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 |
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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. |
doi_str_mv | 10.1097/AAP.0b013e3182052505 |
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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.</description><identifier>ISSN: 1098-7339</identifier><identifier>EISSN: 1532-8651</identifier><identifier>DOI: 10.1097/AAP.0b013e3182052505</identifier><identifier>PMID: 21425510</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>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</subject><ispartof>Regional anesthesia and pain medicine, 2011-03, Vol.36 (2), p.116-120</ispartof><rights>2011 American Society of Regional Anesthesia</rights><rights>Copyright © 2011 by American Society of Regional Anesthesia and Pain Medicine</rights><rights>Copyright © 2011 by American Society of Regional Anesthesia and Pain Medicine2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c338t-49d36de33fba9e70975a78b2b0a19e057ef257cd68bf42c6fc8a249ebada23b53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21425510$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ilfeld, Brian M.</creatorcontrib><creatorcontrib>Shuster, Jonathan J.</creatorcontrib><creatorcontrib>Theriaque, Douglas W.</creatorcontrib><creatorcontrib>Mariano, Edward R.</creatorcontrib><creatorcontrib>Girard, Paul J.</creatorcontrib><creatorcontrib>Loland, Vanessa J.</creatorcontrib><creatorcontrib>Meyer, R. Scott</creatorcontrib><creatorcontrib>Donovan, John F.</creatorcontrib><creatorcontrib>Pugh, George A.</creatorcontrib><creatorcontrib>Le, Linda T.</creatorcontrib><creatorcontrib>Sessler, Daniel I.</creatorcontrib><creatorcontrib>Ball, Scott T.</creatorcontrib><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</title><title>Regional anesthesia and pain medicine</title><addtitle>Reg Anesth Pain Med</addtitle><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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Ambulatory Care - methods</subject><subject>Arthritis</subject><subject>Arthroplasty, Replacement, Knee - adverse effects</subject><subject>Catheters</subject><subject>Female</subject><subject>Femoral Nerve</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Joint replacement surgery</subject><subject>Joint surgery</subject><subject>Knee</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nerve Block - methods</subject><subject>Orthopedics</subject><subject>Osteoarthritis</subject><subject>Pain</subject><subject>Pain, Postoperative - physiopathology</subject><subject>Pain, Postoperative - prevention & control</subject><subject>Prospective Studies</subject><subject>Recovery of Function - drug effects</subject><subject>Recovery of Function - physiology</subject><subject>Regional anesthesia</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1098-7339</issn><issn>1532-8651</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9Uk1v1DAUDAhES-EfIGSJA5dN8Uecjx6QwrYLiC2sYCvEKXKcF-rWsVPbWVh-PV62cOiBk5_teTNPbyZJnhF8THBVvKrr1TFuMWHASEkxpxzz-8kh4YymZc7Jg1jjqkwLxqqD5LH3VxjjssjyR8kBJRnlnODDe8nSmu_pGtyAVkKZGfoSVN8b8H6GhOnQYjIyKGuERqfKi1ZpFbao7gM4tLYhPn8wAKh24dLZUQsff7-qcPmneVfYKcQanf0MYDroUD20kxbBui2aWxOUmezk0QIG6yLZR3AbQG-0ldcnqEYrZ_0IcYANzBBJv4FwaGG1tj_SixHZHgl0PumgJJg40Ax9jqp2UL-gm6G1U6OG9Fz46911pYWE1qY7URcp4igRIfST5GEvtIent-dRcrE4W8_fpctPb9_P62UqGStDmlUdyztgrG9FBUU0gIuibGmLBakA8wJ6ygvZ5WXbZ1TmvSwFzSpoRScoazk7Sl7ueUdnbybwoRmUl6C1MBA30JS8pBWhJI_IF3eQV3Zy0QHfRNMYrhjOdqhsj5JxR95B34xODcJtG4KbXUCaGJDmbkBi2_Nb8qkdoPvX9DcREfB6D4C4jI0C13ipwEjolItONJ1V_1f4DcrQzZ4</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Ilfeld, Brian M.</creator><creator>Shuster, Jonathan J.</creator><creator>Theriaque, Douglas W.</creator><creator>Mariano, Edward R.</creator><creator>Girard, Paul J.</creator><creator>Loland, Vanessa J.</creator><creator>Meyer, R. Scott</creator><creator>Donovan, John F.</creator><creator>Pugh, George A.</creator><creator>Le, Linda T.</creator><creator>Sessler, Daniel I.</creator><creator>Ball, Scott T.</creator><general>Elsevier Inc</general><general>BMJ Publishing Group LTD</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20110301</creationdate><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</title><author>Ilfeld, Brian M. ; Shuster, Jonathan J. ; Theriaque, Douglas W. ; Mariano, Edward R. ; Girard, Paul J. ; Loland, Vanessa J. ; Meyer, R. 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Scott</creatorcontrib><creatorcontrib>Donovan, John F.</creatorcontrib><creatorcontrib>Pugh, George A.</creatorcontrib><creatorcontrib>Le, Linda T.</creatorcontrib><creatorcontrib>Sessler, Daniel I.</creatorcontrib><creatorcontrib>Ball, Scott T.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Regional anesthesia and pain medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ilfeld, Brian M.</au><au>Shuster, Jonathan J.</au><au>Theriaque, Douglas W.</au><au>Mariano, Edward R.</au><au>Girard, Paul J.</au><au>Loland, Vanessa J.</au><au>Meyer, R. Scott</au><au>Donovan, John F.</au><au>Pugh, George A.</au><au>Le, Linda T.</au><au>Sessler, Daniel I.</au><au>Ball, Scott T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Regional anesthesia and pain medicine</jtitle><addtitle>Reg Anesth Pain Med</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>36</volume><issue>2</issue><spage>116</spage><epage>120</epage><pages>116-120</pages><issn>1098-7339</issn><eissn>1532-8651</eissn><abstract>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.</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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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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