LCA Escalation Policy. April 2013

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Transcription:

LCA Escalation Policy April 2013

Contents 1 Background... 3 2 Risk and Issue Identification... 3 2.1 Trust Clinical Director for Cancer... 3 2.2 Pathway and Cross-Cutting Groups... 4 2.3 Commissioners and Other External Bodies... 4 2.4 Clinical Board... 4 3 ESCALATION POLICY... 5 3.1 Alerting Local Clinical Leads... 5 3.2 Alerting Trust Management... 5 3.3 Clinical Board Oversight... 5 3.4 Escalation to the Members Board... 6 3.5 Urgent Escalation... 6 4 ROLES AND RESPONSIBILITIES... 7 4.1 Clinical Director and Associate Clinical Director... 7 4.2 Chair of Clinical Board... 7 4.3 Pathway Groups... 7 4.4 Cross-cutting Groups... 7 4.5 Clinical Board... 8 4.6 Members Board... 8 2

1 Background The London Cancer Alliance is a clinical leadership and accreditation organisation committed to improving clinical standards across the 17 partner organisations. It will set standards that are based on evidence and best practice. Responsibility for delivery lies with individual organisations through their cancer leads supported by the Chief Executive and Boards. Performance issues would be expected to be raised through usual Trust mechanisms. The LCA will however help the partners achieve the required standards. The Clinical Board will lead this process and support the Clinical Director/Associate Clinical Director. On occasions where performance indicators are not within the range of acceptable performance or cannot be achieved by the clinical teams or by providers working individually, issues will be escalated to the Members Board for resolution. Ultimately, for serious concerns that significantly impact on service quality, patient safety or the standards set by the LCA and its members, the Board may decide to notify the commissioners and suggest that a service or range of services should no longer be commissioned from an individual organisation. Where this happens it should be regarded as a failure for the LCA. This protocol is the first statement of how concerns will be handled and it aims to give clinicians, the Clinical Board and Members Board some clarity and consistency of expectation. It will be modified in light of experience, the governance arrangements of the LCA and emerging case law. The policy takes account of existing national guidance and recommendations. The policy is intended to address organisational issues and is not applicable to performance issues relating to individual clinicians. 2 Risk and Issue Identification Risks and issues will be identified by: Clinical Leads of individual providers Chairs of the Pathway and Cross-Cutting Groups Commissioners and other external bodies Clinical Board 2.1 Trust Clinical Director for Cancer Issues identified are likely to involve issues that cannot be resolved by one organisation working alone or where, despite best efforts there has been a failure to improve. Concerns should be raised with the Clinical Director (CD) or Associate Clinical Director (ACD) who will clarify the issue, help identify solutions, organise appropriate peer support (from within the LCA wherever possible) and decide whether to inform the Clinical Board. 3

Where more than one organisation is involved the LCA will organise appropriate crossorganisational discussions and, if appropriate, involve the Pathway Group Chair or Chair of the Clinical Board as a neutral Chair of these meetings APRIL 2013 2.2 Pathway and Cross-Cutting Groups Risk and performance indicator issues will be a standing agenda item for the monthly meetings. This will include analysis and evaluation of the pathway specific metrics. The pathway project manager will ensure the risk/issue is recorded in the risk and issue register. The pathway group will be the usual mechanism by which performance issues are identified for a specific tumour or cross-cutting group. These may either be a local issue or more generalised issues across a number of providers in the LCA. The Chair of the Pathway or Cross-cutting group will discuss with the Clinical Director/Associate Clinical Director linked to that group and they will jointly agree whether this is an issue which can be resolved by the Pathway Group. If not the CD/ACD will notify the Clinical Board at the quarterly presentation on progress and advise whether the issue should be added to the overall LCA risk register. The CD/ACD will keep the Board briefed on progress and resolution of the performance issue and determine when it can be removed from the risk register. 2.3 Commissioners and Other External Bodies Concerns may be expressed about a range of issues. Data accuracy and completeness and waiting times are the most probable issues to be raised but there may be concerns about progress against plans, relationships or, on rare occasions, patient safety. Routine reports on peer review or other quality monitoring may also raise concerns. Initial contact should be through the CD/ACD who will follow the route identified above. 2.4 Clinical Board The Clinical Board is responsible for assessing and commenting on the LCA Performance Scorecard (which will be validated by the 17 provider organisations prior to consideration by the Clinical Board) and identifying concerns of general or service specific level for individual organisations or those which have system wide significance to more than one member of the LCA. The Board will also receive regular updates (specified time intervals) on actions against agreed action plans (for example peer review) and will determine whether there are any causes for concern. If identified these should be added to the corporate risk register until resolved. The CD/ACD will act as Chief Advisers on the level of risk identified. The Clinical Board will identify which of these risks and issues should be reported upwards to the Members Board for resolution. These may involve issues that cannot be resolved by clinicians without the support of the Chief Executive, where several organisations are involved or risks to patient safety or the reputation of the LCA. 4

