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short communication

Indian Pediatr 2008;45: 995-997

Intra-articular Triamcinolone in Juvenile Idiopathic Arthritis

Erbil Ünsal and Balahan Makay

From the Department of Pediatrics, Dokuz Eylul University Hospital, Division of Immunology and Rheumatology,
35340 Balcova, Izmir-Turkey.

Correspondence to: Dr Balahan Makay, Dokuz Eylul University Hospital, Department of Pediatrics, Division of Immunology and Rheumatology, 35340, Balcova, Izmir, Turkey. E-mail: [email protected]

Manuscript received: November 12, 2007;
Initial review completed: February 12, 2008;
Revision accepted: February 27, 2008.

Abstract

Thirty-seven children with juvenile idiopathic arthritis (JIA) who were treated with one or more intra-articular triamcinolone acetonide (TA) injections were evaluated. Ninety-five joints were injected with a total number of 125 injections. Complete remission of the joint inflammation lasting at least 6 months was obtained in 62 of 95 injections (65%). Treatment of the joint contractures was successful in 35 of 51 joints (69%). In patients with oligoarthritis, 21 of 26 injected joints (81%) were in full remission at six-months. The 6-month remission was significantly lower in the other subtypes of JIA (P<0.01), 41 of 69 (59%) injected joints, when compared to oligoarticular patients. Intra-articular TA injection is an effective and safe therapy for inflammatory joint disease in JIA, particularly in the oligoarticular form.

Key words: Intra-articular injection, Juvenile idiopathic arthritis, Triamcinolone acetonide.

Introduction

Intra-articular corticosteroid injection is a well established therapeutic option for treatment of juvenile idiopathic arthritis (JIA). It is even recommended as first-line therapy by some authors in oligoarticular JIA, rather than an option for patients unresponsive to non-steroid anti-inflammatory drugs (NSAIDs)(1). It is also indicated in all forms of JIA patients, whose joint inflammation do not respond well to systemic disease modifying anti-rheumatic drugs (DMARDs). The long-acting steroids are the choice for intra-articular injection. Recent data showed that triamcinolone hexacetonide (THA) is the most effective drug(2,3). However, it is not available in most countries. Another well-known long-acting steroid is triamcinolone acetonide (TA), which can be used as an alternative to THA. We present the intra-articular triamcinolone acetonide experience of a pediatric rheumatology center in patients with JIA.

Methods

Charts of patients in Pediatric Rheumatology Department of Dokuz Eylul University Hospital who fulfilled the JIA criteria(4) were retrospectively evaluated from 2000 to 2005. The patients who were treated with intra-articular TA at least 1 year prior to evaluation period were eligible for the study. The indication for intra-articular injection (IAI) in oligoarticular JIA was the persistence of arthritis in spite of treatment with anti-inflammatory drugs for at least 6 weeks. In the other forms of JIA, the patients whose arthritic signs were unresponsive to DMARDs were treated with TA. Remission was considered as the complete resolution of effusion and other signs of inflammation within the first week. The reappearance of the inflammatory signs was defined as relapse.

Patients with oligoarthritis received only NSAIDs at the time of injection. Among the patients with other subtypes of JIA, 8 were on methotrexate, 9 on sulphasalazine, and 1 on methotrexate and sulpha-salazine treatment. In addition to these, five of them also received low dose oral corticosteroids.

A dose of 0.5 mg/kg and 1mg/kg of triamcinolone acetonide was injected for the small and large joints, respectively. The injections were given under general anesthesia in the operating room in all but 5 adolescent patients. Hips and small joints of the hands were injected under guidance of fluoroscopic radiography. Children were advised not to bear weight for 24 hours following the injection of the lower limb joints. All patients with adjacent muscle atrophy and/or joint contracture were encouraged to start physiotherapy shortly after the injection.

Results

A total of 37 patients (15 girls, 22 boys; mean age 7.3 ± 3.7 yr) with JIA were treated with one or more intra-articular TA injections. The mean duration of illness was 4.7±2.9 yr. Ninety-five joints were injected with a total number of 125 injections. The distribution of the injected joints was shown in Table I. There were contractures of several degrees in 51 joints (54 %) before the first injection. Twenty-two joints of 14 patients required more than one injection. Six oligoarthritis, 3 polyarthritis, 4 enthesitis-related arthritis, and 1 psoriatic arthritis patients required repeated injections. Thirteen joints were injected twice (5 knees, 3 ankles, 2 elbows, 2 hips, and 1 wrist), 5 joints 3 times (3 knees, 2 ankles), 2 joints 4 times (1 knee, 1 ankle), and 2 joints 5 times (2 knees) due to relapse or lack of efficacy.

