Configuring Enterprise authentication Further configuration is required for Enterprise; use the navigation keys to select Enterprise Settings Configure.
Page Other options on the screen will be greyed out. A list of files on the USB device will appear. Filenames can only be 24 characters long. Under the Communications menu, select Cellular Configure. The Cellular menu appears. You can use the arrow keys to enable or disable all cellular functions, and configure your cell phone provider information. To pair a new device, use the navigation keys and select New. Page Select Pair Now to pair the device.
On your Bluetooth device, accept the pairing request and enter the PIN, if prompted. The unit then returns to the list of paired devices. Page Transmit button is enabled. Press Transmit to initiate the lead transmission. While the transmission is in process, the green LED on top of the unit is illuminated and a message appears on the screen. Power cycling the unit may correct the problem. If the problem persists, set the date and time by highlighting the Date and Time display field and pressing Select.
The Print Number of Traces option can be set to , or. Page Printing Reports Use the navigation keys to highlight and select the treatment summary you want to print.
Note: The Treatment Summary Report that you selected has a check mark next to it. Use the navigation keys to highlight and select Print Treatment Summary. The Propaq MD unit enables you to print vital signs data at one selected time or a trend summary showing vital signs values acquired during the current case up to the last 24 hours.
Page Chapter 24 Maintenance Maintenance Resuscitation equipment must be maintained to be ready for immediate use.
To ensure the readiness and optimum working condition of the Propaq MD unit, you should perform the following inspections and tests daily or at each shift change.
In addition to the daily check, authorized personnel should complete performance and calibration testing at regularly scheduled intervals, which should not exceed one year.
Note: If a low battery message appears during any of this testing, the battery is close to depletion and should be replaced or recharged. Damage to the battery packs can occur if they are left in a depleted state for more than 14 days. DO NOT allow cleaning agent or water to run into the crevices or connector openings at any time. Use ZOLL recorder paper part number To load the recorder paper into the printer: 1.
Page Cleaning The Print Head Gently wipe the print head with a cotton swab moistened with isopropyl alcohol, and dry any residual alcohol with another dry cotton swab. Cleaning the Print Head Place the paper back into the unit and close the cover see Fig. Indicate whether all requirements have been met. Note any corrective actions taken. Sign the form. Page Defibrillator R wave and the delivery of energy. Page Propaq MD defibrillation waveforms are considered substantially equivalent.
Figures A-1 through A show the Rectilinear Biphasic waveforms that are produced when the Propaq MD defibrillator is discharged into loads of 25, 50, 75, , , , and ohms at each energy setting. Page Ohm Ohm Figure A Rectilinear Biphasic Waveform at Joules www. Page Ohm Figure A Rectilinear Biphasic Waveform at Joules Rev. Rectilinear Biphasic Waveform at 70 Joules www. Rectilinear Biphasic Waveform at 30 Joules Rev. Rectilinear Biphasic Waveform at 15 Joules www.
Rectilinear Biphasic Waveform at 9 Joules Rev. Rectilinear Biphasic Waveform at 7 Joules A www. Page Figure A Rectilinear Biphasic Waveform at 5 Joules Rev. Rectilinear Biphasic Waveform at 3 Joules A www. Rectilinear Biphasic Waveform at 1 Joule Rev. Responds to a 40 BPM step decrease within 3. Response times include a 1. A www. Burn hazard protection via a 1K current limiting resistor contained in each ECG leadwire.
Page Recorder Proper battery care is required to maintain maximum available capacity. Total System Response Time: 2.
Invasive Pressures The Propaq MD does not add any clinically significant time to obtain accurate readings. Seven 7 patients who did not satisfy all protocol criteria were excluded from the analysis. ZOLL disposable gel electrodes with surface areas of 78 cm anterior and cm posterior were used exclusively for the study. Page Conclusion: The data demonstrate the superior efficacy of low energy rectilinear biphasic shocks compared to high energy monophasic shocks for transthoracic cardioversion of atrial fibrillation.
