Similar clinical outcome after unicompartmental knee arthroplasty using a conventional or accelerated care program A randomized, controlled study of 40 patients

被引:14
作者
Borgwardt, Lotte [1 ]
Zerahn, Bo [2 ]
Bliddal, Henning [3 ]
Christiansen, Christian [4 ]
Sylvest, Jesper [5 ]
Borgwardt, Arne [1 ]
机构
[1] Frederiksberg Univ Hosp, Dept Orthopaed Surg, Frederiksberg, Denmark
[2] Copenhagen Univ Hosp, Dept Clin Physiol & Nucl Med, Herlev, Denmark
[3] Frederiksberg Univ Hosp, Parker Inst, Frederiksberg, Denmark
[4] Frederiksberg Univ Hosp, Dept Anaesthesia, Frederiksberg, Denmark
[5] Frederiksberg Univ Hosp, Dept Rheumatol, Frederiksberg, Denmark
关键词
FAST-TRACK; TOTAL HIP; CONTROLLED-TRIAL; REHABILITATION; REPLACEMENT; MANAGEMENT; INTERVENTION; RECOVERY; SYSTEM;
D O I
10.3109/17453670903035559
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Background and purpose Over the last 5 years, there has been increasing interest in reducing length of hospitalization (LOS) through accelerated programs. We examined the clinical outcome of patients undergoing a unicompartmental knee replacement (UKR) in an accelerated care program (A group) compared to a conventional care program (C group). Methods 40 patients randomized into 2 groups were included (A group: 17 patients; C group: 23 patients). Nausea, micturition problems, lower limb dysfunction, pain (VAS), opiate consumption, Knee Society score (KSS), day of discharge, rehospitalization within 3 months, contact with a general physician or nurse, and level of satisfaction were registered. Patients in the A group attended an information meeting. An intraarticular infiltration with Marcaine and adrenaline was used peroperatively. Patients in the C group had an epidural pump for 2 or 3 days. Patients in the A program were treated with NSAID and paracetamol postoperatively. Opiates were used in both groups in the case of breakthrough pain. The patients were considered ready for discharge when they were able to climb stairs to the second floor within 5 min. Results The median length of stay was 1 (1-3) day in the A group and 6 (4-7) days in the C group. The median pain score (VAS) at day 0 was 1 (0-3) in the A group and 5 (0-8) in the C group (p < 0.001). 11/23 of the patients in the C group had weakness of the lower limbs on day I due to the epidural; all patients in the A group were exercising on the day of the operation. Micturition problems necessitating intermediate catherization were more frequent in patients in the C program (19/23) than in patients in the A programme (3/17) (p = 0.001). There were no statistically significant differences between the two groups concerning nausea, average pain on days I and 2, use of opioids (during the first week postoperatively), KSS, contact with primary sector, level of satisfaction, or level of confidence. Interpretation We achieved a reduction in LOS of 5 days without affecting the clinical outcome.
引用
收藏
页码:334 / 337
页数:4
相关论文
共 15 条
[1]
Accelerated recovery for unicompartmental knee replacement - a feasibility study [J].
Beard, DJ ;
Murray, DW ;
Rees, JL ;
Price, AJ ;
Dodd, CAF .
KNEE, 2002, 9 (03) :221-224
[2]
Fast-track cardiac anesthesia in patients with sickle cell abnormalities [J].
Djaiani, GN ;
Cheng, DCH ;
Carroll, JA ;
Yudin, M ;
Karski, JM .
ANESTHESIA AND ANALGESIA, 1999, 89 (03) :598-603
[3]
Fisher DA, 1997, CLIN ORTHOP RELAT R, P155
[4]
Husted Henrik, 2006, Ugeskr Laeger, V168, P2148
[5]
Fast track in total hip and knee arthroplasty - experiences from Hvidovre University Hospital, Denmark [J].
Husted, Henrik ;
Holm, Gitte .
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, 2006, 37 :S31-S35
[6]
INSALL JN, 1989, CLIN ORTHOP RELAT R, P13
[7]
Accelerated rehabilitation after total knee replacement [J].
Isaac, D ;
Falode, T ;
Liu, P ;
I'Anson, H ;
Dillow, K ;
Gill, P .
KNEE, 2005, 12 (05) :346-350
[8]
Kehlet H, 2005, RECENT RES CANCER, V165, P8, DOI 10.1007/3-540-27449-9_2
[9]
Accelerated perioperative care and rehabilitation intervention for hip and knee replacement is effective - A randomized clinical trial involving 87 patients with 3 months of follow-up [J].
Larsen, Kristian ;
Sorensen, Ole Gade ;
Hansen, Torben B. ;
Thomsen, Per B. ;
Soballe, Kjeld .
ACTA ORTHOPAEDICA, 2008, 79 (02) :149-159
[10]
Parvataneni Hari K, 2007, Instr Course Lect, V56, P125