Mizuhosi
WILSON PLUS and the Radiolucent Frame Model 5321G & 5319G Owner’s Manual Rev E
Owners Manual
23 Pages
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IMPORTANT NOTICES CAUTION: To ensure safe operation of this device, please READ THESE INSTRUCTIONS COMPLETELY and keep this manual for future reference Carefully observe and comply with all warnings, cautions and instructions placed on the equipment or described in this manual. Throughout this manual the Wilson Plus™, Radiolucent Wilson Frame is referred to as the RWF. In this manual, the symbol WARNING is intended to alert the user to the presence of important operating and safety instructions. This device is intended for use by trained personnel only. To schedule an in-service, please contact your Mizuho OSI sales representative or call 1-800-329-4674. The application techniques outlined in this manual comprise the manufacturer’s suggested technique. The final disposition of each patient’s care as related to the use of this equipment rests with the attending physician. Trademarks Wilson Plus™ and TLC are trademarks of Mizuho OSI. GentleTouch® and ShearGuard™ are registered trademarks of Mizuho OSI. OrangeAid® is a registered trademark of Mizuho OSI ProneView® is a registered trademark of Dupaco, Inc.
WARNING: Use of any Wilson Plus™, Radiolucent Wilson Frame with patients weighing more than 300 lbs(136 kg.) would result in damage to the Frame and possible injury to the patient.
WARNING: Before use, inspect the device for possible damage, excessive wear, or nonfunctioning parts. Carefully inspect all critical, inaccessible areas, joints, and all moving parts for possible damage or non function. Damaged or defective parts should not be used or processed. Contact your local Mizuho OSI representative for repair or replacement.
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TABLE OF CONTENTS 1.1 General Description of Radiolucent Wilson Frame Model 5321G & 5319G ... 4 1.2 Assembly & Use of RWF Model 5321G on Mizuho OSI Spinal Table System ... 6 ProneView® Instructions for Use with Model 5321G RWF ... 7 1.3 Patient Transfer onto RWF Model 5321G via Log Roll ... 10 1.4 Patient Transfer onto RWF Model 5321G via Spinal Table System Rotation ... 11 1.5 Patient Positioning on RWF Model 5321G ... 12 1.6 Patient Transfer off the RWF Model 5321G ... 13 1.7 Assembly & Use of RWF Model 5319G for Imaging Top and General Tables ... 13 1.8 Preparation of the Imaging Top and Set-up of RWF Model 5319G ... 14 1.9 Preparation of a General Surgery Table and Set-up of RWF Model 5319G ... 14 1.10 Patient Transfer onto RWF Model 5319G ... 18 1.11 Patient Positioning on RWF Model 5319G ... 18 1.12 Patient Transfer off the RWF Model 5319G ... 19 1.13 Cleaning And Maintenance of RWF Model 5321G & 5319G ... 20 Instant Support Value Package ... 22 To order Replacement Parts (RP) ... 23 To return damaged parts (RGA) ... 23 To send a part for repair (RA) ... 23
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1.1 General Description of Radiolucent Wilson Frame Model 5321G & 5319G Mizuho OSI’s Wilson Plus™ Radiolucent Wilson Frame Positioners are available in two models: 1. Model 5321G is designed for use with the Mizuho OSI Spinal Table System 2. Model 5319G is designed for use with Mizuho OSI’s Modular Imaging Top, General Surgical Tables, or other flat surface surgical platforms. The Radiolucent Wilson Frame (RWF) utilizes carbon composites and high impact plastics that deliver unrestricted radiolucency and C-arm integration while providing a convenient and stable method of maintaining patients in a prone flexed position for laminectomy, decompression, disk surgery and micro-discectomy.
