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  • #70722
    Cath Murphy
    Participant

    Author:
    Cath Murphy

    Email:
    cath@INFECTIONCONTROLPLUS.COM.AU

    Organisation:

    State:

    Greetings all

    One year since their implementation I am wondering how most IPs are coping with the Commission’s national safety and quality standards and in particular Standard 3. As some of you may know I was personally involved in some of their development through membership on two of the Commission’s committees. Yesterday I enquired of the Commission about any publically available information on how the Standards implementation is progressing but they are unable to report anything. To my knowledge there are no papers in peer-reviewed journals either. The Commission’s timeframe for review as stated on their website is 2015.

    I am especially keen to hear in IP-speak 1) the challenges, rewards and obstacles that IPs may have faced as a result of Standard 3. 2)How “usual” ways of work may have changed and 3) any assistance that would make the task of implementing them easier.

    In their Annual Report and at ACIPC 2012 Conference in Sydney the Commission referred to HH compliance, C Diff rates and SAB rates as the markers they will use to assess Stdnard 3’s impact. I’m more interested in the impact on programs or the IP role. Please feel free to share your experiences good, bad or indifferent through discussion here or email me personally.

    And many thanks for those of you who discussed publically or as a sidebar, the issue of single-use pt care equipment – your insights were very illuminating.

    Thanks and warm regards
    Cath

    Dr Cathryn Murphy RN MPH PhD CIC
    Executive Director
    Infection Control Plus Pty Ltd

    Adjunct Professor
    Griffith University, School of Nursing and Midwifery
    http://www.infectioncontrolplus.com.au
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    #70723
    Michael Wishart
    Participant

    Author:
    Michael Wishart

    Email:
    Michael.Wishart@hsn.org.au

    Organisation:

    State:

    Hi Cath

    We were accredited via the new Standards by ACHS late last year, and I think the process of having to demonstrate minimum requirements is good. Most of Standard 3 involves things we have been doing for a while (or should have been doing) in infection control, and most of meeting Standard 3 is just closing the loop with documentation and evaluation of what we do. So mostly good – to have all facilities measured against these Standards can only lead to improved patient outcomes, in my opinion.

    My biggest gripe is AMS – AMS is an important infection prevention issue, don’t get me wrong, but ICP’s don’t prescribe antibiotics. In a facility with a standalone ICP (ie not part of a team with ID Physicians and clinical microbiologists) getting medical staff (who, in the private sector, are not even part of the workforce, really) to prescribe according to guidelines is a target way out of reach. Sure, we can audit and put up posters and stuff, but the responsibility for this part of Standard 3 should NOT be upon the facility, in my view, but put back on the medical staff, at least in the private sector. That’s my main gripe within Standard 3.

    Just some thoughts.

    Cheers
    Michael

    Michael Wishart
    Infection Control Coordinator
    Holy Spirit Northside Private Hospital
    627 Rode Road, Chermside, Qld 4032
    t: (07) 3326 3068 | f: (07) 3607 2226
    e: Michael.Wishart@hsn.org.au
    w:www.holyspiritnorthside.org.au
    Please consider the environment before printing this email

    [cid:image001.png@01CF136C.06F021B0]

    Greetings all

    One year since their implementation I am wondering how most IPs are coping with the Commission’s national safety and quality standards and in particular Standard 3. As some of you may know I was personally involved in some of their development through membership on two of the Commission’s committees. Yesterday I enquired of the Commission about any publically available information on how the Standards implementation is progressing but they are unable to report anything. To my knowledge there are no papers in peer-reviewed journals either. The Commission’s timeframe for review as stated on their website is 2015.

    I am especially keen to hear in IP-speak 1) the challenges, rewards and obstacles that IPs may have faced as a result of Standard 3. 2)How “usual” ways of work may have changed and 3) any assistance that would make the task of implementing them easier.

    In their Annual Report and at ACIPC 2012 Conference in Sydney the Commission referred to HH compliance, C Diff rates and SAB rates as the markers they will use to assess Stdnard 3’s impact. I’m more interested in the impact on programs or the IP role. Please feel free to share your experiences good, bad or indifferent through discussion here or email me personally.

    And many thanks for those of you who discussed publically or as a sidebar, the issue of single-use pt care equipment – your insights were very illuminating.

