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Ultrasound probe cleanign and disinfection

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  • #68999
    Fiona de Sousa
    Participant

    Author:
    Fiona de Sousa

    Position:

    Organisation:

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    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    If you are not the intended recipient you are hereby notified that any dissemination, distribution or reproduction of this message
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    #69002
    Jane Barnett
    Participant

    Author:
    Jane Barnett

    Position:

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    Hi

    We introduced this into our radiology dept for the US probes over a year
    ago now and it seems to work well. The previous processes were really
    inadequate for these items and the chlorine dioxide does achieve high
    level disinfection options without exposure to staff of liquid
    chemicals. The company provided good training to the staff who carry
    this out plus we ensured that there were laminated instruction charts
    with all mobile equipment e.g. used in our gynae emergency area.

    Happy to share the protocol if you contact me.

    Jane Barnett

    Clinical Nurse Specialist

    Infection Prevention & Control

    Christchurch Women’s Hospital

    Private Bag 4711, Christchurch

    Infection Prevention and Control is Everyone’s Business

    Behalf Of Fiona de Sousa
    disinfection

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
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    Adventist Hospital.
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    #69000
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Position:

    Organisation:

    State:

    Hi Fiona

    I have not seen this particular system in Australia, but the questions I would be asking are:

    1. Is the disinfectant licensed with TGA as an instrument-grade disinfectant (ie high level disinfectant)? If not, you cannot proceed as these devices require high level disinfection with a TGA approved disinfectant.

    2. Has the manufacturer / sponsor of the disinfectant provided evidence of materials compatibility with the specific TV probe you use? This preferably would be advice from the probe manufacturer to say the disinfectant is safe to use with the probe.

    Since it is unlikely current Australian guidelines will reference a product that was not on the Australian market when the guidelines were written, this is the process I would follow.

    If both of the above are provided to your satisfaction, form an IC perspective I would be happy to permit the use of the product in a specific situation.

    Cheers

    Michael Wishart

    Public Health Nurse,Communicable Disease Control
    Logan West Moreton PHU
    Ph 34131200 Fax 34131221

    To contact Nursing team:
    LWM_PHN@health.qld.gov.au

    >>> Fiona de Sousa 17/05/2012 1:09 pm >>>

    Hi All,

    I have been asked to review a new cleaning and disinfection system for reprocessing transvaginal ultrasound probes especially those used in IVF related pregnancies where chemical residues are a high concern.
    The system consists of three separate pre-packaged wipes (a cleaner, a disinfectant and a rinse wipe) which I believe is currently used in he UK. The active ingredient in the disinfectant wipe is chlorine dioxide in aqueous solution.

    Has anyone got any experience with this type of system that they would be willing to share with me?

    Kind Regards,

    Fiona De Sousa
    Infection Prevention & Control Coordinator
    Sydney Adventist Hospital
    Mobile: 0408 468 470
    Office: (02) 9487 9732
    Fax: (02) 9472 8053
    Fiona.Desousa@sah.org.au
    185 Fox Valley Road, Wahroonga, NSW, 2076

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    #69001
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Position:

    Organisation:

    State:

    #69004
    Ruth Barratt
    Participant

    Author:
    Ruth Barratt

    Position:

    Organisation:

    State:

    Hi there,

    In Christchurch New Zealand we have introduced this system into our
    radiology unit that undertakes Trans vaginal ultrasonography using
    probes. We investigated the efficacy of the product in depth and it
    seemed to be the best solution for our local area and was an improvement
    on sodium hypochlorite. This was about a year ago. I have no issues with
    the efficacy of Chlorine dioxide for high-level disinfection.

    One of the key things for us is that we have only a few people to train
    to use this system as we have a Hospital Aide who does all the
    reprocessing. As usual any product must be used correctly.

    Hope this helps

    Ruth Barratt

    Ruth Barratt RN, BSc, MAdvPrac (Hons)

    Clinical NurseSpecialist Infection Prevention and Control

    :: ruth.barratt@cdhb.health.nz

    (: + 64 3 3640 083 or ext.80083

    Level 5, Riverside Building

    Christchurch Hospital | Private Bag 4710, Christchurch

    Clean Hands Save Lives!

