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Dive into the research topics where Suzanne DiFilippo is active.

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Featured researches published by Suzanne DiFilippo.


Journal of the American Geriatrics Society | 1998

Identification of medications that cause cognitive impairment in older people: the case of oxybutynin chloride.

Ira R. Katz; Laura P. Sands; Warren B. Bilker; Suzanne DiFilippo; Alice A. Boyce; Kristina D'Angelo

OBJECTIVES: To evaluate the cognitive effects of acute challenges with the antispasmodic agent oxybutynin hydrochloride in normal older volunteers and to compare these effects with those attributable to diphenhydramine, another commonly used medication with anticholinergic (muscarinicblocking) activity.


American Journal of Geriatric Psychiatry | 2000

Heuristic Comparison of Sertraline With Nortriptyline for the Treatment of Depression in Frail Elderly Patients

David W. Oslin; Joel E. Streim; Ira R. Katz; Buster D. Smith; Suzanne DiFilippo; Thomas R. Ten Have; Thomas Cooper

Studies have demonstrated that the selective serotonin reuptake inhibitor antidepressants have similar efficacy to other agents, such as tricyclic antidepressants. However, data are limited for direct comparisons with other antidepressants. The authors conducted a contemporaneous comparison of nursing home residents treated with open-label sertraline in doses up to 100 mg/day with nursing home residents treated in a double-blind randomized study of low vs. regular doses of nortriptyline. There were 97 patients enrolled in the study (28 treated with sertraline), with an average treatment duration of 55 days. There were no differences in the tolerability of sertraline vs. nortriptyline. However, in this group of frail older adults, sertraline was not as effective as nortriptyline for the treatment of depression.


Journal of Geriatric Psychiatry and Neurology | 2002

Pharmacologic treatment of depression in nursing home residents: a mental health services perspective.

Catherine J. Datto; David W. Oslin; Joel E. Streim; Stephen M. Scheinthal; Suzanne DiFilippo; Ira R. Katz

Over the past 10 to 15 years, there has been marked progress in clinical research on depression in nursing home residents. There have also been significant changes in federal regulations designed to improve the quality of care. In 1987, only 10% of nursing home residents diagnosed with depression were receiving treatment, but by 1999, 25% of all residents were receiving antidepressants. We report on two studies: one demonstrating that treatment for depression has a substantial, ecologically relevant impact in the nursing home and another demonstrating that profound changes have occurred in the clinical epidemiology of depression and its treatment in the nursing home. Although the numbers of nursing home residents receiving antidepressants have increased dramatically, there are now second-generation problems that must be addressed to ensure the delivery of effective treatment. Developing models to ensure quality of care will require focused mental health services research.


Journal of the American Geriatrics Society | 2006

Simvastatin Causes Changes in Affective Processes in Elderly Volunteers

Knashawn H. Morales; Marsha N. Wittink; Catherine J. Datto; Suzanne DiFilippo; Mark S. Cary; Thomas TenHave; Ira R. Katz

OBJECTIVES: To test for simvastatin‐induced changes in affect and affective processes in elderly volunteers.


Journal of General Internal Medicine | 2008

A Randomized Controlled Trial of a Close Monitoring Program for Minor Depression and Distress

Jennifer T. Ross; Thomas TenHave; April Eakin; Suzanne DiFilippo; David W. Oslin

ABSTRACTBACKGROUNDMinor depression is almost twice as common in primary care (PC) as major depression. Despite the high prevalence, few evidence-based algorithms exist for managing patients with minor depression or patients presenting solely with distress.OBJECTIVESThe aim of this study was to test the effectiveness of a telephone-based close monitoring program to manage PC patients with minor depression or distress.DESIGNSubjects were randomly assigned to either the control arm (usual care; UC) or the intervention arm (close monitoring; CM). We hypothesized that those randomized to CM would exhibit less depression and be less likely to have symptoms progress to the point of meeting diagnostic criteria.SUBJECTSOverall, 223 PC subjects with minor depression or distress consented to participation in this trial.MEASUREMENTSAt baseline, subjects completed a telephone-based evaluation comprised of validated diagnostic assessments of depression and other MH disorders. Outcomes were assessed at six months utilizing this same battery. Chart reviews were conducted to track care received, such as prescribed antidepressants and MH and primary care visits.RESULTSSubjects in the CM arm exhibited fewer psychiatric diagnoses than those in the UC arm (χ2 = 4.04, 1 df, p = 0.04). In addition, the intervention group showed improved overall physical health (SF-12 PCS scores) (M = 45.1, SD = 11.8 versus M = 41.5, SD = 12.4) (χ2 = 5.90, 1 df, p = .02).CONCLUSIONSThose randomized to CM exhibited less MH problems at the conclusion of the trial, indicating that the close monitoring program is effective, feasible and valuable. The findings of this study will allow us to enhance clinical care and support the integration of mental health services and primary care.


