2010 neurology curriculum

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Neurology August 2010 Page 1 of 46

SPECIALTY TRAINING CURRICULUM

FOR

NEUROLOGY

AUGUST 2010

Joint Royal Colleges of Physicians Training Board

5 St Andrews PlaceRegents Park

London NW1 4LB

Telephone: (020) 79351174Facsimile: (020)7486 4160Email: [email protected]

Website: www.jrcptb.org.uk


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Table of Contents1 Introduction........................................................................................................ 32 Rationale ........................................................................................................... 3

2.1 Purpose of the Curriculum .......................................................................... 32.2 Development............................................................................................... 3

2.3 Training Pathway........................................................................................ 32.4 Enrolment with JRCPTB ............................................................................. 42.5 Duration of Training .................................................................................... 42.6 Less Than Full Time Training (LTFT).......................................................... 42.7 Dual CCT.................................................................................................... 5

3 Content of Learning........................................................................................... 53.1 Programme Content and Objectives ........................................................... 53.2 Good Medical Practice................................................................................ 53.3 Syllabus...................................................................................................... 6

4 Learning and Teaching.................................................................................... 324.1 The Training Programme.......................................................................... 324.2 Teaching and Learning Methods............................................................... 32

4.3 Research .................................................................................................. 344.4 Academic Training .................................................................................... 35

5 Assessment..................................................................................................... 365.1 The Assessment System .......................................................................... 365.2 Assessment Blueprint ............................................................................... 375.3 Assessment Methods................................................................................ 375.4 Decisions on Progress (ARCP)................................................................. 395.5 ARCP Decision Aid ................................................................................... 415.6 Penultimate Year Assessment (PYA)........................................................ 425.7 Complaints and Appeals........................................................................... 42

6 Supervision and Feedback .............................................................................. 426.1 Supervision............................................................................................... 42

6.2 Appraisal................................................................................................... 437 Managing Curriculum Implementation ............................................................. 44

7.1 Intended Use of Curriculum by Trainers and Trainees .............................. 447.2 Recording Progress.................................................................................. 45

8 Curriculum Review and Updating .................................................................... 459 Equality and Diversity ...................................................................................... 45


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1 IntroductionNeurology is the specialty encompassing the diagnosis, investigation and long termmanagement of adults with neurological symptoms and diseases.

The specialty also involves the care of patients with stroke disease and sometrainees may elect to undertake an additional one year training scheme in strokemedicine to achieve subspecialty recognition. Some neurology trainees may alsoelect to undertake dual training in neurology and neurophysiology or othersubspecialty. Equally neurophysiology trainees complete 12 months training inneurology within the neurophysiology training programme.

2 Rationale

2.1 Purpose of the Curriculum

The purpose of this curriculum is to define the process of training and thecompetencies needed for the award of a certificate of completion of training (CCT) inneurology. This curriculum covers the period of training following successfulcompletion of both a two year Foundation Programme and a two year Core MedicalTraining (CMT) Programme, through to the recognised award of CCT.

The curriculum covers training for all four nations of the UK.

2.2 Development

This curriculum was developed in 2009 by the Specialty Advisory Committee (SAC)for neurology under the direction of the Joint Royal Colleges of Physicians TrainingBoard (JRCPTB). It was written by the curriculum sub-committee, which included

both a lay and trainee representative, and reviewed by the full SAC. It replaces theprevious version of the curriculum dated 2007, with changes to ensure the curriculummeets GMCs standards for Curricula and Assessment, and to incorporate revisionsto the content and delivery of the training programme. Major changes from theprevious curriculum include the incorporation of leadership, health inequalities andcommon competencies.

2.3 Training Pathway

Specialty training in Neurology consists of core and higher speciality training. Coretraining provides physicians with: the ability to investigate, treat and diagnose

patients with acute and chronic medical symptoms; and with high quality review skillsfor managing inpatients and outpatients. Higher speciality training then builds onthese core skills to develop the specific competencies required to practiseindependently as a consultant Neurologist.

Core training may be completed in a Core Medical Training (CMT) or Acute CareCommon Stem (ACCS) programme. The full curriculum for specialty training inNeurology therefore consists of the curriculum for either CMT or ACCS plus thisspecialty training curriculum for Neurology.

The approved curriculum for CMT is a sub-set of the Curriculum for General InternalMedicine (GIM). A Framework for CMT has been created for the convenience of

trainees, supervisors, tutors and programme directors. The body of the Frameworkdocument has been extracted from the approved curriculum but only includes the


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syllabus requirements for CMT and not the further requirements for acquiring a CCTin GIM.

For those trainees undertaking CMT or ACCS, acquisition of full MRCP (UK) will berequired before entry into Specialty training at ST3 (2011 onwards).

2.4 Enrolment with JRCPTB

Trainees are required to register for specialist training with JRCPTB at the start oftheir training programmes. Enrolment with JRCPTB, including the complete paymentof enrolment fees, is required before JRCPTB will be able to recommend trainees fora CCT. Trainees can enrol online at www.jrcptb.org.uk.

2.5 Duration of Training

Although this curriculum is competency based, the duration of training must meet theEuropean minimum of 4 years for full time specialty training adjusted accordingly forflexible training (EU directive 2005/36/EC). However the SAC has advised that

training from ST1 will usually be completed in 7 years in full time training (2 yearscore plus 5 years specialty training). This is because the SAC believe it will take 5years of full time specialty training for trainees to achieve all the competencies setout in this curriculum particularly in light of changes in training opportunities as theresult of the European Working Time Directives.

If trainees are undertaking sub-speciality training in Stroke Medicine, the SAC hasadvised a further 12 months training will be required to complete all the necessarycompetencies.

2.6 Less Than Full Time Training (LTFT)

Trainees who are unable to work full-time are entitled to opt for less than full timetraining programmes. EC Directive 2005/36/EC requires that:

LTFT shall meet the same requirements as full-time training, from which it willdiffer only in the possibility of limiting participation in medical activities.

FY2

MRCP

NeurologySpecialtyTraining

Core MedicalTraining or ACCS

Selection Selection

CCT after 84

months

Work place based assessments

SCE


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The competent authorities shall ensure that the competencies achieved and thequality of part-time training are not less than those of full-time trainees.

The above provisions must be adhered to. LTFT trainees should undertake a pro ratashare of the out-of-hours duties (including on-call and other out-of-hourscommitments) required of their full-time colleagues in the same programme and atthe equivalent stage.

EC Directive 2005/36/EC states that there is no longer a minimum time requirementon training for LTFT trainees. In the past, less than full time trainees were required towork a minimum of 50% of full time. With competence-based training, in order toretain competence, in addition to acquiring new skills, less than full time traineeswould still normally be expected to work a minimum of 50% of full time. If you arereturning or converting to training at less than full time please complete the LTFTapplication form on the JRCPTB website www.jrcptb.org.uk .

Funding for LTFT is from deaneries and these posts are not supernumerary. Ideally

therefore 2 LTFT trainees should share one post to provide appropriate servicecover.

Less than full time trainees should assume that their clinical training will be of aduration pro-rata with the time indicated/recommended, but this should be reviewedduring annual appraisal by their TPD and chair of STC and Deanery Associate Deanfor LTFT training. As long as the statutory European Minimum Training Time (ifrelevant), has been exceeded, then indicative training times as stated in curriculamay be adjusted in line with the achievement of all stated competencies.

2.7 Dual CCT

Trainees who wish to achieve a CCT in another speciality as well as neurology musthave applied for and successfully entered a training programme which wasadvertised openly as a dual training programme. Trainees will need to achieve thecompetencies, with assessment evidence, as described in both the neurology andsecond curricula. Individual assessments may provide evidence towardscompetencies from both curricula. Postgraduate Deans wishing to advertise suchprogrammes should ensure that they meet the requirements of both SACs.

If trainees wish to register for dual CCT following appointment to a ST3 post, this willneed approval of the deanery, STC Chair/TPD and SAC. It is not guaranteed thatpost JRCPTB enrolment requests will be granted.

3 Content of Learning

3.1 Programme Content and Objectives

The neurology syllabus below sets out the general and professional content, as wellas specialty specific (major topics and allied topics) content that need to bemastered. Demonstration of completion of all these competencies is required toachieve a CCT in neurology.

3.2 Good Medical Practice

In preparation for the introduction of licensing and revalidation, the General MedicalCouncil has translated Good Medical Practice into a Framework for Appraisal and


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Assessment which provides a foundation for the development of the appraisal andassessment system for revalidation. The Framework can be accessed athttp://www.gmc-uk.org/Framework_4_3.pdf_25396256.pdf

The Framework for Appraisal and Assessment covers the following domains:Domain 1 Knowledge, Skills and PerformanceDomain 2 Safety and QualityDomain 3 Communication, Partnership and TeamworkDomain 4 Maintaining Trust

The GMP column in the syllabus defines which of the 4 domains of the GoodMedical Practice Framework for Appraisal and Assessment are addressed by eachcompetency. Most parts of the syllabus relate to Knowledge, Skills andPerformance but some parts will also relate to other domains.

3.3 Syllabus

In the tables below, the Assessment Methods shown are those that are appropriateas possible methods that could be used to assess each competency. It is notexpected that all competencies will be assessed and that where they are assessednot every method will be used. See section 5.2 for more details.

The assessments are marked as mandatory (M) or recommended (R) within thesyllabus. This reflects the need for trainees to show competencies across the breadthof the curriculum with particular emphasis on the most important topics within thecurriculum. It is expected trainees produce evidence of at least one satisfactoryassessment from all the mandatory topics for the attainment of a CCT in neurology.

GMP defines which of the 4 domains of the Good Medical Practice Framework for

Appraisal and Assessment are addressed by each competency. See section 3.2 formore details.

The Medical Leadership Competency Framework, developed by the Academy ofMedical Royal Colleges and the NHS Institute for Innovation and Improvement, hasinformed the inclusion of leadership competencies in this curriculum. The Frameworkidentified possible assessment methods, but in reviewing these we identified a needfor more specific methods. JRCPTB and the RCP Education Department haveestablished a working group to develop and evaluate leadership assessmentmethods. These may include variants of CbD and ACAT, as well as the CaseConference Assessment Tool currently being piloted.


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Syllabus Content

1. General and Professional Content......................................................................... 91.1 History Taking.............................................................................................. 91.2 Neurological Examination ............................................................................ 9

1.3 Communication Skills .................................................................................. 91.4 Differential Diagnosis, Investigation and Initial Management ..................... 101.5 Personal qualities ...................................................................................... 101.6 Working with others ................................................................................... 111.7 Managing Services .................................................................................... 121.8 Improving Services .................................................................................... 121.9 Setting Direction ........................................................................................ 131.10 Clinical Pharmacology of Neurological Disorders..................................... 141.11 Presentation and Audit Skills ................................................................... 141.12 Special Interest Groups: Women & Pregnancy ........................................ 151.13 Special Interest Groups: Teenagers......................................................... 151.14 Special Interest Groups: Elderly............................................................... 16

1.15 Special Interest Groups: Learning Difficulties........................................... 161.16 Special Interest Groups: Terminally Ill...................................................... 16

2. Major Topics within Neurology Curriculum........................................................... 172.1 Head Injury................................................................................................ 172.2 Headache.................................................................................................. 172.3 Disorders of Consciousness ...................................................................... 172.4 Disorders of Sleep ..................................................................................... 182.5 Disorders of Higher Function & Behaviour ................................................. 182.6 Epilepsy and Loss of Consciousness......................................................... 192.7 Cerebrovascular Disease........................................................................... 192.8 Tumours of the NS, Neurological Complications of Systemic Cancer,

Complications of Treatment of Cancer...................................................... 20

2.9 Infections of Nervous System .................................................................... 202.10 CSF Disorders ......................................................................................... 212.11 Demyelination & Vasculitis....................................................................... 212.12 The Neurological Complications of Immunosuppression.......................... 212.13 Parkinsonism & Movement Disorders ...................................................... 222.14 Motor Neuron Disease............................................................................. 222.15 Toxic & Metabolic States ......................................................................... 222.16 Disorders of the Visual System................................................................ 232.17 Disorders of Cranial Nerves..................................................................... 232.18 Disorders of Spine, Spinal Cord, Roots and Spinal Injury ........................ 232.19 Disorders of Peripheral Nerve.................................................................. 242.20 Disorders of Automatic Nervous System.................................................. 242.21 Disorders of Muscle ................................................................................. 252.22 Pain......................................................................................................... 25

3. Allied Topics within Neurology Curriculum....................................................... 263.1 Clinical Neurophysiology............................................................................ 263.2 Neuroendocrinology................................................................................... 263.3 Neurogenetics ........................................................................................... 273.4 Neurointensive Care.................................................................................. 273.5 Neuro-otology ............................................................................................ 283.6 Neuropaediatrics ....................................................................................... 283.7 Neuropathology ......................................................................................... 283.8 Neuropsychiatry......................................................................................... 29

3.9 Neuropsychology....................................................................................... 293.10 Neuroradiology ........................................................................................ 29


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3.11 Neurorehabilitation................................................................................... 303.12 Neurosurgery........................................................................................... 303.13 Neurourology........................................................................................... 30


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1. General and Professional Content

1.1 History Taking

Knowledge AssessmentMethods

GMP

Ability to take a medical and neurological history. mini-CEX, CbD 1,2,3,4

Understand the differences between open and closed questioning. mini-CEX, CbD 1,2,3,4

Skills

Able to take an appropriate, focussed and comprehensive history,including where appropriate information from others, andcommunicate this verbally or in writing and in summary form.

mini-CEX, CbD (R) 1,2,3,4

Be aware of the possible influence of, and sensitively includequestions about, socio-economic status, household poverty,employment status and social capital in taking a medical history.

mini-CEX, CbD 1,3,4

Behaviours

Ability to listen and deal with complex patients (e.g. angry ordistressed patient). Appropriate use of an interpreter for patients &families when English is not their first language.

mini-CEX, CbD, MSF 1,2,3,4

Be aware of ones own behaviour and how it might impact onpatients health issues.

mini-CEX, CbD, PS 1,3

1.2 Neurological Examination


GMP

A thorough working knowledge of neuroanatomy. SCE, mini-CEX, CbD 1,2,3,4

Skills

Able to undertake an appropriate, focussed and comprehensiveexamination of mental and physical state and communicate thisverbally or in writing and in summary form.

mini-CEX, CbD (R) 1, 2,3,4

Behaviours

Use of chaperone where appropriate, respect for patients personaldignity.


Adopt assessments and interventions that are inclusive, respectful ofdiversity and patient-centred.

mini-CEX, CbD,MSF, PS

1,3

1.3 Communication Skills


GMP

Ability to communicate in English language verbally and in writing. mini-CEX, CbD 1,2,3,4

Skills

Use of a Dictaphone, discharge summaries, legibility of case notes.Ability to negotiate with patients, relatives and fellow healthcareprofessionals.


Consideration and time shown to those with visual and auditoryimpairments.


Communicate effectively with patients from diverse backgrounds and mini-CEX, CbD 1,3


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those with special communication needs, such as the need forinterpreters, etc.

Behaviours

Able to communicate effectively with the patient, their family andcarers and other staff in relation to the individual needs of the patient

and with appropriate regard for confidentiality. Individual cultural,religious & educational parameters must be taken into consideration.

MSF 1,2,3,4

Able to give a prognosis, to explain the patients condition, to breakbad news, to obtain full and informed consent for investigations andtreatment.

MSF 1,2,3,4

Able to inform concerning patient support groups and relevantcharities.

MSF 1,2,3,4

Able to summarise clinical case in a coherent manner to clinicalcolleagues.

MSF 1,2,3,4

1.4 Differential Diagnosis, Investigation and Initial Management


GMP

Knowledge of the different presentations of common and lesscommon neurological diseases.

SCE, mini-CEX, CbD 1,2,3,4

Understanding of the roles and usefulness of investigations includingneuroimaging and neurophysiology.

SCE, mini-CEX, CbD 1,2,3,4

Skills

Able to formulate an appropriately ordered differential diagnosisbased on an appreciation of the patient, their past history and currentproblems and their likely causes. Consideration given for differentracial, social & ethnic groups.

mini-CEX, CbD 1,2,3,4

Able to formulate a focussed and relevant series of investigations. mini-CEX, CbD 1,2,3,4

Adopt assessments and interventions that are inclusive, respectful ofdiversity and patient-centred.

mini-CEX, CbD

Behaviours

Able to plan and order appropriate observations, liaise with membersof the MDT, determine and prescribe immediate treatment, seekappropriate opinions and interventions and with others, develop anoverall plan for the individual patient.

MSF 1,2,3,4

Demonstrate leadership skills including mentorship of junior medicalcolleagues.

MSF 1,2,3,4

1.5 Personal qualities

Identify own strengths, limitations and the impact of their behaviour and is able to change theirbehaviour in light of feedback and reflection

Knowledge

AssessmentMethods

GMP

Demonstrates different methods of obtaining feedback. 1

Awareness of the trainees own values and principles and how thesemay differ from those of other individuals and groups.

MSF, CbD 1,3,4

The importance of best practice transparency and consistency. 1Skills


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Maintain and routinely practice critical self awareness, including beingable to discuss strengths and weaknesses with supervisor andrecognising external influences and changing behaviour accordingly.

1

Use assessment, appraisal, complaints and other feedback to discussand develop an understanding of own development needs.

1.3

Identify own strengths and weaknesses. MSF 1,3

Organise and manage workload effectively and flexibly. 1, 3

Behaviours

Recognising and showing respect for diversity and differences inothers.

1

Shows commitment to continuing professional development whichinvolves seeking training and self development opportunities, learningfrom colleagues and accepting criticism.

1,3

Demonstrate self management: organising and managing themselveswhile taking account of the needs and priorities of others.

CbD, PS 3

1.6 Working with others

Adopt a team approach, acknowledging and appreciating efforts, contributions andcompromises. Continue to recognise the common purpose of the team and respect theirdecisions

Knowledge

AssessmentMethods

GMP

Demonstrates a wide range of leadership styles and approaches andthe applicability to different situations and people.

1

Knowledge of the roles and importance of different members of the

MDT.

MSF 1,2,3,4

Skills

Enable individuals, groups and agencies to implement plans andmake decisions.

1,3

Assessment and appraisal of more junior clinical colleagues orstudents.

1, 3

Build and maintain relationships by listening, supporting others,gaining trust and showing understanding.

MSF 3

Shown willingness to act as a leader, mentor, educator and rolemodel.

MSF 3

Able to liaise with, refer to and communicate with all members of theMDT in a constructive and professional manner in the interests of thepatient and their carers.

MSF 1,2,3,4

Able to liaise with and understand the role of specialist nurses. MSF 1,2,3,4

Behaviours

Showing recognition of a team approach, respecting colleagues,including non-medical professionals.

1,3

Able to contribute to or lead a MDT meeting. MSF 1,2,3,4

Respect diversity of status and values in patients and colleagues. MSF, PS 1,3


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1.7 Managing Services

Support team members to develop their roles and responsibilities and continue to reviewperformance of the team members to ensure that planned service outcomes are met

Knowledge

AssessmentMethods

GMP

Demonstrate knowledge of relevant legislation and HR policies. 1

Show knowledge of the duties, rights and responsibilities of anemployer and co-worker.

1

Demonstrates knowledge of individual performance review. 1

Understand the roles, competences and capabilities of otherprofessionals and support workers.

1,3,4

Understand the role of audit (improving patient care and services, riskmanagement etc).

1

Understand the steps involved in completing the audit cycle. 1

Skills

Continue to contribute towards staff development and training,including mentoring, supervision and appraisal.

1,3

Able to write a job description, including person specification andshort listing criteria.

1

Contribute to the development of an organisational response toemerging health policy.

1

Behaviours

Commitment to good communication whilst also inspiring confidenceand trust.

1,3

Manage resources: know what resources are available and useinfluence to ensure that resources are used efficiently and safely.

1

Manage people: providing direction, reviewing performance andmotivating others.

1,3

Manage performance: hold oneself and others accountable forservice outcomes.

1,3

1.8 Improving Services

Ensure patient safety at all times, continue to encourage innovation and facilitate transformation

Knowledge

AssessmentMethods

GMP

Demonstrate knowledge of risk management issues and riskmanagement tools.

1,2

Demonstrates understanding of how healthcare governanceinfluences patient care.

1

Demonstrates a knowledge of a variety of methodologies fordeveloping creative solutions to improving services.

1,2

Recall principles of risk assessment and management. 1,2

Identify risk management guidance e.g. safe prescribing, sharpsdisposal, needlestick injury.

1,2

Skills


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Reports clinical incidents. 1,2

Be able to assess and manage risk to patients. 2

Monitors the quality of equipment and safety of the environmentrelevant to the specialty.

1,2

Ensure the correct and safe use of medical equipment, ensuringfaulty equipment is reported appropriately.

2

Questions existing practice in order to improve the services. 1,2

Behaviours

Seeks advice and or assistance whenever concerned about patientsafety.

1,2,3

Supports colleagues to voice new ideas and is open minded to newthoughts.

1,3

1.9 Setting Direction

Is able to identify the contexts for change and is able to make decisions

Knowledge

AssessmentMethods

GMP

Demonstrates knowledge of the functions and responsibilities ofnational bodies, College and faculties, representatives, regulatorybodies.

1

Demonstrates effective communication strategies withinorganisations.

1

Skills

The ability to discuss the local, national and UK health priorities and

how they impact on the delivery of health care relevant to thespecialty.

1

Is able to run committee meetings and work collegiately andcollaboratively with a wide range of people outside the immediateclinical setting.

1,3

Behaviours

Willingness to articulate strategic ideas and use effective influencingskills.

1,3

Willingness to participate in decision making processes beyond theimmediate clinical care setting.

1,3

Apply knowledge and evidence: gathering information to produce anevidence-based challenge to systems and processes in order toidentify opportunities for service improvements.

1

Make decisions: integrating values with evidence to inform decisions. 1, 3


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1.10 Clinical Pharmacology of Neurological Disorders


GMP

Principles of neuro-pharmacokinetics and pharmacodynamics. SCE, CbD 1,2,3,4

Understand principles of treatment especially vascular disease,migraine, epilepsy, pain, psychiatric disorders, movement disorders,multiple sclerosis, autoimmune disorders, infections, dementia, motorneuron disease.

SCE, CbD 1,2,3,4

Understand limitations: compliance, adverse effects, interactions, costimplications.

SCE, CbD 1,2,3,4

Skills

Able to plan and administer pharmacological treatments safely andeffectively.


Able to refer to local and national guidelines (NICE) and sources ofevidence and information about treatments.


Understand information needs of patients and others. mini-CEX, CbD (R) 1,2,3,4

Behaviours

Utilise reporting mechanisms for adverse events, both within anorganisation and to national bodies.

CbD 1,2,3,4

1.11 Presentation and Audit Skills


GMP

An understanding of the importance and processes of audit. AA 1,2,3

Skills

Ability to give a range of oral presentations with the use ofappropriate audio-visual aids including Powerpointpresentations.Presentations may involve clinical cases, audits or research papers.

TO 1,3

Ability to instigate and collate an audit project. AA 1,2,3

Ability to answer questions from members of the audience. TO

Behaviours

Ability to adjust level of presentation dependent upon the anticipatedaudience.

TO 1,3

Ability to reflect upon changes in patient management as the result ofa completed audit project.

AA 1,2,3


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Recognise how health systems can discriminate against patients from diversebackgrounds, and how to work to minimise this discrimination. For example, inrespect of age, gender, race, culture, disability, spirituality, religion and sexuality

1.12 Special Interest Groups: Women & Pregnancy


GMP

Understand the effects of menarche, menstrual cycle and menopauseon common neurological disorders.

