| Literature DB >> 35887663 |
Yaron Bar-Ziv1, Eran Beit Ner1, Konstantin Lamykin1, Ahmad Essa1, Ron Gilat1, Gilad Livshits1, Noam Shohat1, Yiftah Beer1.
Abstract
Kinematic alignment (KA) total knee arthroplasty (TKA) has gained popularity in the past decade, but outcomes of KA-TKA in the valgus knee have never been specifically evaluated. In this retrospective single institution study, we analyzed patient reported outcomes and radiographic measurements at minimum 2 years following KA-TKA for valgus knees (n = 51) and compared the results to KA-TKA performed for non-valgus knees (n = 275). The same approach, technique, and implants were used in both groups without the need to release soft tissues or use constrained implants. Surgery duration was similar between groups (p = 0.353). Lateral distal femoral angle was lower in the valgus group postoperatively (p = 0.036). In both groups significant improvement was seen in relieving pain and improving function, while average scores were superior in the non-valgus group for visual analog score (p = 0.005), oxford knee score (p = 0.013), and knee injury and osteoarthritis outcome score (p = 0.009). However, these differences did not translate to statistically significant differences in minimal clinical important difference achievement rates. In conclusion, KA-TKA is efficient in relieving pain and improving function, as reported in subjective questionnaires, and holds advantage in patients with valgus alignment by avoiding soft tissue releases and use of constrained implants. Future studies should examine whether bone loss occurs in the lateral distal femur.Entities:
Keywords: arthroplasty; clinically significant outcomes; function; kinematic alignment; patient reported outcomes; valgus
Year: 2022 PMID: 35887663 PMCID: PMC9318663 DOI: 10.3390/jpm12071164
Source DB: PubMed Journal: J Pers Med ISSN: 2075-4426
Figure 1A 76-year-old female with a preoperative valgus alignment (a). Postoperative radiographic analysis shows a MPTA of 88.1°, LDFA of 83.9°, and HKA of 3.9° (b).
Baseline characteristics, operative factors, and patient reported outcomes in the valgus versus non-valgus groups.
| Variable | Non-Valgus ( | Valgus ( | |
|---|---|---|---|
| Age | 70.37 (8.08) | 70.53 (9.01) | 0.905 |
| Gender (female) | 172 (62.5%) | 39 (76.5%) | 0.058 |
| BMI (kg/m) | 29.86 (4.95) | 32.09 (4.92) | 0.005 |
| CCI | 0.85 (1.08) | 1.15 (1.39) | 0.142 |
| Anesthesia (spinal) | 204 (74.2%) | 32 (62.7%) | 0.124 |
| Operative duration | 82.63 (19.28) | 86.61 (29.02) | 0.353 |
| LOS | 4.09 (2.24) | 4.65 (3.61) | 0.292 |
| Extension | 4.32 (5.42) | 3.53 (4.59) | 0.523 |
| Flexion | 110.48 (15.38) | 106.18 (18.75) | 0.378 |
| VAS | 8.044 (1.45) | 8.314 (1.33) | 0.195 |
| OKS | 13.40 (7.61) | 14.21 (7.84) | 0.497 |
| KOOS TOTAL | 28.64 (15.10) | 28.66 (14.69) | 0.992 |
| KOOS SYMPTOMS | 40.49 (20.74) | 43.02 (22.15) | 0.431 |
| KOOS PAIN | 31.78 (18.95) | 39.16 (17.60) | 0.010 |
| KOOS FUNCTION | 30.32 (15.28) | 32.39 (17.29) | 0.385 |
| KOOS QOL | 16.32 (8.78) | 14.90 (9.10) | 0.293 |
| Time to Follow Up (m) | 40.18 (9.56) | 38.03 (10.00) | 0.144 |
(BMI) Bone Mass Index; (CCI) Charlson Comorbidity Index; (LOS) Length of Stay; (KOOS) Knee injury and Osteoarthritis Outcome Score; (OKS) Oxford Knee Score; (VAS) Visual Analog Scale; (m) months.
Preoperative and postoperative alignment in the valgus and non-valgus groups.
| Preoperative | Postoperative | |||||
|---|---|---|---|---|---|---|
| Non-Valgus ( | Valgus ( | Non-Valgus ( | Valgus ( | |||
| MPTA | 84.33 (3.08) | 89.32 (2.74) | <0.001 | 86.32 (3.11) | 87.05 (3.11) | 0.127 |
| LDFA | 90.10 (3.8) | 86.64 (3.6) | <0.001 | 84.94 (4.1) | 83.59 (4.40) | 0.036 |
| HKA * | −10.78 (4.79) | 5.92 (4.26) | <0.001 | −2.83 (2.81) | 1.36 (4.18) | <0.001 |
| Slope | 11.42 (5.59) | 9.03 (4.44) | <0.001 | 7.01 (4.05) | 7.37 (3.15) | 0.545 |
MPTA (medial proximal tibial angle); LDFA (lateral distal femoral angle); HKA (hip knee angle). * Minus represents varus.
Figure 2Mean (and SD) patient reported outcome scores in the valgus (green columns) versus non-valgus (blue columns) groups; (KOOS) Knee injury and Osteoarthritis Outcome Score; (OKS) Oxford Knee Score; (VAS) Visual Analog Scale; (QOL) Quality of Life.
Number and percentage of patients achieving minimal clinical differences (MCID) of the oxford knee score (OKS) and the Knee injury and Osteoarthritis Outcome Score (KOOS) sub-categories in the valgus versus non-valgus groups.
| MCID | Non-Valgus ( | Valgus ( | |
|---|---|---|---|
| OKS | 262 (95.4%) | 48 (93.9%) | 0.707 |
| KOOS SYMPTOMS | 231 (83.9%) | 42 (82.4%) | 0.831 |
| KOOS PAIN | 215 (78.3%) | 35 (68.6%) | 0.189 |
| KOOS FUNCTION | 236 (85.7%) | 42 (82.4%) | 0.654 |
| KOOS QOL | 243 (88.2%) | 46 (90.2%) | 0.804 |
(KOOS) Knee injury and Osteoarthritis Outcome Score; (OKS) Oxford Knee Score; (QOL) Quality of Life.