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Indian Pediatr 2008;45: 995-997 |
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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.
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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 |
|
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Oligoarticular |
17 |
(46%) |
Entesitis related |
10 |
(27%) |
Polyarticular |
4 |
(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 |
5 |
(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.
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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.
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