SCE, CbD 1,2

Knowledge of methods of contraception, failure rate and interactionwith drugs (especially antiepileptic drugs); teratogenic risks ofcommonly prescribed drugs (especially AEDs) and genetic risks ofneurological diseases; presymptomatic/prenatal diagnosis ofneurological conditions; psychosexual dysfunction in neurologicalillness (especially epilepsy).

SCE, CbD 1,2

Understand the effect of pregnancy on existing neurological disordersand neurological disorders as complications of pregnancy.

SCE, CbD 1,2

Knowledge of the neonatal complications in offspring of affectedwomen with neurological conditions; effects of drugs on pregnancy(foetus and mother) and pregnancy on drugs.

SCE, CbD 1,2

Skills

Ability to evaluate, diagnose and manage women with neurologicaldisease.


Behaviours

Adherence to national guidelines (e.g. NICE guidelines for epilepsy,British National Formulary etc.

MSF 1,2,3,4

Ability to interface with obstetricians. MSF 1,2,3,4

1.13 Special Interest Groups: Teenagers


GMP

Knowledge of neurological disorders presenting in adolescence. SCE, CbD 1,2

Knowledge of childhood neurological disorders presenting in earlyadulthood.

SCE, CbD 1,2

(see neuropaediatric section)

Skills

Understand the special needs of teenagers, particular issues ofconfidentiality, and transition disorders.


Ability to evaluate, diagnose and manage teenagers with neurologicaldisease.


Behaviours

Ability to interface with paediatricians in the handover of patients frompaediatric to adult neurological practice.

MSF 1,2,3,4


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1.14 Special Interest Groups: Elderly


GMP

Understand the normal clinical and radiological findings in the elderly;

special presentations of neurological disease in the elderly; diagnosis,investigation and management of dementia; effects of drugs in theelderly; hospital based & community services; communication withrelatives and care agencies; role of departments of medicine for theelderly.

SCE, CbD 1,2

Skills

Understand the specific issues of the Mental Capacity Act in relationto this patient group.


Ability to evaluate, diagnose and manage the elderly with neurologicaldisease.


Behaviours

Ability to interface with geriatricians and care agencies dealing withthe elderly population.

MSF 1,2,3,4

1.15 Special Interest Groups: Learning Difficulties


GMP

Understanding of the common causes of learning difficulties and thedifferent presentation of symptoms in this group.

SCE, CbD 1,2

(see neuropaediatric section)

Recognise the stigmatising effects of some illnesses and work to helpin overcoming stigma. mini-CEX, CbD 1,2,3,4

Skills

Understand the needs of patients with special educational needs withneurological disorders. Understand the specific issues of the MentalCapacity Act in relation to this patient group.


Behaviours

Ability to interface with fellow professionals and care agencies dealingwith patients with learning difficulties.

MSF 1,2,3,4

1.16 Special Interest Groups: Terminally Ill


GMP

Understand end of life issues in neurological disorders and the role ofpalliative care services and specialist nurses; ethical and legalaspects of terminal care.

SCE, CbD 1,2

Skills

Ability to communicate end of life issues including the withdrawal oftreatment and organ donation with patients and relatives.


Behaviours

Ability to interface with fellow professionals and care agencies dealingwith patients with end of life issues. MSF 1,2,3,4


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2. Major Topics within Neurology Curriculum

2.1 Head Injury


GMP

Knowledge of symptoms and signs of head injury and itscomplications; indications for investigations; indications for medicalinterventions, ITU referral, urgent and delayed neurosurgery.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with acute head injury: performimmediate resuscitative measures; formulate a strategy for immediateand short term management; primary and secondary effects of headinjury.


Ability to evaluate and manage post traumatic change in

consciousness, behaviour and cognition, and other post-traumaticsymptoms (including epilepsy).


Ability to interface with neurosurgeons and ITU staff. mini-CEX, CbD (R) 1,2,3,4

Behaviours

Demonstration of relevant general and professional contentcompetencies.

MSF 1,2,3,4

2.2 Headache


GMP

Knowledge of the clinical features, differential diagnosis and specificpharmacological and general treatment of the causes of headacheand facial pain.

SCE, CbD 1,2

An understanding of the role of relevant investigations: brainscanning, urgent blood tests, lumbar puncture.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with headache & facial pains. mini-CEX, CbD (M) 1,2,3,4

Behaviours


MSF 1,2,3,4

2.3 Disorders of Consciousness


GMP

Knowledge of anatomy and physiology of consciousness, and thepathophysiology of disorders of consciousness; definitions, causes,pathophysiology, clinical features and prognosis of permanentvegetative state, locked in state and brainstem death.

SCE, CbD 1,2

An understanding of the legal issues relating to disorders ofconsciousness.

SCE, CbD 1,2

Skills

Ability to assess the unresponsive patient and to formulate plan ofinvestigation and management.

mini-CEX, CbD (M) 1,2,3,4


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Use of tests for brainstem death. mini-CEX, CbD (M) 1,2,3,4

Development of interpersonal skills for relating to management of thefamily of people with disorders of consciousness.


Behaviours


MSF 1,2,3,4

2.4 Disorders of Sleep


GMP

Knowledge of narcolepsy, daytime hypersomnolence, parasomnias,obstructive sleep apnoea, effects of neurological conditions on sleep;indications, scope and limitations of the sleep laboratory; principles ofphysical and pharmacological treatment.

SCE, CbD 1,2

An understanding of the effects of sleep on the EEG. SCE, CbD 1,2

Knowledge of driving regulations and the consequences andcomplications of sleep disorders.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with sleep disorders. mini-CEX, CbD (R) 1,2,3,4

Behaviours


MSF 1,2,3,4

2.5 Disorders of Higher Function & Behaviour


GMP

An understanding of memory, language, visuospatial function &behaviour; definition and epidemiology of dementia; pathology andclinical features of individual dementias; relevant investigations,specific treatments, genetic aspects, risks and costs of investigations;role of neuropsychological evaluation (inc. dementia and moodscales).

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with disordered higher function& behaviour.


Evaluation of competency (e.g. Mental Capacity Act, enduring powerof attorney).


Ability to work with community and support services. mini-CEX, CbD (R) 1,2,3,4

Behaviours


MSF 1,2,3,4


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2.6 Epilepsy and Loss of Consciousness


GMP

Knowledge of the differential diagnosis of paroxysmal and transient

events; scope and limitations of investigations; use of anti-epilepticdrugs; treatment of refractory seizures; serial seizures and statusepilepticus; role of epilepsy surgery.

SCE, CbD 1,2

Awareness of issues related to women and pregnancy, driving,vocation and sudden death; psychological and social consequencesof epilepsy especially teenagers.

SCE, CbD 1,2

Knowledge and management of other causes of loss ofconsciousness including syncope, drop attacks and vaso-vagalepisodes.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with epilepsy. mini-CEX, CbD (M) 1,2,3,4

Recognise that people can be denied employment opportunitiesunnecessarily through myths, stigma, dogma and insufficientadvocacy and support; be aware of the role of doctors and otherservices in combating this inequality.

mini-CEX, CbD 1,3,4

Behaviours


MSF 1,2,3,4

2.7 Cerebrovascular Disease

Knowledge Assessment

Methods

GMP

Knowledge of the cerebral circulation and its determinants;pathophysiology of cerebral infarction, cerebral haemorrhage,subarachnoid haemorrhage, cerebral venous thrombosis andvascular dementia.

SCE, CbD 1,2

Knowledge of the epidemiology, risk factors and their management;features of stroke /TIA, intracranial haemorrhage and venousthrombosis; investigation and management of acute stroke (includingthrombolysis) and TIA as medical emergencies; the role of medicalsecondary prevention and surgical interventions (e.g.hemicraniectomy, endartectomy).

SCE, CbD 1,2

An understanding of the role and limitation of imaging (e.g. CTA,

DWI); role of evaluation scales.

SCE, CbD 1,2

Cerebral aneurysm and AVM; interventional, surgical andradiotherapy treatment.