RWF Specifications: 300 lb (136 kg.) patient weight capacity and is labeled on base of frame 3-1/2”(8.8 cm) of intraoperative flex of the pads for lordosis control 0” to 6”(0-15.2 cm) of pad width adjustment Model 5321G weighs 40lbs(18 kg.) and the Model 5319G weighs 36 lbs(16 kg)
Standard Components with Model 5321G: P/N 5321-43 Wheeled Storage Cart P/N 5319-36 ShearGuard™ Pads P/N 5319-6 Crank Handle with Torque Limiter P/N 5878PV-2 Patient Care Kit with ProneView® 2/case
Recommended Accessories For Model 5321G: P/N D28705CE ProneView® Helmet & Mirror System for use on the Spinal Table System P/N 5878PV Patient Care Kit with ProneView® 6/case P/N 10604 Patient Safety Strap with OrangeAid® Gel
Standard Components with Model 5319G: P/N 5319-1 Wheeled Storage Case P/N 5319-36 ShearGuard™ Pads P/N 5319-6 Crank Handle with Torque Limiter P/N D28501CE ProneView® Helmet & D28590CE Adjustable ProneView Mirror P/N 5322PV-2 Patient Care Kit with ProneView® 2/case
Recommended Accessories For Model 5319G: P/N 10604 Patient Safety Strap with OrangeAid® Gel P/N 10101 OrangeAid® Gel Pad P/N 5855-550 Safety Strap (used to secure Frame to table) P/N 5322PV Patient Care Kit with ProneView® 6/case
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Sources of Information: In addition to this Owner’s Manual, a Quick Reference is provided on the top of the base of Model 5319G Radiolucent Wilson Frame. (See Figure 1)
Figure 1: Quick Reference Instructions Located on the Base of Model 5319G RWF
The model number for the device, serial number and additional manufacturer information is found on the manufacturer’s label located on the side of the base of the frame and to the right of where the crank handle is utilized. (See Figure 2)
Figure 2: Manufacturer’s Label with Serial Number and Model Number of Device
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1.2 Assembly & Use of RWF Model 5321G on Mizuho OSI Spinal Table System Model 5321G mounts directly onto a Mizuho OSI Spinal Surgery Top.
Figure 3: Wilson Plus™ Model 5321G Radiolucent Wilson Frame for the Spinal Table System
Wheel the RWF into the O.R. on the storage cart provided. (See Figure 4)
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Figure 4: Wilson Plus™ Model 5321G Radiolucent Wilson Frame on Storage Cart
Open the patient care kit. Set the components aside in a convenient location. Position the Modular Table Base and engage all floor locks. Attach the Spinal Surgery Top in the lowest available position on the H-Frame. Visually check and confirm that the table top is level. Model 5321G can be utilized with the Spinal Table System Face Plate and GentleTouch® Pillow or the Proneview® System. Both products are available as optional accessories should you need to purchase. ProneView® Instructions for Use with Model 5321G RWF Components used in the ProneView® System for Model 5321G Wilson Frame: D28501CE Helmet, D28700CE Adjustable Mirror Platform for Spinal Table System, D28503CE Large Cushion Insert or D28507CE Small Cushion Insert. NOTE: Read all instructions on the ProneView® Helmet and Mirror before using the ProneView® System. When using the ProneView® cushion, it is recommended to open the cushion at least 60 minutes prior to use to allow for complete expansion. Follow the instructions on the underside of the ProneView® mirror for proper cushion placement into the helmet. Remove the fastening rod from the ProneView® Mirror Platform by removing one of the black “T” handles. Place the mirror platform onto the Spinal Surgery Top (SST) by aligning the metal rails of the platform over the spinal frame. NOTE: The mirror must align with the helmet when the patient is log rolled onto the Wilson Frame to properly engage the helmet legs with the mirror pegs. Insert the fastening rod through the receptacles of the platform and reattach the black “T” handle.
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WARNING: Visually confirm the fastening rod is under the Spinal Frame and has captured the mirror platform and the rails of the frame. Failure to do so could lead to migration of the mirror platform and injury to the patient. The fastening rod may be kept loosely engaged until the desired platform position is achieved. Keep the helmet in place by holding it onto the patient’s face and log roll the patient onto the Wilson Frame. Align the pegs on the mirror with the helmet and engage. When this is done, use the mirror to visually confirm that the eyes, nose and mouth are completely clear of the cushion Insert. NOTE: It is suggested that the anesthesia provider place the ProneView® cushion with helmet on the patient’s face and adjust the endo-tracheal tube and anesthesia circuit prior to transferring (log rolling) the patient onto the RWF.
