#メディカルテクニカ

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欧州 ハンガリ国 #ラブテック社製

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非観血血圧機能 心電図 3/24チャンエル

24時間から 連続監視機能付き

自律神経ソフトウエア付きデジタル出力ファイル付き

解析機能はパソコンソフトウエア

#ラブテック_ホルターの解析例
#心房細動診断に必須な #P波自動検出機能を有します
#Heart_Rate_Variability 、#TWA_アルタナンス、#Turbulence、#3D可変表示、
#Spectral_Analysis 等が装備されています

Theory of the #P_wave_detection

The algorithm first finds the  the possible positive and negative wave peaks based on zero transition searching, then validates them with comparing to reference P waves.

The P wave detection needs high amplitude resolution. This value is better, than 0.6 uV / bit in the Cardiospy system.  With this resolution and the effective filter system which uses wavelet transformation, the Cardiospy system is able to detect P waves less than 50 uV of amplitude.

 

Validation of the P wave detector

The validation is carried out on 10 pcs 12 channel and 10 pcs 3 channel ECG reference records. The reference records include the P wave  annotation.  12 of the 20 records are taken from the MitBih database, 8 records are taken from the Labtech database (30000 – 30007). 

12 ch records

s0014lre, s0292lre, s0302lre, s0331lre, s0364lre, s0422_re, s0431_re, s0437_re, s0549_re, s0550_re

3 ch records

mgh001, mgh007, 30000, 30001, 30002, 30003, 30004, 30005, 30006, 30007

 

Validation result:

Sensitivity:                       95.42%

Positive predictivity:         97.16%


#Arteriograph #アルテリオグラフ24

診療報酬有 #動脈硬化指標を24時間から72時間トレンド計測 #三分間で測定 
#欧州米国特許有 #日本特許有 携帯電話及びインターネット利用、
高脂血症、高血圧、肥満、生活習慣病、腎臓病、内分泌などが原因か

中心血圧と関連パラメータは検証対象です


#ケアテイカメディカル社 #米国FDA2017年認可 
#Caretaker_type1_type2_type3_type4
#VitalStream_type1_type2_type3
#メディカルテクニカは #2007年から研究向けに導入


httpswww.ncbi.nlm.nih.govpmcarticlesPMC5361833

 BMC Anesthesiol. 2017; 17: 48.

Published online 2017 Mar 21. doi: 10.1186/s12871-017-0337-z

PMCID: PMC5361833

PMID: 28327093

#Continuous_Non-invasive_finger_cuff #CareTaker® comparable to invasive #intra-arterial_pressure in patients undergoing major intra-abdominal surgery

Irwin Gratz,1 Edward Deal,1 Francis Spitz,1 Martin Baruch,2 I. Elaine Allen,3 Julia E. Seaman,4 Erin Pukenas,1 and Smith Jean1

Author information Article notes Copyright and License information Disclaimer

This article has been cited by other articles in PMC.

 

Associated Data

Data Availability Statement

The datasets generated during and analysed for the current study are available from the corresponding author on reasonable request.

 

Abstract

Background

Despite increased interest in non-invasive arterial pressure monitoring, the majority of commercially available technologies have failed to satisfy the limits established for the validation of automatic arterial pressure monitoring by the Association for the Advancement of Medical Instrumentation (AAMI). According to the ANSI/AAMI/ISO 81060–2:2013 standards, the group-average accuracy and precision are defined as acceptable if bias is not greater than 5 mmHg and standard deviation is not greater than 8 mmHg. In this study, these standards are used to evaluate the CareTaker® (CT) device, a device measuring continuous non-invasive blood pressure via a pulse contour algorithm called Pulse Decomposition Analysis.

Methods

A convenience sample of 24 patients scheduled for major abdominal surgery were consented to participate in this IRB approved pilot study. Each patient was monitored with a radial arterial catheter and CT using a finger cuff applied to the contralateral thumb. Hemodynamic variables were measured and analyzed from both devices for the first thirty minutes of the surgical procedure including the induction of anesthesia. The mean arterial pressure (MAP), systolic and diastolic blood pressures continuously collected from the arterial catheter and CT were compared. Pearson correlation coefficients were calculated between arterial catheter and CT blood pressure measurements, a Bland-Altman analysis, and polar and 4Q plots were created.

Results

The correlation of systolic, diastolic, and mean arterial pressures were 0.92, 0.86, 0.91, respectively (p<0.0001 for all the comparisons). The Bland-Altman comparison yielded a bias (as measured by overall mean difference) of −0.57, −2.52, 1.01 mmHg for systolic, diastolic, and mean arterial pressures, respectively with a standard deviation of 7.34, 6.47, 5.33 mmHg for systolic, diastolic, and mean arterial pressures, respectively (p<0.001 for all comparisons). The polar plot indicates little bias between the two methods (90%/95% CI at 31.5°/52°, respectively, overall bias=1.5°) with only a small percentage of points outside these lines. The 4Q plot indicates good concordance and no bias between the methods.

Conclusions

In this study, #blood_pressure_measured using the #non-invasive CT device was shown to correlate well with the arterial catheter measurements. Larger studies are needed to confirm these results in more varied settings. Most patients exhibited very good agreement between methods. Results were well within the limits established for the validation of automatic arterial pressure monitoring by the AAMI.

Keywords: Non-Invasive, CareTaker, Central blood pressure, Finger cuff, Intra-Arterial pressure


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