Posey Wheelchair Lap Trays User Manual

lAp top trAYs
Applicable Products:
REF
8220, 8221
ApplicAtion
DEscription oF proDuct: Activity lap top tray for wheelchairs or similar non-wheelchair applications.
8221
inDicAtions For usE:
• Patientswhohavepooruppertorsoalignmentand/orneeda
LATEX
firm surface to rest their elbows on.
• Patientswhorequireananteriorposturesupport.
• Patientswhorequireaworkareaoreatingareaontheirwheelchairor
similar non-wheelchair applications.
• Productapplicationsconsidered“self-release”or“assisted-release”
must be specified by the ordering physician.
contrAinDicAtions:
• DO NOT use on a patient who is or becomes highly aggressive, combative, agitated, or suicidal.
• STOP USE AT ONCE: if the patient is at risk to slide forward or down in the device.
NOTE: A restraint with a pelvic piece will help to reduce the risk of sliding. See Posey Catalog.
• DO NOT use on a patient who is unwilling or unable to follow instructions, and is at risk of a
fall or re-injury from self-release.
ADVErsE rEActions
• Severeemotional,psychological,orphysicalproblemsmayoccur:iftheapplieddeviceis
uncomfortable; or if it severely limits movement. If symptoms of these problems ever appear
posEY lAp top trAYs
REF
8220 Clear Lap Top Tray
for any reason, get help from a qualified medical authority and find a less restrictive, product or intervention.
22”L x 20½” x ½” ick (56 cm x 52 cm x 1.3 cm)
REF
8221 Padded Lap Top Tray 22”L x 20½” x ½” ick (56 cm x 52 cm x 1.3 cm)
rx onlY
8220
notE: ese products are designed for use on full-length arm
wheelchairs or other similarly equipped non-wheelchair applications.
ApplicAtion instructions:
1. Seat the patient in the chair with the hips resting firmly
against the seat backrest.
2. Put the lap top tray on the armrest, so it doesn’t interfere
with breathing.
3. Secure the lap top tray to the arm rest using the provided
“hook and loop” straps. ere are two straps on each side. Either the front strap, back strap, or both may be used depending on the patient’s assessment.
4. If necessary, use the strap around the back of the chair to
prevent the tray from being pushed forward.
Posey Company • 5635 Peck Road, Arcadia, CA 91006-0020 USA • www.posey.com Phone: 1.800.447.6739 or 1.626.443.3143 • Fax: 1.800.767.3933 or 1.626.443.5014
© 2009 Posey Company. All rights reserved.
be snug, but not interfere with breathing
is device should ALWAYS
or circulation. After application, slide an open hand (flat) between the device and patient to ensure proper fit. ALWAYS monitor a patient to make sure the patient is not able to slide down, under
FiG. 1
the device, and fall off the chair seat (fig. 1). If a patient’s body weight becomes suspended off the chair, chest compression and suffocation could result. Restraints with a pelvic piece may be necessary to reduce sliding down.
ADDitionAl sAFEtY AnD lAunDErinG
instructions on othEr siDE
MDSS GmbH
EC REP
Schiffgraben 41 D-30175 Hannover, Germany
I9248 052009
Safety Information for the Use of Posey Wheelchair/Gerichair Lap Products
WARNING:
Improper application or use of any restraint may result in serious injury or death.
ALWAYS Monitor patients per facility policy.
RX ONLY. NOT FOR HOME USE. Federal law (USA) restricts this
device to sale by or on order of a physician. For use in a licensed healthcare facility only.
STAFF TRAINING: Staff must have on going training and be able to demonstrate competency to use this device in accord with: Posey instructions; your facility policies and state and federal regulations (Federal Register, Part IV, 42 CFR Part 482.13(e)(5) and (f) (6); Posey offers inservice training aids at no charge. Contact Posey online at www.posey.com or call toll-free at 1.800.447.6739 (press 5).
