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The device was not returned for evaluation.The lot number is unknown therefore the device history record could not be reviewed.The instructions for use state the following: "bard® dignishield® stool management system sms002 indications for use: the bard® dignishield® stool management system (sms) with odor barrier properties is intended for fecal management by diverting and collecting liquid or semi-liquid stool to minimize skin contact in bedridden patients and to provide access for the administration of medications.Adult use only.Device description: the bard® dignishield® sms device consists of a catheter tube assembly, a collection bag (figure 1), a 60 ml syringe, a syringe of lubricating jelly and a biological odor eliminator.The device has no components made of natural rubber latex.Figure 1 ¿ catheter tube assembly and collection bag position indicator line contents: ¿ catheter tube assembly (figure 1 includes collection bag) ¿ collection bag ¿ 60 ml syringe ¿ lubricating jelly syringe (10 ml) ¿ instructions for use ¿ 1 bottle (1 oz) of medi-aire® biological odor eliminator ¿ tube clamp the bard® dignishield® sms catheter tube assembly consists of a catheter body and collection bag assembly that is primarily constructed of a proprietary copolymer material called permalene¿, bonded to a low-pressure retention cuff and trans-sphincteric zone (tsz) primarily constructed of silicone material.The permalene¿ catheter and collection bag material is designed to minimize permeation of gas and water vapor.The low-pressure retention cuff is designed to retain the device in the rectum.The tube opening at the cuff is funnel-shaped to aid in diverting the stool into the drainage tube.The cuff leads to the tsz segment, which is designed to minimize dilation of the sphincter during use while providing a channel for fecal matter to pass through drainage tube and into the collection bag.Along the drainage tube are three lumens, each with a separate access port.The green inflation port (¿inf(45ml)/inflate to 45ml¿) is used to inflate/deflate the cuff.The clear irrigation port (¿irrig¿) is used to infuse water at the end of the retention cuff and to provide access for the administration of medication.The purple flush port (¿flush¿) is used to infuse water through slits for the entire length of the drainage tube to assist drainage of fecal matter.(figure 2) a sample port on the drainage tube allows for the collection of stool samples through a slip-tip syringe.A piston valve connector located on the end of the drainage tube of the catheter attaches to the collection bag hub socket.When the collection bag is disengaged from the catheter, the catheter and bag automatically close to prevent spillage.A bag cap is provided to secure the contents of the collection bag when the catheter is removed.The 60 ml syringe and lubricating jelly syringe are used in the preparation and use of the catheter.The medi-aire® biological odor eliminator may be used as an air freshener in the room.Do not spray on patient or device.The tube clamp is used to retain medication during administration of medication.Figure 2 ¿ description of drainage tube ports the catheter contains four ports.Label port color label definition inf(45ml)/inflate to 45 ml green (matches the cuff color) inflation port for retention cuff, specifies recommended inflation volume flush purple flushing port irrig clear irrigation port/port for administration of medication white sampling port contraindications ¿ do not use for more than 29 consecutive days.The uninterrupted use for this device, including immediate replacement with the same or an identical device, is intended to be 29 days or less.¿ do not use on patients known to be sensitive to or allergic to any components within the system.¿ do not use on patients who had lower large bowel or rectal surgery within the last year.¿ do not use on patients with any rectal or anal injury, severe rectal or anal stricture or stenosis (or on any patient if the distal rectum cannot accommodate the inflated cuff), confirmed rectal or anal tumor, severe hemorrhoids, or fecal impaction.¿ do not use on patients with suspected or confirmed rectal mucosa impairment, i.E.Severe proctitis, ischemic proctitis, mucosal ulcerations.¿ do not use on patients with indwelling rectal or anal device (e.G.Thermometer) or delivery mechanism (e.G.Suppositories) or enemas in place.Warnings ¿ there is a potential risk of misconnections with connectors from other healthcare applications, such as intravenous equipment, breathing and driving gas systems, urethral/urinary, limb cuff inflation, neuraxial devices and other enteral and gastric applications.¿ do not use if package is opened or damaged.¿ do not use improper amount or type of fluids for irrigation/flush or cuff inflations.Never use hot liquids.¿ do not over inflate retention cuff.¿ use only gravity or slow manual irrigation.Do not connect mechanical pumping devices to catheter irrigation port.Do not irrigate patient with compromised intestinal wall integrity.¿ rectal bleeding should be investigated to ensure no evidence of pressure necrosis from the device.Discontinuation of use is recommended if pressure necrosis is evident.¿ abdominal distention that occurs while using the device should be investigated.