Name: patient directed recording of a bipolar three-lead electrocardiogram using a smartwatch with ecg function
Uploaded: 2019-12-11T13:00:00
Description: Watch this Scientific Journal Video about Patient Directed Recording of a Bipolar Three-Lead Electrocardiogram using a Smartwatch with ECG Function at JoVE.com

This research received no external funding. We thank Lisa Tiedemann, Ester Krist and Tobias Anke for technical support.

This study was performed according to the Declarations of Helsinki and approved by the Ethics Committee of the Aerztekammer Westfalen-Lippe (reference number 2019-456).
1. Study
<ol>
	<li>Instruct subjects on how to use the smartwatch for proper ECG recording.</li>
</ol>
2. Recording of a standard 12-lead ECG by a common device
<ol>
	<li>Use a common ECG device for standard ECG recording.</li>
	<li>Adjust the paper running speed to 50 mm/s.</li>
	<li>Perform the ECG...

<ol>
	<li>Turakhia, M. P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rationale+and+design+of+a+large-scale,+app-based+study+to+identify+cardiac+arrhythmias+using+a+smartwatch:+The+Apple+Heart+Study.">Rationale and design of a large-scale, app-based study to identify cardiac arrhythmias using a smartwatch: The Apple Heart Study.</a> American Heart Journal. 207, 66-75 (2019).</li><li>Dorr, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+WATCH+AF+Trial:+SmartWATCHes+for+Detection+of+Atrial+Fibrillation.">The WATCH AF Trial: SmartWATCHes for Detection of Atrial Fibrillation.</a> JACC Clinical Electrophysiology. 5 (2), 199-208 (2019).</li><li>Hochstadt, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Continuous+heart+rate+monitoring+for+automatic+detection+of+atrial+fibrillation+with+novel+bio-sensing+technology.">Continuous heart rate monitoring for automatic detection of atrial fibrillation with novel bio-sensing technology.</a> Journal of Electrocardiology. 52, 23-27 (2019).</li><li>Baquero, G. A., Banchs, J. E., Ahmed, S., Naccarelli, G. V., Luck, J. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Surface+12+lead+electrocardiogram+recordings+using+smart+phone+technology.">Surface 12 lead electrocardiogram recordings using smart phone technology.</a> Journal of Electrocardiology. 48 (1), 1-7 (2015).</li><li>Desteghe, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Performance+of+handheld+electrocardiogram+devices+to+detect+atrial+fibrillation+in+a+cardiology+and+geriatric+ward+setting.">Performance of handheld electrocardiogram devices to detect atrial fibrillation in a cardiology and geriatric ward setting.</a> Europace. 19 (1), 29-39 (2017).</li><li>Samol, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Prevalence+of+unknown+atrial+fibrillation+in+patients+with+risk+factors.">Prevalence of unknown atrial fibrillation in patients with risk factors.</a> Europace. 15 (5), 657-662 (2013).</li><li>Nigolian, A., Dayal, N., Nigolian, H., Stettler, C., Burri, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Diagnostic+accuracy+of+multi-lead+ECGs+obtained+using+a+pocket-sized+bipolar+handheld+event+recorder.">Diagnostic accuracy of multi-lead ECGs obtained using a pocket-sized bipolar handheld event recorder.</a> Journal of Electrocardiology. 51 (2), 278-281 (2018).</li><li>Foster, K. R., Torous, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Opportunity+and+Obstacles+for+Smartwatches+and+Wearable+Sensors.">The Opportunity and Obstacles for Smartwatches and Wearable Sensors.</a> IEEE Pulse. 10 (1), 22-25 (2019).</li><li>Lau, J. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=iPhone+ECG+application+for+community+screening+to+detect+silent+atrial+fibrillation:+a+novel+technology+to+prevent+stroke.">iPhone ECG application for community screening to detect silent atrial fibrillation: a novel technology to prevent stroke.</a> International Journal of Cardiology. 165 (1), 193-194 (2013).</li><li>Einthoven, W., Fahr, G., De Waart, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=On+the+direction+and+manifest+size+of+the+variations+of+potential+in+the+human+heart+and+on+the+influence+of+the+position+of+the+heart+on+the+form+of+the+electrocardiogram.">On the direction and manifest size of the variations of potential in the human heart and on the influence of the position of the heart on the form of the electrocardiogram.</a> American Heart Journal. 40 (2), 163-211 (1950).</li><li>Burch, G. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=History+of+precordial+leads+in+electrocardiography.">History of precordial leads in electrocardiography.</a> European Journal of Cardiology. 8 (2), 207-236 (1978).</li><li>Leslie, W. S., Urie, A., Hooper, J., Morrison, C. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Delay+in+calling+for+help+during+myocardial+infarction:+reasons+for+the+delay+and+subsequent+pattern+of+accessing+care.">Delay in calling for help during myocardial infarction: reasons for the delay and subsequent pattern of accessing care.</a> Heart. 84 (2), 137-141 (2000).</li><li>Tison, G. 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O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Novel+Use+of+Apple+Watch+4+to+Obtain+3-Lead+Electrocardiogram+and+Detect+Cardiac+Ischemia.">Novel Use of Apple Watch 4 to Obtain 3-Lead Electrocardiogram and Detect Cardiac Ischemia.</a> Permanente Journal. 23, (2019).</li></ol>

