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  • #69111
    Gerald Cha
    Participant

    Author:
    Gerald Cha

    Email:
    Gerald.Chan@sjog.org.au

    Organisation:

    State:

    Dear all,
    I’m keen to obtain feedback from hospitals currently using the eWater system and from anyone with a good grasp of electrolysed water.
    Having seen a demo, I note that the system utilizes dissolved sodium chloride (stored in a separate container) which is then pumped into a wall mounted unit (eWater system), gets mixed with tap H2O which then goes through electrolysis… thus giving us 2 distinct byproducts comprising of sodium hypochlorite and sodium hydroxide (which the system spits out in 2 separate taps marketed as “sanitising” and “cleaning” solutions respectively).
    The chemistry bit is rather clear, plain water with added salt, gets zapped and we get a weak bleach as well as caustic soda.
    These mild solutions are ideal for sanitising fruits/veggies/meat in the catering industry… and that’s where they’re promoting its key use.
    Aside from washing produce, the rep promoted the use of the supplied spray bottles which you then fill with eWater for disinfecting surfaces in the catering department.
    They were keen on proving the effectiveness of eWater in this respect by doing swabs.
    Obviously culture swabs taken before spraying the surface would yield a higher microbial count as we’re not just spraying plain water but a solution containing either bleach or caustic soda (that plus the rep was scrubbing the surfaces vigorously).
    Where I start questioning this all is when the rep informs me that the eWater solution can be kept for >7 days in the spray bottles without losing its efficacy (these spray bottles get decanted each time).
    Wouldn’t electrolyzed water lose its potency rather quickly? Or is it because we’ve added sodium chloride to the mix that we’ve now obtained a relatively stable bleach solution?
    From the papers provided by the company, it is reported that eWater offers a higher sanitising efficiency due to its “significantly higher Oxidation-Reduction Potential (ORP)”.
    This “significantly higher ORP” apparently offers a higher kill rate when compared to an un-electrolyzed comparable solution of bleach (with similar ppm counts).
    They were also keen to promote the use of eWater as a replacement to handwashing with soap and water (in clinical areas as well!)… eWater does not contain emollients and with prolonged usage (fervent observance of the 5 Moments), IMO there would most definitely be reported skin issues relating to dryness. You can’t replace the effectiveness and convenience of ABHRs.
    I recognise the potential of eWater in the kitchens (from a convenience perspective, space-saving, environmental, etc. compared to current processes) but do not see its use beyond that in a hospital setting.
    Keen to hear the views from hospitals who’ve trialed this system… what’s your experience and has it been used out of the kitchen setting.
    Thanks, all.
    Regards,
    Gerald

    Gerald Chan
    Coordinator Infection Control

    St John of God Murdoch Hospital
    100 Murdoch Drive
    MURDOCH. WA 6150

    P: 9366 1552
    M: 0405 495 906 (7804)
    F: 9311 4685
    E: Gerald.Chan@sjog.org.au
    W: http://www.sjog.org.au/murdoch

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    #69112
    Kevin Griffin
    Participant

    Author:
    Kevin Griffin

    Email:
    Kevin.Griffin@BIOQUELL.COM

    Organisation:

    State:

    Gerald

    As you said the chemistry is pretty clear.

    The resultant sodium Hypochlorite is basically that, normal Sodium Hypochlorite and should have stability and efficacy the same as that as a standard weak bleach solution.

    Regards

    Kevin

    Kevin Griffin
    Bioquell Asia Pacific Pte Ltd

    207 Henderson Road,#01-05

    Singapore 159550

    T: +65 6592 5145
    F: +65 6227 5878
    M: +65 8511 3733

    E: Kevin.Griffin@bioquell.com

    W: http://www.bioquell.asia

    Dear all,

    I’m keen to obtain feedback from hospitals currently using the eWater system and from anyone with a good grasp of electrolysed water.

    Having seen a demo, I note that the system utilizes dissolved sodium chloride (stored in a separate container) which is then pumped into a wall mounted unit (eWater system), gets mixed with tap H2O which then goes through electrolysis… thus giving us 2 distinct byproducts comprising of sodium hypochlorite and sodium hydroxide (which the system spits out in 2 separate taps marketed as “sanitising” and “cleaning” solutions respectively).

    The chemistry bit is rather clear, plain water with added salt, gets zapped and we get a weak bleach as well as caustic soda.

    These mild solutions are ideal for sanitising fruits/veggies/meat in the catering industry… and that’s where they’re promoting its key use.

    Aside from washing produce, the rep promoted the use of the supplied spray bottles which you then fill with eWater for disinfecting surfaces in the catering department.

