Peter Gross
Hackensack University Medical Center
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Infection Control and Hospital Epidemiology | 2008
Deverick J. Anderson; Keith S. Kaye; David C. Classen; Kathleen M. Arias; Kelly Podgorny; Helen Burstin; David P. Calfee; Susan E. Coffin; Erik R. Dubberke; Victoria Fraser; Dale N. Gerding; Frances A. Griffin; Peter Gross; Michael Klompas; Evelyn Lo; Jonas Marschall; Leonard A. Mermel; Lindsay Nicolle; David A. Pegues; Trish M. Perl; Sanjay Saint; Cassandra D. Salgado; Robert A. Weinstein; Robert R. Wise; Deborah S. Yokoe
Previously published guidelines are available that provide comprehensive recommendations for detecting and preventing healthcare-associated infections. The intent of this document is to highlight practical recommendations in a concise format designed to assist acute care hospitals to implement and prioritize their surgical site infection (SSI) prevention efforts. Refer to the Society for Healthcare Epidemiology of America/Infectious Diseases Society of America “Compendium of Strategies to Prevent Healthcare-Associated Infections” Executive Summary and Introduction and accompanying editorial for additional discussion.1. Burden of SSIs as complications in acute care facilities.a. SSIs occur in 2%-5% of patients undergoing inpatient surgery in the United States.b. Approximately 500,000 SSIs occur each year.2. Outcomes associated with SSIa. Each SSI is associated with approximately 7-10 additional postoperative hospital days.b. Patients with an SSI have a 2-11 times higher risk of death, compared with operative patients without an SSI.i. Seventy-seven percent of deaths among patients with SSI are direcdy attributable to SSI.c. Attributable costs of SSI vary, depending on the type of operative procedure and the type of infecting pathogen; published estimates range from
Infection Control and Hospital Epidemiology | 2008
Evelyn Lo; Lindsay E. Nicolle; David C. Classen; Kathleen M. Arias; Kelly Podgorny; Deverick J. Anderson; Helen Burstin; David P. Calfee; Susan E. Coffin; Erik R. Dubberke; Victoria Fraser; Dale N. Gerding; Frances A. Griffin; Peter Gross; Keith S. Kaye; Michael Klompas; Jonas Marschall; Leonard A. Mermel; David A. Pegues; Trish M. Perl; Sanjay Saint; Cassandra D. Salgado; Robert A. Weinstein; Robert J. Wise; Deborah S. Yokoe
3,000 to
Infection Control and Hospital Epidemiology | 2008
Susan E. Coffin; Michael Klompas; David C. Classen; Kathleen M. Arias; Kelly Podgorny; Deverick J. Anderson; Helen Burstin; David P. Calfee; Erik R. Dubberke; Victoria Fraser; Dale N. Gerding; Frances A. Griffin; Peter Gross; Keith S. Kaye; Evelyn Lo; Jonas Marschall; Leonard A. Mermel; Lindsay Nicolle; David A. Pegues; Trish M. Perl; Sanjay Saint; Cassandra D. Salgado; Robert A. Weinstein; Robert J. Wise; Deborah S. Yokoe
29,000.i. SSIs are believed to account for up to
Experimental Gerontology | 2002
Donna M. Murasko; Erica D. Bernstein; Elizabeth M. Gardner; Peter Gross; Gary Munk; Sandra Dran; Elias Abrutyn
10 billion annually in healthcare expenditures.1. Definitionsa. The Centers for Disease Control and Prevention National Nosocomial Infections Surveillance System and the National Healthcare Safety Network definitions for SSI are widely used.b. SSIs are classified as follows (Figure):i. Superficial incisional (involving only skin or subcutaneous tissue of the incision)ii. Deep incisional (involving fascia and/or muscular layers)iii. Organ/space
Infection Control and Hospital Epidemiology | 2008
David P. Calfee; Cassandra D. Salgado; David C. Classen; Kathleen M. Arias; Kelly Podgorny; Deverick J. Anderson; Helen Burstin; Susan E. Coffin; Erik R. Dubberke; Victoria J. Fraser; Dale N. Gerding; Frances A. Griffin; Peter Gross; Keith S. Kaye; Michael Klompas; Evelyn Lo; Jonas Marschall; Leonard A. Mermel; Lindsay Nicolle; David A. Pegues; Trish M. Perl; Sanjay Saint; Robert A. Weinstein; Robert J. Wise; Deborah S. Yokoe
Previously published guidelines are available that provide comprehensive recommendations for detecting and preventing healthcare-associated infections. The intent of this document is to highlight practical recommendations in a concise format designed to assist acute care hospitals in implementing and prioritizing their catheter-associated urinary tract infection (CAUTI) prevention efforts. Refer to the Society for Healthcare Epidemiology of America/Infectious Diseases Society of America “Compendium of Strategies to Prevent Healthcare-Associated Infections” Executive Summary and Introduction and accompanying editorial for additional discussion. 1. Burden of CAUTIs a. Urinary tract infection is the most common hospital-acquired infection; 80% of these infections are attributable to an indwelling urethral catheter. b. Twelve to sixteen percent of hospital inpatients will have a urinary catheter at some time during their hospital stay. c. The daily risk of acquisition of urinary infection varies from 3% to 7% when an indwelling urethral catheter remains in situ. 2. Outcomes associated with CAUTI a. Urinary tract infection is the most important adverse outcome of urinary catheter use. Bacteremia and sepsis may occur in a small proportion of infected patients. b. Morbidity attributable to any single episode of catheterization is limited, but the high frequency of catheter use in hospitalized patients means that the cumulative burden of CAUTI is substantial. c. Catheter use is also associated with negative outcomes other than infection, including nonbacterial urethral inflammation, urethral strictures, and mechanical trauma.