International Journal of Geriatric Psychiatry | 2013

Telephone-based care management for older adults initiated on psychotropic medication

Donovan T. Maust; Shahrzad Mavandadi; Amy Benson; Joel E. Streim; Suzanne DiFilippo; Thomas Snedden; Anita L. Weber; David W. Oslin

This study aimed to explore the longitudinal, 6‐month symptom course of older adults newly started on an antidepressant or anxiolytic by non‐psychiatrist physicians and enrolled in a care management program.


Journal of Geriatric Psychiatry and Neurology | 2003

Effect of Increasing the Dose and Duration of Sertraline Trial in the Treatment of Depressed Nursing Home Residents

Daniel Weintraub; Joel E. Streim; Catherine J. Datto; Ira R. Katz; Suzanne DiFilippo; David W. Oslin

There has been limited research into defining what constitutes an adequate first-line antidepressant trial in elderly patients. The authors report the outcome of extended, high-dosage sertraline treatment in a sample of nursing home residents experiencing residual significant depressive symptoms after 10 weeks of treatment with sertraline at a final dosage of 100 mg/day. Subjects who had a Hamilton Depression Rating Scale score ≥ 12 after 10 weeks of treatment with sertraline were eligible for the 8-week open-label extension phase, which involved titrating the sertraline dosage to 200 mg/day. The cumulative response rate was 52% for the extension phase, compared with 37% for the acute phase. Examining acute phase nonresponders, 39% responded during the extension phase. Rates of discontinuation due to adverse events were comparable in the 2 phases. Our findings suggest that an extended trial or high dosages of sertraline may benefit some depressed elderly patients with persistent depression after acute treatment. (J Geriatr Psychiatry Neurol 2003; 16:109-111)


American Journal of Geriatric Psychiatry | 1996

Use of the Hamilton and Montgomery-Asberg Depression Scales in Institutionalized Elderly Patients

Steven C. Samuels; Ira R. Katz; Patricia A. Parmelee; Alice A. Boyce; Suzanne DiFilippo

In screening for a study of drug treatment of major depression, the authors obtained data on depressive symptoms in elderly residential care patients (N = 116; average age 84 years; 81% women). Principal-components analysis (with varimax rotation) of the Hamilton Rating Scale for Depression yielded a four-factor solution (accounting for 47.2% of variance): core depression, anxiety, insomnia-hypochondriasis, and cognitive-ideational symptoms. The Montgomery-Asberg Depression Scale yielded two factors (54% of variance)-core depression and anxiety. Core depression factor scores from both scales (but not other factor scores) predicted mortality. The association of core depression with mortality (in subsets of patients for which data on these covariates were available) remained significant after measures of illness burden and disability were controlled.


JAMA Psychiatry | 2015

A Telephone-Based Program to Provide Symptom Monitoring Alone vs Symptom Monitoring Plus Care Management for Late-Life Depression and Anxiety: A Randomized Clinical Trial

Shahrzad Mavandadi; Amy Benson; Suzanne DiFilippo; Joel E. Streim; David W. Oslin

