Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Michele L. Pearson is active.

Publication


Featured researches published by Michele L. Pearson.


American Journal of Infection Control | 2002

Guidelines for the Prevention of Intravascular Catheter–Related Infections

Naomi P. O'Grady; Mary Alexander; Lillian A. Burns; E. Patchen Dellinger; Jeffery S. Garland; Stephen O. Heard; Pamela A. Lipsett; Henry Masur; Leonard A. Mermel; Michele L. Pearson; Issam Raad; Adrienne G. Randolph; Mark E. Rupp; Sanjay Saint

Naomi P. O’Grady, Mary Alexander, E. Patchen Dellinger, Julie L. Gerberding, Stephen O. Heard, Dennis G. Maki, Henry Masur, Rita D. McCormick, Leonard A. Mermel, Michele L. Pearson, Issam I. Raad, Adrienne Randolph, and Robert A. Weinstein National Institutes of Health, Bethesda, Maryland; Infusion Nurses Society, Cambridge, and University of Massachusetts Medical School, Worcester, and The Children’s Hospital, Boston, Massachusetts; University of Washington, Seattle; Office of the Director, Centers for Disease Control and Prevention (CDC), and Division of Healthcare Quality Promotion, National Center for Infectious Diseases, CDC, Atlanta, Georgia; University of Wisconsin Medical School and Hospital and Clinics, Madison; Rhode Island Hospital and Brown University School of Medicine, Providence, Rhode Island; MD Anderson Cancer Center, Houston, Texas; and Cook County Hospital and Rush Medical College, Chicago, Illinois


The New England Journal of Medicine | 2008

Emergence of Vancomycin Resistance in Staphylococcus aureus

Theresa L. Smith; Michele L. Pearson; Kenneth R. Wilcox; Cosme Cruz; Michael V. Lancaster; Barbara Robinson-Dunn; Fred C. Tenover; Marcus J. Zervos; Jeffrey D. Band; Elizabeth White; William R. Jarvis

BACKGROUND Since the emergence of methicillin-resistant Staphylococcus aureus, the glycopeptide vancomycin has been the only uniformly effective treatment for staphylococcal infections. In 1997, two infections due to S. aureus with reduced susceptibility to vancomycin were identified in the United States. METHODS We investigated the two patients with infections due to S. aureus with intermediate resistance to glycopeptides, as defined by a minimal inhibitory concentration of vancomycin of 8 to 16 microg per milliliter. To assess the carriage and transmission of these strains of S. aureus, we cultured samples from the patients and their contacts and evaluated the isolates. RESULTS The first patient was a 59-year-old man in Michigan with diabetes mellitus and chronic renal failure. Peritonitis due to S. aureus with intermediate resistance to glycopeptides developed after 18 weeks of vancomycin treatment for recurrent methicillin-resistant S. aureus peritonitis associated with dialysis. The removal of the peritoneal catheter plus treatment with rifampin and trimethoprim-sulfamethoxazole eradicated the infection. The second patient was a 66-year-old man with diabetes in New Jersey. A bloodstream infection due to S. aureus with intermediate resistance to glycopeptides developed after 18 weeks of vancomycin treatment for recurrent methicillin-resistant S. aureus bacteremia. This infection was eradicated with vancomycin, gentamicin, and rifampin. Both patients died. The glycopeptide-intermediate S. aureus isolates differed by two bands on pulsed-field gel electrophoresis. On electron microscopy, the isolates from the infected patients had thicker extracellular matrixes than control methicillin-resistant S. aureus isolates. No carriage was documented among 177 contacts of the two patients. CONCLUSIONS The emergence of S. aureus with intermediate resistance to glycopeptides emphasizes the importance of the prudent use of antibiotics, the laboratory capacity to identify resistant strains, and the use of infection-control precautions to prevent transmission.


Annals of Internal Medicine | 1992

Nosocomial transmission of multidrug-resistant Mycobacterium tuberculosis : a risk to patients and health care workers

Michele L. Pearson; John A. Jereb; Thomas R. Frieden; Jack T. Crawford; Barry J. Davis; Samuel W. Dooley; William R. Jarvis