Smart devices like smartphones and smartwatches are increasingly used in daily life and medical care1. These new devices and apps may have a significant impact on health awareness of the population, but their effective use needs to be tested in studies8. To the best of our knowledge, our group was the first to develop this method of single-lead ECG recordings corresponding to the conventional Einthoven ECG leads I-III using a smartwatch14.
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Smartwatches or other so-called "wearable devices" show increasing popularity and a steeply rising daily use in Western countries. Nearly 80% of US-Americans own a smartphone and more than 10% have a smartwatch1. Due to a photoplethysmographic sensor using LED-light and photodiodes, some smartwatches can record pulse frequency and irregularities1. This feature enables the detection of arrhythmias, especially AF, with high diagnostic accuracy2,3. For authentic ECG arrhythmia detection, portable, handheld, and wearable ECG devices have been developed to enable smartphone-assisted ECG recordings. Nevertheless, these devices allow patient-activated recording of electrocardiograms only if the patients&rsquo; compliance for carrying the ECG device is extremely high4,5,6,7.
Thus, the optimal tool for a patient&rsquo;s medical surveillance would be a smart device for daily use. Some last generation smartwatches enable a single-lead ECG recording comparable to bipolar lead Einthoven I from a standard 12-channel ECG using the backside of the watch as the positive and the crown as the negative electrode8. ECG recording is patient-controlled and activated if symptoms occur. Thereafter, an application creates a PDF document for further analysis by a healthcare professional. Nevertheless, using only a single-lead ECG for discrimination of P waves for diagnosis of sinus rhythm is sometimes insufficient9 for detection of the P wave and often multiple ECG leads are required5. In addition, multichannel ECG recording is mandatory for diagnosis of most acute or chronic structural heart diseases like myocardial infarction (MI), pulmonary embolism, or signs of acute heart failure.
More than 100 years ago, Einthoven developed a method for recording of a bipolar three- channel ECG10. This three-channel ECG offers the opportunity to identify the electrical heart axis and possibly the myocardial ischemia as well, especially in inferior regions of the myocardium11. Therefore, in clinical daily practice bipolar Einthoven leads I-III are essential parts of the 12-lead ECG and enable heart rhythm determination or detection of myocardial ischemia.
Early diagnosis and especially early treatment of myocardial infarction has improved substantially during recent decades. Nevertheless, especially early after the onset of symptoms, many patients hesitate to contact professional help. Thus, first medical contact and initiation of adequate treatment is often delayed12. Registration and transmission of a patient-directed ECG early after the onset of symptoms might accelerate specific treatment and thus enable a better patient outcome7. Until now, ischemia detection by smart devices is limited, because mainly single-lead (Einthoven I), or as in our study, maximal three-lead (Einthoven I-III) ECGs can be recorded, which only represent a limited area of the myocardium.
Several studies used patient-directed devices like portable ECG recorders, smartphones, and very recently smartwatches, for detection of AF in heart patients1,2,5,9. The Apple Heart Study and the WATCH AF trial used the photoplethysmographic LED-light sensor of the smartwatch for detection of an irregular or variable pulse, which correlates with arrhythmia like AF1,2. Insufficient signal quality was the limiting factor in these trials, leading to a high dropout rate2. Another smartwatch trial used photoplethysmography for AF detection, but also showed reduced diagnostic accuracy compared to regular ECGs13.
The detection of AF by the registration of pulse irregularities is the limiting factor of photoplethysmography, because heartbeat variabilities due to extra systoles or sinus arrhythmia may also cause pulse irregularities. Thus, recording of an ECG by a smartphone or smartwatch may increase the sensitivity and specificity of arrhythmia detection. Several smartphone compatible devices can record a bipolar single-lead ECG simulating Einthoven lead I5,9. In one study, a bipolar smartphone ECG device was used for AF screening9. In this trial, a small voltage of P waves in lead I led to incorrect AF determination, a limitation when only a single-lead ECG is available9. ECG devices for AF screening were also tested in hospitalized patients on cardiologic and geriatric wards5. Diagnostic accuracy of the automated algorithms was only suboptimal and additional 12-lead ECGs were often mandatory. Most of these devices have the limitation of only one ECG lead recording (Einthoven I), which is not always sufficient to ensure arrhythmia or repolarization detection.
Only one small case series of five patients demonstrated that a conventional 12 lead ECG is recordable by a conventional bipolar smartphone device after modification for unipolar lead recordings with ECG tabs and wires with alligator clips4. They showed ECG recordings with good signal quality, but the limiting factor is the need for device modifications that complicates patient-directed self-ECG recording.
In contrast, we performed the first study for recording an ECG with a smartwatch with the three bipolar Einthoven leads as a proof of concept in healthy subjects. We were able to show a high grade of consistency between the smartwatch leads and the Einthoven leads from a standard ECG using the following simple protocol.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Apple Watch Series 4</td>
			<td>Apple</td>
			<td>Smartwatch with bipolar ECG function</td>
		</tr>
		<tr>
			<td>IBM SPSS Statistics</td>
			<td>IBM</td>
			<td>version 25 for Mac</td>
		</tr>
		<tr>
			<td>MAC 5500</td>
			<td>GE Healthcare</td>
			<td>Standard 12 channel ECG device</td>
		</tr>
	</tbody>
</table>