    They were keen on proving the effectiveness of eWater in this respect by doing swabs.

    Obviously culture swabs taken before spraying the surface would yield a higher microbial count as we’re not just spraying plain water but a solution containing either bleach or caustic soda (that plus the rep was scrubbing the surfaces vigorously).

    Where I start questioning this all is when the rep informs me that the eWater solution can be kept for >7 days in the spray bottles without losing its efficacy (these spray bottles get decanted each time).

    Wouldn’t electrolyzed water lose its potency rather quickly? Or is it because we’ve added sodium chloride to the mix that we’ve now obtained a relatively stable bleach solution?

    From the papers provided by the company, it is reported that eWater offers a higher sanitising efficiency due to its “significantly higher Oxidation-Reduction Potential (ORP)”.

    This “significantly higher ORP” apparently offers a higher kill rate when compared to an un-electrolyzed comparable solution of bleach (with similar ppm counts).

    They were also keen to promote the use of eWater as a replacement to handwashing with soap and water (in clinical areas as well!)… eWater does not contain emollients and with prolonged usage (fervent observance of the 5 Moments), IMO there would most definitely be reported skin issues relating to dryness. You can’t replace the effectiveness and convenience of ABHRs.

    I recognise the potential of eWater in the kitchens (from a convenience perspective, space-saving, environmental, etc. compared to current processes) but do not see its use beyond that in a hospital setting.

    Keen to hear the views from hospitals who’ve trialed this system… what’s your experience and has it been used out of the kitchen setting.

    Thanks, all.

    Regards,

    Gerald

    Gerald Chan

    Coordinator Infection Control

    St John of God Murdoch Hospital
    100 Murdoch Drive
    MURDOCH. WA 6150

    P: 9366 1552

    M: 0405 495 906 (7804)
    F: 9311 4685

    E: Gerald.Chan@sjog.org.au

    W: http://www.sjog.org.au/murdoch

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    #69114
    Gerald Cha
    Participant

    Author:
    Gerald Cha

    Email:
    Gerald.Chan@sjog.org.au

    Organisation:

    State:

    Thanks Kevin.
    I’ve asked for the MSDS to have a look at the bleach concentrations churned out by this system as that’ll better guide our planning (from an OSH and IC perspective).
    In terms of solely using the eWater for handwashing, has anyone encountered issues with this?
    Would appreciate any feedback you’ve had from your catering staff.
    Cheers,
    Gerald

    Gerald Chan
    Coordinator Infection Control

    St John of God Murdoch Hospital
    100 Murdoch Drive
    MURDOCH. WA 6150

    P: 9366 1552
    M: 0405 495 906 (7804)
    F: 9311 4685
    E: Gerald.Chan@sjog.org.au
    W: http://www.sjog.org.au/murdoch

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    >>> Kevin Griffin 13/06/2012 2:38 PM >>>

    Gerald
    As you said the chemistry is pretty clear.
    The resultant sodium Hypochlorite is basically that, normal Sodium Hypochlorite and should have stability and efficacy the same as that as a standard weak bleach solution.
    Regards
    Kevin

    Kevin Griffin
    Bioquell Asia Pacific Pte Ltd
    207 Henderson Road,#01-05
    Singapore 159550
    T: +65 6592 5145
    F: +65 6227 5878
    M: +65 8511 3733
    E: Kevin.Griffin@bioquell.com ( mailto:firstname.surname@bioquell.com )

    W: http://www.bioquell.asia

    Dear all,

    I’m keen to obtain feedback from hospitals currently using the eWater system and from anyone with a good grasp of electrolysed water.

    Having seen a demo, I note that the system utilizes dissolved sodium chloride (stored in a separate container) which is then pumped into a wall mounted unit (eWater system), gets mixed with tap H2O which then goes through electrolysis… thus giving us 2 distinct byproducts comprising of sodium hypochlorite and sodium hydroxide (which the system spits out in 2 separate taps marketed as “sanitising” and “cleaning” solutions respectively).

    The chemistry bit is rather clear, plain water with added salt, gets zapped and we get a weak bleach as well as caustic soda.

    These mild solutions are ideal for sanitising fruits/veggies/meat in the catering industry… and that’s where they’re promoting its key use.

    Aside from washing produce, the rep promoted the use of the supplied spray bottles which you then fill with eWater for disinfecting surfaces in the catering department.

    They were keen on proving the effectiveness of eWater in this respect by doing swabs.

    Obviously culture swabs taken before spraying the surface would yield a higher microbial count as we’re not just spraying plain water but a solution containing either bleach or caustic soda (that plus the rep was scrubbing the surfaces vigorously).

