Noninvasive Continuous Arterial Pressure Measurement Based on Radial Artery Tonometry
Abstract
Background
Radial artery applanation tonometry technology can be used for continuous non-invasive measurement of arterial pressure (AP). The purpose of this study was to evaluate this AP monitoring technology in intensive care unit (ICU) patients in comparison with invasive AP monitoring using a radial arterial catheter.
Methods
In 24 ICU patients (German university hospital), AP values were simultaneously recorded on a beat-to-beat basis using radial artery applanation tonometry (T-Line system; Tensys Medical, San Diego, CA, USA) and a radial arterial catheter (contralateral arm). The primary endpoint of the study was to investigate the accuracy and precision of the non-invasively assessed AP measurements with the Bland–Altman method based on averaged 10 beat AP epochs (n=2993 10 beat epochs).
Results
For mean AP (MAP), systolic AP (SAP), and diastolic AP (DAP), we observed a bias (±standard deviation of the bias; 95% limits of agreement; percentage error) of +2 mm Hg (±6; −11 to +15 mm Hg; 15%), −3 mm Hg (±15; −33 to +27 mm Hg; 23%), and +5 mm Hg (±7; −9 to +19 mm Hg; 22%), respectively.
Conclusions
In ICU patients, MAP and DAP measurements obtained using radial artery applanation tonometry show clinically acceptable agreement with invasive AP determination with a radial arterial catheter. While the radial artery applanation tonometry technology also allows SAP measurements with high accuracy, its precision for SAP measurements needs to be further improved.
Keywords
- arterial pressure, measurement
- measurement techniques, arterial pressure
- monitoring, intensive care
- T-Line
Editor's key points
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Radial applanation tonometry can be used for non-invasive arterial pressure (AP) measurement.
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In 24 intensive care unit patients, the authors simultaneously recorded AP with a tonometry device and an arterial cannula.
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Bias for non-invasive measurements was low.
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Precision was satisfactory for mean and diastolic pressures, but less satisfactory for systolic pressure.
Continuous arterial pressure (AP) monitoring is fundamental to adequately guide fluid therapy and administration of vasoactive agents in critically ill patients.
Since the placement of an arterial catheter is associated with potential negative short- and long-term side-effects, non-invasive technologies for continuous AP monitoring have been introduced. Besides photoplethysmography technologies,
,
,
,
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radial artery applanation tonometry has been demonstrated to be a promising technology for non-invasive beat-to-beat AP monitoring in anaesthetized patients during surgery compared with invasive AP measurements using a radial arterial catheter.
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
,
8
- Szmuk P
- Pivalizza E
- Warters RD
- Ezri T
- Gebhard R
An evaluation of the T-Line Tensymeter continuous noninvasive blood pressure device during induced hypotension.
- Crossref
- PubMed
- Scopus (40)
- Google Scholar
,
The company Tensys Medical Inc. (San Diego, CA, USA) provides a radial artery applanation tonometry device (T-Line system). When using this uncalibrated applanation tonometry system for continuous non-invasive AP measurement, a raw AP signal (waveform) is obtained using the system's sensor that is placed over the radial artery.
,
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
,
The radial artery site is an ideal choice for applanation tonometry, since it meets the requirements of a superficial artery and a bony structure acting as a counter bearing.
The term 'applanation' illustrates that a prerequisite for this method is that the sensor compresses the artery used for the AP measurement by applying pressure.
In the optimal 'applanation position', the artery is compressed (but not occluded) by the sensor to an extent that the vascular transmural pressure is minimized and the intraluminal AP (waveform with maximized pulse pressure) can be transduced to the pressure sensor placed on the skin.
,
In this position, mean AP (MAP) can then be determined from the raw AP waveform.
The raw AP signal is then scaled using a proprietary 'gain function' resulting in the final AP waveform allowing the derivation of systolic AP (SAP) and diastolic AP (DAP).
In intensive care unit (ICU) patients, radial artery tonometry has been previously compared with invasive central aortic AP readings.
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
However, there is a need for confirmation that AP measurements with radial artery applanation tonometry technology are reliable compared with an arterial catheter placed in the radial artery in an ICU setting. Therefore, in this study we compared radial artery applanation tonometry AP with invasive radial AP.
Methods
Study design and setting
This study comparing non-invasive (radial artery applanation tonometry) with invasive (radial arterial catheter) AP monitoring was performed in ICU patients treated in a German university hospital. It was approved by the appropriate ethics committee (Ethikkommission der Fakultät für Medizin der Technischen Universität München) and all patients (or their legal representatives) gave written informed consent.