Warning: Failure to confirm proper cushion placement may cause injury to the patient. Adjust the helmet height as necessary by turning the knobs on the underside of the mirror clockwise to increase the height. The ProneView® adjustable mirror platform for the Spinal Frame has 2-1/2” (6.4 cm) of height adjustment. Warning: The ProneView® cushion is not to be used without the ProneView® helmet. Do not use the ProneView® helmet without a ProneView® cushion. Place the RWF on the table against the head support plate (face plate). Or, if using the ProneView® System, against the adjustable mirror platform and secure with the hook and loop straps (See Figure 5)
Figure 5: Model 5321G RWF on Spinal Frame with ProneView®
Engage the torque limiter crank and turn counter-clockwise to lower the pads to the lowest position until you hear an audible clicking sound. (See Figure 6) Mizuho OSI 2011
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Figure 6: Engaging the Crank Handle into the Base of the Frame
Disengage the pads from the foot end retention lip of the frame to apply the disposable pad covers found in the patient care kit. To disengage pads, reach under the pad support and lifting up at the center of the pad to release from the retaining lip at the foot end of the base. (See Figure 7)
Pad Disengaged from Retaining Lip of Base
Head End Lateral Adjustment
Foot End
Figure 7: Disengaging the Pads from the Frame of Model 5319G RWF Same Process for Model 5321G
When the foot end of the pad is disengaged from the base, lift each pad towards the head end of the frame and apply the disposable pad covers over the pads and supports. Take care when pulling on the covers to avoid tearing. Confirm that the covers are smooth against the surface of the pad and the elastic of the cover is over the bottom of the pad. While the pads are disconnected from the foot end of the base, set the pads to the surgeon’s preferred width which is usually determined by size of patient. To adjust each pad, push and hold the lateral adjustment release button located on the head end of the frame. Slide the pad supports to the desired location on the cross bar. Release the button to lock the pads. (See Figure 8) Mizuho OSI 2011
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Lateral Adjustment Release Button
Lateral Adjustment Release Button Crossbar at Head End Figure 8: Lateral Adjustment on a RWF
WARNING: Check the pad width setting to ensure there will be no excessive pressure on the patient’s brachial plexus. Excessive pad width may also allow the patient to migrate downward between the pads. Either occurrence may result in injury to the patient. Once you have positioned the pads, re-engage the pad supports to the frame by inserting the pad supports under the retention lip provided in the base of the frame. Apply the foam cross bar protector, from the patient care kit, over the cross bar at the head end of the frame. This protector will help ensure that the patient does not make accidental contact with the metal cross bar (See Figure 8). Depending on the placement of the pads and width between them, the cross bar protector may be trimmed if it is too long.
1.3 Patient Transfer onto RWF Model 5321G via Log Roll Ensure pads are at the lowest position. Orient the patient stretcher or bed along side the Spinal Table System and engage floor locks. Elevate the stretcher or bed so that the patient is level with the RWF pad surface. It is suggested that the anesthetist apply the GentleTouch® headrest pillow or ProneView® helmet with cushion insert to the patient’s face and adjust the endotracheal tube and anesthesia circuit prior to transferring the anesthetized patient onto the RWF. Using adequate help, transfer the patient onto the frame by carefully rolling the supine patient from the stretcher or bed into the prone position on top of the frame. Hold the helmet or pillow securely on the patient’s face during the transfer to the prone position. Make sure that the neck is in a neutral or dependent position. After patient transfer, visually confirm the pad covers are smooth under the patient. Lift the patient up on each side, individually, smooth the pad covers and eliminate any skin folds that may have occurred as a result of the patient transfer.