ESCALATION POLICY 3 ESCALATION POLICY 3.1 Alerting Local Clinical Leads The Clinical Director/Associate Clinical Director will contact the cancer clinical lead and chief operating officer /general manager/divisional director at the relevant Trust to arrange a date to meet. The Trust will provide a written acknowledgement of the concern raised and agree a date to meet within 10 working days of receipt of the request, This meeting will also be attended by any other relevant colleagues from within the LCA (including the Pathway Group Chair), the Trust and the MDT lead of the service. Where appropriate individual clinicians involved in delivering the performance indicator will be invited to attend. The remit of the meeting will be to discuss: Validation of data and assessment of data quality to determine if there is a case to answer Factors leading to performance indicator falling outside the range of acceptable performance, and consideration of justifiable explanations Actions already implemented to resolve issue Unresolved problems: The LCA will offer support and work with the provider to develop an action plan which will include necessary actions, required resources and specified milestone dates The Trust lead clinician or cancer lead will submit progress reports every 10 working days to the CD/ACD to provide assurance that performance is improving. The CD/ACD will determine whether the issue is significant enough to be drawn to the attention of the Clinical Board and added to the risk register. He/she will take appropriate advice as necessary. If raised with the Board, follow up reports will be provided every 20 working days (Clinical Board Meeting - agenda item) until the risk is removed from the register. 3.2 Alerting Trust Management Where issues cannot be resolved at a service level and need raising with the Clinical Board, the LCA Clinical Director/ACD will inform the Medical Director and CEO of the relevant Trust and request a meeting.. The Trust will respond within 5 working days of receipt of the request. The remit of the meeting will be to review the current performance data and potential risks in order to revise the action plan. The Trust will agree to submit progress reports every 10 working days. Following the meeting, if the CEO / Medical Director are unable to provide assurance that that the Trust is able to deliver an effective action plan the issue should be escalated to the Members Board. 3.3 Clinical Board Oversight On the advice from the CD/ACD the Board will receive reports and determine when the actions required are completed and the issue can be removed from the risk register. 5

