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Michael Wishart

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  • in reply to: Surgical hand scrub #69122
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

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    Hi all

    Along the lines of Matthias’ post, has anyone yet seen any standardised protocols for Australian HCW’s from any Australian college or association? I think that ACORN was working on something, and possibly RACS, but I have not yet seen anything. Has any other Australian professional entity produced some usage protocols for surgical antisepsis with waterless agents yet?

    I am not asking about protocols developed by manufacturers or suppliers.

    Thanks
    Michael

    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

    >>> “Matthias Maiwald (KKH)” 15/06/2012 11:05 am >>>

    Dear Prue, dear Colleagues,

    Just wanted to add one aspect to the discussion on alcohol-based surgical hand antisepsis: this is the importance of technique.

    I realise there are differences between countries/settings where this is newly introduced versus those where this has been standard practice in operating theatres for many decades.

    An example where this has been newly introduced and apparently failed due to non-adherence to proper technique is here:

    http://www.ncbi.nlm.nih.gov/pubmed/20103542

    In settings where this has been practiced for a long time such procedures become highly ritualised and are being watched by a number of (sometimes fierce) operating theatre nurses and surgeons, to make sure that every new person adheres to this.

    A fundamental difference between simple ward-based hand antisepsis (such as for the 5 Moments) and surgical hand antisepsis is that for the former, a single volume of hand rub of about 3 mL is applied. For surgical hand antisepsis, the WHO 2009 Guideline recommends repeated application of about 15 mL to hands and forearms, but also states that one study demonstrated that keeping the hands and forearms literally wet with alcohol for the entire duration of the procedure is more important than the actual volume applied.

    The latter would require re-thinking for those who are only used to the 5-Moments-type hand rub with about 3 mL, and is one reason why I do not recommend gels (but instead liquids) for surgical hand antisepsis — gels would just build up too much sludge when applied as required for surgical hand antisepsis.

    As already mentioned, another article is here:

    http://www.ncbi.nlm.nih.gov/pubmed/19716627

    Best regards, Matthias.


    Matthias Maiwald, MD, FRCPA
    Consultant in Microbiology
    Adj. Assoc. Prof., Natl. Univ. Singapore
    Department of Pathology and Laboratory Medicine
    KK Women’s and Children’s Hospital
    100 Bukit Timah Road
    Singapore 229899
    Tel. +65 6394 8725 (Office)
    Tel. +65 6394 1389 (Laboratory)
    Fax +65 6394 1387

    From: ACIPC Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On Behalf Of Prue Wright
    Sent: Friday, 15 June, 2012 5:28 AM
    To: AICALIST@AICALIST.ORG.AU
    Subject: Re: Surgical hand scrub

    Hi All,
    We have introduced Skinman which is an alcoholic based surgical scrub. It is very popular with the surgeons and scrub staff. Many of us have problems with dermatitis from traditional water based scrubbing, these have been resolved with the Skinman.

    Prue Wright
    Infection Control Coordinator
    Hurstville Private Hospital
    37 Gloucester Rd, Hurstville, NSW 2220, Australia
    T +61 2 9579 7780 F +61 2 9579 7466
    E Infection.Control@hurstvilleprivate.com.au W healthecare.com.au

    From: ACIPC Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On Behalf Of Tracy Sloane
    Sent: Wednesday, 13 June 2012 9:19 AM
    To: AICALIST@AICALIST.ORG.AU
    Subject: Re: Surgical hand scrub

    Hi All,
    If you check out the latest edition of Healthcare Infections you will find an article about a study I did prior to TGA approval of a surgical hand rub (SHR) looking at HCW current scrub practices and their knowledge and attitudes about SHR. You might find the reference list helpful.
    Cheers,
    Tracy
    Tracy Sloane
    Senior Infection Control Consultant
    Dandenong Hospital, Southern Health
    T (03) 95548173 F (03) 95541905
    E tracy.sloane@southernhealth.org.au

    From: ACIPC Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On Behalf Of Helen Scott
    Sent: Tuesday, 12 June 2012 2:36 PM
    To: AICALIST@AICALIST.ORG.AU
    Subject: Re: Surgical hand scrub

    Hi Jane,

    The CDC have got a good article on this. It’s their MMWR and in October 2002, Vol 51, page 17 it discusses exactly this. I’m sure there’s a more up to date report somewhere. You could also try Skinman Soft, made by Orion.