¿ prolonged traction on the catheter may result in the retention cuff migrating into the anal canal which may result in mucosal lesion, temporary or permanent clinical sphincter dysfunction, or catheter expulsion.¿ solid or soft-formed stool cannot pass through the catheter and will obstruct the opening.The use of the device is not indicated for patients with solid or soft formed stool.¿ single use only.Do not reuse.Reuse and/or packaging may create a risk possibly resulting in patient or user infection.Structural integrity and/or essential material and design characteristics of the device, may be compromised, which may lead to device failure and/or lead to injury, illness or death of the patient.Precautions ¿ caution: federal (u.S.A.) law restricts this device to sale by or on the order of a physician.¿ do not sterilize.¿ close attention should be paid to the use of the device in patients who have inflammatory bowel conditions.The physician should determine the degree and location of inflammation within the colon/rectum prior to considering use of this device in patients with such conditions.Ensure retention cuff and funnel are folded into a low profile form prior to insertion (as shown in figure 4).¿ patients with very weak sphincter muscles may not be able to retain the device in place and may experience increased leakage of stool.¿ if the catheter becomes blocked with solid particles, it may be flushed with water (see figure 8 - ¿flushing the device¿).If obstruction of the catheter is due to solid stool, use of the device should be discontinued.¿ to avoid injury to the patient, do not insert anything into the anal canal while this device is in place (e.G.Thermometer, suppositories, etc.).Remove the device prior to insertion of anything into the anal canal.¿ notify a physician if any of the following occur: o persistent rectal pain o rectal bleeding o abdominal distension ¿ if the patient¿s bowel control, consistency and frequency of stool begin to return to normal, discontinue use of the device.¿ caution should be exercised in using this device in patients who have a tendency to bleed from either anticoagulant / antiplatelet therapy or underlying disease.¿ when using the tube clamp for medication delivery, ensure the patient is closely monitored and is not allowed to lie on the tube clamp.¿ ensure the tube clamp is only used during medication delivery and for the prescribed dwell time.Do not leave the tube clamp on the drainage tube for longer than the prescribed dwell time.Potential adverse events as with the use of any rectal device, the following adverse events may occur: o excessive leakage of stool around the device o loss of anal sphincter muscle tone which could lead to temporary or permanent anal sphincter dysfunction o pressure necrosis of rectal or anal mucosa o infection o bowel obstruction o perforation of the bowel o rectal bleeding o rectal tear o ulceration of rectal/anal mucosa instructions for use 1.Preparation of sms prior to insertion a.Verify the retention cuff has been completely deflated.This can be done by squeezing the cuff to ensure there is no residual air inside the device.1) if air remains within the cuff, attach the 60 ml syringe to the green inflation port and withdraw all remaining air from the cuff.B.After the cuff has been fully deflated, fill the syringe with 45 ml of water and set aside.C.Using a permanent marker, record the catheter insertion date on the label located on the piston valve connector.2.Collection bag connection a.Attaching the collection bag: 1) attach the collection bag to the piston valve connector on the catheter by pulling back on the green trigger switch and engaging the piston valve connector onto the collection bag hub socket.(figure 3-a, b) 2) ensure that the green ring at the base of the collection bag hub socket is not visible.The green ring at the base of the collection bag hub socket will not be visible when the piston valve is properly connected.Figure 3 ¿ attaching the collection bag a b 3.Preparation of patient a.The preferred patient position for catheter insertion is the left lateral knee-chest position, although the patient¿s clinical situation may dictate the use of an alternate position.The goal of patient positioning is to maximize sphincter relaxation to ease catheter insertion.B.Perform a digital rectal exam to evaluate for fecal impaction.If a fecal impaction is present, disimpaction procedure and device insertion may occur at the discretion of the healthcare professional.4.Insertion of device a.Unfold the length of the catheter to lay flat on the bed, extending the collection bag towards the foot of the bed.B.Attach the 60 ml syringe filled with 45 ml of water to the inflation port, but do not inflate.C.Insert the inflation cuff using a four-step process: 1) as previously stated in step 1, ¿preparation of sms prior to insertion¿, ensure the retention cuff is completely deflated.(figure 4a) 2) holding the left point of the cuff between the thumb and index finger, fold the top right point of the cuff down and to the left in a 45 degree angle (figure 4b), in order to create a conical shape with a leading edge for easy insertion.(figure 4c) 3) generously coat the patient¿s anus with lubricating jelly.4) gently insert the cuff end through the anal sphincter until the cuff is beyond the external orifice and well inside the rectal vault.