patient directed recording of a bipolar three-lead electrocardiogram using a smartwatch with ecg function

Cardiac arrhythmias and cardiovascular diseases are a major public health problem in developed countries. A major goal in preventive medicine is the reduction of cardiovascular death by early detection of atrial fibrillation (AF), which may cause stroke, or early detection of life-threatening myocardial ischemia in acute coronary syndrome. Detection of arrhythmia is often challenging if symptoms occur when patients have no chance for immediate electrocardiogram (ECG) diagnostic testing, or if the observation time period is short or an immediate visit to their doctor is not possible. Smartwatches and other wearable devices are able to record a single lead ECG recording, but a single lead ECG is often not sufficient for diagnosis of cardiovascular disorders. Even diagnosis of AF can be difficult with only information from a single lead bipolar ECG. Some smart devices use photoplethysmography for detection of cardiac rhythm, but this technique can only give indirect hints of the underlying cardiac rhythm, is prone to interferences, and cannot be used for detection of myocardial ischemia. A three-lead bipolar ECG like the Einthoven leads used in regular ECGs can add useful information concerning arrhythmia detection or even diagnosis of other cardiovascular diseases like ischemia. Therefore, we describe a protocol for the patient-directed recording of an Einthoven three-lead ECG using a smartwatch.

In a cohort of 100 healthy subjects (66 female) we investigated the feasibility of our smartwatch recording protocol. The subjects' characteristics are shown in Table 1. After a short tutorial all volunteers managed the ECG recording procedure with the smartwatch. All 300 smartwatch ECGs were useable for further analysis with at least adequate signal quality for diagnostics purposes. Of the total ECGs, 277 (92%) were of good quality and 23 (8%) of moderate signal quality. Three blinded cardiologists were...

