and mortality (five day and one year mortality) between the use of LMWH plus thrombolytic treatment and UFH plus thrombolytic in the treatment of acute massive PE.

  3. Investigational plan 3.1. Study design This is a single-center randomized study in acute PE patients who require thrombolytic treatment and have no contraindication to use of anticoagulation, comparing safety of SC LMWH versus IV UFH when used with thrombolytic treatment.

    After a baseline evaluation for the diagnostic procedures and providing informed consent, eligible patients who are diagnosed as acute PE and require thrombolytic treatment but have no contraindication to use any study drug including alteplase, LMWH (enoxaparin) or heparin will be included in the study.

    3.2. Study setting A tertiary care, university, hospital, which is the biggest hospital in eastern part of Turkey and serving more than 7 cities.

    3.3. Study period Between January 2011 and December 2013 3.4. Rationale of study design LMWHs have been used in the treatment of PE and their use becomes popular in many centers because of practical administration route, SC versus infusion, no need for monitoring and close follow up. However, there is no previous data on the use of LMWHs in the cases who require thrombolytic and, for this reason, no recommendation about their use in the current guidelines. Because some cases were administered LMWH before admission to a hospital for thrombolytic treatment and they were required immediate administration of thrombolytic treatment, their use with thrombolytic is likely although there is no recommendation for such use. Because the adverse events associated with the use of LMWH with thrombolytic treatment in the cases who require thrombolytic were comparable even with the cases who use LMWH alone and do not require thrombolytic (7), we planned to compare LMWH and UFH in the cases who require thrombolytic treatment that the latter is the only choice in those cases according to the current guidelines.

    This study will provide data comparing safety of LMWH versus UFH in the treatment of acute PE cases who require thrombolytic treatment.

    The randomized study was selected to make head to head comparison in the evaluating the safety of LMWH versus UFH in the treatment of acute PE cases who require thrombolytic treatment.

    No stratification was applied for randomization. 3.5. Randomization method The randomization order was determined using a computer-generated list of random numbers.

    3.6. Ethical considerations Local ethical committee approved the protocol of the study.

  4. Population 4.1. Study population: The study population will consist approximately 120 adult cases with a clinical diagnosis of acute PE who require thrombolytic treatment and have no contraindication to use of anticoagulation in a single center, tertiary university hospital. It is anticipated that approximately 150 patients will need to be screened in order to randomize into the 2 treatment arms of the study with a randomization ratio of 1:1; therefore, approximately 60 patients will be assigned to each treatment group.

    4.3. Screening for eligibility All patients with clinical suspicion of PE (major risk factors, clinical manifestations) were underwent chest X-ray, electrocardiogram (ECG), echocardiographic evaluation and computerized thorax (CT) angiography with a 16-slice multidetector CT (if there was no contraindication).

    4.4. Inclusion criteria:

    Key inclusion criteria that the patient must fulfill to be eligible for the study include:

    • Adults, age ≥ 18 years
    • Patients who have signed the study informed consent form prior to initiation of any study-related procedure.
    • Acute massive PE patients who require thrombolytic treatment. 4.5. Exclusion criteria Patients fulfilling any of the following criteria are not eligible for inclusion in this study. No additional exclusions may be applied by the investigator, in order to ensure that the study population will be representative of all eligible patients.
    • Patients who have a contraindication to use of anticoagulation and thrombolysis, such as active bleeding, stroke, cranial trauma, or neurologic surgery within the preceding 6 months, current pregnancy, major surgery, or biopsy within the preceding 7 days, major trauma within the preceding 10 days, gastrointestinal bleeding within the preceding 1 months during their admission.
    • Patients who received any anticoagulation medication prior to admission to the hospital.
  5. Treatment 5.1. Investigational and control treatments (Exposure) Investigational treatment: LMWH, enoxaparin, plus alteplase Control treatment: UFH plus alteplase 5.2. Treatment arms After providing informed consent, patients will be assigned to 1 of the following 2 treatment arms in a ratio 1:1.

    • Fixed dose SC LMWH (enoxaparin)
    • Weight adjusted dose of UFH. In both treatment arms, patients will also receive thrombolytic treatment, a bolus of 10 mg of alteplase followed by 90 mg over 2-h infusion.

5.3. Treatment and monitoring After thrombolytic treatment, a bolus of 10 mg of alteplase followed by 90 mg over 2-h infusion, patients either administered a constant heparin infusion (18 U/Kg per hour) adjusted to maintain an activated partial thromboplastin time of 46-70 s or SC LMWH received enoxaparin. After fibrinolytic therapy (FT), 4-6 hour later, activated partial thromboplastin time (APTT) was checked. According to initial SC LMWH use time, fixed dose SC LMWH, enoxaparin, was administered subcutaneous every 12 hours. Both groups overlapped with warfarin on the 1st day to 5th day or the day achieved targeted international normalized ratio (INR) level. The patients were kept on warfarin, aiming for an INR between 2.0 and 3.0 for 3 months or more, depending on the presence of major risk factors.