    Where I start questioning this all is when the rep informs me that the eWater solution can be kept for >7 days in the spray bottles without losing its efficacy (these spray bottles get decanted each time).

    Wouldn’t electrolyzed water lose its potency rather quickly? Or is it because we’ve added sodium chloride to the mix that we’ve now obtained a relatively stable bleach solution?

    From the papers provided by the company, it is reported that eWater offers a higher sanitising efficiency due to its “significantly higher Oxidation-Reduction Potential (ORP)”.

    This “significantly higher ORP” apparently offers a higher kill rate when compared to an un-electrolyzed comparable solution of bleach (with similar ppm counts).

    They were also keen to promote the use of eWater as a replacement to handwashing with soap and water (in clinical areas as well!)… eWater does not contain emollients and with prolonged usage (fervent observance of the 5 Moments), IMO there would most definitely be reported skin issues relating to dryness. You can’t replace the effectiveness and convenience of ABHRs.

    I recognise the potential of eWater in the kitchens (from a convenience perspective, space-saving, environmental, etc. compared to current processes) but do not see its use beyond that in a hospital setting.

    Keen to hear the views from hospitals who’ve trialed this system… what’s your experience and has it been used out of the kitchen setting.

    Thanks, all.

    Regards,

    Gerald

    Gerald Chan

    Coordinator Infection Control

    St John of God Murdoch Hospital
    100 Murdoch Drive
    MURDOCH. WA 6150

    P: 9366 1552

    M: 0405 495 906 (7804)
    F: 9311 4685

    E: Gerald.Chan@sjog.org.au

    W: http://www.sjog.org.au/murdoch

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    #69135
    GRAYSON, Lindsay
    Participant

    Author:
    GRAYSON, Lindsay

    Email:
    Lindsay.GRAYSON@AUSTIN.ORG.AU

    Organisation:

    State:

    Further to Matthias’ email… His point #16 is correct – namely that
    neither Infection Control nor Infectious Diseases know anything about
    eWater and have never been asked to assess it, let alone approve it!!
    Until this email I had never heard of eWater.

    Needless to say, we are currently investigating how Austin Health
    “approved eWater”, but it was not via any clinical department. I will
    report back since it may be a lesson for others.

    Thanks Matthias

    Kind regards

    Lindsay

    Prof. M. Lindsay Grayson
    Infectious Diseases Department,
    Austin Health
    Department of Medicine, University of Melbourne
    Studley Rd., Heidelberg, VIC 3084
    Australia

    ________________________________

    Dear Colleagues,

    The topic of the eWater System appeared on both the ACIPC and OzBug
    e-mail lists (I overlooked the ACIPC one initially) and I thought it
    would be worth writing a somewhat more detailed joint reply to both
    lists.

    I have previously posted (to ACIPC) on what seemed a similar technology,
    the ActiveIon device.

    I have looked at some of the available information concerning the eWater
    System, and even though I cannot make any final conclusions, I have a
    number of questions and issues of concern that I would like to share. If
    I were to look at purchasing the device, these would be some of the
    points that I would look at more closely.

    (1) The description is that the system performs electrolysis of an NaCl
    solution and creates two solutions, one a (probably weak) bleach (NaOCl)
    and/or hypochlorous acid (HOCl) solution (not sure which one
    predominates), the other a sodium hydroxide (NaOH) solution. The bleach
    solution — according to the description — is microbicidal and can be
    used for disinfection, including disinfection in the food industry, in
    hospitals, even hand antisepsis. The NaOH solution — according to the
    description — is for cleaning.

    (2) The question comes: What would be the difference between using the
    eWater system and just buying bleach and/or hypochlorous acid itself,
    which are cheap standard chemicals that are easily available?

    (3) Has the system been tested by a manufacturer-independent (!)
    disinfectant testing laboratory with relevant expertise? Experience
    tells us that one cannot solely rely on manufacturer-provided test
    reports or manufacturer claims when it comes to disinfectants —
    preferable would be at least two independent test reports from
    experienced reputable labs.

    (4) Has the system been tested by any of the available standardised
    testing protocols for surface disinfection (or other types of
    application, depending on the intended use)? There are, for example, US
    ASTM standards and European EN standards. The EN standard for surface
    disinfection is EN 13697, and such tests are typically done in
    variations (a) with or without organic load (“dirty conditions”) and (b)
    with or without mechanical action (simulating the wiping).

    (5) If, for example, antimicrobial activity would fail in the presence
    of organic load, then a prior cleaning step would become highly
    critical. Organic load is, of course, an issue in the food industry,
    where one of the advertising targets lies.

