Testing of the viQtor in postoperative patiënts: a study utilizing photoplethysmography (PPG) sensor technology

In the pursuit of delivering optimal patient care while adhering to budget
constraints, hospitals must maximize their resources, including staff members
and available beds. This necessitates efficient management of patient
admissions and discharges, often aiming to transition patients to lower levels
of care whenever possible. However, navigating these tasks can be complex and
challenging. One valuable solution that can enhance patient management and
triage is the utilization of wearable monitoring devices for continuous vital
sign measurements.

Continuous vital sign monitoring with wearable devices offers significant
benefits in understanding patients' health conditions more comprehensively.
This deeper insight aids in effective triaging, allowing medical professionals
to make informed decisions about the appropriate level of care for each
patient2. At present, continuous monitoring is predominantly carried out in
medium and intensive care units and recoveries, where (critically ill) patients
are located. However, to effectively and timely detect deterioration, it is
crucial to implement continuous monitoring for patients in general wards as
well. By employing wearable devices, healthcare providers can continue
monitoring patients even in lower care settings, reducing the urgency to keep
patients within the hospital.

The peri-operative period, characterized by high incidences of respiratory and
hemodynamic events, presents a critical time for patient monitoring. Continuous
vital sign monitoring facilitated by wearable devices such as the viQtor*
solution enables early detection of clinical deterioration, providing
opportunities for prompt intervention and preventive adjustments to treatment.
In an ideal scenario, such monitoring would be ongoing, wireless, and
independent of constant supervision.

By implementing wearable monitoring devices, such as the viQtor* solution, in
hospital settings and outside, medical professionals gain a valuable tool to
enhance patient care and resource management. Continuous monitoring can offer a
comprehensive view of patient health, aiding in effective triage on patient
admission and facilitating appropriate discharge decisions. Moreover, the
ability to detect and address clinical deterioration early on through
continuous monitoring contributes possibly to improved patient outcomes.

Given that viQtor* version 1.0 has a CE mark and has successfully undergone
stringent tests for elec-trical safety and performance according to the ISO
60601 standards at an accredited testing facility, our focus shifts to
assessing the accuracy of measuring vital signs within a clinical environment,
in patients who exhibit significant variability in vital functions. Therefore,
we have opt-ed for postoperative patients as this group shows an increased risk
of health deterioration. It is essential to understand how the viQtor* performs
under these conditions to ensure its reliability and effectiveness in a
clinical setting.

To achieve this, we have designed a comprehensive study with the aim of
comparing vital signs data collected during standard postoperative monitoring
with data obtained using the viQtor*.

In this prospective observational data-collection study with retrospective data
analysis, 80 subjects, who have been admitted at the UMC Utrecht because of a
surgery, will be recruited at the pre-operative screening clinic before
surgery. Prior to the surgery procedure, the treating doctor will inquire
whether the researcher may contact the patients for potential participation in
the study. If the participant is interested in participating, the researcher
will approach the participant and provide them with the informed consent form
at least 24 hours prior to the measurements. Participants will, thus, have 24
hour to consider participating in the study.
After the informed consent is signed and after surgery, the participant will be
equipped with the viQtor device (SQ-RD or viQtor 2) on the upper arm and
monitored simultaneously by a hospital reference monitor (Spacelab XPREZZON) in
the recovery department for a minimum of 4 hours and a maximum of 24 hours
until transition to a general ward of the UMCU. It is important to note that
the ward staff will rely solely on the values measured by the hospital's
monitoring device for the assessment of the patient's vital functions. The
values measured by the viQtor SQ-RD and viQtor 2 will only be stored, and
analyzed after the study, exclusively for the purpose of this study. More
information about both viQtor devices and the reference hospital measurement
devices can be found in Chapter 6.

At the end of the study period, following a maximum wear time of 24 hours or
upon transfer to the general ward, the research nurse will ask the patient
three questions about their experience with the viQtor device using a short
5-point Likert Scale questionnaire. During this interview, the nurse will
inquire about the patient's satisfaction of the viQtor. This interview is
expected to take about 3 minutes.

Measuring vital signs
Within the first phase of this study, measurement data will be collected, with
the SQ-RD, from a case mix of 40 postoperative patients in the recovery
department of UMC Utrecht. The photoplethysmogram (PPG) data are needed for the
determination of all three vital sign measurements (SpO2, PR, RR), as the
performance of RR is directly related to the performance of the other two vital
signs algorithms. These measurement data will be used to train/improve the
technical performance of the RR algorithm, and possibly also for the
training/improvement of the algorithms for SpO2 and PR. The
training/improvement of the technical performance of the RR algorithm is based
on comparing measurement values of the SQ-RD with the reference equipment
(Spacelab type XPREZZON ® 91393) at UMC Utrecht.

Based on the collected measurement data in phase 1, the RR algorithm, and
possibly also the PR and SpO2 algorithms, will be optimized by the manufacturer
if needed, with the aim of improving technical performance.

In the second phase of the study, the clinical validation of the technical
performance will take place for the new software version with viQtor 2, which
includes the optimized RR algorithm, as well as previously validated algorithms
for PR and SpO2, possibly with improvements. Measurements will be compared
again with the reference device (Spacelab type XPREZZON ® 91393) at UMC Utrecht
and also with the Smart Advanced CapnoLine® H Plus EtCO* sampling line
(Medtronic, Boulder, CO, USA) to achieve more precise RR measurements. In this
second phase, a new group of 40 postoperative patients will be involved to
prevent bias from the test patient population.

Additionally, it is of ultimate importance that the various time clocks are set
identically in the recovery room and the respective device. Within 2 minutes,
both the viQtor device and the reference device must be initiated. The start
time is manually annotated. Retrospectively, the time matching is determined
based on the correlation of both datasets. The viQtor has a start delay of 1
minute, and there may be missing data points at the beginning. Therefore, we
accept a maximum time difference of 5 minutes in the correlation of the data.

Within this study, the number and type of artifacts are also examined, such as
"no data" or when recorded as an "invalid value." Classification into
valid/invalid or missing data is determined retrospectively, including missing
data since the start of a measurement.

As an additional quality check on the reference measurements, RR annotations
are performed by the research nurse in the recovery department, which are
crucial for establishing and comparing the RR data of the viQtor and the
Spacelab XPREZZON at the specified moments below.
The annotation is conducted through direct observation at three specific points
in the study (5 minutes after the application of the viQtor, after 2 hours of
wearing the viQtor, and during the last 5 minutes before the viQtor is
removed). The RR is manually annotated by counting the number of breaths per
minute. Simultaneously, the research nurse manually records the results of the
respiratory rate measured by the Spacelab XPREZZON at that same moment to
enable a comparison.

Within the framework of this study, the aim is to improve and validate the
technical performance of a new algorithm for determining the respiratory rate
(RR) of the viQtor. This research involves continuous collection of
photoplethysmogram (PPG) data (initially) and vital parameters including pulse
rate (PR), respiratory rate (RR), and blood oxygen saturation (SpO2), from 80
post-operative patients. The data collection will span a minimum of 4 hours and
a maximum of 24 hours during their stay in the recovery department. The study
is divided into two phases, which are further explained below.

Phase 1:
The primary goal of this first phase is to collect measurement data from a case
mix of 40 postoperative patients in the recovery department of the UMC Utrecht.
These measurement data will be used to train/improve the technical performance
of the RR algorithm. During this phase, the viQtor research device (SQ-RD) will
be utilized. The training/improvement of the technical performance of the RR
algo-rithm is based on comparing the measurement values of the SQ-RD with the
reference equipment (Spacelab type XPREZZON ® 91393) at UMC Utrecht. PPG
measurement data will be used for train-ing/improving RR, and possibly also for
the training/improvement of SpO2 and PR. Vital parameters SpO2 and PR are also
measured because the performance of RR is related to them. In this phase, the
research group in terms of size and population will be equal to the group in
phase 2, ensuring both groups have the same level of representativeness of the
collected data.

Optimization:
Based on the collected measurement data in phase 1, if necessary, the RR
algorithm will be optimized by the manufacturer with the aim of improving
technical performance. If applicable, the technical per-formance of the PR and
SpO2 algorithms will also be improved. The result of the optimization is a new
software version that will be clinically validated for technical performance in
phase 2 within a new group of postoperative patients. In phase 2, the viQtor
device, equipped with the new, yet-to-be-certified, software version (viQtor 2)
will be used. ViQtor 2 is identical to the current CE certified device (viQtor
1), with the only difference being that it contains new software that is not
yet CE certified. This new software will have been verified according to the
manufacturer's quality processes, including verification of technical
performance in healthy subjects before phase 2.

Phase 2:
In the second phase of the study, the clinical validation of the technical
performance of the new soft-ware version with viQtor 2, containing the
optimized RR algorithm, as well as previously validated algorithms for PR and
SpO2, will take place. Measurements will again be compared with the reference
device (Spacelab type XPREZZON ® 91393) at UMC Utrecht. Additionally, in phase
2 of the study, we will connecting patients to the Smart Advanced Capno-Line® H
Plus EtCO* sampling line (Medtronic, Boulder, CO, USA) to achieve more precise
RR measurements. Literature and clinical practice indicate that capnography is
the gold standard for measuring RR [1]. These capnography measurements
complement ECG-based data by providing real-time respiratory insights directly
related to ventilation quality and CO* exchange efficiency. In addition, to
using the capo-line for RR measurements, we will continue to measure RR with
the Spacelab system, but will give special attention to applying the
electrodes. In this second phase, a new group of 40 postoperative patients will
be involved to prevent bias from the test patient population. Postoperative
patients are chosen due to the significant variability in vital functions
within this group, allowing for a broader validation of the technical
performance of viQtor 2.

After clinical validation, the obtained results of technical performance will
be used to create a clinical evaluation report, which is part of the
documentation for the modification of viQtor 2 (algorithm adjustment). This
report will then be submitted for approval for CE-certification to the Notified
Body, as viQtor is a Class IIa medical device.

MDR 74.2:
This research is part of the conformity assessment according to MDR 74.2. The
study is conducted with the aim of training and clinically validating the
technical performance of the RR algorithm, and possibly also the algorithms for
PR and SpO2 within the new intended application [2]. It involves assessing
per-formance based on MDR-specified requirements within the new intended
application [MDR Regulation (EU) 2017/745, Appendix II, Chapter 6]. For this
purpose, the recovery department within UMC Utrecht has been selected, where
the accuracy and reliability of viQtor can be well-established given the
strongly varying vital measurement values.

[2] Intended application of viQtor 2 (only the bolded text contains a
modification to the intended application):The intended use of the viQtor
solution is to periodically transfer health data and events to a professional
healthcare organization for assessment by healthcare professionals. It measures
SpO2, pulse rate (PR), respiratory rate (RR) of adult users(18 years and older)
in hospitals, nursing homes, and home settings, allowing remote monitoring and
assessment of trends by healthcare professionals. Ad-ditionally, viQtor
monitors skin temperature, user activity and detects potential falls. In case
of a possi-ble fall, the device sends a request for attention to a professional
healthcare organization. The user also has the option to send a request for
assistance to the professional healthcare organization by pressing the
assistance request button.
The viQtor solution is not intended:
o to detect acute life-threatening situations
o for use in high-acuity environments, such as ICU or operating rooms.
o for use on acutely ill (cardiac) patients with the potential to develop life
threatening deterioration, like arrhythmias or very fast atrial fibrillation.
These patients should be monitored using a device with continuous ECG. The
viQtor solution is not a substitute for an ECG monitor.

Intended use of the viQtor solution for this study is:
The SQ-RD and viQtor 2 (equipped with the new, yet-to-be-certified, software
version) are specifically designed for use in a clinical setting, focusing on a
diverse population of postoperative patients, including those with COPD, which
have undergone various surgi-cal procedures such as cardiac ablation. The
intended application is to capture and analyze data related to vital functions,
including PR, RR, and SPO2, for the detection of cardiac arrhythmias and
decreased oxygen saturation during the postoperative period. To facilitate a
comprehensive evaluation of both the device and the software across various
usage environments, we have decided to conduct the study in a postoperative
setting at the UMC Utrecht with a diverse group of patients. The selection of
post-operative patients is driven by the substantial variability in vital
functions due to an increased risk of health deterioration, allowing for
testing of the medical device across a broad spectrum within the dynamic range
of the device.

Estimated study timelines
First Subject enrolled: February 2024 (pending IRB approval)
Enrolment Period: 1 month
Follow-up duration: min 4 hours and max 24 hours per participant
Total study duration: 2 months
Data cleaning/closeout: 3 months



*

The viQtor wearable will be placed on the upper arm with a band which can be
easily adjusted for comfort. The study participants will wear the viQtor*
wearable 24/7 in the hospital for a minimal of 4 hours and a maximum of 24
hours but this will not affect their clinical care nor impact their activities.
Additionally, in phase 2 of the study, we propose connecting patients to the
Smart Advanced Capno-Line® H Plus EtCO* sampling line to achieve more precise
RR measurements. Research has shown that this capnography line is comfortable
for patients. To minimize patient burden, they will be connected to the
capnoLine for a minimum of 2 hours and up to a maximum of 6 hours. The
capnoLine will be placed immediately after surgery while the patient is often
still sedated, ensuring they experience minimal discomfort from its placement.
Besides potential skin irritation, there is no further burden to the patient.
Measurements obtained with the viQtor* will not be viewed nor analyzed during
the study, and consequently, no clinical decisions will be made based on these
measurements.

In addition, participation in the study incurs a minimal time commitment. The
study participant wears the viQtor device only during their hospital stay.
Additionally, we ask the participant to answer a set of questions at the end of
the study, which are also administered within the hospital setting. The
interview typically takes about 3 minutes.

Participation in the study does not impact the standard care/treatment that the
participant receives at the hospital. Participants receive the regular
treatment or assessments for the condition for which they have been admitted to
the UMC Utrecht.