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Table 1.  

Characteristic Likelihood ratio test aRR (95% CI) p-value
Chi-square p-value
Vascular access type§
Central venous catheter 2,090.2 <0.001 6.2 (5.7–6.7) <0.001
Graft or other 2.2 (2.0–2.4) <0.001
Fistula Ref
Location/Hospital affiliation
Hospital** 113.0 <0.001 1.5 (1.3–1.8) <0.001
Freestanding Ref
Member of group or chain of dialysis centers
No 111.7 <0.001 1.4 (1.2–1.7) <0.001
Yes Ref
Written antibiotic use policy
No 35.1 <0.001 1.3 (1.1–1.4) <0.001
Yes Ref
Quartile of % of persons aged ≥65 yrs††
Quartile 4: 75–100 (highest) 54.3 <0.001 1.4 (1.2–1.6) <0.001
Quartile 3: 50–74 1.3 (1.2–1.5) <0.001
Quartile 2: 25–49 1.3 (1.2–1.4) <0.001
Quartile 1: 0–24 (lowest) Ref

Table 1. Independent factors associated with dialysis-associated Staphylococcus aureus bloodstream infection incidence* — National Healthcare Safety Network, United States, 2020

Abbreviations: aRR = adjusted rate ratio; ATSDR = Agency for Toxic Substances and Disease Registry; NHSN = National Healthcare Safety Network; Ref = referent group; SVI = Social Vulnerability Index.
* Negative binomial regression was used to fit this multivariate model.
Likelihood ratio test evaluates whether a factor is statistically significantly associated with Staphylococcus aureus bloodstream infection incidence. Additionally, Akaike and Bayesian information criteria and Wald and likelihood ratio chi-square tests were used to evaluate model fit. The best candidate model was validated using bootstrap resampling methods and independently assessed by two separate analysts.
§ Source of data was NHSN event surveillance.
Source of data was NHSN Outpatient Dialysis Center Practices Survey. https://www.cdc.gov/nhsn/forms/57.500_outpatientdialysissurv_blank.pdf
** Location could be a hospital or a freestanding location owned by a hospital.
†† Source of data was CDC/ATSDR SVI.

Table 2.  

Characteristic Univariate analysis Multivariable analysis
No. of S. aureus bloodstream infections No. of patient-years Unadjusted rate aRR§ (95% CI) p-value
Age groups, yrs
18–49 736 11,848 6,212 1.7 (1.5–1.9) <0.001
50–64 993 22,312 4,451 1.2 (1.1–1.4) <0.001
≥65 1,071 31,758 3,372 Ref
Sex
Female 1,112** 28,239 3,938 Ref
Male 1,685 37,679 4,472 1.2 (1.1–1.4) <0.001
EIP site
California 822 23,478 3,501 1.1 (0.9–1.4) 0.19
Connecticut 182 4,404 4,133 1.2 (1.0–1.5) 0.12
Georgia 393 6,218 6,320 2.0 (1.6–2.5) <0.001
Maryland 741 15,022 4,933 1.4 (1.1–1.7) 0.003
New York 242 5,024 4,817 1.3 (1.0–1.6) 0.05
Tennessee 183 4,190 4,368 1.2 (1.0–1.5) 0.12
Minnesota 237 7,582 3,126 Ref
Race and ethnicity††
Black, non-Hispanic 1,509 31,762 4,751 1.1 (0.9–1.2) 0.40
Hispanic 321 7,122 4,500 1.4 (1.2–1.7) <0.001
White, non-Hispanic 687 17,764 3,866 Ref
Other, non-Hispanic 284 9,270 3,061 1.0 (0.8–1.2) 0.92
Vascular access types§§
Central venous catheter 1,444 11,963 12,071 4.3 (3.9–4.8) <0.001
Fistula or graft 1,303 48,631 2,679 Ref
Total 2,800 65,918 4,248

Table 2. Staphylococcus aureus bloodstream infections associated with hemodialysis — Emerging Infections Program,* United States, 2017–2020

Abbreviations: aRR = adjusted rate ratio; EIP = Emerging Infections Program; Ref = referent group; S. aureus = Staphylococcus aureus.
* EIP data for January 1, 2017–December 31, 2020.
Per 100,000 hemodialysis person-years.
§ Adjusted for age, race and ethnicity, sex, vascular access type, and EIP site as appropriate.
The median age of patients with hemodialysis S. aureus bacterial infection was 60 years (IQR = 49–70 years); the median age of those aged 18–49 years was 41 years.
** Sex was unknown for three patients.
†† Race and ethnicity were categorized as non-Hispanic Black or African American (Black), Hispanic or Latino (Hispanic), non-Hispanic White, and non-Hispanic other (includes patients with more than one race recorded). Race and ethnicity case counts are averaged over 10 imputations to account for missing values of race and ethnicity. The total sums to >2,800 because of rounding.
§§ Fifty-three cases had unknown vascular access type. The denominator includes 5,324 hemodialysis patient-years with unknown vascular access type.

