2. Please describe the nature of the institution:
public hospital
general gractice
private hospital
dental practice
Other, please specify
Where is the institution located?Ireland UK
3. How long have you been in the institution/organisation? yrs mths
4. How long have you been employed in your current role? yrs mths
5. Do you have sole responsibility for the risk management process? yes no
6. If not, how many other individuals/groups have responsibility over the risk management process?
7. Please state their job title/s (e.g. CEO, member of audit committee etc.)
8. Please describe the nature of your responsibility/tasks in relation to risk management: (tick as necessary)
I am involved in the formulation of policy and strategy in the organisation
I am involved in the carrying out of internal audits
I am involved in the reporting of adverse incidents
I am involved in organising a risk register
I am involved in organising a risk action plan
I am involved in training staff in medico-legal and risk management matters
I am involved in matters of health and safety
I am involved with patient complaints and grievances
I act as a liaison between management and clinical staff
I am involved in making decisions in relation to investment
other, please specify
9. Please describe the organisations over which you have responsibility:
1 hospital
2-5 hospitals
6-15 hospitals
general practice
dental practice
other, please specify
10. Do you have a qualification in risk management? yes no
If yes, from where did you obtain it?
11. How essential is this qualification for your employment?
This was a mandatory requirement
It was not mandatory but desirable
It was not important, I wanted to further my knowledge of risk management
12. Is there an individual(s) specifically appointed for
responsibility over matters of health & safety? (e.g. a health &
safety officer) yes no
13. If yes, does this individual have interaction with the
appointed Risk Manager(s) (where there is one or more) as follows?
the interaction is regular
the interaction is not regular
the interaction only takes place on the occurrence of an adverse incident
there is no interaction
Other, please specify
EMPLOYEE DETAILS
14. How many employees are there in total in the institution/organisation?
15. How many clinical personnel are employed in the institution/organisation?
2. RISK MANAGEMENT AT INSTITUTIONAL /ORGANISATIONAL LEVEL
RISK MANAGEMENT POLICY (THE 'POLICY')
16. Is there a specific 'policy' (i.e. a statement of
objectives/risk management mission statement/risk management statement,
agreed rules and regulations governing procedures on risk management) on
risk management in your institution/organisation?
yes no
THE RISK MANAGEMENT PROCESS ('THE PROCESS')
17. If yes, in what form does this policy exist? (tick as necessary)
a written mission and/statement that is visually displayed
available as part of a written training/induction pack
distributed as part of employment contract or employee handbook
available on institution/organisation internal website
communicated as part of an overall communication strategy (i.e posters, leaflets or newsletters)
discussed at board level
discussed at management level
discussed at staff departmental level
discussed at training courses/lectures
Other, please specify
18. Is there a defined or established risk management process in your organisation?
yes no
19. Which of the following is included in your risk management process? (tick as necessary)
internal audits
external audits
self-assessment
a system of accreditation
defined responsibility of roles
competence assurance
patient complaints procedure
accountability for risk management
early warning systems for adverse incident (adverse events and near misses) reporting
an
annual/regular assurance statement on the risk management process
signed by the CEO/Board of
management/manager of the organisation
Other, please specify
20. Who is/was involved in establishing/drawing up the process? (e.g. CEO, member of audit committee etc.)
21. In which year was the idea of developing the process first introduced?
22. In which year was the actual process introduced?
23. Please rank the following factors in order of the importance to
your institution/organisation, (please rank from 1-7 where 1 is the
most important, 7 being of lesser importance)
quality of patient care
the number of cases/lawsuits taken by patients against your institution/organisation
indemnity and insurance premiums
public liability insurance premiums
staff morale
professional reputation
increase of costs, please specify
24. How was the process evaluated?
the process was not evaluated
an external consultant was used
a user panel was used
meets the standard of an accreditation body, please indicate which body
meets the guidelines of a government department
evaluation took place internally only
Other, please specify
25. Is there a specific budget in place to deal with matters of risk management?
yes no
If yes, what percentage of the total annual budget is allocated to risk management? %
26. Over the last three years, has this budget allocation for risk management increased in your institution/organisation?
yes no
If yes, please indicate by what percentage %
27. Is there an official costing procedure for the process?yes no
28. What is the responsibility of management to this risk management process? (tick as necessary)
management formulate future policy as a result of lessons learnt from the process
management
will vary budgets/investment depending on the requirements and
priorities that result from the process
management will define responsibilities of various members of staff
management communicate the process to all staff
management ensure the commitment of all staff to the process
29. Is management accountable for this process? yes no not sure
30. If no to 29, then who is accountable for this process?
31. Are all clinical staff made aware of this process? yes no not sure
32. If yes, how were they made aware of this process?
through documentation (letters, memos etc)
through staff/departmental meetings
through training and lectures given internally/given by internal staff
through training and lectures given by a third party/external organisation
by means of the organisation's website
Other, please specify
33. Do you believe that the risk management process is satisfactory in your institution/organisation? yes no
3. EDUCATION AND TRAINING
34. Is there a mandatory system of continuing education in place for appointed risk managers? yes no
35. If yes to 34 above, does this system consist of the following? (tick as necessary)
lectures relating to medico-legal matters (good record keeping, patient consent, etc.)
