Patients
We conducted a single-center, retrospective cohort study of patients with follow-up. From January 2014 to December 2017, 21 patients with SA of the hip were eligible for enrolment in our study. Among them, 1 patient decided to leave the hospital and was treated in the local hospital after being diagnosed. A total of 20 patients were finally included. Inclusion criteria were patients who 1) were aged ≥ 18 years; 2) had a definite diagnosis of acute SA of the hip joint; 3) were advanced SA with destruction of hip joint; and 4) had a set of complete medical records (including nursing records), preoperative and postoperative radiographs. Exclusion criteria were patients who 1) were early SA of hip; 2) were multiple arthritis; 3) had incomplete medical records; 4) were not willing to be followed up, 5) had immune deficiency.
Patient diagnosis
Patients with SA of the hip had clinical symptoms of infection including pain, sudden chills and fever; local swelling, and limited range of motion. In addition, complete blood cell count (CBC), C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) were measured. X-ray, CT and MRI were also performed. X-ray showed narrowing of the hip joint space for advanced SA of the hip. CT could detect local edema, osteonecrosis, osteomyelitis, and hip bone destruction. MRI provided good resolution for the detection of joint effusion, bone differentiation, and soft tissue infection. MRI findings of SA patients include joint effusion, cartilage and bone destruction, soft tissue abscess and bone edema [10] (Fig. 1–3). The diagnosis of SA synthesized the results of these tests. If the patient was suspected of having septic arthritis, PPD test, Brucella agglutination test and needle aspiration of the hip were then added. The patient should accept an procedure according to patent’s willing once sepsis is confirmed via aspiration [11].
Surgical technique
All of the 20 patients (20 hips) underwent two-stage surgeries. Among them, 9 cases underwent debridement, 11 cases underwent antibiotic-loaded spacer implantation in the first stage. After a period of time, THA was conducted in all patients in the second stage. Therefore, two procedures were named as debridement with THA group and spacer implantation with THA group, respectively. Patients chose one of two procedures according to patent’s willing. All operations were performed by four professional surgeons in our department.
During the first stage, posterolateral approach was performed in all patients. Debridement was performed in 9 patients (9 hips) and femoral head resection with antibiotic-loaded spacer implantation were performed in 11 patients (11 hips). The inflamed soft tissues, necrotic bones, abscesses, and sinus tracts were totally debrided during the first stage. Then the specimens were taken for pathological examination and tissue bacterial culture. For patients undergoing debridement, irrigation tube were placed in operation and continued to be rinsed with gentamicin solution after operation but not in patients with antibiotic-loaded spacer implantation. For patients undergoing femoral head resection and antibiotic-loaded spacer implantation, femoral head were removed and a cement spacer containing gentamicin were installed (Fig. 1). Susceptible antibiotic drugs were given to patients based on the results of bacterial culture until serological results return to normal. Symptoms disappeared 2 weeks later. Empirical antibiotics (ceftriaxone) was used in patients with negative bacterial culture results [11, 10]. CBC, CRP and ESR were detected for weekly regular monitoring. Patients stopped antibiotic usage and discharged once the vital signs and serological indicators was basically normal and the infection was eradicated. If there was pain in the affected limb within 24–48 hours after operation, patient was conducted for traction of the affected limb. After 48 hours, patient strengthened functional exercise [10, 12].
During the second-stage, all procedures were performed via the posterolateral approach, with the patient in a lateral position.When the joint was opened, no pus and no inflammatory edema of soft tissue around the joint was confirmed under the naked eye. Then the hypertrophic soft tissue and scar was removed as thoroughly as possible in the direct visualization. Odophor and hydrogen peroxide were used ito immerse the hip joint cavity to reduce the probability of infection. Titanium Acetabular Reconstruction Cup was used for 2 cases with deficient acetabular wall, which was fixed with screws. Then acetabular impactors were used to perform impaction graft. The gap between cup and host bone was completely filled by allogeneic morselized bone. On completion of cage placement and bone grafts, an acetabular polyethylene liner was fixed with high radiopaque bone cement conting gentamicin. In addition, central acetabular defect in 3 patients were performed graft impaction using acetabular impactors, and a larger acetabular cup was implanted. Besides, 1 patient had a high hip dislocation secondary to SA of the hip. Structural autograft obtained from the femoral neck was implanted on the patien’s upper acetabular bone and fixed with screws. The remaining 15 patients were operated normal THA. The usage of antibiotics dependeded on the susceptibility of the first-stage organism identified in joint fluid culture. Antibiotics were chosen empirically if no organism was identified.
Data collection
The scanning edition of electronic medical records were reviewed in detail to retrieve pertinent information, including demographic data (gender, age, height and weight), the preoperative and postoperative clinical evaluation (CBC, CRP and ESR), imaging evaluation (X-ray, CT and MRI), Harris hip score and VAS pain score. Clinical data were all recorded during follow-up.
Follow up
Anteroposterior and lateral radiographs of the hip, full-length view of the lower extremities, CT and MRI of the hip were taken for the pre-operation. In our department, patients were required to have regular follow-up in the 1st month, the 3rd month, the 6th month and the 12th month after operation. Anteroposterior and lateral radiographs of the hip were taken at each follow-up. All of the 20 patients had adequate preoperative and postoperative imaging examinations.
Statistical analysis
All data were performed using SPSS 19.0 software (IBM, Armonk, NY, USA). Quantitative data were described using means ± standard deviation (SD). Mann-Whitney U test was used to compare continuous categorical variables, including Harris hip score and VAS pain score between the two groups. A P value of less than 0.05 were considered statistically significant.