Organization for health professions: Implementation
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Consistency with the cultural climate of the organization
Blending between staff management and organization
Enhancement of professional independence
Hierarchical and bureaucratic approach to planning and control
Ability to involve professionals in planning and management processes
Independence and responsibility
The strength of the top management lies in its authority when supervising and managing the compatibilities between different Operating Units
The departmental organization significantly strengthens the middle management, contributing to the integration and coordination process within the organization
Technostructure
Middle line
Staff
Operating core
Clinical governance, considered as the ability to ensure the continuous improvement of the quality of services through the creation of a context where excellence can thrive, is made of the following key elements:
Continuing education
Performance monitoring and measurement
Interdisciplinarity
Efficiency and appropriateness
Research
Risk Management
Risk Management
Technical quality
Technical and allocative efficiency
Quality perceived
What are the most common administrative problems in the running of a hospital?
Little attention is paid to quality processes and results in the services provided
Conflicts between Operating Units
Staff burn-out
Deresposibilization
Litigation with users
What are the main causes?
ENVIRONMENT:
Uncertainty of the position
High variability
PEOPLE:
Understaffing
Demotivation
Errors in the selection and allocation of resources
Lack of appropriate systems of rewards and sanctions
What are the main causes? (2)
ACTIVITY:
Lack of professional differentiation
Fragmentation
Lack of expertise and scientific validation
Rigidity
COORDINATION:
Ambiguous and poor definition of roles and responsibilities
Centralized decision-making
Lack of integration mechanisms
Complex procedures
It is necessary to develop integration tools to overcome difficulties through the redefinition of professional behaviours. Such tools aim at:
In order to choose the tool that best suits the different situations, the following must be taken into account:
Detailed and logical sequence of operations intended for the different operators according to their specific skills
Give precise instructions on the behavioural sequences that do not require discretionary decision-making
PROTOCOL
Predefined pattern of behaviour intended for professionals
Give validated and quite rigid behavioural instructions for specific situations and contexts, leaving little room for professional discretionary decision-making
Recommendations of behaviour aimed at supporting professionals in specific situations
Provide instructions and guidance, derived from the scientific evidences available and validated by experts, on the appropriate behaviours for situations in which the professional has significant discretionary decision-making powers
WORKING PLAN Organizational integration of an Operating Unit
Ensure the achievement of an Operational Unit, define task allocation, their coordination, and the resources needed
CARE PLAN
Planning of the care of a specific patient and documentation by the nurse
Ensure to each patient personalized, safe, effective, continuous and complete care
The systematic processes for the drafting of guidelines differ according to the specific issues and to the contexts (clinical, organizational, teaching, etc.) in which they are implemented. Nevertheless, it is possible to outline some key points for the drafting of guidelines:
Validity
Reproducibility
Applicability
Flexibility
Guidelines are valid only if they bring the benefits expected (in terms of quality of the care provided, of the beneficts expected by one or more patients after one or more specific interventions, and/or in economic terms)
Guidelines are reproducible when, starting from the same scientific evidences and using the same method, different experts come to the same conclusion.
Guidelines should be applicable to populations of patients defined according to scientific evidences and/or clinical experience, and to the resources available
Guidelines should state what clinical situations are an exception to the recommendations, and under what circumstances the patient’s preferences can or have to be taken into account
Guidelines: requirements (2)
Clarity
Documentation
Substantiation
Recommendations
strength
Guidelines should be written with a clear language and in a format making them easy to use in clinical practice
Guidelines should clearly state those who took part in their drafting
Guidelines should clearly state the scientific evidences they are based on, specifying:
• the method used to establish the evidences
• the quality of the evidences (the absolute number of studies available)
• the consistency of the evidences available (degree of homogeneity of the different studies available)
Guidelines should state the quality of the scientific evidences on which their recommendations are based (expert opinions or evidences/facts that are objectively proven)
A The recommendation formulated by the guidelines is supported by good scientific evidences
B The recommendation formulated by the guidelines is supported by fair scientific evidences
C The recommendation formulated by the guidelines is supported by poor scientific evidences, but other considerations make it equally acceptable
D Fair scientific evidences support the recommendation not to perform that intervention
E Good scientific evidences support the recommendation not to perform that intervention
Requirement
Validity
Reproducibility
Applicability
Motivation
Aprocedure is valid when it allows to achieve a goal
Aprocedure is reproducible when, starting from the same scientific evidences and using the same method, different experts come to the same conclusion
Aprocedure is applicable when, for the situation envisaged, it indicates a series of operations that are feasible and for which materials are available
Clarity
The procedure should be written with a clear language and in a format making it easy to use in clinical practice
Requirement Motivation
Conciseness
Completeness
Aprocedure is very concise because it gives direct behavioural instructions
Aprocedure should clearly state the dates of drafting and validation by the authors
Updating Aprocedure should state the date of validity
Systematicity and continuity
Its implementation must be systematic and continuous
Specificity
Aprocedure always refers to a specific context in which it is applicable
Requirement
Validity
Reproducibility
Motivation
Aprotocol is valid only if it brings the benefits expected (in terms of quality of the care provided, and in economic terms)
Aprotocol is reproducible when, starting from the same scientific evidences and using the same method, different experts come to the same conclusion
Applicability
Inapplicable or theoretical protocols should be avoided, as well as those based on unavailable materials and resources
Clarity
Aprotocol must be written in a language leaving no room for arbitrary interpretations and making it easy to use in clinical practice
Requirement Motivation
Conciseness
Completeness
Aprotocol should not be encyclopaedic, but it must be complete
The names of the authors, the date, the methods, the scientific evidences and the study period must be stated
Sharing It must be accepted, rather than imposed
Sistematicity and continuity
Its implementation must be systematic and continuous