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i n d i a n j o u rn a l o f r h e uma t o l o g y 9 ( 2 0 1 4 ) S 7eS 6 7 S57
P170. Systemic onset juvenile idiopathic arthritis (SoJIA):Delayed diagnosis leads to joint damage
Pradeepta Sekhar Patro, Ranjan Gupta, Able Lawrence,
Vikas Agarwal, Ramnath Misra, Amita Aggarwal; Department ofClinical Immunology, Sanjay Gandhi Postgraduate Institute of MedicalSciences, Lucknow, India
Introduction: SoJIA is a systemic inflammatory disease which in-
volves multiple organ systems. Early diagnosis is the key to
effective therapy to suppress inflammation and future damage. In
India the diagnosis is often delayed due to lack of awareness
Methods: Retrospective case records based analysis of 123 pa-
tients with SoJIA was done. Data on baseline clinical features,
duration of symptoms and presence of damage as well as in-
flammatory markers was retrieved.
Results: Of the total 123 patients, 41(33.3%) were girls. Mean age
at the onset of symptoms was 6.75 years and mean delay in
making a diagnosis was 35 months. Fever (98.70%) and inflam-
matory polyarthritis (96.2%) were the most common presenting
symptoms. Lymphadenopathy (58.6%), hepatomegaly (44.60%)
splenomegaly (33.75%) rashes (39.50%) were also common.
Three patients presented first time with macrophage activation
syndrome. Deformities were present in 39 out of 123 children
(32%) at the first visit itself. Wrist (73%) was the most commonly
damaged joint. Investigations revealed high inflammatory
burden: mean CRP of 10.7 mg/dl, mean ESR of 77 mm/hr and
mean platelet count of 4, 29,353/mm3 at the time of
presentation.
Conclusions: Delay in making the correct diagnosis of SoJIA leads
to the high inflammatory burden in these patients and results in
significant joint damage. Thus increased awareness about this
disease is required among pediatricians.
P171. Viscosupplementation in osteoarthritis: A single centerexperience
Darshan Singh Bhakuni, Krishnan Shanmuganandan,
Amar Tej Atal, Arun Hegde, Abhishek Kumar; Army HospitalResearch & Referral, Delhi Cantt, India
Introduction: Viscosupplementation helps to restore the rheo-
logical and physiological state of joints in osteoarthritis. Several
systematic reviews on this modality have offered differing
results.
Methods: We carried out a retrospective analysis of 353 patients of
knee osteoarthritis, given intra-articular Hylan G-F 20 at our
center and evaluated during the period 05 February 2011 to 08
August 2014. Data was collated from patients for each target knee
injected. Response to injection was quantified as ‘improvement’,
‘no change’ and ‘worsening’ of pain and function at baseline and
24 weeks post injection.
Results: Out of a total of 543 knees injected, 216 were Kellgren-
Lawrence grade 2, 299 were grade 3 and 28 were grade 4. Of these
knees, 449 (82.7%) responded favourablyat24weeks.Transientpost
procedure pain was reported over 24-72 hours in 34 knees, while
pain and swelling requiring prolonged rest and NSAIDs were
demonstrable in 2 knees. Response pertaining to 186 knees collated
after the second injection of viscosupplementation, revealed
improvement in 142 knees (76.3%). Response related to 63 knees,
after their third injection of Hylan G-F 20 demonstrated
improvement in 41 (65%). Failure to respond to treatment over 8
weeks was related to lack of improvement or worsening of pain at
24 weeks.
Conclusion: Viscosupplementation with Hylan G- F 20 is safe and
effective in reducing pain and improving function in patients of
knee osteoarthritis.
P172. Is body fat distribution correlated with osteoarthritisand its severity? A preliminary study
Ragini Srivastava, Shweta Agarwal, S.K. Das, R.N. Srivastava;Department of Rheumatology and Orthopedic Surgery, KG MedicalUniversity, Lucknow, India
Introduction: Obesity and quadriceps weakness have been
considered to be important risk factors for osteoarthritis. Osteo-
arthritis also occurs in non-obese persons. Here we have tried to
study if there is any difference in fat distribution pattern and lean
musclemass between non obese OA patients and similar controls.
Methods: Non obese (BMI<30) patients of (a) knee osteoarthritis
and (b) controls were selected from the patients attending Rheu-
matology / Orthopedics OPD. Patients having clinico radiological
OA were evaluated after taking informed consent. 56 patients and
14 controls were studied. Whole body BMD was conducted in
patients and controls by GE Lunar machine. OA disease activity
was assessed using WOMAC and KGMC scale.
Result: Body fat and lean mass of Whole body, Trunk, Legs,
Android and Gynoid distribution of OA patients were compared
with controls of similar BMI. OA patients were divided ac-
cording to disease activity and disease activity compared with
body fat distribution. No difference was observed in patients vs
controls and disease activity and body fat distribution. High
Body fat and less lean muscle mass was reported in females
(n¼42) than males (n¼12) which correlated with Total KGMC
score (p<0.05).
Conclusion: No correlation was observed in OA, disease severity
and Body fat and leg muscle mass. However as expected signifi-
cant difference were observed among the female vsmale patients.
This appeared to be correlated to higher disease activity in fe-
males. The limitations are number of patients is small and sta-
tistical analysis is preliminary.
P173. Leprosy: In disguise and blending in with the crowd
Deepak Rath, Bijit Kumar Kundu; Department of Medicine, PGIMER &Dr RML Hospital, New Delhi, India
Affection of skin and nerves by leprosy is quiet common and
easily diagnosed. However diagnosing musculoskeletal involve-
ment as being due to leprosy is difficult given its protean mani-
festations and the fact that it is a great mimic of many
autoimmune conditions. We present two cases where leprosy
presented with features similar to and were diagnosed and
treated initially as Rheumatoid Arthritis (RA), and Seronegative
Spondyloarthritis (SpA) respectively. Only later was the true
diagnosis revealed. In leprosy endemic areas it is imperative to
keep in mind the myriad presentations of leprosy including its
musculoskeletal manifestations as consequences of misdiagnosis
and hence mistreatment can be catastrophic, especially in the era
of increasing use of biologic disease modifying agents. We
conclude that in endemic areas leprosy should be ‘actively’ ruled
out and should be made an integral part of pre-biologic screening.