    (6) FYI, disinfectant testing and assessment is usually done in two
    steps, step 1 is testing in suspension — like the MBC (minimum
    bactericidal concentration) for antibiotics – and step 2 is testing
    under simulated practice conditions, e.g. surface disinfection on a
    carrier.

    (7) Has any testing employed experimental controls that — in terms of
    biological plausibility — leave no other conclusions than what the
    machine produced killed the microorganisms and not (!) some other part
    of the application? (In the ActiveIon example, the microbial reduction
    achieved by one testing lab was similar to what one would expect from
    applying plain inactive water and wiping, but such a control was
    omitted).

    (8) Is there a way to make sure that the disinfectant concentrations
    coming out of the machine are kept consistent and in an antimicrobially
    active range to fulfill their purpose? Meaning how are concentrations
    monitored and ensured that there is active disinfectant? Is there a
    testing method provided to measure the concentrations in daily use (in
    analogy to checking fridge temperatures in labs on a daily basis as part
    of quality control)? Apparently, electrodes age over time and may
    deliver electrolysis less consistently. Is there experience with
    stability of not only disinfectant concentration but also microbicidal
    activity over the intended period of machine usage (I presume years)?
    Also, how long are the prepared solutions stable after electrolysis and
    before application?

    (9) The company address given on the website is an Australian one, but
    it is unclear to me if they are a distributor or the manufacturer. Some
    of the documentation appears to be from Japan; this may indicate that
    the Australian address may be a distributor.

    (10) I saw two “research” publications on the website, both looked like
    research papers, but none had proper bibliographic information (journal
    name, year, volume, etc.). (I found one of these subsequently, with
    journal information, by putting the title into PubMed).

    (11) A table on the website showing microbial test results (citing an
    article published in Japanese) misspelled quite a number of bacterial
    names. If someone claiming to have microbiological expertise is unable
    to spell some of the most common bacterial names, this should ring alarm
    bells.

    (12) On the eWater website, there are three linked documents from RMIT
    University (origin: School of Civil Engineering). One is a brief
    Executive Summary, another a more comprehensive multi-page document,
    another what appears to be a conference poster. The Executive Summary
    appears to focus on cost, environmental and social factors, the bigger
    document has “report final” in its file name but has oblique “draft”
    written over the pages and no authors specified. The microbiology part
    is dubious. All three are written in a very positive tone, raising the
    question whether they might be industry-sponsored.

    (13) The claim that the system can “sterilise” medical instruments
    appears unsubstantiated. From a solution like the one described, one
    would expect at best (!) high-level disinfection, but not sterilisation.
    Even claims for high-level disinfection would have to be substantiated
    by standardised testing, and it should be specified what types of
    instruments can be treated and under which conditions.

    (14) It is proposed to use the electrolysed water for hand hygiene, but
    it is unclear to me how it should be useful for that purpose. NaOCl
    (bleach) is genuinely unsuitable (!) for hand hygiene, because in higher
    concentrations it would be damaging to hands and in lower concentrations
    it would take too long to kill microorganisms (alcohol hand rubs produce
    several log reduction in about 30 sec). Again, results from standardised
    tests would be needed.

    (15) The main target is apparently the food industry, but it is also
    promoted for hospitals. Even if the product were “only” intended for the
    food industry, one would still expect that the system should fulfill
    basic claims concerning antimicrobial efficacy. Both industries are
    critical in terms of preventing infections.

    (16) The company advertises with an endorsement from Austin Health. That
    would raise the question whether Austin’s Infection Control Department
    and/or Lindsay Grayson’s group has seen and/or endorsed this, or whether
    the company only liaised with scientifically untrained personnel, such
    as the housekeeping or kitchen department. The latter would be quite
    inappropriate. (We had an occasion here where a manufacturer tried to
    market a new product by circumventing the Infection Control Committee
    and went straight to Housekeeping).

    I think that this system should be properly investigated by an
    institution or authority with the competency and clout to do this before
    it is used in the healthcare and food industry.