lectures relating to clinical governance, controls assurance and risk management
practical workshops
by way of interactive training tools
other training
Other, please specify
36. How often do risk managers receive training, as outlined in question 35?
every month
every four months
annually
bi-annually
Other, please specify
37. Is there a mandatory system of continuing education in place for clinical personnel? yes no
38. If yes to 37 above, does this system consist of the following? (tick as necessary)
lectures relating to medico-legal matters (good record keeping, patient consent, etc.)
lectures relating to clinical governance, controls assurance and risk management
practical workshops
by way of interactive training tools
other training
Other, please specify
39. How often do clinical personnel receive the above?
every month
every four months
annually
bi-annually
Other, please specify
40. If the above is not mandatory, do voluntary systems exist? yes no
If yes, please describe
41. If clinical audits are carried out, are the results fed to clinical staff through training and education? yes no
42. Do clinical staff receive the following educational tools?
medico-legal/risk management training manual
any interactive training tools (CD-ROM or Web-based)
Other, please specify
4. SPECIFICS RELATING TO MEDICO-LEGAL ASPECTS FOR MANAGEMENT OF CLINICAL RISKS AND NON-CLINICAL RISKS
43. Is training given in your institution/organisation in relation to the following?
the working of legal systems
medical ethics
patient consent
record keeping and data protection
clinical negligence law and practice
living wills
ethics and law in relation to terminally ill patient
ethics and law in relation to the dying patient
doctor/patient communication
inter-professional communication
clinical trials and clinical research
health and safety legislation and procedures
44. If this training is given, is it given by any of the following methods?
documentation
lectures/training seminars
communicated by an ethics committees
by way of interactive training tools
Other, please specify
45. Do established/defined procedures/protocols exist in your
institution/organisation in relation to the following health and safety
matters? yes no
If yes, please tick and describe:
sharps injuries (e.g. needle stick injuries)
chemical & biological agents
manual handling of loads (e.g. the lifting of patients)
sterilisation of equipment
minimisation of slips and falls
waste management
stress management
violence at work
security in the workplace
infection control policy
emergency plans in cases of fire
Other, please specify
46. Does your institution/organisation have a health and safety statement? yes no
47. If yes, is every employee (clinical and non-clinical) given the health and safety statement? yes no
48. If your Institution/organisation has a health and safety statement, how often is it reviewed?
annually
bi-annually
when considered necessary
Other, please specify
49. Do (clinical and non-clinical) personnel receive training in health and safety? yes no
If yes, do they receive the following types of training? (tick as necessary)
lecture
training workshops
by way of interactive training tools
Other, please specify
If this training is received, is it mandatory? yes no
50. Does the National Agency with responsibility over Health and
Safety in your country visit your institution/organisation? yes no
If yes, how often?
every two years
annually
bi-annually
every four months
every month
Other, please specify
51. Within the last three years, has your institution/organisation or medical personnel experienced:
52. What percentage of your total annual budget is utilised for such litigation? %
53. Has the institution/organisation incorporated the findings of
court decisions to improve the risk management process? yes no
5. BENEFITS/OUTCOMES/FUTURE OUTCOMES/IMPACT
54. Since the introduction of a risk management process have cases
of litigation against your institution/organisation been reduced? yes no difficult to say
have patient complaints reduced in number? yes no difficult to say
do you believe that staff morale increased? yes no difficult to say
is there a measured and definite improvement in the quality of patient care? yes no difficult to say
55. Has there been a reduction in medical indemnity costs? yes no difficult to say
56. Has there been a reduction in public liability insurance costs? yes no difficult to say
57. Has there been a reduction in other costs?yes no
Other, please specify
58. Will the improvement of the risk management process directly reduce costs relating to litigation? yes no not sure
59. If these litigation costs are reduced, will the reduction
further enable the institution/organisation to improve the delivery of
healthcare? yes no
60. What impact has risk management had on patient care in your institution/organisation?
no impact
very little impact
some impact
considerable impact
it is difficult to say what impact it has had
Other, please specify
6. OTHER CONCERNS AND YOUR OPINIONS - LOOKING TO THE FUTURE
61. Do you feel that the Government should have a role in the
regulation of the risk management process? (1 being the most important
and 3 being of lesser importance) yes no not sure
62. Please rank in order of importance, the role you think a court
of law should play in clinical negligence. (1 being the most important
and 3 being of lesser importance)
setting standards of care in the healthcare professions
compensating for loss for injured patients
providing a medium for a fair hearing
63. Do you feel that clinical negligence/litigation should be either:
removed from the court system
maintained within the court system and improved
64. If you feel that clinical negligence/litigation can be improved
within the court system then please rank in order of importance (1
being the most important and 3 being of lesser importance) the
following:
the manner in which damages are paid
speed up the processing of cases
introduce specialised medical courts that will only deal with cases of clinical negligence
65. Do you feel that Alternative Dispute Resolution (ADR) systems
could be utilised in relation to matters of clinical negligence? yes no
66. If yes to the above, please rank in order of importance (1
being the most important and 5 being of lesser importance) the following
ADR systems:
arbitration
mediation
patient complaints system provided by healthcare provider
no-fault liability scheme
medical injuries compensation boards
67. Please describe any concerns you have in relation to the future of clinical governance/risk management.
If you wish to be considered as a 'best practice' organisation for a
video interview and a case study, please include your name,
organisation, address and contact details in the box provided so that we
may contact you.
Name :
Organisation :
Address:
Telephone :
Email :
The form may take up to two minutes to submit. Please press the 'send' button only once.