This is a multi-center cluster-randomized trial with the following Specific Aims: * To evaluate if continuous noninvasive hemoglobin monitoring will reduce the RBC transfusions in patients undergoing surgeries associated with a significant risk of bleeding. * To evaluate if patients monitored with continuous noninvasive hemoglobin experience less frequent complications and shorter hospital stay compared with patients who are not being monitored with continuous noninvasive hemoglobin. Accordingly, the study hypotheses are defined as follows: * The primary null hypothesis is that continuous noninvasive hemoglobin monitoring will not reduce the RBC transfusions in patients undergoing surgeries associated with a significant risk of bleeding. * The secondary hypothesis is that in patients monitored with continuous noninvasive hemoglobin, there will be earlier warning of critical drops in hemoglobin, and thus, there will be less frequent complications compared with patients who are not being monitored with continuous noninvasive hemoglobin.
This is a matched-pair cluster-randomized controlled trial. At each participating centers, consenting eligible Anesthesiologists will be grouped into matched pairs based on their practice characteristics and experience (namely, their main surgical service/procedures and their years of experience working as a clinician responsible for making transfusion decisions). From each pair, Anesthesiologists will be randomly allocated to either treat their patients while having access to data from a continuous noninvasive hemoglobin monitoring device (total hemoglobin \[SpHb\] and Pleth Variability Index \[PVI\]) (SpHb group) or without access to SpHb/PVI data, under standard of care (control group). Regardless of randomization, all patients will be monitored with the device but the data will be blinded and not be available to the Anesthesiologist to be used in the management of the control group. Only in the SpHb group, the SpHb/PVI data will be provided live to the Anesthesiologist, to be used during management of the patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
470
Availability of data from a continuous noninvasive hemoglobin monitoring device (total hemoglobin \[SpHb\] and Pleth Variability Index \[PVI\]) to the clinicians in the operating room
Stanford University
Stanford, California, United States
RECRUITINGMontefiore Medical Center
The Bronx, New York, United States
COMPLETEDDuke University Medical Center
Durham, North Carolina, United States
COMPLETEDThe Ohio State University Wexner Medical Center
Columbus, Ohio, United States
RECRUITINGSwedish Medical Center
Seattle, Washington, United States
COMPLETEDCHU Angers
Angers, France
COMPLETEDIRCCS Policlinico San Donato
San Donato, MI, Italy
COMPLETEDSapporo Medical University School of Medicine
Chuo-ku Sapporo, Hokkaido, Japan
COMPLETEDAmount of Intraoperative RBC Transfusion
Number of allogeneic RBC units transfused intraoperatively per patient
Time frame: From the first surgical incision to the wound closure
Intraoperative RBC Transfusion Rate
Occurrence of any allogeneic RBC transfusions intraoperatively
Time frame: From the first surgical incision to the wound closure
Amount of Perioperative RBC Transfusion
Total number of allogeneic RBC units transfused perioperatively during hospital stay
Time frame: From time of admission to the hospital to the time of discharge or death whichever sooner (an estimated average of 6 days)
Ischemic Events
Incidence of new (or worsening of pre-existing) ischemic events
Time frame: From time of surgery to the time of discharge or death whichever sooner (an estimated average of 5 days)
Mortality
Any death occuring during surgery or within 30-day period following the surgery
Time frame: From time of surgery to 30 days after the surgery
Length of Stay
Length of post-surgery hospital stay
Time frame: From time of surgery to time of discharge from hospital (an estimated average of 5 days)
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