    Behalf Of Fiona de Sousa
    disinfection

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
    dissemination, distribution or reproduction of this message
    is prohibited. If you have received this message in error please notify
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    Any views expressed in this message are solely those of the individual
    sender, except where the sender is specifically authorised
    by Sydney Adventist Hospital to state that they are the views of Sydney
    Adventist Hospital.
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    #69005
    Sue Kelly
    Participant

    Author:
    Sue Kelly

    Position:

    Organisation:

    State:

    Hi Fiona,

    The three separate wipe system I think you are talking is the Tristel
    Wipe System.

    Thanks,

    Sue Kelly.

    Infection Prevention & Control Practioner,

    Seymour Health.

    Seymour 3660

    Behalf Of Fiona de Sousa

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
    dissemination, distribution or reproduction of this message
    is prohibited. If you have received this message in error please notify
    the sender immediately, then destroy the original message.
    Any views expressed in this message are solely those of the individual
    sender, except where the sender is specifically authorised
    by Sydney Adventist Hospital to state that they are the views of Sydney
    Adventist Hospital.
    _____________________________________________________________________
    This e-mail has been scanned for viruses by Symantec Hosted Services
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    #69006
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Position:

    Organisation:

    State:

    Fiona

    I can’t verify the current status of this information, but there has
    been a previous discussion about this product on this list (November
    2011). This is one of the more comprehensive messages in that group.

    From:AICA Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On
    Behalf Of Glenys.Harrington@HEALTH.VIC.GOV.AU

    Maree and Robert,

    Further to my comments earlier today. I have contacted the TGA for
    further clarification.

    The particular product under discussion in this thread is categorised
    as a “medical device” as it is “intended to be used on medical devices”.

    Such products must be included on the Australian Register of
    Therapeutic Goods Devices (ARTG) before they can be supplied in
    Australia.

    The ARTG form will state the following:

    “Product type: Medical Device – Class …… – Included”

    The key word is “included” which confirms that the product is suitable
    for the ” intended purpose” which is also included on the ARTG form.
    For this particular products the intended purpose on the ARTG form is as
    follows:

    “Intended purpose: The Tristel disinfecting wipes system is intended to
    decontaminate and disinfect non-lumened medical devices that cannot be
    fully immersed in liquid disinfectant or sterilant and cannot be
    sterilised by heat. It allows high level disinfection of instruments
    where automated dishwashers, sinks and water supplies are unavailable.
    The system provides high-level disinfection in less than two minutes.
    The Tristel system is not intended for high level disinfection of
    critical medical devices which must be sterilised prior to use on
    patients”.

    The information above is unclear and ideally should have included
    information about semi critical devices (ie contacts mucous membranes,
    non-intact skin) in addition to critical devices (ie enters normally
    sterile tissue or vascular system). It is also unclear in the intended
    purpose statement reference to the use of the product “where ….sinks
    and water supplies are unavailable” as such devices would before high
    level disinfection need to be meticulously pre-cleaned?

    I am providing TGA with additional information (ie Methods of
    sterilization and disinfection, [Modified Spaulding classification
    system]).

    All ARTG forms can be found by searching the ARTG database available on
    the TGA web page.

    https://www.ebs.tga.gov.au/ebs/ANZTPAR/PublicWeb.nsf/cuDevices?OpenView

    For disinfectants not used on medical devices (ie for general, outbreak
    or isolation cleaning and disinfecting purposes) there are 3 categories:

    1. Hospital grade and commercial/household grade disinfectants with
    specific claims
    2. Hospital grade disinfectants without specific claims
    3. Household or commercial grade disinfectant without specific claims
    (that do not make disinfectant claims)

    1 & 2 must be either “listed” or “registered” on the ARTG.

    The ARTG form will include an “ARTG identifier” with either “Aust L”
    or Aust R” (listed or registered with the TGA). Generally products need
    to be registered to make fungicidal, sporicidal, tuberculocidal and
    viricidal claims (ie with specific claims).

    If a product is not registered in Australia and the
    manufacturer/supplier is making fungicidal, sporicidal, tuberculocidal
    and viricidal claims TGA have asked that you let them know via their
    on-line “Report a perceived breach or questionable practices” at the
    following link and they will follow-up.

    http://www.tga.gov.au/about/form-breach-tgact.htm

    The manufacturer/supplier may not be fully aware of the TGA
    requirements as outlined in the TGA “Guidelines for the Evaluation of
    Sterilants and Disinfectants”.

