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Acta Ortopedica Brasileira logoLink to Acta Ortopedica Brasileira
. 2022 Jan 28;30(1):e253870. doi: 10.1590/1413-785220223001e253870

THE RESULTS OF A COMPARISON OF A BRAZILIAN AND AN IMPORTED KNEE PROSTHESIS - 5 YEARS OF FOLLOW-UP

OS RESULTADOS DE UMA COMPARAÇÃO DE UMA PRÓTESE DE JOELHO BRASILEIRA E UMA IMPORTADA - CINCO ANOS DE ACOMPANHAMENTO

JOAO HENRIQUE COSTA CALEGARI 1, THIAGO CAVALCANTE COELHO MARQUEZE 1, OMAR SHARID TEIXEIRA EL KADRI 1, EIKE JEFFERSON GALDINO PEREIRA 2, ALEXANDRE OLIVEIRA QUEIROZ 3, PAULO ROBERTO BIGNARDI 2, MARCUS VINICIUS DANIELI 1,2,3, JOÃO PAULO FERNANDES GUERREIRO 1,2,3
PMCID: PMC8979361  PMID: 35431633

ABSTRACT

Introduction

To compare the functional results, satisfaction rates, and revisions of total knee arthroplasties performed by the same surgical team using either Brazilian or imported implants, with a minimum follow-up of 5 years after surgery.

Materials and Methods

A retrospective cohort study analyzing the medical records and interviews of patients who underwent total knee arthroplasty with Brazilian or imported implants with a minimum of 5 years after surgery.

Results

One hundred and fifty patients were evaluated (164 knees). In the functional questionnaire, 71% of patients had favorable answers in the group of patients who underwent surgery using the Brazilian prosthesis and 74.8% in the group with imported implants (p=0.634). There was no statistical difference in satisfaction between the groups, with 78.4% of patients satisfied or very satisfied in the Brazilian implant group and 90.7% in the imported implant group (p=0.053). Loosening of the implants was reported in 5.3% versus 4.7% (p>0.999).

Conclusion

The total knee arthroplasties performed by the same surgical team with a minimum follow-up period of 5 years showed similar levels of satisfaction, function, and complications with both the Brazilian and imported implants. Level of Evidence III, cohort study.

Keywords: Arthroplasty, Replacement, Knee, Knee prosthesis

INTRODUCTION

Degenerative osteoarthritis affects 4% of the Brazilian population 1 . The best solution found to treat advanced knee osteoarthrosis is total arthroplasty and, in developed countries, the increase in arthroplasties already produces relevant social and economic impacts 1 . A large proportion of total knee arthroplasties in our country is performed with imported implants which, thanks to the exchange rate discrepancy, transportation, taxes and import costs, can cost twice the price of the material manufactured in Brazil 2 . Imported implants are widely used abroad, many cases are monitored and have durability rates that reach up to 82% in 25 years 3 . Some Brazilian implants have shown good durability in biomechanical tests 4 , but we do not have large clinical studies with a long follow-up period proving the same durability and results. Some national case series have already demonstrated good results and low revision rate with some Brazilian implants in a medium-term follow-up 5-6 . The choice of implant impacts health care costs and generates a lot of conflicts between surgeons and health managers 7-8 .

Our objective was to evaluate whether there are differences in functional results, satisfaction rates and revisions between Brazilian and imported implants used by the same surgical team and with a minimum follow-up of 5 years after surgery.

Our hypothesis was that there is no difference in satisfaction, function, and revision rates between imported and Brazilian implants used by the same surgical team with a minimum follow-up time of 5 years.

MATERIALS AND METHODS

A retrospective cohort study was carried out with analysis of medical records of 377 patients who underwent total knee arthroplasty using Brazilian and imported implants. All patients were operated on by the same team, which included three knee surgeons, between 2010 and 2015. The data collection took place between August 2020 and June 2021 after approval by the Research Ethics Committee.

The preoperative inclusion criteria were patients with primary osteoarthritis, Ahlbäck classification 9 of arthrosis type 3, 4 and 5. The postoperative inclusion criteria were a minimum follow-up of 5 years and complete medical records. The preoperative exclusion criteria were valgus deformity, osteoarthritis secondary to inflammatory diseases and fracture sequelae. The postoperative exclusion criteria were patellar replacement, use of an implant with preservation of the posterior cruciate ligament, the impossibility of phone contact for interview and patients who did not agree to participate in the phone interview after reading the informed consent form.

The selected cases were subdivided into two groups: “national” when undergoing surgery with the Brazilian implant (MB®️, Meta Bio Ltd., Rio Claro, São Paulo, Brazil) and “imported” when undergoing with the imported implant (NexGen®️, Zimmer, Warsaw, IN, USA). The two models of prosthesis used have a similar design (Figure 1) and compatible surgical instruments. The choice of the type of implant for each patient was based on the option of the surgeon, the patient, and the health plan at the time of surgery.

Figure 1. A and B: Brazilian Implant; C and D: Imported Implant.

Figure 1

In medical records, we searched for the following information: name, gender, date of birth, date of surgery, type of implant used and whether the patient underwent a new surgery (arthrofibrosis release, cleaning without exchange material, osteosynthesis due to peri-prosthesis fracture or revision surgery), if the patient underwent revision surgery, what was the cause (stiffness, infection, aseptic loosening, peri-prosthetic fracture or anterior pain requiring patellar replacement). In the interview with the patient, we searched for new information about treatments or the need for new surgeries not reported in the medical record and asked about the degree of satisfaction with the procedure (very dissatisfied, a little dissatisfied, a little satisfied, satisfied or very satisfied), if he would underwent the surgery again (if yes or no), and if there were symptoms at that moment related to the operated knee (yes or no), what symptoms were present: any difficulty to walk (yes or no), if he could support his body weight on the operated leg (yes or no), if he had any difficulty using stairs (yes or no), any difficulty to squat (yes or no), the presence of knee swelling (yes or no), if he could bend the knee to 90 degrees of flexion (yes or no), if he felt any disturb such as crackles or “noise” when moving the knee (yes or no).

