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Is there a renoprotective value to leukodepletion during heart valve surgery?: A randomized controlled trial (ROLO)

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Is there a renoprotective value to leukodepletion during heart valve surgery? A randomized controlled trial (ROLO). / Khoshbin, E.; Spencer, S.; Solomon, L. et al.
In: Journal of Cardiothoracic Surgery, Vol. 16, No. 1, 58, 26.03.2021.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Khoshbin, E, Spencer, S, Solomon, L, Tang, A, Clark, S, Stokes, E, Wordsworth, S, Dabner, L, Edwards, J, Reeves, B & Rogers, C 2021, 'Is there a renoprotective value to leukodepletion during heart valve surgery? A randomized controlled trial (ROLO)', Journal of Cardiothoracic Surgery, vol. 16, no. 1, 58. https://doi.org/10.1186/s13019-021-01402-4

APA

Khoshbin, E., Spencer, S., Solomon, L., Tang, A., Clark, S., Stokes, E., Wordsworth, S., Dabner, L., Edwards, J., Reeves, B., & Rogers, C. (2021). Is there a renoprotective value to leukodepletion during heart valve surgery? A randomized controlled trial (ROLO). Journal of Cardiothoracic Surgery, 16(1), Article 58. https://doi.org/10.1186/s13019-021-01402-4

Vancouver

Khoshbin E, Spencer S, Solomon L, Tang A, Clark S, Stokes E et al. Is there a renoprotective value to leukodepletion during heart valve surgery? A randomized controlled trial (ROLO). Journal of Cardiothoracic Surgery. 2021 Mar 26;16(1):58. doi: 10.1186/s13019-021-01402-4

Author

Khoshbin, E. ; Spencer, S. ; Solomon, L. et al. / Is there a renoprotective value to leukodepletion during heart valve surgery? A randomized controlled trial (ROLO). In: Journal of Cardiothoracic Surgery. 2021 ; Vol. 16, No. 1.

Bibtex

@article{f06996debccf4429b37eadba4a4ee8be,
title = "Is there a renoprotective value to leukodepletion during heart valve surgery?: A randomized controlled trial (ROLO)",
abstract = "Background: Acute Kidney Injury (AKI) adversely affects outcomes after cardiac surgery. A major mediator of AKI is the activation of leukocytes through exposure to the cardiopulmonary bypass circuit. We evaluate the use of leukodepletion filters throughout bypass to protect against post-operative AKI by removing activated leukocytes during cardiac surgery. Methods: This is a single-centre, double-blind, randomized controlled trial comparing the use of leukodepletion versus a standard arterial filter throughout bypass. Elective adult patients undergoing heart valve surgery with or without concomitant procedures were investigated. The primary clinical outcome measured was the development of AKI according to the KDIGO criteria. Secondary measures included biomarkers of renal tubular damage (urinary Retinol Binding Protein and Kidney Injury Molecule-1), glomerular kidney injury (urinary Micro Albumin and serum Cystatin C) and urinary Neutrophil Gelatinase Associated Lipocalin, as well as the length of hospital stay and quality of life measures through EQ-5D-5L questionnaires. Results: The ROLO trial randomized 64 participants with a rate of recruitment higher than anticipated (57% achieved, 40% anticipated). The incidence of AKI was greater in the leukodepletion filter group (44% versus 23%, risk difference 21, 95% CI − 2 to 44%). This clinical finding was supported by biomarker levels especially by a tendency toward glomerular insult at 48 h, demonstrated by a raised serum Cystatin C (mean difference 0.11, 95% CI 0.00 to 0.23, p = 0.068) in the leukodepleted group. There was however no clear association between the incidence or severity of AKI and length of hospital stay. On average, health related quality of life returned to pre-operative levels in both groups within 3 months of surgery. Conclusions: Leukocyte depletion during cardiopulmonary bypass does not significantly reduce the incidence of AKI after valvular heart surgery. Other methods to ameliorate renal dysfunction after cardiac surgery need to be investigated. Trial registration: The trial was registered by the International Standard Randomized Controlled Trial Number Registry ISRCTN42121335. Registered on the 18 February 2014. The trial was run by the Bristol Clinical Trials and Evaluation Unit. This trial was financially supported by the National Institute of Health Research (Research for Patient Benefit), award ID: PB-PG-0711-25,090. ",
keywords = "Acute kidney injury, Cardiac surgery, Cardiopulmonary bypass, Heart valve, Leukodepletion",
author = "E. Khoshbin and S. Spencer and L. Solomon and A. Tang and S. Clark and E. Stokes and S. Wordsworth and L. Dabner and J. Edwards and B. Reeves and C. Rogers",
year = "2021",
month = mar,
day = "26",
doi = "10.1186/s13019-021-01402-4",
language = "English",
volume = "16",
journal = "Journal of Cardiothoracic Surgery",
number = "1",

}

RIS

TY - JOUR

T1 - Is there a renoprotective value to leukodepletion during heart valve surgery?

T2 - A randomized controlled trial (ROLO)

AU - Khoshbin, E.

AU - Spencer, S.

