Moderate pulmonary embolism treated with thrombolysis (from the "MOPETT" Trial).
Research article published in The American journal of cardiology (2012)
Abstract
The role of low-dose thrombolysis in the reduction of pulmonary artery pressure in moderate pulmonary embolism (PE) has not been investigated. Because the lungs are very sensitive to thrombolysis, we postulated that effective and safe thrombolysis might be achieved by a lower dose of tissue plasminogen activator. The purpose of the present study was to evaluate the role of this "safe dose" thrombolysis in the reduction of pulmonary artery pressure in moderate PE. During a 22-month period, 121 patients with moderate PE were randomized to receive a "safe dose" of tissue plasminogen activator plus anticoagulation (thrombolysis group [TG], n = 61 patients) or anticoagulation alone (control group [CG], n = 60). The primary end points consisted of pulmonary hypertension and the composite end point of pulmonary hypertension and recurrent PE at 28 months. Pulmonary hypertension and the composite end point developed in 9 of 58 patients (16%) in the TG and 32 of 56 patients (57%) in the CG (p <0.001) and 9 of 58 patients (16%) in the TG and 35 of 56 patients (63%) in the CG (p <0.001), respectively. The secondary end points were total mortality, the duration of hospital stay, bleeding at the index hospitalization, recurrent PE, and the combination of mortality and recurrent PE. The duration of hospitalization was 2.2 ± 0.5 days in the TG and 4.9 ± 0.8 days in the CG (p <0.001). The combination of death plus recurrent PE was 1 (1.6%) in TG and 6 (10%) in the CG (p = 0.0489). No bleeding occurred in any group, and despite a positive trend in favor of a "safe dose" thrombolysis, no significant difference was noted in the rate of individual outcomes of death and recurrent PE when assessed independently. In conclusion, the results from the present prospective randomized trial suggests that "safe dose" thrombolysis is safe and effective in the treatment of moderate PE, with a significant immediate reduction in the pulmonary artery pressure that was maintained at 28 months.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
The role of low-dose thrombolysis in the reduction of pulmonary artery pressure in moderate pulmonary embolism (PE) has not been investigated. Because the lungs are very sensitive to thrombolysis, we postulated that effective and safe thrombolysis might be achieved by a lower dose of tissue plasminogen activator.
Por qué esto importa para la hirudoterapia
El ensayo MOPETT aleatorizó a 121 pacientes con embolia pulmonar moderada a una dosis baja ("segura") de activador del plasminógeno tisular más anticoagulación versus anticoagulación sola, informando que el conjunto de hipertensión pulmonar y EP recurrente se desarrolló en muchos menos pacientes del grupo de trombólisis (16% vs 63%, p<0.001), hospitalización más corta, menos eventos combinados de muerte/EP recurrente y sin sangrado en ninguno de los grupos. Para ASH es una demostración clínicamente significativa de que la terapia fibrinolítica (disolvente de coágulos) puede mejorar los resultados en tromboembolismo venoso — el mismo principio fibrinolítico encarnado por enzimas del secreto de sanguijuelas como la destabilasa, que se estudia por su capacidad de lisar fibrina y que ancla parte de la narrativa de descubrimiento de fármacos derivados de sanguijuelas. Cuidado honesto: MOPETT es un ensayo aleatorizado abierto único, relativamente pequeño de un fármaco trombolítico convencional (alteplasa), no de ningún agente derivado de sanguijuelas, y su resultado de no sangrado proviene de una muestra modesta que estudios más grandes necesitarían confirmar; ASH lo cita solo como contexto de apoyo para el concepto de fibrinólisis, sin establecer equivalencia alguna con la terapia de sanguijuelas.
Citación
Moderate pulmonary embolism treated with thrombolysis (from the "MOPETT" Trial).
Sharifi M et al. · The American journal of cardiology, 2012
Contexto clínico relacionado
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Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026