OBJECTIVE To determine the factors associated with the development of multidrug-resistant tuberculosis among patients at a New York City Hospital and to investigate possible nosocomial transmission. DESIGN A retrospective case-control study and tuberculin skin test survey. PATIENTS Twenty-three patients with tuberculosis whose isolates were resistant to at least isoniazid and rifampin (case patients) were compared with patients with tuberculosis whose isolates were susceptible to all agents tested (controls). Tuberculin skin test conversion rates were compared among health care workers assigned to wards where patients with tuberculosis were frequently or rarely admitted. SETTING A large, teaching hospital in New York City. MEASUREMENTS Mycobacterium tuberculosis isolates from case patients and controls were typed by restriction fragment length polymorphism analysis. RESULTS Case patients were younger (median age, 34 compared with 42 years; P = 0.006), more likely to be seropositive for HIV (21 of 23 compared with 11 of 23 patients; odds ratio, 11.5; 95% CI, 1.9 to 117), and more likely to have had a previous hospital admission within 7 months before the onset of tuberculosis (19 of 23 compared with 5 of 23 patients; odds ratio, 17.1; CI, 3.3 to 97), particularly on one ward (12 of 23 compared with 0 of 23 patients; odds ratio, undefined; P = 0.002). Health care workers assigned to wards housing case patients were more likely to have tuberculin skin test conversions than were health care workers assigned to other wards (11 of 32 compared with 1 of 47 health care workers; P less than 0.001). Few (6 of 23) case patients were placed in acid-fast bacilli isolation, and no rooms tested had negative pressure. Of 16 available multidrug-resistant isolates obtained from case patients, 14 had identical banding patterns by restriction fragment length polymorphism analysis. In contrast, M. tuberculosis isolates from controls with drug-susceptible tuberculosis had patterns distinct from each other and from those of case patients. CONCLUSIONS These data suggest nosocomial transmission of multidrug-resistant tuberculosis occurred from patient to patient and from patient to health care worker and underscore the need for effective acid-fast bacilli isolation facilities and adherence to published infection control guidelines in health care institutions.


Infection Control and Hospital Epidemiology | 2002

Guidelines for the prevention of intravascular catheter-related infections.

Naomi P. O'Grady; Mary Alexander; E. Patchen Dellinger; Julie Louise Gerberding; Stephen O. Heard; Dennis G. Maki; Henry Masur; Rita D. McCormick; Leonard A. Mermel; Michele L. Pearson; Issam Raad; Adrienne G. Randolph; Robert A. Weinstein; Jane D. Siegel; Raymond Chinn; Alfred DeMaria; Elaine Larson; James T. Lee; Ramon E. Moncada; William A. Rutala; William E. Scheckler; Beth H. Stover; Marjorie A. Underwood

BACKGROUND Although many catheter-related bloodstream infections (CRBSIs) are preventable, measures to reduce these infections are not uniformly implemented. OBJECTIVE To update an existing evidenced-based guideline that promotes strategies to prevent CRBSIs. DATA SOURCES The MEDLINE database, conference proceedings, and bibliographies of review articles and book chapters were searched for relevant articles. STUDIES INCLUDED Laboratory-based studies, controlled clinical trials, prospective interventional trials, and epidemiologic investigations. OUTCOME MEASURES Reduction in CRBSI, catheter colonization, or catheter-related infection. SYNTHESIS The recommended preventive strategies with the strongest supportive evidence are education and training of healthcare providers who insert and maintain catheters; maximal sterile barrier precautions during central venous catheter insertion; use of a 2% chlorhexidine preparation for skin antisepsis; no routine replacement of central venous catheters for prevention of infection; and use of antiseptic/antibiotic-impregnated short-term central venous catheters if the rate of infection is high despite adherence to other strategies (ie, education and training, maximal sterile barrier precautions, and 2% chlorhexidine for skin antisepsis). CONCLUSION Successful implementation of these evidence-based interventions can reduce the risk for serious catheter-related infection.


The New England Journal of Medicine | 1999

Emergence of vancomycin resistance in Staphylococcus aureus. Glycopeptide-Intermediate Staphylococcus aureus Working Group.

Theresa L. Smith; Michele L. Pearson; Kenneth R. Wilcox; Cosme Cruz; Michael V. Lancaster; Barbara Robinson-Dunn; Fred C. Tenover; Marcus J. Zervos; Jeffrey D. Band; Elizabeth White; William R. Jarvis