Vaccine | 1999
Erica D. Bernstein; D Kaye; Elias Abrutyn; Peter Gross; M Dorfman; Donna M. Murasko
Previously published guidelines are available that provide comprehensive recommendations for detecting and preventing healthcare-associated infections. The intent of this document is to highlight practical recommendations in a concise format designed to assist acute care hospitals in implementing and prioritizing their ventilator-associated pneumonia (VAP) prevention efforts. Refer to the Society for Healthcare Epidemiology of America/Infectious Diseases Society of America “Compendium of Strategies to Prevent Healthcare-Associated Infections” Executive Summary and Introduction and accompanying editorial for additional discussion.1. Occurrence of VAP in acute care facilities.a. VAP is one of the most common infections acquired by adults and children in intensive care units (ICUs).i. In early studies, it was reported that 10%-20% of patients undergoing ventilation developed VAP. More-recent publications report rates of VAP that range from 1 to 4 cases per 1,000 ventilator-days, but rates may exceed 10 cases per 1,000 ventilator-days in some neonatal and surgical patient populations. The results of recent quality improvement initiatives, however, suggest that many cases of VAP might be prevented by careful attention to the process of care.2. Outcomes associated with VAPa. VAP is a cause of significant patient morbidity and mortality, increased utilization of healthcare resources, and excess cost.i. The mortality attributable to VAP may exceed 10%.ii. Patients with VAP require prolonged periods of mechanical ventilation, extended hospitalizations, excess use of antimicrobial medications, and increased direct medical costs.
Clinical Journal of The American Society of Nephrology | 2006
Alain Soupart; Peter Gross; Jean-Jacques Legros; Sándor Alföldi; Djillali Annane; Hassan M. Heshmati; Guy Decaux
While influenza immunization significantly reduces the risk of pneumonia and associated deaths, vaccination of elderly only affords 30-50% protection against influenza disease. The purpose of this study was to: (1) evaluate the consistency of immune responses across multiple years in young and elderly; (2) determine the contribution of antibody and cell-mediated responses in protection after immunization with influenza vaccine. Independently living healthy elderly (>200/year; mean age 78.8-80.6/year) were recruited yearly in this four year study. The results clearly demonstrate: (1) both young and elderly consistently produced significant antibody and T cell proliferative responses to influenza vaccine upon yearly immunization; however, both responses of elderly were significantly and consistently lower than young. (2) Percentages of both young and elderly demonstrating protective titers (i.e. HI>/=40) increased post-immunization each year, but were consistently higher in young compared to elderly. (3) The risk of developing influenza disease after immunization was highest among elderly demonstrating neither antibody nor cell-mediated responses. Importantly, the risk of influenza disease was comparable in elderly demonstrating a cell-mediated response alone, an antibody response alone, or both cell-mediated and antibody responses. This suggests that cell-mediated responses play a significant role in protection in at least a subset of elderly from influenza disease after immunization.
