Incidence, risk factors, and outcomes of the transition of HIPEC-induced acute kidney injury to acute kidney disease: a retrospective study

Ren Fail. 2024 Dec;46(1):2338482. doi: 10.1080/0886022X.2024.2338482. Epub 2024 Apr 11.

Abstract

Background: Acute kidney injury (AKI) is recognized as a common complication following cytoreductive surgery combined with hyperthermic intraperitoneal chemotherapy (CRS-HIPEC). Characterized by prolonged renal function impairment, acute kidney disease (AKD) is associated with a higher risk of chronic kidney disease (CKD) and mortality.

Methods: From January 2018 to December 2021, 158 patients undergoing CRS-HIPEC were retrospectively reviewed. Patients were separated into non-AKI, AKI, and AKD cohorts. Laboratory parameters and perioperative features were gathered to evaluate risk factors for both HIPEC-induced AKI and AKD, with the 90-day prognosis of AKD patients.

Results: AKI developed in 21.5% of patients undergoing CRS-HIPEC, while 13.3% progressed to AKD. The multivariate analysis identified that ascites, GRAN%, estimated glomerular filtration rate (eGFR), and intraoperative (IO) hypotension duration were associated with the development of HIPEC-induced AKI. Higher uric acid, lessened eGFR, and prolonged IO hypotension duration were more predominant in patients proceeding with AKD. The AKD cohort presented a higher risk of 30 days of in-hospital mortality (14.3%) and CKD progression (42.8%).

Conclusions: Our study reveals a high incidence of AKI and AKI-to-AKD transition. Early identification of risk factors for HIPEC-induced AKD would assist clinicians in taking measures to mitigate the incidence.

Keywords: AKD; AKI; CKD; HIPEC; renal function.

MeSH terms

  • Acute Disease
  • Acute Kidney Injury* / chemically induced
  • Acute Kidney Injury* / epidemiology
  • Humans
  • Hyperthermic Intraperitoneal Chemotherapy / adverse effects
  • Hypotension*
  • Incidence
  • Renal Insufficiency, Chronic* / complications
  • Renal Insufficiency, Chronic* / epidemiology
  • Renal Insufficiency, Chronic* / therapy
  • Retrospective Studies
  • Risk Factors

Grants and funding

The research has received support from the Beijing Natural Science Foundation with a grant number of [7222199], the National Natural Science Foundation of China with a grant number of [81971808], and Peking University People’s Hospital Scientific Research Development Funds with a grant number of [RDGS2023-07].