AU - Solomon, L.

AU - Tang, A.

AU - Clark, S.

AU - Stokes, E.

AU - Wordsworth, S.

AU - Dabner, L.

AU - Edwards, J.

AU - Reeves, B.

AU - Rogers, C.

PY - 2021/3/26

Y1 - 2021/3/26

N2 - Background: Acute Kidney Injury (AKI) adversely affects outcomes after cardiac surgery. A major mediator of AKI is the activation of leukocytes through exposure to the cardiopulmonary bypass circuit. We evaluate the use of leukodepletion filters throughout bypass to protect against post-operative AKI by removing activated leukocytes during cardiac surgery. Methods: This is a single-centre, double-blind, randomized controlled trial comparing the use of leukodepletion versus a standard arterial filter throughout bypass. Elective adult patients undergoing heart valve surgery with or without concomitant procedures were investigated. The primary clinical outcome measured was the development of AKI according to the KDIGO criteria. Secondary measures included biomarkers of renal tubular damage (urinary Retinol Binding Protein and Kidney Injury Molecule-1), glomerular kidney injury (urinary Micro Albumin and serum Cystatin C) and urinary Neutrophil Gelatinase Associated Lipocalin, as well as the length of hospital stay and quality of life measures through EQ-5D-5L questionnaires. Results: The ROLO trial randomized 64 participants with a rate of recruitment higher than anticipated (57% achieved, 40% anticipated). The incidence of AKI was greater in the leukodepletion filter group (44% versus 23%, risk difference 21, 95% CI − 2 to 44%). This clinical finding was supported by biomarker levels especially by a tendency toward glomerular insult at 48 h, demonstrated by a raised serum Cystatin C (mean difference 0.11, 95% CI 0.00 to 0.23, p = 0.068) in the leukodepleted group. There was however no clear association between the incidence or severity of AKI and length of hospital stay. On average, health related quality of life returned to pre-operative levels in both groups within 3 months of surgery. Conclusions: Leukocyte depletion during cardiopulmonary bypass does not significantly reduce the incidence of AKI after valvular heart surgery. Other methods to ameliorate renal dysfunction after cardiac surgery need to be investigated. Trial registration: The trial was registered by the International Standard Randomized Controlled Trial Number Registry ISRCTN42121335. Registered on the 18 February 2014. The trial was run by the Bristol Clinical Trials and Evaluation Unit. This trial was financially supported by the National Institute of Health Research (Research for Patient Benefit), award ID: PB-PG-0711-25,090.

AB - Background: Acute Kidney Injury (AKI) adversely affects outcomes after cardiac surgery. A major mediator of AKI is the activation of leukocytes through exposure to the cardiopulmonary bypass circuit. We evaluate the use of leukodepletion filters throughout bypass to protect against post-operative AKI by removing activated leukocytes during cardiac surgery. Methods: This is a single-centre, double-blind, randomized controlled trial comparing the use of leukodepletion versus a standard arterial filter throughout bypass. Elective adult patients undergoing heart valve surgery with or without concomitant procedures were investigated. The primary clinical outcome measured was the development of AKI according to the KDIGO criteria. Secondary measures included biomarkers of renal tubular damage (urinary Retinol Binding Protein and Kidney Injury Molecule-1), glomerular kidney injury (urinary Micro Albumin and serum Cystatin C) and urinary Neutrophil Gelatinase Associated Lipocalin, as well as the length of hospital stay and quality of life measures through EQ-5D-5L questionnaires. Results: The ROLO trial randomized 64 participants with a rate of recruitment higher than anticipated (57% achieved, 40% anticipated). The incidence of AKI was greater in the leukodepletion filter group (44% versus 23%, risk difference 21, 95% CI − 2 to 44%). This clinical finding was supported by biomarker levels especially by a tendency toward glomerular insult at 48 h, demonstrated by a raised serum Cystatin C (mean difference 0.11, 95% CI 0.00 to 0.23, p = 0.068) in the leukodepleted group. There was however no clear association between the incidence or severity of AKI and length of hospital stay. On average, health related quality of life returned to pre-operative levels in both groups within 3 months of surgery. Conclusions: Leukocyte depletion during cardiopulmonary bypass does not significantly reduce the incidence of AKI after valvular heart surgery. Other methods to ameliorate renal dysfunction after cardiac surgery need to be investigated. Trial registration: The trial was registered by the International Standard Randomized Controlled Trial Number Registry ISRCTN42121335. Registered on the 18 February 2014. The trial was run by the Bristol Clinical Trials and Evaluation Unit. This trial was financially supported by the National Institute of Health Research (Research for Patient Benefit), award ID: PB-PG-0711-25,090.

KW - Acute kidney injury

KW - Cardiac surgery

KW - Cardiopulmonary bypass

KW - Heart valve

KW - Leukodepletion

U2 - 10.1186/s13019-021-01402-4

DO - 10.1186/s13019-021-01402-4

M3 - Journal article

VL - 16

JO - Journal of Cardiothoracic Surgery

JF - Journal of Cardiothoracic Surgery

IS - 1

M1 - 58

ER -