Dr. Beaty graduated from the UMDNJ Robert Wood Johnson Medical School in 1983. He works in Jersey City, NJ and specializes in Internal Medicine. Dr. Beaty is affiliated with Jersey City Medical Center.
Feb 2012 to 2000 National Account ManagerRoche Diabetes Care
Aug 2009 to Jan 2012 National Account ManagerRoche Diabetes Care Minneapolis, MN Jan 2005 to Jul 2009 Regional Business ManagerRoche Diabetes Care
Apr 2001 to Dec 2004 National Account Manager - RetailRoche Diabetes Care
Jan 2000 to Mar 2001 Key Account Business Manager - RetailRoche Diabetes Care
Jan 1998 to Dec 1999 Regional Account Manager - RetailHORMEL FOODS CORPORATION - MEAT PRODUCTS DIVISION Los Angeles, CA Apr 1994 to Jan 1998 Account ExecutiveHORMEL FOODS CORPORATION - MEAT PRODUCTS DIVISION Denver, CO Dec 1991 to Jan 1998 Territory Manager AAHORMEL FOODS CORPORATION - MEAT PRODUCTS DIVISION Denver, CO Nov 1992 to Mar 1994 Territory Manager AAHormel Foods Corporation - Meat Products Division Minneapolis, MN Dec 1991 to Oct 1992 Territory Manager AModern Controls, Inc. Minneapolis, MN Nov 1990 to Nov 1991 Territorial Sales Representative, Permeation Systems
Education:
University of North Dakota Grand Forks, ND Dec 1989 Bachelor of Business Administration in Management
Us Patents
System And Method For Optically Monitoring The Concentration Of A Gas, Or The Pressure, In A Sample Vial To Detect Sample Growth
Nicholas Bachur - Monkton MD, US Patrick Beaty - Felton PA, US Timothy Foley - Forest Hill MD, US
International Classification:
G01N021/84
US Classification:
250/343000, 435/034000
Abstract:
A system and method employing infrared laser spectrography and dual wavelength modulation to monitor the concentration of a gas, such as oxygen or carbon dioxide, in the sample vial, or to monitor the pressure in the sample vial, to thus detect for microorganism growth in the sample vial. The system and method each employ an energy emitting device, such as an infrared laser, a detector and a signal analyzer, such as a spectroscopy device. The infrared laser emits toward the container infrared energy having a substantially single wavelength substantially equal to a wavelength at which the gas absorbs the infrared energy. The detector detects a portion of the energy signal that passes through the container, and the signal analyzer spectroscopically analyzes the detected portion of the energy signal to determine whether the gas exists in the container, or to determine the pressure in the container. The system and method thus determines whether an organism or cell of interest is present or viable in the container based on the results of the gas or pressure detection.
Systems, methods and apparatus for determining an amount of blood in a blood culture are provided where an initial biological state and then periodic measurements of the biological state of the culture are taken. For each respective measurement, a normalization relative value between the respective measurement and the initial measurement is made thereby forming normalization relative values. For each interval of time points represented by the normalization relative values, a first derivative of the normalization relative values in the interval is made thereby forming a plurality of rate transformation values. For each set of rate transformation values in the plurality of rate transformation values, an average relative transformation value is computed, thereby forming average relative transformation values. A lookup table that matches a measure of central tendency of the average relative transformation values to a blood amount is used to determine the amount of blood in the culture.
Systems, methods, and apparatus for determining whether a culture in a vessel contains a plurality of microorganisms are provided. A normalization relative value is calculated for each respective measurement of a biological state of the culture between (i) the respective measurement and (ii) an initial biological state. For each fixed interval of time points, a derivative of the normalization relative values in the interval of time points is calculated, thereby forming a plurality of rate transformation values. For each set of rate transformation values in the plurality of rate transformation values, a measure of central tendency of the values in the set is computed, thereby forming a plurality of average relative transformation values. A determination whether the culture contains the microorganisms is made based on whether any calculated average relative transformation value exceeds a first threshold or whether an extent of growth exhibited by the culture exceeds a second threshold.
Systems And Methods For Presumptive Identification Of Microorganism Type In A Culture
Systems, methods and apparatus for identifying a microorganism type in a culture are provided. A normalization relative value is calculated for each respective measurement of a biological state of the culture between (i) the respective measurement and (ii) an initial biological state. For each fixed interval of time points, a first derivative of the normalization relative values in the interval of time points is calculated, thereby forming a plurality of rate transformation values. For each respective set of rate transformation values in the plurality of rate transformation values, a measure of central tendency of the rate transformation values in the set is computed, thereby forming a plurality of average relative transformation values. A maximum metabolic rate and an extent of growth, determined from the normalization relative values and the average relative transformation values, are compared against a lookup table that matches these values to a microorganism type.
