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Acute ischemic stroke patients are at high risk of devel-oping deep-vein thrombosis (DVT) and pulmonary
embolism (PE), which are the major causes of mortality and morbidity in these patients.1,2 Some consensus guidelines rec-ommend venous thromboembolism (VTE) prophylaxis with unfractionated heparin or low-molecular-weight heparins in acute stroke patients with restricted mobility, although there is no guidance on prophylaxis duration.2
The EXCLAIM (EXtended CLinical prophylaxis in Acutely Ill Medical patients) study reported that extended-duration enoxaparin (for a further 28 days after standard 10-day enoxa-parin prophylaxis) reduced the risk of VTE but increased major bleeding complications. Women, older patients (>75 years), and sedentary patients experienced reduction in risk of VTE.3 This subanalysis assessed the risk of VTE and bleeding
with extended-duration enoxaparin prophylaxis in patients with acute ischemic stroke.
MethodsThe international, multicenter, prospective, double-blind randomized controlled EXCLAIM trial has been previously reported.3 Patients aged over 40 years, hospitalized for an acute medical illness with recent reduced mobility for a maximum of 3 days and an anticipated mobility reduction for a further 3 days, were eligible.3 Eligibility cri-teria were amended after a planned interim analysis (Supplementary Appendix).
Enrolled patients received open-label subcutaneous enoxaparin 40 mg daily for 10±4 days. Patients were then double-blind random-ized to subcutaneous enoxaparin 40 mg daily or placebo for a further 28±4 days.
The primary efficacy end point was centrally adjudicated VTE, defined as the composite of symptomatic or asymptomatic proximal
Background and Purpose—The optimal duration of venous thromboembolism prophylaxis in acute stroke patients is unknown. This subanalysis of the Extended Prophylaxis for Venous ThromboEmbolism in Acutely Ill Medical Patients With Prolonged Immobilization (EXCLAIM) study investigated extended-duration thromboprophylaxis with enoxaparin, compared with placebo following standard-duration enoxaparin, in ischemic stroke patients.
Methods—Acutely ill medical patients with recently reduced mobility received open-label enoxaparin 40 mg for 10±4 days, and they were then randomized to double-blind enoxaparin 40 mg daily or placebo for further 28±4 days. Venous thromboembolism incidence (symptomatic/asymptomatic deep-vein thrombosis, symptomatic/fatal pulmonary embolism) up to day 28 after randomization and major bleeding rates up to 48 h after the last dose of study treatment were reported.
Results—In total, 389 of 5963 (6.5%) randomized patients had ischemic stroke: 198 received extended-duration prophylaxis and 191 placebo. Extended-duration prophylaxis reduced venous thromboembolism incidence versus placebo (2.4% versus 8.0%; absolute risk difference, −5.6%; 95% CI, −10.5% to −0.7%), but it was associated with an increase in major bleeding (1.5% versus 0% in enoxaparin and placebo groups; absolute risk difference, +1.5%; 95% CI, −0.2% to 3.2%).
Conclusion—Extended-duration thromboprophylaxis with enoxaparin was associated with reduced venous thromboembolism risk and increased major bleeding in the subgroup of patients with ischemic stroke in the EXCLAIM study.
Clinical Trial Registration Information—URL: http://clinicaltrials.gov. Unique Identifier: NCT00077753. (Stroke. 2013;44:249-251.)
Key Words: anticoagulants ◼ cerebrovascular disease/stroke ◼ deep-vein thrombosis
Venous Thromboembolism Risk in Ischemic Stroke Patients Receiving Extended-Duration Enoxaparin Prophylaxis:
Results From the EXCLAIM StudyAlexander G.G. Turpie, MD; Russell D. Hull, MBBS; Sebastian M. Schellong, MD;
Victor F. Tapson, MD; Manuel Monreal, MD; Meyer-Michel Samama, MD, Pharm D; Min Chen, PhD; Roger D. Yusen, MD, MPH; for the EXCLAIM Investigators*
*Collaborators listed in Supplementary AppendixFrom McMaster University and HHS McMaster Clinic (A.G.G.T.), Hamilton, Ontario, Canada; University of Calgary (R.D.H.), Foothills Hospital,
Calgary, Alberta, Canada; Municipal Hospital Dresden Friedrichstadt (S.M.S.), Dresden, Germany; Duke University Medical Center (V.F.T.), Durham, NC; Hospital Germans Trias i Pujol (M.M.), Barcelona, Spain; Service d’Hématologie Biologique Hôtel-Dieu (M.-M.S.), Paris, France; Sanofi-aventis (M.C.), Bridgewater, NJ; and Washington University School of Medicine (R.D.Y.), St. Louis, MO.
The online-only Data Supplement is available with this article at http://stroke.ahajournals.org/lookup/suppl/doi: 10.1161/STROKEAHA. 112.659797/-/DCI.
Correspondence to Alexander G.G. Turpie, MD, Department of Medicine, McMaster University, Hamilton Health Sciences-General Hospital, 237 Barton Street East, Hamilton, Ontario L8L 2X2, Canada. E-mail [email protected].
© 2012 American Heart Association, Inc.
Stroke is available at http://stroke.ahajournals.org DOI: 10.1161/STROKEAHA.112.659797
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250 Stroke January 2013
DVT, symptomatic PE, or fatal PE, during the double-blind period of extended prophylaxis.
The primary safety end point was the incidence of major hemor-rhagic complications during, and up to 48 h after, the double-blind treatment period.
Statistical AnalysesVTE and bleeding events were compared between groups using chi-square and Fisher exact tests. Univariate and multivariate logistic re-gression models were employed to look at the association between VTE and risk factors. Cox proportional hazard models were used to analyze the relationship between treatment and all-cause mortality.
ResultsA total of 389 ischemic stroke patients were identified: in the safety population, 198 patients received extended-duration enoxaparin and 191 received placebo; in the efficacy popula-tion, 166 patients received extended-duration enoxaparin and 150 received placebo (Supplementary Appendix, Figure 1). The mean age was 68.1 years (66.9 years in the enoxaparin group; 69.4 years in the placebo group).
In ischemic stroke patients, extended-duration prophy-laxis with enoxaparin was associated with a reduction in the incidence of VTE at 1 month compared with placebo (2.4% versus 8.0%, respectively, Table 1). No cases of symptom-atic VTE were observed in patients who received extended-duration enoxaparin during the double-blind phase versus 2 events (both symptomatic DVT) in those who received placebo (Table 1). There was one fatal PE in the placebo group.
Major bleeding occurred in 1.5% (3/198) of patients who received extended-duration prophylaxis versus none in the placebo (Table 1). There was one fatal intracranial bleeding
event and a trend toward increased rates of total bleeding in patients receiving extended-duration enoxaparin (Table 1).
Prior VTE and obesity were associated with an increased rate of VTE (Supplementary Appendix, Table 1). In the multi-variate analysis, only prior VTE was an independent predictor of VTE (P=0.0088). The multivariate model indicated that the adjusted odds ratio for treatment effect was 0.32, versus 0.28 unadjusted, suggesting that any imbalance in well-recognized VTE risk factors between the treatment groups has a very lim-ited impact on treatment effect.
DiscussionThis subanalysis showed that extended-duration prophylaxis with enoxaparin reduced the VTE incidence and increased major bleeding in the subgroup of patients with ischemic stroke in the EXCLAIM study. Without VTE prophylaxis, ischemic stroke patients remain at high risk of VTE for at least 1 month after the index stroke.
Our findings support earlier data that the risk of VTE is reduced when stroke patients receive extended-duration VTE prophylaxis.4–6 Stroke patients often experience long periods of immobility, a known risk factor for VTE.4,6 Autopsy evi-dence suggests that while fatal PEs are rare in the first week after a stroke, they are most frequent, and become the main cause of mortality, in the second-to-fourth weeks after the stroke.7,8 A previous study reported that prolonged thrombo-prophylaxis during stroke rehabilitation may reduce the inci-dence of VTE in stroke patients.5
Prior VTE was predictive of post–stroke VTE in a multivar-iate analysis. This subanalysis suggests that extended throm-boprophylaxis is associated with a reduced risk of VTE and an increase in major bleeding in ischemic stroke patients. The
Table 1. Efficacy and Safety End Points During the Double-Blind Treatment Phase in Ischemic Stroke Patients
Ischemic Stroke Patients
Parameter, n (%)Extended-Duration
Enoxaparin* Placebo*Absolute Difference
(%) (95% CI) P Value
VTE at day 28 (Efficacy Population) n=166 n=150
VTE all 4 (2.4) 12 (8.0) −5.6 (−10.5 to −0.7) 0.0236
Fatal PE 0 (0.0) 1 (0.7) −0.7 (−2.0 to 0.6) 0.4747
DVT 4 (2.4) 11 (7.3) −4.9 (−9.7 to −0.1) 0.0398
Symptomatic DVT 0 (0.0) 2 (1.3) −1.3 (−3.2 to 0.5) 0.1356
Asymptomatic DVT 4 (2.4) 9 (6.0) −3.6 (−8.0 to 0.9) 0.1086
Symptomatic VTE 0 (0.0) 2 (1.3) −1.3 (−3.2 to 0.5) 0.1356
All-cause mortality (Safety Population) n=198 n=191
30-day 5 (2.6) 8 (4.2) −1.7 (−5.2 to 1.9) 0.369
90-day 8 (4.0) 11 (5.8) −1.7 (−6.0 to 2.6) 0.440
180-day 10 (5.0) 12 (6.3) −1.2 (−5.8 to 3.4) 0.606
Bleeding (Safety Population) n=198 n=191
Total 12 (6.1)† 5 (2.6) 3.4 (−0.6 to 7.5) 0.0972
Major (hemoglobin decrease ≥2 g/dL)‡ 3 (1.5) 0 (0.0) 1.5 (−0.2 to 3.2) 0.0881
Minor 9 (4.5) 5 (2.6) 1.9 (−1.7 to 5.6) 0.3082
CI, confidence interval; DVT, deep-vein thrombosis; VTE, venous thromboembolism.*Two patients in the extended-duration enoxaparin group and 3 patients in the placebo group had a recurrent ischemic stroke during the double-blind period.†Two patients had intracranial bleeding (one was a fatal event); 1 patient had gastrointestinal bleeding.‡Results were the same with the ≥3 g/dL hemoglobin decrease thresholds for major bleeding.
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Turpie et al Extended Enoxaparin Prophylaxis in Stroke Patients 251
question on the optimal duration of VTE prevention in this patient group remains open, calling for additional studies in this setting.
ConclusionsIschemic stroke patients with reduced mobility remain at high risk for VTE for at least 1 month following the index stroke. In the subgroup of patients with ischemic stroke, extended-duration prophylaxis with enoxaparin was associated with a reduction in the incidence of VTE and an increase in major bleeding.
Sources of FundingThe EXCLAIM study was sponsored by Sanofi. The authors received editorial/writing support in the preparation of this article, which was funded by Sanofi.
DisclosuresDr Turpie has worked as a consultant for Sanofi, Bayer, J&J, Astellas, Merck, Takeda, and Portola and has received speaker's bureau fees from Bayer, BMS/Pfizer, Boehringer-Ingelheim, J&J, GSK, and Sanofi; Dr Hull has worked as a consultant for Sanofi, has received honoraria from Sanofi, Leo Pharma, GSK, Bayer, and Pfizer, and has received research grants from Sanofi and Leo Pharma; Dr Schellong has worked as a consultant and received honoraria for lectures from Sanofi, Boehringer-Ingelheim, Bayer, Daiichi Sankyo, BMS, and Pfizer; Dr Tapson has worked as a consultant and received grant sup-port from Sanofi and Bayer; has worked as a consultant for Covidien, Bacchus, and Biolex and has received honoraria from Sanofi, Eisai, and Genentech; Dr Monreal has received consultant fees from Bayer and Boehringer-Ingelheim and honoraria from Sanofi; Dr Samama
has worked as a consultant for Sanofi, Eli Lilly, Pfizer, Boehringer-Ingelheim, and BMS and has received honoraria from GSK, Sanofi, BMS, and Bayer; Dr Chen is an employee of Sanofi US; Dr Yusen has worked as a consultant for Sanofi, has received honoraria from Sanofi and SCIOS, and has received research funding/grant support from Bayer, Pfizer, Amgen, ParinGenix, and Sanofi.
References 1. Davenport RJ, Dennis MS, Wellwood I, Warlow CP. Complications after
acute stroke. Stroke. 1996;27:415–420. 2. Lansberg MG, O’Donnell MJ, Khatri P, et al. Antithrombotic and
thrombolytic therapy for ischemic stroke: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. Chest. 2012;141(2 Suppl):e601S–e636S.
3. Hull RD, Schellong SM, Tapson VF, et al. Extended-duration venous thromboembolism prophylaxis in acutely ill medical patients with recently reduced mobility: a randomized trial. Ann Intern Med. 2010;153:8–18.
4. Salzman EW, Hirsh J. The epidemiology, pathogenesis, and natural his-tory of venous thrombosis. In: Colman RW, Hirsh J, Marder J, Salzman EW, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 3rd ed. Philadelphia, Pa: Lippincott; 1994:1275–1296.
5. Harvey RL, Lovell LL, Belanger N, Roth EJ. The effectiveness of antico-agulant and antiplatelet agents in preventing venous thromboembolism during stroke rehabilitation: a historical cohort study. Arch Phys Med Rehabil. 2004;85:1070–1075.
6. Kamphuisen PW, Agnelli G, Sebastianelli M. Prevention of venous thromboembolism after acute ischemic stroke. J Thromb Haemost. 2005;3:1187–1194.
7. Viitanen M, Winblad B, Asplund K. Autopsy-verified causes of death after stroke. Acta Med Scand. 1987;222:401–408.
8. Kelly J, Rudd A, Lewis R, Hunt BJ. Venous thromboembolism after acute stroke. Stroke. 2001;32:262–267.
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InvestigatorsMonreal, Meyer-Michel Samama, Min Chen, Roger D. Yusen and for the EXCLAIM
Alexander G.G. Turpie, Russell D. Hull, Sebastian M. Schellong, Victor F. Tapson, ManuelEnoxaparin Prophylaxis: Results From the EXCLAIM Study
Venous Thromboembolism Risk in Ischemic Stroke Patients Receiving Extended-Duration
Print ISSN: 0039-2499. Online ISSN: 1524-4628 Copyright © 2012 American Heart Association, Inc. All rights reserved.
is published by the American Heart Association, 7272 Greenville Avenue, Dallas, TX 75231Stroke doi: 10.1161/STROKEAHA.112.659797
2013;44:249-251; originally published online November 1, 2012;Stroke.
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SUPPLEMENTAL MATERIAL
Interim analysis
After a planned interim analysis, eligibility criteria were amended for patients with level 2
immobility (total bed rest or sedentary with bathroom privileges) to include only those with
additional VTE risk factors: age >75 years, a history of VTE, or active or prior cancer.
For further reference please see:
1. Hull RD, Schellong SM, Tapson VF, Monreal M, Samama MM, Nicol P, et al.
EXCLAIM (Extended Prophylaxis for Venous ThromboEmbolism in Acutely Ill Medical
Patients With Prolonged Immobilization) study. Extended-duration venous
thromboembolism prophylaxis in acutely ill medical patients with recently reduced
mobility: a randomized trial. Ann Intern Med. 2010;153:8-18.
2. Hull RD, Schellong SM, Tapson VF, Monreal M, Samama MM, Turpie AGG, et al.
Extended-duration thromboprophylaxis in acutely ill medical patients with recent reduced
mobility: methodology for the EXCLAIM study. J Thromb Thrombolysis. 2006;22:31-
38.
Assessment of outcomes
The primary efficacy endpoint was assessed in the total efficacy population that included all
randomized patients who received at least one dose of study medication during the double-blind
treatment period, had a confirmed VTE within 7 days after cessation of study treatment, or had at
least one interpretable ultrasound evaluation during the double-blind treatment period (day
28±4). Bleeding parameters were assessed in the total safety population, which included the sub-
populations of all randomized ischemic stroke patients and all acutely medically ill non-stroke
patients who received at least one dose of study medication during the double-blind period.
Results – bleeding during open-label treatment
During the open-label phase of the study, 29/454 (6.4%) patients experienced bleeding, of which
6 (1.3%) was adjudicated as major bleeding and 23 (5.1%) were classified as minor bleeds.
Study limitations
There are limitations to this subanalysis. The small sample size and low event rates may reduce
the statistical power of comparisons between treatment groups. Intracranial bleeding was not
assessed by systematic computerized tomography scans. Stroke severity was measured by the
level of resulting immobility instead of using specific scale scores such as the National Institute
of Health Stroke Scale or the modified Rankin scale scores. This may limit the generalizability of
our findings and restricts our ability to comment on the comparative benefits of extended-
duration enoxaparin thromboprophylaxis in patients with severe, compared with less severe,
ischemic stroke.
Enrolling Investigators:
Argentina – J.A. Mazzei, M. Casey, M. del Carmen Gallo, J. Ceresetto, B. Grand.
Australia – H. Salem, C. Denaro, V. Ayyar, T. Brighton, K. Narayan, H. Gibbs, E. Gan, A.
Gallus, S. Dunkley, B. Chong, R. Baker, M. Leahy, U. Hahn, P. Blombery, C. Ward, B.
McGrath, I. Prosser, S. Chunilal.
Austria – J. Patsch, M. Jud, K. Aigner, F. Hoppichler, H. Pall, P. Grabher, P. Kobierski, H.
Zwick, M. Juchum, M.G. Röger, H-R. Schönherr, F. Schmalzl, C. Geyer, B. Kohler.
Belgium – M. Delcroix, M. Vandewoude, J.C. Wautrecht, K. De Boeck, C. Hermans, P. Hainaut.
Brazil – G. Reis, A.C.P. Barreto, M. de Arruda Martins, C. Carvalho, V. Tadini, J.A. de Barros,
L. Moura, A.C. Lopes, C. Pereira da Cunha, C. Gun, R. Milani.
Canada – S. Kahn, M.J. Miron, C. Demers, L. Desjardins, K. Lai, S. Solymoss, J.D. Rolf, R.
Audet, A.G.G. Turpie, T. Wong, I. Kirouac, P. Duffy, S. Dolan, J. Kassis, D. Anderson, A.
Kuchtaruk, J. Berlingieri, G. Gamble, K. Grewal, M. Weigel, J. Biem, R. Labonte, A. Cheung,
A. Forster, A. Panju. J. Villeneuve, B. McCarron.
Colombia – P.M. Pacheco, F. Cuervo, R. Dennis, A. Londoño, E.J. Ruiz, J.C. Velásquez, R.
Acero, R.D. Vargas, U. Largo.
France – D. Mottier, A. Proust, I. Quere, H. Decousus, B. Lorcerie, J.F. Bergmann, J.J. Leduc,
C. Series, G. Dien, E. Duhamel, G. Berrut, T. Prazuck, M. Goralski, J.Y. Hatron, D. Farge, P.
Jego, A. Achkar, P. Lacroix, J. Doucet, O. Bouchard, F. Parent, H. Boccalon, C. Conri, E. Le
Moigne, P. Letellier, O. Sanchez, P. Zuck.
Germany – J. Harenberg, M. Sternkopf, H. Lawall, C. Kelbel, G. Pöhlmann, T. Dorsel, O.
Altmann, W. Sehnert, G. Vossbeck, F. Odemar, W. Oettler, A. Hartmann, K. Nogai, H.
Bechtold, R. Fünfstück, H. Omran, T. Ittel, R. Egger, T. Horacek, J. Cailloud, S. Maier, G.
Hasenfuss, A. Schmidt-Lucke, M. Pfisterer, W. Lengfelder, J. Treib, H-J. Dieckmann, H.
Thomas, T. Ziegler, J. Brachmann, F-L. Dumoulin, G. Cieslinski, B. Schmidt, S. Schellong.
India – P. Mehta, K. Asokan, P.M. Sathe, R.M.P.L. Ramanathan, M.V.S. Subbalaxmi, Z.
Udwadia, S.K. Sharma, N. Ramakrishnan, A. Vigg.
Israel – A. Shlomo Berliner, G. Lugassy, M. Ellis, B. Brenner.
Italy – E. De Gaudenzi, D. Imberti, M. Silingardi, S. Siragusa, C. Cimminiello, P. Prandoni, W.
Ageno, G. Scannapieco, N. Zanatta, M. Pini, S. Testa, L. Lusiani, P. Pola, G. Marchegiani, G.M.
Patrassi.
Mexico – D. Rodriguez-Gonzalez, U. Chavarria-Martinez, J.F. Velasco-Rodriguez, J. Jaimes-
Hernandez, A. Cruz-Diaz, F. Aguilera-Almazan, A. Arauz Góngora, M. Poblano-Morales, G.
Velasco-Sanchez, A. Quesada-Sanchez, R. Lara-Badillo, A. Mireles-Munoz, V. Borja-Sanchez.
Poland – A. Torbicki, P. Psuja, P. Pruszczyk, J. Musial, G. Opolski, M. Dluzniewski, K.
Zawilska.
Russia – V.A. Lyusov, I. Gordeev, P.Y. Dovgalevskiy, S.B. Fitilev, M.G. Glezer, G.I.
Storozhakov, M.A. Karpenko, K.E. Sobolev, O.A. Khrustalev, A.G. Chuchalin, A.L. Vertkin,
S.A. Rumyantseva, U.B. Belousov, D.A. Zateytshikov, M.A. Piradov.
South Africa – J. Verster, J. Engelbrecht, F. Maritz, L. van Zyl, G.H. Latiff, M.M. De Vries
Basson.
Spain – M. Monreal, J. Luis Rodriguez, D. Jimenez, J. Moreno, J. Ramon Calabuig, C. Suarez,
A. Castro, S. Reus, C. Falga, R. Otero, M. Aburto, P. Conthe, A. Page, A. Blanco, A. Valencia,
F. Martos, J. Ruiz Galiana, J. Trujillo.
Tunisia – F. Boujelben, R. Hassine, F. Bahri, A. Derbel, S. Ben Youssef Zouari, S. Othmani, R.
Charfi, M. Chakroun, H. Bouacha, M. Marouane, S. Mahjoub, R. Miladi, C. Laouani Kechrid, N.
Belkhiria, H. Drissa, H. Houman.
United Kingdom – A. Cohen, M. Gormley, A.J. Moriarty.
USA – W. Rodriguez, J. Updegrove, M. Hazelrigg, S. Etezadi, D. Amin, K. Krell, V. Nadar, R.
Yusen, J. Dexter, R. Fei, A. Marinelli, A. Seibert, J. Welker, W. O'Riordan, E. Kolettis, D. Kett,
D. Hill, D. Buchan, T. Morris, M. Siegel, A. Spyropoulos, R. Lerner, W. Leeds, M. Anderson III,
D. Banish, J. Anderson, F. Messina, A. Baker, L. Emdur, V. Robinson, K. Danisa, B. Sangani,
D. Lawler, R. Betzu, L. Gatien, H. Berlin, R. Deichmann, S. Kaatz, M. Amin, H. Fleming, W.
McKenzie, C. Lawton, A.J. Quaranta, A. Shah, M. Rush, R. Snyder, R. Shriver, J. Ansell, V.
Tapson, R.C. Touchon, R.T-P. Chow, H. Thawani, S.J. Simon, S. Deitelzweig, R. McLafferty, S.
Jacobson, B. Davidson, R. Elliott-Mullens, P. Patel, M. Waters, J. Hansbrough, N. Abramson, B.
Lahiri, M. El Shahawy, R. Levine, J. Fenton, W.J. Pendergast, R. Lavender, K.L. Watson-
Ramirez, C. Pollack, B. Chamacho, T. Albertson, D. Beard, J.R. Rehem, D. Elias, M. Pistoria, H.
Chandarana, E. Elamin, W. Miller, C.L. Anderson, K. Leeper, A. Schlau, C. Sotolongo, H.
Karunartne, G.L. Walters, W. Summer, L.C. Faulk, L. Barr, L. Thet, R.D. Hite, D. Ost, G.
Criner, G. Martin, P. Kaboli, D. Brofman, J. Johnson, L. Rink, G. Merli, L. Kendrick, G.
Schuyler, D. Chardon, M.C. Joseph, C. Francis, C. Lewinstein, S. Mauger, A. El-Solh, H. Yu, D.
Green, S. Padove, J. Sippel, P. Norwood, H. Haught, C. Palmer, M. Moncure, P.W. Sturm, A.K.
Gupta, T. Lee, R. Ali, N. Desbiens, J. Witt, L. Greenspon, D. Heiselman.
Underlined names indicate national coordinators.
Table 1. Univariate analysis of the incidence of VTE at day 30 in ischemic stroke patients with
associated risk factors.
n (N) Rate (%) P value
Risk factors
Sex
Male 8 (158) 5.1 1.0000
Female 8 (158) 5.1
Age >75 y
Yes 5 (91) 5.5 0.8241
No 11 (225) 4.9
Cancer
Yes 0 (15) 0.0 0.9794
No 16 (301) 5.3
Chronic heart failure
Yes 0 (18) 0.0 0.9774
No 16 (298) 5.4
History of VTE
Yes 3 (12) 25.0 0.0055
No 13 (304) 4.3
Obesity
Yes 7 (71) 9.9 0.0440
No 9 (245) 3.7
Venous insufficiency
Yes 4 (40) 10.0 0.1388
No 12 (276) 4.3
Chronic respiratory failure
Yes 2 (14) 14.3 0.1288
No 14 (302) 4.6
Immobilization level
Level 1 immobility* 11 (232) 4.7 0.6650
Level 2 immobility† 5 (84) 6.0
Number of risk factors experienced
No risk factor 3 (137) 2.2 0.0885
One risk factor 8 (115) 7.0
Two risk factors 2 (45) 4.4
Three or more risk factors 3 (19) 15.8
VTE, venous thromboembolism
* Total bed rest or sedentary patients without bathroom privileges
† Level 1 with bathroom privileges
Figure 1. EXCLAIM ischemic stroke population
* Randomized patients receiving at least one dose of enoxaparin or placebo
† Randomized patients receiving at least one dose of enoxaparin or placebo and evaluable for the
primary efficacy endpoint
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