Clinical trajectories and impact of acute kidney disease after acute kidney injury in the intensive care unit: a 5-year single-centre cohort study.


Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
23 Jan 2023
Historique:
received: 21 10 2021
pubmed: 4 3 2022
medline: 26 1 2023
entrez: 3 3 2022
Statut: ppublish

Résumé

Patients suffering from acute kidney injury(AKI) in the intensive care unit (ICU) can have various renal trajectories and outcomes. Aims were to assess the various clinical trajectories after AKI in the ICU and to determine risk factors for developing chronic kidney disease (CKD). We conducted a prospective 5-year follow-up study in a medical ICU at Bordeaux University Hospital (France). The patients who received invasive mechanical ventilation, catecholamine infusion or both and developed an AKI from September 2013 to May 2015 were included. In the Cox analysis, the violation of the proportional hazard assumption for AKD was handled using appropriate interaction terms with time, resulting in a time-dependent hazard ratio (HR). A total of 232 patients were enrolled, with an age of 62 ± 16 years and a median follow-up of 52 days (interquartile range 6-1553). On day 7, 109/232 (47%) patients progressed to acute kidney disease (AKD) and 66/232 (28%) recovered. A linear trajectory (AKI, AKD to CKD) was followed by 44/63 (70%) of the CKD patients. The cumulative incidence of CKD was 30% [95% confidence interval (CI) 24-36] at the 5-year follow-up. In a multivariable Cox model, in the 6 months following AKI, the HR for CKD was higher in AKD patients [HR 29.2 (95% CI 8.5-100.7); P < 0.0001). After 6 months, the HR for CKD was 2.2 (95% CI 0.6-7.9; P = 0.21; n = 172 patients). There were several clinical trajectories of kidney disease after ICU-acquired AKI. CKD risk was higher in AKD patients only in the first 6 months. Lack of renal recovery rather than AKD per se was associated with the risk of CKD.

Sections du résumé

BACKGROUND BACKGROUND
Patients suffering from acute kidney injury(AKI) in the intensive care unit (ICU) can have various renal trajectories and outcomes. Aims were to assess the various clinical trajectories after AKI in the ICU and to determine risk factors for developing chronic kidney disease (CKD).
METHODS METHODS
We conducted a prospective 5-year follow-up study in a medical ICU at Bordeaux University Hospital (France). The patients who received invasive mechanical ventilation, catecholamine infusion or both and developed an AKI from September 2013 to May 2015 were included. In the Cox analysis, the violation of the proportional hazard assumption for AKD was handled using appropriate interaction terms with time, resulting in a time-dependent hazard ratio (HR).
RESULTS RESULTS
A total of 232 patients were enrolled, with an age of 62 ± 16 years and a median follow-up of 52 days (interquartile range 6-1553). On day 7, 109/232 (47%) patients progressed to acute kidney disease (AKD) and 66/232 (28%) recovered. A linear trajectory (AKI, AKD to CKD) was followed by 44/63 (70%) of the CKD patients. The cumulative incidence of CKD was 30% [95% confidence interval (CI) 24-36] at the 5-year follow-up. In a multivariable Cox model, in the 6 months following AKI, the HR for CKD was higher in AKD patients [HR 29.2 (95% CI 8.5-100.7); P < 0.0001). After 6 months, the HR for CKD was 2.2 (95% CI 0.6-7.9; P = 0.21; n = 172 patients).
CONCLUSION CONCLUSIONS
There were several clinical trajectories of kidney disease after ICU-acquired AKI. CKD risk was higher in AKD patients only in the first 6 months. Lack of renal recovery rather than AKD per se was associated with the risk of CKD.

Identifiants

pubmed: 35238922
pii: 6541872
doi: 10.1093/ndt/gfac054
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

167-176

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the ERA.

Auteurs

Arthur Orieux (A)

Service de Médecine Intensive Réanimation, Hôpital Pellegrin, CHU Bordeaux, Bordeaux, France.

Mathilde Prezelin-Reydit (M)

AURAD Aquitaine, 2, allée des demoiselles, Gradignan, France.
Unité INSERM U1219 Bordeaux Population Health, ISPED, Université de Bordeaux, Bordeaux, France.

Renaud Prevel (R)

Service de Médecine Intensive Réanimation, Hôpital Pellegrin, CHU Bordeaux, Bordeaux, France.

Christian Combe (C)

Service de Néphrologie, Transplantation, Dialyse, Aphérèses, Hôpital Pellegrin, CHU de Bordeaux, Bordeaux, France.
Unité INSERM Biotis U1026, Université de Bordeaux, Bordeaux, France.

Didier Gruson (D)

Service de Médecine Intensive Réanimation, Hôpital Pellegrin, CHU Bordeaux, Bordeaux, France.
Unité INSERM U1045, Université de Bordeaux, Bordeaux, France.

Alexandre Boyer (A)

Service de Médecine Intensive Réanimation, Hôpital Pellegrin, CHU Bordeaux, Bordeaux, France.
Unité INSERM U1045, Université de Bordeaux, Bordeaux, France.

Sébastien Rubin (S)

Service de Néphrologie, Transplantation, Dialyse, Aphérèses, Hôpital Pellegrin, CHU de Bordeaux, Bordeaux, France.
Unité INSERM U1034, Université de Bordeaux, Bordeaux, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH