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Abstract Number: 187

Revision Arthroplasty in Rheumatoid and Osteoarthritis: Does Methotrexate Decrease Radiographic Lucency in RA Patients?

Mike Wei1, Douglas N. Mintz2, Lisa A. Mandl3, Arielle Fein4, Jayme C. Burket5, Yuo-Yu Lee4, Wei-Ti Huang6, Vivian P. Bykerk4, Mark P. Figgie7, Edward F. DiCarlo8, Bruce N. Cronstein9 and Susan M. Goodman3, 1Weill Cornell Medical College, New York, NY, 2Radiology, Hospital for Special Surgery, New York, NY, 3Rheumatology, Hospital for Special Surgery, New York, NY, 4Hospital for Special Surgery, New York, NY, 5Healthcare Research Institute, Hospital for Special Surgery, New York, NY, 6Biostatistics, Hospital for Special Surgery, New York, NY, 7Orthopedics, Hospital for Special Surgery, New York, NY, 8Pathology, Hospital for Special Surgery, New York, NY, 9NYU School of Medicine, Division of Rheumatology, New York, NY

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: methotrexate (MTX), Osteoarthritis, rheumatoid arthritis (RA) and x-ray

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Session Information

Title: Orthopedics, Low Back Pain and Rehabilitation

Session Type: Abstract Submissions (ACR)

Background/Purpose

Rheumatoid arthritis (RA) patients have excellent total hip arthroplasty (THA) survival, and methotrexate (MTX), an anti-inflammatory disease modifying drug which may affect bone reabsorption, may play a role. The purpose of this study is to determine the diagnosis leading to revision THA (rTHA) in RA patients and to assess the association of radiographic lucency with MTX use.

Methods

All patients with validated diagnosis of RA in the institution’s THA registry undergoing rTHA from May 2007 – February 2011 were eligible. Diagnosis leading to rTHA and medication use was determined by chart review. Osteolysis was evaluated on available radiographs by measuring maximum lucency in each Gruen zone. Differences within RA patients with/without MTX in osteolysis, demographics, and medications were assessed with chi-squared, Fisher’s exact tests or Mann-Whitney U tests as appropriate. The error rate for multiple comparisons of lucency in the different Gruen zones was corrected via false discovery rate methods. A secondary analysis was performed to determine differences in diagnoses leading to revision between RA and matched OA controls (2:1 match by sex age +/- 5 years). OA exclusion criteria included presence of rheumatic diseases, use of MTX, and lack of records.

Results

51 RA rTHA were identified and compared with 103 OA (Table 1). Mean age for RA was 57.7 v 59.4 years for OA (p = 0.240). 82.4% RA were female v 83.5% OA (p = 0.859). RA had lower BMI than OA (25.5 v 28.2; p = 0.166). There was no difference in diagnosis leading to rTHA, including infection (RA 3.9 v OA 6.8%; p = 0.719) or dislocation (RA 23.5 v OA 23.3%; p = 0.975). There was no significant difference in the length of time the implant was in before revision: RA 11.0 v OA 8.8 years (p = 0.060). Among RA with/without MTX, (Table 2) there was no difference in use of biologics (30.0 v 43.3%, p = 0.283), steroids (47.6 v 50.0%, p = 0.867) or bisphosphonates (23.8 v 33.3%, p = 0.543). There was no difference in rTHA diagnosis with/without MTX, including loosening (52.4 v 56.7%, p = 0.762). There was no significant difference in lucencies with MTX use in any Gruen zone. Patients with MTX had femoral stem subsidence of 3.7mm v no subsidence without MTX (p = 0.006).

Conclusion

There was no difference in the diagnosis leading to rTHR in RA and OA, although RA trended longer prior to rTHA. In this small retrospective study, there were no significant differences associated with MTX exposure or radiographic lucency among RA patients. The significance of subsidence is not clear. Further study of arthroplasty survival in RA patients is warranted.

 

Table 1: Demographic characteristics and reason for revision for OA vs. RA patients*

 

RA, N=51

OA, N=103

p-value

Age, Mean (Std Dev)

57.7 (14.1)

59.4 (15.0)

0.240

BMI, Mean (Std Dev)

25.5 (5.2)

28.2 (11.4)

0.166

Female, N (%)

42 (82.4)

86 (83.5)

0.859

Years Implanted, Mean (StDev)

11.0 (8.3)

8.8 (8.8)

0.060

Diagnosis, N (%)

 

 

 

Infection

2 (3.9)

7 (6.8)

0.719

Loosening

28 (54.9)

59 (57.3)

0.779

Fracture

7 (13.7)

7 (6.8)

0.232

Wear

12 (23.5)

19 (18.4)

0.459

Dislocation

12 (23.5)

24 (23.3)

0.975

Mech Failure

2 (3.9)

7 (6.8)

0.862

Other

1 (2.0)

0 (0.0)

0.331

*28 patients were ascribed more than 1 diagnosis. 

 

Table 2: Demographic characteristics and radiographic analysis of RA patients with/without MTX*

 

MTX, N=20

No MTX, N=30

p-value

Age, Mean (Std Dev)

59.3 (14.9)

56.6 (13.7)

0.461

BMI, Mean (Std Dev)

27.2 (5.9)

24.2 (4.3)

0.059

Years Implanted, Mean (Std Dev)

10.7 (9.1)

11.3 (7.9)

0.737

Diagnosis, N (%)

 

 

 

Infection

1 (4.8)

1 (3.3)

>0.999

Loosening

11 (52.4)

17 (56.7)

0.762

Fracture

3 (14.3)

4 (13.3)

>0.999

Wear

6 (28.6)

6 (20.0)

0.351

Dislocation

6 (28.6)

6 (20.0)

0.581

Mech Failure

0 (0.0)

2 (6.7)

0.506

Other

0 (0.0)

1 (3.3)

>0.999

Medication, N (%)

 

 

 

Bisphosphonates

5 (23.8)

10 (33.3)

0.543

Biologics

6 (30.0)

13 (43.3)

0.283

Prednisone

10 (47.6)

15 (50.0)

0.867

Cemented Cup, N (%)

3 (18.8)

5 (22.7)

>0.999

Cemented Femur, N (%)

5 (31.3)

13 (59.1)

0.112

Lucency, Mean (Std Dev) [mm]

 

 

Femur Zone 1

11.4 (16.8)

7.4 (10.2)

0.954

Femur Zone 2

0.0 (0.0)

0.9 (1.7)

0.225

Femur Zone 3

0.2 (0.8)

0.5 (1.8)

0.954

Femur Zone 4

2.7 (8.7)

0.0 (0.0)

0.189

Femur Zone 5

0.3 (0.9)

0.7 (2.6)

0.954

Femur Zone 6

1.3 (3.3)

0.8 (2.8)

0.954

Femur Zone 7

3.7 (5.6)

3.0 (5.5)

0.954

Femur Zone 8

5.7 (7.9)

5.0 (6.3)

0.954

Femur Zone 9

0.0 (0.0)

1.8 (3.5)

0.189

Femur Zone 10

0.2 (0.9)

0.0 (0.0)

0.954

Femur Zone 11

0.8 (2.3)

0.7 (2.4)

0.954

Femur Zone 12

0.1 (0.4)

0.8 (3.6)

0.954

Femur Zone 13

2.2 (5.0)

1.3 (3.6)

0.954

Femur Zone 14

3.5 (6.1)

3.3 (6.3)

0.954

Subsidence (mm)

3.7 (7.1)

0.0 (0.0)

0.006

*11 patients were ascribed more than 1 diagnosis.


Disclosure:

M. Wei,
None;

D. N. Mintz,
None;

L. A. Mandl,
None;

A. Fein,
None;

J. C. Burket,
None;

Y. Y. Lee,
None;

W. T. Huang,
None;

V. P. Bykerk,

Amgen, Pfizer, BMS, Janssen, UCB, Roche/Genentech,

2;

M. P. Figgie,
None;

E. F. DiCarlo,
None;

B. N. Cronstein,

Canfite Pharma,

1,

AstraZeneca,

2,

Cellgene,

2,

Gilead,

2,

NIH,

2,

NYU School of Medicine,

3,

Bristol-Myers Squibb,

5,

Pfizer Inc,

5,

Eli Lilly and Company,

5,

Rheumatology Reseach Foundation,

6,

ACR,

6,

Arthritis Foundation,

6;

S. M. Goodman,
None.

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