(figure 4d and figure 4e).Figure 4 (a-c) ¿ folding the retention cuff fold the top right point of the cuff down and to the left in a 45 degree angle, using the left point as a vertex in order to create a conical shape with a leading edge for easy insertion.Figure 4 (d-e) ¿ inserting the device d e d.Inflate the cuff with 45 ml of water by slowly depressing the syringe plunger.The green inflation port has an external pilot balloon used as a guide to determine proper inflation; as the cuff inflates, the pilot balloon also inflates.The pilot balloon should be used as a reference to determine proper cuff inflation (figure 5).If the pilot balloon indicates over - or under - inflation, use the syringe to withdraw the fluid from the cuff, reposition the cuff in the rectal vault and reinflate.Ensure the inflation port remains parallel to the catheter in order to prevent kinking of the inflation lumen and blockage of injected fluid.Figure 5 ¿ cuff inflation grasp the catheter and gently insert the cuff end through the anal sphincter until the cuff is beyond the external orifice and well inside the rectal vault.Inflate the cuff with 45 ml of water by slowly depressing the syringe plunger.The inflation port has an external pilot balloon as a guide to determine proper inflation; as the cuff inflates, the pilot balloon also inflates.The pilot balloon should be used as a reference to determine proper cuff inflation.Position indicator line pilot balloon e.Remove the syringe from the green inflation port and gently pull on the drainage catheter to check that the cuff is securely in the rectum and that it is positioned against the rectal floor.(figure 6) f.Position the length of the flexible drainage tube along the patient¿s leg, avoiding kinks, obstruction and tension.¿ take note of the black position indicator line that is printed in the proximal segment of the tsz.Observe its relative position to the patient¿s anus.Observe changes in the location of the position indicator band as a means to determine movement of the retention cuff in the patient¿s rectum.This may indicate the need for the cuff or drainage tube to be repositioned.G.Hang the bag using the built-in hanger at a convenient location on the bedside (below the level of the patient¿s rectum).Figure 6 ¿ proper cuff placement against the rectal floor remove the syringe from the inflation port and gently pull on the drainage tube to check that the cuff is securely in the rectum and that it is positioned against the rectal floor.5.Irrigation of the retention cuff if the retention cuff area becomes obstructed with fecal matter, it may be irrigated by filling a syringe with tap water, attaching the syringe to the clear irrigation port and depressing the plunger (figure 7).Make sure the irrigation port remains parallel to the catheter in order to prevent kinking in the tubing and blockage of the injected water.Repeat the procedure as often as necessary to maintain proper functioning of the device.Ensure that water drains.Figure 7 ¿ irrigation of the retention cuff if the funnel or retention cuff area becomes clogged with solid particles, it may be irrigated by filling the syringe with water, attaching the syringe to the clear irrigation port and depressing the plunger.6.Flushing of the drainage tube if the drainage tube becomes obstructed with fecal matter, flush the tube by filling a syringe with tap water, attaching the syringe to the purple ¿flush¿ port, and depressing the plunger.Make sure the flush port remains parallel to the catheter in order to prevent kinking in the tubing and blockage of the injected water.This is used to maintain an unobstructed flow of stool into the collection bag (figure 8).If repeated flushing with water does not return the flow of stool through the catheter, the device should be inspected to determine if there is an external obstruction (i.E.Pressure from a body part or piece of equipment).If no source of obstruction of the device is detected, use of the device should be discontinued.Figure 8 ¿ flushing the device if the drainage tube becomes clogged, flush the device by filling the syringe with tap water, attaching the syringe to the purple ¿flush¿ port, and depressing the plunger.7.Administration of medication a.Confirm the irrigation line is clear by attaching a luer lock syringe to the clear irrigation port (labeled ¿irrig¿) and flushing the system with water.B.Locate the tube clamp and place near the patient.