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1.
Ann Pharmacother ; 26(6): 757-62, 1992 Jun.
Article in English | MEDLINE | ID: mdl-1611155

ABSTRACT

OBJECTIVE: To assess the ability of a combination of insulin and an oral hypoglycemic agent (glyburide) to improve the overall glycemic control in a population of patients with type I diabetes. DESIGN: Randomized, placebo-controlled, double-blind trial. SETTING: Community-based, university-affiliated, family medicine group. PATIENTS: Men and women between 18 and 68 years of age with type I diabetes. INTERVENTIONS: Subjects were observed and titrated on an insulin-only regimen for 12 weeks (phase I). Subjects were then randomized to receive either placebo or glyburide 10 mg/d for an additional 12 weeks (phase II). MAIN OUTCOME MEASURES: Glucose measurements were taken at breakfast, lunch, supper, and bedtime. Each patient also was followed sequentially for serum lipids, glycosylated hemoglobin, (Hb A1c) and daily insulin utilization. RESULTS: Average fasting blood glucose (FBG) measurements were significantly lower in the glyburide-treated group during phase II (9.22 +/- 0.55 mmol/L) compared with baseline (10.27 +/- 0.93 mmol/L) and phase I (10.41 +/- 0.55 mmol/L). A decrease in the average Hb A1c concentration in the glyburide group was evident by week 4 and was sustained for the duration of the study. The average daily insulin dose rose significantly in the glyburide but not the placebo group compared with baseline. Total cholesterol, triglycerides, and low-density lipoprotein cholesterol did not change significantly in either group over the course of the study. High-density lipoprotein cholesterol increased significantly over baseline in the glyburide group during phase II. Several patients experienced dramatic improvements in glycemic parameters after the addition of glyburide to their insulin regimens. CONCLUSIONS: Improvements were observed in the FBG and Hb A1c measurements of this heterogeneous population of patients with type I diabetes after the addition of glyburide to their insulin regimens. The study failed to find consistent trends in glycemic control when evaluating mean changes in FBG measurements.


Subject(s)
Blood Glucose/analysis , Diabetes Mellitus, Type 1/drug therapy , Glyburide/therapeutic use , Insulin/therapeutic use , Adolescent , Adult , Aged , Diabetes Mellitus, Type 1/blood , Double-Blind Method , Drug Therapy, Combination , Female , Glyburide/administration & dosage , Glycated Hemoglobin/analysis , Humans , Insulin/administration & dosage , Lipids/blood , Male , Middle Aged
2.
DICP ; 24(1): 52-9, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2405587

ABSTRACT

A review of the aldosterone antagonist spironolactone is presented. It is effective both as monotherapy and in combination with other hypotensive agents in the control of both essential and hyperaldosterone-induced hypertension. It is useful as a diuretic in conditions such as cirrhosis and congestive heart failure, and is most commonly employed because of its potassium- and magnesium-sparing qualities. Spironolactone also has been used as an antiandrogenic agent in managing hirsutism. Its adverse effect profile, considered somewhat prohibitive in the past, is generally not significant when reasonably low doses (less than 150 mg/d) are used.


Subject(s)
Spironolactone/pharmacology , Humans , Spironolactone/adverse effects , Spironolactone/pharmacokinetics , Spironolactone/therapeutic use
3.
Drug Intell Clin Pharm ; 22(10): 778-80, 1988 Oct.
Article in English | MEDLINE | ID: mdl-3229343

ABSTRACT

A case of a patient who had an acutely toxic reaction to cocaine ingestion and later developed acute renal failure secondary to rhabdomyolysis is described. Evidence of rhabdomyolysis was noted by the combination of myalgia, urine discoloration, and elevated serum concentrations of muscle enzymes. Although the mechanism of the rhabdomyolysis is unknown, the clinical presentation resembled that of a norepinephrine-induced vasoconstrictive effect that alters the metabolic demands of the muscle in such a way that the muscle is damaged.


Subject(s)
Cocaine/adverse effects , Rhabdomyolysis/chemically induced , Adult , Humans , Male , Rhabdomyolysis/blood
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