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Published Online, 18 August 2009, www.theannals.com, DOI 10.1345/aph.1L542.
The Annals of Pharmacotherapy: Vol. 43, No. 9, pp. 1528-1531. DOI 10.1345/aph.1L542
© 2009 Harvey Whitney Books Company.
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Spontaneous Hemothorax Following Anticoagulation with Low-Molecular-Weight Heparin

Amitava Ganguli, BSc(Hons) MBcHB MRCP

Specialist Registrar and Honorary Lecturer in Clinical Pharmacology, Respiratory Medicine and General Internal Medicine, Royal Liverpool University Hospital, Liverpool, UK

Lauren Walker, BSc(Hons) MBcHB(Hons)

Foundation Year 2 Senior House Officer, Royal Liverpool University Teaching Hospital, Liverpool

Richard Joaquim FitzGerald, MBcHB MRCP

Specialist Registrar, Clinical Pharmacology and Therapeutics, and Research Fellow, University of Liverpool, UK

Munir Pirmohamed, MBcHB(Hons) PhD FRCP FRCP(E), NHS

Chair of Pharmacogenetics, Department of Pharmacology, The University of Liverpool, Liverpool

Reprints: Dr. Ganguli, Department of Clinical Pharmacology and Therapeutics, Royal Liverpool University Hospital, Liverpool L7 8XP, fax 00 44 1517 063 061, aganguli05{at}yahoo.co.uk

OBJECTIVE: To report a case of spontaneous hemothorax following anticoagulation with low-molecular-weight heparin (LMWH) for the management of suspected pulmonary embolism.

CASE SUMMARY: A 66-year-old man with a background history of breast carcinoma was admitted with pleuritic chest pain. He was initially managed as a suspected case of pulmonary embolism. Dalteparin, an LMWH, was started at a maximum dose of 18,000 units subcutaneously once daily, according to British national prescribing guidelines. On day 4, following 3 doses of dalteparin, the patient developed acute respiratory distress attributable to a massive right hemothorax confirmed by computed tomography pulmonary angiography (CTPA) and intercostal drainage of 1500 mL of frank blood. CTPA identified no pulmonary embolus or vascular abnormalities. Reaccumulation of hemothorax occurred over the 48 hours following drain removal, necessitating insertion of a second drain, which removed 1400 mL of blood-stained fluid. The patient's hemoglobin decreased from 12.7 to 8.5 g/dL and he received a 3-unit blood transfusion. Histologic assessment of pleural fluid revealed no malignancy and results of video-assisted thoracoscopic surgery were normal. Discontinuation of dalteparin on day 4 led to resolution of symptoms.

DISCUSSION: The causal association between anticoagulant therapy and spontaneous hemothorax remains relatively uncommon. The striking temporal relationship between commencing dalteparin on day 1 and subsequent development of effusion on day 4, following 3 doses of LMWH, led us to believe that the bleed occurred as a result of the therapy. Exclusion of other causes strengthened this conclusion. Application of the Naranjo probability scale categorized this adverse reaction as being probably due to LMWH.

CONCLUSIONS: Spontaneous hemothorax is a rare phenomenon in conjunction with LMWH but should be considered in cases of acute respiratory distress following commencement of LMWH.

Key Words: anticoagulants, dalteparin, hemorrhage, hemothorax, low-molecular-weight heparin

Published Online, August 18, 2009. www.theannals.com, DOI 10.1345/aph.1L542





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