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Pain at the tip of the stem after revision total knee arthroplasty

Abstracts

OBJECTIVE: To correlate parameters of implants with incidence of pain. METHODS: 32 knees (31 patients) operated on between 2006 to 2008 in a serie of cases of TKA revision surgery were monitored for evidence of pain at the tip of the stem.In all we used uncemented stem Scorpio TS Total Knee® Revision System (Stryker®). Criteria assessed: pain in the leg or thigh without other causes, diameter and length of the nail; position of the rod in the medullary canal, intramedullary canal diameter. RESULTS: Mean age was 66.7 years and mean follow-up was 2.6 years.21,87% of patients reported leg pain, 9.37% thigh pain. The group of pacients with leg pain presented with shaft diameter 14.7 mm, length 80 mm in 71.42% and 155 mm in 28,58%, stem diameter/ intramedullary canal diameter average relation of 0,76, 42.8% had stem malalignment. The group without leg pain presented with shaft diameter 15.2 mm, length 80 mm in 68% and 155 mm in 32%, diameters average relation of 0.80, 20.8% had stem malalignment. The group with thigh pain presented with shaft diameter 18.3 mm, length 80 mm in 66.67% and 155 mm in 33,33%,diameters average relation of 0.75, 0% had stem malalignment The group without thigh pain presented with shaft diameter 16.56 mm, length 80 mm in 70.37% and 155 mm in 29,63%, diameters average relation of 0.79, 14,2% had stem malalignment. CONCLUSION: There was no association between the assessed criteria and pain in the tip of the stem.

Arthroplasty, Replacement, Knee; Knee Joint; Pain


OBJETIVO: Correlacionar parâmetros dos implantes com incidência de dor. MÉTODOS: 32 joelhos (31 pacientes), operados entre 2006-2008 em uma série de casos de cirurgia de revisão de ATJ, foram acompanhados quanto ao surgimento de dor na ponta da haste. Em todos utilizou-se haste não cimentada Scorpio® TS Total Knee Revision System (Stryker®). Critérios analisados: presença de dor na perna ou coxa sem outras causas; diâmetro e comprimento da haste utilizada; posicionamento da haste no canal medular; e diâmetro do canal intramedular. RESULTADOS: A idade média foi de 66,7 anos e o seguimento médio foi de 2,6 anos. Dos pacientes, 21,87% referiram dores na perna, 9,37% na coxa. O grupo com dor na perna apresentou haste com diâmetro médio de 14,7mm; comprimento de 80mm em 71,42% e de 155mm em 28,58%, relação diâmetro da haste/diâmetro do canal intramedular média de 0,76, 42,8% apresentavam mau alinhamento. O grupo sem dor na perna apresentou haste com diâmetro de 15,2mm; comprimento de 80mm em 68% e de 155mm em 32%, relação dos diâmetros 0,80, 20,8% apresentavam mau alinhamento. O grupo com dor na coxa apresentou haste com diâmetro de 18,3mm; comprimento de 80mm em 66,67% e de 155mm em 33,33%, relação dos diâmetros 0,75, 0% apresentou mau alinhamento. O grupo sem dor na coxa apresentou haste femoral com diâmetro de 16,56mm; comprimento de 80mm em 70,37% e de 155mm em 29,63%, relação dos diâmetro de 0,79, 14,2% apresentavam mau alinhamento. CONCLUSÃO: Não houve associação entre os critérios avaliados e dor na região da ponta da haste.

Artroplastia do Joelho; Articulação do Joelho; Dor


ORIGINAL ARTICLE

Pain at the tip of the stem after revision total knee arthroplasty

Rômulo Ballarin AlbinoI; Lívia Souza SantosII; Riccardo Gomes GobbiIII; Maurício IamaguchiIII; Marco Kawamura DemangeIII; Luis Eduardo TiricoIII; José Ricardo PécoraIV

IResident Physicians of the Institute of Orthopedics and Traumatology, HC/FMUSP

IIResident Physicians of the Institute of Orthopedics and Traumatology, HC/FMUSP

IIIAssistant Physicians of the Institute of Orthopedics and Traumatology, HC/FMUSP

IVAssistant Physician and Head of the Knee Group of the Institute of Orthopedics and Traumatology, HC/FMUSP

Correspondence

ABSTRACT

OBJECTIVE: To correlate parameters of implants with incidence of pain.