Watch this Scientific Journal Video about Patient Directed Recording of a Bipolar Three-Lead Electrocardiogram using a Smartwatch with ECG Function at JoVE.com

Patient Directed Recording of a Bipolar Three-Lead Electrocardiogram using a Smartwatch with ECG Function

We describe a protocol for the patient-directed registration of a three lead bipolar electrocardiogram by a smartwatch that functions identically to the Einthoven leads from standard electrocardiograms. This enables patients to record electrocardiograms on their own immediately after the onset of symptoms.

Cardiac arrhythmias and cardiovascular diseases are a major public health problem in developed countries. A major goal in preventive medicine is the ...

This protocol enables subjects owning a smartwatch with ECG function to record three bipolar signal lead ECGs comparable to Einthoven leads one to three from a standard ECG. This technique may help to detect cardiac arrhythmias or myocardial ischemia. Subjects could help a doctor identify ECG abnormalities immediately after onset of symptoms.This method can principally be applied to all bipolar ECG recording devices and smartwatches with ECG function, except for the protocol for sending PDF to the doctor, which is specific to the device app. It is important that the subject is able to generate a good skin contact, especially during recording of leads two and three. It may be difficult to record Einthoven leads two and three because the watch has to be placed in the lower abdominal of the individual.Therefore a resting position is mandatory. Demonstrating the procedure will be Sven Kaese, a colleague from our department. To record a standard ECG, use a common ECG device and adjust the paper running speed to 50 millimeters per second.Perform the recording after a five minute resting period in a supine position. Place the right and left arm electrodes near the shoulders and the right and left leg electrodes near the ankles. Then place the V1 and V2 electrodes in the fourth intercostal space at the right and left parasternal lines respectively.Place the V4 electrode in the fifth intercostal space at the midclavicular line and the V3 electrode between the V2 and V4.Then place the V5 electrode in the fifth intercostal space at the anterior axillary line and the V6 electrode at the mid axillary line. Once all electrodes are in place, record a standard 12 lead ECG with the ECG device. Record the smartwatch ECG immediately after recording the standard ECG.Enable the application for ECG recording, which will record a 30 second ECG after proper skin contact with the smartwatch. Record Einthoven one by placing the back of the smartwatch on left wrist and the right index finger on the crown. Then, record Einthoven two by placing it on the left lower abdomen and the right index finger on the crown.Finally, record Einthoven three in the same position, but with the left index finger on the crown. Ensure that the right and left index finger do not contact the skin of the wrist of lower abdomen and that the subject does not move during the recording. Use the Send PDF to Your Doctor function to create a PDF document of every smartwatch ECG lead.Then print the digital ECG on paper for comparison with the standard ECG. Classify all smartwatch ECGs as moderate quality if at least three consecutive QRS complexes show noise free signal quality and there are no artifacts in the isoelectric lines between complexes. If this is true for 10 QRS complexes, classify the ECG as good quality.Then, perform statistical analysis on the ECGs. The smartwatch recording protocol was tested on 100 healthy subjects, all of whom managed the ECG recording procedure after a short tutorial. Of the total recorded ECGs, 92%were of good signal quality and 8%of moderate signal quality.Despite different writing speeds of the standard and smartwatch ECG curves, the morphologies of the three channels were clearly identical. Three blinded cardiologists were asked to assign the smartwatch ECGs to the corresponding Einthoven leads in each subject and all three correctly assigned the ECGs from 89 participants. All assignment errors were made in the ECGs with good signal quality, but the errors occurred in statistically older subjects.When attempting this procedure, the most important thing is to perform recordings under resting conditions to obtain best ECG signal quality. Chest lead ECG recordings may also be recorded with mobile device to give additional informations of the interior wall of the left ventricle. This technique may enable widespread of diagnostic potential in an outpatient setting for cardiac disorders.

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Assessing Endothelial Vasodilator Function with the Endo-PAT 2000

The endothelium is a delicate monolayer of cells that lines all blood vessels, and which comprises the systemic and lymphatic capillaries. By virtue of the panoply of paracrine factors that it secretes, the endothelium regulates the contractile and proliferative state of the underlying vascular smooth muscle, as well as the interaction of the vessel wall with circulating blood elements. Because of its central role in mediating vessel tone and growth, its position as gateway to circulating immune cells, and its local regulation of hemostasis and coagulation, the the properly functioning endothelium is the key to cardiovascular health. Conversely, the earliest disorder in most vascular diseases is endothelial dysfunction.
In the arterial circulation, the healthy endothelium generally exerts a vasodilator influence on the vascular smooth muscle. There are a number of methods to assess endothelial vasodilator function. The Endo-PAT 2000 is a new device that is used to assess endothelial vasodilator function in a rapid and non-invasive fashion. Unlike the commonly used technique of duplex ultra-sonography to assess flow-mediated vasodilation, it is totally non-operator-dependent, and the equipment is an order of magnitude less expensive. The device records endothelium-mediated changes in the digital pulse waveform known as the PAT ( peripheral Arterial Tone) signal, measured with a pair of novel modified plethysmographic probes situated on the finger index of each hand. Endothelium-mediated changes in the PAT signal are elicited by creating a downstream hyperemic response. Hyperemia is induced by occluding blood flow through the brachial artery for 5 minutes using an inflatable cuff on one hand. The response to reactive hyperemia is calculated automatically by the system. A PAT ratio is created using the post and pre occlusion values. These values are normalized to measurements from the contra-lateral arm, which serves as control for non-endothelial dependent systemic effects. Most notably, this normalization controls for fluctuations in sympathetic nerve outflow that may induce changes in peripheral arterial tone that are superimposed on the hyperemic response.
In this video we demonstrate how to use the Endo-PAT 2000 to perform a clinically relevant assessment of endothelial vasodilator function.

A noninvasive procedure to assess endothelial function is demonstrated using the Endo-PAT 2000.

The endothelium is a delicate monolayer of cells that lines all blood vessels, and which comprises the systemic and lymphatic capillaries. By virtue of ...

A Neonatal Mouse Spinal Cord Compression Injury Model

Spinal cord injury (SCI) typically causes devastating neurological deficits, particularly through damage to fibers descending from the brain to the spinal cord. A major current area of research is focused on the mechanisms of adaptive plasticity that underlie spontaneous or induced functional recovery following SCI. Spontaneous functional recovery is reported to be greater early in life, raising interesting questions about how adaptive plasticity changes as the spinal cord develops. To facilitate investigation of this dynamic, we have developed a SCI model in the neonatal mouse. The model has relevance for pediatric SCI, which is too little studied. Because neural plasticity in the adult involves some of the same mechanisms as neural plasticity in early life1, this model may potentially have some relevance also for adult SCI. Here we describe the entire procedure for generating a reproducible spinal cord compression (SCC) injury in the neonatal mouse as early as postnatal (P) day 1. SCC is achieved by performing a laminectomy at a given spinal level (here described at thoracic levels 9-11) and then using a modified Yasargil aneurysm mini-clip to rapidly compress and decompress the spinal cord. As previously described, the injured neonatal mice can be tested for behavioral deficits or sacrificed for ex vivo physiological analysis of synaptic connectivity using electrophysiological and high-throughput optical recording techniques1. Earlier and ongoing studies using behavioral and physiological assessment have demonstrated a dramatic, acute impairment of hindlimb motility followed by a complete functional recovery within 2 weeks, and the first evidence of changes in functional circuitry at the level of identified descending synaptic connections1.

This article describes a method for generating a reproducible spinal cord compression injury (SCI) in the neonatal mouse. The model provides an advantageous platform for studying mechanisms of adaptive plasticity that underlie spontaneous functional recovery.

Spinal cord injury (SCI) typically causes devastating neurological deficits, particularly through damage to fibers descending from the brain to the spinal ...

