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Randomized Controlled Trial
. 2024 Jun;47(6):e24304.
doi: 10.1002/clc.24304.

Randomized Pilot Trial of Pre- and Postoperative Heart Failure Nurse-Supported Care in Heart Failure Patients Requiring Noncardiac Surgery-Feasibility and Results

Affiliations
Randomized Controlled Trial

Randomized Pilot Trial of Pre- and Postoperative Heart Failure Nurse-Supported Care in Heart Failure Patients Requiring Noncardiac Surgery-Feasibility and Results

Ester J Herrmann et al. Clin Cardiol. 2024 Jun.

Abstract

Introduction: The perioperative cardiovascular management of patients undergoing noncardiac surgery is particularly challenging in those with pre-existing heart failure (HF). This study was designed to evaluate the effectiveness of nurse-based pre- and postoperative specialized HF management in reducing postoperative HF-associated complications in patients with known HF undergoing noncardiac surgery.

Methods: This prospective, randomized pilot study included patients with established HF requiring intermediate- to high-risk noncardiac surgery. Patients received postoperatively either standard care (control group, CG) or nurse-supported HF management (intervention group, IG). The primary endpoint was a composite of HF-related postoperative complications at 30 days. Secondary endpoints included length on intensive care unit, length of hospital stay, death, hospitalization for HF, and quality of life assessment using the SF-12 questionnaire.

Results: The trial was halted prematurely for futility. A total of 34 patients (median age 70.5 [IQR 67-75] years; with 15 HfpEF, 9 HfmrEF,10 HfrEF), with an average NT-proBNP of 1.413 [463-2.832] pg/mL were included. The IG had a lower rate of postoperative primary events (25%; n = 4) compared with the CG (33%; n = 6). There were no differences in secondary endpoints between the groups. Quality-of-life scores improved slightly in both groups (δ 5.6 ± 0.9 [CG] and 3.1 ± 1.2 [IG]).

Conclusion: Nurse-based pre- and postoperative HF care appears to be feasible and may reduce HF-associated complications in patients undergoing noncardiac surgery. Larger clinical trials are needed to further evaluate the effectiveness of this approach in reducing postoperative complications in this high-risk patient population.

Keywords: elective noncardiac surgery; heart failure; nurse‐based HF care; preoperative HF screening.

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Conflict of interest statement

B.A. reports having received consulting fees and an unrestricted research grant from St Jude Medical is now Abbott, and lecture fees from Abbott, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Edwards, Novartis, NovoNordisk, CSL Vifor and ZOLL. E.J.H. reports having received lecture fees from Bayer and CSL Vifor.

Figures

Figure 1
Figure 1
Design of the patient recruitment: Recruitment of trial subjects based on inclusion and exclusion criteria.
Figure 2
Figure 2
(A) Days on intensive care unit (ICU) compared for control and intervention group, by type of surgery. (B) Length of hospital stay for control and intervention group, by type of surgery.
Figure 3
Figure 3
Quality of life assessments using the SF12 questionnaire. Quality of life within the different dimensions of the SF 12 and treatment groups comparing baseline to 30‐day follow‐up.

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