Abstract:There were no differences in the efficacy or safety of the isophane and glargine-based insulin regimens. We recommend an initial daily insulin dose of 0.5 units/kg bodyweight if not on insulin, a greater than 30% increase in pre-prednisolone insulin dose and larger insulin dose adjustments in patients with prednisolone-induced hyperglycaemia.
“…Ruiz de Adana et al reported that in patients with type 2 diabetes and respiratory disease treated with methylprednisolone or deflazacort, there was no significant difference in glucose control between patients randomized to glargine-or isophane-based basal bolus insulin (39). Similarly, we reported no difference in mean glucose or hypoglycaemia in patients with hyperglycaemia with or without known diabetes while taking short-term prednisolone who were randomized to insulin glargine and insulin aspart vs insulin isophane and insulin aspart (30).…”
Section: Pharmacokinetics Of Insulin Therapy For Prednisolone-inducedmentioning
confidence: 42%
“…Although there are plausible mechanisms by which short-term hyperglycaemia might increase morbidity and mortality, such as inducing endothelial dysfunction and oxidative stress (29), data on major clinical endpoints are lacking. In our study, the inclusion criteria for hypoglycaemic therapy were one blood glucose level above 15 mmol/L or two blood glucose levels above 10 mmol/L within 24 h, to ensure subjects had either marked or sustained hyperglycaemia (30).…”
Section: Is Treating Hyperglycaemia During Acute Prednisolone Therapymentioning
confidence: 99%
“…Two complementary randomized controlled studies have compared matched doses of isophane-based and glargine-based basal bolus insulin in patients on glucocorticoids (30,39). In both studies, 50% of the daily dose was administered as basal insulin and 50% as short-acting insulin with meals (30,39).…”
Section: Pharmacokinetics Of Insulin Therapy For Prednisolone-inducedmentioning
confidence: 99%
“…Two complementary randomized controlled studies have compared matched doses of isophane-based and glargine-based basal bolus insulin in patients on glucocorticoids (30,39). In both studies, 50% of the daily dose was administered as basal insulin and 50% as short-acting insulin with meals (30,39). Ruiz de Adana et al reported that in patients with type 2 diabetes and respiratory disease treated with methylprednisolone or deflazacort, there was no significant difference in glucose control between patients randomized to glargine-or isophane-based basal bolus insulin (39).…”
Section: Pharmacokinetics Of Insulin Therapy For Prednisolone-inducedmentioning
Glucocorticoids are frequently prescribed to patients with a wide range of inflammatory and autoimmune diseases. The semi-synthetic glucocorticoid prednisolone is most commonly prescribed and in two main patterns. Prednisolone is prescribed short-term at medium-high doses to treat an acute inflammatory illness or long-term at lower doses to attenuate chronic inflammatory disease progression. In hospitalized patients with acute prednisolone-induced hyperglycaemia there is a distinct circadian pattern of glucose elevation, which occurs predominantly in the afternoon and evening. As a morning dose of isophane insulin has a pharmacokinetic pattern that matches this pattern of glucose elevation, treatment comprising a basal dose of morning isophane insulin in combination with short-acting insulin boluses is generally recommended. However, evidence is lacking that isophane-based basal bolus insulin is more efficacious than other insulin regimens. In outpatients, low dose prednisolone causes a small increase in post glucose-load glucose concentration but no change in overall glycaemic control as measured by glycosylated haemoglobin. If treatment is indicated, metformin has been shown to be effective and may attenuate other adverse effects of long-term prednisolone therapy. Further studies are necessary in order to identify factors underlying the variability in response to insulin therapy and clinical benefits of treatment in hospitalized patients with prednisolone-induced hyperglycaemia. In outpatients prescribed low dose prednisolone, the cardiovascular risk associated with postprandial hyperglycaemia and efficacy of hypoglycaemic therapies should be evaluated in future randomized clinical trials.