CME / ABIM MOC / CE

Health Disparities in Hemodialysis-Associated Staphylococcus aureus Bloodstream Infections--United States, 2017-2020

  • Authors: Brian Rha, MD; Isaac See, MD; Lindsay Dunham, MPH, MSDA; Preeta K. Kutty, MD; Lauren Moccia, MA; Ibironke W. Apata, MD; Jennifer Ahern, PhD; Shelley Jung, PhD; Rongxia Li, PhD; Joelle Nadle, MPH; Susan Petit, MPH; Susan M. Ray, MD; Lee H. Harrison, MD; Carmen Bernu, MPH; Ruth Lynfield, MD; Ghinwa Dumyati, MD; Marissa Tracy, MPH; William Schaffner, MD; D. Cal Ham, MD; Shelley S. Magill, MD, PhD; Erin N. O’Leary, MPH; Jeneita Bell, MD; Arjun Srinivasan, MD; L. Clifford McDonald, MD; Jonathan R. Edwards, MStat; Shannon Novosad, MD
  • CME / ABIM MOC / CE Released: 5/13/2023
  • Valid for credit through: 5/13/2024, 11:59 PM EST
Start Activity

  • Credits Available

    Physicians - maximum of 0.50 AMA PRA Category 1 Credit(s)™

    ABIM Diplomates - maximum of 0.50 ABIM MOC points

    Nurses - 0.50 ANCC Contact Hour(s) (0 contact hours are in the area of pharmacology)

    Pharmacists - 0.50 Knowledge-based ACPE (0.050 CEUs)

    You Are Eligible For

    • Letter of Completion
    • ABIM MOC points

Target Audience and Goal Statement

This activity is intended for primary care clinicians, infectious disease specialists, nephrologists, and other healthcare professionals who treat and manage patients with end-stage kidney disease.

The goal of this activity is for learners to be better able to evaluate risk factors of hemodialysis-associated Staphylococcus aureus bloodstream infections in the setting of end-stage kidney disease.

Upon completion of this activity, participants will:

  • Assess the epidemiology of end-stage kidney disease and hemodialysis-associated bloodstream infections in the US
  • Evaluate the prevalence of hemodialysis-associated Staphylococcus aureus bacteremia in the setting of end-stage kidney disease
  • Analyze risk factors for hemodialysis-associated Staphylococcus aureus bacteremia in the setting of end-stage kidney disease


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Faculty

  • Brian Rha, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Brian Rha, MD, has no relevant financial relationships.

  • Isaac See, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Isaac See, MD, has no relevant financial relationships.

  • Lindsay Dunham, MPH, MSDA

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Lindsay Dunham, MPH, MSDA, has no relevant financial relationships.

  • Preeta K. Kutty, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Preeta K. Kutty, MD, has no relevant financial relationships.

  • Lauren Moccia, MA

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Lauren Moccia, MA, has no relevant financial relationships.

  • Ibironke W. Apata, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia
    Division of Renal Medicine
    Emory University School of Medicine
    Atlanta, Georgia

    Disclosures

    The opinions expressed are those of Dr Apata and do not necessarily reflect the views of Emory University or Emory Healthcare. Dr Apata‘s participation in this activity does not constitute or imply endorsement by Emory University or Emory Healthcare.
    Ibironke W. Apata, MD, has no relevant financial relationships.

  • Jennifer Ahern, PhD

    University of California, Berkeley
    Berkeley, California

    Disclosures

    Jennifer Ahern, PhD, has the following relevant financial relationships:
    Received research funding from: Chan Zuckerberg Biohub Investigators Program gift

  • Shelley Jung, PhD

    University of California, Berkeley
    Berkeley, California

    Disclosures

    Shelley Jung, PhD, has no relevant financial relationships.

  • Rongxia Li, PhD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Rongxia Li, PhD, has no relevant financial relationships.

  • Joelle Nadle, MPH

    California Emerging Infectious Program
    Oakland, California

    Disclosures

    Joelle Nadle, MPH, has no relevant financial relationships.

