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Table 1.  

Variable and response Value
Race
   Black or African American 444 (91)
   White 9 (1.8)
   Prefer not to answer 6 (1.2)
   Black and White 2 (0.4)
   Unsure 2 (0.4)
   No response 25 (5.1)
Ethnicity
   Not Hispanic or Latino 407 (83)
   Prefer not to answer 16 (3.3)
   Hispanic or Latino 7 (1.4)
   Unknown 6 (1.2)
   No response 52 (11)
County
   Wilcox 237 (56)
   Lowndes 101 (21)
   Perry 86 (17)
   No response 66 (14)
Household receives water bill
   Yes 385 (79)
   No 67 (14)
   Don’t know 6 (1.2)
   No response 430 (6.1)
Household sanitation
   Septic tank 207 (42)
   Sewer connection 111 (23)
   Don’t know 80 (16)
   Straight pipe 56 (11)
   Cesspit 2 (0.4)
   Other 1 (0.1)
   No response 31 (6.3)
Raw sewage in yard or home in past year
   No 400 (82)
   Yes 38 (7.8)
   No response 50 (10)
History of international travel in past year
   No 448 (92)
   Yes 13 (2.7)
   No response 27 (5.5)
Sex
   M 236 (48)
   F 229 (47)
   No response 23 (4.7)
Daily screen time, h
   <2 72 (15)
   2–4 182 (37)
   >4 203 (42)
   No response 31 (6.4)
Age, y
   Mean (SD) 11 (4.1)
   Median (interquartile range) 11 (8–14)
   Range 2–18
   No response 37 (17.6)
Ever treated for an intestinal parasite
   No 418 (86)
   Don’t know 45 (9.2)
   Yes 12 (2.5)
   No response 13 (2.7)

Table 1. Demographic characteristics of 488 children and water infrastructure summary based on self-administered surveys conducted in Lowndes, Wilcox, and Perry Counties, Alabama, USA, January 2019–December 2021*

*Values are no. (%) except as indicated.

Table 2.  

Type and pathogen Prevalence, no. (%)
Any
   ≥1 pathogen gene detected 127 (26)
Bacteria
   Clostridioides difficile 32 (6.6)
   EPEC (atypical) 30 (6.1)
   EAEC 19 (3.9)
   Helicobacter pylori 11 (2.3)
   EPEC (typical) 7 (1.4)
   Yersinia enterocolitica 5 (1.0)
   E. coli O157:H7 4 (0.8)
   Plesiomonas shigelloides 2 (0.4)
   ETEC 2 (0.4)
   Shigella or EIEC 1 (0.2)
   Salmonella 1 (0.2)
   STEC 1 (0.2)
   Campylobacter jejuni or coli 0
Fungus/algae
   Blastocystis 18 (3.7)
   Enterocytozoon bieneusi 0
   Encephalitozoon intestinalis 0
Protozoa
   Balantidium coli 3 (0.6)
   Acanthamoeba 2 (0.4)
   Giardia spp. 2 (0.4)
   Entamoeba hystolytica 1 (0.2)
   Cystoisospora belli 0
   Cyclospora cayetanensi 0
   Cryptosporidium 0
   Entamoeba 0
Virus
   Norovirus GI or GII 7 (1.4)
   SARS-CoV-2 3 (0.6)
   Rotavirus 2 (0.4)
   Sapovirus 2 (0.4)
   Astrovirus 1 (0.2)

Table 2. Prevalence of enteric pathogens in stool specimens of children in a study conducted in Lowndes, Wilcox, and Perry Counties, Alabama, USA, January 2019–December 2021*

*EAEC, enteroaggregative Escherichia coli; EIEC, enteroinvasive E. coli; EPEC, enteropathogenic E. coli; ETEC, enterotoxigenic E. coli; GI/GII, genotype group I and II; STEC, Shiga toxin–producing E. coli.

Table 3.  