METHODS: 32 knees (31 patients) operated on between 2006 to 2008 in a serie of cases of TKA revision surgery were monitored for evidence of pain at the tip of the stem.In all we used uncemented stem Scorpio TS Total Knee ® Revision System (Stryker ®). Criteria assessed: pain in the leg or thigh without other causes, diameter and length of the nail; position of the rod in the medullary canal, intramedullary canal diameter.

RESULTS: Mean age was 66.7 years and mean follow-up was 2.6 years.21,87% of patients reported leg pain, 9.37% thigh pain. The group of pacients with leg pain presented with shaft diameter 14.7 mm, length 80 mm in 71.42% and 155 mm in 28,58%, stem diameter/ intramedullary canal diameter average relation of 0,76, 42.8% had stem malalignment. The group without leg pain presented with shaft diameter 15.2 mm, length 80 mm in 68% and 155 mm in 32%, diameters average relation of 0.80, 20.8% had stem malalignment. The group with thigh pain presented with shaft diameter 18.3 mm, length 80 mm in 66.67% and 155 mm in 33,33%,diameters average relation of 0.75, 0% had stem malalignment The group without thigh pain presented with shaft diameter 16.56 mm, length 80 mm in 70.37% and 155 mm in 29,63%, diameters average relation of 0.79, 14,2% had stem malalignment.

CONCLUSION: There was no association between the assessed criteria and pain in the tip of the stem.

Keywords - Arthroplasty, Replacement, Knee; Knee Joint; Pain

INTRODUCTION

Total knee arthroplasty (TKA) is an effective procedure for controlling pain and improving the quality of life of patients with advanced-stage arthrosis. TKA revision surgery, which is necessary in cases of loosening, infection, material failure and periprosthetic fracture, is a challenge to surgeons because of the technical difficulty and because the functional and patient satisfaction results are inferior to the results from primary prostheses(1,2). IN an attempt to improve stability and facilitate alignment, present-day knee revision prosthesis models provide the option of using an intramedullary nail in the tibial and femoral components(3).

It has been noted that, after primary and revision arthroplasty, some patients persist with pain after the surgery. Even after investigation with physical examinations, imaging examinations and laboratory tests in an attempt to find a triggering factor such as poor positioning, loosening, instability and inflammatory or infectious causes, many cases of pain remain without defined etiology. Pain located in the diaphyseal portion of the femur and tibia has been correlated with the presence of the nail in revision arthroplasty(4,5). Likewise, pain in the thigh has been correlated with hip arthroplasty, and variations in the material, design, size and module of elasticity have been regarded as possible associated factors(6-9).

The objectives of this study were to analyze the incidence of pain at the nail tip in patients who underwent knee arthroplasty revision at our service between 2006 and 2008 and to investigate a possible relationship between pain at the nail tip and the percentage filling of the medullary canal or nail length.

MATERIALS AND METHODS

We followed up 31 patients who underwent TKA revision surgery between 2006 and 2008, who were evaluated prospectively regarding occurrences of lower-leg and thigh pain that possibly resulted from the intramedullary nails of the implants.

All the patients were operated using tibial and femoral implants that included uncemented nails (Scorpio® TS Total Knee Revision System; Stryker®).

In all the patients, we evaluated the following parameters:

- component positioning

- nail length

- nail diameter

- medullary canal diameter, measured by means of radiographs

- nail diameter, measured by means of radiographs

- nail positioning in relation to the orientation of the diaphysis

- occurrences of pain in the lower leg resulting from the nail

- occurrences of pain in the thigh resulting from the nail.

