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The Utility of Oral Nonsteroidal Anti-inflammatory Drugs Compared With Standard Opioids Following Arthroscopic Meniscectomy: A Prospective Observational Study

Pham, Hien; Pickell, Michael; Yagnatovsky, Michelle; Kramarchuk, Mark; Alaia, Michael J; Strauss, Eric J; Jazrawi, Laith M; Campbell, Kirk A
PURPOSE/OBJECTIVE:To evaluate the efficacy of oral nonsteroidal anti-inflammatory drugs (NSAIDs) as the primary postoperative pain medication compared with standard oral opioids following arthroscopic partial meniscectomy. METHODS:This was a single-center, prospective, nonrandomized, comparative observational study. Patients ages 18 to 65 years who were indicated for arthroscopic meniscectomy were included. Postoperatively, patients were prescribed 1 of 2 analgesic regimens: (1) ibuprofen (600 mg every 6-8 hours as needed) and 10 tablets of oxycodone/acetaminophen (5/325 mg as needed for breakthrough pain) or (2) 30 to 40 tablets oxycodone/acetaminophen (5/325 mg every 6 hours as needed). Subjects completed questionnaires at 8 hours, 24 hours, 48 hours, and 1 week after surgery, which included medication usage, visual analog scale pain score, incidence of adverse events, and patient satisfaction. RESULTS:Sixty-eight patients with mean age 51.2 years (±10.4 years) were enrolled between October 2016 and February 2017. Enrollment in the opioid group continued until 30 patients were enrolled in the NSAID group, and at final analysis there were 28 patients in the NSAID group and 40 in the opioid group. There were no significant differences in sex, visual analog scale pain score, or patient satisfaction between the 2 groups at any time point. Patients in the opioid group had a significantly higher mean opioid consumption on postoperative day 1 (1.1 vs 0.5 tablets, P < .03) and postoperative days 3 to 7 (2.6 vs 0.5 tablets, P < .02) compared with NSAID group patients. There was a trend toward greater total (1 week) opioid usage (4.7 vs 2.0 tablets) in the opioid group; however, this was not statistically significant (P < .08). Fifty-three percent of opioid group patients independently chose to forego their opioid medication for an over-the-counter NSAID and/or acetaminophen instead. No patients requested a medication refill. CONCLUSIONS:We found no significant difference in pain control, satisfaction, and total 1-week opioid use between patients prescribed NSAIDs with opioids and those prescribed opioids alone. All patients used only limited amounts of opioids to control postoperative pain, suggesting we are currently overprescribing opioids after arthroscopic partial meniscectomy. LEVEL OF EVIDENCE/METHODS:Level II, prospective comparative study.
PMID: 30733030
ISSN: 1526-3231
CID: 3632382

Biological Effects of Bone Marrow Concentrate in Knee Pathologies

Fortier, Lisa A; Strauss, Eric J; Shepard, David O; Becktell, Liliya; Kennedy, John G
With our aging population desiring to remain active, the incidence and costs associated with managing knee pain from both acute injury and symptomatic knee osteoarthritis continue to dramatically increase. Current treatment methods fall short with respect to their ability to improve the intra-articular environment and restore normal joint homeostasis. With increasing basic science and clinical evidence showing efficacy, cell-based therapies such as bone marrow concentrate (BMC) hold promise as a nonsurgical joint preserving treatment approach. BMC has inherent advantages over other treatments commonly used for various knee pathologies because it is a point-of-care orthobiologic product that uniquely and simultaneously delivers growth factors, anti-inflammatory proteins, and mesenchymal stem cells. There is increasing evidence for the use of BMC for repair of focal cartilage defects and for the treatment of generalized knee pain. However, continued high-quality studies are necessary for the clinical utility of BMC to be critically assessed with particular attention paid to appropriate patient selection, standardized aspiration, and processing and reporting of both functional and imaging-based outcomes.
PMID: 30500973
ISSN: 1938-2480
CID: 3524902

