Andreas Coppi
Yale University
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Publication
Featured researches published by Andreas Coppi.
Biomedical optics | 2003
Richard A. DeVerse; Frank Geshwind; Ronald R. Coifman; William G. Fateley; Andreas Coppi
We have constructed an adaptive digitally tuned light source in the form of a de-dispersive imaging spectrograph in both the visible and near infrared spectral regions capable of illuminating a sample with appropriate energy weighted spectral bands or spatio-spectral bands that relate only to the constituents of interest to the investigator. The energy from each of the spectral resolution elements can be digitally modulated to provide a tuned weighted spectral output. A tuned light source based on this technology was adapted for use in a conventional imaging microscope system to enable direct measure of spatio-spectral features of interest. Some imagery resulting from preliminary tests on colon tissue biopsies are presented.
Biomedical optics | 2006
Mauro Maggioni; Gustave L. Davis; Frederick Warner; Frank Geshwind; Andreas Coppi; Richard A. DeVerse; Ronald R. Coifman
We apply a unique micro-optoelectromechanical tuned light source and new algorithms to the hyper-spectral microscopic analysis of human colon biopsies. The tuned light prototype (Plain Sight Systems Inc.) transmits any combination of light frequencies, range 440nm 700nm, trans-illuminating H and E stained tissue sections of normal (N), benign adenoma (B) and malignant carcinoma (M) colon biopsies, through a Nikon Biophot microscope. Hyper-spectral photomicrographs, randomly collected 400X magnication, are obtained with a CCD camera (Sensovation) from 59 different patient biopsies (20 N, 19 B, 20 M) mounted as a microarray on a single glass slide. The spectra of each pixel are normalized and analyzed to discriminate among tissue features: gland nuclei, gland cytoplasm and lamina propria/lumens. Spectral features permit the automatic extraction of 3298 nuclei with classification as N, B or M. When nuclei are extracted from each of the 59 biopsies the average classification among N, B and M nuclei is 97.1%; classification of the biopsies, based on the average nuclei classification, is 100%. However, when the nuclei are extracted from a subset of biopsies, and the prediction is made on nuclei in the remaining biopsies, there is a marked decrement in performance to 60% across the 3 classes. Similarly the biopsy classification drops to 54%. In spite of these classification differences, which we believe are due to instrument and biopsy normalization issues, hyper-spectral analysis has the potential to achieve diagnostic efficiency needed for objective microscopic diagnosis.
Journal of the American Heart Association | 2017
Chenxi Huang; Sanket S. Dhruva; Andreas Coppi; Frederick Warner; Shu-Xia Li; Haiqun Lin; Khurram Nasir; Harlan M. Krumholz
Background SPRINT (Systolic Blood Pressure Intervention Trial) and the ACCORD (Action to Control Cardiovascular Risk in Diabetes) blood pressure trial used similar interventions but produced discordant results. We investigated whether differences in systolic blood pressure (SBP) response contributed to the discordant trial results. Methods and Results We evaluated the distributions of SBP response during the first year for the intensive and standard treatment groups of SPRINT and ACCORD using growth mixture models. We assessed whether significant differences existed between trials in the distributions of SBP achieved at 1 year and the treatment‐independent relationships of achieved SBP with risks of primary outcomes defined in each trial, heart failure, stroke, and all‐cause death. We examined whether visit‐to‐visit variability was associated with heterogeneous treatment effects. Among the included 9027 SPRINT and 4575 ACCORD participants, the difference in mean SBP achieved between treatment groups was 15.7 mm Hg in SPRINT and 14.2 mm Hg in ACCORD, but SPRINT had significantly less between‐group overlap in the achieved SBP (standard deviations of intensive and standard groups, respectively: 6.7 and 5.9 mm Hg in SPRINT versus 8.8 and 8.2 mm Hg in ACCORD; P<0.001). The relationship between achieved SBP and outcomes was consistent across trials except for stroke and all‐cause death. Higher visit‐to‐visit variability was more common in SPRINT but without treatment‐effect heterogeneity. Conclusions SPRINT and ACCORD had different degrees of separation in achieved SBP between treatment groups, even as they had similar mean differences. The greater between‐group overlap of achieved SBP may have contributed to the discordant trial results.
Hypertension | 2017
Sanket S. Dhruva; Chenxi Huang; Erica S. Spatz; Andreas Coppi; Frederick Warner; Shu-Xia Li; Haiqun Lin; Xiao Xu; Curt D. Furberg; Barry R. Davis; Sara L. Pressel; Ronald R. Coifman; Harlan M. Krumholz
Randomized trials of hypertension have seldom examined heterogeneity in response to treatments over time and the implications for cardiovascular outcomes. Understanding this heterogeneity, however, is a necessary step toward personalizing antihypertensive therapy. We applied trajectory-based modeling to data on 39 763 study participants of the ALLHAT (Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial) to identify distinct patterns of systolic blood pressure (SBP) response to randomized medications during the first 6 months of the trial. Two trajectory patterns were identified: immediate responders (85.5%), on average, had a decreasing SBP, whereas nonimmediate responders (14.5%), on average, had an initially increasing SBP followed by a decrease. Compared with those randomized to chlorthalidone, participants randomized to amlodipine (odds ratio, 1.20; 95% confidence interval [CI], 1.10–1.31), lisinopril (odds ratio, 1.88; 95% CI, 1.73–2.03), and doxazosin (odds ratio, 1.65; 95% CI, 1.52–1.78) had higher adjusted odds ratios associated with being a nonimmediate responder (versus immediate responder). After multivariable adjustment, nonimmediate responders had a higher hazard ratio of stroke (hazard ratio, 1.49; 95% CI, 1.21–1.84), combined cardiovascular disease (hazard ratio, 1.21; 95% CI, 1.11–1.31), and heart failure (hazard ratio, 1.48; 95% CI, 1.24–1.78) during follow-up between 6 months and 2 years. The SBP response trajectories provided superior discrimination for predicting downstream adverse cardiovascular events than classification based on difference in SBP between the first 2 measurements, SBP at 6 months, and average SBP during the first 6 months. Our findings demonstrate heterogeneity in response to antihypertensive therapies and show that chlorthalidone is associated with more favorable initial response than the other medications.
PLOS ONE | 2017
Julian S. Haimovich; Arjun K. Venkatesh; Abbas Shojaee; Andreas Coppi; Frederick Warner; Shu-Xia Li; Harlan M. Krumholz
Identifying temporal variation in hospitalization rates may provide insights about disease patterns and thereby inform research, policy, and clinical care. However, the majority of medical conditions have not been studied for their potential seasonal variation. The objective of this study was to apply a data-driven approach to characterize temporal variation in condition-specific hospitalizations. Using a dataset of 34 million inpatient discharges gathered from hospitals in New York State from 2008–2011, we grouped all discharges into 263 clinical conditions based on the principal discharge diagnosis using Clinical Classification Software in order to mitigate the limitation that administrative claims data reflect clinical conditions to varying specificity. After applying Seasonal-Trend Decomposition by LOESS, we estimated the periodicity of the seasonal component using spectral analysis and applied harmonic regression to calculate the amplitude and phase of the condition’s seasonal utilization pattern. We also introduced four new indices of temporal variation: mean oscillation width, seasonal coefficient, trend coefficient, and linearity of the trend. Finally, K-means clustering was used to group conditions across these four indices to identify common temporal variation patterns. Of all 263 clinical conditions considered, 164 demonstrated statistically significant seasonality. Notably, we identified conditions for which seasonal variation has not been previously described such as ovarian cancer, tuberculosis, and schizophrenia. Clustering analysis yielded three distinct groups of conditions based on multiple measures of seasonal variation. Our study was limited to New York State and results may not directly apply to other regions with distinct climates and health burden. A substantial proportion of medical conditions, larger than previously described, exhibit seasonal variation in hospital utilization. Moreover, the application of clustering tools yields groups of clinically heterogeneous conditions with similar seasonal phenotypes. Further investigation is necessary to uncover common etiologies underlying these shared seasonal phenotypes.
Pharmacoepidemiology and Drug Safety | 2018
Jonathan Bates; Craig S. Parzynski; Sanket S. Dhruva; Andreas Coppi; Richard E. Kuntz; Shu-Xia Li; Danica Marinac-Dabic; Frederick A. Masoudi; Richard E. Shaw; Frederick Warner; Harlan M. Krumholz; Joseph S. Ross
To estimate medical device utilization needed to detect safety differences among implantable cardioverter defibrillators (ICDs) generator models and compare these estimates to utilization in practice.
Journal of the American College of Cardiology | 2017
Sanket S. Dhruva; Chenxi Huang; Erica S. Spatz; Andreas Coppi; Frederick Warner; Shu-Xia Li; Haiqun Lin; Xiao Xu; Curt Furberg; Barry Davis; Sara Pressel; Ronald R. Coifman; Harlan M. Krumholz
Background: Prior randomized trials of hypertension have rarely examined patient heterogeneity in response to treatments and the implications for outcomes. Methods: We applied growth mixture modeling to identify distinct SBP trajectory classes within the first 6 months of ALLHAT. We assessed the
IEEE Journal of Biomedical and Health Informatics | 2017
Bobak Mortazavi; Nihar R. Desai; Jing Zhang; Andreas Coppi; Frederick Warner; Harlan M. Krumholz; Sahand Negahban
Electronic health records (EHR) provide opportunities to leverage vast arrays of data to help prevent adverse events, improve patient outcomes, and reduce hospital costs. This paper develops a postoperative complications prediction system by extracting data from the EHR and creating features. The analytic engine then provides model accuracy, calibration, feature ranking, and personalized feature responses. This allows clinicians to interpret the likelihood of an adverse event occurring, general causes for these events, and the contributing factors for each specific patient. The patient cohort considered was 5214 patients in Yale-New Haven Hospital undergoing major cardiovascular procedures. Cohort-specific models predicted the likelihood of postoperative respiratory failure and infection, and achieved an area under the receiver operating characteristic curve of 0.81 for respiratory failure and 0.83 for infection.
Archive | 2005
Frank Geshwind; Andreas Coppi; William G. Fateley; Nicholas Black; Zydrunas Gimbutas; Marya R. Doery
Archive | 2005
Andreas Coppi; Ronald R. Coifman; Jonathan Berger; Frank Geshwind; William G. Fateley