infection prevention & control 1 infection prevention & control · 2020. 11. 9. ·...

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t: 0333 405 33 33 e: [email protected] w: www.qcs.co.uk Introduction Purpose Good infection prevention and control is essential to ensure that people who use Primary Care services receive safe and effective care. Effective prevention and control of infection must be part of everyday practice and be applied consistently by everyone. The Care Quality Commission (CQC) will assess a registered provider on how it complies with the infection prevention requirements, including environmental cleanliness. The purpose of this audit is to: Ensure an infection prevention and control (IPC) audit is conducted on a six-monthly basis – as a minimum Ensure the audit accurately reflects findings, with reference to supportive information as examples of evidence of good practice Promote a standardised approach to evidence gathering and supportive documentation when preparing for and undertaking an Infection Prevention & Control Audit Ensure responsive action is taken and recorded to demonstrate delivery and progress for all findings recorded as ‘No’ Infection Prevention & Control (IPC) Audit for Dental

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Page 1: Infection Prevention & Control 1 Infection Prevention & Control · 2020. 11. 9. · Infection Prevention & Control (IPC) Audit for Dental 1 t: 0333 405 33 33 e: info@qcs.co.uk w:

Infection Prevention & Control(IPC) Audit for Dental

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t: 0333 405 33 33 e: [email protected] w: www.qcs.co.uk

Introduction

Purpose

Good infection prevention and control is essential to ensure that people who use Primary Care services receive safe and effective care. Effective prevention and control of infection must be part of everyday practice and be applied consistently by everyone. The Care Quality Commission (CQC) will assess a registered provider on how it complies with the infection prevention requirements, including environmental cleanliness.

The purpose of this audit is to:

Ensure an infection prevention and control (IPC) audit is conducted on a six-monthly basis – asa minimumEnsure the audit accurately reflects findings, with reference to supportive information as examplesof evidence of good practicePromote a standardised approach to evidence gathering and supportive documentation whenpreparing for and undertaking an Infection Prevention & Control AuditEnsure responsive action is taken and recorded to demonstrate delivery and progressfor all findings recorded as ‘No’

Infection Prevention & Control(IPC) Audit for Dental

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Approach

Feedback

A dedicated inspection date(s) will need to be identified, with named auditors identified to conduct the audit. On the agreed day(s), the allocated auditor(s) will:

Ensure the completed audit tool is reviewed and the findings shared with the Practice Managerand/or Registered Manager.

This audit template covers the following areas:

Ensure the auditor(s) answer the questions honestly and objectivelyIn the event of answering ‘Yes’ to any question, the auditor(s) will need to document andcollate examples of their findings in the ‘Comments’ column and/or refer to examples ofsupportive evidence where appropriate e.g. meeting minutes and date of meeting

1. Prevention of Bloodborne Virus Exposure2. Decontamination3. Environmental Design and Cleaning4. Hand Hygiene5. Management of Dental Medical Devices6. Personal Protective Equipment7. Waste Management8. Infection Prevention & Control (IPC) Inspection – Action Plan

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Actions

Draft an action plan in response to all questions answered ‘No’, to demonstrate improvements, management of risk and delivery of progressThe action plan must identify:

Give a copy of the audit findings plus action plan to the Practice Manager and/orRegistered ManagerEnsure the Practice Manager shares the audit findings and actions required with staff,celebrating success, and identifying areas of improvements required

The issueThe action(s) taken/to be takenNamed individuals responsible for managing and delivering the actionsAnticipated delivery timeframes

Name of person carryingout the audit

Date Completed Signature on completionJob role of the persondoing the audit

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

Section 1: Prevention of Bloodborne Virus Exposure

1. Does the practice have a policy and procedure in place for the prevention of blood borne virus exposure? Does it include the management of spillages, sharps and inoculation incidents in accordance with national guidance?

3. Have all staff at risk from sharps injuries received an occupational health check in relation to risk reduction in blood borne virus transmission and general infection?

4. Can decontamination and clinical staff demonstrate current immunisation with the hepatitis B vaccine? Can the Practice Manager provide documented proof?