5.4. Schedule of measurements The clinical evaluation (physical exam, blood pressure, pulse rate & oxygen saturation) was performed before and after starting fibrinolytic treatment.

The echocardiographic examination and interpretation were performed before starting fibrinolytic treatment.

5. 5. Data collection and follow-up Data collection was performed on admission, during hospitalization and at discharge. At least a year-follow up was planned.

6. Definitions 6.1. Adverse Events Major hemorrhage; stroke (confirmed by computed tomography), hematoma>5 cm, oral or gastrointestinal bleeding or another bleeding with concomitant hypotension that required treatment with intravenous fluids, blood transfusion, surgical control, discontinuation of FT regimen, decrease >15% points in hematocrit or >5 g/dl reduction in hemoglobin [9].

Minor hemorrhage; decrease between 10-15% points in hematocrit or 3-5 g/dl reduction in hemoglobin [9].

Mortality: Hospital mortality on day 5 and one year mortality. 6.2. Other definitions Massive PE; is defined as acute PE with sustained hypotension (systolic arterial pressure <90 mm Hg or a drop in systolic arterial pressure of at least 40 mm Hg for at least 15 minutes) and cardiogenic shock (including an altered level of consciousness, oliguria, or cool, clammy extremities) [8].

Recurrent PE; clinical suspicion of new PE symptoms, new signs on electrocardiogram in-hospital with or without clinical instability, or death.

7. Statistical Analysis Plan 7.1. Sample size and power: 120 acute massive PE patients. We should have >80% power (2-sided testing and significance level <0.05) to detect a 20% absolute bleeding risk increase.

7.2. Statistical methods Statistical analysis will be performed with SPSS for Windows version 17.0 (SPSS Inc., Chicago, USA).

Data will be expressed in percent, mean and standard deviation, odds ratio and 95% confident interval.

We will use the two-tailed Student t test for comparisons of continuous variables between patients with SC LMWH plus thrombolytic and UFH plus thrombolytic and Pearson Chi square test for comparisons of categorical variables.

Survival estimations will be done by Kaplan-Meier Survival Probability estimates and Cox regression.

Findings will be considered statistically significant if a P value of <0.05 was obtained.

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

150

Fase

  • Fase 4

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Erzurum, Pavo, 25240
        • Reclutamiento
        • Ataturk University Faculty of Medicine Pulmonary Disease Department
        • Contacto:
          • Elif Yilmazel Ucar, Assit prof
          • Número de teléfono: 0090442 344 7447
          • Correo electrónico: eucar1979@yahoo.com
        • Investigador principal:
          • Elif Yilmazel Ucar, Assit prof

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

19 años a 85 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Adults, age ≥ 18 years
  • Patients who have signed the study informed consent form prior to initiation of any study-related procedure.
  • Acute massive PE patients who require thrombolytic treatment.

Exclusion Criteria:

  • Patients who have a contraindication to use of anticoagulation and thrombolysis, such as active bleeding, stroke, cranial trauma, or neurologic surgery within the preceding 6 months, current pregnancy, major surgery, or biopsy within the preceding 7 days, major trauma within the preceding 10 days, gastrointestinal bleeding within the preceding 1 months during their admission.
  • Patients who received any anticoagulation medication prior to admission to the hospital.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador activo: enoxaparin and alteplase
After alteplase therapy , 4-6 hour later, activated partial thromboplastin time (APTT) was checked. According to initial SC LMWH use time, fixed dose SC LMWH, enoxaparin, was administered subcutaneous every 12 hours.
Comparador activo: Unfractionated heparin and alteplase
After thrombolytic treatment, a bolus of 10 mg of alteplase followed by 90 mg over 2-h infusion, patients either administered a constant heparin infusion (18 U/Kg per hour) adjusted to maintain an activated partial thromboplastin time of 46-70 s.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The primary aim of the study is to compare the major hemorrhage risk between the use of LMWH plus thrombolytic treatment and UFH plus thrombolytic in the treatment of acute massive PE.
Periodo de tiempo: 7 day
Number of patients with adverse events
7 day

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The secondary aim of the study is to compare the minor hemorrhage risk between the use of LMWH plus thrombolytic treatment and UFH plus thrombolytic in the treatment of acute massive PE.
Periodo de tiempo: 7 day
Number of patients with adverse events
7 day

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Mortality
Periodo de tiempo: 5 day
Number of patients with mortality
5 day

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de enero de 2011

Finalización primaria (Anticipado)

1 de diciembre de 2013

Finalización del estudio (Anticipado)

1 de enero de 2014

Fechas de registro del estudio

Enviado por primera vez

27 de septiembre de 2013

Primero enviado que cumplió con los criterios de control de calidad

7 de octubre de 2013

Publicado por primera vez (Estimar)

8 de octubre de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

8 de octubre de 2013

Última actualización enviada que cumplió con los criterios de control de calidad

7 de octubre de 2013

Última verificación

1 de octubre de 2013

Más información

Términos relacionados con este estudio

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir