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Letters to the Editor   |    
Perioperative Use of Low-Molecular-Weight Heparin
Dominick Cannavo, M.D.; Eduardo A. Salvati, M.D.; Vincent D. PellegriniJr., M.D.; Nigel E. Sharrock, M.B., Ch.B.; Paul A. Lotke, M.D.; David W. Murray, F.R.C.S.; Hollis Potter, M.D.; Geoffrey H. Westrich, M.D.
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Department of Anesthesiology, Hospital for Joint Diseases Orthopaedic Institute, New York University Medical Center, 301 East 17th Street, New York, N.Y. 10003
Corresponding author: Nigel E. Sharrock, M.B., Ch.B., Department of Anesthesiology, The Hospital for Special Surgery, 535 East 70th Street, New York, N.Y. 10021

The Journal of Bone & Joint Surgery.  2000; 82:1673-a-1673 
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To The Editor:
I found the recent Symposium entitled "Recent Advances in Venous Thromboembolic Prophylaxis During and After Total Hip Arthroplasty" (82-A: 252-270, Feb. 2000), by Salvati et al., very informative. Their technique is innovative and their discussion, intelligent and convincing. I do, however, feel that in the section entitled "The Role of Anesthesia," the authors were incorrect in saying that "it is unsafe to administer epidural anesthesia to a patient who has received low-molecular-weight heparin preoperatively or to use low-molecular-weight heparin postoperatively before removal of an epidural catheter. Low-molecular-weight heparin is suitable for use in patients receiving general anesthesia, provided that it is administered twelve hours after the operation."
When one examines the case reports on epidural hematoma from 1993 through 1998 as presented by Horlocker and Wedel2, it is clear that at least some of the epidural hematomas occurred from misuse of the drug. Specifically, considering that the peak activity of the drug is three to four hours after administration and that the half-life is 3.5 hours, any neuraxial intervention (spinal or epidural) within twelve hours (less than three half-lives) is contraindicated. To say that these drugs are contraindicated preoperatively if regional anesthesia is anticipated is wrong. What if the patient received the drug three days or three weeks prior to surgery? At the Hospital for Joint Diseases, we have routinely treated hip-fracture patients preoperatively with Lovenox (enoxaparin) and safely administered spinal anesthetics twelve hours later. We have used this approach on hundreds of patients and have not observed a single epidural hematoma. In addition, the majority of total joint arthroplasties at our institution are performed with the patient under spinal anesthesia, and low-molecular-weight heparin is administered postoperatively as prophylaxis against deep-vein thrombosis. Considering our volume of cases, this amounts to thousands of patients, again, without a single epidural hematoma. According to published guidelines, low-molecular-weight heparins are not contraindicated in patients with epidural catheters in place. One must simply recognize that withdrawing an epidural catheter is also a traumatic event, wait twelve hours after the previous dose before withdrawing the catheter, and wait an additional two hours before redosing. When one examines the aforementioned case reports on epidural hematoma, it becomes clear that epidural catheters were placed or removed well short of the safe twelve-hour window and sometimes right at the peak activity of the drug. The obvious conclusion is that the anesthesiologists involved did not know that their patients had received this drug.
In May 1998, at the urging of the Food and Drug Administration, the American Society of Regional Anesthesia convened a panel to evaluate the use of low-molecular-weight heparins and to formulate guidelines for their safe use with neuraxial anesthesia. A consensus statement was published in December 1998, to which I would refer the reader2.
I believe, as does the American College of Chest Physicians and the American Society of Regional Anesthesia, that the use of low-molecular-weight heparins is a safe and efficacious means of venous thromboembolic prophylaxis. Further, these drugs can be used safely in the context of regional anesthesia as long as the published guidelines are followed. Statements to the contrary are simply untrue and serve only to create more confusion, which many in the fields of anesthesia and orthopaedics have spent the past two years trying to eliminate.
Dominick Cannavo, M.D.
Department of Anesthesiology Hospital for Joint Diseases Orthopaedic Institute New York University Medical Center 301 East 17th Street New York, N.Y. 10003
E. A. Salvati, V. D. Pellegrini, Jr., N. E. Sharrock, P. A. Lotke, D. W. Murray, H. Potter, and G. H. Westrich reply:
Dr. Cannavo raises a very important unresolved issue in anesthetic practice - namely, how can one safely use conduction anesthetics in conjunction with low-molecular-weight heparin? This is extremely important due to the rare but potentially tragic consequences of epidural hematoma. Epidural hematomas are distinctly rare in patients managed with aspirin or Coumadin (warfarin), but a significant number were described after the introduction of low-molecular-weight heparin. Some occurred after spinal anesthesia, but most were noted in association with the use of epidural catheters. Cases were more frequent when higher doses of low-molecular-weight heparin were utilized.
The use of spinal anesthesia according to the guidelines described by Dr. Cannavo is probably safe, as his experience would suggest. However, placing an epidural catheter entails more trauma than placing a spinal needle. Our concern relates to two issues. The first issue relates to dosage. If higher doses, such as forty milligrams twice a day, caused a significant number of epidural hematomas, how certain can one be that a dose of forty milligrams once a day will completely eliminate the risk? Adjusting the dose according to weight may be another option to reduce risk. The second issue relates to the time when the epidural catheter is removed. The recommendation is to withdraw the catheter twelve hours after the administration of low-molecular-weight heparin. The problem is that catheters become dislodged spontaneously in up to 10 percent of cases1.
It is likely that, with judicious management, low-molecular-weight heparin can be used effectively with spinal anesthesia. However, due to difficulties with epidural catheters and unpredictable patient responsiveness to low-molecular-weight heparin, epidural anesthesia and analgesia should be approached with considerable caution, if at all, when patients are receiving low-molecular-weight heparin.
Eduardo A. Salvati, M.D. Vincent D. Pellegrini, Jr., M.D. Nigel E. Sharrock, M.B., Ch.B. Paul A. Lotke, M.D. David W. Murray, F.R.C.S. Hollis Potter, M.D. Geoffrey H. Westrich, M.D.
Corresponding author: Nigel E. Sharrock, M.B., Ch.B. Department of Anesthesiology The Hospital for Special Surgery 535 East 70th Street New York, N.Y. 10021
Burstal, R.; Wegener, F.; Hayes, C.; and Lantry, G.: Epidural analgesia: prospective audit of 1062 patients. Anaesth. and Intensive Care,26: 165-172, 1998.26165  1998 
 
Horlocker, T. T., and Wedel, D. J.: Neuraxial block and low-molecular-weight heparin: balancing perioperative analgesia and thromboprophylaxis. Reg. Anesth. and Pain Med.,23 (6 Supplement 2): 164-177, 1998.23 (6 Supplement 2)164  1998 
 

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Burstal, R.; Wegener, F.; Hayes, C.; and Lantry, G.: Epidural analgesia: prospective audit of 1062 patients. Anaesth. and Intensive Care,26: 165-172, 1998.26165  1998 
 
Horlocker, T. T., and Wedel, D. J.: Neuraxial block and low-molecular-weight heparin: balancing perioperative analgesia and thromboprophylaxis. Reg. Anesth. and Pain Med.,23 (6 Supplement 2): 164-177, 1998.23 (6 Supplement 2)164  1998 
 
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These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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