The largest database of trusted experimental protocols

Finometer device

Manufactured by Finapres Medical Systems
Sourced in Netherlands

The Finometer device is a non-invasive medical instrument designed to continuously monitor and record blood pressure and other cardiovascular parameters. It provides a real-time analysis of beat-to-beat blood pressure changes. The device utilizes a finger cuff to measure these parameters without the need for an intravenous line or arterial catheter.

Automatically generated - may contain errors

Lab products found in correlation

3 protocols using finometer device

1

Cardiovascular Hemodynamics and Carotid Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
The validated Finometer device [15 (link), 16 (link)] was used to measure systolic blood pressure (SBP) and diastolic blood pressure (DBP) after 5 min resting period (Finapres Medical Systems, Amsterdam, The Netherlands). Total peripheral resistance (TPR) and Windkessel compliance (Cwk) were calculated using the Fast Modelflo computer software program from the Finometer data. The Sonosite Micromaxx ultrasound system (SonoSite Inc., Bothell, WA) and a 6-13 MHz linear array transducer was used to measure carotid intima media thickness (cIMT), by obtaining a high resolution image from two angles from the left and right carotid artery. A 10 mm segment with good image quality was chosen after the images were imported into the Artery Measurement System (AMS) II v1.139 (Gothenburg, Sweden). The mean cIMT were calculated through determining the borders of the far and near wall and the inner diameter of the vessel from 100 discrete measurements through the 10 mm segment for each participant. The analysis of the cIMT was done by one observer and the intra-observer variability was 0.04 mm between two measurements made 4 weeks apart (n = 10).
+ Open protocol
+ Expand
2

Noninvasive Cardiovascular Monitoring

Check if the same lab product or an alternative is used in the 5 most similar protocols
Heart rate was monitored by electrocardiography and BP was measured by finger plethysmography (Finometer; TNO, Amsterdam, Netherlands) of the right index or middle finger intermittently recalibrated against oscillometry. Beat-to-beat arterial BP was noninvasively and continuously measured by a fully automated Finometer® device (Finapres Medical Systems, TNO-BMI, Netherlands), which uses a volume clamp technique and has been well-validated against intra-arterial BP measurements. Systolic BP (SBP) and diastolic BP (DBP) were measured on a beat-by-beat basis. The beat-by-beat stroke volume was derived from the blood pressure waveform using Beatscope® software (1.1a, TNO-BMI, Amsterdam, Netherlands), a program that employs the Modelflow technique computing cardiac output (CO) by simulating a nonlinear three-element Windkessel model of aortic input impedance.
+ Open protocol
+ Expand
3

Cardiovascular and Hemostatic Stress Response

Check if the same lab product or an alternative is used in the 5 most similar protocols
Participants were administered the Stroop Color-Word Conflict test to induce mental stress, which provokes reproducible cardiovascular reactivity30 (link) and hemostatic activation31 (link). For one minute, words on a cardboard describing a specific color, but written in different colors, were shown to participants. They were asked to verbally indicate the ink color of a given word but not to read the color represented by the word. In order to increase the stress/ challenge level, participants were asked to progress as fast as possible and to correct answers that were wrong; they received a monetary incentive according to their performance on completion of the task. To determine cardiovascular reactivity, beat-to-beat BP and heart rate were recorded with the Finometer device at baseline and during stress (Finapres Medical Systems, Amsterdam, the Netherlands). For this purpose, the average of the recordings of the last minute of the 5-min baseline phase and of the last 20 s of the 1-min stress phase was calculated. To determine hemostatic reactivity, citrated blood samples to assay hemostatic factors were collected immediately before the Stroop test and 10 min thereafter.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!