Adipose-to-muscle area ratio at the knee is superior to BMI in predicting post-operative outcome following arthroscopic meniscectomy

Dai, Amos Z; Breite, Joshua; Pham, Hien; Pickell, Michael; Kramarchuk, Mark; Vaca, Eduardo; Strauss, Eric J
PURPOSE/OBJECTIVE:To determine if measurement of leg adipose tissue area by MRI is a better predictor of post-operative clinical outcome compared to body mass index (BMI) following arthroscopic meniscectomy. METHODS:Patients that underwent an arthroscopic partial meniscectomy between 2011 and 2016 were identified and a retrospective chart review was performed. Patients with additional knee pathology other than a meniscal tear with or without associated articular cartilage injury were excluded. Leg adipose tissue and muscle area measurements at the level of the knee joint were performed for patients on their preoperative axial magnetic resonance imaging (MRI) study and adipose-to-muscle area ratio (AMR) was calculated. Correlations among AMR, BMI, and post-operative clinical outcomes were compared. RESULTS:compared to those with no cartilage damage. AMR was also significantly correlated to age and BMI. CONCLUSIONS:The current study demonstrates that compared to BMI, leg adiposity as determined by the ratio of adipose tissue to muscle area on axial MRI (AMR), is a stronger predictor of functional outcome following meniscectomy. This suggests a role of obesity in the progression of OA beyond the increased joint forces associated with increased BMI. LEVEL OF EVIDENCE/METHODS:IV, retrospective case series.
PMID: 30167858
ISSN: 1434-3916
CID: 3256232

The Utility of Biologics, Osteotomy, and Cartilage Restoration in the Knee

Frank, Rachel M; Cotter, Eric J; Strauss, Eric J; Gomoll, Andreas H; Cole, Brian J
The management of complex cartilage and meniscal pathology in young, athletic patients is extremely challenging. Patients with concomitant knee pathologies, including cartilage defects, meniscal deficiency, malalignment, and/or ligamentous insufficiency, are the patients in whom joint preservation surgery is most difficult. Clinical decision making for these patients is further complicated by articular cartilage lesions, which often are incidental findings; therefore, treatment decisions must be based on the confirmed contribution of articular cartilage lesions to symptomatology. Surgical management of any of the aforementioned knee pathologies that is performed in isolation typically results in acceptable patient outcomes; however, concomitant procedures for the management of concomitant knee pathologies often are essential to the success of any single procedure. The use of biologic therapy as an alternative to or to augment more conventional surgical management has increased in popularity in the past decade, and indications for biologic therapy continue to evolve. Orthopaedic surgeons should understand knee joint preservation techniques, including biologic and reconstructive approaches in young, high-demand patients.
PMID: 31411433
ISSN: 0065-6895
CID: 6061242

Siponimod versus placebo in secondary progressive multiple sclerosis (EXPAND): a double-blind, randomised, phase 3 study