Inclusion and exclusion criteria
Inclusion criteria included age 18 yr or older, body weight 40–180 kg, height 1.37–1.98 m, and the presence of an arterial catheter previously placed in the radial artery for routine clinical reasons. Patients in whom an arteriovenous shunt was present were not eligible for study enrolment, as were patients with anatomical abnormalities or injuries of the wrist. A history of peripheral vascular disease or cardiovascular disease was not an exclusion criterion for study enrolment.
Non-invasive and invasive AP measurements
The T-Line system (TL-200 or TL-200pro; Tensys Medical Inc.) was used for continuous non-invasive assessment of AP, as described previously.
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
Simultaneously, AP values were measured using an arterial catheter placed in the radial artery of the patient's contralateral arm. In each patient, three 5 min intervals of AP measurements (resulting in a total of 15 min) were recorded.
Data extraction, data processing, and statistical analysis
After simultaneous recording of invasive and non-invasive AP data, a beat-to-beat report containing numeric AP values was extracted from the raw data sets using computer software as previously described.
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
All recorded AP data were included in the statistical analysis.
For statistical analyses, we used IBM SPSS Statistics 20 (SPSS Inc., Chicago, IL, USA) and the statistical software package R (The R Foundation for Statistical Computing, Vienna, Austria). When describing patients' characteristics, the median and 25–75% percentile range (i.e. interquartile range) was used for continuous data and absolute frequencies with percentages were computed for qualitative measures. Non-invasively and invasively assessed AP values are described by mean [standard deviation (sd)]. AP measurements obtained continuously on a beat-to-beat basis were averaged (10 beat epochs) for comparative statistical analyses.
For each individual patient, radial artery applanation tonometry-derived AP measurements (SAP, MAP, and DAP) were plotted against invasively assessed AP measurements as a scatter plot.
For the comparison of AP measurements using the two methods, we performed a Bland–Altman analysis [mean difference (bias), sd, and 95% limits of agreement] for multiple measurements in one individual as described by Bland and Altman in 2007
(section 3). To assess potential non-uniform relations between the bias and mean AP measurements, we additionally performed mixed models analysis as described before.
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
The percentage error (2×sd of the differences/mean of measurements) was also calculated. In addition, modified Bland–Altman plots showing individual mean AP measurements, the intra-individual AP variability, the individual mean difference, and the intra-individual mean difference variability were computed.
Based on the averaged 10 beat epochs, four-quadrant plot analysis was performed to investigate the concordance of the AP measurements obtained with radial artery applanation tonometry and the radial arterial catheter-derived AP measurements regarding the direction of AP changes. For this AP concordance analysis, we computed four-quadrant plots with an exclusion zone of 3 mm Hg and calculated concordance between the two AP measurement methods as described previously.
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
Results
Patients
Twenty-eight patients were eligible for study inclusion. Four patients could not be included in the study because they (or their legal representatives) refused to give written informed consent. Therefore, 24 patients (15 males, nine females) were enrolled in the study. These patients had a median age of 67 (54–77) yr, a median body weight of 82 (73–93) kg, and a median height of 1.74 (1.67–1.85) m. On the day of study inclusion, 11 patients were on mechanical ventilation and six patients were receiving norepinephrine. Six patients had atrial fibrillation during study recordings. Patients were treated in the ICU for the following reasons: pneumonia/respiratory insufficiency (nine patients), admission after major surgery (five patients), central nervous system affection (four patients), gastrointestinal bleeding (three patients), or other (three patients).
AP measurements
A total of 2993 averaged 10 beat AP epochs were recorded in 24 patients. Using invasive AP measurements (radial arterial catheter), we observed a mean (sd) (minimum, maximum) for MAP, SAP, and DAP of 86 (15) (62, 137), 133 (20) (82, 192), and 63 (13) (41, 109) mm Hg, respectively. Radial artery applanation tonometry measurements resulted in a mean (sd) (minimum, maximum) for MAP, SAP, and DAP of 88 (13) (67, 126), 130 (18) (88, 184), and 68 (11) (49, 103) mm Hg, respectively.
For each patient, individual scatter plots with radial artery applanation tonometry-derived MAP, SAP, and DAP plotted against invasively assessed MAP, SAP, and DAP are presented in Figure 1.
Fig 1 Scatter plots with non-invasive AP measurements plotted against invasive AP measurements. For each individual patient we computed an individual scatter plot with radial artery applanation tonometry-derived AP measurements (non-invasive, y-axis) plotted against invasively assessed AP measurements (invasive, x-axis). One plot provides information on MAP, SAP, and DAP. In each figure, the diagonal represents perfect concordance.