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Visually confirm the female breasts are positioned in a comfortable and natural position and also check to ensure that the foam cross bar protector is in place and no part of the patient is in contact with the metal crossbar. Re-position the patient as necessary and utilize additional padding to support and protect the patient from contact with the parts of the frame other than the pads. Visually confirm there is no excess pressure on the patient’s anterior thigh. Use pillows or gel positioners as needed with the leg sling or leg boards to raise and support the patient legs and reduce pressure.
WARNING: Inadequate lifting help can result in injury to both patient and staff.
WARNING: Failure to confirm appropriate patient positioning after patient transfer onto the frame, may result in patient injury. 1.4 Patient Transfer onto RWF Model 5321G via Spinal Table System Rotation To avoid lifting the patient, you may elect to use the rotational capabilities of the Spinal Table System to position the patient. To do so, follow the instructions in the Spinal Table System Owner’s Manual. A thorough understanding of the use of the Mizuho OSI Modular Table System is required to perform this procedure. Extra caution should be used when rotating with the RWF. The RWF has a higher profile than the chest, hip and thigh pads it replaces. Some adjustment must be made in the standard rotational technique. The imaging top must be attached approximately two holes lower to the H-frames to allow for the higher profile. More pillows will be needed to fill in the additional space and ensure proper control of the patient during rotation. Finally, pillows should be placed under the patient’s head, shoulders, hips and legs before rotation to help mold the patient to the frame. NOTE: Make certain the RWF frame pads are in their lowest position during rotation. WARNING: All patient safety straps must be used before rotation. Failure to properly control the patient during rotation could result in the patient being dropped and cause harm to the patient and/or healthcare worker. After patient rotation, visually confirm the pad covers are smooth under the patient. Lift the patient up on each side, individually, smooth the pad covers and eliminate any skin folds that may have occurred as a result of the patient transfer. Visually confirm the female breasts are positioned in a comfortable and natural position and also check to ensure that the foam cross bar protector is in place and no part of the patient is in contact with the metal crossbar. Mizuho OSI 2011
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Re-position the patient as necessary and utilize additional padding to support and protect the patient from contact with the parts of the frame other than the pads. Visually confirm there is no excess pressure on the patient’s anterior thigh. Use pillows or gel positioners as needed with the leg sling or leg boards to raise and support the patients legs and reduce pressure. 1.5 Patient Positioning on RWF Model 5321G After confirming the patients’ position on the frame, the pads can be flexed to the desired height. Engage the torque limiter crank handle into the base of the frame and turn it clockwise until the desired flexion is achieved. Once the desired flexion has been achieved, remove the crank and set it aside. (See Figure 9) NOTE: Do not place the crank handle into its storage slot in the base of the frame during surgery because it will interfere with radiolucency. NOTE: Do not place the crank handle in the quiver it can result in damage to the crank handle.
Head End
Foot End
Crank Handle
Figure 9: 5321G RWF Use of Crank Handle with Torque Limiter
WARNING: As the pads are flexed and un-flexed, the patient’s head will shift. Failure to maintain appropriate alignment of the patient’s head could result in undue strain and injury to the patient. Some patients will naturally bear weight at the knees, while for others pillows or rolled gel pads may be needed. If the knees are weight bearing, a Mizuho OSI Gel Pad, Mizuho OSI P/N 10101, or its equivalent is recommended under the knees. Additional pillows may be used to elevate the legs and achieve the desired hip flexion. Place a pillow under the lower leg to elevate the toes off the table surface. Adjust the arm boards and apply the TLC™ Arm Cradles from the patient care kit. The Arm Cradles should contour the entire length of the arm. Mizuho OSI 2011
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WARNING: Apply a circumferential patient safety strap, Mizuho OSI P/N 10604 or equivalent under the pad supports and around the patient’s thighs. All patient safety straps must be used before rotation. Failure to properly control the patient during rotation could result in the patient being dropped and cause harm to the patient and/or healthcare worker. 1.6 Patient Transfer off the RWF Model 5321G After the surgery has concluded, position the patient’s stretcher or bed along side the table and engage floor locks. Adjust the height of the stretcher/bed so that it is level with the surface of the frame pads. Enlist appropriate personnel to assist and maintain the patient on the RWF and remove the circumferential patient safety strap. Using adequate help, roll the patient from the frame to a supine position on to the stretcher/bed. NOTE: You may use the lateral tilt feature of the Mizuho OSI Advanced Control Base to facilitate patient transfer. Position the stretcher or bed lower than the frame pad height and, while maintaining the patient on the RWF, tilt the table until the lateral edge of the frame pad contacts the edge of the stretcher or bed pad. Then roll the patient off the frame tand to a supine position on the stretcher or bed. 1.7 Assembly & Use of RWF Model 5319G for Imaging Top and General Tables
Figure 10: Model 5319G RWF on Imaging Top of the Mizuho OSI Modular Table System
The Model 5319G Wilson Plus™ Radiolucent Wilson Frame can be used on any general surgery table. However, to ensure the full benefit of all of its design advantages, it is best to interface it with the Radiolucent Imaging Top of the Mizuho OSI Modular Table System. The unique characteristics of the imaging table, including the totally radiolucent carbon composite top, carbon composite side rails, narrow top width, low operating height and unrestricted C-arm access allow for full realization of all of the advantages of the Wilson Plus™.
