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289


Gaps in Medical Therapy for Patients with Heart Failure and Reduced Ejection Fraction (HFrEF) in a Large, Diverse, Electronically Identified Cohort [Meeting Abstract]

Mukhopadhyay, Amrita; Reynolds, Harmony; Phillips, Lawrence M.; Nagler, Arielle; Horwitz, Leora; Katz, Stuart D.; Blecker, Saul
ISI:000752020001276
ISSN: 0009-7322
CID: 5263712

CHARACTERISTICS OF MYOCARDIAL INFARCTION AND EARLY PRESENTATION AFTER PREGNANCY AMONG WOMEN WITH PRIOR ADVERSE PREGNANCY OUTCOMES [Meeting Abstract]

Countouris, Malamo; Koczo, Agnes; Reynolds, Harmony; Hausvater, Anais; Mulukutla, Suresh; Catov, Janet
ISI:000647487503082
ISSN: 0735-1097
CID: 5285742

SEX DIFFERENCES IN EVALUATION AND MANAGEMENT OF YOUNG ADULTS PRESENTING TO THE EMERGENCY DEPARTMENT WITH CHEST PAIN [Meeting Abstract]

Banco, Darcy; Chang, Jerway; Talmor, Nina; Lu, Xinlin; Wadhera, Priya; Reynolds, Harmony
ISI:000648571300005
ISSN: 0735-1097
CID: 4929652

Psychosocial Factors Amongst Women with MINOCA [Meeting Abstract]

Hausvater, Anais; Spruill, Tanya; Park, Ki; Smilowitz, Nathaniel; Shah, Binita; Marzo, Kevin; Jhalani, Nisha; Giesler, Caitlin; Mehta, Laxmi S.; Ahmed, Bina; Merz, C. Noel Bairey; Thomas, Dwithiya; Trost, Jeff; Mehta, Puja; Har, Bryan; Bainey, Kevin R.; Xia, Yuhe; Zhong, Hua; Hada, Ellen; Hochman, Judith S.; Reynolds, Harmony
ISI:000752020003325
ISSN: 0009-7322
CID: 5285762

Assessment of Racial/Ethnic Disparities in Hospitalization and Mortality in Patients With COVID-19 in New York City

Ogedegbe, Gbenga; Ravenell, Joseph; Adhikari, Samrachana; Butler, Mark; Cook, Tiffany; Francois, Fritz; Iturrate, Eduardo; Jean-Louis, Girardin; Jones, Simon A; Onakomaiya, Deborah; Petrilli, Christopher M; Pulgarin, Claudia; Regan, Seann; Reynolds, Harmony; Seixas, Azizi; Volpicelli, Frank Michael; Horwitz, Leora Idit
Importance/UNASSIGNED:Black and Hispanic populations have higher rates of coronavirus disease 2019 (COVID-19) hospitalization and mortality than White populations but lower in-hospital case-fatality rates. The extent to which neighborhood characteristics and comorbidity explain these disparities is unclear. Outcomes in Asian American populations have not been explored. Objective/UNASSIGNED:To compare COVID-19 outcomes based on race and ethnicity and assess the association of any disparities with comorbidity and neighborhood characteristics. Design, Setting, and Participants/UNASSIGNED:This retrospective cohort study was conducted within the New York University Langone Health system, which includes over 260 outpatient practices and 4 acute care hospitals. All patients within the system's integrated health record who were tested for severe acute respiratory syndrome coronavirus 2 between March 1, 2020, and April 8, 2020, were identified and followed up through May 13, 2020. Data were analyzed in June 2020. Among 11 547 patients tested, outcomes were compared by race and ethnicity and examined against differences by age, sex, body mass index, comorbidity, insurance type, and neighborhood socioeconomic status. Exposures/UNASSIGNED:Race and ethnicity categorized using self-reported electronic health record data (ie, non-Hispanic White, non-Hispanic Black, Hispanic, Asian, and multiracial/other patients). Main Outcomes and Measures/UNASSIGNED:The likelihood of receiving a positive test, hospitalization, and critical illness (defined as a composite of care in the intensive care unit, use of mechanical ventilation, discharge to hospice, or death). Results/UNASSIGNED:Among 9722 patients (mean [SD] age, 50.7 [17.5] years; 58.8% women), 4843 (49.8%) were positive for COVID-19; 2623 (54.2%) of those were admitted for hospitalization (1047 [39.9%] White, 375 [14.3%] Black, 715 [27.3%] Hispanic, 180 [6.9%] Asian, 207 [7.9%] multiracial/other). In fully adjusted models, Black patients (odds ratio [OR], 1.3; 95% CI, 1.2-1.6) and Hispanic patients (OR, 1.5; 95% CI, 1.3-1.7) were more likely than White patients to test positive. Among those who tested positive, odds of hospitalization were similar among White, Hispanic, and Black patients, but higher among Asian (OR, 1.6, 95% CI, 1.1-2.3) and multiracial patients (OR, 1.4; 95% CI, 1.0-1.9) compared with White patients. Among those hospitalized, Black patients were less likely than White patients to have severe illness (OR, 0.6; 95% CI, 0.4-0.8) and to die or be discharged to hospice (hazard ratio, 0.7; 95% CI, 0.6-0.9). Conclusions and Relevance/UNASSIGNED:In this cohort study of patients in a large health system in New York City, Black and Hispanic patients were more likely, and Asian patients less likely, than White patients to test positive; once hospitalized, Black patients were less likely than White patients to have critical illness or die after adjustment for comorbidity and neighborhood characteristics. This supports the assertion that existing structural determinants pervasive in Black and Hispanic communities may explain the disproportionately higher out-of-hospital deaths due to COVID-19 infections in these populations.
PMID: 33275153
ISSN: 2574-3805
CID: 4694552

