Introduction

Mid- and long-term follow-up of Charnley’s hip arthroplasty demonstrates good functional results as shown in different studies. A French series from Lyon assessed an 85% survivorship at 25 years [5]. Older reported 96% after 25 years, while Berry et al. reported 86.5% [1], and Callaghan et al. found 78% survivorship after 35 years [2]. Wrobleski et al. reported Charnley low friction arthroplasty survival patterns to 38 years. They concluded that a regular follow-up after hip replacement is essential [7]. Both authors, Jacques Caton (Lyon study) and Jean Louis Prudhon (Grenoble study) followed-up two different series of long-term Charnley’s hip arthroplasty [35].

The purpose of this study was to analyse function and radiological component status after very long-term follow-up (more than 25 years in the Lyon study and 30 years in the Grenoble study).

First patient series from Grenoble

Eighty-six Charnley’s total hip arthroplasties (THA) implanted from January 1972 to December 1972 were followed-up in a retrospective study by J.L. Prudhon, MD. Data were collected in 2003 and 2004. All the implants were cemented original Charnley’s components manufactured by Thackray’s company Leeds, UK. Only two sizes of femoral components were available at that time. Two sizes of full polyethylene cemented acetabular cups were used. A senior surgeon, René Vidil, MD, performed all the procedures.

Surgery was routinely performed using Charnley’s enclosure system with a general anaesthesia, through a postero lateral approach without capsular repair. The cementing technique used a high viscosity cement introduced into the femoral shaft with the fingers without pressurisation. The acetabular cup was implanted after reaming the acetabular bone with an expanding Charnley’s reamer fixed in the acetabular bone through a central hole as described in original Charnley’s technique. The hole was sealed with a metallic mesh “Mexican hat” included in the cement mantle.

Patients were discharged on average, 28 days after surgery. Full weight bearing was allowed after three weeks. Patients did not receive any antibiotics pre- or post-operatively.

Material

Eighty-six THA were performed between January 1972 and December 1972. Three patients had both hips replaced during this period. Nine patients had the contralateral hip replaced in 1973. Twelve patients had the contralateral hip replaced later on. Fifty patients were female, and 33 were male. The average age at surgery was 66 years, ranging from 54 to 84.

The hip diseases were:

  • 70 osteoarthrosis

  • five avascular osteonecrosis

  • three dysplasic osteoarthritis

  • one femoral neck fracture

  • two post-traumatic osteoarthritis

  • one rheumatoid arthritis

  • three hip osteotomy failure

  • one hip revision

Thirty-nine patients were totally and definitely lost for follow-up. Of these patients according to the patient chart we could see that two THA had been revised and one THA had been removed for deep infection. Information on those patients, excepted the three patients revised, who were lost to follow-up or suspected to have died was collected by mail or phone, extending the contact to the family or the general physician of their country. In 11 cases we were able to obtain information from the family after the patient had died. The replaced hip was still working nicely when the patient died in nine cases. One THA had been revised by another team for loosening, and one case was removed due to a late infection. Forty-seven patients could be included in the long-term follow-up. Data were collected from the patient chart and the end point (patient death) was known. Two THAs had been revised for severe acetabular wear with bipolar loosening (Figs. 1 and 2).

Fig. 1
figure 1

Significant wear of the cup and femoral component loosening at 28 years post-op

Fig. 2
figure 2

Bone scan showing wear and loosening of both components after 26 years

One THA was simply removed because of late infection. Forty-four THA were still working with a good functional result. The average wear was between 1 and 3 mm. There were no signs of loosening in either component. Three patients had recurrent dislocations but no revision surgery was performed because of the poor general health. Of these, two patients one had severe weight loss due to a neurological disease and two had significant cup wear, without loosening. Three patients are still alive. They are respectively 83, 83, and 85 years old. The THA is functioning well. There is no loosening nor are there radiolucent lines. The cup wear is 3 mm in one case and between 3 and 5 mm in two cases.

At the time of that study patients expected age would be between 88 to 113 years old with a median of 104 years (Graph 1).

Graph 1
figure 3

Expected age of the patients in 2004 patient series from Grenoble

Second patient series from Lyon

Material

We reviewed 25 patients operated upon from 1969 to 1974 by a senior surgeon, Pr. Claude Regis Michel, in the same conditions as patients from Grenoble with immediate full weight bearing. Thirty-seven hips have been replaced in 19 females and six males. Average body mass index was 26. The preoperative function was evaluated according to the Merle D’Aubigne scoring system. The patient’s age at surgery ranged from 37 to 73 with an average of 55. The average pre op PMA score was 10.76. Mean follow-up was 26 years.

Clinical results

Four THA with severe cup wear and loosening of acetabular components have been revised after 17 years (one case), 24 years (two cases) and 31 years (one case). The average post op PMA score at last follow-up was 16.86 (range 14–18).

Radiological results

PE wear has been measured according to Livermore and Chevrot-Kerboul's methods. Cup wear ranged from 0 mm to 6.8 mm. The median was 2.69 mm. PE wear in this series was comparable with that observed in other LFA series (0.1 mm a year).

Radiolucency had been analysed in 31 cases. Five cups demonstrated radiolucency in zone 1. In the femoral components, we could see lucent lines in Gruen’s zone 1 in six cases and in zone 7 in eight cases. In two cases we noted heterotopic bone Brooker 1 in one case, and Brooker 2 in two cases.

Discussion

This study is anecdotal and emphasises how difficult it is to strictly follow-up patients following hip replacement as noted by M. Wrobleski [7]. At that time patients were not informed of the necessity to be reviewed with X-ray examination every two years.

PE wear is an unpredictable process. In all our different series of hip arthroplasty of full polyethylene cemented or uncemented metal back socket, the wear ranges were in three categories:

  • One third with an excessive wear pattern over 0.1 mm a year, with early revision.

  • One third with a "regular" wear pattern of 0.1 mm a year. Revision surgery needed after 25 years.

  • One third of patients with no wear at all. Wear undetectable during the life of the THA and patient death as the end point (Figs. 3 and 4).

Fig. 3
figure 4

No cup wear and no radiolucent lines at 30 years follow-up

Fig. 4
figure 5

No detectable wear after 30 years follow-up with original Charnley’s total hip arthroplasty (THA)

Many factors can influence PE longevity. At the time of surgery PE was sterilised by a gamma irradiation process without vacuum protection. The head was finished by hand, and the sphericity of the ball could have influenced arthroplasty longevity (Fig. 5).

Fig. 5
figure 6

Unpredictable wear process at 26 years follow-up in a female patient who was 36 years old at the time of surgery. The same surgeon and the same implants were used for both sides. The right hip was operated upon in January 1984, and the left in June 1984. Significant wear and a loosened cup occurred in the right hip. The cup was revised

The revue also shows that many patients can derive functional benefits from Charnley’s THA. First symptoms such as pain, dislocation and snapping regularly appear when the socket becomes loose and, as such, alert the patient.

Conclusion

All the long-term series have shown that PE wear is the weak point of joint replacement. Low friction arthroplasty can be considered a good and reliable solution for degenerative disease of the hip.

Will the new polyethylene be better in the future? Improvements in the PE manufacturing processes might be significant in the next few years according to the works of Triclot et al. [6].