IMPORTANCE Mental health (MH) conditions are undertreated in late life. It is important to identify treatment strategies that address variability in treatment content and delivery and take individual-specific symptoms into account, particularly among low-income, community-dwelling older adults. OBJECTIVE To evaluate program feasibility and MH outcomes among community-dwelling older adults randomized to 1 of 2 treatment arms of varying intensity of evidence-based, collaborative MH care management services (ie, the Supporting Seniors Receiving Treatment and Intervention [SUSTAIN] program) that provide standardized, measurement-based, software-aided MH assessment and symptom monitoring and connection to community resources via telephone. DESIGN, SETTING, AND PARTICIPANTS Trial participants were 1018 older, community-dwelling, low-income adults prescribed an antidepressant or anxiolytic by a primary care or non-MH professional and experiencing clinically significant MH symptoms at intake. The participant subsample was drawn from a larger parent sample of older adults enrolled in the SUSTAIN program. Individuals were randomized to receive MH symptom monitoring alone (hereafter monitoring alone) or MH symptom monitoring plus care management (hereafter care management) provided by an MH professional. Baseline characteristics were examined, and changes in clinical MH outcomes were evaluated at 3-month and 6-month follow-up. The study dates were August 5, 2010, to May 5, 2014. INTERVENTIONS Monitoring alone or care management delivered by an MH professional. MAIN OUTCOMES AND MEASURES Overall MH functioning (primary) and depressive and anxiety symptoms. RESULTS A total of 509 participants were randomized to the monitoring alone group and 509 to the care management group; 377 and 401 completed ≥2 research assessments in the monitoring alone and case management groups, respectively. Compared with those randomized to monitoring alone, individuals randomized to care management showed greater improvements in the 3 domains of MH functioning (β [SE], 0.36 [0.12]; 95% CI, 0.12 to 0.60; P = .004), depressive symptoms (β [SE], -0.20 [0.06]; 95% CI, -0.32 to -0.09; P < .001), and anxiety symptoms (β [SE], -0.23 [0.05]; 95% CI, -0.33 to -0.14; P < .001) over time. CONCLUSIONS AND RELEVANCE The SUSTAIN program, which provides assessment, monitoring, care management, and brief therapies for MH symptoms and needs in primary care settings, is feasible and scalable. A more intense level of care (ie, symptom monitoring plus care management) is associated with more favorable individual outcomes for low-income, community-dwelling older adults experiencing clinically significant MH symptoms. TRIAL REGISTRATION clinicaltrials.gov Identifier: NCT02440594.


Neuropsychopharmacology | 2005

Probing for Affective Side Effects of Drugs Used in Geriatric Practice: Use of Daily Diaries to Test for Effects of Metoclopramide and Naproxen

Ira R. Katz; Knashawn H. Morales; Catherine J. Datto; Joel E. Streim; David W. Oslin; Suzanne DiFilippo; Thomas R. Ten Have

The aim of this study was to develop the use of daily diaries of affects and events as measures of pharmacological effects on affective processes and to apply them to evaluate the possible affective toxicity of metoclopramide and naproxen, two medications commonly used in geriatric practice. In all, 105 adults aged 65 years or older were randomized to receive metoclopramide (up to 40 mg/day), naproxen (up to 1000 mg/day), or placebo under double-blind conditions for a period of 5 weeks. Patients were seen weekly for evaluations of affective and cognitive outcomes as well as safety. In addition, patients kept diaries with daily records of positive and negative affect and reports of significant daily events. Findings included mixed model analyses of drug assignment, time, events, and interactions for both positive affect and days with significant negative affect. Subjects exhibited high levels of adherence in completing daily diaries. Neither the pattern of dropouts nor the weekly assessments demonstrated significant drug effects on mood or affect. However, diary data demonstrated that metoclopramide increased the apparent impact of negative events on both positive and negative affect relative to placebo, and that naproxen increased the apparent impact of positive events on positive affect and, possibly, of negative events on negative affect relative to placebo. The findings confirm the utility of diary methods for studying drug effects on affective processes in normal elderly subjects. They suggest that both metoclopramide and naproxen can affect the associations between daily events and affects. If replicated, they would demonstrate that drug effects can extend beyond the intensity of affect and/or the emergence of full-fledged psychiatric disorders to include moderation of the interactions between daily events and affect.

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David W. Oslin

University of Pennsylvania

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Joel E. Streim

University of Pennsylvania

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Ira R. Katz

University of Pennsylvania

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Amy Benson

University of Pennsylvania

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Kristina D'Angelo

University of Pennsylvania

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Shirley H. Leong

University of Pennsylvania

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Alice A. Boyce

University of Pennsylvania

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