There were no unsafe outcomes or adverse events due to the use of Rectilinear Biphasic Waveform. Page Synchronized Cardioversion Of Atrial Fibrillation Place the front apex pad on the third intercostal space, mid clavicular line on the right anterior chest. The customer or the user of the Propaq MD unit should assure that it is used in such an environment.
The customer or the user of the Propaq MD should assure that it is used in such an environment. Immunity test Page Electromagnetic Immunity: Life-Supporting Functions The life-supporting functions of the Propaq MD are intended for use in the electromagnetic environment specified below. The customer or user of the Propaq MD should ensure that it is used in such an environment. Page Electromagnetic Immunity: Non Life-Supporting Functions The non life-supporting functions of the Propaq MD are intended for use in the electromagnetic environment specified below.
Page The life-supporting functions of the Propaq MD are intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The customer or user of the Propaq MD can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the Propaq MD as recommended below, according to the maximum output power of the communications equipment.
Page Propaq MD The non life-supporting functions of the Propaq MD are intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The customer or user of the Propaq MD can help prevent Page Ecg Analysis Algorithm Accuracy as a percentage of the total number of non-shockable rhythms.
To order any of these items, contact your local ZOLL representative. Print page 1 Print document pages. Rename the bookmark. Delete bookmark? Cancel Delete. Delete from my manuals? Sign In OR. Don't have an account? Sign up! Restore password. Upload manual. Upload from disk. Bluetooth Device Pairing Sending a Lead Report Sending Disclosure Logs Supervisor Communications Menu Accessing the Communications Menu Wi-Fi Access Point Profiles Setting up Cellular Communications Setting up an Ethernet Connection Configuring Lead Report Transmissions Configuring Disclosure Log Transmissions Data Services Configuring Clock Synchronization Communications System Messages Printing Patient Data Printer Setup Automatic Prints Printing Waveforms Printing Reports Printing Trends Inspection and Cleaning instructions Cleaning the Propaq M unit Cleaning SpO2 Sensors Cleaning Cables and Accessories Loading Recorder Paper Cleaning the Print Head Recommended Minimum Preventive Maintenance Schedule Guidelines for Maintaining Peak Battery Performance Impedance Pneumography Printer Recorder Non-Invasive Blood Pressure Invasive Pressures FCC Notice Temperature, and Respiration.
It has been designed for all resuscitation situations and its rugged, compact, lightweight design makes it ideal for transport situations. It is powered by auxiliary power and an easily replaced battery pack that is quickly recharged in the device when it is connected to auxiliary power.
Note: Some of the monitoring functions are optional features. See the complete list of options in Fig. All features are included in this manual, but only purchased features will be available on your unit. The product is designed for use in hospital, EMS, and rugged military environments. The unit has a large colorful LCD display of numerics and waveform data that provides easy visibility from across the room and at any angle. ECG, plethysmograph, and respiration waveform traces can be displayed simultaneously, giving easy access to all patient monitoring data at once.
The display screen is configurable, so you can choose the best visual layout to fit your monitoring needs. The Propaq M has a patient data review and collection system that allows you to view, store, and transfer patient data.
The Propaq M unit contains a USB port, which you can use to transfer data to a PC and, optionally, a printer, that you can use to print patient data. The Propaq M unit can send data through a wireless connection to remote locations. The unit can send lead report snapshots including trend data or disclosure logs to a recipient via a ZOLL server. Note: All features are included in this manual, but only purchased features will be available on your unit. The Propaq M Operator's Guide provides information operators need for the safe and effective use and care of the Propaq M product.
It is important that all persons using this device read and understand all the information contained within. Procedures for daily checkout and unit care are located in the Chapter 17, "Cleaning and Maintenance". An issue or revision date for this manual is shown on the front cover. If more than three years have elapsed since this date, contact ZOLL Medical Corporation to determine if additional product information updates are available. All users should carefully review each manual update to understand its significance and then file it in its appropriate section within this manual for subsequent reference.
Product documentation is available through the ZOLL website at www. From the Products menu, choose Product Manuals. Carefully inspect each container for damage. If the shipping container or cushion material is damaged, keep it until the contents have been checked for completeness and the instrument has been checked for mechanical and electrical integrity.