Kappos, Ludwig; Bar-Or, Amit; Cree, Bruce A C; Fox, Robert J; Giovannoni, Gavin; Gold, Ralf; Vermersch, Patrick; Arnold, Douglas L; Arnould, Sophie; Scherz, Tatiana; Wolf, Christian; Wallström, Erik; Dahlke, Frank; Achiron, Anat; Achtnichts, Lutz; Agan, Kadriye; Akman-Demir, Gulsen; Allen, Alison B; Antel, Jack P; Antiguedad, Alfredo Rodriguez; Apperson, Michelle; Applebee, Angela M; Ayuso, Guillermo Izquierdo; Baba, Masayuki; Bajenaru, Ovidiu; Balasa, Rodica; Balci, Belgin Petek; Barnett, Michael; Bass, Ann; Becker, Veit U; Bejinariu, Mihaela; Bergh, Florian Then; Bergmann, Arnfin; Bernitsas, Evanthia; Berthele, Achim; Bhan, Virender; Bischof, Felix; Bjork, Randall John; Blevins, Gregg; Boehringer, Matthias; Boerner, Thomas; Bonek, Robert; Bowen, James D; Bowling, Allen; Boyko, Alexey N; Boz, Cavit; Bracknies, Vera; Braune, Stefan; Brescia Morra, Vincenzo; Brochet, Bruno; Brola, Waldemar; Brownstone, Paul Kenneth; Brozman, Miroslav; Brunet, Donald; Buraga, Ioan; Burnett, Margaret; Buttmann, Mathias; Butzkueven, Helmut; Cahill, Jonathan; Calkwood, Jonathan C; Camu, William; Cascione, Mark; Castelnovo, Giovani; Centonze, Diego; Cerqueira, Joao; Chan, Andrew; Cimprichova, Andrea; Cohan, Stanley; Comi, Giancarlo; Conway, Jill; Cooper, Joanna A; Corboy, John; Correale, Jorge; Costell, Brian; Cottrell, David A; Coyle, Patricia K; Craner, Matthew; Cui, Liying; Cunha, Luis; Czlonkowska, Anna; da Silva, Ana Martins; de Sa, Joao; de Seze, Jérôme; Debouverie, Marc; Debruyne, Jan; Decoo, Danny; Defer, Gilles; Derfuss, Tobias; Deri, Norma H; Dihenia, Bhupesh; Dioszeghy, Peter; Donath, Vladimir; Dubois, Benedicte; Duddy, Martin; Duquette, Pierre; Edan, Gilles; Efendi, Husnu; Elias, Stanton; Emrich, Peter J; Estruch, Bonaventura Casanova; Evdoshenko, Evgeniy P; Faiss, Juergen; Fedyanin, Alexander S; Feneberg, Wolfgang; Fermont, Jiske; Fernandez, Oscar Fernandez; Ferrer, Francisco Coret; Fink, Katharina; Ford, Helen; Ford, Corey; Francia, Ada; Freedman, Mark; Frishberg, Benjamin; Galgani, Simonetta; Garmany, George P; Gehring, Klaus; Gitt, Jeffrey; Gobbi, Claudio; Goldstick, Lawrence P; Gonzalez, Rafael Arroyo; Grandmaison, Francois; Grigoriadis, Nikolaos; Grigorova, Olga; Grimaldi, Luigi Maria Edoardo; Gross, Jeffrey; Gross-Paju, Katrin; Gudesblatt, Mark; Guillaume, Daniel; Haas, Judith; Hancinova, Viera; Hancu, Anca; Hardiman, Orla; Harmjanz, Arndt; Heidenreich, Fedor R; Hengstman, G J D; Herbert, Joseph; Herring, Mark; Hodgkinson, Suzanne; Hoffmann, Olaf M; Hofmann, Werner E; Honeycutt, William D; Hua, Le Hanh; Huang, Dehui; Huang, Yining; Huang, DeRen; Hupperts, Raymond; Imre, Piroska; Jacobs, Alan Keith; Jakab, Gabor; Jasinska, Elzbieta; Kaida, Kenichi; Kalnina, Jolanta; Kaprelyan, Ara; Karelis, Guntis; Karussis, Dimitrios; Katz, Amos; Khabirov, Farit