SCE, CbD 1,2

Multidisciplinary stroke care, organisation of stroke units, nutritionafter stroke, rehabilitation techniques, community stroke care.

SCE, CbD 1,2

Skills

Ability to work competently within a stroke MDT and on-call setting. MSF 1,2,3,4

Ability to evaluate and mange people with stroke disease CbD, mini-CEX (M) 1,2,3,4

Behaviours


MSF 1,2,3,4


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2.8 Tumours of the NS, Neurological Complications of Systemic Cancer,Complications of Treatment of Cancer


GMP

Neuropathological classification of brain tumours; clinical features of

the common tumours of the nervous system including malignantmeningitis.

SCE, CbD 1,2

Clinical features and immunology of paraneoplastic syndromes;benefits and risks of therapies including surgery and radiotherapy;neurological complications of chemotherapy and radiotherapy.

SCE, CbD 1,2

Understanding the role of the neuro-oncology MDT. SCE, CbD 1,2

Skills

Ability to evaluate and manage people with primary tumours of theNS or effects of systemic tumours or their treatment.


Behaviours


MSF 1,2,3,4

2.9 Infections of Nervous System


GMP

Principles of neurological infectious disease; clinical features of thesediseases and their causes (including meningitis, encephalitis, TB,HIV, neurosyphilis).

SCE, CbD 1,2

Diagnostic techniques and their appropriate use; anti-microbialtherapies and their use; the importance of liaison with infectious

disease physicians, microbiologists, public health and occupationalhealth medicine in relation to neurological infections.

SCE, CbD 1,2

Knowledge of prion disorders and its wider implications, such asinfection control risk.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with infections of NS.Demonstrate appropriate history and communication skills (i.e. sexualand travel history, or need for HIV testing) in a patient with suspectedNS infection.


Based on an understanding of risk, be able to apply epidemiologicalprinciples and public health approaches so as to reduce and prevent

disease and improve the health of populations.


Behaviours


MSF 1,2,3,4


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2.10 CSF Disorders


GMP

CSF composition and dynamics; anatomy and radiology of the

ventricular system; genesis of hydrocephalus; biochemistry andimmunology of CSF; blood brain barrier; indications, techniques, andcontraindications of CSF examination.

SCE, CbD 1,2

Methods of intracranial pressure monitoring; treatments of raisedintracranial pressure, management of shunts.

SCE, CbD 1,2

Skills

Able to evaluate and manage people with disorders of CSF includingdiagnostic and therapeutic lumbar punctures.

mini-CEX, CbD (R)

DOPS (R)

1,2,3,4

Behaviours

Demonstration of relevant general and professional content

competencies.

MSF 1,2,3,4

2.11 Demyelination & Vasculitis


GMP

Biology of demyelination & vasculitis; clinical features of multiplesclerosis, related demyelinating disorders and vasculitic and arteriticdisorders.

SCE, CbD 1,2

Management of specific impairments and disabilities arising in MS;role of disease modifying drugs, symptomatic treatments andtherapies.

SCE, CbD 1,2

Use of disability rating scales. SCE, CbD 1,2

Skills

Ability to evaluate & manage people with demyelinating & vasculiticdisorders.


Behaviours


MSF 1,2,3,4

2.12 The Neurological Complications of Immunosuppression


GMP

Principles of immune responses in relation to the NS; immunologicalbasis underlying auto-immune neurological disease; clinical featuresof these diseases; diagnostic techniques and their appropriate use.

SCE, CbD 1,2

Immunosuppressive and immunomodulatory therapies; their actions,side effects and indications.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with immunological disorderscaused by disease or treatment.


Behaviours

Demonstration of relevant general and professional content MSF 1,2,3,4


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competencies.

2.13 Parkinsonism & Movement Disorders


GMP

Clinical features and differential diagnosis of parkinsonism,chorea/athetosis, dystonia, tics and tremor; role of investigations indiagnosis (including DAT scans).

SCE, CbD 1,2

Treatment (and complications of treatment) of movement disorders;role of neurosurgical interventions.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with Parkinsonism andMovement Disorders.


Ability to liaise with other members of MDT (e.g. PD specialist nurse). mini-CEX, CbD (M) 1,2,3,4

Behaviours


MSF 1,2,3,4

2.14 Motor Neuron Disease


GMP

Clinical features and differential diagnosis of motor neuronsyndromes; disease modifying and symptomatic treatments (e.g.NIV).

SCE, CbD 1,2

Special issues of breaking bad news and prognosis; palliative care

aspects; knowledge of advanced directives and living wills.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with motor neuron disease. mini-CEX, CbD (M) 1,2,3,4

Behaviours


MSF 1,2,3,4

2.15 Toxic & Metabolic States


GMP

Biochemistry and neuropathology of exposure to alcohol and otherrecreational drugs (cocaine, amphetamine, opiates), heavy metals,pesticides and therapeutic agents; clinical features of alcohol,cocaine, opiate, amphetamine neurotoxicity; of heavy metal, CO, NOand organophosphate poisoning; of therapeutic agent neurotoxicity(e.g. vincristine, lithium, radiation).

SCE, CbD 1,2

Psychiatric morbidity associated with substance abuse. SCE, CbD 1,2

Neurological presentations of renal & hepatic failure, nutritionaldeficiencies and porphyria.

SCE, CbD 1,2

Role and value of blood and urine toxicology, imaging andneurophysiology; assessment of other organ damage; clinical

features and management of hyper/hypo-thermia, sodium, potassium,calcium and acid base disorders.

SCE, CbD 1,2


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Skills

Ability to evaluate and manage people with metabolic/toxic states. mini-CEX, CbD (R) 1,2,3,4

Behaviours


competencies.

MSF 1,2,3,4

2.16 Disorders of the Visual System


GMP

Applied anatomy and physiology of the visual and oculomotorsystems; clinical evaluation of the eye and adnexae, vision (acuity,fields and higher function); clinical features and conditions which mayaffect these systems.

SCE, CbD 1,2

Driving regulations. SCE, CbD 1,2

SkillsAbility to evaluate and manage people with disorders of the visualsystem including visual failure, oculomotor disorders & pituitarydisease.


Behaviours


MSF 1,2,3,4

2.17 Disorders of Cranial Nerves


GMP

Anatomy of the skull base, particularly the orbit, cavernous sinus,pituitary fossa, foramen magnum and jugular foramen; pathologicalprocesses involving cranial nerves and their central connections;clinical features & clinical assessment of cranial nerve function.

SCE, CbD 1,2

Management of cranial nerve disorders including multidisciplinaryapproaches to visual, hearing & balance, speech & swallowingdisorders.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with disorders of cranial nervefunction.


BehavioursDemonstration of relevant general and professional contentcompetencies.

MSF 1,2,3,4

2.18 Disorders of Spine, Spinal Cord, Roots and Spinal Injury


GMP

Anatomy of the spine, spinal cord, roots; clinical features of spinalcord, root and cauda equina syndromes; indications for urgentinvestigation; potential and limitations of spinal CT, MRI, myelographyand spinal angiography.

SCE, CbD 1,2

Emergency management of spinal cord or root compression, of spinalinjury; management of neck and low back pain and sciatica.

SCE, CbD 1,2


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Skills

Ability to evaluate and manage people with disorders of the spine,spinal cord and roots, and the acute & chronic consequences of acutespinal cord injury including effects of paralysis, autonomic dysfunctionand sensory loss.


Behaviours


MSF 1,2,3,4

2.19 Disorders of Peripheral Nerve


GMP

Anatomy and pathology of peripheral nerves; clinical features &investigation of genetic and acquired axonal and demyelinatingneuropathies, traumatic & entrapment neuropathies, plexopathies and

mononeuritis multiplex; management of Guillain-Barr syndrome andother severe paralysing neuropathies; general management of acuteneuromuscular paralysis.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with disorders of peripheralnerves (including plexus lesions).


