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Case Reports  |   December 2004
Spinal Epidural Hematoma after Spinal Anesthesia in a Patient Treated with Clopidogrel and Enoxaparin
Author Affiliations & Notes
  • Rainer J. Litz, M.D.
    *
  • Birgit Gottschlich, M.D.
    *
  • Sebastian N. Stehr, M.D.
  • * Staff Anesthesiologist, † Resident, Department of Anesthesiology and Critical Care Medicine, University Hospital Dresden, Technical University Dresden.
Article Information
Case Reports
Case Reports   |   December 2004
Spinal Epidural Hematoma after Spinal Anesthesia in a Patient Treated with Clopidogrel and Enoxaparin
Anesthesiology 12 2004, Vol.101, 1467-1470. doi:
Anesthesiology 12 2004, Vol.101, 1467-1470. doi:
IN recent years newly developed antiplatelet drugs such as the thienopyridine derivatives ticlopidine and clopidogrel are being increasingly used in patients with cardiovascular disease. Knowledge of their pharmacokinetics is crucial for appropriate perioperative care. Therefore, updated guidelines for the concomitant use of these drugs and locoregional anesthesia have been issued by the American Society of Regional Anesthesia and Pain Medicine1 and by European societies of anesthesiologists2 concerning a risk-benefit ratio as well as specific time intervals that should be maintained between the last drug administration and performance of neuroaxial blocks or withdrawal of catheters. Because of differences in pharmacokinetics, a free interval of at least 7 days for clopidogrel and of 10–14 days for ticlopidine is recommended before performance of central neuraxial blocks (provided that platelet count and coagulation time are in a normal range). Concurrent use of additional medication affecting clotting mechanisms may increase the risk of bleeding disorders. We report a patient transferred to our hospital with a history of clopidogrel intake who received low molecular weight heparin for prophylaxis of thromboembolism in the perioperative course of difficult and traumatic spinal anesthesia. Despite maintaining a free interval of 7 days after the last clopidogrel intake, adhering to guidelines concerning low molecular heparin application, and despite the fact that clotting tests were normal, spinal epidural hematoma developed after spinal anesthesia.
Case Report
A 81-yr-old woman (height, 160 cm; weight, 75 kg) with American Society of Anesthesiologists physical status III had received spinal anesthesia for elective fasciotomy and perforator vein ligation because of a lower limb ulceration. Her medical history included ischemic heart disease grade II (Canadian Cardiovascular Society angina classification) with atrial fibrillation, compensated renal insufficiency (creatinine clearance 34 ml/min), hypertension, and insulin-dependent diabetes. Her oral medication included molsidomine (Corvaton™; Aventis Pharma Deutschland GmbH, Bad Soden, Germany), piretanide/ramipril (Arelix ACE™; Aventis Pharma Deutschland GmbH), spironolactone/furosemide (Furorese™; Hexal AG, Holzkirchen, Germany), metoprolol (Beloc zok™;AstraZeneca GmbH, Wedel, Germany), and xipamid (Aquaphor™;Lilly Deutschland GmbH, Bad Homburg, Germany) for treatment of hypertension, ischemic heart disease, and renal insufficiency. Diabetes was treated with subcutaneous insulin. In addition, she was treated daily with 75 mg clopidogrel (Iscover™;Bristol-Myers Squibb GmbH, München, Germany) for ischemic heart disease which was discontinued 7 days before surgery.
Preoperatively the activated partial thromboplastin time was 39 s (normal range, 30–40 s), the prothrombin time was 85% (normal range, 70–120%) and the international normalized ratio was 1.02 (therapeutic level, 2–4.5), platelet count was 161 × 109/l, at the lower limit of the normal range (150 × 109/l – 400 × 10/l).
Spinal anesthesia was performed by an experienced staff anesthesiologist using a 22-gauge Sprotte needle. However, the first attempt failed at L3–4 because of repeated bone contact as well as a sanguine puncture presumed to be outside the epidural space. At the L4–5 level subarachnoid puncture was performed uneventfully in the first attempt and 3 ml of plain bupivacaine 0.5% was injected. Within 10 min maximum level of sensory block reached the T8 dermatome. Surgery was performed uneventfully and the regression of the block was complete within 4 h. The patient was mobilized on the evening of the day of surgery. For prophylaxis of thromboembolism the patient received two doses of low molecular weight heparin (enoxaparin) 40 mg 8 and 36 h after lumbar puncture. During the second postoperative night, 4 h after the second enoxaparin administration, the patient complained of voiding difficulty, and a urinary catheter was applied. At that time neither sensory nor motor deficiency was observed. On the morning of the second postoperative day the patient complained of numbness and weakness in both lower limbs. No back pain was reported. Emergency magnetic resonance imaging revealed spinal epidural hematoma extending from T12 to L3, with a maximum diameter between T12 and L1 (figs. 1–3). The patient was transferred to the university hospital and presented with lower paraplegia and a Th12 sensory loss. Emergency decompressive laminectomy was performed 20 h after the first signs of bladder dysfunction were observed. Before the second surgical procedure coagulation profile was documented as activated partial thromboplastin time 44, prothrombin time 81, international normalized ratio 1.22, and a platelet count of 216 × 109/l. The operative site showed a partially liquid and partially organized hematoma, which was difficult to resect as organized parts showed strong adhesion to the conus and seemed to obstruct epidural veins. No lesions related to puncture or vessel malformations were seen.
