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1.
Diabet Med ; 18(8): 614-8, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11553197

ABSTRACT

AIMS: We have evaluated the local tolerance and the metabolic efficacy of a lyophilized nasal insulin preparation in 10 severely hyperglycaemic Type 2 diabetic patients. METHODS: The study included two 4-month randomized periods: (A) three preprandial doses of nasal insulin secondarily combined with one evening subcutaneous NPH if the desired glycaemic control was not achieved; (B) two NPH injections daily. We assessed: (i) diabetes control on monthly HbA1c levels and occurrence of hypoglycaemic events; (ii) local tolerance on clinical symptoms, rhinoscopy, nasal muco-ciliary clearance and nasal biopsies; (iii) insulin absorption at months 0 and 4. RESULTS: One patient was withdrawn because of cough and dizziness after each nasal application. HbA1c was not significantly different at month 4 (9.4 +/- 0.5% vs. 8.8 +/- 0.2%, A vs. B). Blood glucose control remained only fair in the majority of our patients. Nasal insulin was able to replace the daytime fraction of the subcutaneous insulin with a 18% efficacy. Side-effects included transient nasal hyperactivity (pruritus, sneezing and rhinorrhoea) and chronic persistence of nasal crusts. Plasma insulin profiles were not significantly different between months 0 and 4. CONCLUSIONS: The utilization of nasal insulin (with or without NPH) was associated with similar diabetes control compared with NPH twice daily. Nasal insulin alone was able to achieve an adequate glycaemic control in three of the 10 patients.


Subject(s)
Administration, Intranasal , Diabetes Mellitus, Type 2/drug therapy , Hyperglycemia/blood , Hypoglycemic Agents/therapeutic use , Insulin, Isophane/administration & dosage , Adult , Aged , Cross-Over Studies , Diabetes Mellitus, Type 2/blood , Glycated Hemoglobin/metabolism , Humans , Insulin/blood , Insulin, Isophane/adverse effects , Insulin, Isophane/pharmacokinetics , Insulin, Isophane/therapeutic use , Middle Aged , Patient Selection , Treatment Failure
2.
Diabetes Metab ; 27(3): 372-7, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11431603

ABSTRACT

OBJECTIVE: Nasal insulin administration is a potential route for intensive insulin management, less invasive and more rapid than subcutaneous injections. Previous studies have shown poor bioavailability (less than 15%) with nasal insulin administration with various absorption enhancers. The aim of the study was to evaluate in type 1 diabetic patients, the metabolic efficacy and local tolerance of a new gelified sprayed nasal insulin containing glychocolate and methylcellulose as absorption promoters. MATERIAL AND METHODS: The study was conducted in 16 type 1 diabetic patients (HbA1c 8.6+/-0.2%) in a cross-over trial including 2 six month randomized periods: a) NPH twice daily + 3 pre-prandial nasal insulin doses + nasal supplementation in case of unexpected hyperglycaemia; b) NPH twice daily + 3 pre-prandial regular insulin injections. End points were HbA1c levels, hypoglycaemic episodes and tolerance evaluated at month 0, 2, 6 and 8 on clinical symptoms and objective nasal assessments. RESULTS: Four patients were withdrawn because of nasal burning (3 cases) and persistent sinusitis (1 case), and one patient had purulent sinusitis at the month 6 examination. At month 6, HbA1c levels were comparable (8.3 +/- 0.1 vs 8.6 +/- 0.1%, m +/- SEM, NS) for nasal and subcutaneous period respectively. The number of hypoglycaemic events was identical during the 2 periods (88 episodes). Nasal tolerance with the gelified form was better than with the already reported lyophilized form but, when present, symptoms were more marked, suggesting a potentiating additional role of methylcellulose excipient on nasal intolerance. CONCLUSIONS: 1) Gelified nasal insulin is as efficient as subcutaneous regular insulin in type 1 diabetic patients. 2) Other galenic forms should be investigated to improve nasal tolerance and bioavailability.


Subject(s)
Diabetes Mellitus, Type 1/drug therapy , Insulin, Isophane/administration & dosage , Administration, Intranasal , Adult , Cross-Over Studies , Diabetes Mellitus, Type 1/blood , Drug Administration Schedule , Glycated Hemoglobin/analysis , Humans , Hyperglycemia/epidemiology , Hypoglycemic Agents/administration & dosage , Hypoglycemic Agents/adverse effects , Hypoglycemic Agents/therapeutic use , Inflammation , Injections, Subcutaneous , Insulin, Isophane/adverse effects , Insulin, Isophane/therapeutic use , Nasal Mucosa/drug effects , Nasal Mucosa/pathology , Sinusitis/etiology
3.
Diabetes Metab ; 26(5): 416-20, 2000 Nov.
Article in French | MEDLINE | ID: mdl-11119023

ABSTRACT

Diabetes can induce sexual disorders by different mechanisms. These troubles are more frequent in diabetics subjects. Thus, management of sexual impotence is an important aspect of diabetes care. However, most diabetologists are not trained to treat sexual disorders. The recent availability of oral drugs, i. e. Sildenafil (Viagra), has partly simplified the treatment of sexual impotence, particularly in diabetic patients. However, Viagra is efficient in only 60% cases in diabetic subjects. In the remaining cases, intracavernosal injections or vacuum can be used. Since Viagra has been available, more diabetic patients complained with sexual disorders, and ask for treatment of impotence. Cardio-vascular diseases must retain more attention in diabetic patients who are exposed to silencious myocardial ischemia. In such subjects, Viagra is not contra-indicated, but must be used after myocardial explorations, especially if the patients have cardio-vascular risk factors. However, patients and their doctors have been threatened by death cases reported with Viagra in United States. The lack of detailed informations has restrained Viagra's prescription. The following explains how to manage sexual disorders as part of diabetes care, and suggests rules for Viagra's prescription in diabetic patients.


Subject(s)
Diabetes Mellitus/physiopathology , Erectile Dysfunction/drug therapy , Phosphodiesterase Inhibitors/therapeutic use , Piperazines/therapeutic use , Cardiovascular Diseases/complications , Cardiovascular Diseases/physiopathology , Contraindications , Diabetes Complications , Diabetic Angiopathies/physiopathology , Erectile Dysfunction/etiology , Humans , Male , Myocardial Ischemia/complications , Myocardial Ischemia/physiopathology , Purines , Sildenafil Citrate , Sulfones
4.
Diabetes Metab ; 23(6): 533-6, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9496561

ABSTRACT

Management of very high insulin requirements in rare extreme insulin resistance syndromes is difficult and poorly documented. We report a case of a type B insulin-resistant patient requiring approximately 10,000 units of insulin per day, i.e. beyond the possibilities of current insulin formulations and delivery devices. Only the Panomat C10 portable pump model (Disetronic) and U500 Humulin (Lilly) allowed the required rate of 400 units per hour to be attained only when the reservoir was changed twice daily and the site and catheter were changed once daily. Three months after discharge, the patient was in good general and local condition, but with only fair diabetes control (glycated haemoglobin 9.5%).


Subject(s)
Diabetes Mellitus, Type 1/drug therapy , Insulin Infusion Systems , Insulin Resistance , Insulin/administration & dosage , Adult , Blood Glucose/metabolism , Body Weight , Diabetes Mellitus, Type 1/physiopathology , Female , Glycated Hemoglobin/analysis , Glycosuria , Humans , Infusions, Intravenous , Injections, Subcutaneous , Insulin/therapeutic use , Plasma Exchange
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