5. Are chlorine releasing agents available for blood/bodily fluid spillages and used as per the manufacturer’s instructions? Is a spillage kit readily available?

6. Are sharps containers correctly assembled and labelled with the date, location and a signature?

7. Can you confirm that all sharps containers are not filled beyond the indicator mark? Are they locked shut when filled to the indicator mark?

8. Are full sharps containers stored in a secure place away from public access ready for collection?

9. Is there a readily available protocol and flowchart in place providing information on what to do in the event of a sharps injury

10. Are inoculation injuries recorded?

2. Have all staff received training on the prevention and management of blood borne virus exposure?

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YES NO Comments

YES NO Comments

YES NO Comments

11. Can you confirm only the clinician using syringes is fully responsible for disposing of them?

12. Are safer sharps syringes used?

13. Are sharps containers available at the point of use and positioned safely? For example, wall mounted near the clinician

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

Section 2: Decontamination

1. Does the practice have a policy and procedure in place that includes all aspects of the decontamination process?

2. Have all clinical and sterilisation team members received training on decontamination processes they are expected to perform?

3. Do you keep a record of instruments that are single use and therefore cannot be re-processed?

4. Are all wrapped, sterilised instruments date stamped with the date sterilised, use by date and name and signature of the decontaminator operator?

5. Does the practice have a nominated lead responsible for infection control and decontamination?

6. Can you provide evidence that all decontamination equipment (autoclaves, washer disinfectors etc.) are validated and serviced regularly as per the manufacturer’s instructions?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

7. Is there a procedure for the transportation ofinstruments to and from other locations thatensures the segregation of contaminatedinstruments from clean/sterilised instruments?

8. Is all documentation (including testing, servicing,maintenance and repair records) retained in thepractice for at least two years?

9. Are reusable instrument traysdecontaminated and sterilised after each use?

10. Are any instruments (used or unused) left ontrays at the end of each session sterilised beforefurther use?

11. Are instruments that are not decontaminatedimmediately kept moist until they aredecontaminated?

12. Are instruments inspected underilluminated magnification for cleanliness andcondition following cleaning?

13. Are handpieces decontaminated in betweeneach patient in accordance with manufacturers’instructions?

14. Are separate canisters of lubricant used forunclean, cleaned and sterilised instruments?

15. Are those handpieces that are manuallycleaned, wiped and lubricated with oil beforesteam sterilisation in accordance withmanufacturers’ instructions?

16. Are handpieces decontaminated by anautomated washer disinfector lubricated withoil before steam sterilisation in accordancewith manufacturers’ instructions?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

17. Are handpieces decontaminated by anautomated washer-disinfector (with a specifichandpiece irrigation system) lubricated withoil before steam?

18. Are all instruments washed in awasher-disinfector before they are sterilised?

19. If the practice does not have awasher-disinfector are all instruments cleanedmanually before they are sterilised?

20. When manual cleaning, are two sinks (or twobowls in a single unit) used? One for washing andthe other for rinsing?

21. Are specially formulated detergents used formanually cleaning instruments and is it used at thespecified concentration according to themanufacturer’s instructions?

22. When manual cleaning is the water temperaturechecked and recorded to make sure it is 45°Cor lower?

23. Are instruments fully submerged whenmanually cleaned? (unless the manufacturer’sinstructions suggest otherwise)

24. Are brushes used to manually cleaninstruments either single use or washed aftereach use and replaced at the manufacturer’srecommended intervals or when damaged?

25. Are there contractual validation and testingarrangements in place to ensure all autoclavesare routinely maintained and validated inaccordance with HTM-01-05 and manufacturers’instructions?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

26. Are daily, weekly, quarterly and annualinspection testing and maintenance recordsavailable for autoclaves as described in section 12of HTM-01-05?

27. Are fault logs kept for all autoclaves and are theyremoved from use until the fault has been rectified?

28. Are there arrangements to ensure all ultrasoniccleaners are maintained and validated inaccordance with HTM-01-05 requirementsand manufacturers’ instructions?