Variable Reference Exposure RR (95% CI) aRR (95% CI)
Pay a water bill Yes No 1.8 (1.2–2.5) 1.7 (1.1–2.5)
Sanitation Sewer connection Cesspit NA NA
Other 3.4 (0.57–20) 5.2 (0.88–30)
Septic tank 0.89 (0.61–1.3) 0.95 (0.64–1.4)
Straight pipe 0.95 (0.55–1.6) 0.95 (0.55–1.7)
Child’s screen time <2 h 2–4 h 0.74 (0.48–1.1) 0.79 (0.51–1.2)
>4 h 0.74 (0.48–1.1) 0.73 (0.47–1.1)
Child’s sex Male Female 0.89 (0.65–1.2) 0.89 (0.65–1.2)
International travel in past year No Yes 0.89 (0.32–2.5) 0.93 (0.34–2.5)
Raw sewage in home or yard in past year No Yes 1.1 (0.68–1.9) 1.1 (0.66–2.0)
Child’s age <5 y 5–10 y 0.71 (0.40–1.3) 0.76 (0.41–1.4)
>10 y 0.82 (0.47–1.4) 0.90 (0.49–1.6)

Table 3. Risk factors for detection of ≥1 enteric pathogen in stool specimens of children in a study conducted in Lowndes, Wilcox, and Perry Counties, Alabama, USA, January 2019–December 2021*

*Unadjusted RRs are from bivariate models, whereas aRRs are from full model including all covariates. aRR, adjusted risk ratio; RR, risk ratio.

CME / ABIM MOC

Risk Factors for Enteric Pathogen Exposure Among Children in Black Belt Region of Alabama, USA

  • Authors: Drew Capone, PhD; Toheedat Bakare; Troy Barker, MPH; Amy Hutson Chatham, PhD; Ryan Clark, BS; Lauren Copperthwaite, BS; Abeoseh Flemister, BS; Riley Geason, BS; Emery Hoos; Elizabeth Kim, BS; Alka Manoj, BS; Sam Pomper, BS; Christina Samodal, BS; Simrill Smith, BS; Claudette Poole, MD; Joe Brown, PhD
  • CME / ABIM MOC Released: 11/15/2023
  • Valid for credit through: 11/15/2024, 11:59 PM EST
Start Activity

  • Credits Available

    Physicians - maximum of 1.00 AMA PRA Category 1 Credit(s)™

    ABIM Diplomates - maximum of 1.00 ABIM MOC points

    You Are Eligible For

    • Letter of Completion
    • ABIM MOC points

Target Audience and Goal Statement

This activity is intended for primary care clinicians, pediatricians, infectious disease specialists, and other healthcare professionals who treat and manage children and adolescents, particularly in poor and rural areas.

The goal of this activity is for members of the healthcare team to be better able to assess the prevalence of and risk factors for positive testing for enteric pathogens among Black children in Alabama.

Upon completion of this activity, participants will:

  • Assess characteristics of the current study examining the prevalence of enteric pathogens among children and adolescents
  • Distinguish the prevalence of enteric pathogens among children and adolescents in the current study
  • Compare rates of positive tests for different enteric pathogens in the current study
  • Evaluate variables associated with a higher rate of positive testing for at least 1 pathogen in the current study


Disclosures

Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated. Others involved in the planning of this activity have no relevant financial relationships.


Faculty

  • Drew Capone, PhD

    Department of Environmental and Occupational Health
    School of Public Health
    Indiana University
    Bloomington, Indiana

  • Toheedat Bakare

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Troy Barker, MPH

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Amy Hutson Chatham, PhD

    Department of Environmental Health Sciences
    School of Public Health
    University of Alabama at Birmingham
    Birmingham, Alabama

  • Ryan Clark, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Lauren Copperthwaite, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Abeoseh Flemister, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Riley Geason, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Emery Hoos

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Elizabeth Kim, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Alka Manoj, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Sam Pomper, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Christina Samodal, BS

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

  • Simrill Smith, BS

    School of Civil and Environmental Engineering
    Georgia Institute of Technology
    Atlanta, Georgia

  • Claudette Poole, MD

    Department of Pediatrics
    Heersink School of Medicine
    University of Alabama at Birmingham
    Birmingham, Alabama

  • Joe Brown, PhD

    Department of Environmental Sciences and Engineering
    Gillings School of Public Health
    University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina

Editor

  • Jude Rutledge, BA

    Copyeditor
    Emerging Infectious Diseases

CME Author

  • Charles P. Vega, MD

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

    Disclosures

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

Compliance Reviewer

  • Maria Morales, MSN, RN, CLNC

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Maria Morales, MSN, RN, CLNC, has no relevant financial relationships.


Accreditation Statements

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Interprofessional Continuing Education

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    For Physicians

  • Medscape, LLC designates this Journal-based CME activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)™ . Physicians should claim only the credit commensurate with the extent of their participation in the activity.