Clinical Infectious Diseases | 2007
Peter Gross; Brijesh Patel
Previously published guidelines are available that provide comprehensive recommendations for detecting and preventing healthcare-associated infections (HAIs). Our intent in this document is to highlight practical recommendations in a concise format to assist acute care hospitals in their efforts to prevent transmission of methicillin-resistant Staphylococcus aureus (MRSA). Refer to the Society for Healthcare Epidemiology of America/Infectious Diseases Society of America “Compendium of Strategies to Prevent Healthcare-Associated Infections” Executive Summary, Introduction, and accompanying editorial for additional discussion. 1. Burden of HAIs caused by MRSA in acute care facilities a. In the United States, the proportion of hospital-associated S. aureus infections that are caused by strains resistant to methicillin has steadily increased. In 2004, MRSA accounted for 63% of S. aureus infections in hospitals. b. Although the proportion of S. aureus –associated HAIs among intensive care unit (ICU) patients that are due to methicillin-resistant strains has increased (a relative measure of the MRSA problem), recent data suggest that the incidence of central line–associated bloodstream infection caused by MRSA (an absolute measure of the problem) has decreased in several types of ICUs since 2001. Although these findings suggest that there has been some success in preventing nosocomial MRSA transmission and infection, many patient groups continue to be at risk for such transmission. c. MRSA has also been documented in other areas of the hospital and in other types of healthcare facilities, including those that provide long-term care.
Vaccine | 2001
Elizabeth M. Gardner; Erica D. Bernstein; Sandra Dran; Gary Munk; Peter Gross; Elias Abrutyn; Donna M. Murasko
Elderly individuals not only demonstrate a greater risk of morbidity and mortality from influenza than the young, but also have greater difficulty mounting a protective response to influenza vaccine. The mechanism of the decreased efficacy of influenza vaccination in the elderly is not well understood. The present study was designed to assess the interaction between cell-mediated and humoral immune responses to influenza vaccine in a large population (n = 233) of healthy elderly individuals (mean age = 80.7) living in six continuing care retirement communities (CCRCs). While influenza vaccination resulted in significant increases in the mean anti-influenza antibody titres and mean proliferative responses of peripheral blood mononuclear cells to purified subvirion trivalent influenza vaccine one month after vaccination, only 48.9% and 30.0% of subjects had intact humoral and cell-mediated immune responses, respectively. No association was observed between intact cell-mediated and humoral responses: 14.7% of subjects had an intact cell-mediated, but not humoral response, and 32.6% of subjects had an intact humoral, but not cell-mediated response. However, IFNgamma production was significantly correlated with both antibody and cell-mediated responses to influenza vaccination, a finding not previously reported in the elderly. These results indicate that there is considerable heterogeneity among immune responses of the elderly to influenza vaccination. This heterogeneity needs to be a major consideration in evaluation of new vaccine preparations.
Annals of Internal Medicine | 2013
Lori-Ann Linkins; Shannon M. Bates; Eddy Lang; Susan R. Kahn; James D. Douketis; Jim A. Julian; Sameer Parpia; Peter Gross; Jeffrey I. Weitz; Frederick A. Spencer; Agnes Y.Y. Lee; Martin O'Donnell; Mark Crowther; Howard H.W. Chan; Wendy Lim; Sam Schulman; Jeffrey S. Ginsberg; Clive Kearon
The effects of satavaptan (SR121463B), a novel long-acting orally active vasopressin V(2)-receptor antagonist, were investigated in patients with the syndrome of inappropriate antidiuretic hormone secretion (SIADH). In the first part of this randomized, double-blind study, 34 patients first were treated with satavaptan (versus placebo) for up to 5 d and then during 23 d of open-label dosage-adjustment period. In the second part of the study, long-term efficacy and safety of satavaptan was assessed in an open-label trial during at least 12 mo. Mean (+/-SD) serum sodium (SNa) levels before treatment were 127 +/- 2 mmol/L (placebo, n = 8), 125 +/- 6 mmol/L (25 mg, n = 14), and 127 +/- 5 mmol/L (50 mg, n = 12). Responders (patients SNa levels normalized or increased by at least 5 mmol/L from baseline during the double-blind period) were 79% in the 25-mg group (SNa 136 +/- 3 mmol/L; P = 0.006), 83% in the 50-mg group (SNa 140 +/- 6 mmol/L; P = 0.005), and 13% in the placebo group (SNa 130 +/- 5 mmol/L). No drug-related serious adverse events were recorded. During the long-term treatment, 15 of 18 enrolled patients achieved 6 mo and 10 achieved 12 mo of treatment. The SNa response was maintained during this time with a good tolerance. The new oral vasopressin V(2)-receptor antagonist satavaptan adequately corrects mild or moderate hyponatremia in patients with SIADH and has a good safety profile.