29. Are daily, weekly, quarterly and annualinspections, testing and maintenance recordsavailable for ultrasonic cleaners?

30. Are there contractual arrangements in placeto ensure all automated washer-disinfectors areroutinely maintained and validated in line withmanufacturers’ instructions?

31. Are daily, weekly, quarterly and annualvalidation and testing results recorded forautomated washer-disinfectors?

32. When using ultrasonic cleaners, areinstruments placed in an instrument basket orcassette and fully immersed ensuring that allsurfaces are in contact with the solution?

33. When using ultrasonic cleaners (and when notin use) is the lid closed to preventcontamination of the ultrasonic cleaning solution?

34. Is the ultrasonic cleaner solution emptiedwhen visibly contaminated or otherwise at theend of every clinical session?

35. Where instruments are manually cleaned, arethey rinsed after removing from the ultrasoniccleaner?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

36. Are the relevant staff aware of the instrumentloading procedure for the washer disinfector?(spray arms are free to rotate, cannulatedinstruments are loaded correctly)

37. Are washer-disinfector cycle parametersrecorded?

38. For autoclaves, are there daily recordsavailable for the past two years of thetemperature and pressure achieved on completionof each cycle

39. Can you confirm that autoclaves are neverused if they display faults?

40. When using autoclaves, can you confirm thatonly pre-wrapped instruments are used invacuum type sterilisers?

41. Is distilled water or RO (reverse osmosis) waterused in the autoclave?

42. Are opened bottles of distilled water discardedat the end of each working day?

43. Are autoclave reservoirs drained and left cleanand dry at the end of each day?

44. Is there a separate dedicated decontaminationroom which is restricted to those performingdecontamination duties?

45. Is the decontamination room clearly zonedinto clean and dirty areas?

46. Are decontamination areas and worksurfaces clean and uncluttered?

47. Is there adequate ventilation in thedecontamination room?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

48. Where full mechanical ventilation is used in thedecontamination room, is the direction of airflowing from the clean to the dirty area?

49. Where full mechanical ventilation is used in thedecontamination room, is the direction of air flowingfrom the clean to the dirty area?

50. Are instruments maintained in a moist conditionbetween use and decontamination?

51. Are instrument transport containers lidded,clean, leak proof and cleaned, disinfected anddried following each use?

52. Are instruments processed in a non-vacuum(type N) autoclave dried prior to packing using adisposable lint free cloth?

53. Does the practice have a system in place toensure that the storage of non-wrappedinstruments does not exceed 1 day if stored in aclinical area?

54. Does the practice have a system in place toensure that the storage of wrapped instrumentsdoes not exceed 1 year?

55. Is there a system in place to identify instrumentstorage time, including the date by which theyshould be used or re-processed?

56. Are instruments stored in a dedicated secure,dry and cool environment?

YES NO Comments

Section 3: Environmental Design and Cleaning

1. Does the practice have a policy and procedurefor cleaning and maintaining the environment?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

2. Are daily cleaning and decontamination checklistspresent and filled in for all clinical areas? Can youprovide two years of evidence of this?

3. Does the practice have a daily checklist forthe cleaner?

4. Does the practice have a COVID-19 Policy andProcedure in place?

5. Are two metre social distancing markers onthe floor in all areas during the pandemic?

6. Is hand sanitising gel readily available in allrooms?

7. Is there a clear shield in front of the receptiondesk to protect staff and patients?

8. Have staff undertaking cleaning duties beenfully trained to undertake such duties?undertakesuch duties?

9. Are surgery floors mopped after each session?

10. Is the overall appearance of the clinical anddecontamination environment tidy and uncluttered?

11. Are all dental chairs free of rips or tears andcleaned in between each patient?

12. Are all walls, floors, ceilings, fixtures and fittingsfree from damage?

13. Are all work surface joints intact, seamlessand with no visible damage?

14. Are all surfaces free from dust and visible dirt?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

15. Are the surfaces of accessible ventilationfittings cleaned weekly?

16. Are easy clean keyboards used in all clinicalareas?

17. Can you confirm that none of the clinicalareas are carpeted?

18. Do all floor coverings in the clinical anddecontamination areas have coved edges thatare sealed?

19. Is cleaning equipment colour coded todetermine what area it should be used in?

20. Is general cleaning equipment stored in anon-clinical area?

21. Where disposable single-use covers are usedare they discarded after each patient contact?

22. Are surfaces and equipment cleaned inbetween each patient? (dental chairs, curinglamps, light handles, the dental cart, spittoon etc.)

23. Is fallow time used where needed followingthe latest guidelines during the pandemic?

24. Are AGP - Do not enter signs placed on doorswhen being undertaken?

25. Are all taps, drainage points, splashbacks, sinks,aspirators, drains and spittoons cleaned after everysession with a surface disinfectant?

26. Are floors, cupboard doors and accessiblehigh level surfaces cleaned daily?

27. Is there a designated area for the disposal ofdirty water which is separate to the kitchen, clinicaland decontamination areas?

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YES NO Comments

YES NO Comments

28. Does the practice have a COSHH Policyand Procedure?

29. Are frequently touched sites/points, inparticular waiting room areas cleaned regularlythroughout the day?

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

Section 4: Hand Hygiene

1. Does the practice have a policy and procedure for hand hygiene?

2. Is hand hygiene an integral part of staff induction?

3. Is hand hygiene training provided periodicallythroughout the year?

4. Are hand hygiene audits performed regularlyfor all staff?

5. Is hand hygiene carried out before donninggloves and after removing them?

6. Do all staff involved in any clinicaland decontamination procedures have shortnails that are clean and free from nail extensionsand varnish?

7. Do all clinical and decontamination staffremove watches and rings with stones duringclinical and decontamination procedures?

9. Is there a separate dedicated hand basin provided for hand hygiene in each surgery and is it clearly marked?

8. Are laminated or wipe clean hand hygiene posters on display by all sinks?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

10. Are no contact liquid soap dispensersavailable in all surgeries and decontaminationareas?

11. Are elbow or foot operated electronic mixersor thermostatically controlled taps available atall hand wash sinks in clinical anddecontamination areas?

12. Can you confirm that nail brushes arenever used?

13. Are good quality disposable and absorbentpaper towels used when drying hands?

14. Is hand cream available for all clinical anddecontamination staff?

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

Section 5: Management of Dental Medical Devices

1. Does the practice’s infection control policy includeprocedures for the use, maintenance, service and repair of all medical devices?

2. Does the practice have an individual responsible for ensuring that all staff comply with medical device procedures?

3. Has the practice had a legionella riskassessment of the building carried out?

4. Does the practice have a legionella policyand procedure?

5. Are regular temperature checks carried outand recorded according to the risk assessment?

6. Are all new reusable instruments sterilisedprior to use?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

7. Are instruments sent for repair labelled toidentify they have been through thedecontamination process?

8. Are contaminated patient devices (dentures,impressions etc.) decontaminated and labelledbefore being sent to the laboratory?

9. Are patient devices returned from the laboratorydisinfected before being placed in the patient’smouth?

10. Are single use items always discarded after use?

11. Can you confirm that single use endodonticinstruments are never re-used?

12. Are contaminated intra-oral x-ray digitalsensor wrappers discarded after use, the sensorcleaned according to the manufacturer’sinstructions then re-wrapped?

13. Are x-ray film holders sterilised after everyuse according to the manufacturer’s instructions?

14. Are difficult to clean instruments and devicesidentified as single use?

15. Are dental chair filters cleaned and replacedas per the manufacturer’s instructions?

16. Does the dental chair have an independentbottled water system to dispense distilled orreverse osmosis water?

17. Is the bottle removed, cleaned and driedat the end of each day?

18. If a bottled water chair system is notused is there a physical air gap separating dentalunit water lines from the mains water system?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

19. For surgical procedures involving irrigation,is sterile saline available?

20. Are dental unit water lines flushed throughfor a minimum of two minutes at the start of theday and for a minimum of 20-30 secondsbetween every patient?