“…Ruiz de Adana et al reported that in patients with type 2 diabetes and respiratory disease treated with methylprednisolone or deflazacort, there was no significant difference in glucose control between patients randomized to glargine-or isophane-based basal bolus insulin (39). Similarly, we reported no difference in mean glucose or hypoglycaemia in patients with hyperglycaemia with or without known diabetes while taking short-term prednisolone who were randomized to insulin glargine and insulin aspart vs insulin isophane and insulin aspart (30).…”
Section: Pharmacokinetics Of Insulin Therapy For Prednisolone-inducedmentioning
confidence: 42%
“…Although there are plausible mechanisms by which short-term hyperglycaemia might increase morbidity and mortality, such as inducing endothelial dysfunction and oxidative stress (29), data on major clinical endpoints are lacking. In our study, the inclusion criteria for hypoglycaemic therapy were one blood glucose level above 15 mmol/L or two blood glucose levels above 10 mmol/L within 24 h, to ensure subjects had either marked or sustained hyperglycaemia (30).…”
Section: Is Treating Hyperglycaemia During Acute Prednisolone Therapymentioning
confidence: 99%
“…Two complementary randomized controlled studies have compared matched doses of isophane-based and glargine-based basal bolus insulin in patients on glucocorticoids (30,39). In both studies, 50% of the daily dose was administered as basal insulin and 50% as short-acting insulin with meals (30,39).…”
Section: Pharmacokinetics Of Insulin Therapy For Prednisolone-inducedmentioning
confidence: 99%
“…Two complementary randomized controlled studies have compared matched doses of isophane-based and glargine-based basal bolus insulin in patients on glucocorticoids (30,39). In both studies, 50% of the daily dose was administered as basal insulin and 50% as short-acting insulin with meals (30,39). Ruiz de Adana et al reported that in patients with type 2 diabetes and respiratory disease treated with methylprednisolone or deflazacort, there was no significant difference in glucose control between patients randomized to glargine-or isophane-based basal bolus insulin (39).…”
Section: Pharmacokinetics Of Insulin Therapy For Prednisolone-inducedmentioning
Glucocorticoids are frequently prescribed to patients with a wide range of inflammatory and autoimmune diseases. The semi-synthetic glucocorticoid prednisolone is most commonly prescribed and in two main patterns. Prednisolone is prescribed short-term at medium-high doses to treat an acute inflammatory illness or long-term at lower doses to attenuate chronic inflammatory disease progression. In hospitalized patients with acute prednisolone-induced hyperglycaemia there is a distinct circadian pattern of glucose elevation, which occurs predominantly in the afternoon and evening. As a morning dose of isophane insulin has a pharmacokinetic pattern that matches this pattern of glucose elevation, treatment comprising a basal dose of morning isophane insulin in combination with short-acting insulin boluses is generally recommended. However, evidence is lacking that isophane-based basal bolus insulin is more efficacious than other insulin regimens. In outpatients, low dose prednisolone causes a small increase in post glucose-load glucose concentration but no change in overall glycaemic control as measured by glycosylated haemoglobin. If treatment is indicated, metformin has been shown to be effective and may attenuate other adverse effects of long-term prednisolone therapy. Further studies are necessary in order to identify factors underlying the variability in response to insulin therapy and clinical benefits of treatment in hospitalized patients with prednisolone-induced hyperglycaemia. In outpatients prescribed low dose prednisolone, the cardiovascular risk associated with postprandial hyperglycaemia and efficacy of hypoglycaemic therapies should be evaluated in future randomized clinical trials.
“…Aunque se ha aducido que el uso de NPH podría asociarse a un menor riesgo de hipoglucemias frente a insulina glargina o detemir 17 , en nuestro estudio, basado en una terapia basal-bolo, solo hubo una hipoglucemia grave en el grupo del PC, a pesar de las altas dosis de insulina administrada. Radhakutty et al, en su análisis de control glucémico los días 1 y 3 del ingreso aplicando una pauta basal-bolo versus insulina NPH, no observaron diferencias significativas ni en el control glucémico ni en la incidencia de hipoglucemias 19 . Otros estudios también han encontrado una eficacia similar entre NPH y pauta basal-bolo 16,18 .…”
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