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Clinical Care
Part I
INSULIN THERAPY IN TYPE 2 DM
A JUDICIOUS USE OF INSULIN THERAPY MAY BE NECESSARY FOR OPTIMAL MANAGEMENT
IN MANY PEOPLE WITH TYPE 2 DIABETES!
A table listing some of the types of T2DM patients who should receive
insulin is given in Appendix 6a
| Types of INSULINS available for
clinical use: |
Although animal insulins made from beef and pig pancreas may still be
found, the vast majority of the insulins used now are of the "human"
variety. Recently there has been an increasing emphasis on the use of
the newly available insulin analogs and the clinical question is to place
them correctly in the therapeutic armamentarium.
It would not be correct to totally replace the use of human insulins with
analogs in routine therapy, especially as one has to factor in the costs
to the patient and in many cases the use of human insulins would offer
good control.
Table Showing Commonly used Insulin Preparations:
| Type of Insulin |
Human |
Analogues |
| Long acting |
|
Detemir, Glargine |
| Intermediate acting |
NPH |
|
| Short acting |
Regular Human Insulin |
Insulin Aspart, Lispro, Glulisine |
| Premixed |
Biphasic Human Insulin (30/70,50/50) |
Biphasic Insulin Aspart (30/70), Biphasic Insulin Lispro (25/75
and 50/50) |
Long acting analogs
They exhibit a relatively constant glucose-lowering profile over 24 hours
that permits once-daily dosing, although some patients may do better with
a twice daily dose of levemir insulin. Clinically, its potency is approximately
the same as human insulin and it does not lead to a better glycemic control.
Rapid acting analogs
Their use in place of the human insulins does not always lead to a better
control, but their rapid onset and short duration of action make them
of particular use in some clinical situations.
For a list of some clinical scenarios where it may be better to use
insulin analogs, see Appendix 6b
| "ONCE A CLINICAL DECISIONS TAKEN THAT THE PATIENT REQUIRES
INSULIN FOR OPTIMAL MANAGEMENT, ALL EFFORTS SHOULD BE MADE TO USE
THE GENETICALLY DERIVED PURE HUMAN INSULINS. IN A SIGNIFICANT NUMBER
OF CLINICAL SCENARIOS, PATIENTS WOULD DO BETTER WITH THE USE THE ANALOG
INSULINS, IF FEASIBLE." |
| TIME-ACTIVITY CHARACTERISTICS |
| |
Begins Working |
Peaks At |
Ends Working |
Lows Occur At |
| Insulin-Lyspro |
15-20 minutes |
30-90 min |
3-4 hours |
2 to 4 hr |
| Insulin- aspart |
15-20 minutes |
40-50 min |
3-4 hours |
2 to 4 hr |
| Regular |
30-60 minutes |
80-120 min |
4-6 hours |
3 to 7 hr |
| NPH |
2-4 hours |
6-10 hours |
14-16 hours |
6 to 12 hr |
| Lente |
3-4 hours |
6-12 hours |
16-18 hours |
7 to 14 hr |
| Ultralente |
4-6 hours |
10-16 hours |
18-20 hours |
12 to 24 hr |
| Insulin Glargine/Levemir |
2-3 hours |
almost no peak |
18-26 hours |
4 to 24 hr |
However, each person responds to insulin in his or her own way. That
is why onset, peak time, and duration are given as ranges.
It is important to have an understanding of the time-activity characteristics
of the available insulins. When blood glucose levels are not well controlled
at certain times during the day, or if hypoglycemic reactions are occurring,
the knowledge of the action and characteristics of each insulin being
taken will help to determine where changes need to be made.
Fortunately, the picture becomes much more clear, if it is realised that
from a practical and clinical viewpoint, human insulins can be divided
into two main groups, depending on their time course of action. These
are the "short-acting (SAI)" and the "intermediate acting
(IAI)" insulins.

* Rosiglitazone should not be used along with insulin and the dose
of pioglitazone should not exceed 30mg/day.
In most patients with a significant degree of symptoms, or in whom the
fasting blood glucose values are higher than 250-300mg%, insulin therapy,
if indicated in a particular patient, may be started along with the diet
and exercise prescription.
Start with a small dose and gradually titrate upwards depending on the
time characteristics of the insulins used as well as the individual response
of a patient.
With increasing use, it would be possible to cut out some of the initial
steps outlined above and start with a twice daily mixture of SAI and IAI
insulins, especially in insulin requiring patients.
The most commonly used regimen is the Premixed regimen:
It is the most convenient and effective insulin regimen for initiation
of insulin therapy. In this there is dual coverage as it is a combination
of short acting and intermediate acting insulin preparations in fixed
ratio like 30:70 or 50:50 respectively (options for different food habits).
So the same preparation is able to give both basal and meal related coverage
and helps to mimic physiology to a great extent. There for these are considered
as the effective and compliant insulin preparations for initiation as
well as intensification of insulin therapy.

* Rosiglitazone should not be used along with insulin and the dose
of pioglitazone should not exceed 30mg/day.
Other Regimens
Basal Only Regimen:
In this patients on OHAs who are not optimally managed are supplemented
with just basal insulin. This is done with the help of NPH or the modern
insulins. With NPH patients usually require 2 doses per day where as with
insulin analogues with one injection per day you can achieve the desired
targets in most of the patients, if chosen appropriately.
Basal Bolus Regimen:
Very rarely required for T2DM patients, but may be necessary in certain
clinical scenarios. In this a basal insulin supplementation given with
the help of long acting insulins either two or one (with insulin analogues)
injections and then three meal related short acting insulin injections.

The sites where the injections can be given. Efforts must be made to
rotate the site of the injection throughout the permissible areas and
not inject only into one region.
| COMMONLY SEEN SIDE EFFECTS |
Hypoglycemia
Edema
Allergy
Lipodystrophy and scar formation
| The use of insulin therapy is often required to
achieve optimal blood glucose control. In most T2DM patients this
should be accompanied by using insulin sensitizers, which would lower
the insulin resistance seen in the patients with T2DM and allow a
much smoother control at the minimal possible dosages. |
|