  • Susan Petit, MPH

    Connecticut Department of Public Health
    Hartford, Connecticut

    Disclosures

    Susan Petit, MPH, has no relevant financial relationships.

  • Susan M. Ray, MD

    Division of Infectious Diseases
    Emory University School of Medicine
    Atlanta, Georgia

    Disclosures

    The opinions expressed are those of Dr Ray and do not necessarily reflect the views of Emory University or Emory Healthcare. Dr Ray‘s participation in this activity does not constitute or imply endorsement by Emory University or Emory Healthcare.

    Susan M. Ray, MD, has no relevant financial relationships.

  • Lee H. Harrison, MD

    University of Pittsburgh
    Pittsburgh, Pennsylvania
    Johns Hopkins Bloomberg School of Public Health
    Baltimore, Maryland

    Disclosures

    Participation by Dr Harrison does not constitute or imply endorsement by the Johns Hopkins University or the Johns Hopkins Hospital and Health System.

    Lee H. Harrison, MD, has the following relevant financial relationships:
    Received transportation expenses from: GlaxoSmithKline, Merck, Pfizer, and Sanofi Pasteur

  • Carmen Bernu, MPH

    Minnesota Department of Health
    St. Paul, Minnesota

    Disclosures

    Carmen Bernu, MPH, has no relevant financial relationships.

  • Ruth Lynfield, MD

    Minnesota Department of Health
    St. Paul, Minnesota

    Disclosures

    Ruth Lynfield, MD, has no relevant financial relationships.

  • Ghinwa Dumyati, MD

    University of Rochester Medical Center
    Rochester, New York

    Disclosures

    Ghinwa Dumyati, MD, has no relevant financial relationships.

  • Marissa Tracy, MPH

    University of Rochester Medical Center
    Rochester, New York

    Disclosures

    Marissa Tracy, MPH, has no relevant financial relationships.

  • William Schaffner, MD

    Vanderbilt University Medical Center
    Nashville, Tennessee

    Disclosures

    William Schaffner, MD, has no relevant financial relationships.

  • D. Cal Ham, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    D. Cal Ham, MD, has no relevant financial relationships.

  • Shelley S. Magill, MD, PhD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Shelley S. Magill, MD, PhD, has no relevant financial relationships.

  • Erin N. O’Leary, MPH

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Erin N. O’Leary, MPH, has no relevant financial relationships.

  • Jeneita Bell, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Jeneita Bell, MD, has no relevant financial relationships.

  • Arjun Srinivasan, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Arjun Srinivasan, MD, has no relevant financial relationships.

  • L. Clifford McDonald, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    L. Clifford McDonald, MD, has no relevant financial relationships.

  • Jonathan R. Edwards, MStat

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Jonathan R. Edwards, MStat, has no relevant financial relationships.

  • Shannon Novosad, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    Centers for Disease Control and Prevention
    Atlanta, Georgia

    Disclosures

    Shannon Novosad, MD, has no relevant financial relationships.

CME Author

  • Charles P. Vega, MD

    Health Sciences Clinical Professor of Family Medicine
    University of California, Irvine School of Medicine

    Disclosures

    Charles P. Vega, MD, has the following relevant financial relationships:
    Consultant or advisor for: Boehringer Ingelheim; GlaxoSmithKline; Johnson & Johnson

Editor/Compliance Reviewer/Nurse Planner

  • Leigh Schmidt, MSN, RN, CNE, CHCP

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Leigh Schmidt, MSN, RN, CNE, CHCP, has no relevant financial relationships.


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CME / ABIM MOC / CE

Health Disparities in Hemodialysis-Associated Staphylococcus aureus Bloodstream Infections--United States, 2017-2020

Authors: Brian Rha, MD; Isaac See, MD; Lindsay Dunham, MPH, MSDA; Preeta K. Kutty, MD; Lauren Moccia, MA; Ibironke W. Apata, MD; Jennifer Ahern, PhD; Shelley Jung, PhD; Rongxia Li, PhD; Joelle Nadle, MPH; Susan Petit, MPH; Susan M. Ray, MD; Lee H. Harrison, MD; Carmen Bernu, MPH; Ruth Lynfield, MD; Ghinwa Dumyati, MD; Marissa Tracy, MPH; William Schaffner, MD; D. Cal Ham, MD; Shelley S. Magill, MD, PhD; Erin N. O’Leary, MPH; Jeneita Bell, MD; Arjun Srinivasan, MD; L. Clifford McDonald, MD; Jonathan R. Edwards, MStat; Shannon Novosad, MDFaculty and Disclosures

CME / ABIM MOC / CE Released: 5/13/2023

Valid for credit through: 5/13/2024, 11:59 PM EST

processing....

