| Literature DB >> 23248725 |
Seema Malvankar1, Wasim S Khan, Anant Mahapatra, George Se Dowd.
Abstract
Lateral wedges were originally proposed to manage medial compartment osteoarthritis of the knee but recent reviews suggest that lateral wedges do not affect disease progression. We performed a systematic review to analyse the recent literature and define how effective, if at all, lateral wedges are in the management of medial compartment osteoarthritis of the knee. The inclusion criteria were defined as any study published within the last decade, using a sample size of at least twenty patients, and investigating the effect of insoles or wedges on either unilateral or bilateral knee varus osteoarthritis. The standardised keyword term 'lateral*wedge*OR insole*OR orthotic* OR medial compartment OR varus OR osteoarthri* OR knee*' was used. We identified 10 studies that fitted our inclusion criteria. Although there is not enough evidence in the literature to prove that lateral wedge orthotics are an effective treatment for varus osteoarthritis of the knee, there is some evidence to suggest that they do have some symptomatic effect. Patients with early osteoarthritis and higher BMI may benefit to a greater extent than those with a greater extent of degenerative changes and lower BMI. The literature is unclear as to what the optimal duration for the use of lateral wedges is, but does support the prolonged use of the wedges as the benefits at one month are maintained at one year. Future studies should be randomised controlled trials with a large sample size with long follow-up, and use objective clinical, biomechanical and radiological outcome measures.Entities:
Keywords: Osteoarthritis; knee; lateral wedge; orthotic.; varus
Year: 2012 PMID: 23248725 PMCID: PMC3522189 DOI: 10.2174/1874325001206010544
Source DB: PubMed Journal: Open Orthop J ISSN: 1874-3250
Details of the 10 Studies Identified Including Type of Study, Number of Subjects and Numbers Lost to Follow-Up, Duration of Follow-Up and Outcome Measures Used
| Study | Type of Study | Number of Subjects | Number of Subjects Lost to Follow-Up | Follow-Up | Outcome Measures Used |
|---|---|---|---|---|---|
| Pham | Prospective double-blind randomised control trial | 156 | 50 | 2 years | Patients’ overall assessment of disease activity (5 grade scale), WOMAC index subscales and need for concomitant treatments. |
| Butler | Prospective single-blind randomised control trial | 30 | N/A | N/A | Gait analysis study with kinematic and force measurements to determine the hind foot, knee and hip moment. |
| Kakihana | Prospective non randomised, cross-over study | 70 | N/A | N/A | Gait analyses to determine the knee and subtalar joint moments, and centre of pressure. Blinded radiological assessment with Kellgren and Lawrence grading. |
| Shimada | Prospective case-control study | 65 | N/A | N/A | Gait analyses study that measured peak external adduction moment at the knee during the stance phase of gait and the first acceleration peak after heal strike at the lateral side of the femoral condyles. Kellgren and Lawrence grading system for radiographic assessment of osteoarthritis. |
| Baker | Prospective double-blind randomised crossover trial | 90 | 4 | 16 weeks | WOMAC pain and disability scale, the overall knee pain with a 50 feet walk and any medication for knee pain taken. |
| Toda | Prospective randomised control trial | 81 | 0 | 2 weeks | Femorotibial angle on blinded weight-bearing radiographs, and the remission scores of the Lequesne index. |
| Hinman | Prospective randomised control trial | 20 | 0 | 1 month | Gait analyses study measuring knee adduction moments and adduction angular impulse. |
| Barrios | Prospective single-blinded block randomised control trial | 66 | 10 | 1 year | WOMAC index, six minute walk distance and pain change, and chair negotiation time and pain change. |
| Toda | Prospective single-blinded block randomised control trial | 227 | 20 | 12 weeks | Pain using the Lequesne index and the Visual analogue score (VAS), and last assessment of material wear of the insole. |
| Toda | Prospective randomised control trial | 90 | 0 | 8 weeks | Femorotibial angle and talar tilt angle using weight-bearing radiographs, and VAS. |