Cost Effectiveness of Glargine Insulin Versus NPH Insulin in Diabetic Patients in Iran

This was a randomized double blind controlled clinical trial of 12months on subjects with type 2 diabetes. Two hundred diabetic subjects, 18-65 years of age, were included in the study. Subjects were willing to initiate insulin therapy and had A1C >8.0%. Any current and prior medications were acceptable for participant inclusion other than any type of insulin being evaluated. Demographic and anthropometric variables were recorded. Paraclinical data including glucose and lipid profile were measured every three months.In addition, quality of life was assessed with self-administered standard EQ-5D questionnaire.

Subjects were excluded for any of the following criteria: Alteration in insulin sensitivity such as major surgery, infection, renal failure (Glomerular Filtration Rate < 50), glucocorticoid treatment, recent (within 2 weeks) serious hypoglycemic episode (requires assistance of another), simultaneous participating in another clinical study, using any type of insulin, sight or hearing impaired, active proliferative retinopathy or maculopathy require treatment within 6 months prior to screening, breast feeding, pregnancy or nursing of the intention of becoming pregnant or not using adequate contraceptive measures.

Participants were recruited between July 2011 and October 2012. They were randomly allocated to two groups using a simple randomization method The insulin therapies were prescribed by a physician in the clinic. The starting dose of insulin Glargine was 24 units per day (0.2-0.6 unit/kg) in 2 divided doses in the intervention group. The control group received NPH/Reg insulin (2:1) with initiation dose of 0.2-0.6 unit/kg in 2 divided doses.Two-thirds of the dose was given before breakfast and the remainder before dinner. In the study, insulin analogues were used in accordance with the licensed approval from the local regulatory authority. Changes to OGLDs at the time of starting the insulin analogue, or thereafter, were entirely at the discretion of the participant and physician. Paraclinical data were measured in a referral laboratory every three months. Trial visits were defined as 0, 12, 24, 36 and 48 weeks from baseline. All participants were asked to record their 7-point blood glucose values in three consecutive days before each visit. Seven-point self-monitoring blood glucose includes three pre-meals, three post-meals, and bedtime blood glucose values during each day.Insulin doses were adjusted by a titration regimen according to self-monitored blood glucose.For both groups, treatment goals were as follows: fasting blood glucose of 80-120 mg/dl, postprandial glucose <160 mg/dl, A1C<7% We collected medical costs of each patient by a checklist. All patients had been asked to attend in our clinic every one month during the study. Clinical events or hospital episodes and also all related costs were determined at each visit. Any pharmaceutical, laboratory/diagnostic and rehabilitative care, as well as any contact with specialists, general practitioners, nurses, opticians, podiatrists, and dieticians were recorded for patients with/without complication.Finally total costs were calculated.

Direct nonmedical costs:

Any services such as transportation for patients and their family to clinic and taking care of dependents were assessed for non-medical expenditures by a patient self-estimate questionnaire.