Abstract | INTRODUCTION: MATERIALS AND METHODS: Patients with acute PE at multiple Chinese teaching hospitals had been randomized to UFH or LMWH for initial treatment. These treatment cohorts had baseline measurement of pulmonary artery obstruction (PAO) score, which was prospectively separated into quartiles, lowest to highest PAO. All patients were followed for bleeding episodes, which were subsequently analyzed by quartile of PAO. RESULTS: Two hundred seventy-four patients divided between the two groups had similar efficacy and safety outcomes (12 clinically significant bleeds in the UFH group vs 15 in the LMWH group). LMWH recipients with the smallest clot burdens (lowest PAO quartiles) had highest bleeding rates (Cochran-Armitage trend test, P trend = 0.048), but there was no such trend for UFH recipients. CONCLUSIONS: For UFH, excess anticoagulant pro-hemorrhagic potential is down-adjusted via activated partial thromboplastin time monitoring, but for LMWH it is not. For PE patients at high bleeding risk, UFH may be safer if the clot burden is small.
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Authors | Chen Wang, Zhenguo Zhai, Yuanhua Yang, Zhaozhong Cheng, Kejing Ying, Lirong Liang, Huaping Dai, Kewu Huang, Weixuan Lu, Zhonghe Zhang, Xiansheng Cheng, Ying Hu Shen, Bruce L Davidson, China National Venous Thromboembolism (VTE) Study Group |
Journal | The clinical respiratory journal
(Clin Respir J)
Vol. 10
Issue 5
Pg. 596-605
(Sep 2016)
ISSN: 1752-699X [Electronic] England |
PMID | 25619125
(Publication Type: Comparative Study, Journal Article, Observational Study)
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Copyright | © 2015 John Wiley & Sons Ltd. |
Chemical References |
- Anticoagulants
- Fibrinolytic Agents
- Heparin, Low-Molecular-Weight
- Heparin
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Topics |
- Adult
- Aged
- Anticoagulants
(administration & dosage, adverse effects)
- Female
- Fibrinolytic Agents
(administration & dosage, adverse effects)
- Hemorrhage
(chemically induced)
- Heparin
(administration & dosage, adverse effects)
- Heparin, Low-Molecular-Weight
(administration & dosage, adverse effects)
- Humans
- Male
- Middle Aged
- Pulmonary Embolism
(blood, drug therapy, pathology)
- Venous Thrombosis
(etiology, prevention & control)
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