setting up the service by lynn tobin. how did we get here? abundence of evidence providing...
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BOWEL CANCER-THE FACTS• THIRD MOST COMMON FORM OF
CANCER• SECOND LEADING CAUSE OF CANCER
RELATED DEATHS IN THE WEST• USUALLY ASYMPOTOMATIC IN EARLY
STAGES• 95% OF COLO-RECTAL CANCERS ARISE
FROM ADENOMATOUS POLYPS
BOWEL CANCER- THE FACTSIN THE UK1 IN 20 FEMALES AND 1 IN 18 MALES
WILL DEVELOP BOWEL CANCER IN THEIR LIFETIME
EVERY DAY 50 PEOPLE DIE FROM BOWEL CANCER
THIS EQUATES TO 18,000 DEATHS PER YEAR
C & M DUKES STAGES
• DUKES A = 53%• DUKES B = 21.4%• DUKES C = 21.4%• DUKES D = 4.2%• THESE STATS ARE BASED UPON THE
FIRST 115 PATIENTS IN THE PROGRAMME BUT WE HAVE HAD 247 CANCERS TO DATE
SETTING UP THE SERVICE
• PUT OVERALL PATHWAY SLIDE IN HERE
1st nurse clinic appointment letter sent to patient from Rugby
1st appointment nurse clinic
Referral forCT ACE
Patient refuses colonoscopy
Disclaimer
Unfit for colonoscopy
BOWEL CANCER SCREENING PROGRAMME PATIENT JOURNEY
DNA
Nurse to discuss assessmentwith BCSP clinician
Cancelled
NAD Polyps
Nurse telephoneClinic
Incomplete colonoscopy
Administrator to phone patient and offer new appointment
Suspected tumour Other
Referral to local MDT for CT
staging.Histology within 1
week.
Surveillance colonoscopy
Colonoscopy GP information fax
Intermediate risk polyp repeat colonoscopy 3
yearly
Ba Enemawithin 2 weeks
3 Year surveillance until 2 normal examinations
Rugby rebook 1st nurse clinic appointment
Routinescreening
2 year FOBTinvitation
Referral back to local speciality
Pre appointment
Day of appointment
Administrator to phone patient and offer new
appointment
High risk polyp repeat colonoscopy 1 year
Routine screening2 year FOBT
Invitation
Screening centre to offer 2nd
appointment
NAD Routine screening
2 Year FOBT invitation
Abnormal repeat colonoscopy
Low risk polyps routine screening 2 year FOBT
invitation
3 Yearly surveillance until2 normal examinations
Listed for colonoscopy
DNA
Attended
SETTING UP CLINICS.CONSIDERATIONS;• HOW MANY CLINICS WILL YOU NEED TO
FACILITATE YOUR POPULATION?• WHERE WILL YOU HOLD CLINIC?• IF YOU HAVE A SURGE IN FOBT + DO
YOU AVAILABILTY FOR EXTRA CLINICS?• DO YOUR PATIENTS HAVE A CHOICE OF
WHICH CLINIC THEY WISH TO ATTEND?
WHAT MUST BE IN PLACE BEFORE WE SEE A PATIENT• AGREED PATHWAYS/ PROFORMAS• AGREED MANAGEMENT PLANS FOR PATIENTS WITH
COMPLEX CO-MORBIDITY• PGD• TCI PATHWAY• ANTI-COAGULATION POLICY (NEW BSG GUIDELINES)• DIABETIC POLICY• NOMINATED LEADS FOR;• CT• X-RAY• PATHOLOGY• PHARMACY
WHAT DO I NEED TO BRING TO CLINIC WITH ME?
• PATIENT ASSESSMENT FORMS/LAPTOPS• MOBILE PHONES• PATIENT JOURNEY STORY BOOKS• AGREED HEALTH PROMOTION LEAFLETS• CONSENT INFORMATION LEAFLETS• RELEVENT LOCAL HOSPITAL INFORMATION• C&M HAVE CONDENSED THIS INFORMATION
INTO BOOKLETS SPECIFIC TO EACH SCREENING SITE
WHO IS INELIGABLE?
• IBD PATIENTS ALREADY IN SURVEILLANCE PROGRAMME
• BARIUM ENEMA WITH FLEXI SIGMOIDOSCOPY OR COLONOSCOPY WITHIN PAST 2 YEARS
• CURRENTLY UNDER TREATMENT FOR COLO-RECATL CANCER OR ALREADY IN SURVEILLANCE PROGRAMME
• TOTAL COLECTOMY
COMMONLY ASKED QUESTIONS/ANSWERS
• WHAT IS MY CHANCE OF HAVING;• CANCER = 1 IN 10 (10%)• POLYPS = 1 IN 4 (40%)• NORMAL RESULT = 1IN 5 (50%)
COMMONLY ASKED QUESTIONS/ANSWERS
• HOW MANY PEOPLE HAVE ABNORMAL FOBT RESULTS?
• 2 OUT OF 100 WILL HAVE ABNORMAL RESULTS SO 98 OUT OF 100 WILL BE NORMAL
HOW RELIABLE/EFFECTIVE IS THE FOBT TEST KIT?• PROS;• NON-INVASIVE• CAN DO AT HOME• REFLECTS COMPLETE
COLON• CHEAP AND EASY (£5)• COLONOSCOPY £424
• CONS;• POOR SENSITIVITY AND
SPECIFICITY• - 10% FOR Ca• - 40% FOR ADENOMAS• SENSITIVITY• 55-92% COLORECTAL
CANCERS• 10-32% ADENOMAS• 12-53% ADENOMAS
GREATER THAN 1 CM
COMMONLY ASKED QUESTIONS/ANSWERS
• IF MY COLONOSCOPY IS NORMAL, WILL YOU DO ANY FURTHER INVESTIGATIONS TO LOOK FOR POSSIBLE EXPLANATIONS OF FOBT POSITIVITY?
COLONOSCOPY
• INVESTIGATION DATASET• CONSENT• MDT PATHWAYS, REFERRAL FORMS AND
PATIENT CONTACT LETTERS POST SUSPECTED DIAGNOSIS USEFUL TO HAVE AT EACH SCREENING SITE.
• BCSP STAMPS• POST COLONOSCOPY DOCUMENTATION
POST COLONOSCOPY/TELEPHONE CLINICS• IT PROFORMAS• POST INVESTIGATION DATASET• SIGNED/DISCUSSED HISTOLOGY• 8 PATIENTS PER CLINIC WITH 20/30
MINUTE SLOTS (DEPENDING UPON EXPERIENCE OF SSP)
MALIGNANT POLYPS. WHO TELLS THE PATIENT?
• LIAISE WITH SCREENING CONSULTANT RE; MALIGNANT HISTOLOGY
• ASSESS SUITABILITY OF SSP GIVING THE RESULT
• BRING THE PATIENT INTO FACE TO FACE CLINIC
WHAT THE SSP MUST UNDERSTAND BEFORE GIVING MP DIAGNOSIS;• CLINICAL DETAILS• MACROSCOPIC DESCRIPTION• TYPE OF CARCINOMA• DIFFERENTIATION• RESECTION MARGINS• HAGITT STAGE• KIKUCHI STAGE• NO SPECULATION ON PART OF SSP