Convalescent Kelly. Directions for Use

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Transcription:

Convalescent Kelly Directions for Use

302-00001 2

Table of Contents Recommends 4 Items Included 5 Skills Taught 5 Airway System 6 Arms 7 Legs 7 Colon Reservoir 8 Genitalia 8 Urinary Catheterization and Enema Simulation 9 Care and Maintenance 10 AHA and ARC Guidelines 10 Warranty 12 Replacement Parts 13 302-00001 3

Convalescent Kelly is a full-body, lifelike manikin, which realistically simulates a hospital patient. It is specifically designed for training professionals in the practice of both CPR and basic nursing skills. The manufacturing quality of this simulator should provide many sessions of training when reasonable care and maintenance are practiced. Recommends: Urinary catheterization - Size 16 French Enema simulation Size 7mm catheter 302-00001 4

Items Included: (1) Convalescent Kelly Manikin (1) Upper Teeth (1) Lower Teeth (3) Reusable Mouthpieces (1) Airway Bags (100) (1) Female Genitalia (1) Male Genitalia (1) Colostomy Plug (1) Gown Skills Taught: Basic Nursing Skills Subcutaneous and intramuscular injection External denture care Catheterization Enema simulation Ostomy irrigation CPR Skills Head tilt/chin lift Obstructed airway CPR Chest Compressions Carotid pulse simulation Abdominal thrust Bandaging and dressing Bed baths Patient moving and lifting 302-00001 5

Preparing the Manikin for Use: Airway System: 1. Unfasten chest skin at shoulders and pull back to expose chest cavity. (Figure1) 2. Attach airway bag to mouthpiece. Fig. 1 (Figure 2) Fig. 2 3. Fold airway bag, being careful not to twist neck of bag. (Figure 3) Fig. 3 4. Insert airway bag through face and under neckpiece of manikin, being careful not to twist or knot airway. 5. Lift flesh colored ventilation cover and spread airway over metal compression plate. (Figure 4) 6. Return flesh colored ventilation cover to its original position. 7. Insert mouthpiece into face of manikin. 8. Reattach chest skin at shoulders. Fig. 4 302-00001 6

To remove, reverse the procedure. Attaching Arms: 1. Unfasten chest skin at shoulders. 2. Pull back to expose flesh colored ventilation cover. 3. Lift ventilation cover. 4. Remove two screws that will release metal ventilation plate - set aside. (Figure 5) 5. Locate hole in shoulder. 6. Remove deltoid injection pad from arm. 7. Unscrew wing nut from bolt in arm. 8. Remove wing nut, two washers and spring. 9. Insert bolt through hole in shoulder. 10. Slide one washer, spring and second washer back over bolt. Use a screwdriver to hold bolt steady while tightening wing nut. Metal Ventilation Fig. 5 To remove, reverse procedure. Attaching Legs: 1. Remove abdominal thrust module and belly plate from manikin. 2. Locate hole in hip. 3. Remove thigh injection pad from leg. 4. Remove wing nut and washer from bolt already inserted in leg. (Leave spring assembly in thigh of leg). 5. Insert bolt through hole in pelvis. 302-00001 7

6. Slide washer and wing nut back over bolt. Use a screwdriver to drive the bolt into wing nut. (Figure 6) Fig. 6 To remove, reverse procedure. Colon Reservoir: Colon reservoir inserts into pelvic cavity with narrow end downward and connector pointing outward. This connector attaches reservoir to rectal valve on genitalia. Reservoir should be removed from manikin, inverted and drained completely before storage. Genitalia: Male and female genitalia have been provided for urinary catheterization and enema training procedures. They are connected with valves. Longer valve connects urethra to urinary reservoir. Shorter valve connects anus to colon reservoir. To attach: Connect cap end of valve screws onto reservoir. Attach other end to genitalia by sliding it on connector and tightening with c-clamp. Before pressing belly plate into position, replace pelvic support pin. 302-00001 8