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1.8 Preparation of the Imaging Top and Set-up of RWF Model 5319G Position the Modular Table Base in the O. R. suite and engage all floor locks. Attach the Radiolucent Imaging Top in the lowest available position on the H-frame. Visualize and confirm that the table top is level. WARNING: Failure to support the frame on a level surface could cause premature failure of the frame. Wheel the frame into the room. Place the wheeled case on the table top. The handle built into the cover is oriented to the foot end of the table. (See Figure 11)
RWF in Case can be Wheeled to Storage
Head End, Wheels of Case Up in Position for Top of Case to be Removed
Foot End where Handle is Located
Figure 11: Model 5319G RWF Wheeled Case Oriented on Table Top
Remove the protective cover and secure the frame to the table with a patient safety strap, Mizuho OSI P/N 5855-550 or equivalent. (See Figure 10) Apply a Safety Strap P/N 5855-550 or equivalent. NOTE: Visualize that the Safety Strap does not impede the pad range of motion. 1.9 Preparation of a General Surgery Table and Set-up of RWF Model 5319G
Figure 12: Model 5319G RWF with ProneView® and Patient Kit Components on General Surgical Table
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Prepare the O.R. table as per manufacturer’s instructions. Position it as desired and engage all floor locks. Because the Radiolucent Wilson Frame holds the patient above the table surface, you may wish to remove any cassette tunnels to lower the table height. If possible orient the frame on the table top to maximize radiolucency at the operative site. Visualize that the table top is level and bring it to level.
WARNING: Failure to support the frame on a level surface could cause premature failure of the frame. Wheel the RWF case into the room, and place the case on the table top. The handle built into the cover is oriented to the foot end of the table. Remove the protective cover and secure the frame to the table with a patient safety strap, Mizuho OSI P/N 5855-550 or equivalent
WARNING: Failure to properly control the patient could result in the patient being dropped and cause harm to the patient and/or healthcare worker. ProneView® Instructions for Use with Model 5319G Components Used in the ProneView® System for 5319G RWF: D28501CE Helmet, D287590CE Adjustable Mirror, D28503CE Large Cushion Insert or D28507CE Small Cushion Insert. NOTE: Read all instructions on the ProneView® helmet and mirror before using the ProneView® System. Open the Patient Care Kit. When using the ProneView® cushion, it is recommended to open the cushion at least 60 Minutes prior to use to allow for complete expansion. Follow the instructions on the underside of the ProneView® mirror for proper cushion placement into the helmet. NOTE: It is suggested that the anesthesia provider place the ProneView® cushion with helmet on the patient’s face and adjust the endo-tracheal tube and anesthesia circuit prior to transferring the patient onto the RWF.
Engage the torque limiter crank handle and turn counter-clockwise to lower the pads to the lowest position until you hear an audible clicking sound. (See Figure 13)
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Figure 13: Engaging the Crank Handle into the Base of the Frame
Pad Disengaged from Retaining Lip of Base
Head End Lateral Adjustment
Foot End
Figure 14: Disengaging the Pads from the Frame of Model 5319G RWF
Disengage the pads from the foot end retention lip of the frame to apply the disposable pad covers found in the patient care kit. To disengage pads, reach under the pad support and lifting up at the center of the pad to release from the retaining lip at the foot end of the base. (See Figure 14) When the foot end of the pads is disengaged from the base, lift them head-ward and apply the disposable pad covers over the pads and supports. Take care when pulling on the covers to avoid tearing. The elastic should be on the bottom. While the pads are disconnected from the foot end of the base, set the pads to the surgeon’s preferred width. To adjust each pad, push and hold the lateral adjustment release button located on the lateral adjustment assembly. Slide the pad supports to the desired location on the cross bar. Release the button to lock the pads. (See Figure 15)
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Lateral Adjustment Release Button
Lateral Adjustment Release Button Crossbar at Head End Figure 15: RWF Lateral Release Button
WARNING: Check the pad width setting to ensure there will be no excessive pressure on the brachial plexus. Excessive pad width may allow the patient to migrate downward between the pads. Either occurrence may result in injury to the patient. Once you have positioned the pads, re-engage the pad supports by inserting the pad supports under the retention lip provided in the base. Apply the cross bar protector, from the patient care kit, over the cross bar. This protector will help ensure that the patient does not make accidental contact with the metal cross bar (See Figure 15). The cross bar protector may be trimmed if too long. Remove the crank from its storage slot in the base and apply the base cover from the patient care kit across the base attaching it with the adhesive hook and loop provided.
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1.10 Patient Transfer onto RWF Model 5319G Orient the patient stretcher or bed along the side of the O.R. table and engage floor locks. Elevate the stretcher or bed so that the patient is level with the frame pad surface. It is suggested that the anesthetist apply the GentleTouch® headrest pillow, or if using ProneView®, apply the helmet with cushion insert to the patient’s face and adjust the endo-tracheal tube and anesthesia circuit prior to transferring the anesthetized patient onto the RWF. Using adequate help, transfer the patient onto the frame by carefully rolling the supine patient from the stretcher or bed into a prone position on top of the frame. Make sure that the neck is in a neutral or dependent position. WARNING: Inadequate lifting help can result in injury to both patient and staff.
After patient transfer, visually confirm the pad covers are smooth under the patient. Lift the patient up on each side, individually, smooth the pad covers and eliminate any skin folds that may have occurred as a result of the patient transfer. Visually confirm the female breasts are positioned in a comfortable and natural position and also check to ensure that the foam cross bar protector is in place and no part of the patient is in contact with the metal crossbar. Re-position the patient as necessary and utilize additional padding to support and protect the patient from contact with the parts of the frame other than the pads. Visually confirm there is no excess pressure on the patient’s anterior thigh. Use pillows or gel positioners as needed with the leg sling or leg boards to raise and support the patients legs and reduce pressure. 1.11 Patient Positioning on RWF Model 5319G Engage the torque limiter crank handle and turn it clockwise until the desired flexion is achieved. The crank has a built in torque limiter that makes a clicking noise when the pads reach the limit of travel. Once the desired flexion has been achieved, remove the crank handle and set it aside.
WARNING: As the pads are flexed and un-flexed, the patient’s head will shift. Failure to maintain appropriate alignment of the patient’s head could result in undue strain and injury to the patient.
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NOTE: Do not place the crank handle into its storage slot in the base of the frame during surgery because it will interfere with radiolucency. NOTE: Do not place the crank handle in the quiver it can result in damage to the crank handle. Some patients will naturally bear weight at the knees, while for others pillows or rolled gel pads may be needed. If the knees are weight bearing, a Mizuho OSI Gel Table Pad, Mizuho OSI P/N 10101, or its equivalent is recommended under the knees. Additional pillows may be used to elevated the legs and achieve the desired hip flexion. Place a pillow under the lower leg to elevate the toes off the table surface. Adjust the arm boards and apply the TLC™ Arm Cradles from the patient care kit. The Arm Cradles should contour the entire length of the arm.
