Date: {{$ActivityAssignDate}}

Dear Dr. {{$doctorName}},


Subject: Evaluation of Lipid levels and Associated Risk Markers in Indian dyslipidemia Patients treated with Atorvastatin (LIPIMAP III) – A retrospective, cross-sectional, real world study


Dyslipidemia is the major condition responsible for the atherosclerotic process, the prevalence of dyslipidemia in Indians is very high with 79% of subjects having at least one lipid abnormality, with decreased high density lipoprotein cholesterol (HDL-C) levels in 72.3% subjects, hypertriglyceridemia in 29.5% subjects and elevated low density lipoprotein cholesterol (LDL-C) levels in 11.8% of subjects. Statins remain main line of treatment, with lifestyle modification. Intensified statin therapy by increasing dose, switching to a more potent statin or addition of Ezetimibe should be considered to achieve further reduction in LDL-C levels, and thereby prevention of ASCVD.

In India the prevalence of Ischemic Heart Disease is around 23.8 million, the prevalence of Coronary artery Disease (CAD) is 21.4% for diabetics and 11% for non-diabetics. The prevalence of CAD in rural parts of country is nearly half than that in urban population.

In secondary prevention cardiovascular disease (CVD), clinical trials have demonstrated that higher intensity levels of statin therapy are more effective than lower levels in reducing mortality rates. In post-MI cases, guideline compliant high intensity statins & adherence significantly lowers risk of MACE by 16% & adherence of statins lowers MACE by 7%.

Additionally, recent guideline statements have recommended high-intensity statin therapy (i.e., atorvastatin 80 mg or rosuvastatin 20-40 mg) for nearly all patients who have undergone cardiac intervention. For patients who cannot tolerate high-dose statins and those with contraindications, Ezetimibe may also be considered.

Risk factors like smoking, sedentary lifestyle, obesity, hypertension and diabetes are all important contributors to ASCVD. In The Dyslipidemia International Study (DYSIS II) hypertension and diabetes were identified as common risk factors seen in patients with coronary heart disease.

Currently there is limited evidence on prevalence of risk factors like hypertension, diabetes and obesity, as well as level of lipid control in Indian patients with dyslipidemia. Thus in lieu of the above, the present study is planned to evaluate the prevalence of ASCVD or ASCVD risk factors, level of lipid control and current management practices of dyslipidemia in Indian patients with or without ASCVD or ASCVD risk factors.

We invite you to participate in this study. On acceptance, you will need to capture the relevant data as mentioned in the standard Data Collection Form (DCF) provided, from the patient’s medical records (case papers and investigational reports – hereafter referred as source documents).

We would recommend you to capture data fulfilling the criteria as outlined in the protocol and whose relevant laboratory investigations are available for the preceding 3 months.

We wish to inform you that the DCF will capture all data in de-identified form and any identifiable parameters which may potentially disclose the identity of the patient such as name or address will strictly not be captured so as to ensure we maintain patient confidentiality. We would encourage you to carefully fill all available information to the fullest as recommended in the DCF.


In alignment with good clinical research practices, an independent Contract Research Organization (CRO) will monitor this study and do the source data verification of the data captured in the DCF with copies of the patients’ source medical records (case papers and investigational reports) to ensure that the data entered in the DCFs are accurate and in alignment with the patients’ medical records. The study is approved by independent ethics committee.

If you agree to participate in the said study, we would request you to sign and return the enclosed reply along with your visiting card for accuracy of records.





With regards,




Sun Pharma Laboratories Limited
Sun House, 201/B1, Western Express Highway,
Goregaon (East), Mumbai,
Maharashtra (India) – 400 063