Blood Culture Bottles With Mechanisms For Controlled Release Of Substances Into Culture Media
- Franklin Lakes NJ, US Brent Pohl - Timonium MD, US Gary F. Hershner - Red Lion PA, US Dwight Livingston - Fallston MD, US Eric Ursprung - Camp Hill PA, US Gerard Lotz - Fallston MD, US Kevin Bailey - Monkton MD, US Ammon David Lentz - York PA, US Michael A. Brasch - Gaithersburg MD, US Ming-hsiung Yeh - New Freedom PA, US Patrick Shawn Beaty - Dallastown PA, US Charles C. Yu - Lutherville MD, US Timothy M. Wiles - Manchester MD, US Liping Feng - Baltimore MD, US Ben Turng - Tucson AZ, US Xiaofei Chang - Timonium MD, US Patrick R. Murray - Gibson Island MD, US
An apparatus and associated methods of use for a controlled combination of reagents is disclosed. The apparatus includes a vessel , a vessel insert , and a cap element . The vessel has a body portion for receiving a biological sample. The vessel insert receives at least one reagent therein. Preferably, the vessel insert is received in a portion of the vessel . The cap element is attached to the vessel to secure the vessel insert in the vessel . During use, the vessel insert is adapted to release its contents when the biological sample is introduced into the body portion of the vessel upon application of an intermixing force to the vessel insert . A variety of intermixing forces may be applied, depending upon the embodiment of the present invention and its associated methods of use.
Formulations And Process For Isolating Viable Microorganisms From Positive Blood Cultures
- Franklin Lakes NJ, US Vanda White - Baltimore MD, US William B. Brasso - Columbia MD, US Dyan Luper - Cockeysville MD, US James Y. Zhou - Columbia MD, US Julie L. Rosales - Randallstown MD, US Jeffery H. Bruton - Randallstown MD, US John D. Mantlo - Sykesville MD, US Adrien P. Malick - Granite MD, US Donald R. Callihan - Cockeysville MD, US Ben Turng - Tucson AZ, US Liping Feng - Baltimore MD, US Curtis M. Gosnell - Fallston MD, US Patrick Shawn Beaty - Dallastown PA, US John P. Douglass - York PA, US
Assignee:
BECTON DICKINSON AND COMPANY - Franklin Lakes NJ
International Classification:
C12Q 1/14 C12Q 1/24 C12N 1/02 C12N 1/20
Abstract:
Various embodiments disclosed herein provide for reagents and methods for rapidly isolating viable microbial cells, including , from positive blood culture samples. The resulting microbial pellet can be used for both identification and growth-based methods such as antimicrobial susceptibility testing. The buffers described herein may contain a base solution, non-ionic detergents, thiols, and optionally, ammonium chloride. The disclosed methods provide a process for rapidly isolating and concentrating viable microorganism(s) from PBC samples using only one sample preparation tube and centrifugation while removing cellular debris from the mammalian blood cells that may interfere with identification methods.
Systems And Methods For Identifying A Culture As Positive For Microorganisms With High Confidence
- Franklin Lakes NJ, US Patrick Shawn Beaty - Dallastown PA, US
Assignee:
BECTON DICKINSON AND COMPANY - Franklin Lakes NJ
International Classification:
C12Q 1/04
Abstract:
Systems, methods, and apparatus for determining whether a culture in a vessel contains a plurality of microorganisms are provided. A normalization relative value is calculated for each respective measurement of a biological state of the culture between (i) the respective measurement and (ii) an initial biological state. For each fixed interval of time points, a derivative of the normalization relative values in the interval of time points is calculated, thereby forming a plurality of rate transformation values. For each set of rate transformation values in the plurality of rate transformation values, a measure of central tendency of the values in the set is computed, thereby forming a plurality of average relative transformation values. A determination whether the culture contains the microorganisms is made based on whether any calculated average relative transformation value exceeds a first threshold or whether an extent of growth exhibited by the culture exceeds a second threshold.
Blood Culture Bottles With Mechanisms For Controlled Release Of Substances Into Culture Media
- Franklin Lakes NJ, US Brent Pohl - Timonium MD, US Gary F. Hershner - Red Lion PA, US Dwight Livingston - Fallston MD, US Eric Ursprung - Camp Hill PA, US Gerard Lotz - Fallston MD, US Kevin Bailey - Cockeysville MD, US Ammon David Lentz - York PA, US Michael A. Brasch - Gaithersburg MD, US Ming-hsiung Yeh - New Freedom PA, US Patrick Shawn Beaty - Dallastown PA, US Charles C. Yu - Lutherville MD, US Timothy M. Wiles - Manchester MD, US Liping Feng - Baltimore MD, US Ben Turng - Tucson AZ, US Xiaofei Chang - Timonium MD, US Patrick R. Murray - Gibson Island MD, US
An apparatus and associated methods of use for a controlled combination of reagents is disclosed. The apparatus includes a vessel , a vessel insert , and a cap element . The vessel has a body portion for receiving a biological sample. The vessel insert receives at least one reagent therein. Preferably, the vessel insert is received in a portion of the vessel . The cap element is attached to the vessel to secure the vessel insert in the vessel . During use, the vessel insert is adapted to release its contents when the biological sample is introduced into the body portion of the vessel upon application of an intermixing force to the vessel insert . A variety of intermixing forces may be applied, depending upon the embodiment of the present invention and its associated methods of use.
Beaty Patrick (1976-1980), Jim Kelly (1976-1980), Mark Russo (1973-1977), Doug Shipe (1977-1981), Chester Pabin (1965-1969), Chuck Riesbeck (1971-1975)