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Dive into the research topics where Kenneth I. Shulman is active.

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Featured researches published by Kenneth I. Shulman.


International Journal of Geriatric Psychiatry | 2000

Clock-drawing: is it the ideal cognitive screening test?

Kenneth I. Shulman

Objective. The clock‐drawing test has achieved widespread clinical use in recent years as a cognitive screening instrument and a significant amount of literature relates to its psychometric properties and clinical utility. This review aims to synthesize the available evidence and assess the value of this screening test according to well‐defined criteria.


International Journal of Geriatric Psychiatry | 2010

Brief cognitive screening instruments: an update

Zahinoor Ismail; Tarek K. Rajji; Kenneth I. Shulman

To review the recent literature on cognitive screening with a focus on brief screening methods in primary care as well as geriatric services.


International Journal of Geriatric Psychiatry | 1996

A validation study of The Geriatric Depression Scale short form

Nathan Herrmann; Nicole Mittmann; Ivan L. Silver; Kenneth I. Shulman; Usoa A. Busto; Neil H. Shear; Claudio A. Naranjo

The validity of the Geriatric Depression Scale (GDS) short form was assessed in a geriatric affective disorders outpatient clinic (N = 116). The GDS was highly correlated with the Montgomery Asberg Depression Rating Scale (MADRS), and with optimal cutoff scores of 5/6, demonstrated a sensitivity of 85% and a specificity of 74.0%. The GDS appears to be a useful, valid screening instrument in this population.


Journal of the American Geriatrics Society | 2004

Drug‐Induced Lithium Toxicity in the Elderly: A Population‐Based Study

David N. Juurlink; Muhammad Mamdani; Alexander Kopp; Paula A. Rochon; Kenneth I. Shulman; Donald A. Redelmeier

Objectives: To study the association between hospital admission for lithium toxicity and the use of diuretics, angiotensin‐converting enzyme (ACE) inhibitors, and nonsteroidal antiinflammatory drugs (NSAIDs) in the elderly.


Journal of Affective Disorders | 1997

The efficacy, safety and tolerability of antidepressants in late life depression : a meta-analysis

Nicole Mittmann; Nathan Herrmann; Thomas R. Einarson; Usoa E. Busto; Krista L. Lanctôt; Barbara A. Liu; Kenneth I. Shulman; Ivan L. Silver; Claudio A. Naranjo; Neil H. Shear

BACKGROUND To determine the efficacy, safety and tolerability of antidepressants in depressed elderly patients. METHODS Search for randomized controlled double-blind studies evaluating atypical antidepressants (ATYPs), reversible inhibitors of monoamine oxidase-A, selective serotonin reuptake inhibitors (SSRIs) and tricyclic antidepressants in moderate/severe depressed patients > or = 60 years for > or = four weeks. The random effects model (single-arm; comparative) was used to aggregate efficacy, safety and dropout. RESULTS No difference in single-arm aggregation of outcomes for four antidepressant classes. Comparative analyses showed no statistical difference between outcomes, except SSRIs had a higher response rate than ATYPs. CONCLUSION Elderly show no differences in antidepressant class outcomes. LIMITATIONS Heterogeneity and lack of power. CLINICAL RELEVANCE There is little advantage for antidepressant classes over another in the aged.


Drugs & Aging | 2000

Differential Pharmacokinetics of Lithium in Elderly Patients

Beth Sproule; Brian G. Hardy; Kenneth I. Shulman

The pharmacotherapeutic use of lithium in the elderly as acute and maintenance therapy in bipolar disorder and augmentation therapy for major depression is well documented. Differences in the response to lithium are explained, in part, by the effect of age-related physiological changes, comorbid conditions, and concurrent medications on the pharmacokinetics of lithium in the elderly. The pharmacokinetic profile of lithium has been studied for many years, primarily in younger adult populations. Lithium pharmacokinetics may be influenced by a number of factors including age. It was first noted several years ago that elderly individuals required lower doses of lithium to achieve serum concentrations similar to those observed in younger adults. This is due to the combination of a reduced volume of distribution and reduced renal clearance. The composition of the human body changes with aging producing an increase in body fat, a decrease in fat-free mass and a decrease in total body water. Lithium clearance decreases as the glomerular filtration rate decreases with increasing age.The effects of other medical conditions in the elderly on the pharmacokinetics of lithium are less well delineated. Reduced lithium clearance is expected in patients with hypertension, congestive heart failure or renal dysfunction. Larger lithium maintenance doses are required in obese compared with non-obese patients.The most clinically significant pharmacokinetic drug interactions associated with lithium involve drugs which are commonly used in the elderly. Thiazide diuretics, ACE inhibitors, and nonsteroidal anti-inflammatory drugs can increase serum lithium concentrations.The tolerability of lithium is lower in the elderly. Neurotoxicity clearly occurs in the elderly at concentrations considered ‘therapeutic’ in general adult populations. There are no placebo-controlled randomised trials of lithium in old age and recommendations for clinical use are based on extrapolations from pharmacokinetic studies, anecdotal reports from mixed age populations and clinical experience in old age psychiatry. Serum concentrations of lithium need to be markedly reduced in the elderly population and particularly so in the very old and frail elderly.


