Glenna A. Dowling
University of California, San Francisco
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Featured researches published by Glenna A. Dowling.
Journal of the American Geriatrics Society | 2008
Glenna A. Dowling; Robert L. Burr; Eus J. W. Van Someren; Erin M. Hubbard; Jay S. Luxenberg; Judy Mastick; Bruce A. Cooper
OBJECTIVES: To test whether the addition of melatonin to bright‐light therapy enhances the efficacy in treating rest–activity (circadian) disruption in institutionalized patients with Alzheimers disease (AD).
Cancer | 2005
Catherine E. Jansen; Christine Miaskowski; Marylin Dodd; Glenna A. Dowling; Joel H. Kramer
Little is known about the effects of chemotherapy on cognitive function. The purposes of this metaanalysis were to estimate the effect sizes for the effect of chemotherapy on each domain of cognitive function and to differentiate effect sizes by each method of comparison of effects (i.e., normative data, control group, or baseline data).
International Psychogeriatrics | 2005
Glenna A. Dowling; Erin M. Hubbard; Judy Mastick; Jay S. Luxenberg; Robert L. Burr; Eus J. W. Van Someren
BACKGROUND Disturbances in rest-activity rhythm are prominent and disabling symptoms in Alzheimers disease (AD). Nighttime sleep is severely fragmented and daytime activity is disrupted by multiple napping episodes. In most institutional environments, light levels are very low and may not be sufficient to enable the circadian clock to entrain to the 24-hour day. The purpose of this randomized, placebo-controlled, clinical trial was to test the effectiveness of morning bright light therapy in reducing rest-activity (circadian) disruption in institutionalized patients with severe AD. METHOD Subjects (n = 46, mean age 84 years) meeting the NINCDS-ADRDA (National Institute of Neurological and Communicative Disorders and Stroke--the Alzheimers Disease and Related Disorders Association) AD diagnostic criteria were recruited from two large, skilled nursing facilities in San Francisco, California. The experimental group received one hour (09:30-10:30) of bright light exposure (> or = 2500 lux in gaze direction) Monday through Friday for 10 weeks. The control group received usual indoor light (150-200 lux). Nighttime sleep efficiency, sleep time, wake time and number of awakenings and daytime wake time were assessed using actigraphy. Circadian rhythm parameters were also determined from the actigraphic data using cosinor analysis and nonparametric techniques. Repeated measures analysis of variance (ANOVA) was used to test the primary study hypotheses. RESULTS AND CONCLUSION Although significant improvements were found in subjects with aberrant timing of their rest-activity rhythm, morning bright light exposure did not induce an overall improvement in measures of sleep or the rest-activity in all treated as compared to control subjects. The results indicate that only subjects with the most impaired rest-activity rhythm respond significantly and positively to a brief (one hour) light intervention.
Psycho-oncology | 2008
Catherine E. Jansen; Marylin Dodd; Christine Miaskowski; Glenna A. Dowling; Joel H. Kramer
Objectives: Recent studies suggest that standard dose chemotherapy for breast cancer may cross the blood–brain barrier. However, the evidence for chemotherapy‐induced cognitive impairments in breast cancer patients is inconsistent. The purposes of this study in a sample of newly diagnosed patients with breast cancer were to (1) evaluate cognitive function prior to the administration of chemotherapy; (2) assess changes in cognitive function over time; and (3) evaluate potential relationships between cognitive function and anxiety, depression, fatigue, hemoglobin level, menopausal status, and perception of cognitive function.
Oncology Nursing Forum | 2005
Catherine E. Jansen; Christine Miaskowski; Marylin Dodd; Glenna A. Dowling; Joel H. Kramer
PURPOSE/OBJECTIVES To review the domains of cognitive function and their corresponding neuroanatomic structures as well as present current evidence for neurotoxicity associated with specific chemotherapeutic agents and potential mechanisms for chemotherapy-induced cognitive impairments. DATA SOURCES Published research articles, review articles, and textbooks. DATA SYNTHESIS Chemotherapy does not appear to cross the blood-brain barrier when given in standard doses; however, many chemotherapy drugs have the potential to cause cognitive impairments through more than one mechanism. In addition, patient factors may be protective or place individuals at higher risk for cognitive impairments. CONCLUSIONS Although evidence of chemotherapy-induced impairments in cognitive function exists, no clinical studies have attempted to elucidate the mechanisms for chemotherapy-induced impairments in cognitive function. In addition, further studies are needed to determine predictive factors, potential biomarkers, and relevant assessment parameters. IMPLICATIONS FOR NURSING The ability to identify high-risk patients has important implications for practice in regard to informed consent, patient education about the effects of treatment, and preventive strategies.
