Arteriovenous Fistula Maturation, Functional Patency, and Intervention Rates.


Journal

JAMA surgery
ISSN: 2168-6262
Titre abrégé: JAMA Surg
Pays: United States
ID NLM: 101589553

Informations de publication

Date de publication:
01 12 2021
Historique:
pubmed: 23 9 2021
medline: 27 1 2022
entrez: 22 9 2021
Statut: ppublish

Résumé

National initiatives have emphasized the use of autogenous arteriovenous fistulas (AVFs) for hemodialysis, but their purported benefits have been questioned. To examine AVF usability, longer-term functional patency, and remedial procedures to facilitate maturation, manage complications, or maintain patency in the Hemodialysis Fistula Maturation (HFM) Study. The HFM Study was a multicenter (n = 7) prospective National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases cohort study performed to identify factors associated with AVF maturation. A total of 602 participants were enrolled (dialysis, kidney failure: 380; predialysis, chronic kidney disease [CKD]: 222) with AVF maturation ascertained for 535 (kidney failure, 353; CKD, 182) participants. All clinical decisions regarding AVF management were deferred to the individual centers, but remedial interventions were discouraged within 6 weeks of creation. In this case series analysis, the primary outcome was unassisted maturation. Functional patency, freedom from intervention, and participant survival were summarized using Kaplan-Meier analysis. Most participants evaluated (n = 535) were men (372 [69.5%]) and had diabetes (311 [58.1%]); mean (SD) age was 54.6 (13.6) years. Almost two-thirds of the AVFs created (342 of 535 [64%]) were in the upper arm. The AVF maturation rates for the kidney failure vs CKD participants were 29% vs 10% at 3 months, 67% vs 38% at 6 months, and 76% vs 58% at 12 months. Several participants with kidney failure (133 [37.7%]) and CKD (63 [34.6%]) underwent interventions to facilitate maturation or manage complications before maturation. The median time from access creation to maturation was 115 days (interquartile range [IQR], 86-171 days) but differed by initial indication (CKD, 170 days; IQR, 113-269 days; kidney failure, 105 days; IQR, 81-137 days). The functional patency for the AVFs that matured at 1 year was 87% (95% CI, 83.2%-90.2%) and at 2 years, 75% (95% CI, 69.7%-79.7%), and there was no significant difference for those receiving interventions before maturation. Almost half (188 [47.5%]) of the AVFs that matured had further intervention to maintain patency or treat complications. The findings of this study suggest that AVF remains an accepted hemodialysis access option, although both its maturation and continued use require a moderate number of interventions to maintain patency and treat the associated complications.

Identifiants

pubmed: 34550312
pii: 2784421
doi: 10.1001/jamasurg.2021.4527
pmc: PMC8459303
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1111-1118

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK079626
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008721
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082232
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Auteurs

Thomas S Huber (TS)

Division of Vascular Surgery and Endovascular Therapy, Department of Surgery, University of Florida College of Medicine, Gainesville.

Scott A Berceli (SA)

Division of Vascular Surgery and Endovascular Therapy, Department of Surgery, University of Florida College of Medicine, Gainesville.

Salvatore T Scali (ST)

Division of Vascular Surgery and Endovascular Therapy, Department of Surgery, University of Florida College of Medicine, Gainesville.

Dan Neal (D)

Division of Vascular Surgery and Endovascular Therapy, Department of Surgery, University of Florida College of Medicine, Gainesville.

Erik M Anderson (EM)

Division of Vascular Surgery and Endovascular Therapy, Department of Surgery, University of Florida College of Medicine, Gainesville.

Michael Allon (M)

Division of Nephrology, University of Alabama at Birmingham.

Alfred K Cheung (AK)

Nephrology and Hypertension Division, University of Utah School of Medicine, Salt Lake City.

Laura M Dember (LM)

Renal, Electrolyte and Hypertension Division, University of Pennsylvania Perelman School of Medicine, Philadelphia.

Jonathan Himmelfarb (J)

Kidney Research Institute, Division of Nephrology, University of Washington, Seattle.

Prabir Roy-Chaudhury (P)

University of North Carolina Kidney Center, Chapel Hill.

Miguel A Vazquez (MA)

Division of Nephrology, University of Texas Southwestern, Dallas.

Charles E Alpers (CE)

Department of Pathology, University of Washington, Seattle.

Michelle L Robbin (ML)

Department of Radiology, University of Alabama at Birmingham.

Peter B Imrey (PB)

Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.

Gerald J Beck (GJ)

Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.

Alik M Farber (AM)

Division of Vascular and Endovascular Surgery, Boston Medical Center, Boston, Massachusetts.

James S Kaufman (JS)

Renal Section, Veterans Affairs New York Harbor Healthcare System, New York.

Larry W Kraiss (LW)

Division of Vascular Surgery, University of Utah, Salt Lake City.

Wanpen Vongpatanasin (W)

Division of Nephrology, University of Texas Southwestern, Dallas.

John W Kusek (JW)

Division of Kidney, Urologic, and Hematologic Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

Harold I Feldman (HI)

Renal, Electrolyte and Hypertension Division, University of Pennsylvania Perelman School of Medicine, Philadelphia.
Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania Perelman School of Medicine, Philadelphia.

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Classifications MeSH