For the analysis of qualitative variables, the Chi-square test or Fisher’s Exact test was used. For quantitative variables, the Shapiro-Wilk test was first applied to verify normality, then the Mann-Whitney test was used for non-normal data and t test for variables with Gaussian distribution. The results were analyzed using the Statistical Package for Social Sciences program (SPSS Inc., Chicago, IL, USA) – 18.0, with a confidence level of 5% being established for all applied tests.

RESULTS

We selected 125 patients (143 knees) that met the inclusion and exclusion criteria. There were 57 patients in national group and 86 in the imported group. The two groups matched in age, sex, and follow up (Table 1).

Table 1. Demographic data.

  National Imported P Value
Age (years) 76,1 ± 6.5 74,8 ± 7,7 0.294
Gender (F/M) 43/14 67/21 0.698
Follow-up (years) 6,85 (5,2 - 9,64)* 6,56 (5,18 - 9,96)* 0.292

*Average (IQR).

Regarding the answers to the functional questionnaire that we created, we found 71% of patients with favorable responses in the group of patients submitted to the Brazilian prosthesis and 74.8% in the group with imported implants, with no statistical difference between the groups (Figure 2). Regarding satisfaction, there was also no statistical difference between the groups with 78.4% of satisfied or very satisfied patients in the group with Brazilian implants and 90.7% in the group of patients with imported prosthesis (Figure 3).

Figure 2. Function Questionnaire (p=0.634).

Figure 2

Figure 3. Satisfaction Index (p=0.053).

Figure 3

Evaluating new surgeries, aseptic loosening and other causes, we found similar rates between the implants (Table 2).

Table 2. Complications.

  National Imported P Value
New surgery 11/57 (19,3%) 12/86 (14,0%) 0.725
Infection 3/57 (5,3%) 4/86 (4,7%) >0,999
Aseptic loosening 3/57 (5,3%) 4/86 (4,7%) >0,999
Arthrofibrosis 2/57 (3,5%) 2/86 (2,3%) >0,999
Fracture 0/57 (0%) 1/86 (1,2%) >0,999
Haematoma 3/57 (5,3%) 1/86 (1,2%) 0,301

DISCUSSION

This study shows that, in a medium-term follow up, the results of surgeries with Brazilian and imported implants performed by the same medical team had statistically similar results regarding satisfaction rate, functional results and complications.

Our results of satisfaction and functional questionnaire were comparable to the national and international literature and regardless the type of implant used 5-6,10-12 . Kahlenberg et al. 12 shows, in a retrospective cohort, similar results of improvement in function and satisfaction among 4069 patients undergoing five of the most common different international brands of implant.

Aseptic loosening rate in this study was 4.8% in the evaluated patients. In a literature review, Labek et al. 13 found a 12% rate of revisions in 10 years in the largest international series. We found good results regarding aseptic loosening in two case series with Brazilian implants with a mean follow-up of 5 years 5-6 and in another national case series that used the imported implant 10 with similar follow-up. Barreto et al. 5 presents in his series 58 knees and no revision due to aseptic loosening. He reports only 3 cases of asymptomatic patients with radiolucents on radiographs. Vasconcelos et al. 6 presents the results of 53 knees and does not report loosening or revisions. Fuchs et al. 10 with imported implants presents 68 knees and 2 cases (2,9%) of aseptic loosening. One case with loosening due to wear of the patellar component and another case in a patient with rheumatoid arthritis.

This study has several limitations. First, the mean follow-up time was 6.6 years, while we predict a durability of more than 15 years in most cases. Second, the number of patients is limited for a retrospective cohort on this topic. Third, we didn’t do any objective functional tests on the patients, just a simplified questionnaire about function, so the patient could understand and answer on the phone. This can make it difficult to compare our results with other studies. Due to the fact that we evaluated a population of patients from the same center and operated by the same team, we believe there was an advantage in making these comparison.

We know that the implant is just one of the factors that lead to a successful procedure 7-8 . There are several other factors that hinder the analysis of the results of arthroplasties in our country, such as: the heterogeneous characteristics of the services that perform arthroplasties; the lack of documentation of results; the low adherence of patients to long-term follow-ups (especially in cases with good results); cultural, structural, and socioeconomic issues that limits the access to medical services 1,14 . Our study showed, as well as the few previous case series using Brazilian implants 5-6 that the Brazilian implant has results comparable to the imported. A better investment in registries and in follow-up of patients using these implants can lead to an increase in the reliability of the Brazilian implant. This can contribute to cost reduction and economic improvement for our healthcare system.

CONCLUSION

Total knee arthroplasty performed by the same surgical team in a minimum follow-up period of 5 years showed similar levels of satisfaction, function, and complications between the Brazilian and imported implants used.

Footnotes

The study was conducted at the Hospital de Ortopedia Uniort.e and the Hospital Evangélico de Londrina.

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Articles from Acta Ortopedica Brasileira are provided here courtesy of Department of Orthopedics and Traumatology, Faculdade de Medicina da Universidade de São Paulo

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