(the tube clamp comes preattached to the piston valve hanger string.) c.Attach a luer lock syringe with the medication to be delivered (dosage as indicated and as prescribed by the treating physician) to the clear irrigation port (labeled ¿irrig¿).Elevate the drainage tubing to facilitate medication retention and infuse the prescribed amount of medication.To ensure delivery of medication into the rectum, immediately flush the irrigation line with at least 10 ml of water (or volume per physician's orders).Note: some medication will reside between the clamp and the device opening.D.Slide the tube clamp onto the drainage tube until the drainage tube contacts the hinge (figure 9).Position the tube clamp as close to the patient¿s buttocks as possible without touching the patient¿s skin.E.Using two hands to facilitate ease of closure, place thumb on thumb to snap the tube clamp shut (figure 10).Ensure the patient does not lie on the tube clamp.If the clamp is difficult to close or excessive leakage of medication is observed, reposition the tube clamp on the drainage tube.F.Dispose of the syringe according to institutional policy.G.After the prescribed dwell time, remove the tube clamp and reattach to the piston valve hanger string.Verify unobstructed flow from the patient into the collection bag.Figure 9 - positioning the tube clamp.Figure 10 - securing the tube clamp.8.Stool sampling a.Uncap the white sample port (figure 11a).B.Gently kink the catheter segment between the piston valve connector and the sample port (figure 11b).C.Tilt or milk the catheter to collect fecal matter around the sample port.D.Insert a slip-tip syringe into the sample port valve and draw the appropriate sample of fecal matter into the syringe (figure 11c).Withdraw the syringe.E.Secure the white cap back onto the sample port (figure 11d).Figure 11 ¿ stool sampling 9.Removal/replacement of the collection bag to remove the collection bag, grab the piston valve connector, gently pull backward on the switch located on the slide of the connector until the piston ejects from the collection bag hub.The piston valve and bag hub should close off automatically in this process.Once the bag is removed, insert the bag cap into the hub connector (figure 12) and dispose of the collection bag in accordance with institutional protocol for disposal of medical waste.Replace the collection bag by securely snapping a new bag to the connector (reference step 2).Collection bag reorder # is sms2b1l.A.Collection bag removal / replacement: 1) remove the collection bag by pulling back on the green slide and the piston valve until it disengages from the collection bag hub socket (figure 12a).2) insert the bag cap onto the bag hub socket and dispose of the bag in accordance with hospital policy and protocols (figure 12b).3) collection bag reorder number: sms2b1l.Figure 12 ¿ bag removal and cap plugging 10.Removal of device a.To remove the catheter from the rectum, the retention cuff must be deflated.1) attach the 60 ml syringe to the green inflation port, and slowly withdraw all water from the retention cuff.(figure 13) b.Make sure the inflation port remains parallel to the catheter in order to prevent kinking in the tubing and blockage of fluid.Refer to ideal patient positioning described in step 3a.1) once you have ensured the cuff is fully deflated, disconnect the syringe and discard.2) to facilitate removal, you may add an appropriate amount of lubricant to the anal sphincter prior to pulling back on the catheter to remove the cuff.3) grasp the catheter as close to the patient as possible and slowly slide the cuff out of the anus.Dispose of the device in accordance with institutional protocol for disposal of medical waste.Figure 13 ¿ deflating retention cuff to remove the catheter from the rectum, the retention cuff must be deflated.Attach the syringe to the green inflation port, and slowly withdraw all water from the retention cuff.11.System care, maintenance, and monitoring of device a.Take note of the black position indicator line that is printed in the proximal segment of the tsz.Observe its relative position to the patient¿s anus.Observe changes in the location of the position indicator band as a means to determine movement of the retention cuff in the patient¿s rectum.This may indicate the need for the cuff or drainage tube to be repositioned.B.Change the collection bag as needed.C.Secure the bag cap onto each used collection bag and discard according to institutional protocol for disposal of medical waste.D.To ensure unobstructed flow of fecal matter from the drainage tube to the collection bag, frequently verify that the catheter and collection bag are positioned so that the catheter is not twisted, kinked, or externally compressed.E.Frequently verify that waste is not accumulating in the catheter drainage tube.F.Verify patient is not lying on drainage tube or ports in such a manner as to potentially cause discomfort or localized prolonged pressure.G.Check the retention cuff volume regularly to ensure proper inflation.Medi-aire® biological odor eliminator net contents: 1 fl oz (30 ml) medi-aire® spray is a unique, powerful odor eliminator formulated to quickly counteract offensive odors from urine, feces, emesis and even necrotic tissue.Directions for use: pump sprayer once or twice.Direct spray away from patient.Contains: water, sd alcohol 40, triethylene glycol, benzethonium chloride, d&c color, tetrasodium edta.Caution: may be harmful if swallowed.Avoid eye contact.Keep out of reach of children.General guidelines: the device may be replaced as needed, to perform patient assessment.For medical or technical questions, please contact medical services and support 800-227-3357.If further information or guidelines are needed, please contact bard medical, at the address below: c.R.Bard, inc.Covington, ga 30014 usa 1-800-526-4455 assembled in mexico www.Bardmedical.Com bard, dignishield, medi-aire and permalene are trademarks and/or registered trademarks of c.R.Bard, inc.©2015 c.R.Bard, inc.All rights reserved.".
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