Vascular access for renal replacement therapy among 459 critically ill patients: a pragmatic analysis of the randomized AKIKI trial.

Acute kidney injury Catheter Critical care Renal replacement therapy Vascular access

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
08 Apr 2021
Historique:
received: 05 01 2021
accepted: 24 03 2021
entrez: 8 4 2021
pubmed: 9 4 2021
medline: 9 4 2021
Statut: epublish

Résumé

Vascular access for renal replacement therapy (RRT) is routine question in the intensive care unit. Randomized trials comparing jugular and femoral sites have shown similar rate of nosocomial events and catheter dysfunction. However, recent prospective observational data on RRT catheters use are scarce. We aimed to assess the site of RRT catheter, the reasons for catheter replacement, and the complications according to site in a large population of critically ill patients with acute kidney injury. We performed an ancillary study of the AKIKI study, a pragmatic randomized controlled trial, in which patients with severe acute kidney injury (KDIGO 3 classification) with invasive mechanical ventilation, catecholamine infusion or both were randomly assigned to either an early or a delayed RRT initiation strategy. The present study involved all patients who underwent at least one RRT session. Number of RRT catheters, insertion sites, factors potentially associated with the choice of insertion site, duration of catheter use, reason for catheter replacement, and complications were prospectively collected. Among the 619 patients included in AKIKI, 462 received RRT and 459 were finally included, with 598 RRT catheters. Femoral site was chosen preferentially (n = 319, 53%), followed by jugular (n = 256, 43%) and subclavian (n = 23, 4%). In multivariate analysis, continuous RRT modality was significantly associated with femoral site (OR = 2.33 (95% CI (1.34-4.07), p = 0.003) and higher weight with jugular site [88.9 vs 83.2 kg, OR = 0.99 (95% CI 0.98-1.00), p = 0.03]. Investigator site was also significantly associated with the choice of insertion site (p = 0.03). Cumulative incidence of catheter replacement did not differ between jugular and femoral site [sHR 0.90 (95% CI 0.64-1.25), p = 0.67]. Catheter dysfunction was the main reason for replacement (n = 47), followed by suspected infection (n = 29) which was actually seldom proven (n = 4). No mechanical complication (pneumothorax or hemothorax) occurred. Femoral site was preferentially used in this prospective study of RRT catheters in 31 French intensive care units. The choice of insertion site depended on investigating center habits, weight, RRT modality. A high incidence of catheter infection suspicion led to undue replacement.

Sections du résumé

BACKGROUND BACKGROUND
Vascular access for renal replacement therapy (RRT) is routine question in the intensive care unit. Randomized trials comparing jugular and femoral sites have shown similar rate of nosocomial events and catheter dysfunction. However, recent prospective observational data on RRT catheters use are scarce. We aimed to assess the site of RRT catheter, the reasons for catheter replacement, and the complications according to site in a large population of critically ill patients with acute kidney injury.
PATIENTS AND METHODS METHODS
We performed an ancillary study of the AKIKI study, a pragmatic randomized controlled trial, in which patients with severe acute kidney injury (KDIGO 3 classification) with invasive mechanical ventilation, catecholamine infusion or both were randomly assigned to either an early or a delayed RRT initiation strategy. The present study involved all patients who underwent at least one RRT session. Number of RRT catheters, insertion sites, factors potentially associated with the choice of insertion site, duration of catheter use, reason for catheter replacement, and complications were prospectively collected.
RESULTS RESULTS
Among the 619 patients included in AKIKI, 462 received RRT and 459 were finally included, with 598 RRT catheters. Femoral site was chosen preferentially (n = 319, 53%), followed by jugular (n = 256, 43%) and subclavian (n = 23, 4%). In multivariate analysis, continuous RRT modality was significantly associated with femoral site (OR = 2.33 (95% CI (1.34-4.07), p = 0.003) and higher weight with jugular site [88.9 vs 83.2 kg, OR = 0.99 (95% CI 0.98-1.00), p = 0.03]. Investigator site was also significantly associated with the choice of insertion site (p = 0.03). Cumulative incidence of catheter replacement did not differ between jugular and femoral site [sHR 0.90 (95% CI 0.64-1.25), p = 0.67]. Catheter dysfunction was the main reason for replacement (n = 47), followed by suspected infection (n = 29) which was actually seldom proven (n = 4). No mechanical complication (pneumothorax or hemothorax) occurred.
CONCLUSION CONCLUSIONS
Femoral site was preferentially used in this prospective study of RRT catheters in 31 French intensive care units. The choice of insertion site depended on investigating center habits, weight, RRT modality. A high incidence of catheter infection suspicion led to undue replacement.

Identifiants

pubmed: 33830370
doi: 10.1186/s13613-021-00843-3
pii: 10.1186/s13613-021-00843-3
pmc: PMC8032839
doi:

Types de publication

Journal Article

Langues

eng

Pagination

56

Subventions

Organisme : Ministère de la Santé, France
ID : AOM12456

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Auteurs

Nicolas Benichou (N)

AP-HP, Hôpital Européen Georges Pompidou, Service de Néphrologie, 75015, Paris, France.
Université de Paris, Paris, France.
French National Institute of Health and Medical Research (INSERM), UMR_S1155, Remodeling and Repair of Renal Tissue, Hôpital Tenon, Sorbonne Université, 75020, Paris, France.