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The Bland–Altman analyses were performed for MAP, SAP, and DAP. The mean difference (bias) between the radial artery applanation tonometry-derived AP measurements and the AP measurements obtained using the arterial catheter placed in the contralateral radial artery and the corresponding sd, 95% limits of agreement, and the percentage error are presented in Table 1 and Figure 2. For MAP, SAP, and DAP, we observed a mean difference (sd) of +2 (6), −3 (15), and +5 (7) mm Hg, respectively. This resulted in 95% limits of agreement and a percentage error of −11 to +15 mm Hg and 15% for MAP, −33 to +27 mm Hg and 23% for SAP, and −9 to +19 mm Hg and 22% for DAP. The modified Bland–Altman plots showing individual mean AP measurements, the intra-individual AP variability, the individual mean difference, and the intra-individual mean difference variability are presented in Figure 3.
Table 1 Radial artery applanation tonometry-derived and invasively assessed AP recordings. AP values [mean (sd)] recorded with radial artery applanation tonometry and a radial arterial catheter and comparison of the two methods with the Bland–Altman method (bias, sd of the difference, 95% limits of agreement) and the percentage error. Analyses are based on 2993 averaged 10 beat epochs in the 24 patients included in the study
| Radial artery applanation tonometry | Radial arterial catheter | Bias (sd) of the difference | 95% limits of agreement | Percentage error (%) | |
|---|---|---|---|---|---|
| Mean arterial pressure | 88 (13) mm Hg | 86 (15) mm Hg | +2 (6) mm Hg | −11 to +15 mm Hg | 15 |
| Systolic arterial pressure | 130 (18) mm Hg | 133 (20) mm Hg | −3 (15) mm Hg | −33 to +27 mm Hg | 23 |
| Diastolic arterial pressure | 68 (11) mm Hg | 63 (13) mm Hg | +5 (7) mm Hg | −9 to +19 mm Hg | 22 |
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Fig 2 Bland–Altman plots illustrating accuracy and precision of radial artery applanation tonometry. For the 24 patients enrolled in the study, we computed the Bland–Altman plots for repeated measurements in one individual to investigate the accuracy (mean difference; continuous line) and precision [95% limits of agreement, i.e. mean difference ±(1.96× sd); dashed lines] of radial artery applanation tonometry compared with reference AP measurements from a radial arterial catheter for MAP (a), SAP (b), and DAP (c). Potential non-uniform relations between the bias and mean AP measurements were assessed by mixed models analysis and are illustrated by the diagonal black lines, with the diagonal dashed lines representing the respective 95% confidence interval. MAP-ni, non-invasively assessed mean arterial pressure; MAP-i, invasively assessed mean arterial pressure; SAP-ni, non-invasively assessed systolic arterial pressure; SAP-i, invasively assessed systolic arterial pressure; DAP-ni, non-invasively assessed diastolic arterial pressure; DAP-i, invasively assessed diastolic arterial pressure.
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Fig 3 Modified Bland–Altman plots showing individual mean AP measurements, the intra-individual AP variability, the individual mean difference, and the intra-individual mean difference variability. Bland–Altman plots showing the accuracy (mean difference; continuous line) and precision [95% limits of agreement, i.e. mean difference ±(1.96×sd); dashed lines] of radial artery applanation tonometry compared with reference AP measurements from a radial arterial catheter for MAP (a), SAP (b), and DAP (c). One data point in these Bland–Altman plots represents a patient's individual mean AP value. In addition, the intra-individual AP variability (sd in parallel to the x-axis), the individual mean difference, and the intra-individual mean difference variability (sd in parallel to the y-axis) are shown. MAP-ni, non-invasively assessed mean arterial pressure; MAP-i, invasively assessed mean arterial pressure; SAP-ni, non-invasively assessed systolic arterial pressure; SAP-i, invasively assessed systolic arterial pressure; DAP-ni, non-invasively assessed diastolic arterial pressure; DAP-i, invasively assessed diastolic arterial pressure.
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Figure 4 (four-quadrant plots) illustrates the concordance regarding AP changes between the two AP measurement techniques. This analysis revealed a concordance of 0.882 for MAP, 0.763 for SAP, and 0.824 for DAP.
Fig 4 Four-quadrant plots illustrating the ability of radial artery applanation tonometry to follow AP changes. We computed four-quadrant plots to evaluate the ability of radial artery applanation tonometry to follow changes in MAP (a), SAP (b), and DAP (c). An exclusion zone of 3 mm Hg was used. MAP-ni, non-invasively assessed mean arterial pressure; MAP-i, invasively assessed mean arterial pressure; SAP-ni, non-invasively assessed systolic arterial pressure; SAP-i, invasively assessed systolic arterial pressure; DAP-ni, non-invasively assessed diastolic arterial pressure; DAP-i, invasively assessed diastolic arterial pressure.
