Searched for: Department/Unit:Population Health
The authors reply [Letter]
Duncan, Dustin T; Kawachi, Ichiro; Subramanian, S V; Aldstadt, Jared; Melly, Steven J; Williams, David R
PMCID:3927981
PMID: 24693551
ISSN: 0002-9262
CID: 1028782
Electrocardiographic predictors of adverse cardiovascular events in acute drug overdose: A validation study [Meeting Abstract]
Manini, Alex F; Stimmel, Barry; Nair, Ajith; Vedanthan, Rajesh; Vlahov, David; Hoffman, Robert S
ISI:000335007100261
ISSN: 1556-9519
CID: 1019612
Defining the clinical course of multiple sclerosis: The 2013 revisions
Lublin, Fred D; Reingold, Stephen C; Cohen, Jeffrey A; Cutter, Gary R; Sorensen, Per Soelberg; Thompson, Alan J; Wolinsky, Jerry S; Balcer, Laura J; Banwell, Brenda; Barkhof, Frederik; Bebo, Bruce Jr; Calabresi, Peter A; Clanet, Michel; Comi, Giancarlo; Fox, Robert J; Freedman, Mark S; Goodman, Andrew D; Inglese, Matilde; Kappos, Ludwig; Kieseier, Bernd C; Lincoln, John A; Lubetzki, Catherine; Miller, Aaron E; Montalban, Xavier; O'Connor, Paul W; Petkau, John; Pozzilli, Carlo; Rudick, Richard A; Sormani, Maria Pia; Stuve, Olaf; Waubant, Emmanuelle; Polman, Chris H
Accurate clinical course descriptions (phenotypes) of multiple sclerosis (MS) are important for communication, prognostication, design and recruitment of clinical trials, and treatment decision-making. Standardized descriptions published in 1996 based on a survey of international MS experts provided purely clinical phenotypes based on data and consensus at that time, but imaging and biological correlates were lacking. Increased understanding of MS and its pathology, coupled with general concern that the original descriptors may not adequately reflect more recently identified clinical aspects of the disease, prompted a re-examination of MS disease phenotypes by the International Advisory Committee on Clinical Trials of MS. While imaging and biological markers that might provide objective criteria for separating clinical phenotypes are lacking, we propose refined descriptors that include consideration of disease activity (based on clinical relapse rate and imaging findings) and disease progression. Strategies for future research to better define phenotypes are also outlined.
PMCID:4117366
PMID: 24871874
ISSN: 0028-3878
CID: 1018782
Solid renal masses: what the numbers tell us
Kang, Stella K; Huang, William C; Pandharipande, Pari V; Chandarana, Hersh
OBJECTIVE. Solid renal masses are most often incidentally detected at imaging as small (= 4 cm) localized lesions. These lesions comprise a wide spectrum of benign and malignant histologic subtypes, but are largely treated with surgical resection given the limited ability of imaging to differentiate among them with consistency and high accuracy. Numerous studies have thus examined the ability of CT and MRI techniques to separate benign lesions from malignancies and to predict renal cancer histologic grade and subtype. This article synthesizes the evidence regarding renal mass characterization at CT and MRI, provides diagnostic algorithms for evidence-based practice, and highlights areas of further research needed to drive imaging-based management of renal masses. CONCLUSION. Despite extensive study of morphologic and quantitative criteria at conventional imaging, no CT or MRI techniques can reliably distinguish solid benign tumors, such as oncocytoma and lipid-poor angiomyolipoma, from malignant renal tumors. Larger studies are required to validate recently developed techniques, such as diffusion-weighted imaging. Evidence-based practice includes MRI to assess renal lesions in situations where CT is limited and to help guide management in patients who are considered borderline surgical candidates.
PMCID:4174582
PMID: 24848816
ISSN: 0361-803x
CID: 1005042
Bisphenol A Exposure Is Associated with Decreased Lung Function
Spanier, Adam J; Fiorino, Elizabeth K; Trasande, Leonardo
OBJECTIVE: To examine the associations of bisphenol A (BPA) exposure with lung function measures and exhaled nitric oxide (FeNO) in children. STUDY DESIGN: We performed a cross-sectional analysis of a subsample of US children age 6-19 years who participated in the 2007-2010 National Health and Nutrition Examination Survey. We assessed univariate and multivariable associations of urinary BPA concentration with the predicted pulmonary function measures for age, sex, race/ethnicity and height (forced expiratory volume in 1 second [FEV1], forced vital capacity [FVC], forced expiratory flow 25%-75%, and FEV1 divided by FVC) and with FeNO. RESULTS: Exposure and outcome data were available for 661 children. Median BPA was 2.4 ng/mL (IQR: 1.3, 4.1). In multivariable analysis, a larger urinary BPA concentration was associated with significantly decreased percent predicted forced expiratory flow 25%-75% (%FEF2575) (3.7%, 95% CI 1.0, 6.5) and percent predicted FEV1 divided by FVC (%FEV1/FVC) (0.8%, 95% CI 0.1, 1.7) but not percent predicted FEV1, percent predicted FVC, or FeNO. A child in the top quartile of BPA compared with the bottom quartile had a 10% decrease in %FEF2575 (95% CI -1, -19) and 3% decrease in %FEV1/FVC (95% CI -1, -5). CONCLUSIONS: BPA exposure was associated with a modest decrease in %FEF2575 (small airway function) and %FEV1/FVC (pulmonary obstruction) but not FEV1, FVC, or FeNO. Explanations of the association cannot rule out the possibility of reverse causality.
