Methods

3,155 unilateral primary THAs performed via DA or posterior approaches between 1/1/2017 and 06/30/2019 at nine hospitals and ambulatory surgery centers (ASC) in a large metropolitan healthcare system were retrospectively reviewed. All surgeons were experienced and beyond learning curves. 247 cases were excluded to eliminate confounds. Operating room (OR) in and out times and surgical times were collected via EMR electronic and manual data extraction with verification. Multivariate statistical analyses were utilized with p<0.05 significant.

Methods

A consecutive series of 174 THAs performed without TXA were compared to a consecutive series of 156 THAs performed with topical TXA. Procedures were performed by a single surgeon using identical perioperative medical and pain control protocols. Inpatient pain scores (VAS 0 to 10), opioid consumption (morphine equivalents, Meq), time to first opioid, and drop in hemoglobin (Hgb) were evaluated. Univariate analysis of topical TXA and 20 potential covariates of pain and blood loss was performed, followed by logistic and linear regression with p≤0.250.

Methods

One hundred thirty-one consecutive manual UKAs performed by a single surgeon using a cemented, fixed bearing implant were radiographically reviewed by an independent reviewer to avoid surgeon bias. Native and tibial implant slope and coronal alignment were measured on pre- and postoperative lateral and anteroposterior radiographs, respectively. Manual targets were set within 2° of native tibial slope and 0 to 2° varus tibial component alignment. Deviations from target were calculated as root mean square (RMS) errors and were compared to robotic-assisted UKA data.

Methods

Sixty-one consecutive two-stage resection and reimplantation THAs for PJI between 2011 and 2017 were retrospectively reviewed in a prospectively collected registry database. Patients were categorized with McPherson's Staging System and infection was defined by MSIS criteria. Contemporary standardized protocols were adhered to including implant resection and meticulous surgical debridement, six-week intravenous antibiotics with a high-dose antibiotic spacer, a two-week drug holiday, and laboratory assessment of infection eradication prior to reimplantation. Extended antibiotics after reimplantation were not routinely used. Successful treatment was defined as reimplantation with component retention at minimum two-year follow-up.

Methods

A retrospective review of consecutive TKA's performed by two surgeons was performed. After final components were implanted and balanced, sensor-embedded tibial trials were inserted and kinematic patterns were recorded through range-of-motion. Femoro-tibial contact points were recorded at four distinct flexion points (0°, 45°, 90° and full flexion). Center of rotation kinematic patterns were calculated and categorized as medial pivot, lateral pivot or translation at each measurement range via established criteria. Knees with lateral (L) pivot in early flexion between 0 and 45 ° and medial (M) pivot beyond 90°, regardless of the mid-flexion pivot pattern, formed the experimental group designated as LXM. All other patterns were designated non-LXM and formed the control group. Modern, validated clinical outcome measures (Knee Society Score, EQ5D, UCLA) were obtained preoperatively and at minimum one-year postoperatively.

METHODS

We reviewed data on 185 consecutive primary TKAs in which sensor-embedded tibial trials were used to evaluate kinematic patterns following traditional ligament balancing. Procedures were performed by two board-certified arthroplasty surgeons. The same implant design and surgical approach was used for all knees.

Contact locations on the medial and lateral condyles were recorded for each patient at 0°, 45° and 90° of flexion, and full flexion. Vector equations were created by contact locations on the medial and lateral sides and the vector intersections determined the center of rotation between each measurement position. Center of rotation was calculated as the average of vector intersections at 0 to 45°, 45 to 90°, and 90° to full flexion. If the average center of rotation was between 16 and 1000 mm of the contact location on the medial side it was considered a medial pivot knee. Knees were also classified as medial (16 to 200 mm on medial side), lateral (16 to 200 mm on lateral side), translating (> 200 mm medially or laterally), and other (< 16 mm on both medial and lateral sides). The new Knee Society Scoring System (KSSO objective score, KSSS satisfaction score, KSSF function score), the EQ-5D™ Health Status Index, and the University of California Los Angeles (UCLA) Activity Level Score were measured preoperatively and at minimum one-year follow-up (average 20.4 months).