A; Khatri, Bhupendra; Kimura, Takashi; Kister, Ilya; Kizlaitiene, Rasa; Klimova, Eleonora; Koehler, Juergen; Komatineni, Aparna; Kornhuber, Anselm; Kovacs, Krisztina; Koves, Agnes; Kozubski, Wojciech; Krastev, Georgi; Krupp, Lauren B; Kurca, Egon; Lassek, Christoph; Laureys, Guy; Lee, Liesly; Lensch, Eckart; Leutmezer, Fritz; Li, Hongzeng; Linker, Ralf A; Linnebank, Michael; Liskova, Petra; Llanera, Cristina; Lu, Jiahong; Lutterotti, Andreas; Lycke, Jan; Macdonell, Richard; Maciejowski, Maciej; Maeurer, Mathias; Magzhanov, Rim V; Maida, Eva-Maria; Malciene, Lina; Mao-Draayer, Yang; Marfia, Girolama Alessandra; Markowitz, Clyde; Mastorodimos, Vasileios; Matyas, Klotild; Meca-Lallana, Jose; Merino, Juan Antonio Garcia; Mihetiu, Ioan Gheorghe; Milanov, Ivan; Miller, Aaron E; Millers, Andrejs; Mirabella, Massimiliano; Mizuno, Masanori; Montalban, Xavier; Montoya, Lilina; Mori, Masahiro; Mueller, Stefanie; Nakahara, Jin; Nakatsuji, Yuji; Newsome, Scott; Nicholas, Richard; Nielsen, A Scott; Nikfekr, Esmaeil; Nocentini, Ugo; Nohara, Chiyoko; Nomura, Kyoichi; Odinak, Miroslav M; Olsson, Tomas; van Oosten, B W; Oreja-Guevara, Celia; Oschmann, Patrick; Overell, James; Pachner, Andrew; Panczel, Gyula; Pandolfo, Massimo; Papeix, Caroline; Patrucco, Liliana; Pelletier, Jean; Piedrabuena, Raul; Pless, Misha; Polzer, Udo; Pozsegovits, Krisztian; Rastenyte, Daiva; Rauer, Sebastian; Reifschneider, Gerd; Rey, Roberto; Rizvi, Syed A; Robertson, Derrick; Rodriguez, Jose Martinez; Rog, David; Roshanisefat, Homayoun; Rowe, Vernon; Rozsa, Csilla; Rubin, Susan; Rusek, Stanislaw; Saccà, Francesco; Saida, Takahiko; Salgado, Antonio Vasco; Sanchez, Victoria Eugenia Fernandez; Sanders, Kalina; Satori, Maria; Sazonov, Denis V; Scarpini, Elio Angelo; Schlegel, Eugen; Schluep, Myriam; Schmidt, Stephan; Scholz, Erich; Schrijver, H M; Schwab, Matthias; Schwartz, Raymond; Scott, James; Selmaj, Krzysztof; Shafer, Stuart; Sharrack, Basil; Shchukin, Ivan A; Shimizu, Yuko; Shotekov, Penko; Siever, Arno; Sigel, Karl-Otto; Silliman, Scott; Simo, Magdolna; Simu, Mihaela; Sinay, Vladimiro; Siquier, Antonio Escartin; Siva, Aksel; Skoda, Ondrej; Solomon, Andrew; Stangel, Martin; Stefoski, Dusan; Steingo, Brian; Stolyarov, Igor D; Stourac, Pavel; Strassburger-Krogias, Katrin; Strauss, Erik; Stuve, Olaf; Tarnev, Ivaylo; Tavernarakis, Antonios; Tello, Cristina Ramo; Terzi, Murat; Ticha, Veronika; Ticmeanu, Marina; Tiel-Wilck, Klaus; Toomsoo, Toomas; Tubridy, Niall; Tullman, Mark J; Tumani, Hayrettin; Turcani, Peter; Turner, Ben; Uccelli, Antonio; Urtaza, Francisco Javier Olascoaga; Vachova, Marta; Valikovics, Attila; Walter, Silke; Van Wijmeersch, Bart; Vanopdenbosch, Ludo; Weber, Joerg R; Weiss, Sara; Weissert, Robert; Vermersch, Patrick; West, Timothy; Wiendl, Heinz; Wiertlewski, Sandrine; Wildemann, Brigitte; Willekens, Barbara; Visser, L H; Vorobeychik, Galina; Xu, Xianhao; Yamamura, Takashi; Yang, Yi N; Yelamos, Sergio Martinez; Yeung, Michael; Zacharias, Alan; Zelkowitz, Marvin; Zettl, Uwe; Zhang, Meini; Zhou, Hongyu; Zieman, Ulf; Ziemssen, Tjalf
