Seroprevalence of Strongyloides stercoralis and Evaluation of Universal Screening in Kidney Transplant Candidates: A Single-Center Experience in Houston (2012-2017).

kidney transplant candidate pretransplant screening strongyloidiasis

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
01 Jul 2019
Historique:
received: 14 02 2019
accepted: 11 04 2019
entrez: 1 8 2019
pubmed: 1 8 2019
medline: 1 8 2019
Statut: ppublish

Résumé

Disseminated strongyloidiasis in solid organ transplant recipients is a rare but devastating infection. In our center, we implemented a universal screening of all candidates for kidney transplantation. We assessed the seroprevalence and utility of universal screening for strongyloidiasis in our center. Patients were identified from our transplant referral list (from July 2012 to June 2017). Demographics, pretransplant laboratory, and serological screenings were retrospectively collected. For Strongyloides-seropositive (SSp) patients, data on travel history, symptoms, treatment, and stool ova and parasite examinations were extracted. Logistic regression and multiple imputation for missing data were performed. A total of 1689 patients underwent serological screening, of whom 168 (9.9%) were SSp. Univariate analysis revealed that SSp patients had higher rates of eosinophilia, diabetes mellitus, latent tuberculosis and were likely to be either Hispanic or Asian (P < .05). In multivariate analysis, eosinophilia (P = .01), diabetes mellitus (P = .02), and Asian race (P = .03) were associated with being SSp, but 45 (27%) of the SSp patients did not have any of these 3 factors, and 18 SSp patients (11%) had no epidemiological risk factors. All patients received ivermectin, and none developed disseminated strongyloidiasis. Of patients who underwent serological screening on multiple occasions, 6.8% seroconverted while waiting for kidney transplantation. We found a high rate of Strongyloides seropositivity among our kidney transplantation candidates. No epidemiological risk factors effectively predicted SSp status in our population, and universal screening identified a large number of patients without such factors. Serial screening should be considered when a long wait time is expected before transplantation.

Sections du résumé

BACKGROUND BACKGROUND
Disseminated strongyloidiasis in solid organ transplant recipients is a rare but devastating infection. In our center, we implemented a universal screening of all candidates for kidney transplantation. We assessed the seroprevalence and utility of universal screening for strongyloidiasis in our center.
METHODS METHODS
Patients were identified from our transplant referral list (from July 2012 to June 2017). Demographics, pretransplant laboratory, and serological screenings were retrospectively collected. For Strongyloides-seropositive (SSp) patients, data on travel history, symptoms, treatment, and stool ova and parasite examinations were extracted. Logistic regression and multiple imputation for missing data were performed.
RESULTS RESULTS
A total of 1689 patients underwent serological screening, of whom 168 (9.9%) were SSp. Univariate analysis revealed that SSp patients had higher rates of eosinophilia, diabetes mellitus, latent tuberculosis and were likely to be either Hispanic or Asian (P < .05). In multivariate analysis, eosinophilia (P = .01), diabetes mellitus (P = .02), and Asian race (P = .03) were associated with being SSp, but 45 (27%) of the SSp patients did not have any of these 3 factors, and 18 SSp patients (11%) had no epidemiological risk factors. All patients received ivermectin, and none developed disseminated strongyloidiasis. Of patients who underwent serological screening on multiple occasions, 6.8% seroconverted while waiting for kidney transplantation.
CONCLUSIONS CONCLUSIONS
We found a high rate of Strongyloides seropositivity among our kidney transplantation candidates. No epidemiological risk factors effectively predicted SSp status in our population, and universal screening identified a large number of patients without such factors. Serial screening should be considered when a long wait time is expected before transplantation.

Identifiants

pubmed: 31363770
pii: 5452022
doi: 10.1093/ofid/ofz172
pmc: PMC6656655
pii:
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

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Auteurs

Mohanad Al-Obaidi (M)

Division of Infectious Diseases, McGovern Medical School, University of Texas Health Science Center at Houston.

Rodrigo Hasbun (R)

Division of Infectious Diseases, McGovern Medical School, University of Texas Health Science Center at Houston.

Karen J Vigil (KJ)

Division of Infectious Diseases, McGovern Medical School, University of Texas Health Science Center at Houston.

Angelina R Edwards (AR)

Division of Renal Disease and Hypertension, McGovern Medical School, University of Texas Health Science Center at Houston.

Violeta Chavez (V)

Department of Pathology and Laboratory Medicine, McGovern Medical School, University of Texas Health Science Center at Houston.

David R Hall (DR)

Division of Immunology and Organ Transplantation, McGovern Medical School, University of Texas Health Science Center at Houston.

Wasim A Dar (WA)

Division of Immunology and Organ Transplantation, McGovern Medical School, University of Texas Health Science Center at Houston.

Aleksandra De Golovine (A)

Division of Renal Disease and Hypertension, McGovern Medical School, University of Texas Health Science Center at Houston.

Luis Ostrosky-Zeichner (L)

Division of Infectious Diseases, McGovern Medical School, University of Texas Health Science Center at Houston.

John S Bynon (JS)

Division of Immunology and Organ Transplantation, McGovern Medical School, University of Texas Health Science Center at Houston.

Masayuki Nigo (M)

Division of Infectious Diseases, McGovern Medical School, University of Texas Health Science Center at Houston.

Classifications MeSH