1988
DOI: 10.1177/107110078800800603
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New Jersey Low Contact Stress Total Ankle Replacement: Biomechanical Rationale and Review of 23 Cementless Cases

Abstract: A congruent contact, unconstrained, multiaxial ankle replacement has been developed for use without cement. A talar onlay component with a trochlear surface and central fixation fin uses a cylindrical articulating axis that reproduces the lateral talar curvature. A tibial inlay component with a 7 degree anteriorly inclined short fixation stem uses a flat loading plate, recessed anatomically into the distal tibia to distribute tibial loads to the ankle joint. For both components, made of cast cobalt-chromium-mo… Show more

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Cited by 197 publications
(83 citation statements)
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“…2 This graph shows the distribution of the outcome instruments used among the TAA studies in this review. AOFAS = American Orthopaedic Foot and Ankle Society hindfoot score (region-specific) [21]; VAS pain = visual analog scale pain; SF-36 = Short Form 36 (generic) [43]; NJOH = New Jersey Orthopaedic Hospital ankle score (region-specific) [5]; Evanski = outcome instrument of Evanski and Waugh [11]; Takakura = outcome instrument of Takakura et al [39]; Mazur = outcome instrument of Mazur et al [29]; FFI = Foot Function Index (region-specific) [3]; AOS = Ankle Osteoarthritis Scale (disease-specific) [9]; MFA = Musculoskeletal Functional Assessment (generic) [10]; UCLA = University of California at Los Angeles activity scale (physical activity assessing) [31]; ''Oxford'' = questionnaire (region-specific) developed by the authors [18], modeled to the original Oxford Hip Score [7]; IPAQ = International Physical Activity Questionnaire (physical activity assessing) [31]; HAQ = Health Assessment Questionnaire (generic) [12]. [4]; AOS = Ankle Osteoarthritis Scale [9]; ICC = intraclass correlation coefficient; total = total score; pain = pain subscale; limit = limitations subscale; disab = disability subscale.…”
Section: Discussionmentioning
confidence: 99%
“…2 This graph shows the distribution of the outcome instruments used among the TAA studies in this review. AOFAS = American Orthopaedic Foot and Ankle Society hindfoot score (region-specific) [21]; VAS pain = visual analog scale pain; SF-36 = Short Form 36 (generic) [43]; NJOH = New Jersey Orthopaedic Hospital ankle score (region-specific) [5]; Evanski = outcome instrument of Evanski and Waugh [11]; Takakura = outcome instrument of Takakura et al [39]; Mazur = outcome instrument of Mazur et al [29]; FFI = Foot Function Index (region-specific) [3]; AOS = Ankle Osteoarthritis Scale (disease-specific) [9]; MFA = Musculoskeletal Functional Assessment (generic) [10]; UCLA = University of California at Los Angeles activity scale (physical activity assessing) [31]; ''Oxford'' = questionnaire (region-specific) developed by the authors [18], modeled to the original Oxford Hip Score [7]; IPAQ = International Physical Activity Questionnaire (physical activity assessing) [31]; HAQ = Health Assessment Questionnaire (generic) [12]. [4]; AOS = Ankle Osteoarthritis Scale [9]; ICC = intraclass correlation coefficient; total = total score; pain = pain subscale; limit = limitations subscale; disab = disability subscale.…”
Section: Discussionmentioning
confidence: 99%
“…The control group consisted of 11 healthy participants without any impairment of the lower extremities. Inclusion criteria for the TAA group were: a primary diagnosis of osteoarthritis or rheumatoid arthritis of the ankle joint; a good clinical outcome as defined by ankle scores of more than 80 points 6 on both the Low Contact Stress (LCS) ankle score (Buechel, Pappas, & Iorio, 1988) and the American Orthopaedic Foot and Ankle Society (AOFAS) ankle-hindfoot score (Kitaoka et al, 1994). Furthermore, alignment of the ankle-hindfoot complex should be neutral and range-of-motion, as measured by manual goniometry, should be a minimum of 10 degrees of dorsiflexion and 20 degrees of plantarflexion.…”
Section: Participantsmentioning
confidence: 99%
“…The first report is a 29 year follow-up of the first cementless mobile-bearing shallow-sulcus device developed by the authors in 1978 [11]. The second report describes the improved deep-sulcus device [12] developed in 1989 which has functioned well for 22 years in this patient.…”
Section: Introductionmentioning
confidence: 99%