Movement Disorders | 2006
Kevin M. Biglan; Steven R. Schwid; Shirley Eberly; Karen Blindauer; Stanley Fahn; Tamar Goren; Karl Kieburtz; David Oakes; Sandra Plumb; Andrew Siderowf; Matthew B. Stern; Ira Shoulson; Denni Day; Aileen Shinaman; Mark F. Lew; Connie Kawai; Howard I. Hurtig; Mary Lloyd; Robert A. Hauser; Lisa Gauger; Robert E. Wood; Lawrence I. Golbe; Joanne Wojcieszek; Joann Belden; Andrew Feigin; Mary Lou Klimek; Barbara Shannon; William G. Ondo; Christine Hunter; Vincent Calabrese
The objective of this study was to determine the effects of rasagiline as monotherapy on quality of life (QOL) in patients with early Parkinsons disease (PD). Rasagiline, a potent, second‐generation, irreversible, selective monoamine oxidase B inhibitor improves PD symptoms in patients with early PD. Patients with early untreated PD were randomly assigned to once‐daily rasagiline 1 mg/day, rasagiline 2 mg/day, or placebo in a 6‐month, double‐blind trial (n = 404). At the end of 6 months, patients entered the preplanned, active‐treatment phase in which those receiving 1 mg/day and 2 mg/day of rasagiline continued on their previously assigned dosages and those receiving placebo switched to rasagiline 2 mg/day, while maintaining blinding to treatment assignments. QOL was measured with the Parkinsons Disease Quality of Life questionnaire (PDQUALIF) at 0, 14, 26, and 52 weeks after randomization. Analysis of the change in PDQUALIF scores from baseline to 6 months showed adjusted treatment effects (with 95% confidence interval) favoring rasagiline over placebo of −2.91 units (−5.19, −0.64, P = 0.01) for the 1 mg/day group and −2.74 units (−5.02, −0.45, P = 0.02) for the 2 mg/day. Subscore analysis attributed most of this benefit to the self‐image/sexuality domain. At 12 months (n = 266), with all groups receiving rasagiline for at least 6 months, no significant differences in PDQUALIF scores were seen between groups. Rasagiline improved QOL compared with placebo. This QOL improvement appears to be accounted for primarily by the symptomatic benefit of rasagiline.
Western Journal of Nursing Research | 2007
Glenna A. Dowling; Carla Graf; Erin M. Hubbard; Jay S. Luxenberg
Neuropsychiatric behaviors are common in people with Alzheimers disease (AD) and make both professional and lay caregiving difficult. Light therapy has been somewhat successful in ameliorating disruptive behaviors. This randomized trial tested the effects of morning or afternoon bright light exposure compared with usual indoor light on the presence, frequency, severity, and occupational disruptiveness of neuropsychiatric behaviors in nursing home residents with AD. Light was administered for 1 hr daily (Monday-Friday) for 10 weeks. The Neuropsychiatric Inventory—Nursing Home was used to assess behavior at baseline and end of the intervention. Analyses revealed statistically significant differences between groups on agitation/aggression, depression/dysphoria, aberrant motor behavior, and appetite/eating disorders. The magnitude of change was small and may not represent clinically significant findings. Agitation/aggression and nighttime behaviors commonly occurred and were highly correlated with occupational disruptiveness. Interventions that decrease the presence and/or severity of neuropsychiatric behaviors have the potential to significantly decrease caregiver burden.
Oncology Nursing Forum | 2007
Catherine E. Jansen; Christine Miaskowski; Dodd Mj; Glenna A. Dowling
PURPOSE/OBJECTIVES To identify which neuropsychological tests have been used to evaluate chemotherapy-induced impairment in various domains of cognitive function in patients with breast cancer and to determine the sensitivity of each of the tests through estimation of effect size. DATA SOURCES Original studies published from 1966-June 2006. DATA SYNTHESIS Although an array of neuropsychological tests are available to measure the various domains of cognitive function, information is lacking regarding the sensitivity and specificity of the tests to detect changes in cognitive function from chemotherapy. CONCLUSIONS This meta-analysis provides initial data on the sensitivity of some neuropsychological tests to determine chemotherapy-induced changes in cognitive function in patients with breast cancer. IMPLICATIONS FOR NURSING The identification of sensitive neuro-psychological tests is crucial to further understanding of chemotherapy-induced cognitive impairments.
Journal of Psychosocial Nursing and Mental Health Services | 1996
Robin Buccheri; Louise Trygstad; Nick Kanas; Bernice Waldron; Glenna A. Dowling
Persistent auditory hallucinations can be brought under self-control using behavioral strategies. In this study, all participants found at least one strategy that decreased the distress associated with their symptoms. Both participants and facilitators reported that working within a group to lessen the distress associated with auditory hallucinations was a positive experience. An interactive process of teaching and learning enhanced the learning of both participants and facilitators.
Journal of Neuroscience Nursing | 2010
Yeonsu Song; Glenna A. Dowling; Margaret I. Wallhagen; Kathryn A. Lee; William J. Strawbridge
Sleep in older adults with Alzheimers disease can often be extremely fragmented, thus disturbing normal sleep-wake rhythms. This poor-quality sleep is challenging for caregivers and frequently results in admitting older adults to long-term care institutions. Many variables, such as genes, medications, depression, and environmental factors, influence sleep in persons with Alzheimers disease. Interventions, such as exposure to light, melatonin therapy, sleep hygiene, and physical activity, are commonly used to treat or to prevent sleep problems. Neuroscience nurses can play an important role in assessing sleep characteristics and related factors, educating caregivers and staff, providing family members with emotional support, and conducting research.