Behaviours


MSF 1,2,3,4

2.20 Disorders of Automatic Nervous System


GMP

Anatomy and physiology of ANS; clinical features of ANS disordersalone and as part of other condition e.g. multi-system atrophy;investigations including autonomic function tests.

SCE, CbD 1,2

Pharmacological and physical managements of urinary retention,erectile disorder, constipation, postural hypotension, autonomicdysreflexia.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with disorders of the

autonomic nervous system.


Behaviours


MSF 1,2,3,4


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2.21 Disorders of Muscle


GMP

Clinical features and investigation of genetic and acquired disorders

of the neuromuscular junction and voluntary muscle including periodicdisorders and disorders of energy metabolism (e.g. mitochondrialdisorders).

SCE, CbD 1,2

Management including cardio-respiratory and anaestheticconsiderations.

SCE, CbD 1,2

Skills

Ability to evaluate and manage people with disorders of muscle. mini-CEX, CbD (R) 1,2,3,4

Behaviours


MSF 1,2,3,4

2.22 Pain


GMP

Theories of pain generation; pain patterns in neurological andsystemic diseases; effective use of pharmacological agents and othermeasures for pain relief including nerve blocks, TNS, acupunctureand neurosurgical interventions.

SCE, CbD 1,2

Role of Pain Clinic; psychological and social effects of chronic pain,understanding of MDT approach.

SCE, CbD 1,2

SkillsAbility to evaluate and manage people with neurological disorderscausing pain and common non neurological causes of pain includingmusculoskeletal disease.


Behaviours


MSF 1,2,3,4


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3. Allied Topics within Neurology Curriculum

3.1 Clinical Neurophysiology


GMP

EEG - normal range of EEG findings; common epileptiformabnormalities; capabilities and limitations in neurological disorders;role of monitoring techniques (telemetry, ambulatory); evaluation ofsleep disorders; neurological emergencies.

SCE, CbD 1,2

EMG/NCS/repetitive stimulation principles of techniques;abnormalities in common nerve entrapments, peripheralneuropathies; motor neuron disease; disorders of neuromuscularjunction; muscle disease.

SCE, CbD 1,2

Evoked potentials - common abnormalities in neurological diseases,

particularly demyelination; role of intraoperative EP.SCE, CbD 1,2

Skills

Understand role and practice of neurophysiological investigations indisorders of the nervous system; ability to interpret a neurophysiologyreport.

(see sections on epilepsy, sleep disorders, peripheral nerve andmuscle).


Ability to interface with neurophysiology colleagues. mini-CEX, CbD (M) 1,2,3,4

Behaviours


competencies.

MSF 1,2,3,4

3.2 Neuroendocrinology


GMP

Clinical features and investigations in endocrine disorders;emergency management of disorders; relationships with neurologicaldisorders.

SCE, CbD 1,2

Steroid therapy and its complications. SCE, CbD 1,2

Skills

Understand the principles of the NS in endocrine function andneurological features of endocrine disorder particularly pituitarydisease.


Ability to interface with endocrinological colleagues. mini-CEX, CbD (R) 1,2,3,4

Behaviours


MSF 1,2,3,4


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3.3 Neurogenetics


GMP

Basic genetic principles including inheritance patterns and common

diagnostic methods; roles of a detailed family history and of DNAbased diagnostic tests.

SCE, CbD 1,2

Genetic contribution to multifactorial neurological disease (e.g. stroke,multiple sclerosis, subarachnoid haemorrhage, epilepsy).

SCE, CbD 1,2

Clinical features of common genetic conditions (hereditary ataxias,Huntingtons disease, hereditary neuropathies, muscle diseases, andneurocutaneous syndromes).

SCE, CbD 1,2

An understanding of the role of bioinformatic databases of humandisease.

SCE, CbD 1,2

Skills

Understand the principles of genetics as applied to neurologicaldisorder; ability to interpret a genetics report.


Ability to counsel and consent patients and families prior toundergoing genetic testing.


Ability to interface with genetic colleagues. mini-CEX, CbD (M) 1,2,3,4

Behaviours


MSF 1,2,3,4

3.4 Neurointensive Care

Knowledge AssessmentMethods GMP

Clinical features, causes, investigation and management of coma(including epilepsy and raised intracranial pressure), failure to regainconsciousness and paralysis; diagnosis of and ability to define thevegetative state; management of status epilepticus; the principles ofcardiovascular and respiratory support; indications for and methods ofartificial nutrition.

(see sections on epilepsy, head injury & disorders of consciousness).

SCE, CbD 1,2

ICU neurological complications of major surgery, sepsis, drugs &medical disorders.

SCE, CbD 1,2

Clinical, legal and ethical issues in brain death, coma and vegetativestate.

SCE, CbD 1,2

Skills

Ability to evaluate and manage (with others) people in ICU. mini-CEX, CbD (M) 1,2,3,4

Ability to interface and communicate with patients, relatives and staffin ICU.


Behaviours


MSF 1,2,3,4


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3.5 Neuro-otology


GMP

Applied anatomy and physiology of hearing and balance; history and

examination techniques including vestibular manoeuvres; conditionsaffecting the vestibulocochlear system.

SCE, CbD 1,2

Skills

Ability to evaluate the deaf and / or dizzy person and interpret reportsincluding audiograms.


Ability to perform diagnostic and therapeutic vestibular manoeuvres. mini-CEX, CbD (R)

Ability to interface with ENT and audiological colleagues. mini-CEX, CbD (R)

Behaviours


MSF 1,2,3,4

3.6 Neuropaediatrics


GMP

Understanding of neurological disorders in intrauterine life andchildhood; key stages of development and range of normality;knowledge of developmental disorders (including effects ofintrauterine and perinatal factors on neural development), metabolicconditions, cerebral palsy, learning disability and autism.

SCE, CbD 1,2

Knowledge of paediatric conditions that can present in adulthood. SCE, CbD 1,2

Skills

Ability to evaluate and manage neurological disorders in teenagers inliaison with paediatric neurologists.


Ability to examine teenage children. mini-CEX, CbD (R) 1,2,3,4

Behaviours


MSF 1,2,3,4

3.7 Neuropathology


GMP

Understand the pathological and biochemical basis of neurologicaldisorders; anatomy of brain sections, brain preparation, histological,histochemical, immunocytochemical and E.M. techniques;biochemical, immunological & microbiological techniques; understandand interpret reports issued; role of and consent process for necropsyexamination: role of a coroner.

SCE, CbD 1,2

Skills

Ability to appropriately request pathological investigations andinterpret pathology reports.


Understand the importance of clinico-pathological conferences. mini-CEX, CbD (R) 1,2,3,4

BehavioursDemonstration of relevant general and professional content MSF 1,2,3,4


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competencies.

3.8 Neuropsychiatry


GMP

Understanding of common psychiatric disorders (including learningdisability), neurological features which may have psychiatric causes(including medically unexplained symptoms, conversion disorder,somatisation); the mental health act and when it can be used.

SCE, CbD 1,2

Skills

Ability to evaluate and interpret psychiatric symptoms in and aspresentations of neurological disorders, psychiatric consequences ofneurological disease and neurological features in people withpsychiatric disorders. Ability to evaluate and manage acute organicbrain syndromes.


Ability to liaise effectively and appropriately with psychiatry services. mini-CEX, CbD (R) 1,2,3,4

Behaviours


MSF 1,2,3,4

3.9 Neuropsychology


GMP

Understanding of neuroanatomical and neurophysiological basis ofmemory, attention, language and perception; understand the valueand limitations of neuropsychological interventions such as Cognitive

Behavioural Therapy; understand mini-mental state examination andbasic neuropsychological tests employed by Clinical Psychologists,e.g. NART, WAIS.

SCE, CbD 1,2

Skills

Ability to utilise basic clinical tests of cognitive function, tounderstand the need to refer to and the role of the ClinicalNeuropsychologist, and to interpret reports.