All the data relating to implant size were registered during the surgical procedures.

Information on the diameter and length of the nails used was specified in the surgical register and obtained from the medical file (real measurements of the implants). We analyzed the degree of filling of the tibial medullary canal by the nail, using the following method: the diameters of the nail and medullary canal were measured with a ruler on radiographs, and the point chosen for this was the end of the intramedullary nail. Both of these were measured directly from the radiographs, in order to avoid errors in comparing the real value of the nail diameter (not subject to radiographic megnification) with the value of the medullary canal diameter on the radiograph (subject to this effect). The percentage filling of the medullary canal by the nail was then calculated.

The nail positioning was evaluated from radiographs. Positioning that showed abnormalities in the coronal plane (varus and valgus) and sagittal plane (anteroposterior deviation) of the nail in relation to the orientation of the tibial diaphysis was considered to be inadequate.

To analyze the data, the patients were divided into groups according to the following criteria: presence or absence of pain in the thigh and presence or absence of pain in the lower leg (Figure 1).


For the statistical analysis on the data relating to diameter and percentage filling, the t test was used. For the data on nail length and positioning, the x²(chi-square) test was used.

RESULTS

Thirty-one patients were evaluated, of whom 17 were women and 14 were men (total of 32 knees, given that one male patient underwent bilateral revision arthroplasty), with a mean age of 66.7 years (patients with ages ranging from 45 to 82 years).

After evaluation and follow-up (mean follow-up of 2.6 years), we observed that three patients (three knees) or 9.37% presented thigh pain and seven patients (seven knees) or 21.87% presented lower-leg pain, with different intensities. Two patients (two knees) or 6.25% presented thigh and lower-leg pain simultaneously; and eight patients (eight knees) or 25% presented diaphyseal pain, independent of the site (Box 1).


The group of patients with lower-leg pain presented a mean diameter of the tibial nail of 14.7 mm (range: 13 to 18 mm); the nail length was 80 mm in 71.42% and 155 mm in 28.58% of the patients; and the mean diameter of the medullary canal was 15.6 mm (range: 12 to 18 mm). The ratio of nail diameter/mean intramedullary canal diameter was 0.76. Three patients or 42.8% presented poor nail alignment.

The group of patients without lower-leg pain presented a mean diameter of the tibial nail of 15.2 mm (range: 10 to 21 mm); the nail length was 80 mm in 68% and 155 mm in 32% of the patients; and the mean diameter of the medullary canal was 17.7 mm (range: 13 to 21 mm). The ratio of nail diameter/mean intramedullary canal diameter was 0.79. Five patients or 20.8% presented poor nail alignment.

The group of patients with thigh pain presented a mean diameter of the femoral nail of 18.3 mm (range: 14 to 23 mm); the nail length was 80 mm in 66.67% and 155 mm in 33.33% of the patients; and the mean diameter of the medullary canal was 31.0 mm (range: 21 to 38 mm). The ratio of nail diameter/mean intramedullary canal diameter was 0.75. None of the patients presented poor nail alignment.

The group of patients without thigh pain presented a mean diameter of the femoral nail of 16.56 mm (range: 13 to 23 mm); the nail length was 80 mm in 70.37% and 155 mm in 29.63% of the patients; and the mean diameter of the medullary canal was 21.1 mm (range: 12 to 34 mm). The ratio of nail diameter/mean intramedullary canal diameter was 0.79. Four patients or 14.2% presented poor nail alignment (Tables 1 and 2).