Saïd Lebbah (S)

Département de Biostatistiques, Santé Publique Et Information Médicale, AP-HP, Hôpital Pitié-Salpêtrière, 75013, Paris, France.

David Hajage (D)

Département de Biostatistiques, Santé Publique Et Information Médicale, AP-HP, Hôpital Pitié-Salpêtrière, 75013, Paris, France.
INSERM, ECEVE, U1123, CIC 1421, F-75013, Paris, France.
Faculté de Médecine Sorbonne, Sorbonne Université, Université, Paris, France.

Laurent Martin-Lefèvre (L)

Réanimation Médico-Chirurgicale, CHG, La Roche-sur-Yon, France.

Bertrand Pons (B)

Service de Réanimation, CHU de Pointe À Pitre-Abymes, CHU de La Guadeloupe, Pointe-à-Pitre, France.

Eric Boulet (E)

Réanimation Polyvalente, CH René Dubos, 95301, Pontoise, France.

Alexandre Boyer (A)

Réanimation Médicale CHU Bordeaux, Hôpital Pellegrin, 33000, Bordeaux, France.

Guillaume Chevrel (G)

Service de Réanimation, Centre Hospitalier Sud Francilien, Corbeil Essonne, France.

Nicolas Lerolle (N)

Département de Réanimation Médicale Et Médecine Hyperbare, CHU Angers, Université D'Angers, Angers, France.

Dorothée Carpentier (D)

Réanimation Médicale, CHU Rouen, 76000, Rouen, France.

Nicolas de Prost (N)

Assistance Publique-Hôpitaux de Paris, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, France.
CARMAS Research Group and UPEC-Université Paris-Est Créteil Val de Marne, Créteil, France.

Alexandre Lautrette (A)

Réanimation Médicale, Hôpital Gabriel Montpied, CHU de Clermont-Ferrand, Clermont-Ferrand, France.

Anne Bretagnol (A)

Réanimation Médico-Chirurgicale, Hôpital de La Source, Centre Hospitalier Régional D'Orléans, BP 6709, 45067, Orléans Cedex, France.

Julien Mayaux (J)

Service de Pneumologie Et Réanimation Médicale, APHP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

Saad Nseir (S)

Centre de Réanimation, CHU de Lille, Faculté de Médecine, Université de Lille, 59000, Lille, France.

Bruno Megarbane (B)

Réanimation Médicale Et Toxicologique, Hôpital Lariboisière, INSERM U1144, Université Paris-Diderot, Paris, France.

Marina Thirion (M)

Réanimation Polyvalente, CH Victor Dupouy, 95107, Argenteuil Cedex, France.

Jean-Marie Forel (JM)

Service de Réanimation Des Détresses Respiratoires Aiguës Et Infections Sévères, Hôpital Nord Marseille, 13015, Marseille, France.

Julien Maizel (J)

Service de Réanimation Médicale INSERM U1088, Centre Hospitalier Universitaire de Picardie, Amiens, France.

Hodane Yonis (H)

Réanimation Médicale, Hôpital de La Croix Rousse, 69004, Lyon, France.

Philippe Markowicz (P)

Réanimation, CH Cholet, 49300, Cholet, France.

Guillaume Thiery (G)

Service de Réanimation, CHU de Pointe À Pitre-Abymes, CHU de La Guadeloupe, Pointe-à-Pitre, France.

Frederique Schortgen (F)

Centre Hospitalier Inter-Communal, Service de Réanimation Polyvalente Adulte, Créteil, France.

Florence Tubach (F)

Département de Biostatistiques, Santé Publique Et Information Médicale, AP-HP, Hôpital Pitié-Salpêtrière, 75013, Paris, France.
INSERM, ECEVE, U1123, CIC 1421, F-75013, Paris, France.
Univ Pierre Et Marie Curie, Sorbonne Universités, 75013, Paris, France.

Jean-Damien Ricard (JD)

Univ Paris Diderot, Sorbonne Paris Cité, IAME, UMRS 1137, 75018, Paris, France.
AP-HP, Service de Réanimation Médico-Chirurgicale, Hôpital Louis Mourier, 92700, Colombes, France.

Didier Dreyfuss (D)

AP-HP, Service de Réanimation Médico-Chirurgicale, Hôpital Louis Mourier, 92700, Colombes, France.
Université de Paris, Paris, France.
French National Institute of Health and Medical Research (INSERM), UMR_S1155, Remodeling and Repair of Renal Tissue, Hôpital Tenon, Sorbonne Université, 75020, Paris, France.

Stéphane Gaudry (S)

French National Institute of Health and Medical Research (INSERM), UMR_S1155, Remodeling and Repair of Renal Tissue, Hôpital Tenon, Sorbonne Université, 75020, Paris, France. stephanegaudry@gmail.com.
AP-HP, Service de Réanimation Médico-Chirurgicale, Hôpital Avicenne, 93008, Bobigny, France. stephanegaudry@gmail.com.
Service de Réanimation Médico-Chirurgicale, Hôpital Avicenne, 125 Rue de Stalingrad, 93000, Bobigny, France. stephanegaudry@gmail.com.

Classifications MeSH