    Cheers,
    Helen.

    Helen Scott
    Infection Control Co-ordinator
    Nepean Private Hospital
    Penrith, NSW.
    0247 327333
    Helen.Scott@healthscope.com.au

    Please consider the environment before printing this message

    >>> On 11/06/2012 at 5:50 am, in message , Jane Barnett wrote:
    Hi
    Weve got some staff who can only use the PCMX scrub product as they are sensitive to both chlorhex and betadine but BD have advised that they are withdrawing this product. Can I ask what other centres are doing for staff with allergies would plain soap and water washed followed by plain alcohol (without antiseptic additive) be sufficient for surgical procedures? Thoughts/ideas welcome.
    Thanks

    Jane Barnett
    Clinical Nurse Specialist
    Infection Prevention & Control
    Christchurch Women’s Hospital
    Private Bag 4711, Christchurch
    Tel: 03 364 4510 (int 85510)
    Fax: 03 364 4607

    Infection Prevention and Control is Everyone’s Business

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    kkh

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    in reply to: Re: Surgical hand scrub #69096
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

    State:

    Hi Matthias

    I think the HH guideline is what she is referring to.

    http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5116a1.htm

    Cheers
    Michael

    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

    >>> “Matthias Maiwald (KKH)” 12/06/2012
    3:39 pm >>>

    Dear Helen,
    Yes, Skinman Soft N (Ecolab, formerly Henkel, distributed in Australia
    by Orion) is one of the formulations that are suitable for surgical hand
    antisepsis and it fulfils EN 12791.
    Sorry, which article in MMWR do you mean? I could not find it in the
    2002 list of articles:
    http://www.cdc.gov/mmwr/index2002.htm
    Note, there is also another article from a US perspective in the AORN
    Journal in 2004:
    http://www.sciencedirect.com/science/article/pii/S0001209206606194
    Best regards, Matthias.


    Matthias Maiwald, MD, FRCPA
    Consultant in Microbiology
    Adj. Assoc. Prof., Natl. Univ. Singapore
    Department of Pathology and Laboratory Medicine
    KK Women’s and Children’s Hospital
    100 Bukit Timah Road
    Singapore 229899
    Tel. +65 6394 8725 (Office)
    Tel. +65 6394 1389 (Laboratory)
    Fax +65 6394 1387

    From:ACIPC Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On
    Behalf Of Helen Scott

    Hi Jane,

    The CDC have got a good article on this. It’s their MMWR and in October
    2002, Vol 51, page 17 it discusses exactly this. I’m sure there’s a more
    up to date report somewhere. You could also try Skinman Soft, made by
    Orion.

    Cheers,

    Helen.

    Helen Scott

    Infection Control Co-ordinator

    Nepean Private Hospital

    Penrith, NSW.

    0247 327333

    Helen.Scott@healthscope.com.au

    Please consider the environment before printing this message

    >>> On 11/06/2012 at 5:50 am, in message
    , Jane
    Barnett wrote:

    Hi
    Weve got some staff who can only use the PCMX scrub product as they
    are sensitive to both chlorhex and betadine but BD have advised that
    they are withdrawing this product. Can I ask what other centres are
    doing for staff with allergies would plain soap and water washed
    followed by plain alcohol (without antiseptic additive) be sufficient
    for surgical procedures? Thoughts/ideas welcome.
    Thanks

    Jane Barnett
    Clinical Nurse Specialist
    Infection Prevention & Control
    Christchurch Women’s Hospital
    Private Bag 4711, Christchurch

