Resumen:
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[EN] Type 2 diabetes is characterized by insulin resistance and progressive b-cell deterioration. As b-cell function
declines, most patients with type 2 diabetes treated with oral agents, in monotherapy or combination, ...[+]
[EN] Type 2 diabetes is characterized by insulin resistance and progressive b-cell deterioration. As b-cell function
declines, most patients with type 2 diabetes treated with oral agents, in monotherapy or combination, will
require insulin therapy. Addition of basal insulin (glargine, detemir, or NPH/neutral protamine lispro insulin) to
previous treatment is accepted as the simplest way to start insulin therapy in those patients. But even when basal
insulin is adequately titrated, some patients will also need prandial insulin to achieve or maintain individual
glycemic targets over time. Starting with premixed insulin is an effective option, but it is frequently associated
with increased hypoglycemia risk, ¿xed meal schedules, and weight gain. As an alternative, a novel approached
known as ``basal plus strategy¿¿ has been developed. This approach considers the addition of increasing injections of prandial insulin, beginning with the meal that has the major impact on postprandial glucose values.
Finally, if this is not enough intensi¿cation to basal¿bolus will be necessary. In reducing hyperglycemia, this
modality still remains the most effective option, even in people with type 2 diabetes. This article will review the
currently evidence on the basal plus strategy and also its progression to basal¿bolus therapy. In addition,
practical recommendations to start and adjust basal plus therapy will be provided.
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Agradecimientos:
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F.J.A.-B. has received honoraria as speaker and/or consultant from Abbott, AstraZeneca, Bristol-Myers Squibb, Glaxo-SmithKline, LifeScan, Lilly, Madaus, MannKind Corp., Medtronic, Menarini, Merch Farma y Quimica, SA, MSD, ...[+]
F.J.A.-B. has received honoraria as speaker and/or consultant from Abbott, AstraZeneca, Bristol-Myers Squibb, Glaxo-SmithKline, LifeScan, Lilly, Madaus, MannKind Corp., Medtronic, Menarini, Merch Farma y Quimica, SA, MSD, Novartis, Novo Nordisk, Pfizer, Roche, sanofi-aventis, Schering-Plough, and Solvay. In addition, F.J.A.-B. has participated in clinical trials supported totally or partially by AstraZeneca, Glaxo-SmithKline, LifeScan, Lilly, MSD, Novo Nordisk, Pfizer, sanofi-aventis, and Servier. P. R. has no potential conflicts of interest to declare. J.F.A. has received honoraria as speaker and/or consultant form AstraZeneca, Ferrer, Glaxo-SmithKline, Laboratorios Dr. Esteve, Lilly, MSD, and Solvay.
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