To disassemble: Lift up on belly module and pull upper portion of genitalia back enough to remove pelvic support pin. Belly module, genitalia with conectors and colon reservoir may now be removed simultaneously. Twist cap to release valve from reservoir. Twist c-clamp to release valve from genitalia. Recommends: The pelvic support pin must be replaced. Failure to replace pin will result in pelvic spread. If this occurs, genitalia will no longer fit properly in manikin. Colostomy Plug Colon Reservoir Urinary Reservoir Blank M d l Abdominal Thrust Module Convalescent Kelly P l i Instructions for Use: Urinary Catheterization and Enema Simulation: After several uses, catheter may tend to hang when water has washed away lubricant, causing friction and binding. If this occurs, generously lubricate a hard catheter and insert into urethra several times. If catheter hangs during removal, work with an in and out motion. Use warm water in reservoirs when possible to keep soap from clogging catheters. Recommends: Catheters should be well lubricated with manikin lubricant or liquid soap prior to use. A size 16 French catheter is recommended for urethral catheterization. A 7mm catheter is recommended for enema simulation. 302-00001 9

Reservoirs must be well drained of all water before disconnecting valves. Care and Maintenance: 1. Clean with mild soap and water; do not submerse manikin or parts in cleaning fluids or water. 2. Use only on clean surface. Avoid felt tipped markers, ink pens, acetone, iodine or other staining products and avoid placing the manikin on newsprint or inked lines of any kind. 3. To ensure longevity, each manikin should be cleaned after each training session and a general inspection should be conducted regularly. 4. Modules and all other parts should be drained and air-dried thoroughly before storage and disinfected when needed. After use of injection pads (use water only), accumulated water should be squeezed out. Do not store wet foam pads in the skin. To prevent mildew or mold, pads can be soaked in a mild solution of disinfectant and water or bleach and water. Squeeze excess solution from pads, allow them to dry, then store or reinsert in manikin. 5. Articulating parts will benefit from a light application of talcum powder prior to training sessions. 6. Store properly between teaching sessions. Follow AHA and ARC guidelines on the cleaning of all CPR manikins as follows: a. Thoroughly wash all external and internal surfaces (also reusable mouthpieces) with warm, soapy water. b. Rinse all surfaces with clean, fresh water. c. Wet all surfaces with a sodium hydrochloride solution having at least 500 ppm free available chlorine (e.g., ¼ cup or 60ml of liquid household bleach to approximately 4 liters of tap water for 10 minutes). This solution must be made fresh at each class and discarded after each use. d. Rinse with fresh water and immediately dry all external surfaces. Rinsing with alcohol will aid in drying internal surfaces. This drying will prevent the survival and growth of bacterial fungal pathogens. e. Each time a different student uses the manikin in a training class, the individual mouthpiece and airway should be changed. 302-00001 10

f. People responsible for the use and maintenance of CPR manikins should be encouraged not to rely totally on the mere presence of a disinfectant to protect them and their students from cross infection during training programs. Emphasis should be placed on the necessity of thorough physical cleaning (scrubbing and wiping) as the first step in an effective decontamination protocol. Microbial contamination is easily removed from smooth, nonporous surfaces by using disposable cleaning cloths moistened with a detergent solution. There is no evidence that a soaking procedure alone in any liquid is as effective as the same procedure accompanied by vigorous scrubbing. g. Thoroughly wash all external and internal surfaces (also reusable mouthpieces) with warm, soapy water. h. Rinse all surfaces with clean, fresh water. i. Wet all surfaces with a sodium hydrochloride solution having at least 500 ppm free available chlorine (e.g., ¼ cup or 60ml of liquid household bleach to approximately 4 liters of tap water for 10 minutes). This solution must be made fresh at each class and discarded after each use. j. Rinse with fresh water and immediately dry all external surfaces. Rinsing with alcohol will aid in drying internal surfaces. This drying will prevent the survival and growth of bacterial fungal pathogens. k. Each time a different student uses the manikin in a training class, the individual mouthpiece and airway should be changed. l. People responsible for the use and maintenance of CPR manikins should be encouraged not to rely totally on the mere presence of a disinfectant to protect them and their students from cross infection during training programs. Emphasis should be placed on the necessity of thorough physical cleaning (scrubbing and wiping) as the first step in an effective decontamination protocol. Microbial contamination is easily removed from smooth, nonporous surfaces by using disposable cleaning cloths moistened with a detergent 302-00001 11

solution. There is no evidence that a soaking procedure alone in any liquid is as effective as the same procedure accompanied by vigorous scrubbing. 302-00001 12

Warranty Medical warrants to the purchaser that its products are free from defects in material and workmanship for a period of one (1) year from the date of purchase by the original user. During the designated one (1) year period, Medical will, upon receipt of a product found to be defective due to materials or workmanship from the purchaser and notification in writing of the defect, at its option repair or replace any parts found to be defective or the entire product. Warranty period does not renew with replacement or repair of original product. Products found to be defective and notification of defects may also be sent to the authorized Medical dealer from whom the product was purchased. All postage, shipping or handling charges shall be the sole responsibility of the purchaser. Medical is responsible for the effects of safety, reliability and performance of its product(s) only if: service, repair, readjustment or modification is carried out by Medical or persons authorized by Medical. the electrical installation of the room where the product is used complies with pertinent equipment requirements. the product is used in the proper manner in strict compliance with its Directions for Use. Medical shall not be liable under this warranty for incidental or consequential damages, or in the event any unauthorized repairs or modifications have been made or attempted, or when the product, or any part thereof, has been damaged by accident, misuse or abuse. This warranty does not cover batteries, fuses, normal wear and tear, excessive use, staining, discoloration or other cosmetic irregularity which does not impede or degrade product performance. Some states in the USA do not allow the exclusion or limitation of incidental or consequential damages, so those limitations or exclusions may not apply to you. 302-00001 13

There are no other express or implied warranties, whether of merchantability, fitness or purpose, or otherwise, on the product, its parts and accessories. 302-00001 14

Replacement Parts: Product Number: Description: 300-01850 Upper Teeth 300-01950 Lower Teeth 100-00150 Mouthpieces (6) 100-00450 Airways (100) 300-00450 Valve/Clamp Set 300-03850 Male Genitalia 300-03950 Female Genitalia 300-04950 Stoma 300-04850 Hospital Gown Please contact Customer Service Representatives for more information on Replacement Parts if needed. (C) Copyright Medical Plastics Laboratory, Inc., Gatesville TX Document #1001620 rev B April 30, 2004 302-00001 15