Using Saccadometry with Deep Brain Stimulation to Study Normal and Pathological Brain Function

The oculomotor system involves a large number of brain areas including parts of the basal ganglia, and various neurodegenerative diseases including Parkinson's and Huntington's can disrupt it. People with Parkinson's disease, for example, tend to have increased saccadic latencies. Consequently, the quantitative measurement of saccadic eye movements has received considerable attention as a potential biomarker for neurodegenerative conditions. A lot more can be learned about the brain in both health and disease by observing what happens to eye movements when the function of specific brain areas is perturbed. Deep brain stimulation is a surgical intervention used for the management of a range of neurological conditions including Parkinson's disease, in which stimulating electrodes are placed in specific brain areas including several sites in the basal ganglia. Eye movement measurements can then be made with the stimulator systems both off and on and the results compared. With suitable experimental design, this approach can be used to study the pathophysiology of the disease being treated, the mechanism by which DBS exerts it beneficial effects, and even aspects of normal neurophysiology.

This paper describes the use of quantitative measurement of eye movements in conjunction with stimulation of focal areas of the deep brain in order to study physiology, pathophysiology, and the mechanisms of deep brain stimulation.

The oculomotor system involves a large number of brain areas including parts of the basal ganglia, and various neurodegenerative diseases including ...

A Computerized Functional Skills Assessment and Training Program Targeting Technology Based Everyday Functional Skills

Today, many functional skills are technology-based, so development of a technology-based training program has broad importance. Here we present a computerized functional skills training program that was paired in half of the participants with a commercially available cognitive training (CCT) program.
Non-impaired older individuals (NC) aged 60+ (n=45) and similarly aged individuals with mild cognitive impairment (MCI; n=50) were randomized to receive 12 weeks of twice-weekly computerized functional skills training (CFST) or 12 weeks of twice-weekly sessions split between CCT and CFST. Skills trained were use of an ATM; internet banking; ticket kiosk; telephone and internet prescription refill; medication management; and internet shopping. As with previous functional capacity assessments, we focus on completion time for each simulation.
51 participants completed the training program, either by mastering all 6 tasks (34) or completing 12 weeks of training. 44 more participants completed 4 or more training sessions so they were also analyzed for improvement up to their last training session. Completion time for all 6 tests significantly improved from the baseline assessment to the final training session in both groups of participants (all p&#60;0.001 with an average improvement in task completion time of 45%). Further, there was no differential improvement in MCI and NC in the 6 tests from baseline to end of training (all t&#60;1.66, all p&#62;0.12). Finally, combined CCT plus CFST did not differ from CSFT alone on any of the percent-change score measures (all t&#60;1.64, all p&#62;0.11).
Both NC and MCI groups evidenced substantial improvements in performance. CCT supplementation led to similar functional gains with half as many training sessions. The NC participants proceeded through the training fairly rapidly even without CCT supplementation; MCI participants required more training but learned equivalently. These findings suggest that even in cases with memory impairments, functional skills can be efficiently learned with training.

This training protocol uses computerized training to teach technology-related everyday functional skills. These skills include financial skills, travel and transit, as well as medication management.

Today, many functional skills are technology-based, so development of a technology-based training program has broad importance. Here we present a ...

Electrocardiogram Recordings in Anesthetized Mice using Lead II

The electrocardiogram is a valuable tool for evaluating the cardiac conduction system. Animal research has helped generate novel genetic and pharmacological information regarding the electrocardiogram. However, making electrocardiogram measurements in small animals in vivo, such as mice, has been challenging. To this end, we used an electrocardiogram recording method in anesthetized mice with many advantages: it is a technically simple procedure, is inexpensive, has short measuring time, and is affordable, even in young mice. Despite the limitations with using anesthesia, comparisons between control and experimental groups can be performed with enhanced sensitivity. We treated mice with agonists and antagonists of the autonomic nervous system to determine the validity of this protocol and compared our results with previous reports. Our ECG protocol detected increased heart rates and QTc intervals on treatment with atropine, decreased heart rates and QTc intervals after carbachol treatment, and higher heart rates and QTc intervals with isoprenaline but did not note any change in ECG parameters on administration of propranolol. These results are supported by previous reports, confirming the reliability of this ECG protocol. Thus, this method can be used as a screening approach to making ECG measurements that otherwise would not be attempted due to high cost and technical difficulties.

We present an ECG protocol that is technically easy, inexpensive, fast, and affordable in small mice, and can be performed with enhanced sensitivity. We suggest this method as a screening approach for studying pharmacological agents, genetic modifications, and disease models in mice.

The electrocardiogram is a valuable tool for evaluating the cardiac conduction system. Animal research has helped generate novel genetic and ...

Evaluation of Capnography Sampling Line Compatibility and Accuracy when Used with a Portable Capnography Monitor

Capnography is commonly used to monitor patient&#8217;s ventilatory status. While sidestream capnography has been shown to provide a reliable assessment of end-tidal CO2 (ETCO2), its accuracy is commonly validated using commercial kits composed of a capnography monitor and its matching disposable nasal cannula sampling lines. The purpose of this study was to assess the compatibility and accuracy of cross-paired capnography sampling lines with a single portable bedside capnography monitor. A series of 4 bench tests were performed to evaluate the tensile strength, rise time, ETCO2 accuracy as a function of respiratory rate, and ETCO2 accuracy in the presence of supplemental O2. Each bench test was performed using specialized, validated equipment to allow for a full evaluation of sampling line performance. The 4 bench tests successfully differentiated between sampling lines from different commercial sources and suggested that due to increased rise time and decreased ETCO2 accuracy, not all nasal cannula sampling lines provide reliable clinical data when cross-paired with a commercial capnography monitor. Care should be taken to ensure that any cross-pairing of capnography monitors and disposable sampling lines is fully validated for use across respiratory rates and supplemental O2 flow rates commonly encountered in clinical settings.

The goal of this study was to evaluate the accuracy of capnography sampling lines used in conjunction with a portable bedside capnography monitor. Sampling lines from 7 manufacturers were evaluated for tensile strength, rise time, and ETCO2 accuracy as a function of respiratory rate or supplemental oxygen flow rate.

Capnography is commonly used to monitor patient&#8217;s ventilatory status. While sidestream capnography has been shown to provide a reliable assessment ...

Real-Time Dynamic Navigation System for the Precise Quad-Zygomatic Implant Placement in a Patient with a Severely Atrophic Maxilla

Zygomatic implants (ZIs) are an ideal way to address cases of a severely atrophic edentulous maxilla and maxilla defects because they replace extensive bone augmentation and shorten the treatment cycle. However, there are risks associated with the placement of ZIs, such as penetration of the orbital cavity or infra-temporal fossa. Furthermore, the placement of multiple ZIs makes this surgery risky and more difficult to perform. Potential intraoperative complications are extremely dangerous and may cause irreparable losses. Here, we describe a practical, feasible, and reproducible protocol for a real-time surgical navigation system for precisely placing quad-zygomatic implants in the severely atrophic maxilla of patients with residual bone that does not meet the requirements of conventional implants. Hundreds of patients have received ZIs at our department based on this protocol. The clinical outcomes have been satisfactory, the intraoperative and postoperative complications have been low, and the accuracy indicated by infusion of the designed image and postoperative three-dimensional image has been high. This method should be utilized during the entire surgical procedure to ensure ZI placement safety.

Here, we present a protocol to achieve precise quad-zygomatic implant placement in patients with severely atrophic maxilla using a real-time dynamic navigation system.

Zygomatic implants (ZIs) are an ideal way to address cases of a severely atrophic edentulous maxilla and maxilla defects because they replace extensive ...

