Renal Manifestations of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome: A Systematic Review of 71 Cases.

DIHS DRESS syndrome acute kidney injury drug hypersensitivity syndrome drug reaction eosinophilia glomerulonephritis hematuria kidney proteinuria renal

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
10 Jul 2023
Historique:
received: 02 06 2023
revised: 26 06 2023
accepted: 02 07 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

Unlike other adverse drug reactions, visceral organ involvement is a prominent feature of drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome and correlates with mortality. The aim of this study was to systematically review cases published in PubMed-indexed, peer-reviewed journals in which patients had renal injury during the episode of DRESS syndrome (DS). We found 71 cases, of which 67 were adults and 56% were males. Female sex was associated with higher mortality. Chronic kidney disease (CKD) was present in 14% of patients who developed acute kidney injury (AKI) during DS. In 21% of cases, the kidneys were the only visceral organ involved, while 54% of patients had both liver and kidney involvement. Eosinophilia was absent in 24% of patients. The most common classes of medication associated with renal injury in DS were antibiotics in 34%, xanthine oxidase inhibitors in 15%, and anticonvulsants in 11%. Among antibiotics, vancomycin was the most common culprit in 68% of patients. AKI was the most common renal manifestation reported in 96% of cases, while isolated proteinuria or hematuria was present in only 4% of cases. In cases with AKI, 88% had isolated increase in creatinine and decrease in glomerular filtration (GFR), 27% had AKI concomitantly with proteinuria, 18% had oliguria, and 13% had concomitant AKI with hematuria. Anuria was the rarest manifestation, occurring in only 4% of patients with DS. Temporary renal replacement therapy was needed in 30% of cases, and all but one patient fully recovered renal function. Mortality of DS in this cohort was 13%, which is higher than previously reported. Medication class, latency period, or pre-existing CKD were not found to be associated with higher mortality. More research, particularly prospective studies, is needed to better recognize the risks associated with renal injury in patients with DS. The development of disease-specific biomarkers would also be useful so DS with renal involvement can be easier distinguished from other eosinophilic diseases that might affect the kidney.

Identifiants

pubmed: 37510691
pii: jcm12144576
doi: 10.3390/jcm12144576
pmc: PMC10380880
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Marilia Dagnon da Silva (M)

Municipal University of São Caetano do Sul-USCS Bela Vista, São Paulo 09521-160, Brazil.

Sidney Marcel Domingues (SM)

Municipal University of São Caetano do Sul-USCS Bela Vista, São Paulo 09521-160, Brazil.

Stevan Oluic (S)

Department of Internal Medicine, Loyola University Medical Center, Maywood, IL 60402, USA.

Milan Radovanovic (M)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Hospital Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Pratyusha Kodela (P)

Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Terri Nordin (T)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Family Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Margaret R Paulson (MR)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Hospital Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Bojan Joksimović (B)

Faculty of Medicine Foca, University of East Sarajevo, 73300 Foca, The Republic of Srpska, Bosnia and Herzegovina.

Omobolanle Adetimehin (O)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Hospital Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Devender Singh (D)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Nephrology, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Cristian Madrid (C)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Hospital Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Milena Cardozo (M)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Hospital Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Marko Baralic (M)

Department of Nephrology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.
School of Medicine, University of Belgrade, 11000 Belgrade, Serbia.

Igor Dumic (I)

Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
Department of Hospital Medicine, Mayo Clinic Health System, Eau Claire, WI 54703, USA.

Classifications MeSH