Mark S Lipton

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Mark S Lipton, M.D.

Clinical Associate Professor;
Department of Medicine (Cardio Div)

Clinical Addresses

635 MADISON AVENUE 3RD FLOOR
NEW YORK, NY 10022
Hours: Mon. 8 - 5; Tue. 8 - 5; Wed. 8 - 5; Thu. 8 - 5
Phone: 212-570-2077
Fax: 212-249-6856

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Medical Specialties

Cardiology, Internal Medicine

Medical Expertise

Echocardiogram, General Internal Medicine, Coronary Disease Csurg, Lipid Metabolism, Acute Myocardial Infarction, Valvular Disease, Lipid Disorders, Arteriosclerosis, General Cardiology

Languages

Russian

Insurance

UHC EPO, UHC HMO, UHC POS, UHC PPO, UHC TOP TIER

Insurance Disclaimer: Insurance listed above may not be accepted at all office locations. Please confirm prior to each visit. The information presented here may not be complete or may have changed.

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Board Certification

1981 — Internal Medicine
1985 — Cardiovascular Disease (Internal Med)

Education

1978 — New York University School of Medicine, Medical Education
1978-1979 — NYU Medical Center, Internship
1979-1981 — NYU Medical Center, Residency Training
1983-1985 — NYU Medical Center (Cardiology), Clinical Fellowships

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All data from NYU Health Sciences Library Faculty Bibliography — -

Contact:
http://hsl.med.nyu.edu/faculty-bibliography-search#about

Approaches to patient health information exchange and their impact on emergency medicine
Shapiro, Jason S; Kannry, Joseph; Lipton, Mark; Goldberg, Eric; Conocenti, Paul; Stuard, Susan; Wyatt, Brian M; Kuperman, Gilad
2006 Oct;48(4):426-432, Annals of emergency medicine
Regional health information organizations and electronic health information exchange may have an important impact on the practice of emergency medicine in the United States. Regional health information organizations are local or regional information-sharing networks that enable electronic data interchange among stakeholders in a given geographic area. These stakeholders may include hospitals, skilled nursing facilities, clinics, private physicians' offices, pharmacies, laboratories, radiology facilities, health departments, payers, and possibly the patients themselves. Regional health information organizations are being formed across the country to improve the safety and efficiency of clinical care; improve public health efforts, biosurveillance, and disaster management response; and potentially create large databases of deidentified aggregate data for research. Because of the unique need for rapid access to information and the acuity of the clinical environment, few areas of the health care delivery system stand to change and benefit more from health information exchange than our nation's emergency departments. This article will explain the motivation for the development of regional health information organizations, identify some of the important issues in their formation, and discuss how their development might affect the practice of emergency medicine
— id: 113897, year: 2006, vol: 48, page: 426, stat: Journal Article,

NORMAL LEFT-VENTRICULAR ECHOCARDIOGRAMS IN PATIENTS WITH AORTIC-STENOSIS
Lipton, M; Slater, J; Kramer, P; Schwartz, W; Winer, H; Kronzon, I; Glassman, E
1986 FEB ;7(2):A30-A30, Journal of the American College of Cardiology
— id: 51208, year: 1986, vol: 7, page: A30, stat: Journal Article,

THE INFLUENCE OF CORONARY-ARTERY DISEASE ON THE HEMODYNAMIC PROFILE OF PATIENTS WITH ANGINA AND AORTIC-STENOSIS
Lipton, M; Slater, J; Kramer, P; Schwartz, W; Winer, H; Kronzon, I; Glassman, E
1986 FEB ;7(2):A171-A171, Journal of the American College of Cardiology
— id: 51209, year: 1986, vol: 7, page: A171, stat: Journal Article,