DISCUSSION

Pain at the nail tip after TKA revision is a frequent complication. Barrack(4) observed that the incidence of pain at the nail tip was 11% in the femur and 14% in the tibia, while in the present study we observed that 9.37% of the cases presented pain in the femoral nail and 21.87% in the tibial nail. With the growing numbers of TKA revisions, this may be a worrying problem and the causes need to be correctly established. The large difference in Young's modulus of elasticity between the nail tip and the bone at their point of contact may be the main factor causing the pain, especially if associated with deficient fixation of the metaphysis(4,7-12). The factors that increase the modulus of elasticity of the nail tip relate to the material used and to increasing nail diameter. The contact pressure between the nail tip and the bone increases in relation to the implant geometry, bone geometry and great degrees of filling of the intramedullary canal by the implant.

The first point for discussion was how to determine whether there is any pain at the nail tip without significant errors. For this, before assessing the patients, we gave them explanations regarding the difference between pain in the diaphyseal region of the femur or tibia, called pain at the nail tip, and other possible pains in the knee and hip regions. Furthermore, the physician who made the assessments was the same in all cases, to avoid inter-observer subjectivity. Anamnesis and detailed clinical examination were conducted.

We had imagined that nails of greater diameter would correlate with greater incidence of pain. However, we did not observe any association between the incidence of pain and the diameters of the nails, or between the pain and the ratio of filling of the medullary canal with the nail.

The intramedullary canals of the femur and tibia present progressively smaller diameters going away from the knee, i.e. with a shape resembling a funnel. They are widest in the metaphyseal region and reach a parallel-sided shape bordered by cortical bone in the diaphyseal region. Thus, from a geometrical and biomechanical point of view, a short "press fit" nail presents a greater chance of becoming supported in the metaphyseal-diaphyseal region, thus concentrating the stress and causing a painful area in this region. Theoretically, it would be expected that a longer nail would cause less pain, since its tip would be located in a region where the cortical bone walls were more parallel, with less concentration of the forces. On the other hand, during our follow-up, we did not observe any association between occurrences of pain and the lengths of the femoral and tibial nails.

In relation to inadequate nail positioning (lack of parallelism between the nail and the cortical bone), we again did not observe any association between these parameters and occurrences of complaints of pain. In these cases, a concentration of mechanical stress may form at the point of contact between the nail and cortical bone, which may induce greater incidence of pain. Despite this, we did not observe any statistically significant correlation in any of the parameters evaluated.

Some new types of implant have been developed, with slits at the nail tip in the coronal plane for the femur and the sagittal plane for the tibia, or with slits in both planes(13). These implants tend to diminish the modulus of elasticity of the nail tip and decrease the chance of a painful point of contact, but the benefits have not yet been scientifically proven.

For as long as the causes of thigh and lower-leg pain in patients undergoing TKA revision using nails are not clearly understood, further studies will be needed to try to elucidate the causes. This, together with the development of new materials and changes to prosthesis design, may lead to lower rates for the frequent complaint of diaphyseal pain.

CONCLUSION

Pain reported in the region of the tip of the femoral or tibial nail is a very common complication after TKA revision, and it affects more than 20% of the patients. There was no association between the diameter or length of the fixation nail and pain in the region of the nail tip. There was also no association between the ratio of nail diameter/intramedullary canal diameter and pain at the nail tip, or in relation to nail positioning.

REFERENCES

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  • Correspondência:

    Rua Dr. Ovídio Pires de Campos, 333, Cerqueira César – 05403-010 – São Paulo, SP.
    E-mail:
    Trabalho realizado no LIM 41 – Laboratório de Investigação Médica do Sistema Musculoesquelético do Departamento de Ortopedia e Traumatologia da Faculdade de Medicina da Universidade de São Paulo
  • Publication Dates

    • Publication in this collection
      12 Apr 2012
    • Date of issue
      Feb 2012

    History

    • Received
      31 May 2011
    • Accepted
      26 July 2011
    Sociedade Brasileira de Ortopedia e Traumatologia Al. Lorena, 427 14º andar, 01424-000 São Paulo - SP - Brasil, Tel.: 55 11 2137-5400 - São Paulo - SP - Brazil
    E-mail: rbo@sbot.org.br