BACKGROUND:modulator, on disability progression in patients with SPMS. METHODS:This event-driven and exposure-driven, double-blind, phase 3 trial was done at 292 hospital clinics and specialised multiple sclerosis centres in 31 countries. Using interactive response technology to assign numbers linked to treatment arms, patients (age 18-60 years) with SPMS and an Expanded Disability Status Scale score of 3·0-6·5 were randomly assigned (2:1) to once daily oral siponimod 2 mg or placebo for up to 3 years or until the occurrence of a prespecified number of confirmed disability progression (CDP) events. The primary endpoint was time to 3-month CDP. Efficacy was assessed for the full analysis set (ie, all randomly assigned and treated patients); safety was assessed for the safety set. This trial is registered with ClinicalTrials.gov, number NCT01665144. FINDINGS:1651 patients were randomly assigned between Feb 5, 2013, and June 2, 2015 (1105 to the siponimod group, and 546 to the placebo group). One patient did not sign the consent form, and five patients did not receive study drug, all of whom were in the siponimod group. 1645 patients were included in the analyses (1099 in the siponimod group and 546 in the placebo). At baseline, the mean time since first multiple sclerosis symptoms was 16·8 years (SD 8·3), and the mean time since conversion to SPMS was 3·8 years (SD 3·5); 1055 (64%) patients had not relapsed in the previous 2 years, and 918 (56%) of 1651 needed walking assistance. 903 (82%) patients receiving siponimod and 424 (78%) patients receiving placebo completed the study. 288 (26%) of 1096 patients receiving siponimod and 173 (32%) of 545 patients receiving placebo had 3-month CDP (hazard ratio 0·79, 95% CI 0·65-0·95; relative risk reduction 21%; p=0·013). Adverse events occurred in 975 (89%) of 1099 patients receiving siponimod versus 445 (82%) of 546 patients receiving placebo; serious adverse events were reported for 197 (18%) patients in the siponimod group versus 83 (15%) patients in the placebo group. Lymphopenia, increased liver transaminase concentration, bradycardia and bradyarrhythmia at treatment initiation, macular oedema, hypertension, varicella zoster reactivation, and convulsions occurred more frequently with siponimod than with placebo. Initial dose titration mitigated cardiac first-dose effects. Frequencies of infections, malignancies, and fatalities did not differ between groups. INTERPRETATION:Siponimod reduced the risk of disability progression with a safety profile similar to that of other S1P modulators and is likely to be a useful treatment for SPMS. FUNDING:Novartis Pharma AG.
PMID: 29576505
ISSN: 1474-547x
CID: 5348122

