2019
DOI: 10.1016/j.jaci.2019.01.045
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HLA-A*32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms

Abstract: Australia. Some of the data set(s) used for the analyses described were obtained from Vanderbilt University Medical Center's Synthetic Derivative and BioVU, which are supported by numerous sources: institutional funding, private agencies, and federal grants. These include the National Institutes of Health (NIH)-funded Shared Instrumentation grant S10RR025141 and CTSA grants UL1TR002243, UL1TR000445, and UL1RR024975. Genomic data are also supported by investigator-led projects that include U01HG004798,

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Cited by 138 publications
(105 citation statements)
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“…Use of EHR data may facilitate PD analyses as clinical observations for drug effects or adverse events are often documented as part of clinical care (e.g., recurrent cardiac events, 20 ACE inhibitor-induced cough, 21 and vancomycin-induced drug reaction). 22 However, phenotyping can impose different challenges depending on how it is defined. A sophisticated phenotyping algorithm may need to be developed to abstract PD measures, and further development of NLP may be necessary in order to utilize EHR data for more diverse population PD studies.…”
Section: Discussionmentioning
confidence: 99%
“…Use of EHR data may facilitate PD analyses as clinical observations for drug effects or adverse events are often documented as part of clinical care (e.g., recurrent cardiac events, 20 ACE inhibitor-induced cough, 21 and vancomycin-induced drug reaction). 22 However, phenotyping can impose different challenges depending on how it is defined. A sophisticated phenotyping algorithm may need to be developed to abstract PD measures, and further development of NLP may be necessary in order to utilize EHR data for more diverse population PD studies.…”
Section: Discussionmentioning
confidence: 99%
“…Recent literature suggests a strong association of the HLA-A*32:01 alleles in patients of European ancestry who develop DRESS while on vancomycin. The risk of DRESS approaches 20% at four weeks of therapy in those carrying the HLA-A*32:01 allele [58]. While the current HLA allele testing turnaround time is often too prolonged to lead to clinically relevant data, the long latency period of DRESS may allow for testing after initiation of vancomycin in patients who will require a long treatment course and a cost effective HLA gene panel with a 48-h turnaround time is in development [54,58].…”
Section: Drug Rash With Eosinophilia and Systemic Symptomsmentioning
confidence: 99%
“…DRESS syndrome is a rare but potentially lethal drug-induced hypersensitivity leading to multisystem compromise. Vancomycin is an uncommon cause of DRESS syndrome, but some patients may be genetically predisposed due to human leukocyte antigen (HLA) variations 1. Vancomycin-induced DRESS tends to present with greater incidence of renal impairment compared with other drugs 2.…”
Section: Descriptionmentioning
confidence: 99%