Fig. 1. T2 sagittal magnetic resonance image showing the large extension of the hematoma  (arrows  ), as well as its heterogeneity. 
Fig. 1. T2 sagittal magnetic resonance image showing the large extension of the hematoma 
	(arrows  ), as well as its heterogeneity. 
Fig. 1. T2 sagittal magnetic resonance image showing the large extension of the hematoma  (arrows  ), as well as its heterogeneity. 
×
Fig. 2. T2 axial magnetic resonance image showing the hematoma (L2). 
Fig. 2. T2 axial magnetic resonance image showing the hematoma (L2). 
Fig. 2. T2 axial magnetic resonance image showing the hematoma (L2). 
×
Fig. 3. T1 axial magnetic resonance image showing the hematoma (L2). 
Fig. 3. T1 axial magnetic resonance image showing the hematoma (L2). 
Fig. 3. T1 axial magnetic resonance image showing the hematoma (L2). 
×
Postoperatively, the patient could partially be mobilized and only slowly recovered from her neurologic deficiencies. Three weeks after laminectomy sensory deficiency up to T12 and motor block Bromage 2 were documented.
Discussion
Beneficial effects have been demonstrated for new antiplatelet drugs in cardiovascular patients, especially for thienopyridine derivatives in preventing stroke.3–5 As an increasing number of patients is treated with these drugs, anesthetists must be familiar with their mechanism of action. In Europe two orally applicable adenosine diphosphate receptor antagonists are available that differ in clinical pharmacology. Both drugs inhibit platelet aggregation by noncompetitive nonreversible interaction with the adenosine diphosphate (P2Y12) receptor on the outer platelet surface. Blockade leads to an inhibition of adenosine diphosphate mediated platelet activation via  an increase in intracellular cyclic adenine monophosphate. In addition, release of calcium, fibrinogen, and serotonin that usually boost platelet activation is averted. Concurrently, alteration of GP IIb/IIIa conformation is inhibited.6 
Clopidogrel is six times more potent than ticlopidine7 and is therefore effective within 3–7 (ticlopidine, 8–10) days after its application.8 Normalization of platelet function is restored accordingly to the half-life time of platelets within 7 days (ticlopidine, 7–14 days).9 In an animal model high-dose aprotinin partially reversed the effects of clopidogrel.10 Platelet transfusion is the only effective treatment in cases of severe bleeding in humans.6 
For clopidogrel a therapy-free interval of 7 days is recommended before performance of neuraxial blocks.1,11 In our patient 7 days, as recommended, were maintained and no sustaining clopidogrel impact was suspected.
Nevertheless, an epidural hematoma developed after spinal anesthesia. No case of epidural hematoma occurrence after central neuraxial block performance has been previously reported in patients shortly after a 7 day clopidogrel therapy-free interval. The first sign of epidural bleeding was bladder dysfunction, which was not considered unusual by the nursing staff at that time after spinal anesthesia in a patient of that age. Onset of sensory and motor deficiencies were delayed by approximately 12 h. Once discovered, magnetic resonance imaging was performed immediately and the patient was transferred to our hospital for laminectomy.
We consider four points to be of possible importance in this case:
  • First, sanguine puncture occurred, which has been shown to be a general risk factor in development of spinal hematoma.12,13 Even though in the first attempt it was presumed that the epidural space was not reached, puncture of an epidural vein can not be excluded.

  • Second, as the platelet count was at the lower limit of normal range, platelet regeneration may have been reduced, hence prolonging the effect of the adenosine diphosphate antagonist.

  • Third, the exact response to subcutaneous low molecular weight heparin therapy in our patient remains speculative, as subcutaneous blood flow may vary considerably interindividually in the elderly and may result in therapeutic anticoagulation. A further risk factor might have been the moderate impairment of renal function. A linear correlation between antifactor Xa concentrations and renal function has recently been demonstrated in patients receiving low molecular weight heparin, and the authors concluded that a dose adjustment is necessary in patients with a creatinine clearance of less than 30 ml/min.14 In an older retrospective study even clearance rates lower than 40 ml/min were associated with higher antifactor Xa concentrations.15 In our patient the clearance was slightly greater than 30 ml/min.

  • Finally, a 7–10 day therapy-free interval before operative procedures is recommended according to some manufacturer guidelines.16 The additive effect of anticoagulatory drugs acting at different sites of the coagulatory cascade should not be underestimated.

In summary, several factors may have equally contributed to the occurrence of an epidural hematoma in our patient. For thienopyridine derivatives clinical possibilities of testing thrombocyte function are limited.17 This case further underscores the necessity of close neurologic monitoring after spinal anesthesia, especially in applying locoregional anesthetic techniques shortly after the recommended therapy-free interval of clopidogrel.
References
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Buerkle H, Van Aken H, Buettner J, Riess H: Regional anaesthesia and thromboembolism prophylaxis/anticoagulation: Revised guidelines of the German Society of Anaesthesiology and Intensive Care Medicine [in German] Anästhesiologie und Intensivmedizin 2003; 44:218–30Buerkle, H Van Aken, H Buettner, J Riess, H
Hass WK, Easton JD, Adams HP Jr, Pryse-Phillips W, Molony BA, Anderson S, Kamm B: A randomized trial comparing ticlopidine hydrochloride with aspirin for the prevention of stroke in high-risk patients. Ticlopidine Aspirin Stroke Study Group. N Engl J Med 1989; 321:501–7Hass, WK Easton, JD Adams, HP Pryse-Phillips, W Molony, BA Anderson, S Kamm, B
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A randomised, blinded, trial of clopidogrel versus aspirin in patients at risk of ischaemic events (CAPRIE). CAPRIE Steering Committee. Lancet 1996; 348:1329–39
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Steinhubl SR, Tan WA, Foody JM, Topol EJ: Incidence and clinical course of thrombotic thrombocytopenic purpura due to ticlopidine following coronary stenting. EPISTENT Investigators. Evaluation of Platelet IIb/IIIa Inhibitor for Stenting. JAMA 1999; 281:806–10Steinhubl, SR Tan, WA Foody, JM Topol, EJ
Savcic M, Hauert J, Bachmann F, Wyld PJ, Geudelin B, Cariou R: Clopidogrel loading dose regimens: Kinetic profile of pharmacodynamic response in healthy subjects. Semin Thromb Hemost 1999; 25 Suppl 2:15–9Savcic, M Hauert, J Bachmann, F Wyld, PJ Geudelin, B Cariou, R
Weber AA, Braun M, Hohlfeld T, Schwippert B, Tschope D, Schror K: Recovery of platelet function after discontinuation of clopidogrel treatment in healthy volunteers. Br J Clin Pharmacol 2001; 52:333–6Weber, AA Braun, M Hohlfeld, T Schwippert, B Tschope, D Schror, K
Herbert JM, Bernat A, Maffrand JP: Aprotinin reduces clopidogrel-induced prolongation of the bleeding time in the rat. Thromb Res 1993; 71:433–41Herbert, JM Bernat, A Maffrand, JP
Gogarten W, Van Aken H, Buettner J, Riess H, Buerkle H: Neuroaxial regional anaesthesia in patients receiving antithrombotic drugs [in German]. Anästhesiologie und Intensivmedizin 2003; 44:218–30Gogarten, W Van Aken, H Buettner, J Riess, H Buerkle, H
Vandermeulen EP, Van Aken H, Vermylen J: Anticoagulants and spinal-epidural anesthesia. Anesth Analg 1994; 79:1165–77Vandermeulen, EP Van Aken, H Vermylen, J
Schmidt A, Nolte H: Subdural and epidural hematomas following epidural anesthesia: A literature review [in German]. Anaesthesist 1992; 41:276–84Schmidt, A Nolte, H
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Becker RC, Spencer FA, Gibson M, Rush JE, Sanderink G, Murphy SA, Ball SP, Antman EM: Influence of patient characteristics and renal function on factor Xa inhibition pharmacokinetics and pharmacodynamics after enoxaparin administration in non-ST-segment elevation acute coronary syndromes. Am Heart J 2002; 143:753–9Becker, RC Spencer, FA Gibson, M Rush, JE Sanderink, G Murphy, SA Ball, SP Antman, EM
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Fig. 1. T2 sagittal magnetic resonance image showing the large extension of the hematoma  (arrows  ), as well as its heterogeneity. 
Fig. 1. T2 sagittal magnetic resonance image showing the large extension of the hematoma 
	(arrows  ), as well as its heterogeneity. 
Fig. 1. T2 sagittal magnetic resonance image showing the large extension of the hematoma  (arrows  ), as well as its heterogeneity. 
×
Fig. 2. T2 axial magnetic resonance image showing the hematoma (L2). 
Fig. 2. T2 axial magnetic resonance image showing the hematoma (L2). 
Fig. 2. T2 axial magnetic resonance image showing the hematoma (L2). 
×
Fig. 3. T1 axial magnetic resonance image showing the hematoma (L2). 
Fig. 3. T1 axial magnetic resonance image showing the hematoma (L2). 
Fig. 3. T1 axial magnetic resonance image showing the hematoma (L2). 
×