Behaviours


MSF 1,2,3,4

3.10 NeuroradiologyKnowledge Assessment

MethodsGMP

Request, interpret and utilise neuro-radiological investigationsappropriately; explain the nature, risks and benefits of neuro-radiological investigations (CT scan cranial/angiography, MR scancranial/spinal/angiography, catheter angiographydiagnostic/interventional, myelography, ultrasound carotid/trans-cranial/cardiac, other special investigations e.g. PET, SPECT) topatients.

SCE, CbD 1,2

Skills

Ability to request and evaluate neuroradiological investigations andreports; liaise effectively with the neuroradiologist; understand the



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role, risks and limitations of common techniques.

Behaviours


MSF 1,2,3,4

3.11 Neurorehabilitation


GMP

Understand the difference between pathology, impairment, activity &participation; understand the potential and limitations ofneurorehabilitation; understand the social perspective, relevant socialwork legislation and availability of care in the community.

SCE, CbD 1,2

Skills

Ability to evaluate the requirement for rehabilitation in people withneurological disorders (including stroke, head injury, spinal injury and

MS) in the context of a multidisciplinary team and make appropriatereferrals. Ability to perform and utilise a functional assessment.


Contribute to and, if appropriate, lead an MDT meeting being awareof the different roles, skills, approach and agenda of rehabilitationteams.


Behaviours


MSF 1,2,3,4

3.12 Neurosurgery

Knowledge AssessmentMethods GMP

Understand the role of neurosurgery in the management of headinjury, raised intracranial pressure, intracranial haemorrhage andischaemic stroke, aneurysm, vascular malformation and tumours,spinal cord and root disorder and peripheral nerve lesions.

SCE, CbD 1,2

Understand the purpose, limitations, process and complications ofbiopsy procedures (brain, muscle, nerve).

SCE, CbD 1,2

Understanding of the principles of general and specific risks andcomplications of neurosurgical interventions.

SCE, CbD 1,2

Skills

Ability to evaluate the requirement for neurosurgical interventions inpeople with neurological disorders and to liaise effectively with theneurosurgeon.


Behaviours


MSF 1,2,3,4

3.13 Neurourology


GMP

Understand normal control of micturition and sexual function;differential diagnosis of causes of disordered micturition and erectiledysfunction; understand hypo- and hyper-sexuality; understand

SCE, CbD 1,2


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treatment strategies for disorders of micturition and sexual function.

Skills

Ability to evaluate, manage and or refer people with disorderedmicturition and sexual function due to neurological disorder.


Ability to refer appropriately to Urology, Genitourinary Medicine orUroneurologist.


Behaviours


MSF 1,2,3,4


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4 Learning and Teaching

4.1 The Training Programme

The organisation and delivery of postgraduate training is the statutory responsibilityof the General Medical Council (GMC) which devolves responsibility for the localorganisation and delivery of training to the deaneries. Each deanery oversees aSchool of Medicine which is comprised of the regional Specialty TrainingCommittees (STCs) in each medical specialty. Responsibility for the organisation anddelivery of specialty training in neurology in each deanery is, therefore, the remit ofthe regional neurology STC. Each STC has a Training Programme Director whocoordinates the training programme in the specialty.

Clinical placements will usually be for between 3 and 12 months as directed by theSTC Chair/TPD and all trainees will spend time in a minimum of two neurologicaltraining sites. At least one site must include the allied specialties of neurosurgery,

neuroradiology, neurophysiology, neuropsychology and neuropathology.

All trainees should have exposure to a DGH type setting for the minimum of a 12month period or equivalent total time period. This setting may vary between differenttraining programmes, but for the purpose of this document is defined as a trainingsite with unselected neurological exposure and training opportunities.

All trainees will have the option of Out Of Programme Experience (OOPE)appropriate to their training needs and aspirations. This may include time spent inresearch or experience in other deaneries or overseas and will be determinedfollowing discussions between the trainee, their educational supervisor and STCChair/TPD. Prospective approval should be sought from GMC/JRCPTB to determineif time spent, and experience gained, during an OOPE can be counted towards theattainment of a CCT in neurology.

The sequence of training should ensure appropriate progression in experience andresponsibility. The training to be provided at each training site is defined to ensurethat, during the programme, the entire curriculum is covered and also thatunnecessary duplication and educationally unrewarding experiences are avoided.However, the sequence of training should ideally be flexible enough to allow thetrainee to develop a special interest.

4.2 Teaching and Learning MethodsThe curriculum will be delivered through a variety of learning experiences. Traineeswill learn from practice, clinical skills appropriate to their level of training and to theirattachment within the department.

Trainees will achieve the competencies described in the curriculum through a varietyof learning methods. There will be a balance of different modes of learning fromformal teaching programmes to experiential learning on the job. The proportion oftime allocated to different learning methods may vary depending on the nature of theattachment within a rotation.

This section identifies the types of situations in which a trainee will learn.


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Learning with Peers - There are many opportunities for trainees to learn with theirpeers. Local postgraduate teaching opportunities allow trainees of varied levels ofexperience to come together for small group sessions. Examination preparationencourages the formation of self-help groups and learning sets.

Trainees will be encouraged to create local forums for peer learning opportunities.These include trainee led journal clubs, discussion of cases and participation inregional or departmental grand round presentations

Work-based Experiential Learning - The content of work-based experientiallearning is decided by the local faculty for education but includes active participationin: Medical clinics including specialty clinics. After initial induction, trainees will

review patients in outpatient clinics, under direct supervision. The degree ofresponsibility taken by the trainee will increase as competency increases. Asexperience and clinical competence increase trainees will assess new andreview patients and present their findings to their clinical supervisor. It is

expected trainees will complete the equivalence of 2.5 out patient clinics perweek (max 4 per week) throughout the full training programme. 2 of these perweek will be general neurology clinics and the remainder will allow opportunitiesto attend sub-specialty clinics.

Specialty-specific takes Post-take consultant ward-rounds

Personal ward rounds and provision of ongoing clinical care on specialist medicalward attachments. Every patient seen, on the ward or in out-patients, provides alearning opportunity, which will be enhanced by following the patient through thecourse of their illness: the experience of the evolution of patients problems overtime is a critical part both of the diagnostic process as well as management.Patients seen should provide the basis for critical reading and reflection of clinical

problems. Consultant-led ward rounds. Every time a trainee observes another doctor,

consultant or fellow trainee, seeing a patient or their relatives there is anopportunity for learning. Ward rounds, including those post-take, should be led bya consultant and include feedback on clinical and decision-making skills. It isexpected trainees attend a minimum of 2 consultant-led ward rounds per weekthroughout the majority of time in training.

Multi-disciplinary team meetings. There are many situations where clinicalproblems are discussed with clinicians in other disciplines. These provideexcellent opportunities for observation of clinical reasoning.

Provision of a ward referral service for the in-patients of other hospital specialties.

The complexity of these will vary enormously and close supervision fromconsultants will ensure every training opportunity is realised. It is expectedtrainees keep a record of all ward referrals and on call emergency admissionsseen within their portfolios.

Trainees have supervised responsibility for the care of in-patients for a minimum of 2out of the 5 years training programme. This includes day-to-day review (i.e. providingcontinuity of care) of clinical conditions, note keeping, and the initial management ofthe acutely ill patient with referral to and liaison with clinical colleagues as necessary.The degree of responsibility taken by the trainee will increase as competencyincreases. There should be appropriate levels of clinical supervision throughouttraining with increasing clinical independence and responsibility as learning

outcomes are achieved (see Section 6.1 Supervision and Feedback).


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Formal Postgraduate Teaching The content of these sessions are determined bythe local faculty of medical education and will be based on the curriculum. There aremany opportunities throughout the year for formal teaching in the local postgraduateteaching sessions and at regional, national and international meetings. Many of theseare organised by the Royal Colleges of Physicians.

Suggested activities include:

A programme of formal bleep-free regular teaching sessions to cohorts oftrainees (e.g. a weekly core training hour of teaching within a Trust)

Case presentations Journal clubs

Research and audit projects

Lectures and small group teaching Grand Rounds

Clinical skills demonstrations and teaching Critical appraisal and evidence based medicine and journal clubs

Joint specialty meetings

Attendance at training programmes organised on a deanery or regional basis,which are designed to cover aspects of the training programme outlined in thiscurriculum.