Management of Meniscal Pathology: From Partial Meniscectomy to Transplantation

Pickell, Michael; Jejurikar, Neha; Anil, Utkarsh; Salata, Michael; Davidson, Philip A; Jazrawi, Laith M; Strauss, Eric J
Meniscal tears are common injuries that may result in functionally limiting pain, swelling, and mechanical symptoms. The management of meniscal pathology has evolved as surgeons' understanding of the important role the menisci play in normal knee kinematics increases. Recent emphasis on partial meniscectomy, expanding indications for meniscal repair, and the increased use of meniscal allograft transplantation have helped improve the outcomes of patients with a meniscal tear who undergo treatment. Orthopaedic surgeons should understand meniscal function, pathology, and treatment approaches.
PMID: 31411434
ISSN: 0065-6895
CID: 4042422

Management of Biceps Tendon Pathology: From the Glenoid to the Radial Tuberosity

Frank, Rachel M; Cotter, Eric J; Strauss, Eric J; Jazrawi, Laith M; Romeo, Anthony A
Management of proximal and distal biceps tendon pathology is evolving. The long head of the biceps tendon, if inflamed, may be a pain-producing structure. In appropriately indicated patients, a symptomatic long head of the biceps tendon can be surgically managed via tenotomy, tenodesis, and/or superior labrum anterior to posterior repair. In some patients, primary superior labrum anterior to posterior pathology can be managed via biceps tenodesis. Determining which procedure is most appropriate for and which technique and implant are preferred in a given patient with biceps tendon pathology is controversial. Less debate exists with regard to the timing of distal biceps tendon repair; however, considerable controversy exists with regard to selection of an appropriate surgical technique and implant. In addition, the treatment of patients with a chronic and/or retracted distal biceps tendon tear and patients in whom distal biceps tendon repair fails is extremely challenging. Orthopaedic surgeons should understand the anatomy of, nonsurgical and surgical treatment options for, and outcomes of patients with proximal or distal biceps tendon pathology.
PMID: 31411431
ISSN: 0065-6895
CID: 4042412

When and why should bone marrow concentrate be used to augment bone integration in osteochondral grafting? [Editorial]

Fortier, Lisa A.; Strauss, Eric J.; Kennedy, John G.
ISI:000452891200012
ISSN: 2415-6809
CID: 3700732

Donor-Site-Related Mechanical Symptoms Following Osteochondral Autograft Transfer: A Case Report

Anil, Utkarsh; Strauss, Eric J
CASE/METHODS:A 37-year-old woman presented with repetitive catching of the right knee 4 weeks after implantation of a 2-plug osteochondral autograft into the medial femoral condyle. The workup indicated that the symptoms were secondary to patellar engagement with the donor sites of the lateral aspect of the trochlea. She subsequently underwent osteochondral allograft implantation, resulting in painless, full range of motion with complete resolution of the mechanical symptoms. CONCLUSION/CONCLUSIONS:It is important to consider donor-site morbidity following osteochondral autograft implantation, especially in patients with a relatively narrow distal aspect of the femur. Implantation of osteochondral allograft plugs in the symptomatic donor site is a feasible management option for this rarely reported complication.
PMID: 30601767
ISSN: 2160-3251
CID: 3562852

Knee stiffness following tibial plateau fractures: Predictors and outcomes (OTA-41)

Kugelman, David N; Qatu, Abdullah M; Strauss, Eric J; Konda, Sanjit R; Egol, Kenneth A
OBJECTIVES/OBJECTIVE:What patient characteristics and injury factors predict decreased knee range of motion (ROM) following operative management of tibial plateau fractures? DESIGN/METHODS:Prospective cohort study. SETTING/METHODS:Academic medical center. PATIENTS/METHODS:Over 11 years, tibial plateau fractures at a single academic institution were prospectively followed. A total of 266 patients were included in this study. INTERVENTION/METHODS:Surgical repair of tibial plateau fractures and secondary interventions due to arthrofibrosis. MAIN OUTCOME MEASURE/METHODS:Clinical outcomes were evaluated using the Short Musculoskeletal Function Assessment (SMFA) and range of motion (ROM) at 3-month, 6-month and long-term follow-up. Secondary outcomes were considered as the need for a subsequent procedure due to arthrofibrosis. RESULTS:At 3-month follow-up, the mean ROM was 113°. By long-term follow-up (mean=17 months), the mean ROM improved to 125°. Independent predictors of decreased knee ROM were the following: At 3-month follow-up, open fractures (P=0.047), application of a knee spanning external fixator (P=0.026), orthopaedic poly trauma (P=0.003), and tibial spine involvement (P=0.043). At long-term follow-up, non-Caucasian ethnicity (P=0.003), increasing age (P=0.003), and a deep infection (P=0.002). Ten patients (3.7%required a secondary procedure for arthrofibrosis. There was a significant improvement in the knee ROM (P<0.001) and functional outcomes (P=0.004) following the intervention. CONCLUSIONS:At long-term follow-up, independent predictors of decreased knee ROM were non-Caucasian ethnicity, increasing age, and sustaining a post-operative complication of a deep infection. Secondary interventions were reliable treatments for arthrofibrosis. LEVEL OF EVIDENCE/METHODS:Prognostic level III.
PMID: 30277989
ISSN: 1531-2291
CID: 3327912