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Management of Systemic Lupus Erythematosus

           In  a  landmark  study  on  non-renal  SLE  (The  Exploratory  Phase  II/III
           SLE Evaluation of Rituximab [EXPLORER] trial), rituximab showed no
           significant difference with placebo in major or partial clinical response
           via the BILAG at week 52. 75, level I  However a systematic review of mainly
           moderate  quality  observational  studies  showed  that  rituximab  had  a
           steroid-sparing effect, in addition to improvement in disease activity and
           immunologic parameters. 76, level I

           Two  guidelines  support  the  use  of  rituximab  in  organ  threatening,
           refractory  moderate  and  severe  lupus,  intolerance/contraindications
           to  standard  immunosuppressive  agents  and  as  steroid  sparing
           therapy. 21; 50
           Rituximab also had good safety profile where most frequent AEs were
           infusion reactions and infections. 76, level I


           Recommendation 8
           •  Biologics may be used as an adjunct therapy in active systemic lupus
             erythematosus (SLE) despite standard therapy with corticosteroids
             and immunosuppressants.
           •  Biologics may be considered in refractory disease of SLE, intolerance
             or contraindication to standard treatment.


           e.  Nonsteroidal anti-inflammatory drugs
           Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used to
           relieve pain and reduce inflammation due to their analgesic and anti-
           inflammatory  effects.  There  is  no  retrievable  latest  evidence  on  its
           effectiveness  as  its  use  has  been  established  and  well-tolerated  for
           short-term symptomatic relief. NSAIDs may be used cautiously in non-
           renal mild SLE (e.g. inflammatory arthralgia or myalgia) when there is
           intolerance or poor response to paracetamol. There is also potential
           increased risk of renal, hepatic and CV toxicity when NSAIDs are used
           in SLE patients. 21; 61, level II-2

           f.  Others
           i)   Plasma exchange/Plasmapheresis
           Plasma exchange (PE) or plasmapheresis is a therapeutic intervention
           that  involves  extracorporeal  removal  of  high  molecular  weight
           substances  (e.g.  circulating  immune  complexes,  autoantibodies  and
           other  immune  reactants)  involved  in  the  pathogenesis  of  SLE  with
           subsequent return or exchange of blood plasma or components. It has
           been utilised as an alternative therapeutic modality in selected patients
           with  acute  life-threatening  manifestations,  rare  complications  and
           severe treatment-refractory disease, in particular LN.



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