Table I



Characteristics of Study Children
JIA subtype    
Oligoarticular 17 (46%)
Entesitis related 10  (27%)  
Polyarticular (11%)
Psoriatic 4 (11%)
Systemic 2 (5%)
Type of joint injected
Knee 48 (   %)
Ankle 13 (   %)
Wrist 8 (   %)
PIP 8 (   %)
Hip 6 (   %)
Elbow 6 (   %)
Subtalar 4 (   %)
MCP 2 (   %)
Current systemic treatment  
NSAIDs 17 (46%)
NSAIDs + DMARD¹ 15 (40%)
NSAIDs + Low dose corticosteroid
+ DMARD¹ (14%)
1 Methotrexate or sulphasalazine; MCP: Metacarpo-phalyngeal  joint; 

NSAIDS: Non steroidal anti inflammatory drugs.

Complete remission of the joint inflammation lasting at least for 6 months was obtained in 62 of 95 injections (65%). In patients with oligoarthritis, 21 of 26 injected joints (81%) were in full remission at six-months. However, only 41 of 69 (59%) injected joints in the other subtypes of JIA were in remission at six-month time period, and this rate was significantly lower (P<0.01) when compared to oligoarticular patients. The rate of ongoing remission in oligoarticular group at 12-month time point was 69%, whereas this rate was 52% in the other subgroups (P<0.01).

Joint contraction was corrected in 35 of 51 joints (69%). Two patients had leg-length discrepancy due to chronic unilateral knee inflammation, which remained unchanged in the 3-years follow-up period. One of these patients had complete remission after the first injection, however; the other required two additional injections.

Regarding the complications, there were only two wrists with subcutaneous atrophy. None of the patients experienced infection at the injection site. Cushing syndrome was not observed in any of the 5 patients who received multiple joint injections (more than 2 joints at once). None of the patients who underwent hip injection developed avascular necrosis of femoral head.

Discussion

During the past 50 years, intra-articular corticosteroid administration has gained an important role in the management of inflammatory arthritis. Several studies demonstrated long-lasting remission in the majority of the injected joints in JIA patients, with good pain relief, improved mobility and a significant delay or prevention of further joint destruction(5-7).

This report describes our experience with intra-articular TA injection in children with JIA. The remission rate in this study is higher than previously reported(2,3). The largest single cohort study about IAI in JIA, which was reported by Breit, et al.(8) demonstrated that patients with oligoarthritis responded better to therapy than other subgroups of JIA. In this study also, the remission rates were higher in oligoarticular patients than the other groups, supporting the previous literature. Systemic onset JIA has been reported to have the worst response to IAI(8,9). However, because of small number of patients in each subgroup, we could not compare all of them separately.

The present data indicates that intra-articular TA injection is an effective and safe therapy for inflammatory joint disease in JIA, particularly in the oligoarticular form.


What This Study Adds?

• Intra-articular injection of triamcinolone acetonide is an effective and safe therapy for inflammatory joint disease in JIA, particularly in the oligoarticular form.
 

Contributors: EÜ designed the study and revised the manuscript for important intellectual content. BM collected data and drafted the paper.

Funding: None.

Competing interest: None stated.

References

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2. Zulian F, Martini G, Gobber D, Agosto C, Giante C, Zacchello F. Comparison of intraarticular triamcinolone acetonide and hexacetonide in oligoarticular juvenile arthritis. Rheumatology 2003; 42: 1254-1259.

3. Zulian F, Martini G, Gobber D, Plebani M, Zacchello F, Manners P. Triamcinolone acetonide and hexacetonide intraarticular treatment of symmetrical joints in juvenile idiopathic arthritis: a double blind trial. Rheumatology 2004; 43: 1288-1291.

4. Petty RE, Southwood TR, Baum J, Bhettay E, Glass DN, Manners P, et al. Revision of the proposed classification criteria for juvenile idiophatic arthritis. J Rheumatol 1998; 25: 1991-1994.

5. Honkanen VEA, Rautonen JK, Pelkonen PM. Intra-articular glucocorticoids in early juvenile chronic arthritis. Acta Paediatr 1993; 82: 1072-1074.

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7. Huppertz HI, Tschammler A, Horwitz, AE, Schwab O. Intraarticular corticosteroids for chronic arthritis in children: efficacy and effects on cartilage and growth. J Pediatr 1995; 127: 317-321.

8. Breit W, Frosch M, Meyer U, Heinecke A, Ganser G. A subgroup-specific evaluation of the efficacy of intraarticular triamcinolone hexacetonide in juvenile chronic arthritis. J Rheumatol 2000; 27: 2696-2702.

9. Garcia-Consuegra Molina J, Merino Munoz R. Treatment of idiopathic juvenile arthritis with intraarticular triamcinolone acetonide injections. An Esp Pediatr 2000; 53: 314-317.

10. Job-Deslandre C, Menkes CJ. Complications of intra-articular injections of triamcinolone hexacetonide in chronic arthritis in children. Clin Exp Rheum 1990; 8: 413-416.

 

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