    Find below additional information provide by the TGA this morning:

    Disinfectants are regulated in a variety of ways in Australia,
    depending on the claims made in the instructions for use, labelling and
    promotional material.

    Type of disinfectant
    How is it regulated?
    Comments

    Sterilants and instrument grade disinfectants (all levels) – intended
    to be used on medical devices
    An accessory to a medical device – Class IIb Must be included on the
    ARTG before they can be supplied in Australia.
    In Europe are regulated as Class IIa. Sponsors importing these products
    need to ensure that the Australian regulatory requirements have been met
    by the manufacturer.
    Undergo a mandatory Level 2 Application Audit.

    Cleaners intended to be used on medical devices

    An accessory to a medical device – Class I
    Must be included on the ARTG before they can be supplied in
    Australia.

    Hospital grade and commercial/household grade disinfectants with
    specific claims*
    ‘Other Therapeutic Goods’ – registered
    Must be registered on the ARTG before they can be supplied in
    Australia.
    Must comply with TGO 54 (
    http://www.tga.gov.au/docs/html/tgo/tgo54.htm ).
    Information to be submitted for review includes instructions for
    use, promotional material, labels, product specifications, and efficacy,
    stability and quality control data.

    Hospital grade disinfectants without specific claims*
    ‘Other Therapeutic Goods’ – listed Must be listed on the ARTG before
    they can be supplied in Australia.
    Must comply with TGO 54 ( http://www.tga.gov.au/docs/html/tgo/tgo54.htm
    ).
    Information to be submitted for review includes instructions for use,
    promotional material and labels.

    Household or commercial grade disinfectant without specific claims*
    ‘Other Therapeutic Goods’ – exempt from listing or registration
    Exempt disinfectants are not required to be entered on the ARTG
    however they still must comply with certain parts of TGO 54 (
    http://www.tga.gov.au/docs/html/tgo/tgo54.htm ), including the
    labelling requirements, and are expected to comply with performance
    requirements.

    Antibacterial cleaning wipes
    Sanitisers
    Sanitary fluids/powders
    (that do not make disinfectant claims)
    Exempt or excluded depending on claims
    Claims determine if exempt from entry on the ARTG or excluded from
    the Therapeutic Goods Act 1989.

    * ‘specific claims’ cover virucidal, sporicidal, tuberculocidal,
    fungicidal or other biocidal activity. Except where claims of activity
    against fungi (yeast and mould) for excluded products are concerned,
    these claims mean a product is registered.
    http://www.tga.gov.au/industry/disinfectants-regulation.htmhttp://www.tga.gov.au/industry/disinfectants-hard-surface.htm

    A hospital grade disinfectant with non-specific claims is a listable
    product
    A hospital grade disinfectant with specific claims is a registerable
    product
    A “non-specific claim” is a claim which includes general antibacterial
    action or activity against bacteria covered by the battery of test
    organisms included in the specified test, or bacteria of the same
    family. Claims for bacteria other than these are allowable and do not
    cause the product to become registerable, but the specific organism
    against which activity is claimed must be included as an extra organism
    in the test battery e.g. E. coli O157, Salmonella spp, Streptococcus
    spp, etc.
    A “specific claim” is one which covers virucidal, sporicidal,
    tuberculocidal, fungicidal or other biocidal activity. Except where
    claims of activity against fungi (yeast and mould) for excluded products
    are concerned, such claims lift a product into the registerable category
    of goods.

    For information on disinfectants:

    Please see TGO 54/54A/54B, which can be accessed at
    http://www.comlaw.gov.au/Details/F2009C00327
    Please see the “Guidelines for evaluation of sterilants and
    disinfectants”, which can be accessed at
    http://www.tga.gov.au/industry/disinfectants-evaluation-guidelines.htm.
    These guidelines describe the information to be supplied to the TGA for
    the registration or listing of disinfectants on the ARTG.