BACKGROUND Since the emergence of methicillin-resistant Staphylococcus aureus, the glycopeptide vancomycin has been the only uniformly effective treatment for staphylococcal infections. In 1997, two infections due to S. aureus with reduced susceptibility to vancomycin were identified in the United States. METHODS We investigated the two patients with infections due to S. aureus with intermediate resistance to glycopeptides, as defined by a minimal inhibitory concentration of vancomycin of 8 to 16 microg per milliliter. To assess the carriage and transmission of these strains of S. aureus, we cultured samples from the patients and their contacts and evaluated the isolates. RESULTS The first patient was a 59-year-old man in Michigan with diabetes mellitus and chronic renal failure. Peritonitis due to S. aureus with intermediate resistance to glycopeptides developed after 18 weeks of vancomycin treatment for recurrent methicillin-resistant S. aureus peritonitis associated with dialysis. The removal of the peritoneal catheter plus treatment with rifampin and trimethoprim-sulfamethoxazole eradicated the infection. The second patient was a 66-year-old man with diabetes in New Jersey. A bloodstream infection due to S. aureus with intermediate resistance to glycopeptides developed after 18 weeks of vancomycin treatment for recurrent methicillin-resistant S. aureus bacteremia. This infection was eradicated with vancomycin, gentamicin, and rifampin. Both patients died. The glycopeptide-intermediate S. aureus isolates differed by two bands on pulsed-field gel electrophoresis. On electron microscopy, the isolates from the infected patients had thicker extracellular matrixes than control methicillin-resistant S. aureus isolates. No carriage was documented among 177 contacts of the two patients. CONCLUSIONS The emergence of S. aureus with intermediate resistance to glycopeptides emphasizes the importance of the prudent use of antibiotics, the laboratory capacity to identify resistant strains, and the use of infection-control precautions to prevent transmission.


American Journal of Infection Control | 1998

Guideline for infection control in health care personnel, 1998

Elizabeth A. Bolyard; Ofelia C. Tablan; Walter W. Williams; Michele L. Pearson; Craig N Shapiro; Scott Deitchman

I. Infection control issues for health care personnel: An overview A. EXECUTIVE SUMMARY 291 B. INTRODUCTION 292 C. INFECTION CONTROL OBJECTIVES FOR A PERSONNEL HEALTH SERVICE 292 D. ELEMENTS OF A PERSONNEL HEALTH SERVICE FOR INFECTION CONTROL 293 1. Coordination with other departments 293 2. Medical evaluations 293 3. Personnel health and safety education 293 4. Immunization programs 296 5. Management of job-related illnesses and exposures 298 6. Health counseling 301 7. Maintenance of records, data management, and confidentiality 301 E. EPIDEMIOLOGY AND CONTROL OF SELECTED INFECTIONS TRANSMITTED AMONG HEALTH CARE PERSONNEL AND PATIENTS 302 1. Bloodborne pathogens 302 Affiliations: National Center for Infectious Diseases, National Immunization Program, National Institute of Occupational Safety and Health.


Infection Control and Hospital Epidemiology | 2005

Guidance on public reporting of healthcare-associated infections : recommendations of the Healthcare Infection Control Practices Advisory Committee

Linda McKibben; Teresa C. Horan; Jerome I. Tokars; Gabrielle Fowler; Denise M. Cardo; Michele L. Pearson; Patrick J. Brennan

ed from medical records Numerators: Number of surgical patients: Risk-adjustment is unnecessary d Who received AMP within 1 hour prior to surgical incision (or 2 hours if receiving vancomycin or a


Clinical Infectious Diseases | 2011

Summary of Recommendations: Guidelines for the Prevention of Intravascular Catheter-related Infections

Naomi P. O'Grady; Mary Alexander; Lillian A. Burns; E. Patchen Dellinger; Jeffrey Garland; Stephen O. Heard; Pamela A. Lipsett; Henry Masur; Leonard A. Mermel; Michele L. Pearson; Issam Raad; Adrienne G. Randolph; Mark E. Rupp; Sanjay Saint

These guidelines have been developed for healthcare personnel who insert intravascular catheters and for persons responsible for surveillance and control of infections in hospital, outpatient, and home healthcare settings. This report was prepared by a working group comprising members from professional organizations representing the disciplines of critical care medicine, infectious diseases, healthcare infection control, surgery, anesthesiology, interventional radiology, pulmonary medicine, pediatric medicine, and nursing. The working group was led by the Society of Critical Care Medicine


Infection Control and Hospital Epidemiology | 1998

Guideline for Infection Control in Healthcare Personnel, 1998

Elizabeth A. Bolyard; Ofelia C. Tablan; Walter W. Williams; Michele L. Pearson; Craig N. Shapiro; Scott Deitchman

This guideline updates and replaces the previous edition of the Centers for Disease Control and Prevention (CDC) “Guideline for Infection Control in Hospital Personnel,” published in 1983. The revised guideline, designed to provide methods for reducing the transmission of infections from patients to healthcare personnel and from personnel to patients, also provides an overview of the evidence for recommendations considered prudent by consensus of the Hospital Infection Control Practices Advisory Committee members. A working draft of this guideline was also reviewed by experts in infection control, occupational health, and infectious diseases; however, all recommendations contained in the guideline may not reflect the opinion of all reviewers.


Annals of Internal Medicine | 1995

Efficacy of Control Measures in Preventing Nosocomial Transmission of Multidrug-Resistant Tuberculosis to Patients and Health Care Workers

Susan A. Maloney; Michele L. Pearson; Marcia T. Gordon; Rachel Del Castillo; John F. Boyle; William R. Jarvis

Nosocomial transmission of Mycobacterium tuberculosis, particularly transmission of multidrug-resistant strains, to patients and health care workers is a major public health problem [1-12]. From 1990 through 1992, the Centers for Disease Control and Prevention (CDC) investigated eight outbreaks of multidrug-resistant tuberculosis in U.S. hospitals (1-6; CDC, unpublished data). More than 300 patients with multidrug-resistant tuberculosis were identified during these investigations; most (87%) were infected with human immunodeficiency virus (HIV). Their clinical course was characterized by rapid progression from infection to active tuberculosis and their mortality rate was high [9]. Additionally, more than 100 health care workers at hospitals where outbreaks of multidrug-resistant tuberculosis had occurred had conversion of their tuberculin skin tests, suggesting recently acquired M. tuberculosis infection. At least 17 of these newly infected health care workers developed active multidrug-resistant M. tuberculosis, and at least 7 of them died with multidrug-resistant tuberculosis [10]. Because of the explosive and fatal nature of these recent nosocomial outbreaks of multidrug-resistant tuberculosis, questions have been raised about the most effective interventions and control measures necessary to prevent institutional transmission of tuberculosis [13-15]. We evaluated the efficacy of control measures for decreasing the transmission of these multidrug-resistant M. tuberculosis strains in one of the hospitals that had had an outbreak. Methods In May 1991, we investigated an outbreak of multidrug-resistant tuberculosis at Cabrini Medical Center, a teaching hospital in New York City. In that investigation, epidemiologic and laboratory data showed the occurrence of nosocomial transmission of multidrug-resistant tuberculosis to patients and health care workers [5]. Risk factors for acquisition of multidrug-resistant tuberculosis by patients included age, HIV seropositivity, and hospital admission to Cabrini Medical Center within 7 months before onset of multidrug-resistant tuberculosis. Additionally, health care workers assigned to the medical or HIV wards (primary wards housing patients with tuberculosis) were identified as being at increased risk for tuberculin skin test conversion. Conditions facilitating tuberculosis transmission included delayed identification, isolation, or treatment of patients with infectious tuberculosis; lapses in tuberculosis isolation practices; and inadequate isolation facilities for patients with tuberculosis. In response to the outbreak, control measures similar to those recommended in the CDCs 1990 tuberculosis guidelines were instituted to prevent further nosocomial transmission of tuberculosis [16]. Control Measures Numerous measures were introduced to decrease transmission of multidrug-resistant tuberculosis, including source controls, environmental controls, and respiratory protection for health care workers (Table 1). Source control measures included improved isolation precautions and expanded treatment regimens for patients with suspected or confirmed tuberculosis and included routine use of acid-fast bacilli smears to determine length of isolation and to establish treatment efficacy. To expedite the identification of patients with infectious tuberculosis and the determination of the antimicrobial susceptibility of M. tuberculosis isolates, laboratory procedures were also modified. Thus, personnel and workday hours devoted to processing of mycobacterial isolates were expanded; a hospital-wide computerized database of patients with tuberculosis was developed; a gene probe was introduced; and the reporting of acid-fast bacilli smear results to requesting physicians was standardized. Table 1. Infection Control Measures* Environmental modifications included installing exhaust fans in isolation rooms to increase the number of acid-fast bacilli isolation rooms with negative pressure and included using portable Aeroguard (HR Incorporated, Bellevue, Washington) chambers to do cough-inducing procedures, such as sputum induction or aerosolized pentamidine administration. Finally, to further decrease the risk for occupational acquisition of tuberculosis, the respiratory protection worn by health care workers was changed from nonmolded to molded surgical masks (3M 1800+ Aseptex, 3M Incorporated, St. Paul, Minnesota). To assess compliance with these control measures, we examined the hospitals isolation facilities, reviewed patient charts for documentation of initiation and discontinuation of acid-fast bacilli isolation precautions, interviewed infection control and laboratory personnel, observed isolation practices on hospital wards containing patients with tuberculosis, and evaluated the ventilation system in acid-fast bacilli isolation rooms by testing air-flow direction using smoke tubes. Epidemiologic Studies A case-patient was defined as any Cabrini Medical Center patient whose M. tuberculosis isolate was resistant to at least isoniazid and rifampin and as any patient whose clinical course was consistent with active tuberculosis during the study period (1 January 1990 to 11 August 1992). Case-patients and all other patients with tuberculosis were identified by reviewing