The role of infliximab in rheumatoid arthritis associated non infectious ocular inflammatory disease
The role of infliximab in rheumatoid arthritis associated non infectious ocular inflammatory disease
Purpose: To evaluate the safety and efficacy of standard DMARD compared with biologic immunosuppression agents for the treatment of Rheumatoid arthritis (RA) associated ocular surface inflammatory disease.Methods: Retrospective analysis of a cohort of 16 patients with RA undergoing immunosuppression for ocular surface associated non infectious inflammatory disease was under-taken. Patients were split equally between standard DMARD therapy alone or the addition of biologic immunosuppres-sant, Infliximab, to induce ocular disease remission. Disease activity was assessed clinically and with Visante imaging. Serological assessment of ESR, CRP and Rheumatoid ELISA titre was also evaluated. Initial and repeat surgical interven-tions and time to remission were also analysed.Results: A median follow up after onset of ocular disease was recorded for Standard (30 months) and Infliximab groups (53 months). Average follow up on Infliximab was 15 months. Infliximab induced remission within 2 weeks (1–8), standard DMARD therapy took 9 months (4–20). The standard DMARD treated group fared worse for mortality (22% v 0%) and ocular loss (11% v 0%) compared to the Infliximab treated group.Severity of the ocular morbidity but not the level of any raised systemic inflammatory markers correlated with final mortality.Conclusions: Infliximab was safe and well tolerated. Rapid and total remission of the ocular inflammatory disease occurred with Infliximab only. Surgical intervention, ocular morbidity and mortality were all more prominent in the ‘standard DMARD’ group though still less than in compara-ble published literature. This data provides evidence for the use of biologics for ocular manifestations of severe RA over current standard DMARD therapy alone.
A709
McAlister, J C
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Konstantopoulos, Aristides
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Ardjomand, Navid
2991b041-58a0-41dd-a254-27bbf7220685
Dansingani, K
aae18123-3cdc-4bf1-86ce-9e89bd4dcb6d
Anderson, David F.
de3b2d61-3698-4c8f-adcf-604483666fda
Hossain, Parwez
563de5fc-84ad-4539-9228-bde0237eaf51
24 November 2008
McAlister, J C
7829ee39-b6ca-4210-8f03-e657d231b9a9
Konstantopoulos, Aristides
c54185a9-1ef3-4b6d-91a3-38de444cc4fb
Ardjomand, Navid
2991b041-58a0-41dd-a254-27bbf7220685
Dansingani, K
aae18123-3cdc-4bf1-86ce-9e89bd4dcb6d
Anderson, David F.
de3b2d61-3698-4c8f-adcf-604483666fda
Hossain, Parwez
563de5fc-84ad-4539-9228-bde0237eaf51
McAlister, J C, Konstantopoulos, Aristides, Ardjomand, Navid, Dansingani, K, Anderson, David F. and Hossain, Parwez
(2008)
The role of infliximab in rheumatoid arthritis associated non infectious ocular inflammatory disease.
Clinical and Experimental Dermatology, 36 (suppl 2), .
(doi:10.1111/j.1442-9071.2008.01849.x).
Record type:
Meeting abstract
Abstract
Purpose: To evaluate the safety and efficacy of standard DMARD compared with biologic immunosuppression agents for the treatment of Rheumatoid arthritis (RA) associated ocular surface inflammatory disease.Methods: Retrospective analysis of a cohort of 16 patients with RA undergoing immunosuppression for ocular surface associated non infectious inflammatory disease was under-taken. Patients were split equally between standard DMARD therapy alone or the addition of biologic immunosuppres-sant, Infliximab, to induce ocular disease remission. Disease activity was assessed clinically and with Visante imaging. Serological assessment of ESR, CRP and Rheumatoid ELISA titre was also evaluated. Initial and repeat surgical interven-tions and time to remission were also analysed.Results: A median follow up after onset of ocular disease was recorded for Standard (30 months) and Infliximab groups (53 months). Average follow up on Infliximab was 15 months. Infliximab induced remission within 2 weeks (1–8), standard DMARD therapy took 9 months (4–20). The standard DMARD treated group fared worse for mortality (22% v 0%) and ocular loss (11% v 0%) compared to the Infliximab treated group.Severity of the ocular morbidity but not the level of any raised systemic inflammatory markers correlated with final mortality.Conclusions: Infliximab was safe and well tolerated. Rapid and total remission of the ocular inflammatory disease occurred with Infliximab only. Surgical intervention, ocular morbidity and mortality were all more prominent in the ‘standard DMARD’ group though still less than in compara-ble published literature. This data provides evidence for the use of biologics for ocular manifestations of severe RA over current standard DMARD therapy alone.
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e-pub ahead of print date: 3 November 2008
Published date: 24 November 2008
Identifiers
Local EPrints ID: 448169
URI: http://eprints.soton.ac.uk/id/eprint/448169
ISSN: 0307-6938
PURE UUID: effcca8c-e4e7-4ac0-8a5a-87313b99ead1
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Date deposited: 13 Apr 2021 16:32
Last modified: 17 Mar 2024 03:04
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Contributors
Author:
J C McAlister
Author:
Aristides Konstantopoulos
Author:
Navid Ardjomand
Author:
K Dansingani
Author:
David F. Anderson
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