    Yours sincerely,

    Medical Devices Information Line

    Information http://www.tga.gov.au/devices/devices.htm (
    http://aicalist.org.au/scripts/www.tga.gov.au/devices/devices.htm )
    e-Business http://www.ebs.tga.gov.au (
    http://aicalist.org.au/scripts/www.ebs.tga.gov.au )

    Hope this clarifies further.

    regards

    Glenys
    Glenys Harrington, Infection Control Consultant |Communicable Disease
    Prevention and Control | Public Health
    Department of Health | Level 14 50 Lonsdale Street Melbourne Victoria
    3000 Australia
    t. 03 909 65094 | f. 1300 651 170 | e.
    glenys.harrington@health.vic.gov.au | http://www.health.vic.gov.au/ (
    http://aicalist.org.au/scripts/www.health.vic.gov.au/ideas )

    Based on the above, it may be prudent to contact TGA to discuses the
    status of this product prior to approving it’s use within your
    facility.

    Cheers
    Michael Wishart
    ACIPC Infexion Connexion Administrator

    Michael Wishart

    Public Health Nurse,Communicable Disease Control
    Logan West Moreton PHU
    Ph 34131200 Fax 34131221

    To contact Nursing team:
    LWM_PHN@health.qld.gov.au

    >>> Fiona de Sousa 17/05/2012 1:09 pm >>>

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.
    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa
    Infection Prevention & Control Coordinator
    Sydney Adventist Hospital
    ( blocked::blocked::mailto:Fiona.Desousa@sah.org.au
    )Fiona.Desousa@sah.org.au ( blocked::mailto:Fiona.Desousa@sah.org.au
    )
    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
    dissemination, distribution or reproduction of this message
    is prohibited. If you have received this message in error please notify
    the sender immediately, then destroy the original message.
    Any views expressed in this message are solely those of the individual
    sender, except where the sender is specifically authorised
    by Sydney Adventist Hospital to state that they are the views of Sydney
    Adventist Hospital.
    _____________________________________________________________________
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    #69007
    Glenys Harrington
    Participant

    Author:
    Glenys Harrington

    Position:
    Consultant

    Organisation:
    Infection Control Consultancy (ICC)

    State:

    Hi Fiona,

    Three points to add to the discussion:

    1.The particular product under discussion in this thread is categorised as a
    “medical device” as it is “intended to be used on medical devices”. Such
    products must be included on the Australian Register of Therapeutic Goods
    Devices (ARTG) before they can be supplied in Australia. The ARTG form will
    state the following: “Product type: Medical Device – Class …… –
    Included” The key word is “included” which confirms that the product is
    suitable for the ” intended purpose” which is also included on the ARTG
    form. For the particular product that has been named in the thread the
    intended purpose on the ARTG form is as follows:

    “Intended purpose: The ….. disinfecting wipes system is intended to
    decontaminate and disinfect non-lumened medical devices that cannot be fully
    immersed in liquid disinfectant or sterilant and cannot be sterilised by
    heat. It allows high level disinfection of instruments where automated
    dishwashers, sinks and water supplies are unavailable. The system provides
    high-level disinfection in less than two minutes. The Tristel system is not
    intended for high level disinfection of critical medical devices which must
    be sterilised prior to use on patients”.

    2. Another point I would like to raise is do such wipes remove bacteria from
    a surface by the mechanical action of wiping or is the bacteria being
    removed from a surface by the bactericidal action of the ingredient in the
    wipes?

    Microbiological testing results available online indicate that the
    ingredient in the wipes was active against the target organisms that were
    tested in what looks like a suspension tests not a testing method that
    mimics an in use environment/situation. A presentation recently by Dr
    Jean-Yves Maillard in a webber training telecast (
    http://webbertraining.com/index.php
    “Innate Resistance to Sporicides and Potential Failure to Decontaminate”)
    included discussion relating to a 3-step test method to determine efficacy
    of disinfectant wipes using a method described by Williams et al. J Hosp
    Infect 2007;67:329-35. It seems from this presentation that wipes should
    undergo a “3-step wipe testing method” not a suspension test method.

    This would seem reasonable to me particularly for those wipes that are going
    to be used on medical devices and hence have to be registered as a medical
    device.

