Treatment with somatostatin

StudyPopulationInterventionOutcomesResultsCommentsDesignEL
Yun et al, 199951823 patients with type 1 diabetes
Aged 36.1 ± 10.73 with octreotide, 33.25 ± 13.4 years with no octreotide
Korea
Patients with stuporous or comatose mental state were excluded
  1. IV infusion of low-dose insulin and 50 μg of SC octreotide every 6 hours
  2. IV infusion of low-dose insulin, no octreotide
    Octreotide is a synthetic long- acting somatostatin
Time to recovery of clinical and laboratory signs of ketoacidosis, hypoglycaemia, acidosis and ketosisNo statistically significant difference seen in the time to recovery of hypoglycaemia: octreotide (n = 7) 8.9 ± 3.21 vs. no octreotide (n = 8) 18.8 ± 13.2 hours, p = 0.089
No statistically significant difference seen in the time to recovery of acidosis: octreotide 24.0 ± 12.6 vs. no octreotide 33.2 ± 13.9 hours, p = 0.82
Difference seen in the time to recovery of ketonuria: octreotide 38.0 ± 32.0 vs. no octreotide 68.3 ± 26.0 hours, p = 0.049, borderline statistically significant
Unknown how allocation to groups took place
Possibly groups were biased as 3/7 in the octreotide group had alcohol as a precipitating factor whereas this was not the case in the no octreotide group
Numbers in study do not add up: 8 patients in the no octreotide group were not included in the results but it was not explained why
Intervention study not randomisedIIa

From: Evidence tables

Cover of Type 1 Diabetes
Type 1 Diabetes: Diagnosis and Management of Type 1 Diabetes in Children and Young People.
NICE Clinical Guidelines, No. 15.2.
National Collaborating Centre for Women's and Children's Health (UK).
London: RCOG Press; 2004 Sep.
Copyright © 2004, National Collaborating Centre for Women’s and Children’s Health.

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