Premium
Dramatic Worsening of Type 2 Diabetes Mellitus Due to Olanzapine After 3 Years of Therapy
Author(s) -
Bechara Christopher I.,
GoldmanLevine Jennifer D.
Publication year - 2001
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1592/phco.21.17.1444.34423
Subject(s) - olanzapine , medicine , discontinuation , orthostatic vital signs , extrapyramidal symptoms , diabetes mellitus , atypical antipsychotic , dopamine antagonist , clozapine , complication , anticholinergic , antipsychotic , type 2 diabetes mellitus , anesthesia , schizophrenia (object oriented programming) , endocrinology , psychiatry , antagonist , blood pressure , receptor
Olanzapine, a serotonin‐dopamine‐receptor antagonist, is an atypical antipsychotic agent used to treat schizophrenia and other psychotic disorders. It is preferred over older antipsychotics because of its relatively low frequency of sedation, orthostatic hypotension, extrapyramidal symptoms, and anticholinergic side effects. A 45‐year‐old man with well‐controlled type 2 diabetes mellitus experienced an abrupt worsening of his diabetes after 3 years of olanzapine therapy. His hemoglobin A 1c (HbA 1c ) level rose from a baseline of 5.9–6.2% to 12.5%. Discontinuation of olanzapine by means of a 3‐month taper resulted in a reduction in HbA 1c to pretreatment levels. Although cases of olanzapine‐induced hyperglycemia have been documented in the literature, this complication has not been reported in a patient maintained on therapy for this duration. Clinicians should be aware of this possible complication in patients receiving long‐term olanzapine therapy.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom