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Pvm 2701

Manufactured by Nihon Kohden
Sourced in Japan

The PVM-2701 is a patient vital signs monitor from Nihon Kohden. It is designed to continuously measure and display a patient's vital signs, including heart rate, respiratory rate, and blood pressure.

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3 protocols using pvm 2701

1

Verification of Pulse Oximeter Accuracy

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The verification equipment is capable of verifying a transmission-type pulse oximeter. Therefore, we decided to verify the accuracy by employing a pulse oximeter whose accuracy was verified by the verification device.
We evaluated the accuracy of the pulse oximeter (PVM-2701, Nihon Kohden, Tokyo, Japan) in advance using the validation device (vPad-A1, Metts, Tokyo, Japan) and confirmed that there were no problems with accuracy. The pseudo-signal of light transmitted through living tissue, such as a fingertip, emitted from the verification device was read by the pulse oximeter. We verified whether the value was the same as the vital sign of the validation device.
The PVM-2701 pulse oximeter was then attached to the middle finger of the right hand, while the developed SpO2 sensor was grasped with the index finger of the right hand so that it contacted the palm surface. SpO2 values were simultaneously monitored using the two sensors for 30 s (Figure 6). Bland–Altman analysis was performed to determine the agreement between the developed SpO2 sensor and the commercial pulse oximeter [23 (link),24 (link)]. JMP Pro® 16.0.0 software (SAS Institute Inc., Cary, NC, USA) was used for all statistical analyses.
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2

Anesthesia and Monitoring in Pig Model

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The animals were made to fast for 24 h before anesthesia. We performed the operation under anesthesia with a solution of 3% pentobarbital sodium injected intramuscularly. Subsequently, the pigs were treated with an oxygen mask and isoflurane inhalation anesthesia. Each pig was intubated with an endotracheal tube and maintained under inhalation anesthesia without a muscle relaxant (Kaiser et al., 2006 (link)). The depth of anesthesia was monitored using pain and corneal reflex tests. The depth of anesthesia was adjusted at all times to ensure that the pig breathed smoothly to prevent convulsions during image acquisition. Three vital signs, including rectal temperature, respiratory rate, and heart rate, were continuously monitored using a multifunctional bedside physiological monitor (PVM-2701; Nihon Kohden Corporation, Tokyo, Japan).
At the end of the DSCI model generation surgery, a wake-up test was carried out to prevent any false-negative or false-positive MEP signals from occurring. Approximately 30 min after osteotomy stabilization in animal model generation surgery, the pigs were awakened from anesthesia. We tested and observed lower extremity movements and sensory responses to mechanical stimulation.
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3

Cardiovascular Responses to Induced Seizures

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Pulse oximetry and electrocardiograms monitored heart rate (HR), systolic blood pressure (SBP), and DBP using the Nihon bedside monitor, PVM-2701 (Nihon Kohden Corp., Japan). Heart rate, SBP, and DBP were recorded at 6 time points: before induction of anesthesia (baseline, T0), after the induction of anesthesia but before electrical stimulation (T1), during convulsion (T2), 2 minutes after cessation of motor seizure (T3), 5 minutes after cessation of motor seizure (T4), and 10 minutes after cessation of motor seizure (T5). The CVS measurements at T2 were conducted immediately after the MST or ECT stimulation was administered.9 (link) The rate pressure product (RPP) was calculated as the product of HR and SBP, and is considered a measure of the energy consumption of the cardiac workload.9 (link)
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