    Infection Prevention and Control is Everyone’s Business

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    kkh

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    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

    State:

    Matthew

    The original discussion is concerning port disinfection, and the same CDC HICPAC guidelines you refer to state:

    ‘Minimize contamination risk by scrubbing the access port with an appropriate antiseptic (chlorhexidine, povidone iodine, an iodophor, or 70% alcohol) and accessing the port only with sterile devices [189, 192, 194196]. Category IA’

    Guidelines for the Prevention of Intravascular Catheter-Related Infections, 2011
    http://www.cdc.gov/hicpac/pdf/guidelines/bsi-guidelines-2011.pdf

    Cheers
    Michael

    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

    >>> “Richards, Matthew” 25/05/2012 8:30 am >>>

    Tim
    just a point of reference
    The CDC 2011 guidelines recommendation for skin prep prior to the insertion of a CVC is “>0.5% CHG with alcohol….if there is a contraindication to CHG, tincture of iodine, an iodophor, or 70% alcohol can be used as an alternative”. The reality is 2% CHG in 70% alcohol is most commonly available and used.
    The recommended CDC guidleiens for peripheral skin prep is with an antiseptic “70% alcohol….or alcoholic CHG gluconate solution”

    regards

    Matthew Richards
    Clinical Nurse Consultant
    Infection Prevention and Surveillance Service
    Melbourne Health
    T: 9342 8325 F: 9342 8484
    http://info2.mh.org.au/IPSS/NewWEB/default.htm

    From: ACIPC Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On Behalf Of Tim Spencer
    Sent: Thursday, 24 May, 2012 4:39 PM
    To: AICALIST@AICALIST.ORG.AU
    Subject: Re: [ACIPC_Infexion_Connexion] cvc & other IV device bung/port cleaning protocol

    Hi Jayne,
    Currently, the CDC Guidelines, along with NICE (UK), SHEA (USA), INS (USA) and AVA (USA), ESPEN (Europe) and IVNNZ (New Zealand) all recommend 2% CHG with 70% IPA.
    It’s is pretty much the worldwide standard for skin antisepsis prior to inserion of a IV device (peripheral or central), as well as hub/cap/valve decontamination on any IV device.

    Never heard of it being injected into the patient! I would be interested to see your ID physicians supportive evidence to show any accidental injection of CHG & IPA into the patient and any detriments it may have.

    The evidence speaks correctly. I would base your policy from “evidence-based research and practices’, not speculation from various individuals.

    There is plenty of supportive literature.
    Regards,
    Tim..

    Timothy R. Spencer, RN, APN, DipAppSci, Bach.Health, ICCert.
    Clinical Nurse Consultant | Central Venous Access & Parenteral Nutrition Service
    Conjoint Lecturer, University of NSW
    Dept of Critical Care, Level 2, Clinical Building, Liverpool Hospital, Elizabeth Street, Liverpool, 2170, NSW, Australia
    Tel 02 8738 3603 | Fax 02 8738 3551 | Mob 0409 463 428 | Tim.Spencer@sswahs.nsw.gov.au | Timothy.Spencer@unsw.edu.au

    From: ACIPC Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On Behalf Of Jayne OConnor
    Sent: Thursday, May 24, 2012 4:15 PM
    To: AICALIST@AICALIST.ORG.AU
    Subject: cvc & other IV device bung/port cleaning protocol

    Dear All,

    We are currently revising our CVC policy and just wondering what everyone used for cleaning the ports? All evidence points to 2% Chlorhexidine in 70% alcohol, but we have had conflicting advice from our ID physicians due to safety issues of injecting chlorhexidine into lines?

    Look forward to responses.

    Kind Regards

    Jayne

    Jayne O’Connor RN, BSc.in Infection Control
    Clinical Nurse Consultant- Infection Prevention & Control
    Sydney Adventist Hospital,
    185 Fox Valley Rd,.
    Wahroonga,
    NSW 2076.

    Tel: (02) 9487 9433
    Mobile: 0406 752 685
    Email: jayne.oconnor@sah.org.au

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    in reply to: cvc & other IV device bung/port cleaning protocol #69036
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

    State:

    Hi Jayne

    I recall an anecdotal report of a patient with a chlorhexidine allergy who had a chlorhexidine containing wipe used prior to venepunture and suffered anaphylaxis. The swab used did not clearly identify chlorhexidine content and looked like a alcohol only swab, apparently. Not sure if this incident was every documented publicly.

    This clearly highlights the dangers of chlorhexidine, but anaphylaxis due to chlorhexidine is rare, and the potential for blood-stream infection is much higher. It would be appropriate to ensure all chlorhexidine containing swabs and solutions are clearly unidentified as containing chlorhexidine, and that there is a process (similar to latex allergy I would suggest) of identifying patients with chlorhexidine allergy and managing them appropriately.

    I would not support a blanket ban of chlorhexidine containing products in line management, given the good evidence of their efficacy in reducing blood-stream infection risks associated with intravascular lines.

    You also may want to consider an audit of line management which includes the appropriate drying of solutions used prior to manipulating lines.

    Cheers
    Michael Wishart
    Infection Control Professional

    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

    >>> Jayne OConnor 24/05/2012 4:15 pm >>>

    Dear All,

    We are currently revising our CVC policy and just wondering what everyone used for cleaning the ports? All evidence points to 2% Chlorhexidine in 70% alcohol, but we have had conflicting advice from our ID physicians due to safety issues of injecting chlorhexidine into lines?

    Look forward to responses.

    Kind Regards

    Jayne

    Jayne O’Connor RN, BSc.in Infection Control
    Clinical Nurse Consultant- Infection Prevention & Control
    Sydney Adventist Hospital,
    185 Fox Valley Rd,.
    Wahroonga,
    NSW 2076.

    Tel: (02) 9487 9433
    Mobile: 0406 752 685
    Email: jayne.oconnor@sah.org.au

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    in reply to: Ultrasound probe cleanign and disinfection #69006
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    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
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    by Sydney Adventist Hospital to state that they are the views of Sydney
    Adventist Hospital.
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    If not an intended recipient of this email, you must not copy, distribute or take any action(s) that relies on it; any form of disclosure, modification, distribution and/or publication of this email is also prohibited.
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    Unless stated otherwise, this email represents only the views of the sender and not the views of the Queensland Government.
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    in reply to: Ultrasound probe cleanign and disinfection #69001
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

    State:

    in reply to: Ultrasound probe cleanign and disinfection #69000
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    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

    CAUTION: This message may contain both confidential and privileged 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
    Scanning Services – powered by MessageLabs. For further information
    visit http://www.messagelabs.com
    Messages posted to this list are solely the opinion of the authors, and do not represent the opinion of AICA.
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    If you are not the intended recipient(s), or if you have received this email in error, you are asked to immediately notify the sender by telephone collect on Australia +61 1800 198 175 or by return email. You should also delete this email, and any copies, from your computer system network and destroy any hard copies produced.
    If not an intended recipient of this email, you must not copy, distribute or take any action(s) that relies on it; any form of disclosure, modification, distribution and/or publication of this email is also prohibited.
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    Unless stated otherwise, this email represents only the views of the sender and not the views of the Queensland Government.
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    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

    State:

    Hi Sony

    If scabies s the major concern, and the fabrics are heat-labile and
    will not survive a hot water wash at 75C or above, then you could simply
    quarantine the fabrics in sealed plastic bags for 72 hours as scabies
    mites will not survive away from the human body for longer than that.
    They could then be washed at a low temperature as normal. Another option
    is dry cleaning, where the fabrics are able to withstand the dry
    cleaning process.