    Thanks and warm regards
    Cath

    Dr Cathryn Murphy RN MPH PhD CIC
    Executive Director
    Infection Control Plus Pty Ltd

    Adjunct Professor
    Griffith University, School of Nursing and Midwifery
    http://www.infectioncontrolplus.com.au
    [Description: twitter logo][Description: FB logo][Description: icp icon]

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    #70730
    Jennifer McCarthy
    Participant

    Author:
    Jennifer McCarthy

    Email:
    jenny@maryvaleph.com.au

    Organisation:
    Maryvale Private Hospital

    State:

    Hi Cath
    We are a small stand alone private facilty (47 acute beds) and have just
    gone through the accreditation process (all 10 Standards and just having
    changed over to ISO – great fun!!)
    and I agree with Micheal – I have found the AMS component very hard to
    demonstrate. While the guide for smaller facilities was very helpful I
    felt there was no where to go when there was non compliance with the
    antibiotic guidelines (just have to continue to report it at the
    relevant commitees).
    Having said that the one area we did not get compliance in was 3.19!
    regards
    Jenny

    Jenny McCarthy

    OR Manager/Infection Prevention and Control Coordinator

    Maryvale Private Hospital

    ________________________________

    Behalf Of Michael Wishart

    Hi Cath

    We were accredited via the new Standards by ACHS late last year, and I
    think the process of having to demonstrate minimum requirements is good.
    Most of Standard 3 involves things we have been doing for a while (or
    should have been doing) in infection control, and most of meeting
    Standard 3 is just closing the loop with documentation and evaluation
    of what we do. So mostly good – to have all facilities measured against
    these Standards can only lead to improved patient outcomes, in my
    opinion.

    My biggest gripe is AMS – AMS is an important infection prevention
    issue, don’t get me wrong, but ICP’s don’t prescribe antibiotics. In a
    facility with a standalone ICP (ie not part of a team with ID Physicians
    and clinical microbiologists) getting medical staff (who, in the private
    sector, are not even part of the workforce, really) to prescribe
    according to guidelines is a target way out of reach. Sure, we can audit
    and put up posters and stuff, but the responsibility for this part of
    Standard 3 should NOT be upon the facility, in my view, but put back on
    the medical staff, at least in the private sector. That’s my main gripe
    within Standard 3.

    Just some thoughts.

    Cheers

    Michael

    Michael Wishart

    Infection Control Coordinator

    Holy Spirit Northside Private Hospital

    627 Rode Road, Chermside, Qld 4032

    t: (07) 3326 3068 | f: (07) 3607 2226

    e: Michael.Wishart@hsn.org.au

    w:www.holyspiritnorthside.org.au

    Please consider the environment before printing this email

    Behalf Of Cath Murphy

    Greetings all

    One year since their implementation I am wondering how most IPs are
    coping with the Commission’s national safety and quality standards and
    in particular Standard 3. As some of you may know I was personally
    involved in some of their development through membership on two of the
    Commission’s committees. Yesterday I enquired of the Commission about
    any publically available information on how the Standards implementation
    is progressing but they are unable to report anything. To my knowledge
    there are no papers in peer-reviewed journals either. The Commission’s
    timeframe for review as stated on their website is 2015.

    I am especially keen to hear in IP-speak 1) the challenges, rewards and
    obstacles that IPs may have faced as a result of Standard 3. 2)How
    “usual” ways of work may have changed and 3) any assistance that would
    make the task of implementing them easier.

    In their Annual Report and at ACIPC 2012 Conference in Sydney the
    Commission referred to HH compliance, C Diff rates and SAB rates as the
    markers they will use to assess Stdnard 3’s impact. I’m more interested
    in the impact on programs or the IP role. Please feel free to share your
    experiences good, bad or indifferent through discussion here or email me
    personally.

    And many thanks for those of you who discussed publically or as a
    sidebar, the issue of single-use pt care equipment – your insights were
    very illuminating.

    Thanks and warm regards

    Cath

    Dr Cathryn Murphy RN MPH PhD CIC

    Executive Director

    Infection Control Plus Pty Ltd

    Adjunct Professor

    Griffith University, School of Nursing and Midwifery

    http://www.infectioncontrolplus.com.au

    FB logo Description: icp
    icon

    MESSAGES POSTED TO THIS LIST ARE SOLELY THE OPINION OF THE AUTHOR, AND
    DO NOT REPRESENT THE OPINION OF ACIPC.

    The use of trade/product/commercial brand names through the list is
    discouraged by ACIPC. If you wish to discuss specific reference to
    products or services by brand or commercial names, please do this
    outside the list.

    Archive of all messages are available at http://aicalist.org.au/archives
    – registration and login required.

