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Solid organ transplant recipients are vulnerable to the most severe manifestations of strongyloidiasis.
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Travel to or residence in an endemic region is a risk factor for disease among donors and recipients.
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Limited diagnostic strategies and lack of alternative agents to oral ivermectin make the diagnosis and management of strongyloidiasis challenging.
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Targeted screening for Strongyloides stercoralis infection in the solid organ transplant population is recommended, but universal screening may be
Management of Strongyloides in Solid Organ Transplant Recipients
Section snippets
Key points
Epidemiology and risk factors
Strongyloides is present in temperate, tropical, and subtropical environments3 and is believed to infect as many as 30 to 100 million individuals globally.1 In North America, Strongyloides is endemic to the southeast, particularly Appalachia,4 and to the Caribbean. Although the published studies confirming the presence of S stercoralis in the soil of Appalachia were performed in the 1980s,4 as recently as 2013, surveillance of 102 residents in rural Kentucky showed evidence of S stercoralis
Clinical manifestations
Strongyloides infection after solid organ transplantation may occur by (1) de novo acquisition via travel or residence in endemic areas after transplantation,10 (2) reactivation of disease in the recipient, or (3) donor-derived transmission. Reactivation of prior disease in the recipient is most common. Donor-derived strongyloidiasis typically presents early after transplantation, although there are some reports of diagnosis as late as 9 months after transplantation.11 Reactivation disease
Host response to Strongyloides
Limited animal models have compromised our ability to understand the Strongyloides host–pathogen interaction. In rodents, S stercoralis penetrate skin, migrate to the lungs, and move to skeletal muscle.26 Other species of Strongyloides—Strongyloides ratti and Strongyloides venezuelensis—also infect rodents, but lack an autoinfective cycle.26 Thus, rodent models neither reproduce the intestinal phase of S stercoralis infection nor the autoinfective cycle seen in humans. Only severe combined
Diagnosis
At present, noninvasive diagnostic modalities include parasitologic and serologic tests for the diagnosis of S stercoralis. Unfortunately, the performance of existing noninvasive tests is not optimal. In addition, there are no pathognomonic radiologic findings to assist in diagnosis of S stercoralis.2 The current reference standard, fecal microscopy, has limited sensitivity because there is only intermittent shedding of rhabditiform larvae into stool during the acute, chronic, or autoinfective
Screening strategies
Screening strategies for Strongyloides infection in the context of solid organ transplantation fall into 2 categories: (1) screening of the donor and (2) screening of the recipient. Screening is generally performed via commercial serology. Screening of donors and at-risk recipients is critical to the prevention of hyperinfection or dissemination syndromes after immunosuppression as well as to the rapid evaluation and initiation of appropriate therapy should S stercoralis infection disseminate
Antimicrobial Chemotherapy
Available agents with targeted antihelminth properties to treat strongyloidiasis are the azole drugs—namely, thiabendazole, mebendazole, and albendazole—as well as ivermectin. The calcineurin inhibitor, cyclosporine, may actually have intrinsic antihelminth activity.2 Importantly, antihelminth agents have largely been studied only in the context of chronic Strongyloides infection and there are limited evidence based-data to guide agent selection or duration for treatment of hyperinfection
Summary
Infection with S stercoralis after organ transplantation carries a high mortality. A high index of suspicion is necessary to identify and treat patients with chronic infection owing to S stercoralis before the start of immunosuppression. Delayed diagnosis owing to imperfect diagnostics and limited alternative therapies to oral ivermectin render management of strongyloidiasis challenging. Recent advances in molecular diagnostics, newly identified preclinical therapeutic compounds with
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