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Figure.  Clinician Knowledge of Chagas Disease at Baseline and After Training
Clinician Knowledge of Chagas Disease at Baseline and After Training

Error bars represent SEs. ECG indicates electrocardiogram; NS, not significant; TORCH, toxoplasmosis, other agents (syphilis, hepatitis B), rubella, cytomegalovirus, and herpes simplex.

Table.  Associations Between Participant Characteristics and Baseline Knowledge
Associations Between Participant Characteristics and Baseline Knowledge
1.
Irish  A, Whitman  JD, Clark  EH, Marcus  R, Bern  C.  Updated estimates and mapping for prevalence of Chagas disease among adults, United States.   Emerg Infect Dis. 2022;28(7):1313-1320. doi:10.3201/eid2807.212221PubMedGoogle ScholarCrossref
2.
Rassi  A  Jr, Marin  JA, Rassi  A.  Chronic Chagas cardiomyopathy: a review of the main pathogenic mechanisms and the efficacy of aetiological treatment following the Benznidazole Evaluation for Interrupting Trypanosomiasis (BENEFIT) trial.   Mem Inst Oswaldo Cruz. 2017;112(3):224-235. doi:10.1590/0074-02760160334PubMedGoogle ScholarCrossref
3.
Forsyth  C, Meymandi  S, Moss  I, Cone  J, Cohen  R, Batista  C.  Proposed multidimensional framework for understanding Chagas disease healthcare barriers in the United States.   PLoS Negl Trop Dis. 2019;13(9):e0007447. doi:10.1371/journal.pntd.0007447PubMedGoogle ScholarCrossref
4.
Manne-Goehler  J, Reich  MR, Wirtz  VJ.  Access to care for Chagas disease in the United States: a health systems analysis.   Am J Trop Med Hyg. 2015;93(1):108-113. doi:10.4269/ajtmh.14-0826PubMedGoogle ScholarCrossref
5.
LaVeist  TA, Pérez-Stable  EJ, Richard  P,  et al.  The economic burden of racial, ethnic, and educational health inequities in the US.   JAMA. 2023;329(19):1682-1692. doi:10.1001/jama.2023.5965PubMedGoogle ScholarCrossref
6.
Hasslocher-Moreno  AM, Saraiva  RM, Sangenis  LH,  et al.  Benznidazole decreases the risk of chronic Chagas disease progression and cardiovascular events: a long-term follow up study.   EClinicalMedicine. 2020;31:100694. doi:10.1016/j.eclinm.2020.100694PubMedGoogle ScholarCrossref
Research Letter
Medical Education
July 2, 2024

Clinician Knowledge of Chagas Disease After an Educational Intervention

Author Affiliations
  • 1Department of Tropical Medicine and Infectious Disease, School of Public Health and Tropical Medicine, and Vector-Borne and Infectious Disease Research Center, Tulane University, New Orleans, Louisiana
JAMA Netw Open. 2024;7(7):e2419906. doi:10.1001/jamanetworkopen.2024.19906
Introduction

Chagas disease is a major neglected parasitic infection, affecting an estimated 287 711 people in the US.1 Delayed diagnosis and treatment is associated with increased risk of cardiac, gastrointestinal, and neurological alterations with severe morbidity and mortality.2 Chagas disease remains underdiagnosed (<1%)3 and untreated (<0.3%)4 due to structural, psychosocial, clinical, and systemic barriers and disproportionately affects Hispanic or Latino populations in the US.5 Limited efforts exist to educate physicians on this disease; thus, patient screening is lacking. We evaluated the extent of Chagas disease testing and measured medical knowledge before and after a training lecture.

Methods

In this survey study, the number of Chagas disease tests ordered in major hospitals in New Orleans, including Tulane Medical Center (TMC), University Medical Center (UMC), and Veterans Affair Medical Center (VAMC), was ascertained using electronic health records (EHRs). Patient screening is described in eMethods in Supplement 1. To assess medical knowledge, anonymous cross-sectional surveys were administered to physicians from multiple medical specialties (eTable in Supplement 1) before and after training. The Tulane Institutional Review Board deemed this survey study exempt from review and waived informed consent because it was not human participant research. We followed the AAPOR reporting guideline.

Frequencies were computed for demographics. Survey responses before and after training were compared using McNemar χ2 tests. Association between physician characteristics and knowledge was evaluated using χ2 tests. Results were cross-tabulated and reported as counts. Two-sided P < .05 indicated statistical significance. Data analysis was performed with R 4.3.1 (R Core Team).

Results

Between 2007 and 2023, 1242 tests were ordered at TMC, 48 at UMC, and 6 at VAMC. At TMC, 30 of 1242 (2%) screened were Hispanic or Latino patients, 385 (31%) were transplant recipients or donors, 326 (26%) had cancer, 199 (16%) had preoperative examinations or substance use disorder, and 11 (<1%) had a diagnosis compatible with Chagas disease. Six adults (0.5%) and 1 pediatric patient (0.1%) had positive test results; 4 of these were Hispanic or Latino patients and 1 had a diagnosis compatible with Chagas disease. At UMC, 36 of 48 (75%) screened identified as Hispanic or Latino patients, and 28 (58%) had a diagnosis compatible with Chagas disease. No pregnant patient was screened.

Of 474 physicians who attended the Chagas disease lecture, 280 (59%) completed the baseline survey and 181 of 280 (65%) completed the posttraining survey, and represented various medical specialties, experience levels, races, and ethnicities (Table). At baseline, physicians had adequate general knowledge of Chagas disease but lower percentages of correct answers for aspects such as transmission routes (56%); diagnostic methods (25%); treatment for adult, pediatric, or pregnant patients (17%-49%); disease reactivation (32%); and recognition of Chagas cardiomyopathy (20%-40%) (Figure). Baseline knowledge was higher for clinicians with prior vs without training (345 [65%] vs 422 [51%]), and significantly differed among medical specialties (eg, cardiology: 82 [61%]; pediatrics: 79 [40%]) (Table). Experience level, race and ethnicity, and estimated proportion of Hispanic or Latino patients had no association with Chagas disease knowledge. After training, knowledge significantly increased (>82% correct answers), except for clinical manifestations in infants (28%). Insufficient knowledge remained regarding disease reactivation (45%), diagnostics (75%), and congenital risk (68%). Physicians expressed concerns about access to rapid screening, performance of tests, and algorithm to confirm diagnosis.

Discussion

Current testing for Chagas disease is either targeted and limited in scale or missing most at-risk populations, resulting in low detection of cases. Improved screening is needed, particularly for young adult, pregnant, and pediatric patients who would most benefit from early diagnosis and treatment.6

Limited knowledge of Chagas disease restricts clinicians’ ability to offer optimum patient screening and care. A study limitation is that selection bias can only be inferred because the demographics of nonparticipants were not collected.

Our findings indicate that continued medical education can mitigate knowledge gaps on Chagas disease, at least in the short-term. Educating physicians can potentially change clinical practice to one with more screening, better care, and less health disparities for patients with Chagas disease.

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Article Information

Accepted for Publication: May 1, 2024.

Published: July 2, 2024. doi:10.1001/jamanetworkopen.2024.19906

Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2024 Bernabé KJ et al. JAMA Network Open.

Corresponding Authors: Claudia Herrera, PhD (cherrera@tulane.edu); and Eric Dumonteil, PhD (edumonte@tulane.edu), Department of Tropical Medicine and Infectious Disease, School of Public Health and Tropical Medicine, and Vector-Borne and Infectious Disease Research Center, Tulane University, 1440 Canal St, New Orleans, LA 70112.

Author Contributions: Dr Dumonteil had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: All authors.

Acquisition, analysis, or interpretation of data: Bernabé, Dumonteil.

Drafting of the manuscript: Bernabé.

Critical review of the manuscript for important intellectual content: All authors.

Statistical analysis: Bernabé.

Obtained funding: Herrera.

Administrative, technical, or material support: Bernabé, Herrera.

Supervision: Dumonteil, Herrera.

Conflict of Interest Disclosures: None reported.

Funding/Support: This research was supported by a grant from the Tulane Bywater Institute-Faculty Fellowships in Interdisciplinary Collaboration and the University Senate Committee on Research, in conjunction with the Provost’s Office of Tulane University (Dr Herrera).

Role of the Funder/Sponsor: The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Data Sharing Statement: See Supplement 2.

Additional Contributions: We thank all participants and the department chairs who helped us host Chagas disease training sessions. Crystal Zheng, MD, Tulane School of Medicine, provided helpful feedback on executing this intervention and editing medical content in the survey instrument. She received no additional compensation, outside of her usual salary, for her contributions.

References
1.
Irish  A, Whitman  JD, Clark  EH, Marcus  R, Bern  C.  Updated estimates and mapping for prevalence of Chagas disease among adults, United States.   Emerg Infect Dis. 2022;28(7):1313-1320. doi:10.3201/eid2807.212221PubMedGoogle ScholarCrossref
2.
Rassi  A  Jr, Marin  JA, Rassi  A.  Chronic Chagas cardiomyopathy: a review of the main pathogenic mechanisms and the efficacy of aetiological treatment following the Benznidazole Evaluation for Interrupting Trypanosomiasis (BENEFIT) trial.   Mem Inst Oswaldo Cruz. 2017;112(3):224-235. doi:10.1590/0074-02760160334PubMedGoogle ScholarCrossref
3.
Forsyth  C, Meymandi  S, Moss  I, Cone  J, Cohen  R, Batista  C.  Proposed multidimensional framework for understanding Chagas disease healthcare barriers in the United States.   PLoS Negl Trop Dis. 2019;13(9):e0007447. doi:10.1371/journal.pntd.0007447PubMedGoogle ScholarCrossref
4.
Manne-Goehler  J, Reich  MR, Wirtz  VJ.  Access to care for Chagas disease in the United States: a health systems analysis.   Am J Trop Med Hyg. 2015;93(1):108-113. doi:10.4269/ajtmh.14-0826PubMedGoogle ScholarCrossref
5.
LaVeist  TA, Pérez-Stable  EJ, Richard  P,  et al.  The economic burden of racial, ethnic, and educational health inequities in the US.   JAMA. 2023;329(19):1682-1692. doi:10.1001/jama.2023.5965PubMedGoogle ScholarCrossref
6.
Hasslocher-Moreno  AM, Saraiva  RM, Sangenis  LH,  et al.  Benznidazole decreases the risk of chronic Chagas disease progression and cardiovascular events: a long-term follow up study.   EClinicalMedicine. 2020;31:100694. doi:10.1016/j.eclinm.2020.100694PubMedGoogle ScholarCrossref
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