SELECTING THE RIGHT POSEY PRODUCT: Refer to the Posey catalog to help select the right device to meet individual patients’ needs.
BEFORE APPLYING ANY RESTRAINT:
• Make a complete assessment of the patient to ensure restraint use is appropriate.
• Identify the patient’s symptoms and, if possible, remove the cause. You may need to: cater to individual needs and routines; increase rehabilitation and restorative nursing; modify the environment; or increase supervision.
• Use a restraint only when all other options have failed. Use the least restrictive device, for the shortest time, until you find a less restrictive alternative. Patients have the right to be free from restraint.
• Obtain informed consent from the patient or guardian prior to use. Explain the reason for restraint use to the patient and/or guardian to help ensure cooperation.
• A restraint must only be used in accord with the patient’s Individualized Care Plan (ICP). The ICP is an assessment by an interdisciplinary team, which may include, but is not limited to: PT, OT, Nursing, the Physician, and Social Services. The ICP should include: restorative nursing; patient release; and pressure sore prevention.
NOTE: Just as patient behavior is not 100% predictable, no product is
100% foolproof. Patient safety requires regular reassessment and monitoring per facility policy. A product that worked in the past may be inappropriate if the patient’s mental or physical health status changes. NEVER apply any product that you feel is unsafe. Consult with the proper medical authority if you have questions about patient safety.
ADDITIONAL WARNINGS:
1. ALWAYS monitor patient per facility policy. Be aware that constant monitoring may be required for:
• Aggressive or agitated patients; and
• Patients deemed at risk of aspirating their vomit. This includes patients who are not able to sit up. If
the patient vomits, he or she could aspirate the vomit and
suffocate.
• Be prepared to intervene at the first sign of danger. Such patients require frequent review and evaluation of their physical and psychological status.
2. This device should ALWAYS be snug, but not interfere with breathing or circulation. After application, slide an open hand (flat) between the device and patient to ensure proper fit. ALWAYS monitor a patient to make sure the patient is not able to slide down, under the device, and fall off the chair seat. If a patient’s body weight becomes suspended off the chair, chest compression and suffocation could result. Restraints with a pelvic piece may be necessary to reduce sliding down.
3. NEVER alter or repair this product. ALWAYS Inspect before each use: Check for broken stitches
or parts; torn, cut or frayed material; or locks, buckles, or hook and loop fasteners that do not hold securely. DO NOT use soiled or damaged products. Doing so may result in serious injury or death. Dispose of damaged products per facility policy for BIOHAZARDOUS material.
4. NEVER use Posey products on toilets, or on any chair or furniture that does not allow proper application as directed in the Application Instructions. DO NOT use at home.
5. NEVER expose this product to open flame, fire, smoking materials, or high heat sources. Some
products may melt or ignite and burn. The facility smoking/no smoking policy should be strictly enforced.
6. NEVER use a Posey product as a seat belt in a moving vehicle. Posey products are not designed to withstand the force of a crash or sudden stop.
CLEANING INSTRUCTIONS:
Vinyl Products:
• Wipe Clean with mild detergent. OSHA approved intermediate level disinfectants can be used per manufacturer instructions. DO NOT use phenol and benzyl based disinfectants.
• After cleaning, products MUST be rinsed with water to remove any residual chemicals.
• Make sure products are completely dry before use.
Test Zippers and hook and loop fasteners before each use. DISCARD device if it does not fasten securely.
STORAGE AND HANDLING:
• This device is designed for use in normal indoor environments.
• This device may be stored in ambient warehouse temperatures at normal humidity levels. Avoid excess moisture or high humidity that may damage product materials.
Posey Company • 5635 Peck Road, Arcadia, CA 91006-0020 USA • www.posey.com Phone: 1.800.447.6739 or 1.626.443.3143 • Fax: 1.800.767.3933 or 1.626.443.5014
© 2012 Posey Company. All rights reserved.
EC REP
MDSS GmbH Schiffgraben 41 D-30175 Hannover, Germany
I9200C REV B 092412
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