Norway: LAERDAL MEDICAL AS P.O. Box 377, N-4002 Stavanger Tel. +47 51 51 17 00, Fax +47 51 52 35 57 E-mail: laerdal.norway@laerdal.no Australia: LAERDAL Pty. Ltd. (ABN 47 003 817 490) 23 Edward Street, Oakleigh, Victoria 3166 Tel. +61 3 9569 4055, Toll free 1800 331 565 Fax +61 3 9569 4028, Toll free 1800 635 835 E-mail: customer.service@laerdal.com.au Benelux: "The BeNeLux House" Dijkstraat 54, NL-5554 PS VALKENSWAARD Tel. +31 40 208 58 00, Fax +31 40 208 58 02 E-mail: laerdal.benelux@laerdal.nl Benelux: Belgium and Luxembourg LAERDAL BeNeLux NV Mechelsesteenweg 277, B-1800 VILVOORDE Tel. +32 2 253 36 96, Fax +32 2 253 36 90 E-Mail: info@laerdal.be Canada and Latin America: LAERDAL MEDICAL CANADA LTD. 151 Nashdene Rd., Unit #45 Toronto, ON, Canada, M1V 4C3 Tel. +1 (416) 298-9600, Toll free 888/LAERDAL (523-7325) ou en français (800) 567-9987 Fax +1 (416) 298-8016 E-mail: savelives@laerdal.ca Denmark: LAERDAL DANMARK Postbox 225, DK-8600 Silkeborg Tel. +45 80 333 112, Fax +45 80 333 555 E-mail: laerdal.denmark@laerdal.no Eastern Europe: LAERDAL C.E. EUROPE A-1060 Vienna, Mariahilferstr. 1d/1/3 Tel - Fax +43 15877140, Tel. +43 15815927 E-mail: mstam@aon.at Far East: LAERDAL Singapore Pte Ltd No 1 Marine Parade Central #13-05, Parkway Centre Singapore 449408 Tel. +65 63464259, Fax +65 63467523 E-mail: admin@laerdal.com.sg Finland: LAERDAL OY Vattuniemenranta 2, 00210 HELSINKI Puhelin +358 (0)9-612 99 80, Telekopio +358 (0)9-692 77 99 E-mail: laerdal.finland@laerdal.no France: LAERDAL MEDICAL FRANCE 1 rue des Vergers - Bâtiment n 5-69578 Limonest Cedex Tél. +33 (0)4 72 52 02 52, Fax +33 (0)4 78 35 38 45 E-mail: laerdal.france@laerdal.no Germany: LAERDAL MEDICAL DEUTCHLAND GmbH Am Loferfeld 56, 81249 München Tel. +49 (0)89 / 864 954-0, Fax +49 (0)89 / 864 34 84 E-mail: info@laerdal.de Italy: LAERDAL ITALIA s.r.l. Via Piero Gobetti 52/2 int.z, 40129 Bologna Tel. +39 051-355587, Fax +39 051-355598 E-mail: laerdal.italia@laerdal.no. Japan: LAERDAL MEDICAL JAPAN K..K.. Shinjuku IS Bldg.. 8F 2-13-12, Shinjuku, Shinjuku-ku, Tokyo 160-0022 Tel. 81-3-5919-2121, Fax: 81-3-5919-2122 E-mail: laerdal.japan@laerdal.co.jp Malaysia: LAERDAL HOSPILINE Sdn Bhd 12 Jalan Titir 33/25, Section 33, Shah Alam Technology Park, 40400 Shah Alam, Selangor Darul Ehsan, Tel +60 (3) 5122-7002, Fax +60 (3) 5122-5650 E-mail: customer.service@.com.my New Zealand: LAERDAL NEW ZEALAND Ltd (GST Number 79-403-636) PO Box 302664, North Harbour, Auckland 1330 Tel. +61 3 9564 4066, Toll free 0800 523 732 Fax +61 3 9563 3368, Toll free 0800 528 852 E-mail: customer.service@laerdal.co.nz Portugal: LAERDAL ESPANA, Sucursal em Portugal Rua da Bela Vista à Graca, no.31 A. Escritorio 9, 1170-054 Lisboa Tel. (+351)-21-816-6567, Fax (+351)-21-816-6568, Mob. (+351)-918765367 Spain: LAERDAL ESPANA, S.L. Manuel Tovar 19, 28034 Madrid Tel. (+34) 902-291110, Fax (+34) (91)-7291125 E-mail: laerdal.spain@laerdal.no Sweden: LAERDAL MEDICAL AB Box 2064, Paviljongvägen 3-5, 132 02 Saltsjö-Boo Tel. +46 (0)8-55614610, Fax +46 (0)8-55614619 E-mail:.sweden@laerdal.se United Kingdom: LAERDAL MEDICAL LTD. House, Goodmead Road, Orpington, Kent BR6 0HX Tel. +44 (0)1689 876634, Fax +44 (0)1689 873800 E-mail: customer.service@laerdal.co.uk USA LAERDAL MEDICAL CORPORATION 167 Myers Corners Road, P.O. Box 1840 Wappingers Falls, New York 12590-8840 Tel. (800) 431-1055, +1 (845) 297-7770 Fax (800) 227-1143, +1 (845) 298-4545 E-mail: customerservice@laerdal.com LAERDAL TEXAS P.O. Box 38, 226 FM 116 South Gatesville, Texas 76528-0038 Tel. (800) 433-5539, (254) 865-7221 Telefax (254) 865-8011 E-mail: services@laerdaltx.com 302-00001 16