    Replies to this message will be directed back to the list. To create a
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    contain copyright material of St Vincent’s Health & Aged Care(“SVHAC”),
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    from errors, viruses or interference. Thank-you.

    ________________________________

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    #70732
    Rebecca O’Donnell
    Participant

    Author:
    Rebecca O’Donnell

    Email:
    Rebecca.O'Donnell@STVINCENTS.ORG.AU

    Organisation:

    State:

    Well said Michael..AMS in a private sector is difficult and has proved a huge amount of time taken away from IPCs day. In particular my colleague who has been getting AMS off the ground…she has spent days upon days refining and reviewing procedures, guidelines etc….The workload has been huge….

    Rebecca O’Donnell | Infection Prevention and Control Co-ordinator
    St Vincent’s Hospital Toowoomba | 22-36 Scott Street TOOWOOMBA 4350
    T 07 4690 4042 | F 07 46904400
    E rebecca.o’donnell@stvincents.org.au | W http://www.stvincents.org.au

    P Please consider the environment before printing this email.
    This e-mail and any attachments to it (the “Communication”) is confidential and is for the use only of the intended recipient, and may not be duplicated or used by any other party without the express consent of the sender. The Communication may contain copyright material of St Vincent’s Health & Aged Care (“SVHAC”), or any of its related entities or of third parties. If you are not the intended recipient of the Communication, please notify the sender immediately by return e-mail, delete the Communication, and do not read, copy, print, retransmit, store or act in reliance on the Communication. Any views expressed in the Communication are those of the individual sender only, unless expressly stated to be those of SVHAC. SVHAC does not guarantee the integrity of the Communication, or that it is free from errors, viruses or interference.

    Hi Cath

    We were accredited via the new Standards by ACHS late last year, and I think the process of having to demonstrate minimum requirements is good. Most of Standard 3 involves things we have been doing for a while (or should have been doing) in infection control, and most of meeting Standard 3 is just closing the loop with documentation and evaluation of what we do. So mostly good – to have all facilities measured against these Standards can only lead to improved patient outcomes, in my opinion.

    My biggest gripe is AMS – AMS is an important infection prevention issue, don’t get me wrong, but ICP’s don’t prescribe antibiotics. In a facility with a standalone ICP (ie not part of a team with ID Physicians and clinical microbiologists) getting medical staff (who, in the private sector, are not even part of the workforce, really) to prescribe according to guidelines is a target way out of reach. Sure, we can audit and put up posters and stuff, but the responsibility for this part of Standard 3 should NOT be upon the facility, in my view, but put back on the medical staff, at least in the private sector. That’s my main gripe within Standard 3.

    Just some thoughts.

    Cheers
    Michael

    Michael Wishart
    Infection Control Coordinator
    Holy Spirit Northside Private Hospital
    627 Rode Road, Chermside, Qld 4032
    t: (07) 3326 3068 | f: (07) 3607 2226
    e: Michael.Wishart@hsn.org.au
    w:www.holyspiritnorthside.org.au
    Please consider the environment before printing this email

    [cid:image001.png@01CF136C.06F021B0]

    Greetings all

    One year since their implementation I am wondering how most IPs are coping with the Commission’s national safety and quality standards and in particular Standard 3. As some of you may know I was personally involved in some of their development through membership on two of the Commission’s committees. Yesterday I enquired of the Commission about any publically available information on how the Standards implementation is progressing but they are unable to report anything. To my knowledge there are no papers in peer-reviewed journals either. The Commission’s timeframe for review as stated on their website is 2015.

    I am especially keen to hear in IP-speak 1) the challenges, rewards and obstacles that IPs may have faced as a result of Standard 3. 2)How “usual” ways of work may have changed and 3) any assistance that would make the task of implementing them easier.

    In their Annual Report and at ACIPC 2012 Conference in Sydney the Commission referred to HH compliance, C Diff rates and SAB rates as the markers they will use to assess Stdnard 3’s impact. I’m more interested in the impact on programs or the IP role. Please feel free to share your experiences good, bad or indifferent through discussion here or email me personally.

    And many thanks for those of you who discussed publically or as a sidebar, the issue of single-use pt care equipment – your insights were very illuminating.

    Thanks and warm regards
    Cath

    Dr Cathryn Murphy RN MPH PhD CIC
    Executive Director
    Infection Control Plus Pty Ltd

    Adjunct Professor
    Griffith University, School of Nursing and Midwifery
    http://www.infectioncontrolplus.com.au
    [Description: twitter logo][Description: FB logo][Description: icp icon]

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