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Discussion
To the best of our knowledge, this is the first evaluation of the radial artery applanation tonometry technology with the T-Line system in comparison with invasive AP measurements obtained using an arterial catheter in the radial artery in ICU patients. According to our findings, MAP and DAP measurements obtained using radial artery applanation tonometry showed clinically acceptable agreement with invasive AP determination. Furthermore, the radial artery applanation tonometry technology provided accurate SAP measurements. However, the precision for SAP measurements using this non-invasive approach needs to be further improved.
Previous studies have reported data on the AP measurement performance of radial artery applanation tonometry using the T-Line system in comparison with radial artery catheter-derived measurements in the operating theatre in surgical patients.
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
,
8
- Szmuk P
- Pivalizza E
- Warters RD
- Ezri T
- Gebhard R
An evaluation of the T-Line Tensymeter continuous noninvasive blood pressure device during induced hypotension.
- Crossref
- PubMed
- Scopus (40)
- Google Scholar
,
While the bias for SAP, MAP, and DAP and also the 95% limits of agreement for MAP and DAP determinations were comparably low in the ICU patients enrolled in our study and the surgical patients evaluated in these previous studies, the studies of Janelle and Gravenstein,
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
Szmuk and colleagues,
8
- Szmuk P
- Pivalizza E
- Warters RD
- Ezri T
- Gebhard R
An evaluation of the T-Line Tensymeter continuous noninvasive blood pressure device during induced hypotension.
- Crossref
- PubMed
- Scopus (40)
- Google Scholar
and Dueck and colleagues
resulted in closer 95% limits of agreement for SAP measurements compared with our results.However, differences in the study settings between these studies and our study in ICU patients need to be emphasized. Considering that radial artery applanation tonometry systems are sensitive to motion of the studied limb, one important difference is that our ICU patients'in contrast to the patients reported in these studies'were not anaesthetized. Only five patients included in the present study were sedated during study measurements. In addition, in our study, all recorded AP data were included in the final analysis without deleting any recording episodes.
When evaluating continuous non-invasive AP monitoring systems in clinical studies, one fundamental problem is that definitions for inter-changeability or for clinically acceptable agreement are not available.
15
- Broch O
- Bein B
- Gruenewald M
- et al.
A comparison of continuous non-invasive arterial pressure with invasive radial and femoral pressure in patients undergoing cardiac surgery.
- PubMed
- Google Scholar
Therefore, some authors suggest defining clinically acceptable agreement between a non-invasive AP monitoring device and arterial catheter-derived AP values according to American National Standards Institute/Association for the Advancement of Medical Instrumentation (ANSI/AAMI) standards.
,
,
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
When using these ANSI/AAMI standards for the evaluation of a test device with an arterial catheter as the reference method (criterion standard), clinically acceptable agreement is defined as a mean difference (bias) of less than or equal to ±5 mm Hg with a sd of ≤8 mm Hg.
Considering these ANSI/AAMI performance requirements, in our study, non-invasively and invasively assessed MAP and DAP values were interchangeable. While the bias for SAP also fulfilled the strict ANSI/AAMI standards for clinical acceptability, we observed a sd of >8 mm Hg for SAP. Nevertheless, it has to be emphasized that the ANSI/AAMI guidelines only cover non-automated, automated, or electronic sphygmomanometers 'that are used with an occluding cuff for the indirect determination of arterial blood pressure'.
Measurement requirements for the use of devices obtaining continuous non-invasive AP based on either radial artery applanation tonometry or finger plethysmography are therefore not covered in the ANSI/AAMI guidelines. In addition, the ANSI/AAMI standard explicitly discourages placing the arterial catheter in the radial artery when invasive AP measurements are used as a reference in method comparison studies evaluating non-invasive technologies for continuous AP monitoring.
Considering the increasing number of available devices using different technologies for continuous non-invasive AP monitoring and the increasing number of validation studies evaluating these technologies,
,
,
,
7
- Janelle GM
- Gravenstein N
An accuracy evaluation of the T-Line Tensymeter (continuous noninvasive blood pressure management device) versus conventional invasive radial artery monitoring in surgical patients.
- Crossref
- PubMed
- Scopus (55)
- Google Scholar
,
8
- Szmuk P
- Pivalizza E
- Warters RD
- Ezri T
- Gebhard R
An evaluation of the T-Line Tensymeter continuous noninvasive blood pressure device during induced hypotension.
- Crossref
- PubMed
- Scopus (40)
- Google Scholar
,
,
10
- Saugel B
- Fassio F
- Hapfelmeier A
- Meidert AS
- Schmid RM
- Huber W
The T-Line TL-200 system for continuous non-invasive blood pressure measurement in medical intensive care unit patients.
- Crossref
- PubMed
- Scopus (41)
- Google Scholar
15
- Broch O
- Bein B
- Gruenewald M
- et al.
A comparison of continuous non-invasive arterial pressure with invasive radial and femoral pressure in patients undergoing cardiac surgery.
- PubMed
- Google Scholar
standards defining clinically acceptable agreement/inter-changeability between the non-invasive AP measurements and AP assessment with an arterial catheter (criterion standard) are therefore eagerly awaited. Despite the fact that there are no standards defining acceptable agreement, the low bias observed for AP determination in our study contributes to the increasing body of evidence that radial artery applanation tonometry is capable of providing AP data with good agreement. Therefore, this technology might contribute to an improvement in patient safety in various clinical scenarios. Patients treated in the emergency department or a neurological stroke unit and also patients in need for haemodynamic monitoring in the operating theatre or in the ICU in whom arterial line placement is difficult or impossible might therefore benefit from continuous non-invasive AP monitoring.
In our study we performed concordance analysis based on the computation of four-quadrant plots in order to investigate the ability of radial artery applanation tonometry to adequately follow AP changes. Considering the paramount importance of MAP determination in critical care, a concordance of 88% for MAP also indicates that radial artery applanation tonometry is able to provide real-time MAP data for guidance of haemodynamic treatment in good agreement with the reference method. However, it has to be mentioned that there are no generally accepted cut-off values defining good agreement for the interpretation of four-quadrant plots in the evaluation of continuous non-invasive AP monitoring technologies. In addition, the optimal value to use as an exclusion zone in this kind of concordance analyses is also not yet defined.
Some methodological limitations of our study need to be pointed out. The major limitation of our study is the relatively small sample size. Our results were obtained in critically ill patients with in part markedly altered haemodynamic state. These limitations might therefore influence the generalizability of our results to other patient collectives like surgical patients or patients treated in the emergency department. The relatively short time of AP recordings in our study limits the possibility of drawing definite conclusions about the measurement performance and trending abilities of the evaluated technology. Therefore, further studies in clinical scenarios where continuous AP monitoring is needed for a longer period of time (e.g. emergency department, operating theatre, ICU) are needed.
Conclusions
In ICU patients, MAP and DAP measurements obtained using radial artery applanation tonometry show clinically acceptable agreement with invasive AP determination with a radial arterial catheter. While the radial artery applanation tonometry technology allows SAP measurements with high accuracy, its precision for SAP measurements needs to be further improved.
Authors' contributions
A.S.M.: study design and conception, patient recruitment, data collection, analysis and interpretation of data, drafting of the article. W.H.: study design and conception, revising the article for important intellectual content. J.N.M.: patient recruitment, data collection, revising the article for important intellectual content. M.S.: analysis and interpretation of data, revising the article for important intellectual content. A.H.: study design and conception, analysis and interpretation of data, drafting of the article. N.L.: analysis and interpretation of data, revising the article for important intellectual content. J.Y.W.: analysis and interpretation of data, revising the article for important intellectual content. F.E.: analysis and interpretation of data, revising the article for important intellectual content. R.M.S.: study design and conception, revising the article for important intellectual content. B.S.: study design and conception, patient recruitment, data collection, analysis and interpretation of data, drafting of the article. All authors approved the version of the manuscript for publication.
Declaration of interest
A.S.M. and B.S. received unrestricted research grants from Tensys Medical Inc. (San Diego, CA, USA).
Funding
A.S.M. and B.S. received unrestricted research grants from Tensys Medical Inc. (San Diego, CA, USA). Tensys Medical Inc. (San Diego, CA, USA) provided the technical equipment for recording and extraction of arterial pressure measurements. The company was not involved in study conception, data analysis and interpretation, writing of the manuscript, or the decision to submit the manuscript for publication.
Acknowledgement
Tensys Medical Inc. (San Diego, CA, USA) provided the technical equipment for recording and extraction of arterial pressure measurements.
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Article Info
Publication History
Accepted: August 20, 2013
Handling editor: A. R. Absalom
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DOI: https://doi.org/10.1093/bja/aet400
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© 2014 The Author(s). Published by Elsevier Inc.
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