Searching for Underlying Causes of MINOCA With Multi-Modality Imaging [Editorial]

Reynolds, Harmony R
PMID: 32828765
ISSN: 1876-7591
CID: 4614402

RAAS Inhibitors and Risk of Covid-19. Reply [Comment]

Reynolds, Harmony R; Adhikari, Samrachana; Iturrate, Eduardo
PMID: 33108107
ISSN: 1533-4406
CID: 4646512

Thrombosis in Hospitalized Patients with Viral Respiratory Infections versus COVID-19 [Letter]

Smilowitz, Nathaniel R; Subashchandran, Varun; Yuriditsky, Eugene; Horowitz, James M; Reynolds, Harmony R; Hochman, Judith S; Berger, Jeffrey S
BACKGROUND:Thrombosis is a prominent feature of the novel Coronavirus disease 2019 (COVID-19). The incidence of thrombosis during hospitalization for non-COVID-19 viral respiratory infections is uncertain. We evaluated the incidence of thrombosis in patients hospitalized with non-COVID-19 acute viral respiratory illnesses compared to COVID-19. METHODS:Adults age >18 years hospitalized with a non-COVID-19 viral respiratory illness between 2002-2014 were identified. The primary study outcome was a composite of venous and arterial thrombotic events, including myocardial infarction (MI), acute ischemic stroke, and venous thromboembolism, as defined by ICD-9 codes. The incidence of thrombosis in non-COVID-19 viral respiratory illnesses was compared to the recently published incidence of thrombosis in COVID-19 from 3,334 patients hospitalized in New York in 2020. RESULTS:Among 954,521 hospitalizations with viral pneumonia from 2002 to 2014 (mean age 62.3 years, 57.1% female), the combined incidence of arterial and venous thrombosis was 5.0%. Acute MI occurred in 2.8% of hospitalizations, VTE in 1.6%, ischemic stroke in 0.7%, and other systemic embolism in 0.1%. Patients with thrombosis had higher in-hospital mortality (14.9% vs. 3.3%, p<0.001) than those without thrombosis. The proportion of hospitalizations complicated by thrombosis was lower in patients with viral respiratory illness in 2002-2014 than in COVID-19 (median age 64; 39.6% female) in 2020 (5% vs. 16%; p<0.001) CONCLUSION: In a nationwide analysis of hospitalizations for viral pneumonias, thrombosis risk was lower than that observed in patients with COVID-19. Investigations into mechanisms of thrombosis and risk reduction strategies in COVID-19 and other viral respiratory infections are necessary. SHORT ABSTRACT/UNASSIGNED:We evaluated the incidence of thrombosis in patients hospitalized with non-COVID-19 acute viral respiratory illnesses nationwide from 2012 to 2014 and compared this to the incidence among patients hospitalized with COVID-19 at a large health system in New York. Non-COVID-19 viral respiratory illness was complicated by acute MI in 2.8% of hospitalizations, VTE in 1.6%, ischemic stroke in 0.7%, and other systemic embolism in 0.1%. The proportion of hospitalizations complicated by thrombosis was lower in patients with viral respiratory illness in 2002-2014 than in COVID-19 (5% vs. 16%; p<0.001).
PMCID:7654304
PMID: 33181067
ISSN: 1097-6744
CID: 4665432