APRIL 2013 Where the Clinical Board is concerned about the failure of the Trust to comply with the agreed action plan with the agreed timeline the Board will ask the Chair of the Clinical Board, supported by the CD/ACD to raise the concerns directly with the Cancer Lead and the CEO. The Trust will respond within 5 working days of receipt of the request This will result in either: Agreement that adequate progress is being made against the action plan despite failure to meet timeline. The LCA will determine whether additional support is required to enable the Trust to improve performance or Decision that the Trust is failing to improve performance as required and that the issue will be escalated to the Members Board. 3.4 Escalation to the Members Board The Clinical Board will advise whether failure of the Trust to improve performance indicators following support from the Clinical Board should result in escalation to the Members Board. Risks and issues will be reported to the Members Board when: The risk/issue has not or cannot be resolved at Clinical Board level and requires the intervention of the Members Board The risk/issue is so significant that it needs to be brought to the attention of the Members Board, irrespective of on-going resolution The risk/issue falls outside the direct remit of the Clinical Board The Members Board will trigger appropriate action to resolve the issue with specified milestone dates. Where there is no resolution despite involvement of the Members Board the Clinical Board will provide clear advice about whether the continued failure of a Trust to meet performance standards on quality of services should result in the LCA informing the commissioners that there are serious concerns about the quality of cancer services at the relevant Trust and whether contracts should be withdrawn. Whilst this is the last resort and will happen rarely it is an important part of the system. If a member organisation fails to respond within the specified time period of the request, the LCA will escalate to next level. 3.5 Urgent Escalation In some cases, for example if patient safety is at risk urgent action may be needed. The CD/ACD will identify these issues and alert the Chair of the Clinical Board. The Clinical Board will send a formal letter to the Trust(s) Chief Executive(s) and Clinical Lead copied to the relevant pathway group chair and to the Chair of the Members Board outlining the concerns and setting a timescale for response as currently mandated by the peer review process where urgent issues are identified. The Trust will respond within 5 working days of receipt of the request. 6

ROLES AND RESPONSIBILITIES LCA will expect follow-up correspondence, within the requested timescales and the Clinical Director/Associate Clinical Director will organise an urgent meeting (within 5 working days) to discuss action. For issues of this degree of significance the Clinical Board will monitor progress and report monthly to the Members Board. 4 ROLES AND RESPONSIBILITIES 4.1 Clinical Director and Associate Clinical Director These are the key advisers to the Clinical Board and Members Board. They will work with Pathway Chairs and Clinical leads to identify issues of concern and determine proportionate action. To advise on progress against plans and whether this is satisfactory To trigger urgent escalation process for issues of major concern Represent the Clinical Board s view at the Members Board 4.2 Chair of Clinical Board Support the work of the Board and ensure CEOs are alerted to issues that might need their resolution or might affect patient safety or the reputation or financial position of the organisation. 4.3 Pathway Groups To be responsible for identifying pathway specific risks To agree mitigating actions for identified risks To monitor progress of mitigating actions at each pathway group meeting To ensure all risks are on the pathway risk register and that significant issues are also included on the LCA risk register Significant risks including those requiring immediate intervention should be discussed by the Pathway Group Chair with the Clinical Director or Associate Clinical Director with oversight for that group 4.4 Cross-cutting Groups To be responsible for identifying cross cutting risks To agree mitigating actions for identified risks To monitor progress of mitigating actions aimed at minimising risk at each cross cutting group meeting 7

To ensure all risks are on the pathway risk register and that significant issues are also included on the LCA risk register APRIL 2013 Significant risks including those requiring immediate intervention should be discussed by the Pathway Group Chair with the Clinical Director or Associate Clinical Director with oversight for that group 4.5 Clinical Board To review the LCA Performance Scorecard, concerns raised by Pathway or Cross-cutting Groups and progress against peer review and/ or other agreed action plans at agreed regular intervals To consider significant risks and performance issues on a monthly basis at the Clinical Board meeting To monitor progress of mitigating actions aimed at minimising risk on a monthly basis Where required, to agree interventions to address significant risks To identify risks that should be reported up to the Members Board To agree any required mitigating actions for these identified risks 4.6 Members Board To consider significant risks highlighted by the Clinical Board To monitor progress of mitigating actions aimed at minimising risk Where required, to agree interventions to address significant risks which may include notification of other parties including commissioners and the Care Quality Commission/ Monitor. Referenced documents Department of Health/Healthcare Quality Improvement Partnership (2011), Detection and Management of Outliers, DH, London National Cancer Action Team (2011) National Cancer Peer Review Programme: Handbook, NHS 8