PMCID:4035373
PMID: 24657123
ISSN: 0022-3476
CID: 1004052
Comparison of 2 Informant Questionnaire Screening Tools for Dementia and Mild Cognitive Impairment: AD8 and IQCODE
Razavi, Mehrdad; Tolea, Magdalena I; Margrett, Jennifer; Martin, Peter; Oakland, Andrew; Tscholl, David W; Ghods, Sarah; Mina, Mazdak; Galvin, James E
BACKGROUND: Dementia and mild cognitive impairment (MCI) are underrecognized in community settings. This may be due in part to the lack of brief dementia screening tools available to clinicians. We compared 2 brief, informant-based screening tests: the AD8 and the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) in a community-based neurology practice in the midwestern United States. METHODS: We examined 186 consecutive patients (44 controls, 13 with MCI, and 129 with dementia). Receiver operator characteristic curves were used to examine the ability of AD8 and IQCODE to discriminate between controls and MCI or dementia. Sensitivity, specificity, predictive values, and likelihood ratios were reported. RESULTS: AD8 differentiated healthy controls from MCI (P<0.001) or dementia (P<0.001), and MCI from dementia (P=0.008). The IQCODE differentiated controls and MCI from dementia (both P<0.001), and between controls and MCI (P=0.002). Both AD8 (AUC=0.953; 95% confidence interval, 0.92-0.99) and IQCODE (AUC=0.930, 95% confidence interval, 0.88-0.97) provided discrimination between controls and patients with dementia; however, the AD8 had superior sensitivity detecting dementia (99.2%) and MCI (100%) compared with the IQCODE (79.1% for dementia, 46.1% for MCI) with nonoverlapping confidence intervals. Using published cut-offs (AD8>/=2, IQCODE>/=3.4), only 1 case of dementia was missed with the AD8, whereas the IQCODE failed to detect dementia in 27 individuals. The AD8 detected MCI in all 13 individuals, whereas the IQCODE misclassified 7 individuals. CONCLUSIONS: Both the AD8 and IQCODE were able to detect dementia in a community setting. The AD8, however, was more successful than IQCODE in detecting MCI. If simple and efficient screening for early cognitive impairment is the goal, particularly in the early stages (eg, for prevention trials or public screening), the combination of an informant interview (the AD8) and a brief performance measure could be considered as they meet the basic requirements of the Personalized Prevention Plan for Medicare beneficiaries.
PMCID:3981951
PMID: 24113559
ISSN: 0893-0341
CID: 996642
Chronic Granulomatous Mastitis: An Uncommon Breast Disorder? [Meeting Abstract]
Luu, Xuan; Mor, Adam; Joseph, Kathie-Ann P.
ISI:000334211800096
ISSN: 1068-9265
CID: 997192
Changing the research landscape: the New York City Clinical Data Research Network
Kaushal, Rainu; Hripcsak, George; Ascheim, Deborah D; Bloom, Toby; Campion, Thomas R Jr; Caplan, Arthur L; Currie, Brian P; Check, Thomas; Deland, Emme Levin; Gourevitch, Marc N; Hart, Raffaella; Horowitz, Carol R; Kastenbaum, Isaac; Levin, Arthur Aaron; Low, Alexander F H; Meissner, Paul; Mirhaji, Parsa; Pincus, Harold A; Scaglione, Charles; Shelley, Donna; Tobin, Jonathan N
The New York City Clinical Data Research Network (NYC-CDRN), funded by the Patient-Centered Outcomes Research Institute (PCORI), brings together 22 organizations including seven independent health systems to enable patient-centered clinical research, support a national network, and facilitate learning healthcare systems. The NYC-CDRN includes a robust, collaborative governance and organizational infrastructure, which takes advantage of its participants' experience, expertise, and history of collaboration. The technical design will employ an information model to document and manage the collection and transformation of clinical data, local institutional staging areas to transform and validate data, a centralized data processing facility to aggregate and share data, and use of common standards and tools. We strive to ensure that our project is patient-centered; nurtures collaboration among all stakeholders; develops scalable solutions facilitating growth and connections; chooses simple, elegant solutions wherever possible; and explores ways to streamline the administrative and regulatory approval process across sites.
PMCID:4078297
PMID: 24821739
ISSN: 1067-5027
CID: 985652
The spectrum of cognitive impairment in Lewy body diseases
Goldman, Jennifer G; Williams-Gray, Caroline; Barker, Roger A; Duda, John E; Galvin, James E
Cognitive impairment represents an important and often defining component of the clinical syndromes of Lewy body disorders: Parkinson's disease and dementia with Lewy bodies. The spectrum of cognitive deficits in these Lewy body diseases encompasses a broad range of clinical features, severity of impairment, and timing of presentation. It is now recognized that cognitive dysfunction occurs not only in more advanced Parkinson's disease but also in early, untreated patients and even in those patients with pre-motor syndromes, such as rapid eye movement behavior disorder and hyposmia. In recent years, the concept of mild cognitive impairment as a transitional or pre-dementia state in Parkinson's disease has emerged. This has led to much research regarding the diagnosis, prognosis, and underlying neurobiology of mild cognitive impairment in Parkinson's disease, but has also raised questions regarding the usefulness of this concept and its application in clinical and research settings. In addition, the conundrum of whether Parkinson's disease dementia and dementia with Lewy bodies represent the same or different entities remains unresolved. Although these disorders overlap in many aspects of their presentations and pathophysiology, they differ in other elements, such as timing of cognitive, behavioral, and motor symptoms; medication responses; and neuropathological contributions. This article examines the spectrum and evolution of cognitive impairment in Lewy body disorders and debates these controversial issues in the field using point-counterpoint approaches. (c) 2014 International Parkinson and Movement Disorder Society.
PMCID:4126402
PMID: 24757110
ISSN: 0885-3185
CID: 981052
Reconsidering against medical advice discharges
Alfandre, David
PMCID:4000332
PMID: 24526543
ISSN: 0884-8734
CID: 969922