Publications

2020

Ganatra, Sarju, Sourbha S Dani, Robert Redd, Kimberly Rieger-Christ, Rushin Patel, Rohan Parikh, Aarti Asnani, et al. (2020) 2020. “Outcomes of COVID-19 in Patients With a History of Cancer and Comorbid Cardiovascular Disease.”. Journal of the National Comprehensive Cancer Network : JNCCN, 1-10. https://doi.org/10.6004/jnccn.2020.7658.

BACKGROUND: Cancer and cardiovascular disease (CVD) are independently associated with adverse outcomes in patients with COVID-19. However, outcomes in patients with COVID-19 with both cancer and comorbid CVD are unknown.

METHODS: This retrospective study included 2,476 patients who tested positive for SARS-CoV-2 at 4 Massachusetts hospitals between March 11 and May 21, 2020. Patients were stratified by a history of either cancer (n=195) or CVD (n=414) and subsequently by the presence of both cancer and CVD (n=82). We compared outcomes between patients with and without cancer and patients with both cancer and CVD compared with patients with either condition alone. The primary endpoint was COVID-19-associated severe disease, defined as a composite of the need for mechanical ventilation, shock, or death. Secondary endpoints included death, shock, need for mechanical ventilation, need for supplemental oxygen, arrhythmia, venous thromboembolism, encephalopathy, abnormal troponin level, and length of stay.

RESULTS: Multivariable analysis identified cancer as an independent predictor of COVID-19-associated severe disease among all infected patients. Patients with cancer were more likely to develop COVID-19-associated severe disease than were those without cancer (hazard ratio [HR], 2.02; 95% CI, 1.53-2.68; P<.001). Furthermore, patients with both cancer and CVD had a higher likelihood of COVID-19-associated severe disease compared with those with either cancer (HR, 1.86; 95% CI, 1.11-3.10; P=.02) or CVD (HR, 1.79; 95% CI, 1.21-2.66; P=.004) alone. Patients died more frequently if they had both cancer and CVD compared with either cancer (35% vs 17%; P=.004) or CVD (35% vs 21%; P=.009) alone. Arrhythmias and encephalopathy were also more frequent in patients with both cancer and CVD compared with those with cancer alone.

CONCLUSIONS: Patients with a history of both cancer and CVD are at significantly higher risk of experiencing COVID-19-associated adverse outcomes. Aggressive public health measures are needed to mitigate the risks of COVID-19 infection in this vulnerable patient population.

Riley, Elise D, Eric Vittinghoff, Alan H B Wu, Phillip O Coffin, Priscilla Y Hsue, Dhruv S Kazi, Amanda Wade, Carl Braun, and Kara L Lynch. (2020) 2020. “Impact of Polysubstance Use on High-Sensitivity Cardiac Troponin I over Time in Homeless and Unstably Housed Women.”. Drug and Alcohol Dependence 217: 108252. https://doi.org/10.1016/j.drugalcdep.2020.108252.

INTRODUCTION: The use of controlled substances like cocaine increases the risk of cardiovascular disease (CVD) and myocardial infarction (MI). However, outside of alcohol and tobacco, substance use is not included in CVD risk assessment tools. We identified the effects of using multiple substances (nicotine/cotinine, cannabis, alcohol, cocaine, methamphetamine, heroin and other opioids) on cardiac injury measured by high-sensitivity troponin (hsTnI) in homeless and unstably housed women.

METHODS: We recruited 245 homeless and unstably housed women from shelters, free meal programs and street encampments. Participants completed six monthly study visits. Adjusting for traditional CVD risk factors, we examined longitudinal associations between substance use and hsTnI.

RESULTS: Median participant age was 53 years and 74 % were ethnic minority women. At baseline, 76 % of participants had hypertension, 31 % were HIV-positive, 8% had a history of a prior MI and 12 % of prior stroke. The most commonly used substances were cotinine/nicotine (80 %), cannabis (68 %) and cocaine (66 %). HsTnI exceeding the 99th percentile (14.7 ng/L) - a level high enough to signal possible MI - was observed in 14 participants during >1 study visit (6%). In adjusted analysis, cocaethylene and fentanyl were significantly associated with higher hsTnI levels.

CONCLUSIONS: Fentanyl use and the co-use of cocaine and alcohol are associated with myocardial injury, suggesting that the use of these substances may act as long-term cardiac insults. Whether risk counseling on these specific substances and/or including their use in CVD risk stratification would improve CVD outcomes in populations where substance use is high merits further investigation.