If the contents are incomplete, if there is mechanical damage, or if the monitor does not pass its electrical self-test, U. Customers outside of the U. If the shipping container is damaged, also notify the carrier. Any or all of the following symbols may be used in this manual or on this equipment:.
Return to a collection site intended for waste electrical and electronic equipment WEEE. Do not dispose of in unsorted trash. Warning statements alert you to conditions or actions that can result in personal injury.
Caution Caution statements alert you to conditions or actions that can result in damage to the unit. The Propaq M is intended for use by trained medical personnel who are familiar with basic monitoring, vital sign assessment, and the use of the Propaq M. The Propaq M is also intended for use by or on the order of physicians at the scene of an emergency or in a hospital emergency room, intensive care unit, cardiac care unit, or other similar areas of a hospital.
The usage may be in an ambulance or at the scene of an emergency. It is also intended to be used during the transport of patients. The Propaq M will be used whenever it is required to monitor any of those functions that are included as options in the device.
The Propaq M unit can be used on pediatric patients as described in the following table and on adult patients 21 years of age or older with and without heart dysfunction. The patient population will range from newborn neonate to adult, with and without heart dysfunction. Measurements are made using an inflatable cuff on the patient's arm or leg.
The patient population will range from newborn neonate to adult. The Propaq M is intended for use to make continuous temperature measurements of rectal, esophageal, or surface temperatures, and to alarm if the temperature is outside of the limits set by the user. The pulse CO-oximeter and accessories are indicated for use on adult, pediatric, and neonatal patients during both no motion and motion conditions, and for patients who are well or poorly perfused, in hospitals, hospital-type facilities, or in mobile environments.
The Propaq M is intended for use to continuously monitor respiration rate and to alarm if the rate falls outside of the range set by the operator. Because the measurement method actually measures respiratory effort, apnea episodes with continued respiratory effort such as obstructive apnea may not be detected. It is not intended to be used as an apnea monitor. The Propaq M is intended for use to make continuous noninvasive measurement and monitoring of carbon dioxide concentration of the expired and inspired breath and breath rate.
The Propaq M is intended for use to display and make continuous invasive pressure measurements from any compatible pressure transducer. The primary intended uses are arterial blood pressure, central venous pressure and intracranial pressure monitoring.
Any contraindications of the particular transducer selected by the user shall apply. The lead ECG Analysis is intended for use in acquiring, analyzing and reporting ECG data, and to provide interpretation of the data for consideration by caregivers.
The interpretations of ECG data offered by the device are only significant when used in conjunction with caregiver overread as well as consideration of all other relevant patient data. The ECG waveform is presented on the display along with the following information:. A new, fully charged battery pack typically delivers more than 8 hours of ECG monitoring.
Use of other functions such as higher screen brightness or shorter NIBP intervals reduces this time. The front panel battery indicator operates as follows:. Note: Upon power up, it takes approximately 45 seconds for the LEDs on the battery to accurately display run time.
The Recalibration LED icon lights for approximately 10 seconds after you press and release the Display button if the battery needs to be calibrated.
If the Recalibration LED lights, the runtime indicator will not display run time for that battery. For best performance of the battery, you should recalibrate the battery as soon as possible. After you recalibrate the battery, the Recalibration LED will only flash when you press the.
The RFU indicator has three states which are described in the following table. They are not a substitute for a formal patient care training course. Operators should obtain formal training from an appropriate authority before using this monitor for patient care. Operators must be thoroughly familiar with proper device operation.
A shock hazard exists. Refer all problems to authorized service personnel. If a problem occurs, obtain service immediately. Do not use the monitor until it has been inspected by appropriate personnel. The Propaq M unit should not be stored or used outside of the environmental limits provided in Appendix A of this manual. If unavoidable, verify that the unit operates normally in this configuration before clinical use. Dedicated pacemaker detection circuitry may not detect all implanted pacemaker spikes.
Check the patient's pulse; do not rely solely on heart rate meters. Patient history and physical examination are important factors in determining the presence of an implanted pacemaker.