Operation for chronic constrictive pericarditis: Do the surgical approach and degree of pericardial resection influence the outcome significantly?
Culliford AT; Lipton M; Spencer FC
1980 Feb;29(2):146-152, Annals of thoracic surgery
Our experience with 27 patients undergoing pericardiectomy at New York University Medical Center over the past 13 years has evolved a radical pericardiectomy operation suggesting that two traditional concepts are erroneous: (1) pericardiectomy limited to the anterior and lateral surfaces of the ventricles is an adequate operation and (2) delayed recovery is due to myocardial 'atrophy' and not to inadequate operation. Radical pericardiectomy entails removal of virtually the entire parietal pericardium from all cardiac surfaces including that of both ventricles, the right atrium, and the venae cavae. Performed in 22 patients by dissecting a cleavage plane between the thickened parietal pericardium and underlying epicardium, all procedures were done through a sternotomy. Intraoperative monitoring of arterial pressure, cardiac output, and wedge pressure is essential because of displacement of the left ventricle. The left ventricle can be completely mobilized so that at the end of the operation the entire heart can be lifted upward and the course of the coronary sinus fully visualized. Intraoperative pressure measurements demonstrate that this radical resection immediately corrects hemodynamic abnormalities (elevated right atrial and ventricular end-diastolic pressures), as demonstrated in 10 patients. Most patients undergo massive diuresis (7 to 16 kg) within two weeks, with an uneventful recovery. These findings contrast markedly with early experiences using a conventional limited pericardiectomy
— id: 28941, year: 1980, vol: 29, page: 146, stat: Journal Article,

Surgery for chronic constrictive pericarditis. Does surgical approach and degree of pericardial resection significantly influence outcome?
Culliford AT; Lipton M; Isom OW; Cunningham J; Boyd AD; Adams P; Reed G; Spencer FC
1978 Sep;78(11):1719-1721, New York state journal of medicine
— id: 28945, year: 1978, vol: 78, page: 1719, stat: Journal Article,

A specific inhibitor of complement (C5)-derived chemotactic activity in serum from patients with systemic lupus erythematosus
Perez, H D; Lipton, M; Goldstein, I M
1978 Jul;62(1):29-38, Journal of clinical investigation
In the course of examining polymorphonuclear leukocyte (PMN) chemotaxis in patients with systemic lupus erythematosus (SLE), we have found a previously undescribed serum inhibitor of complement (C5)-derived chemotactic activity. Serum from a 25-yr-old Black female with untreated SLE, when activated with zymosan, failed completely to attract either her own or normal PMN. Incubation of normal PMN with the patient's serum did not affect their subsequent random motility or chemotactic response toward normal zymosan-treated serum (ZTS). The patient's serum, however, did inhibit the chemotactic activity of normal ZTS and of column-purified C5-derived peptide(s), but had no effect on the chemotactic activity of either the synthetic peptide, N-formylmethionyl leucyl-phenylalanine or a filtrate prepared from a culture of Escherichia coli (bacterial chemotactic factor). The inhibitory activity in the patient's serum resisted heating at 56 degrees C for 30 min and could be separated from C5-derived chemotactic activity in the patient's ZTS (or normal ZTS that had been incubated with the patient's serum) by chromatography on Sephadex G-75. Despite its effect on C5-derived chemotactic activity, the patient's serum did not influence two other C5-derived biologic activities: PMN lysosomal enzyme-releasing activity and PMN-aggregating activity. Chromatography of the patient's serum (65% ammonium sulfate pellet) on Sephadex G-200 yielded three distinct peaks of inhibitory activity. Two were heat labile and exhibited other properties of the previously described chemotactic factor inactivators of normal human serum. The third and most active peak, however, resisted heating at 56 degrees C for 30 min, eluted with an apparent mol wt of 50,000-60,000, and acted specifically on C5-derived chemotactic activity. This uniquely specific, heat-stable inhibitor of C5-derived chemotactic activity has been found thus far in serum from 4 of 11 patients with active SLE and may account, in part, for altered host defenses against infections caused by pyogenic microorganisms
— id: 130396, year: 1978, vol: 62, page: 29, stat: Journal Article,