Interview questions Flashcards
(57 cards)
Explain why you would want to do clinical oncology as a career?
Interest in oncology
- MRes
- Clinical attachements
- Work as registrar
Quickly evolving field with many new treatments coming through
Ability to help and impact patients and make meaningful treatments
Follow patients through their treatment and help support them
Team working
Please outline a difficult case you have had to manage
GRI case
50 year old admitted with worsening neuropathic right arm pain
Previous visit to ED which on retrospect showed lesion at apex of right lung - awaiting CT thorax
On Ct thorax reported Friday afternoon - showed probable lung malignancy with erosion into T4 body with probably MSCC
Discussions with neurosurgery and oncology
Discussions with husband and wife and breaking bad news
Starting treatment
Please give an example of an mistake you have made and your actions following this
During receiving shift on a medical assessment ward a woman was referred in with a history of abdominal pain with a family history of AAA rupture from the rheumatology clinic
I was handed over to chase the report of the CT scan which in the conclusion did not show any evidence of acute coronary syndrome. However in the body for eh report it was noted that the Aorta was enlarged at around 6cm
The following day, the report was amended by the radiology consultant regarding this and advised urgent referral to the vascular service
Please describe a weakness of yours
Over critical
Self-confidence
Please give an example showing how you are a team player
While working in radiation oncology in NZ, we had a patient undergoing curative chemoradiotherapy for a HNSCC.
In the centre we treated patients for across a wide geographic area, and so some patients stayed in temporary accommodation while completed longer courses of radiotherapy
This patient did not have much family support with her and struggled through treatment with a number of side effects to be expected. She unfortunately did miss a number of fractions because of this.
We would see her regularly to evaluate her symptoms, and worked closely with the nurse specialists, radiotherapy technicians, nurses on the ward, cultural liaison for Maori people in the hospital as well as involving her family with her consent
Please give an example where you showed team leadership
Undertaking a respiratory QIP in the inhaler management of COPD to ensure up titration of inhaler therapy to triple therapy inhalers for COPD patients admitted to hospital
Working with pharmacists and more junior staff
Delegating jobs
Please give an example where you showed empathy
While covering medical HDU, there were a number of seriously ill patients, often at the ceiling of their care
A 55 year old man, very comorbid with servere LVSD and COPD was admitted from home with necrotising fasciitis, felt that would not be a surgical candidate due to comorbidities and had been having IV antibiotic treatment
Unfortunately was worsening despite this. His wife was with him
Spoke to her of his deterioration with nursing staff present
Offered support and to call his extended family
Offered chaplain
Would check on her throughout the evening
Organised room in the hospital for her to have a bed
Please explain a situation where you had to consent a patient in a vulnerable situation
Schizophrenia patient with fungating tumour
Patient in NZ with history of schizophrenia attended with CPN
Not sought medical treatment earlier, had been encouraged by CPN, but had been mistrustful and did not wish to seek advice
At point of referral had a large fumigating breast tumour, for which he had been prescribed a palliative dose of radiotherapy
Explained process and involved CPN
Invited questions
Tried to build rapport
Tell us what you know of the training programme in clinical oncology
Enter into ST3 oncology common stem year
- Development of CiPs related to areas of overlap between medical and clinical oncology
Requiring to enrol with the Royal College of Radiologists
Clinical oncology specific ST4-7
- Clinical oncology specific CiPs
Four exams to obtain FRCR (oncology):
- FRCR Part 1 - Oncology - investigation and management of cancer patients, tumour biology, mechanism of cytotoxic drugs, statistics and physics - usually done in ST4
- FRCR Part 2A - radiotherapy and drug therapy - Usually done in ST5-6
- FRCR Part 2B - Usually done in ST5-6
Tell us of your teaching experience
During university:
- SSC with university - anatomy demonstrator for medical/Dental and biomedical students, and clinical skills
Teach the teacher course online
Teaching at hospital:
- ICI with case study of triple M syndrome
Teaching medical students in hospital and online e.g. Haematology and oncology SBAs for medical finals - universities throughout the UK
Tell us the qualities of a good teacher
Sets specific and challenging goals
Able to give good quality feedback
Encouraging
Enthusiasm and shows enjoyment in their topic
Adapts the teaching for the students
Involving
Please describe your experiences with QIP/audits
QIP in F2:
- Immunisation in <5 year olds
Audit in radiation oncology:
- Treatment with RAI in thyroid cancer - presented at national meeting
Audit of ophthalmology reviews with hydroxychloroquine in a rheumatology department
QIP in resp:
- COPD
Difference between audit and research
Audit - Process comparing clinical practice against set standards
Research - Aimed to create new knowledge that can be used to develop new standards of car
Please outline your research experience
MRes
Attendance at journal clubs
Please outline why research is important in oncology
Evolving medical field, with many new treatments and technologies becoming available
New treatments help with patient survival and outcomes
Example in the ICIs
Please outline your interest in research
Know that it is important
Outline reasons you wouldn’t necessarily be involved in research
- Prefer to be patient facing
What is research governance
A framework setting out principles of good practice in the management and conduct of health and social care research in the UK
Full guidelines set out in the Health Research Authority document
Principles include safety, competence of the staff undertaking the trial, scientific and ethical conduct, patient, service user and public involvement and integrity quality and transparency
What is evidence based medicine
The use of best evidence in making decisions about the care of individual patients, alongside your own clinical expertise and judgement
This is applied to a specific case, taking into account patient values
What are the different levels of evidence available
1a. Systematic review or meta-analysis of RCTs
1b. At least one RCT
IIa. At least one well-designed controlled study without randomisation
IIb. At least one well designed quasi-experimental study e.g. cohort study
III Well designed non experimental descriptive studies e.g. comparative studies, correlation studies, case-control studies and case series
IV. expert committee reports, opinions and/or clinical experience of respected authorities
Please outline types of clinical trials
Randomised controlled study:
- Two or more study groups followed up over time which differ in interventions. Usually introduction of new therapy in one group with standard of care in other
- Can be blinded with use of placebo and double-blinded in which clinicians do not know where patients have been allocated
Cohort study:
- Follows a group of people over a period of time
- e.g. identifying risk factors over time in a population in who develops cancer
Case-controlled study:
- Looks at people who have a disease and assess against a control group over risk factors developing the disease. Opposite of cohort study
- Quicker and cheaper than cohort studies but often less reliable
Cross-sectional study:
- Carried out at one point in time, or over a short period of time. They find out who has been exposed to a risk factor and who has developed cancer, and see if there is a link.
What is clinical governance
Quality assurance process, in which clinicians should be involved to maintain and improve the quality of care that patients receive and ensure that the NHS is accountable to the public
Outline the ethical principles
Beneficence - act in patient’s best interest
Non-maleficence - do no harm to patients
Justice
Autonomy
Outline the different stages of clinical trials
Pre-clincial trials:
- animal models/ex-vivo/in-vivo/AI assisted
Phase I;
- Tests small number of people with trial drug to ensure safety and identify side effects, and identify dose
Phase II:
- Given to medium size group to identify effectiveness an for safety profiles
Phase III:
- Large groups comparing to gold standard treatment to identify effectiveness
Phase IV:
- Following approval of medication, long term study of side effects
How can you assess capacity
Understand
Weigh up risks
Retain
Communicate