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                 (ASCVD) risk. Since the publication of that document,   5.  Fruchart JC, Sacks  F, Hermans  MP, et  al.  The  Residual  Risk  Reduction
                 additional evidence and perspectives have emerged     Initiative:  a  call to action to reduce residual vascular risk in patients
                 from  randomized clinical trials  and other sources,   with dyslipidemia. Am J Cardiol. 2008;102(10 Suppl):1K-34K.
                 particularly considering the longer-term efficacy and   6.  Lee M et al.Atherosclerosis 2011;217; 492– 8
                 safety  of  proprotein  convertase subtilisin  /  kexin  9   7.  N Engl J Med. 2010:363(7):692-4 Diabetes Care 32:493–498, 2009
                 (PCSK9)  inhibitors  in secondary prevention of ASC-  8.  Børge G Nordestgaard, Anette Varbo Lancet 2014; 384: 626–635
                 VD. Most  notably,  the FOURIER (Further Cardiovas-
                 cular Outcomes  Research with  PCSK9 Inhibition  in   9.  Terry  A. Jacobson  et  al , National  Lipid Association  recommendations
                                                                       for patient-centered  management of dyslipidemia:  Part 1 – executive
                 Subjects with Elevated Risk) trial and SPIRE-1 and -2   summary* Journal of Clinical Lipidology 2014 ;8 473 – 488 .
                 (Studies of PCSK9 Inhibition and  the  Reduction  of
                 Vascular Events), assessing  evolocumab and boco-  10.  An International Atherosclerosis Society Position Paper 2013,Global Rec-
                                                                       ommendations for the  Management of Dyslipidemia [ Full report ]
                 cizumab, respectively, have published final results of
                 cardiovascular outcomes trials in patients with clinical   11.  Kausik  K.Ray et  al , European  Heart  Journal  doi : 10.1093  /eurheartj
                                                                       / ehu 107 .
                 ASCVD and in a smaller number of high-risk primary
                 prevention  patients. In addition, further evidence on   12.    12.  SS Iyengar,Raman  Puri ,S.N.Narasingan  ,Lipid Association  of  India
                 the types of patients most likely to benefit from the   Expert Consensus Statement on  Management of  Dyslipidemia  in Indi-
                                                                       ans 2016 : Part 1 Journal  of Association  of Physicians  of India [JAPI]
                 use of ezetimibe in addition to statin  therapy  after   Supplement copy March 2016 ,Vol : 64 Issue No.3
                 acute coronary syndrome has been published. Based
                 on results from these important analyses, the ECDP
                 writing  committee  judged  that  it would be  desirable
                 to provide a focused update to help guide clinicians
                 more  clearly  on decision  making  regarding  the use
                 of  ezetimibe  and PCSK9 inhibitors  in patients with
                 clinical ASCVD with or without comorbidities.
                 Conclusion

                 There is a need for absolute risk assessment in ev-
                 eryone  and this is  the best  approach  in  managing
                 Lipids . We need to assess the risk and then go with
                 which ever is greater i.e. a 50% LDL-C reduction or a
                 target . In those at highest absolute risk we have to
                 maximise the dose of the statin. We need to decide
                 whether this is enough for this person’s level of risk
                 or  should we go  lower  ? Lower  could  be a greater
                 percentage reduction in LDL-C or a target .LAI Con-
                 sensus statement  in the  management  of Lipids  for
                 Indians has solved many issues pertaining to bring-
                 ing down LDL –c goal to 50 mg in very high risk group
                 . Almost all academic bodies are now recommending
                 55 mgs of LDL goal for very high risk group . Infact ,
                 LAI gets the credit in recommending such low levels
                 before any other academic bodies attempted to do .
                 Refer : www.lipid.net.in

                 References:
                 1.  Grundy SM et al. Circulation.  2004;110:227–239.  Smith SC Jr et al.
                    Circulation, 2006; 113:2363–2372
                 2.  Prakash Deedwania &  Rajiv Gupta et al 2014  Diabetes  &  Metabolic
                    Syndrome Clinical  Research & Reviews  Volume 8 , Issue 3 , July Sep
                    2014 .Pages 156 – 161 ,ELSEVIER
                 3.  Endocrine Practice 2013;19 (Suppl 2):1-48.
                 4.  JAMA 2005; 294: 326-333 , Circulation 2005; 112: 3375-3383 & Na-
                    tional  Lipid  Association  recommendation . Kastelein  JJ, Van der steeg
                    WA, Holme L, et al: Circulation 2008;117: 3002-3009 .


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