WARNING: Apply a circumferential patient safety strap, Mizuho OSI P/N 10604 or equivalent under the pad supports and around the patient’s thighs and under the pad support. Failure to use safety straps may cause the patient to move, drop or fall and cause harm to themselves and/or the healthcare workers. NOTE: If x-ray is needed during surgery, a cassette may be positioned between the pad supports and the frame base. 1.12 Patient Transfer off the RWF Model 5319G After the surgery has concluded, position the stretcher or bed along the side the table and engage floor locks. Adjust the height of the stretcher or bed so that it is level with the surface of the frame pads. Assign an attendant to maintain the patient on the frame and remove the circumferential patient safety strap. Using adequate help, roll the patient from the frame to the supine position on the stretcher or bed. NOTE: You may use the lateral tilt feature of the Mizuho OSI Modular Table or general surgery table to facilitate transfer. Position the stretcher or bed lower than the frame pad height and while maintaining the patient on the frame, tilt the table until the lateral edge of the frame pad contacts the edge of the gurney pad. Then roll the patient off the frame as described.
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1.13 Cleaning And Maintenance of RWF Model 5321G & 5319G
After each use, remove and discard all patient care kit components. Clean the entire unit with a quaternary disinfectant (ammonium chloride). Ensure the cleaning solution is labeled for use as a surface disinfectant and utilize per manufacture’s label instructions. Always rinse and wipe dry with a lint free cloth. Avoid the use of alcohol, bleach or other highly concentrated chemicals. Do not soak or place the device in a washer or flood with water or cleaning solutions. Damage to the device due to improper care and cleaning can void the warranty.
Store the crank handle of Model 5321G in the receptacle of the base. Always store the unit with the provided cover in place. The crank handle for Model 5319G should be stored on the storage cart. Utilizing the provided storage for the frame between uses will help protect the frame and minimize breakage and damage. NOTE: Do not place the crank handle into its storage slot in the base of the frame during surgery because it will interfere with radiolucency. NOTE: Do not place the crank handle in the quiver it can result in damage to the crank handle. Before and after each use, inspect the device for damage, excessive wear, or nonfunctioning parts. Carefully inspect all critical, inaccessible areas, joints, and all moveable parts for possible damage or non-function, damaged or defective products should not be used or processed. Contact your local Mizuho OSI representative for repair or replacement.
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1.14 Replacement Parts for RWF Model 5321G & 5319G For detailed repair information and to order replacement parts contact the MIZUHO OSI Customer Resource Group as outlined in Section 1.15 of this manual.
Model 5319G Wilson Frame Replacement Parts Base Channel Assembly 5319-58 (replacement) Case Cover 5319-2
Model 5321G Wilson Frame Replacement Parts Base Channel Assembly 5321-1 (replacement) Cart Assembly 5321-43
Cover Wheel & Axle
Caster Wheel, 2in (4x)
ND0434
Crank Handle w/ Torque Limiter 5319-6
Crank Handle w/ Torque Limiter
5319-6
Gearbox Assembly
5319-7
Gearbox Assembly
5321-7
Lateral Adjustment Assembly
5319-5
Lateral Adjustment Assembly
5321-5
Pad Set (includes R/L pads & installation tool) Gel Pad, Left
5319-36
5319-36
5319-44
Pad Set (includes R/L pads & installation tool) Gel Pad, Left
Gel Pad, Right
5319-45
Gel Pad, Right
5319-45
Pad Installation Tool
5323-84
Pad Installation Tool
5323-84
Patient Care Kit (Case of 6)
5322PV
Patient Care Kit (Case of 6)
5322PV
5319-60
Wilson Plus™ Spring Sleeve, 1 pr. 5319-67
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5319-44
HB5323-51
Security Strap, Hook (2x)
SB200BHZP
Security Strap, Loop (2x)
SB200BLZP
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