Long-Term Pain, Stiffness, and Functional Disability After Total Knee Arthroplasty With and Without an Extended Ambulatory Continuous Femoral Nerve Block: A Prospective, 1-Year Follow-Up of a Multicenter, Randomized, Triple-Masked, Placebo-Controlled Trial

Previously, we have demonstrated that extending a continuous femoral nerve block (cFNB) from overnight to 4 days after total knee arthroplasty (TKA) provides clear benefits during the infusion, but not subsequent to catheter removal. However, there were major limitations in generalizing the results...

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Veröffentlicht in:Regional anesthesia and pain medicine 2011-03, Vol.36 (2), p.116-120
Hauptverfasser: Ilfeld, Brian M., Shuster, Jonathan J., Theriaque, Douglas W., Mariano, Edward R., Girard, Paul J., Loland, Vanessa J., Meyer, R. Scott, Donovan, John F., Pugh, George A., Le, Linda T., Sessler, Daniel I., Ball, Scott T.
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container_end_page 120
container_issue 2
container_start_page 116
container_title Regional anesthesia and pain medicine
container_volume 36
creator Ilfeld, Brian M.
Shuster, Jonathan J.
Theriaque, Douglas W.
Mariano, Edward R.
Girard, Paul J.
Loland, Vanessa J.
Meyer, R. Scott
Donovan, John F.
Pugh, George A.
Le, Linda T.
Sessler, Daniel I.
Ball, Scott T.
description Previously, we have demonstrated that extending a continuous femoral nerve block (cFNB) from overnight to 4 days after total knee arthroplasty (TKA) provides clear benefits during the infusion, but not subsequent to catheter removal. However, there were major limitations in generalizing the results of that investigation, and we subsequently performed a very similar study using a multicenter format, with many health care providers, in patients on general orthopedic wards, thus greatly improving inference of the results to the general population. Not surprisingly, the perioperative/short-term outcomes differed greatly from the first, more limited study. We now present a prospective follow-up study of the previously published, multicenter, randomized controlled clinical trial to investigate the possibility that an extended ambulatory cFNB decreases long-term pain, stiffness, and functional disability after TKA, which greatly improves inference of the results to the general population. Subjects undergoing TKA received a cFNB with ropivacaine 0.2% from surgery until the following morning, at which time patients were randomized to continue either perineural ropivacaine (n = 28) or normal saline (n = 26). Patients were discharged with their catheter and a portable infusion pump, and catheters were removed on postoperative day 4. Health-related quality of life was measured using the Western Ontario and McMaster Universities Osteoarthritis Index preoperatively and then at 7 days, as well as 1, 2, 3, 6, and 12 months after surgery. This index evaluates pain, stiffness, and physical functional disability. For inclusion in the analysis, we required a minimum of 4 of the 6 time points, including day 7 and at least 2 of months 3, 6, and 12. The 2 treatment groups had similar Western Ontario and McMaster Universities Osteoarthritis scores for the mean area-under-the-curve calculations (point estimate for the difference in mean area under the curve for the 2 groups [overnight infusion group − extended infusion group] = 3.8; 95% confidence interval, −3.8 to +11.3; P = 0.32) and at all individual time points ( P > 0.05). This investigation found no evidence that extending an overnight cFNB to 4 days improves (or worsens) subsequent pain, stiffness, or physical function after TKA in patients of multiple centers convalescing on general orthopedic wards.
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However, there were major limitations in generalizing the results of that investigation, and we subsequently performed a very similar study using a multicenter format, with many health care providers, in patients on general orthopedic wards, thus greatly improving inference of the results to the general population. Not surprisingly, the perioperative/short-term outcomes differed greatly from the first, more limited study. We now present a prospective follow-up study of the previously published, multicenter, randomized controlled clinical trial to investigate the possibility that an extended ambulatory cFNB decreases long-term pain, stiffness, and functional disability after TKA, which greatly improves inference of the results to the general population. Subjects undergoing TKA received a cFNB with ropivacaine 0.2% from surgery until the following morning, at which time patients were randomized to continue either perineural ropivacaine (n = 28) or normal saline (n = 26). Patients were discharged with their catheter and a portable infusion pump, and catheters were removed on postoperative day 4. Health-related quality of life was measured using the Western Ontario and McMaster Universities Osteoarthritis Index preoperatively and then at 7 days, as well as 1, 2, 3, 6, and 12 months after surgery. This index evaluates pain, stiffness, and physical functional disability. For inclusion in the analysis, we required a minimum of 4 of the 6 time points, including day 7 and at least 2 of months 3, 6, and 12. The 2 treatment groups had similar Western Ontario and McMaster Universities Osteoarthritis scores for the mean area-under-the-curve calculations (point estimate for the difference in mean area under the curve for the 2 groups [overnight infusion group − extended infusion group] = 3.8; 95% confidence interval, −3.8 to +11.3; P = 0.32) and at all individual time points ( P &gt; 0.05). This investigation found no evidence that extending an overnight cFNB to 4 days improves (or worsens) subsequent pain, stiffness, or physical function after TKA in patients of multiple centers convalescing on general orthopedic wards.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>21425510</pmid><doi>10.1097/AAP.0b013e3182052505</doi><tpages>5</tpages></addata></record>
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identifier ISSN: 1098-7339
ispartof Regional anesthesia and pain medicine, 2011-03, Vol.36 (2), p.116-120
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subjects Adolescent
Adult
Aged
Ambulatory Care - methods
Arthritis
Arthroplasty, Replacement, Knee - adverse effects
Catheters
Female
Femoral Nerve
Follow-Up Studies
Humans
Joint replacement surgery
Joint surgery
Knee
Male
Middle Aged
Nerve Block - methods
Orthopedics
Osteoarthritis
Pain
Pain, Postoperative - physiopathology
Pain, Postoperative - prevention & control
Prospective Studies
Recovery of Function - drug effects
Recovery of Function - physiology
Regional anesthesia
Time Factors
Treatment Outcome
Young Adult
title Long-Term Pain, Stiffness, and Functional Disability After Total Knee Arthroplasty With and Without an Extended Ambulatory Continuous Femoral Nerve Block: A Prospective, 1-Year Follow-Up of a Multicenter, Randomized, Triple-Masked, Placebo-Controlled Trial
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