Hammond, Michael M, Changyu Shen, Stephanie Li, Dhruv S Kazi, Marwa A Sabe, Reshad Garan, Lawrence J Markson, et al. (2020) 2020. “Retrospective Evaluation of Echocardiographic Variables for Prediction of Heart Failure Hospitalization in Heart Failure With Preserved versus Reduced Ejection Fraction: A Single Center Experience.”. PloS One 15 (12): e0244379. https://doi.org/10.1371/journal.pone.0244379.

BACKGROUND: Limited data exist on the differential ability of variables on transthoracic echocardiogram (TTE) to predict heart failure (HF) readmission across the spectrum of left ventricular (LV) systolic function.

METHODS: We linked 15 years of TTE report data (1/6/2003-5/3/2018) at Beth Israel Deaconess Medical Center to complete Medicare claims. In those with recent HF, we evaluated the relationship between variables on baseline TTE and HF readmission, stratified by LVEF.

RESULTS: After excluding TTEs with uninterpretable diastology, 5,900 individuals (mean age: 76.9 years; 49.1% female) were included, of which 2545 individuals (41.6%) were admitted for HF. Diastolic variables augmented prediction compared to demographics, comorbidities, and echocardiographic structural variables (p < 0.001), though discrimination was modest (c-statistic = 0.63). LV dimensions and eccentric hypertrophy predicted HF in HF with reduced (HFrEF) but not preserved (HFpEF) systolic function, whereas LV wall thickness, NT-proBNP, pulmonary vein D- and Ar-wave velocities, and atrial dimensions predicted HF in HFpEF but not HFrEF (all interaction p < 0.10). Prediction of HF readmission was not different in HFpEF and HFrEF (p = 0.93).

CONCLUSIONS: In this single-center echocardiographic study linked to Medicare claims, left ventricular dimensions and eccentric hypertrophy predicted HF readmission in HFrEF but not HFpEF and left ventricular wall thickness predicted HF readmission in HFpEF but not HFrEF. Regardless of LVEF, diastolic variables augmented prediction of HF readmission compared to echocardiographic structural variables, demographics, and comorbidities alone. The additional role of medication adherence, readmission history, and functional status in differential prediction of HF readmission by LVEF category should be considered for future study.

Stone, J, P Priya, M. Wong, P Stanbrige, N Lee-Walsh, and A Li. 2020. “Povutpat Egestas Erat Rhoncus Dapibus Senectus Fringippa..”
Turpis senectus amet tortor in sodates odio tettus. Pretium id amet, euismod sceteriscue vetit. Imperdiet senectus ornare augue donec cuis. Uttrices ut nist egestas eros, nam sceteriscue. Uttricies tacus, nutta cras eget dotor ptacerat. Et in nutta fetis pettentescue augue. Porttitor hendrerit congue morbi proin aticuam.
Stone, J, P Priya, M. Wong, P Stanbrige, N Lee-Walsh, and A Li. 2020. “Povutpat Egestas Erat Rhoncus Dapibus Senectus Fringippa..”
Turpis senectus amet tortor in sodates odio tettus. Pretium id amet, euismod sceteriscue vetit. Imperdiet senectus ornare augue donec cuis. Uttrices ut nist egestas eros, nam sceteriscue. Uttricies tacus, nutta cras eget dotor ptacerat. Et in nutta fetis pettentescue augue. Porttitor hendrerit congue morbi proin aticuam.
Stone, J, P Priya, M. Wong, P Stanbrige, N Lee-Walsh, and A Li. 2020. “Povutpat Egestas Erat Rhoncus Dapibus Senectus Fringippa..”
Turpis senectus amet tortor in sodates odio tettus. Pretium id amet, euismod sceteriscue vetit. Imperdiet senectus ornare augue donec cuis. Uttrices ut nist egestas eros, nam sceteriscue. Uttricies tacus, nutta cras eget dotor ptacerat. Et in nutta fetis pettentescue augue. Porttitor hendrerit congue morbi proin aticuam.
Stone, J, P Priya, M. Wong, P Stanbrige, N Lee-Walsh, and A Li. 2020. “Povutpat Egestas Erat Rhoncus Dapibus Senectus Fringippa..”
Turpis senectus amet tortor in sodates odio tettus. Pretium id amet, euismod sceteriscue vetit. Imperdiet senectus ornare augue donec cuis. Uttrices ut nist egestas eros, nam sceteriscue. Uttricies tacus, nutta cras eget dotor ptacerat. Et in nutta fetis pettentescue augue. Porttitor hendrerit congue morbi proin aticuam.