Pacemaker patients should be carefully observed. It does not detect a pulse effective circulatory perfusion. Always verify pulse and heart rate by physical assessment of the patient.
Never assume that the display of a nonzero heart rate means that the patient has a pulse. Ensure adequate separation between such emitters, the device, and the patient when performing rhythm analysis. Move sensor every 4 hours to reduce possibility of tissue damage. MRI procedures can cause conducted current to flow through the sensors, causing patient burns.
These breathing attempts can still produce chest size changes, creating impedance changes, which can be detected by the respiration detector. It is best to use the pulse oximeter whenever monitoring respirations, to accurately depict the patient's respiratory condition.
Use only ZOLL-approved cuffs and hoses. Medication may also affect pressure readings. The correct size cuff is essential for accurate blood pressure readings.
If the repeated measurement result is still questionable, use another blood pressure measurement method. Do not reuse sampling lines. The two devices could affect the respiration accuracy. Biomedical equipment and accessories, such as ECG electrodes, cables, and oximeter probes contain ferromagnetic materials.
Ferromagnetic equipment must not be used in the presence of high magnetic fields created by magnetic resonance imaging MRI equipment. The large magnetic fields generated by an MRI device can attract ferromagnetic equipment with an extremely violent force, which could cause serious personal injury or death to persons between the equipment and the MRI device. Operating the unit with a battery provides a backup in case of AC power shortage, and results in faster charge time. The battery can be automatically recharged while it is installed in the unit.
Keep a fully charged spare battery pack with the monitor at all times. When the warning low battery shutdown prompt appears, immediately replace the battery pack with a fully charged pack or plug the Propaq M unit into a power source, as unit shut down due to a low battery condition is imminent. Do not disassemble a battery pack or dispose of it in fire. Using the unit in such environments might cause an explosion.
Electrical safety might be compromised when the monitor is wet. When choosing accessory equipment, consider the following:. You can only view or download manuals with. Sign Up and get 5 for free. Upload your files to the site. You get 1 for each file you add. Get 1 for every time someone downloads your manual.
Buy as many as you need. View and download manuals available only for. Register and get 5 for free. Once you have obtained a copy, save it on a USB thumb drive. This test allows you to perform the USB test to make sure it is working correctly.
When these tests are completed, use the navigation keys to exit out of the Service menu. Create a Text file using Microsoft Notebook.
Open new file in Notebook. III I, II, on the Propaq MD unit and. The Alarm Suspend key flashes. Turn off the Power Supply output. Wait five seconds, then press the charge capacity switch on the Battery Current Test Fixture and verify that the green LEDs momentarily turn on.
Perform these tests at the line-power voltage and frequency used in your. Take the necessary precautions to guard against shock or injury before you start conducting the defibrillator tests. Keep hands and all other objects clear of the multi-function cable connections and defibrillator analyzer when discharging the defibrillator. Select Sync mode on analyzer. Welcome to ManualMachine. We have sent a verification link to to complete your registration.
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Propaq MD Rev B. April Rev. Table of Contents Preface Overview Chapter 3 Disassembly Procedures Overview Safety Considerations The following section describes general warnings and safety considerations for operators and patients. Only qualified personnel should disassemble the Propaq MD unit. Do not use the unit near or within puddles of water. Service Policy Warranty In North America: Consult your purchasing agreement for terms and conditions associated with your warranty.
Propaq MD Overview 2. Use the navigation keys to select Yes. Keypad Test This test checks all the front panel buttons on the unit to make sure they are working correctly. Note: The speed of the flash varies by color. Audio Test This test checks the audio tones on the unit to make sure they are working correctly. Printer Test This test checks the printer to make sure it is working correctly. Follow the instructions on the display.
Fan Test This test checks the fan in the unit to make sure it is working correctly. Creating a Test File 1. Propaq MD Overview 3. Do this Observe this Propaq MD unit: Press the More quick access key key to access the second set of quick access keys. Press the Alarm quick access key. Press the Alarm Cancel quick access key.
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