A Non-Invasive Method for Generating the Cyclic Loading-Induced Intra-Articular Cartilage Lesion Model of the Rat Knee

The pathophysiology of primary osteoarthritis (OA) remains unclear. However, a specific subclassification of OA in relatively younger age groups is likely correlated with a history of articular cartilage damage and ligament avulsion. Surgical animal models of OA of the knee play an important role in understanding the onset and progression of post-traumatic OA and aid in the development of novel therapies for this disease. However, non-surgical models have been recently considered to avoid traumatic inflammation that could affect the evaluation of the intervention. 
In this study, an intra-articular cartilage lesion rat model induced by in vivo cyclic compressive loading was developed, which allowed researchers to (1) determine the optimal magnitude, speed, and duration of load that could cause focal cartilage damage; (2) assess post-traumatic spatiotemporal pathological changes in chondrocyte vitality; and (3) evaluate the histological expression of destructive or protective molecules that are involved in the adaptation and repair mechanisms against joint compressive loads. This report describes the experimental protocol for this novel cartilage lesion in a rat model.

Here, we present the cyclic loading-induced intra-articular cartilage lesion model of the rat knee, generated by 60 cyclic compressions over 20 N, resulting in damage to the femoral condylar cartilage in rats.

The pathophysiology of primary osteoarthritis (OA) remains unclear. However, a specific subclassification of OA in relatively younger age groups is likely ...

Laryngeal Mask Airway (LMA) Placement in a Neonatal Patient Simulator Using a Non-Inflatable Supraglottic Airway (SGA)

The effective delivery of positive pressure ventilation (PPV) can be challenging during neonatal resuscitation. Achieving a patent airway through an appropriate interface during neonatal resuscitation is critical for avoiding airway obstruction and leakage and optimizing access to PPV. Due to the complexity of face mask ventilation, providers have explored corrective steps. However, these methods are difficult to master and thus may present a risk for ventilation delay and/or interruptions at the critical time of resuscitation and the development of complications. In addition, neonatal endotracheal intubation is an invasive procedure that requires significant practice and training. The supraglottic airway (SGA) is a useful laryngeal mask airway (LMA) interface that decreases the time required to achieve a secure airway and reduces the need for endotracheal intubation. Despite the available evidence regarding its effectiveness, insufficient training and awareness limit SGA use in the real world, and frontline providers report low confidence in SGA placement. Here we provide a detailed description of SGA placement, the instruction of which requires only minimal training and leads to a short time to proficiency. Briefly, after the administration of initial ventilatory corrective steps in a neonatal manikin, a provider inserts a non-inflatable SGA into the larynx. This method allows for a single individual to provide effective delivery of PPV in a noninvasive manner without the need for expensive equipment such as video laryngoscopy. Instructors can easily teach this technique with ease and little cost in any clinical and research setting. This is also true for different income settings, including high-, middle-, and low-income countries.

Laryngeal Mask Airway LMA Placement in a Neonatal Patient Simulator Using a Non-Inflatable Supraglottic Airway SGA

This protocol is designed to describe a method to place and establish a supraglottic (alternative) airway during neonatal resuscitation. It can be used in situations where frontline providers cannot ventilate or endotracheally intubate neonates requiring resuscitation.

The effective delivery of positive pressure ventilation (PPV) can be challenging during neonatal resuscitation. Achieving a patent airway through an ...

Acupoint Application Combined with Acupoint Massage for Treating Constipation in a Patient with Chronic Obstructive Pulmonary Disease

Chronic obstructive pulmonary disease (COPD) is a common and frequent disease in elderly patients, with a tendency for progressive exacerbation. Constipation that reduces the quality of life and triggers the risk of diseases is a common concomitant symptom in patients with COPD. Currently, western medical treatment does not achieve the desired results for patients. A high recurrence rate accompanies it, whereas traditional Chinese medicine (TCM) has a long history and rich experience in treating chronic diseases. Both acupoint application and acupoint massage are characteristic therapies of TCM, with minor side effects, high safety, simple operation, and outstanding advantages. They are effective in treating constipation for patients with COPD and are considered an ideal alternative therapy for patients with chronic constipation. The purpose of this article is to introduce the method of acupoint application combined with acupoint massage for the treatment of constipation in patients with COPD, including the selection of points, items, treatment time, and operation procedure.

Here we demonstrate acupoint application combined with acupoint massage for treating constipation in a patient with chronic obstructive pulmonary disease (COPD).