21. Are handpieces fitted with anti-retraction valves?

22. Are dental unit water lines purged usingthe manufacturer’s recommended disinfectants?

23. Are dental unit water line filterschanged according to the manufacturer’sguidelines?

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

Section 6: Personal Protective Equipment

1. Does the practice have a PPE policy andprocedure that includes COVID government guidelines?

2. Are FFP3 masks/hoods, gloves,disposable aprons and visors worn for all AGPs

3. Are PPE donning and doffing areas clearly marked?

4. Are staff trained in the use of PPE as part oftheir practice induction?

5. Are powder free and latex free CE markedgloves used?

6. Are all single use PPE items disposed ofafter each episode of patient care?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

7. Are heavy duty gloves available fordecontamination processes where necessary,and washed with detergent and hot water andleft to dry after each use?

8. Are visors, masks, gloves and disposableaprons worn during all decontamination procedures?

9. Are single use disposable aprons and masksdisposed of as clinical waste after each procedure?

10. Are uniforms worn by staff changed at theend of each day and when visibly contaminated?

11. Can you confirm that staff uniforms arenever worn outside of the practice?

12. Are staff uniforms washed separately and atthe highest temperature possible for the fabric?

13. Are all PPE items stored in accordance withthe manufacturer’s instructions?

14. Are visors decontaminated after clinicalsessions and decontamination procedures?

15. Is eye protection provided for the patientdecontaminated after each use?

16. Are posters about the need to cover the noseand mouth during the pandemic present in thepractice?

17. Do all patients wear a face mask on enteringand exiting the building?

YES NO Comments

Section 7: Waste Management

1. Does the practice have a policy and procedurefor the management and disposal of waste?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

2. Have all staff been trained at their induction onthe process of waste disposal?

3. Is there evidence that your waste contractorsare registered waste carriers?

4. Is there a contract in place for the removalof clinical waste, sharps, amalgam filledextracted teeth and out of date medicines?

5. Is the practice registered with the environmental agency if generating over 500KG of hazardouswaste per year?

6. Are orange clinical waste bags used for infectious category B waste such as blood swabs,blood contaminated gloves and teethwithout amalgam fillings?

7. Are yellow (with a black stripe) bags used foroffensive/hygiene waste that is not contaminated with saliva, blood, medicines, chemicalsor amalgam? for example, tissues andnon-contaminated gloves

8. Are black or clear bags used for domesticwaste including paper towels?

9. Are bins foot operated or sensor controlled,lidded and in good working order?

10. Are local anaesthetic cartridges disposedof in yellow sharps containers that conformto guidelines?

11. Are clinical waste bags tied securely andsharps containers clicked shut before theyare collected by the waste company?

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YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

YES NO Comments

12. Are all clinical waste bags and sharps binslabelled with the practice name, address anddate before they are collected?

13. Is waste awaiting collection stored in a safeand secure location away from the public withinthe practice premises?

14. Are waste consignment notes available for allhazardous waste for the past 3 years?

15. Is there evidence that the practice issegregating waste in accordance with HTM-07-01?

16. Has the practice been assured that a duty ofcare audit has been carried out and recordedfrom the producer to the final disposal?

Audit Results and Action Plan:

The purpose of this audit is to see what you are already doing well and identify areas for improvement. For all questions you should be aiming for a ‘yes’ answer.

The below table is broken down into sections for you to fill in so you can clearly see which areasneed improvement and form an action plan to turn the ‘no’ answers into ‘yes’ answers.

Section

1

2

14

56

Number ofquestions

Numberof questionsansweredyes

Number ofquestionsansweredno

Questionnumberswith ‘no’answersrequiringfurther action

Action plan Date to becompletedby

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3

5

7

4

6

29

23

16

14

17

Section

Total overall % of yes answers

Next audit review date:____________________________________________________(6 months from now)

1

3

6

2

5

4

7

% of yes answers