The frequency, format and range of formal postgraduate teaching opportunities willvary between different training programmes and different clinical placements.

All trainees will be expected to attend the regional training days for neurologytrainees. It is expected a register of attendance at these training will be collated forthe STC Chair/TPD.

Independent Self-Directed Learning -Trainees will use this time in a variety of waysdepending upon their stage of learning. Suggested activities include: Reading, including web-based material

Maintenance of personal portfolio (self-assessment, reflective learning, personaldevelopment plan)

Audit and research projects Reading journals Achieving personal learning goals beyond the essential, core curriculum

Formal Study Courses - Time to be made available for formal courses isencouraged, subject to local conditions of service. Examples include managementcourses and communication courses.

Trainees will also be encouraged to attend relevant national training coursescovering the major topics within the curriculum utilising their study leave entitlements.

4.3 Research

Trainees who wish to acquire research competencies, in addition to those specifiedin their specialty curriculum, may undertake a research project as an ideal way ofobtaining those competencies. For those in specialty training, one option to beconsidered is that of taking time out of programme to complete a specified project orresearch degree. Applications to research bodies, the deanery (via an OOPR form)

and the JRCPTB (via a Research Application Form) are necessary steps, which arethe responsibility of the trainee. The JRCPTB Research Application Form can beaccessed via the JRCPTB website. It requires an estimate of the competencies that


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will be achieved and, once completed, it should be returned to JRCPTB together witha job description and an up to date CV. The JRCPTB will submit applications to therelevant SACs for review of the research content including an indicative assessmentof the amount of clinical credit (competence acquisition) which might be achieved.This is likely to be influenced by the nature of the research (e.g. entirely laboratory-based or strong clinical commitment), as well as duration (e.g. 12 month Masters, 2-year MD, 3-Year PhD). On approval by the SAC, the JRCPTB will advise the traineeand the deanery of the decision. The deanery will make an application to the GMCfor approval of the out of programme research. All applications for out of programmeresearch must be prospectively approved.

Upon completion of the research period the competencies achieved will be agreed bythe OOP Supervisor, Educational Supervisor and communicated to the SAC,accessing the facilities available on the JRCPTB ePortfolio. The competenciesachieved will determine the trainees position on return to programme; for example ifan ST3 trainee obtains all ST4 competencies then 12 months will be recognisedtowards the minimum training time and the trainee will return to the programme at

ST5. This would be corroborated by the subsequent ARCP.

This process is shown in the diagram below:

Funding will need to be identified for the duration of the research period. Traineesneed not count research experience or its clinical component towards a CCTprogramme but must decide whether or not they wish it to be counted on applicationto the deanery and the JRCPTB.

A maximum period of 3 years out of programme is allowed and the SACs willrecognise up to 12 months towards the minimum training times.

4.4 Academic Training

For those contemplating an academic career path, there are now well-defined postsat all levels in the Integrated Academic Training Pathway (IATP) involving the

OOPR Applicantseeks approvalfrom Deanery

Deanery granttime to go OOP

OOPR Applicantapplies to JRCPTBfor OOP approval

SAC decide onresearch content

OOPR Applicantobtainscompetencieswhilst OOP

SAC decide how manycompetencies can becounted towards minimumtraining time

OOP applicant returns toprogramme atappropriate competencylevel


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National Institute for Health Research (NIHR) and the Academy of Medical Sciences(AMS). For full details see http://www.nccrcd.nhs.uk/intetacatrain andhttp://www.academicmedicine.ac.uk/uploads/A-pocket-guide.pdf. Academic traineesmay wish to focus on education or research and are united by the target of aconsultant-level post in a university and/or teaching hospital, typically starting as asenior lecturer and aiming to progress to readership and professor. A postgraduatedegree will usually be essential (see out of programme experience) and academicmentorship is advised (see section 6.1). Academic competencies have been definedby the JRCPTB in association with AMS and the Colleges and modes of assessmenthave been incorporated in the latest edition of the Gold Guide (section 7, see http://www.jrcptb.org.uk/forms/Documents/GoldGuide2009.pdf).

Academic integrated pathways to CCT are a) considered fulltime CCTs as the defaultposition and b) are run through in nature. The academic programmes are CCTprogrammes and the indicative time academic trainees to achieve the CCT is thesame as the time set for non-academic trainees. If a trainee fails to achieve all therequired competencies within the notional time period for the programme, this would

be considered at the ARCP, and recommendations to allow completion of clinicaltraining would be made (assuming other progress to be satisfactory). An academictrainee working in an entirely laboratory-based project would be likely to requireadditional clinical training, whereas a trainee whose project is strongly clinicallyoriented may complete within the normal time (see the guidelines for monitoringtraining and progress)http://www.academicmedicine.ac.uk/careersacademicmedicine.aspx. Extension of aCCT date will be in proportion depending upon the nature of the research and willensure full capture of the specialty outcomes set down by the Royal College andapproved by GMC.

All applications for research must be prospectively approved by the SAC and the

regulator, see www.jrcptb.org.uk for details of the process.

5 Assessment

5.1 The Assessment System

The purpose of the assessment system is to: enhance learning by providing formative assessment, enabling trainees to receive

immediate feedback, measure their own performance and identify areas fordevelopment;

drive learning and enhance the training process by making it clear what is

required of trainees and motivating them to ensure they receive suitable trainingand experience;

provide robust, summative evidence that trainees are meeting the curriculumstandards during the training programme;

ensure trainees are acquiring competencies within the domains of Good MedicalPractice;

assess trainees actual performance in the workplace;

ensure that trainees possess the essential underlying knowledge required fortheir specialty;

inform the Annual Review of Competence Progression (ARCP), identifying anyrequirements for targeted or additional training where necessary and facilitatingdecisions regarding progression through the training programme;

identify trainees who should be advised to consider changes of career direction.


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The integrated assessment system comprises workplace-based assessments andknowledge based assessments. Individual assessment methods are described inmore detail below.

Workplace-based assessments will take place throughout the training programme toallow trainees to continually gather evidence of learning and to provide trainees withformative feedback. They are not individually summative but overall outcomes from anumber of such assessments provide evidence for summative decision making. Thenumber and range of these will ensure a reliable assessment of the training relevantto their stage of training and achieve coverage of the curriculum.

5.2 Assessment Blueprint

In the syllabus (3.3) the Assessment Methods shown are those that are appropriateas possible methods that could be used to assess each competency. It is notexpected that all competencies will be assessed and that where they are assessednot every method will be used.

5.3 Assessment Methods

The following assessment methods are used in the integrated assessment system:

Examinations

The Federation of Royal Colleges of Physicians of the UK, in association with theAssociation of British Neurologists (ABN) has developed a Specialty CertificateExamination. The SCE in neurology is a summative assessment that is a prerequisitefor attainment of the CCT.

The aim of this national assessment is to assess a trainees knowledge and

understanding of the clinical sciences relevant to specialist medical practice and ofcommon or important disorders to a level appropriate for a newly appointedconsultant.

Information about the SCE in neurology, including guidance for candidates, isavailable on the MRCP(UK) website www.mrcpuk.org

Workplace-based assessments

Multi-Source Feedback (MSF)

mini-Clinical Evaluation Exercise (mini-CEX) Direct Observation of Procedural Skills (DOPS) Case-Based Discussion (CbD) Patient Survey (PS) Audit Assessment (AA)

Teaching Observation (TO)

These methods are described briefly below. More information about these methodsincluding guidance for trainees and assessors is available in the ePortfolio and on theJRCPTB website www.jrcptb.org.uk. Workplace-based assessments should berecorded in the trainees ePortfolio. The workplace-based assessment methodsinclude feedback opportunities as an integral part of the assessment process. This isexplained in the guidance notes provided for the techniques.

Multisource Feedback (MSF)


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This tool is a method of assessing generic skills such as communication, leadership,team working, reliability etc, across the domains of Good Medical Practice. Thisprovides objective systematic collection and feedback o