2019

Meyer, Nicole, Oth Tran, Cindy Hartsfield, Linda Nguyen, Dhruv S Kazi, and Bruce Koch. (2019) 2019. “Revascularization Rates and Associated Costs in Patients With Stable Ischemic Heart Disease Initiating Ranolazine Versus Traditional Antianginals As Add-on Therapy.”. The American Journal of Cardiology 123 (10): 1602-9. https://doi.org/10.1016/j.amjcard.2019.02.014.

To assess the frequency and costs of revascularization procedures in patients with stable ischemic heart disease (SIHD) initiating ranolazine versus traditional antianginals. Adults (≥18 years) with a diagnosis of SIHD who initiated ranolazine or a traditional antianginal (beta-blocker [BB], calcium channel blocker [CCB], or long-acting nitrate [LAN]) as second or third line therapy between 2008 and 2016, were selected from the IBM MarketScan Databases. Inverse probability weighting based on propensity score was employed to balance the ranolazine and traditional antianginals cohorts on patient clinical characteristics. Outcomes assessed were frequency and total cost of revascularization procedures over a 12-month follow-up. A total of 108,741 patients with SIHD were included. Of these, 18% initiated treatment with ranolazine, 21% received BBs, 24% received CCBs, and 37% were treated with LANs. Revascularization rates were significantly lower in ranolazine patients (11%) than in BB (16%) and LAN (14%) patients (both p <0.001), and more comparable to CCB patients (10%; p = 0.007). Compared with BB and LAN, those in the ranolazine cohort were less likely to have a revascularization procedure during hospitalization and had a shorter length of stay if hospitalized (all p <0.001). The mean healthcare costs associated with revascularization were lower in ranolazine patients ($2,933) than in BB ($4,465) and LAN ($3,609) patients (p <0.001), but similar to CCB patients ($2,753; p = 0.29). In conclusion, ranolazine treatment in patients with SIHD was associated with fewer revascularization procedures and lower associated healthcare costs compared with patients initiating BB or LAN, and comparable to patients initiating CCBs.

Kazi, Dhruv S, Joanne Penko, Pamela G Coxson, David Guzman, Pengxiao C Wei, and Kirsten Bibbins-Domingo. (2019) 2019. “Cost-Effectiveness of Alirocumab: A Just-in-Time Analysis Based on the ODYSSEY Outcomes Trial.”. Annals of Internal Medicine 170 (4): 221-29. https://doi.org/10.7326/M18-1776.

BACKGROUND: The ODYSSEY Outcomes (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab) trial included participants with a recent acute coronary syndrome. Compared with participants receiving statins alone, those receiving a statin plus alirocumab had lower rates of a composite outcome including myocardial infarction (MI), stroke, and death.

OBJECTIVE: To determine the cost-effectiveness of alirocumab in these circumstances.

DESIGN: Decision analysis using the Cardiovascular Disease Policy Model.

DATA SOURCES: Data sources representative of the United States combined with data from the ODYSSEY Outcomes trial.

TARGET POPULATION: U.S. adults with a recent first MI and a baseline low-density lipoprotein cholesterol level of 1.81 mmol/L (70 mg/dL) or greater.

TIME HORIZON: Lifetime.

PERSPECTIVE: U.S. health system.

INTERVENTION: Alirocumab or ezetimibe added to statin therapy.

OUTCOME MEASURES: Incremental cost-effectiveness ratio in 2018 U.S. dollars per quality-adjusted life-year (QALY) gained.

RESULTS OF BASE-CASE ANALYSIS: Compared with a statin alone, the addition of ezetimibe cost $81 000 (95% uncertainty interval [UI], $51 000 to $215 000) per QALY. Compared with a statin alone, the addition of alirocumab cost $308 000 (UI, $197 000 to $678 000) per QALY. Compared with the combination of statin and ezetimibe, replacing ezetimibe with alirocumab cost $997 000 (UI, $254 000 to dominated) per QALY.

RESULTS OF SENSITIVITY ANALYSIS: The price of alirocumab would have to decrease from its original cost of $14 560 to $1974 annually to be cost-effective relative to ezetimibe.

LIMITATION: Effectiveness estimates were based on a single randomized trial with a median follow-up of 2.8 years and should not be extrapolated to patients with stable coronary heart disease.

CONCLUSION: The price of alirocumab would have to be reduced considerably to be cost-effective. Because substantial reductions already have occurred, we believe that timely, independent cost-effectiveness analyses can inform clinical and policy discussions of new drugs as they enter the market.

PRIMARY FUNDING SOURCE: University of California, San Francisco, and Institute for Clinical and Economic Review.