    See the US CDC fact sheet for this information:
    http://www.cdc.gov/parasites/scabies/gen_info/faqs.html#clothes

    Cheers
    Michael

    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

    >>> “N Y SO, KWH NO(ICN)” 14/05/2012 12:36 pm >>>

    Dear Fiona.

    Thank for your sharing.

    Australian / New Zealand Standards for Laundry Practice AS/NZS
    4146:2000, Section 3.5.2, which states:
    The minimum time/temperature combinations are therefore
    (a) 65C maintained for not less than 10 minutes; minimum cycle time 14
    minutes forlow loading or 18 minutes for high loading; or
    (b) 71C maintained for not less than 3 minutes; minimum cycle time 7
    minutes for lowloading or 11 minutes for high loading.

    My raised question is for the heat liable fabricand it is contaminated
    with scabies. Because the concerned fabrics laundry label states the
    fabric is not suitable for temperature which is greater than 65C.

    So, we would like to know the temperature requirements for washing and
    ironing process of this heat labile fabric.

    Regards,

    Sony SO
    Nursing Officer, Infection Control Team
    Kwong Wah Hospital
    Tel:+ 852 3517-2409 Fax: +852 2332-3348 email:sony@ha.org.hk

    From:AICA Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On
    Behalf Of Fiona de Sousa
    fabric

    Hi Sony,

    Refer to the Australian / New Zealand Standards for Laundry Practice
    AS/NZS 4146:2000. Section 3 outlines the requirements for thermal and
    chemical disinfection.

    Kind Regards,

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

    From:AICA Infexion Connexion [mailto:AICALIST@AICALIST.ORG.AU] On
    Behalf Of Sony SO
    process for different fabric

    HI All,

    I am reviewing our hospitals laundry practices, and I would like to
    knowthe temperature for laundry – drying process for different fabric.
    (1) for heat liable fabric that is treated by low temperature.
    (2) for general fabric that would stand for higher temperature.

    Yours sincerely,

    Sony SO
    Nursing Officer, Infection Control Team
    Kwong Wah Hospital
    Tel:+ 852 3517-2409 Fax: +852 2332-3348 email:sony@ha.org.hk
    Please consider the environment before printing this e-mail

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    action in reliance on it. If you have received this Email by mistake,
    please notify the sender and then delete this Email from your computer.
    The Hospital Authority does not accept liability arising from Email
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    virus or other defects that might affect any computer system into which
    it is received and opened, it is the responsibility of the recipient to
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    information intended for the addressee named above.
    If you are not the intended recipient you are hereby notified that any
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    in reply to: assist dogs in acute hospital #68917
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael_Wishart@health.qld.gov.au

    Organisation:

    State:

    Hi Nicky

    The legislation that surrounds assistance dogs in QLD was updated a couple of years ago. (http://www.legislation.qld.gov.au/LEGISLTN/ACTS/2009/09AC004.pdf) Hospitals can still maintain zones that assistance dogs may not enter (eg kitchens, CSD, theatres, acute wards) as long as they have a clear policy and a process of assisting the person without their animal and somewhere for the animal to be managed.

    I don’t have a policy available to me right now, but hopefully someone else will be able to give you an example. If all else fails, ring the Disability Information Service (http://www.communities.qld.gov.au/disability/support-and-services/our-services/disability-information-service) to get details on what should be in such a policy.

    Cheers
    Michael

    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

    >>> Nicola Swindells 20/03/2012 8:04 am >>>

    Hi All,

    Does anyone have guidelines or a policy they would like to share with me regarding assist/guide dogs in an acute hospital? Also is anyone aware of any discrimination legislation attached to the visits of these dogs in hospitals. Many thanks in advance for any assistance you may be able to offer me.

    Kind Regards

    Nicky Swindells CNC
    Infection Control Coordinator/Wound Management
    Mater Hospitals Central Queensland
    Rockhampton Yeppoon Gladstone

    nswindells@mercycq.com
    07 49313420

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