BMJ | 2003

Changing prescription patterns for lithium and valproic acid in old age: shifting practice without evidence.

Kenneth I. Shulman; Paula A. Rochon; Kathy Sykora; Geoffrey M. Anderson; Muhammad Mamdani; Susan E. Bronskill; Chau T.T. Tran

Over the past decade, valproic acid (prescribed as divalproex in North America) has been marketed as an alternative to lithium for treating bipolar disorders. For elderly patients, however, there is no clear evidence that valproic acid is more beneficial than lithium. Moreover, the evidence for the superiority of valproic acid in treating bipolar disorders—mixed episodes and rapid cycling—has been challenged in a recent Cochrane review.1 Valproic acid has not benefited patients with manic and psychiatric symptoms in dementia, despite the growing use of the drug in the management of these conditions.2 Recently, the relatively rapid shift in prescription patterns has been questioned.3 We describe trends in the use of lithium and valproic acid in a large population of people over 65. We obtained information on drug use from the Ontario Drug Benefit Program, which provides comprehensive drug benefits to all residents aged 65 or older in Ontario, Canada. …


American Journal of Geriatric Psychiatry | 2004

Pharmacotherapy of Bipolar Disorder in Old Age Review and Recommendations

Robert C. Young; Laszlo Gyulai; Benoit H. Mulsant; Alastair J. Flint; John L. Beyer; Kenneth I. Shulman; Charles F. Reynolds

The authors reviewed the evidence-base for pharmacological treatment of mania and bipolar (BP) depression in late life. Treatment benefits and side effects may be modified by age-associated factors, such as neurocognitive impairments. Lithium and divalproex have most often been studied in elderly patients, and both may be efficacious in acute treatment of mania, but there are no controlled efficacy or effectiveness trials. The role of atypical antipsychotic agents remains to be clarified. Similarly, there are no systematic studies of the treatment of BP depression in elderly patients. The authors make suggestions for management and delineate priorities for research.


Journal of the American Geriatrics Society | 2007

A Population-Based Study of Cholinesterase Inhibitor Use for Dementia

Nathan Herrmann; Sudeep S. Gill; Chaim M. Bell; Geoffrey M. Anderson; Susan E. Bronskill; Kenneth I. Shulman; Hadas D. Fischer; Kathy Sykora; Haijiang Steven Shi; Paula A. Rochon

OBJECTIVES: To examine current utilization patterns of cholinesterase inhibitor (ChEI) therapy for dementia to determine treatment duration, use in long‐term care, how often patients receive these drugs until death, and frequency of switching between the available ChEIs.


CNS Drugs | 2013

Current place of monoamine oxidase inhibitors in the treatment of depression.

Kenneth I. Shulman; Nathan Herrmann; Scott E. Walker

This paper reviews the discovery and history of the use of irreversible monoamine oxidase (MAO) inhibitors (MAOIs) such as phenelzine, tranylcypromine and isocarboxazid, as well as the second generation selective and reversible MAOIs such as the MAO-A inhibitor, moclobemide and the MAO-B inhibitor, selegiline. Data for review were identified from a literature search of OvidSP Medline and PsycInfo performed in July 2012, using the subject terms and keywords of ‘monoamine oxidase inhibitors’, ‘major depression’, ‘depressive disorder’ and ‘depression (emotion)’. The search was limited to papers published in the English language and from 2007 onward only.Irreversible MAOIs have the potential to treat the most challenging mood disorder patients including those with treatment-resistant depression, atypical depression and bipolar depression. Unfortunately, the use of irreversible MAOIs has been declining sharply due to lack of marketing and the excessive fears of clinicians. Moreover, few clinicians now have any experience, let alone comfort, in prescribing this class of antidepressants. The newer MAOIs are available as another option for the treatment of major depression but have not replaced the irreversible MAOIs for the specific sub-types of depression for which they are now recommended in most consensus guidelines and treatment algorithms.The pharmacology, drug interactions and dietary recommendations associated with the use of MAOIs are reviewed. With the appropriate dietary restrictions and attention to potential drug interactions with serotonin and noradrenaline agents this class of drugs can be used effectively and safely. The MAOIs still represent an important element in our therapeutic armamentarium. Despite recommendations by opinion leaders and consensus guidelines for the use of MAOIs in specific sub-types of depression, the prescription rate of MAOIs is far less than expected and is decreasing. The “bad reputation” and the lack of industry support for this class of agents (especially the irreversible MAOIs) must be overcome in order to continue to provide a potentially useful treatment for a very vulnerable yet substantial sub-population of mood disorder patients.

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Nathan Herrmann

Sunnybrook Health Sciences Centre

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David Ames

University of Melbourne

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Edmond Chiu

University of Melbourne

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Scott E. Walker

Sunnybrook Health Sciences Centre

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