renal transplant patients
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2022 ◽  
Vol 145 ◽  
pp. 112407
Author(s):  
Huijie Lu ◽  
Haixia Jiang ◽  
Siyao Yang ◽  
Chengcheng Li ◽  
Chuanjiang Li ◽  
...  

Author(s):  
Alexandre Destere ◽  
Charlotte Salmon Gandonnière ◽  
Anders Åsberg ◽  
Véronique Loustaud‐Ratti ◽  
Paul Carrier ◽  
...  

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
José Medina-Pestana ◽  
Dimas Tadeu Covas ◽  
Laila Almeida Viana ◽  
Yasmim Cardoso Dreige ◽  
Monica Rika Nakamura ◽  
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María Molina ◽  
Carolina Sorolla ◽  
Elisabet Samsó ◽  
Monserrat Carcaña ◽  
María Luisa Martín ◽  
...  

2021 ◽  
pp. jim-2021-001933
Author(s):  
Melissa Rachel Downey ◽  
Varsha Taskar ◽  
Daniel F Linder ◽  
Stephanie L Baer ◽  
Jennifer L Waller ◽  
...  

AbstractBackgroundRenal transplant patients are at increased risk for mucormycosis. Diabetes, neutropenia, deferoxamine therapy, and immunosuppressive medications have been associated with increased risk of mucormycosis in studies of solid organ transplant recipients. To focus on renal transplant patients, the US Renal Data System (USRDS) was queried to determine the incidence and risk factors for mucormycosis.MethodsAll renal transplant patients in the USRDS from 1988 to 2015 were queried for a diagnosis of mucormycosis after the first transplant date using ICD-9 and ICD-10 codes. The International Classification of Diseases (ICD) codes, which currently exist in the ninth and tenth revisions, are a global system of classification used to code diagnoses, procedures, and symptoms. We defined proven mucormycosis by a histopathologic or fungal stain procedure code within 7 days of the diagnosis code. Logistic regression controlling for person-years at risk was used to examine demographic and clinical diagnosis risk factors for mucormycosis.ResultsOf the 306,482 renal transplant patients, 222 (0.07%) had codes consistent with proven mucormycosis. The incidence of mucormycosis increased from 1990 to 2000 (peak 17.6 per 100,000 person-years) and subsequently demonstrated more variability. Hispanic ethnicity (OR=1.45), age 65 years or greater (OR=1.64), other or black race compared with white race (OR=1.96 and 1.74), cadaver or other donor type (OR=2.41), and receiving tacrolimus (OR=2.09) were associated with increased risk. Comorbidities associated with decreased risk of mucormycosis included female sex (OR=0.68), iron overload (OR=0.56), and receiving mycophenolate mofetil (OR=0.67) or azathioprine (OR=0.53).ConclusionsIn renal transplant patients, age, deceased donor graft transplant, tacrolimus administration, race other than white, and Hispanic ethnicity were associated with increased risk of mucormycosis. Unexpectedly, iron overload was protective. Mucormycosis is a rare infection in renal transplant patients which should be considered in patients with the above risk factors after more common infections have been ruled out.


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