Abstract and Introduction

Abstract

Introduction: Racial and ethnic minorities are disproportionately affected by end-stage kidney disease (ESKD). ESKD patients on dialysis are at increased risk for Staphylococcus aureus bloodstream infections, but racial, ethnic, and socioeconomic disparities associated with this outcome are not well described.

Methods: Surveillance data from the 2020 National Healthcare Safety Network (NHSN) and the 2017–2020 Emerging Infections Program (EIP) were used to describe bloodstream infections among patients on hemodialysis (hemodialysis patients) and were linked to population-based data sources (CDC/Agency for Toxic Substances and Disease Registry [ATSDR] Social Vulnerability Index [SVI], United States Renal Data System [USRDS], and U.S. Census Bureau) to examine associations with race, ethnicity, and social determinants of health.

Results: In 2020, 4,840 dialysis facilities reported 14,822 bloodstream infections to NHSN; 34.2% were attributable to S. aureus. Among seven EIP sites, the S. aureus bloodstream infection rate during 2017–2020 was 100 times higher among hemodialysis patients (4,248 of 100,000 person-years) than among adults not on hemodialysis (42 of 100,000 person-years). Unadjusted S. aureus bloodstream infection rates were highest among non-Hispanic Black or African American (Black) and Hispanic or Latino (Hispanic) hemodialysis patients. Vascular access via central venous catheter was strongly associated with S. aureus bloodstream infections (NHSN: adjusted rate ratio [aRR] = 6.2; 95% CI = 5.7–6.7 versus fistula; EIP: aRR = 4.3; 95% CI = 3.9–4.8 versus fistula or graft). Adjusting for EIP site of residence, sex, and vascular access type, S. aureus bloodstream infection risk in EIP was highest in Hispanic patients (aRR = 1.4; 95% CI = 1.2–1.7 versus non-Hispanic White [White] patients), and patients aged 18–49 years (aRR = 1.7; 95% CI = 1.5–1.9 versus patients aged ≥65 years). Areas with higher poverty levels, crowding, and lower education levels accounted for disproportionately higher proportions of hemodialysis-associated S. aureus bloodstream infections.

Conclusions and implications for public health practice: Disparities exist in hemodialysis-associated S. aureus infections. Health care providers and public health professionals should prioritize prevention and optimized treatment of ESKD, identify and address barriers to lower-risk vascular access placement, and implement established best practices to prevent bloodstream infections.

Introduction

More than 800,000 persons in the United States live with ESKD, 70% of whom are treated with dialysis (89% hemodialysis and 11% peritoneal dialysis); 30% have a functioning kidney transplant[1]. Race, ethnicity, and social determinants of health* affect development of ESKD[1–4]. ESKD prevalence is fourfold higher among Black persons and more than twofold higher among Hispanic than among White persons[1], disparities which are thought to be attributable at least in part to underlying conditions such as hypertension and diabetes mellitus[1–3]. Furthermore, disparities in pre-ESKD nephrology care and receipt of ESKD therapies exist for these same groups, as well as those with lower income and insurance coverage[1,5–9]. Black persons constitute 33% of all U.S. patients receiving dialysis[1], but only 12% of the U.S. population[10].

Infections are a leading cause of morbidity and mortality in hemodialysis patients[1]. S. aureus is the most commonly isolated pathogen among bloodstream infections in hemodialysis patients reported to NHSN; 40% of those infections are methicillin resistant (MRSA)[11]. Higher rates of invasive S. aureus infections have been observed in dialysis patients compared with nondialysis patients[12].

Type of hemodialysis access is a well-established risk factor for infections; risk is highest for central venous catheters (CVCs), lower for grafts, and lowest for fistulas[11]. Although elevated rates have been reported for both invasive MRSA infections among Black dialysis patients[13] and hospitalizations for dialysis-related infections among adult Black patients and older Hispanic patients (aged >60 years)[14], the association among hemodialysis-related infections, race and ethnicity, and social determinants of health is largely undescribed. To identify groups experiencing high numbers and risk of infections and to determine which preventive interventions should be prioritized, this study used a national facility-level reporting system and a laboratory- and population-based surveillance network to understand markers of disparities in the risk for S. aureus bloodstream infections in hemodialysis patients. This activity was reviewed by CDC and was conducted consistent with applicable federal law and CDC policy.§