    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

    kkh

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    #69137
    Gerald Cha
    Participant

    Author:
    Gerald Cha

    Email:
    Gerald.Chan@sjog.org.au

    Organisation:

    State:

    Thanks Matthias for further identifying the many gaps in the eWater
    system and their “research”.
    It is alarming to note that Austin Health’s approval was not sought
    (from its clinical departments) as the company often quotes its use
    there in marketing its product.
    I have declined their request to allow my organisation’s letterhead to
    be used by them for the informal random swabs they’d conducted in our
    catering department.
    As mentioned to the rep then, there will obviously be a microbial count
    reduction noted in the swab results (post-eWater) as we are not dealing
    with plain water but either hypochlorous acid/hydrochloric acid or
    caustic soda (depending on which tap the “water” is from).
    That plus vigorous scrubbing of the surfaces to be swabbed when eWater
    was applied.
    I think with the discussion points raised, there is an obvious lack of
    supporting evidence to pursue a trial at this stage.
    Thanks Matthias and Lindsay for your feedback.
    Kind regards,
    Gerald

    Gerald Chan
    Coordinator Infection Control

    St John of God Murdoch Hospital
    100 Murdoch Drive
    MURDOCH. WA 6150

    P: 9366 1552
    M: 0405 495 906 (7804)
    F: 9311 4685
    E: Gerald.Chan@sjog.org.au
    W: http://www.sjog.org.au/murdoch

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    >>> “GRAYSON, Lindsay” 26/06/2012 12:44
    PM >>>

    Dear All,
    Further to Matthias email His point #16 is correct namely that
    neither Infection Control nor Infectious Diseases know anything about
    eWater and have never been asked to assess it, let alone approve it!!
    Until this email I had never heard of eWater.
    Needless to say, we are currently investigating how Austin Health
    approved eWater, but it was not via any clinical department. I
    will report back since it may be a lesson for others.
    Thanks Matthias
    Kind regards
    Lindsay

    Prof. M. Lindsay Grayson
    Infectious Diseases Department,
    Austin Health
    Department of Medicine, University of Melbourne
    Studley Rd., Heidelberg, VIC 3084
    Australia

    Dear Colleagues,
    The topic of the eWater System appeared on both the ACIPC and OzBug
    e-mail lists (I overlooked the ACIPC one initially) and I thought it
    would be worth writing a somewhat more detailed joint reply to both
    lists.
    I have previously posted (to ACIPC) on what seemed a similar
    technology, the ActiveIon device.
    I have looked at some of the available information concerning the
    eWater System, and even though I cannot make any final conclusions, I
    have a number of questions and issues of concern that I would like to
    share. If I were to look at purchasing the device, these would be some
    of the points that I would look at more closely.
    (1) The description is that the system performs electrolysis of an NaCl
    solution and creates two solutions, one a (probably weak) bleach (NaOCl)
    and/or hypochlorous acid (HOCl) solution (not sure which one
    predominates), the other a sodium hydroxide (NaOH) solution. The bleach
    solution — according to the description — is microbicidal and can be
    used for disinfection, including disinfection in the food industry, in
    hospitals, even hand antisepsis. The NaOH solution — according to the
    description — is for cleaning.
    (2) The question comes: What would be the difference between using the
    eWater system and just buying bleach and/or hypochlorous acid itself,
    which are cheap standard chemicals that are easily available?
    (3) Has the system been tested by a manufacturer-independent (!)
    disinfectant testing laboratory with relevant expertise? Experience
    tells us that one cannot solely rely on manufacturer-provided test
    reports or manufacturer claims when it comes to disinfectants —
    preferable would be at least two independent test reports from
    experienced reputable labs.
    (4) Has the system been tested by any of the available standardised
    testing protocols for surface disinfection (or other types of
    application, depending on the intended use)? There are, for example, US
    ASTM standards and European EN standards. The EN standard for surface
    disinfection is EN 13697, and such tests are typically done in
    variations (a) with or without organic load (“dirty conditions”) and (b)
    with or without mechanical action (simulating the wiping).
    (5) If, for example, antimicrobial activity would fail in the presence
    of organic load, then a prior cleaning step would become highly
    critical. Organic load is, of course, an issue in the food industry,
    where one of the advertising targets lies.
    (6) FYI, disinfectant testing and assessment is usually done in two
    steps, step 1 is testing in suspension — like the MBC (minimum
    bactericidal concentration) for antibiotics and step 2 is testing
    under simulated practice conditions, e.g. surface disinfection on a
    carrier.
    (7) Has any testing employed experimental controls that — in terms of
    biological plausibility — leave no other conclusions than what the
    machine produced killed the microorganisms and not (!) some other part
    of the application? (In the ActiveIon example, the microbial reduction
    achieved by one testing lab was similar to what one would expect from
    applying plain inactive water and wiping, but such a control was
    omitted).
    (8) Is there a way to make sure that the disinfectant concentrations
    coming out of the machine are kept consistent and in an antimicrobially
    active range to fulfill their purpose? Meaning how are concentrations
    monitored and ensured that there is active disinfectant? Is there a
    testing method provided to measure the concentrations in daily use (in
    analogy to checking fridge temperatures in labs on a daily basis as part
    of quality control)? Apparently, electrodes age over time and may
    deliver electrolysis less consistently. Is there experience with
    stability of not only disinfectant concentration but also microbicidal
    activity over the intended period of machine usage (I presume years)?
    Also, how long are the prepared solutions stable after electrolysis and
    before application?
    (9) The company address given on the website is an Australian one, but
    it is unclear to me if they are a distributor or the manufacturer. Some
    of the documentation appears to be from Japan; this may indicate that
    the Australian address may be a distributor.
    (10) I saw two “research” publications on the website, both looked like
    research papers, but none had proper bibliographic information (journal
    name, year, volume, etc.). (I found one of these subsequently, with
    journal information, by putting the title into PubMed).
    (11) A table on the website showing microbial test results (citing an
    article published in Japanese) misspelled quite a number of bacterial
    names. If someone claiming to have microbiological expertise is unable
    to spell some of the most common bacterial names, this should ring alarm
    bells.
    (12) On the eWater website, there are three linked documents from RMIT
    University (origin: School of Civil Engineering). One is a brief
    Executive Summary, another a more comprehensive multi-page document,
    another what appears to be a conference poster. The Executive Summary
    appears to focus on cost, environmental and social factors, the bigger
    document has “report final” in its file name but has oblique “draft”
    written over the pages and no authors specified. The microbiology part
    is dubious. All three are written in a very positive tone, raising the
    question whether they might be industry-sponsored.
    (13) The claim that the system can “sterilise” medical instruments
    appears unsubstantiated. From a solution like the one described, one
    would expect at best (!) high-level disinfection, but not sterilisation.
    Even claims for high-level disinfection would have to be substantiated
    by standardised testing, and it should be specified what types of
    instruments can be treated and under which conditions.
    (14) It is proposed to use the electrolysed water for hand hygiene, but
    it is unclear to me how it should be useful for that purpose. NaOCl
    (bleach) is genuinely unsuitable (!) for hand hygiene, because in higher
    concentrations it would be damaging to hands and in lower concentrations
    it would take too long to kill microorganisms (alcohol hand rubs produce
    several log reduction in about 30 sec). Again, results from standardised
    tests would be needed.
    (15) The main target is apparently the food industry, but it is also
    promoted for hospitals. Even if the product were “only” intended for the
    food industry, one would still expect that the system should fulfill
    basic claims concerning antimicrobial efficacy. Both industries are
    critical in terms of preventing infections.
    (16) The company advertises with an endorsement from Austin Health.
    That would raise the question whether Austin’s Infection Control
    Department and/or Lindsay Grayson’s group has seen and/or endorsed this,
    or whether the company only liaised with scientifically untrained
    personnel, such as the housekeeping or kitchen department. The latter
    would be quite inappropriate. (We had an occasion here where a
    manufacturer tried to market a new product by circumventing the
    Infection Control Committee and went straight to Housekeeping).
    I think that this system should be properly investigated by an
    institution or authority with the competency and clout to do this before
    it is used in the healthcare and food industry.
    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

    kkh

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    available at the Healthcare infection control special interest group
    (HICSIG) wiki – http://www.hicsiganz.org. Use the left menu item to link to
    ‘AICA OZBUG talk’ or Search by a key word(s).
    ———————————————————————————————————————————————————————

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    intended recipient. They may contain confidential or privileged
    information. This information may not necessarily be the view of St John
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    #69138
    Thomson, Rachel EA
    Participant

    Author:
    Thomson, Rachel EA

    Email:
    Rachel.Thomson@DHHS.TAS.GOV.AU

    Organisation:

    State:

    Hi all,

    I also value the questions and comments from our ID colleagues on this
    matter. The need for rigorous and critical consideration of newer
    technologies is so important and the right questions so clearly need to
    be asked!

    On another matter which is largely unrelated but I would value any
    comments that either Lindsay, Matthias or any other ASID member might be
    willing to make relates to a sporicidal wipe system for disinfection of
    non-lumened scopes, which uses a patented chlorine dioxide agents
    (Tristel). These wipes are currently being promoted by a company in
    Australia and adopted by some centres. I harbour grave concerns in
    relation to this product and its use. Would it be possible to have this
    request cross-posted to the asid-ozbug members as I wonder what view is
    held in this community in relation to this product? Specifically, I
    wonder if there is comment that any ID person might make on the use of a
    sporicidal agent applied by a “wipe” rather than through an automated
    system and the apparent absence or any validation for a
    clean/disinfection process?

    I look forward to some possible replies/responses

    Kind regards

    Rachel

    Rachel Thomson

    Nurse Unit Manager

    Infection Prevention & Control Unit

    Royal Hobart Hospital

    E: rachel.thomson@dhhs.tas.gov.au

    ________________________________

    Behalf Of Gerald Chan

    Thanks Matthias for further identifying the many gaps in the eWater
    system and their “research”.

    It is alarming to note that Austin Health’s approval was not sought
    (from its clinical departments) as the company often quotes its use
    there in marketing its product.

    I have declined their request to allow my organisation’s letterhead to
    be used by them for the informal random swabs they’d conducted in our
    catering department.

    As mentioned to the rep then, there will obviously be a microbial count
    reduction noted in the swab results (post-eWater) as we are not dealing
    with plain water but either hypochlorous acid/hydrochloric acid or
    caustic soda (depending on which tap the “water” is from).

    That plus vigorous scrubbing of the surfaces to be swabbed when eWater
    was applied.

    I think with the discussion points raised, there is an obvious lack of
    supporting evidence to pursue a trial at this stage.

    Thanks Matthias and Lindsay for your feedback.

    Kind regards,

    Gerald

    Gerald Chan

    Coordinator Infection Control

    St John of God Murdoch Hospital
    100 Murdoch Drive
    MURDOCH. WA 6150

    P: 9366 1552

    M: 0405 495 906 (7804)
    F: 9311 4685

    E: Gerald.Chan@sjog.org.au

    W: http://www.sjog.org.au/murdoch

    Murdoch

    facebook facebook.com/stjohnofgodmurdoch

    twitter twitter.com/sjgh_murdoch

    >>> “GRAYSON, Lindsay” 26/06/2012 12:44
    PM >>>

    Dear All,

    Further to Matthias’ email… His point #16 is correct – namely that
    neither Infection Control nor Infectious Diseases know anything about
    eWater and have never been asked to assess it, let alone approve it!!
    Until this email I had never heard of eWater.

    Needless to say, we are currently investigating how Austin Health
    “approved eWater”, but it was not via any clinical department. I will
    report back since it may be a lesson for others.

    Thanks Matthias

    Kind regards

    Lindsay

    Prof. M. Lindsay Grayson
    Infectious Diseases Department,
    Austin Health
    Department of Medicine, University of Melbourne
    Studley Rd., Heidelberg, VIC 3084
    Australia

    ________________________________

    Dear Colleagues,

    The topic of the eWater System appeared on both the ACIPC and OzBug
    e-mail lists (I overlooked the ACIPC one initially) and I thought it
    would be worth writing a somewhat more detailed joint reply to both
    lists.

    I have previously posted (to ACIPC) on what seemed a similar technology,
    the ActiveIon device.

    I have looked at some of the available information concerning the eWater
    System, and even though I cannot make any final conclusions, I have a
    number of questions and issues of concern that I would like to share. If
    I were to look at purchasing the device, these would be some of the
    points that I would look at more closely.

    (1) The description is that the system performs electrolysis of an NaCl
    solution and creates two solutions, one a (probably weak) bleach (NaOCl)
    and/or hypochlorous acid (HOCl) solution (not sure which one
    predominates), the other a sodium hydroxide (NaOH) solution. The bleach
    solution — according to the description — is microbicidal and can be
    used for disinfection, including disinfection in the food industry, in
    hospitals, even hand antisepsis. The NaOH solution — according to the
    description — is for cleaning.

    (2) The question comes: What would be the difference between using the
    eWater system and just buying bleach and/or hypochlorous acid itself,
    which are cheap standard chemicals that are easily available?

    (3) Has the system been tested by a manufacturer-independent (!)
    disinfectant testing laboratory with relevant expertise? Experience
    tells us that one cannot solely rely on manufacturer-provided test
    reports or manufacturer claims when it comes to disinfectants —
    preferable would be at least two independent test reports from
    experienced reputable labs.

    (4) Has the system been tested by any of the available standardised
    testing protocols for surface disinfection (or other types of
    application, depending on the intended use)? There are, for example, US
    ASTM standards and European EN standards. The EN standard for surface
    disinfection is EN 13697, and such tests are typically done in
    variations (a) with or without organic load (“dirty conditions”) and (b)
    with or without mechanical action (simulating the wiping).

    (5) If, for example, antimicrobial activity would fail in the presence
    of organic load, then a prior cleaning step would become highly
    critical. Organic load is, of course, an issue in the food industry,
    where one of the advertising targets lies.

    (6) FYI, disinfectant testing and assessment is usually done in two
    steps, step 1 is testing in suspension — like the MBC (minimum
    bactericidal concentration) for antibiotics – and step 2 is testing
    under simulated practice conditions, e.g. surface disinfection on a
    carrier.

    (7) Has any testing employed experimental controls that — in terms of
    biological plausibility — leave no other conclusions than what the
    machine produced killed the microorganisms and not (!) some other part
    of the application? (In the ActiveIon example, the microbial reduction
    achieved by one testing lab was similar to what one would expect from
    applying plain inactive water and wiping, but such a control was
    omitted).

    (8) Is there a way to make sure that the disinfectant concentrations
    coming out of the machine are kept consistent and in an antimicrobially
    active range to fulfill their purpose? Meaning how are concentrations
    monitored and ensured that there is active disinfectant? Is there a
    testing method provided to measure the concentrations in daily use (in
    analogy to checking fridge temperatures in labs on a daily basis as part
    of quality control)? Apparently, electrodes age over time and may
    deliver electrolysis less consistently. Is there experience with
    stability of not only disinfectant concentration but also microbicidal
    activity over the intended period of machine usage (I presume years)?
    Also, how long are the prepared solutions stable after electrolysis and
    before application?

    (9) The company address given on the website is an Australian one, but
    it is unclear to me if they are a distributor or the manufacturer. Some
    of the documentation appears to be from Japan; this may indicate that
    the Australian address may be a distributor.

    (10) I saw two “research” publications on the website, both looked like
    research papers, but none had proper bibliographic information (journal
    name, year, volume, etc.). (I found one of these subsequently, with
    journal information, by putting the title into PubMed).

    (11) A table on the website showing microbial test results (citing an
    article published in Japanese) misspelled quite a number of bacterial
    names. If someone claiming to have microbiological expertise is unable
    to spell some of the most common bacterial names, this should ring alarm
    bells.

    (12) On the eWater website, there are three linked documents from RMIT
    University (origin: School of Civil Engineering). One is a brief
    Executive Summary, another a more comprehensive multi-page document,
    another what appears to be a conference poster. The Executive Summary
    appears to focus on cost, environmental and social factors, the bigger
    document has “report final” in its file name but has oblique “draft”
    written over the pages and no authors specified. The microbiology part
    is dubious. All three are written in a very positive tone, raising the
    question whether they might be industry-sponsored.

    (13) The claim that the system can “sterilise” medical instruments
    appears unsubstantiated. From a solution like the one described, one
    would expect at best (!) high-level disinfection, but not sterilisation.
    Even claims for high-level disinfection would have to be substantiated
    by standardised testing, and it should be specified what types of
    instruments can be treated and under which conditions.

    (14) It is proposed to use the electrolysed water for hand hygiene, but
    it is unclear to me how it should be useful for that purpose. NaOCl
    (bleach) is genuinely unsuitable (!) for hand hygiene, because in higher
    concentrations it would be damaging to hands and in lower concentrations
    it would take too long to kill microorganisms (alcohol hand rubs produce
    several log reduction in about 30 sec). Again, results from standardised
    tests would be needed.

    (15) The main target is apparently the food industry, but it is also
    promoted for hospitals. Even if the product were “only” intended for the
    food industry, one would still expect that the system should fulfill
    basic claims concerning antimicrobial efficacy. Both industries are
    critical in terms of preventing infections.

    (16) The company advertises with an endorsement from Austin Health. That
    would raise the question whether Austin’s Infection Control Department
    and/or Lindsay Grayson’s group has seen and/or endorsed this, or whether
    the company only liaised with scientifically untrained personnel, such
    as the housekeeping or kitchen department. The latter would be quite
    inappropriate. (We had an occasion here where a manufacturer tried to
    market a new product by circumventing the Infection Control Committee
    and went straight to Housekeeping).

    I think that this system should be properly investigated by an
    institution or authority with the competency and clout to do this before
    it is used in the healthcare and food industry.

    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

    kkh

    ________________________________

    The information contained in this e-mail and the attachments (if any)
    may be privileged and confidential and is intended solely for the named
    addressee. If you are not the intended recipient, please do not print,
    retain copy, disseminate, distribute, or use this e-mail or any part
    thereof. Please notify the sender immediately by replying to this e-mail
    and delete all copies of this e-mail and the attachments.

    _______________________________________________ asid-ozbug mailing list
    asid-ozbug@burnet.edu.au http://lists.burnet.edu.au/listinfo/asid-ozbug
    ————————————————————————
    ————————————————————————
    —————————————————— Edited archives
    of most past OZBUG/ASPID/AICA topic discussions are available at the
    Healthcare infection control special interest group (HICSIG) wiki –
    http://www.hicsiganz.org. Use the left menu item to link to ‘AICA OZBUG talk’
    or Search by a key word(s).
    ————————————————————————
    ————————————————————————
    ———————

    *****************************************************************

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