    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 1.0 MOC points in the American Board of Internal Medicine’s (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider’s responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit. Aggregate participant data will be shared with commercial supporters of this activity.

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CME / ABIM MOC

Risk Factors for Enteric Pathogen Exposure Among Children in Black Belt Region of Alabama, USA

Authors: Drew Capone, PhD; Toheedat Bakare; Troy Barker, MPH; Amy Hutson Chatham, PhD; Ryan Clark, BS; Lauren Copperthwaite, BS; Abeoseh Flemister, BS; Riley Geason, BS; Emery Hoos; Elizabeth Kim, BS; Alka Manoj, BS; Sam Pomper, BS; Christina Samodal, BS; Simrill Smith, BS; Claudette Poole, MD; Joe Brown, PhDFaculty and Disclosures

CME / ABIM MOC Released: 11/15/2023

Valid for credit through: 11/15/2024, 11:59 PM EST

processing....

Abstract and Introduction

Absract

We collected stool from school-age children from 352 households living in the Black Belt region of Alabama, USA, where sanitation infrastructure is lacking. We used quantitative reverse transcription PCR to measure key pathogens in stool that may be associated with water and sanitation, as an indicator of exposure. We detected genes associated with ≥1 targets in 26% of specimens, most frequently Clostridioides difficile (6.6%), atypical enteropathogenic Escherichia coli (6.1%), and enteroaggregative E. coli (3.9%). We used generalized estimating equations to assess reported risk factors for detecting ≥1 pathogen in stool. We found no association between lack of sanitation and pathogen detection (adjusted risk ratio 0.95 [95% CI 0.55–1.7]) compared with specimens from children served by sewerage. However, we did observe an increased risk for pathogen detection among children living in homes with well water (adjusted risk ratio 1.7 [95% CI 1.1–2.5]) over those reporting water utility service.

Introduction

Outside cities and towns served by conventional sewerage, many residents in the rural Black Belt region of Alabama, USA, have failing or inadequate sanitation infrastructure[1,2]. This region was named after its rich black soils, which are typically high in clay content, limiting subsurface infiltration[3] and leading to surface discharge of domestic wastewater. Compounding those challenges is a high rate of poverty; 9 of the 10 poorest counties in Alabama are in the Black Belt region[2,4]. Because common alternatives to septic systems are unaffordable[5,6], many residents use failing systems or lack systems altogether[7,8]. Straight piping (i.e., direct discharge of untreated fecal wastes to the environment) of domestic wastewater is common[7].

When human fecal wastes are not safely managed, they may be transported to the environment through well-understood fecal–oral pathways (i.e., drinking water, soils, flies, food, fomites, and hands)[9,10]. For households reliant on straight pipe discharge of wastewater, direct exposure to this waste may be more likely than for households served by a septic system[8]. Those same households and their communities may also suffer from exposures further downstream. Inadequate treatment of fecal wastes can result in enteric pathogen transport through soil into groundwater and exposure through drinking water (e.g., well water)[11,12]. Other exposures may include fecally contaminated soils[13], flies that feed on and reproduce in human feces[14,15], and contaminated food[10]. Such exposures can result in infection with enteric pathogens, which is a necessary precondition for diarrheal disease and other sequelae, including environmental enteric dysfunction[16], growth deficits[17], cognitive impairment[18], and negative effects on the immune system[19].

Poor sanitation and persistent exposure to fecal wastes, particularly in the context of a state and nation with ample resources to address the issue[20], represents a public policy failure[7,21] affecting human health, dignity, and quality of life. Although the evidence base for public investment in sanitation on health grounds has a long history[22], the health burden attributable to poor rural sanitation in the United States remains poorly characterized, constraining the case for action. To determine the potential roles of rural sanitation improvements or other interventions in controlling disease transmission, a useful first step is estimating prevalence of enteric infections and identifying risk factors associated with them. Because of documented poor sanitation conditions in Alabama’s Black Belt region[5,7,8] and the associated potential persistence of endemic enteric infection[23–25], we conducted a cross-sectional study to assess the prevalence of stool-based enteric pathogen detection in children using molecular methods, as an indicator of previous exposure. We further sought to identify potential household-level environmental risk factors for exposure to those pathogens to understand the potential role of infrastructure in protecting public health in this underserved region.