Cabrini Medical Center laboratory and infection control records during the study period. Medical records of all potential case-patients were reviewed to verify a clinical course consistent with tuberculosis. To determine whether a decrease had occurred in the incidence of multidrug-resistant tuberculosis after the institution of control measures, we compared the proportion of patients with tuberculosis who had multidrug-resistant strains before (preintervention period) and after (intervention period) the implementation of control measures. The preintervention period (January 1990 to June 1991) was defined as the time from the onset of the outbreak until the formal institution of recommended control measures; the intervention period (July 1991 to 11 August 1992) was defined as the time during and after the institution of recommended control measures until our follow-up study. Patient-to-Patient Transmission To investigate possible patient-to-patient transmission of multidrug-resistant tuberculosis, we evaluated case-patient medical records to determine if case-patients had been hospitalized at Cabrini Medical Center within 7 months before onset of tuberculosis. For those case-patients who had been previously hospitalized, we determined whether they had been hospitalized on the same ward at the same time or whether they had a documented nosocomial exposure to another patient with culture-confirmed multidrug-resistant tuberculosis during a previous hospitalization. Data collected included age, sex, race, HIV serologic status, previous opportunistic infections, dates and results of acid-fast bacilli smears and mycobacterial cultures, M. tuberculosis antimicrobial susceptibilities, dates of admission and discharge, hospital room assignments, dates of isolation for tuberculosis, nursing documentation of proper application of isolation precautions, antituberculous medications prescribed, clinical course, and outcome. Patient-to-Health Care Worker Transmission To evaluate whether the risk for transmission of multidrug-resistant tuberculosis from patients to health care workers had been reduced, we compared conversion rates of tuberculin skin tests in health care workers during the preintervention and intervention periods. During both periods, the tuberculin skin testing program at Cabrini Medical Center required annual testing of all hospital employees and additional testing of health care workers after a known tuberculosis exposure. A tuberculin skin test conversion was defined as induration of 10 mm or more to purified protein derivative in a Cabrini Medical Center employee with a documented tuberculin skin test result that was negative within the previous 24 months. Employees without negative skin test results at baseline were excluded from our analyses. Conversion rates were compared by period, by job category (frequent direct patient contact compared with infrequent or no direct patient contact), and by ward assignment (primary wards housing patients with tuberculosis [medical and HIV wards] compared with wards infrequently housing patients with tuberculosis). Health care workers with direct patient contact included physicians, nurses, nursing aides, respiratory therapists, and social workers; workers without direct patient contact included administrative staff, clerks, dieticians, housekeepers, engineers, and laboratory personnel. Health care workers with tuberculin skin-test conversions or active tuberculosis or both were identified by reviewing employee health and infection control records during the study period. Data collected included age, sex, race, history of bacille CalmetteGurin (BCG) vaccination or tuberculosis exposure or both, country of origin, job title, duration of employment, and work location at time of tuberculin skin-test conversion. Statistical Analysis Data were collected on standardized forms, entered into Epi Info Version 5.01b software, and analyzed [17]. Categorical variables were compared by the Fisher exact or chi-square test, and relative risks (RRs) were calculated. Continuous variables were compared by the Student t-test or the Kruskal-Wallis rank-sum test. Results Case-Patients Forty patients met the case definition (Figure 1). Case-patients in the preintervention and intervention periods were similar in age, race, sex, HIV serologic status, and diagnosis of AIDS (data not shown). However, case-patient mortality decreased in the intervention compared with the preintervention period (4 of 10 [40%] compared with 25 of 30 [83%] deaths; P = 0.01). Further, in the preintervention period, 20 of 25 (80%) case-patient deaths were attributed to tuberculosis, whereas in the intervention period, only

Collaboration


Dive into the Michele L. Pearson's collaboration.

Top Co-Authors

Avatar

William R. Jarvis

Centers for Disease Control and Prevention

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Henry Masur

National Institutes of Health

View shared research outputs
Top Co-Authors

Avatar

Issam Raad

University of Texas MD Anderson Cancer Center

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Mary Alexander

National Institutes of Health

View shared research outputs
Top Co-Authors

Avatar

Naomi P. O'Grady

National Institutes of Health

View shared research outputs
Top Co-Authors

Avatar

Stephen O. Heard

University of Massachusetts Medical School

View shared research outputs
Top Co-Authors

Avatar

Teresa C. Horan

Centers for Disease Control and Prevention

View shared research outputs
Researchain Logo
Decentralizing Knowledge