    3. As you mention in additional to using the “Sporicidal Wipe” you are
    required to use the following:

    . Activated Sporicidal Wipes using a reusable foam pump (? is this
    a time dependent procedure)

    . Pre-Clean Wipe/s and

    . Rinse Wipe/s

    All the wipes are packaged in the one box.

    The method of use as described online would raise the following questions
    for me:

    a) Is there a risk of human error in selecting the wrong wipe during a
    procedure?

    b) The Sporicidal Wipes is activated with what looks like a reusable
    foam pump – is there any risk that this reusable pump can become
    contaminated during use?

    Regards

    Glenys

    Glenys Harrington

    Consultant

    Infection Control Consultancy (ICC)

    PO Box 5202

    Middle Park

    Victoria, 3206

    Australia

    H: +61 3 96902216

    M: +61 404 816 434

    infexion@ozemail.com.au

    ABN 47533508426

    Fiona de Sousa
    disinfection

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he UK.
    The active ingredient in the disinfectant wipe is chlorine dioxide in
    aqueous solution.

    Has anyone got any experience with this type of system that they would be
    willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
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    #69010
    Maree Sommerville
    Participant

    Author:
    Maree Sommerville

    Position:

    Organisation:

    State:

    My organisation made a decision very recently on this subject.

    The 2 choices were the Tristel Wipe system and the Trophon system.

    Both systems are listed on the ARTG and are readily searchable.

    I prepared a paper to present to my committee in order for the committee
    to make a decision as to which is the best choice for us.

    I can send an edited version of this paper upon request. I tried to be
    as unbiased as possible in order for my committee to make an impartial
    decision.

    The decision made was for the Trophon and the rationale was because it
    was automated.

    The weakness with the Tristel system is ‘user’ fallibility.

    There is no doubt the Tristel is easy and significantly cheaper.
    However it is harder to measure that correct contact time for the active
    ingredient to be effective. What happens in a busy unit with a doctor/
    sonographer in a hurry to complete the list?

    Trophon has significant ongoing cost implications with consumables and
    once the warranty is expired, ongoing service costs.

    It is a tough decision. Cost of product versus a guarantee of user
    compliance with the process.

    As one of my colleagues said … if we can’t get hand hygiene right
    among some staff, can we expect them to get this right!!!

    Maree Sommerville

    Infection Control Nurse Consultant

    Mercy Hospital for Women

    8458 4759

    ________________________________

    Behalf Of Fiona de Sousa

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
    dissemination, distribution or reproduction of this message
    is prohibited. If you have received this message in error please notify
    the sender immediately, then destroy the original message.
    Any views expressed in this message are solely those of the individual
    sender, except where the sender is specifically authorised
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    Adventist Hospital.
    _____________________________________________________________________
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    DISCLAIMER This email and any files transmitted with it
    may be confidential and intended solely for the use of the
    individual or entity to whom they are addressed. If you have
    received this email in error please notify the sender immediately
    by return email and delete or destroy this message and its
    attachments. While this email and any attachments have
    been cleared by Mercy Health’s virus protection systems, recipients
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    #69011
    Glenys Harrington
    Participant

    Author:
    Glenys Harrington

    Position:
    Consultant

    Organisation:
    Infection Control Consultancy (ICC)

    State:

    Maree,

    An interesting observation made by your colleagues.

    With the introduction of any new system/equipment it is important to evaluate any potential risks that may be associated with human error and where possible consider alternative engineering controls that have been designed to engineer out such risks.

    Regards

    Glenys

    Glenys Harrington

    Consultant

    Infection Control Consultancy (ICC)

    PO Box 5202

    Middle Park

    Victoria, 3206

    Australia

    H: +61 3 96902216

    M: +61 404 816 434

    infexion@ozemail.com.au

    ABN 47533508426

    My organisation made a decision very recently on this subject.

    The 2 choices were the Tristel Wipe system and the Trophon system.

    Both systems are listed on the ARTG and are readily searchable.

    I prepared a paper to present to my committee in order for the committee to make a decision as to which is the best choice for us.

    I can send an edited version of this paper upon request. I tried to be as unbiased as possible in order for my committee to make an impartial decision.

    The decision made was for the Trophon and the rationale was because it was automated.

    The weakness with the Tristel system is user fallibility.

