Abstract

BackgroundIndices of global tissue oxygen delivery and utilization such as mixed venous oxygen saturation, serum lactate concentration, and arterial hematocrit are commonly used to determine the adequacy of tissue oxygenation during cardiopulmonary bypass (CPB). However, these global measures may not accurately reflect regional tissue oxygenation and ischemic organ injury remains a common and serious complication of CPB. Near-infrared spectroscopy (NIRS) is a noninvasive technology that measures regional tissue oxygenation. NIRS may be used alongside global measures to optimize regional perfusion and reduce organ injury. It may also be used as an indicator of the need for red blood cell transfusion in the presence of anemia and tissue hypoxia. However, the clinical benefits of using NIRS remain unclear and there is a lack of high-quality evidence demonstrating its efficacy and cost effectiveness.ObjectiveThe aim of the patient-specific cerebral oxygenation monitoring as part of an algorithm to reduce transfusion during heart valve surgery (PASPORT) trial is to determine whether the addition of NIRS to CPB management algorithms can prevent cognitive decline, postoperative organ injury, unnecessary transfusion, and reduce health care costs.MethodsAdults aged 16 years or older undergoing valve or combined coronary artery bypass graft and valve surgery at one of three UK cardiac centers (Bristol, Hull, or Leicester) are randomly allocated in a 1:1 ratio to either a standard algorithm for optimizing tissue oxygenation during CPB that includes a fixed transfusion threshold, or a patient-specific algorithm that incorporates cerebral NIRS monitoring and a restrictive red blood cell transfusion threshold. Allocation concealment, Internet-based randomization stratified by operation type and recruiting center, and blinding of patients, ICU and ward care staff, and outcome assessors reduce the risk of bias. The primary outcomes are cognitive function 3 months after surgery and infectious complications during the first 3 months after surgery. Secondary outcomes include measures of inflammation, organ injury, and volumes of blood transfused. The cost effectiveness of the NIRS-based algorithm is described in terms of a cost-effectiveness acceptability curve. The trial tests the superiority of the patient-specific algorithm versus standard care. A sample size of 200 patients was chosen to detect a small to moderate target difference with 80% power and 5% significance (two tailed).ResultsOver 4 years, 208 patients have been successfully randomized and have been followed up for a 3-month period. Results are to be reported in 2015.ConclusionsThis study provides high-quality evidence, both valid and widely applicable, to determine whether the use of NIRS monitoring as part of a patient-specific management algorithm improves clinical outcomes and is cost effective.Trial RegistrationInternational Standard Randomized Controlled Trial Number (ISRCTN): 23557269; http://www.isrctn.com/ISRCTN23557269 (Archived by Webcite at http://www.webcitation.org/6buyrbj64)

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Summary

The relevance of the proposed research to the priorities and needs of the NHS

Whilst blood transfusions are a life-saving treatment, there is increasing awareness of the importance of not using transfusions indiscriminately in surgery because of the associated adverse effects on patients and the diminishing availability of blood supplies. The applicants state that this cannot happen within the time frame of the programme but would happen subsequently It is clear, and the applicants emphasize, that the benefits of the proposed research would not be limited to patients within the host division of cardiac surgery, UBHT, but findings could be translated both to other NHS trusts across the UK and to other types of surgery. The applicants emphasize, that the benefits of the proposed research would not be limited to patients within the host division of cardiac surgery, UBHT, but findings could be translated both to other NHS trusts across the UK and to other types of surgery This is apparent for project A1 which envolves validation of a risk score in several different populations including use of data from the Edinburgh cardiac unit, the North West Quality Improvement Programme and the Society for Cardiothoracic Surgery in Great Britain and Ireland National Audit

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