Initial Invasive Versus Conservative Management of Stable Ischemic Heart Disease in Patients With a History of Heart Failure or Left Ventricular Dysfunction: Insights From the ISCHEMIA Trial

Lopes, Renato D; Alexander, Karen P; Stevens, Susanna R; Reynolds, Harmony R; Stone, Gregg W; Piña, Ileana L; Rockhold, Frank W; Elghamaz, Ahmed; Lopez-Sendon, Jose Luis; Farsky, Pedro S; Chernyavskiy, Alexander M; Diaz, Ariel; Phaneuf, Denis; De Belder, Mark A; Ma, Yi-Tong; Guzman, Luis A; Khouri, Michel; Sionis, Alessandro; Hausenloy, Derek J; Doerr, Rolf; Selvanayagam, Joseph B; Maggioni, Aldo Pietro; Hochman, Judith S; Maron, David J
BACKGROUND:Whether an initial invasive strategy in patients with stable ischemic heart disease and at least moderate ischemia improves outcomes in the setting of a history of heart failure (HF) or left ventricular dysfunction (LVD) when ejection fraction is ≥35% but <45% is unknown. METHODS:Among 5179 participants randomized into ISCHEMIA (International Study of Comparative Health Effectiveness With Medical and Invasive Approaches), all of whom had left ventricular ejection fraction (LVEF) ≥35%, we compared cardiovascular outcomes by treatment strategy in participants with a history of HF/LVD at baseline versus those without HF/LVD. Median follow-up was 3.2 years. RESULTS:interaction = 0.055). A similar differential effect was seen for the primary outcome, all-cause mortality, and cardiovascular mortality when invasive versus conservative strategy-associated outcomes were analyzed with LVEF as a continuous variable for patients with and without previous HF. CONCLUSIONS:ISCHEMIA participants with stable ischemic heart disease and at least moderate ischemia with a history of HF or LVD were at increased risk for the primary outcome. In the small, high-risk subgroup with HF and LVEF 35% to 45%, an initial invasive approach was associated with better event-free survival. This result should be considered hypothesis-generating. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01471522.
PMID: 32862662
ISSN: 1524-4539
CID: 4683762

Randomized evaluation of beta blocker and ACE-inhibitor/angiotensin receptor blocker treatment in patients with myocardial infarction with non-obstructive coronary arteries (MINOCA-BAT): Rationale and design

Nordenskjöld, Anna M; Agewall, Stefan; Atar, Dan; Baron, Tomasz; Beltrame, John; Bergström, Olle; Erlinge, David; Gale, Chris P; López-Pais, Javier; Jernberg, Tomas; Johansson, Pelle; Ravn-Fisher, Annica; Reynolds, Harmony R; Somaratne, Jithendra B; Tornvall, Per; Lindahl, Bertil
Myocardial infarction with non-obstructive coronary arteries (MINOCA) is common and occurs in 6-8% of all patients fulfilling the diagnostic criteria for acute myocardial infarction (AMI). This paper describes the rationale behind the trial 'Randomized Evaluation of Beta Blocker and ACE-Inhibitor/Angiotensin Receptor Blocker Treatment (ACEI/ARB) of MINOCA patients' (MINOCA-BAT) and the need to improve the secondary preventive treatment of MINOCA patients. METHODS: MINOCA-BAT is a registry-based, randomized, parallel, open-label, multicenter trial with 2:2 factorial design. The primary aim is to determine whether oral beta blockade compared with no oral beta blockade, and ACEI/ARB compared with no ACEI/ARB, reduce the composite endpoint of death of any cause, readmission because of AMI, ischemic stroke or heart failure in patients discharged after MINOCA without clinical signs of heart failure and with left ventricular ejection fraction ≥40%. A total of 3500 patients will be randomized into four groups; e.g. ACEI/ARB and beta blocker, beta blocker only, ACEI/ARB only and neither ACEI/ARB nor beta blocker, and followed for a mean of 4 years. SUMMARY: While patients with MINOCA have an increased risk of serious cardiovascular events and death, whether conventional secondary preventive therapies are beneficial has not been assessed in randomized trials. There is a limited basis for guideline recommendations in MINOCA. Furthermore, studies of routine clinical practice suggest that use of secondary prevention therapies in MINOCA varies considerably. Thus results from this trial may influence future treatment strategies and guidelines specific to MINOCA patients.
PMID: 33203618
ISSN: 1097-6744
CID: 4716502