    There is no doubt the Tristel is easy and significantly cheaper. However it is harder to measure that correct contact time for the active ingredient to be effective. What happens in a busy unit with a doctor/ sonographer in a hurry to complete the list?

    Trophon has significant ongoing cost implications with consumables and once the warranty is expired, ongoing service costs.

    It is a tough decision. Cost of product versus a guarantee of user compliance with the process.

    As one of my colleagues said if we cant get hand hygiene right among some staff, can we expect them to get this right!!!

    Maree Sommerville

    Infection Control Nurse Consultant

    Mercy Hospital for Women

    8458 4759

    _____

    Hi All,

    I have been asked to review a new cleaning and disinfection system for reprocessing transvaginal ultrasound probes especially those used in IVF related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a disinfectant and a rinse wipe) which I believe is currently used in he UK. The active ingredient in the disinfectant wipe is chlorine dioxide in aqueous solution.

    Has anyone got any experience with this type of system that they would be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    If you are not the intended recipient you are hereby notified that any dissemination, distribution or reproduction of this message
    is prohibited. If you have received this message in error please notify the sender immediately, then destroy the original message.
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    by Sydney Adventist Hospital to state that they are the views of Sydney Adventist Hospital.
    _____________________________________________________________________
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    been cleared by Mercy Health’s virus protection systems, recipients
    should use their own systems to detect computer viruses or other
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    #69016
    Anonymous
    Inactive

    Author:
    Anonymous

    Position:

    Organisation:

    State:

    Dear Jayne
    Would this be the Tristel Wipes System? AshMed are canvassing all
    hospitals I believe. We have a trophon EPR and prcessor. We have been
    canvassed but I am a little trepiditious despite the supporting
    literature re introducing. Would love it if you would be happy to share
    your protocol?….and any other feedback/evidence of efficacy etc.

    Cheers

    Liz Vanderlinde
    Infection Control Officer
    North West Private Hospital

    Brickport Road, Burnie TAS 7320, Australia
    T +61 3 6432 6022 F +61 3 6431 6158
    E Liz.Vanderlinde@healthecare.com.au W

    is intended only for the use of the addressee(s) named above and may
    contain information that is privileged or subject to copyright. If you
    are not the intended recipient of this message you are hereby notified
    that you must not disseminate, copy or take any action based upon it.
    Please delete and destroy the message from your computer. If you
    received this message in error please notify Healthe Care Australia
    immediately.

    ________________________________

    Behalf Of Jane Barnett

    Hi

    We introduced this into our radiology dept for the US probes over a year
    ago now and it seems to work well. The previous processes were really
    inadequate for these items and the chlorine dioxide does achieve high
    level disinfection options without exposure to staff of liquid
    chemicals. The company provided good training to the staff who carry
    this out plus we ensured that there were laminated instruction charts
    with all mobile equipment e.g. used in our gynae emergency area.

    Happy to share the protocol if you contact me.

    Jane Barnett

    Clinical Nurse Specialist

    Infection Prevention & Control

    Christchurch Women’s Hospital

    Private Bag 4711, Christchurch

    Infection Prevention and Control is Everyone’s Business

    Behalf Of Fiona de Sousa
    disinfection

    Hi All,

    I have been asked to review a new cleaning and disinfection system for
    reprocessing transvaginal ultrasound probes especially those used in IVF
    related pregnancies where chemical residues are a high concern.

    The system consists of three separate pre-packaged wipes (a cleaner, a
    disinfectant and a rinse wipe) which I believe is currently used in he
    UK. The active ingredient in the disinfectant wipe is chlorine dioxide
    in aqueous solution.

    Has anyone got any experience with this type of system that they would
    be willing to share with me?

    Kind Regards,

    Fiona De Sousa

    Infection Prevention & Control Coordinator

    Sydney Adventist Hospital

    Fiona.Desousa@sah.org.au

    185 Fox Valley Road, Wahroonga, NSW, 2076

    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
    dissemination, distribution or reproduction of this message
    is prohibited. If you have received this message in error please notify
    the sender immediately, then destroy the original message.
    Any views expressed in this message are solely those of the individual
    sender, except where the sender is specifically authorised
    by Sydney Adventist Hospital to state that they are the views of Sydney
    Adventist Hospital.
    _____________________________________________________________________
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