“working together better” dermatology 12 th april 2007
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“Working together better” Dermatology 12 th April 2007. Catherine Smith Clinical Lead for Dermatology St Johns Institute of Dermatology GSTT. St Johns Institute of Dermatology: what are we?. Largest UK centre for patients with skin disease Clinical service (GSTT) - PowerPoint PPT PresentationTRANSCRIPT
“Working together better”Dermatology
12th April 2007
Catherine SmithClinical Lead for Dermatology
St Johns Institute of DermatologyGSTT
St Johns Institute of Dermatology: what are we?
• Largest UK centre for patients with skin disease
• Clinical service (GSTT)• Research (GKT, Kings College London)• Training and education
Clinical Service• General Dermatology• Specialist Services* Skin Cancer: lymphoma, melanoma Inflammatory Skin Disease: Psoriasis, Eczema Blistering disease Cutaneous Allergy: Contact dermatitis, urticaria Mastocytosis Genetic Skin Disease Vulval and Oral Dermatoses Specialised Diagnostic Laboratory services
*includes all those cited in the National Specialist Services Definition Set for Dermatology
Clinical Service: Access • General dermatology
– Standard referral letter– Choose and Book– Current waiting times 5-6 weeks for routine OPD
• Suspected skin cancer– via standard 2WW proforma
• Emergency referrals– On call SpR available 9am-9pm Monday to Friday 9am-1pm Saturday, Sunday
Current Issues for Dermatology Services: Background• ‘Our health, our care, our say: a new direction for community
services’ (2006)– ‘…to ensure the delivery of the most appropriate care to patients in the
most appropriate setting in clinical terms, whilst demonstrating the most effective use of available resources’
• New Targets– By 2008, no one will wait longer than 18 weeks from GP referral to
hospital treatment– 5 weeks for first outpatient consultation– 6 weeks for diagnostics
• New guidelines relevant to dermatology services – Improving Outcomes Guidance (IOG) for skin cancer (2006)– Management of paediatric atopic eczema (expected 2008)
• New funding arrangements – Payment By Results– Practice Based Commissioning
Drive for major service redesign and effective referral management
Current Issues for Dermatology Services: Background
• Dermatology services remain a major focus in the context of this agenda
• Two out of ‘Top Ten Tips’ in DOH guide to practice based commissioning focus on dermatology services
Nurse led community services for childhood atopic eczema
GPSI led ‘intermediary’ community services• Implications for Education, Training, Research and
provision of Specialist Services not addressed in detail
Plans and progress to date• Established Dermatology Steering Group • Purpose: to develop and implement strategy to ensure continued
access to comprehensive dermatology services for patients• Progress to date:
– Agree referral criteria for atopic dermatitis, psoriasis, acne (checklists)
– Agree conditions for which treatment is not available on the NHS – Audited current referral practice against national benchmarks to
meet demand management agenda– Develop strategy for training and education of primary health care
professionals
Methods• Proforma developed and reviewed by St Johns staff, PCT
(Southwark and Lambeth), interested GPs• Layout and data fields revised following pilot in 2 general
clinics • Period of data collection:
– 2 weeks– November 13th -24rd 2006– 16 lists cancelled due to A/L, S/L (representative)
• General clinics only• Proforma attached to all clinic notes• Data entry completed by clinicians in clinic• Entered onto spreadsheet; descriptive data analysis
Type of referral
• Total number of news 164 (41%) – Two week cancer wait 14– New 150– Re-referral 10
• Total number of follow ups 227 (59%)• New : follow up ratio 1.38
Completed proformas returned for 75% of those attending
Diagnosis*• Benign lumps & bumps 78• Cancer 98• Eczema 53• Psoriasis 35• Acne 19• Urticaria 10• Blisters 3• Leg ulcers 4• Other and not specified** 91
*Diagnosis following dermatology consultation** includes where no data entry given
Inflammatory skin disease(ie: excluding benign skin lesions
and skin cancer)
0
10
20
30
40
50
60
Psoriasis Eczema Acne Urticaria Blisters Leg Ulcer
No. patients
total followup
no data
Re-referral
New
No. of patients seen according to diagnostic category*
(*excluding benign lesions, skin cancer and ‘other’)
Number of follow up appointments
0
2
4
6
8
10
12
1 2nd 3rd 4th 5th 6-10. >10
Psoriasis
Eczema
AcneUrticaria
Blisters
Leg Ulcer
Number of follow up appointments
No. of patients*
(* Total number of follow ups seen in any of 6 diagnostic categories given = 128)
Indications for secondary care*(*as defined by PCDS/BAD guidelines)
0
5
10
15
20
25
Diagnostic uncertainty
Failure of topical Rx
Advice on topicals
Psychological/work impact
Exclude CD
Day unit Rx
Phototherapy
Systemic Rx
Admission
Unstable disease
EczemaPsoriasisAcne Urticaria
Summary (1)• Response rate 74%• 45% of total referrals seen relate to skin tumours
(benign and malignant)• Of the remaining 55% of patients seen, 29% (n=
114) had eczema, psoriasis and acne• New to follow up ratios are below national
average• A significant cohort of high need patients with
skin cancer, psoriasis and eczema are currently on continued, long term follow up in secondary care
Summary (2)
• Of those patients falling into one of the 6 primary diagnostic categories (eczema, psoriasis, acne, urticaria, blisters, leg ulcer, n= 131)– 81% fulfilled PCDS criteria for secondary care– 18% (n=24) no data available/no reason given– Commonest reasons cited for for secondary care
(across all skin diseases) were• Diagnostic uncertainty (30%)• Failure of topicals (23%)• Need for systemic or phototherapy (22%)• Psychological co-morbidity (8%)
Training and education
• 3 year GSTT charity funded bid developed in collaboration with Lambeth PCT, post graduate centre (VTS) and St Johns‘Improving dermatology training for general
practitioners’• Dermatology Care Module (Nursing and
Midwifery, KCL)
Other Service Developments• Skin Cancer
– Expansion of specialised dermatologic surgery provision– Rapid access skin cancer screening clinic – one of first four services to be integrated into the new cancer centre
(Guys)• Chronic skin disease
– Day Centre for high need patients – Nursing: outreach team, nurse consultant – Chronic disease management pathways
• Paediatric Dermatology– Paediatric Eczema Clinic– Paediatric Dermatology to be developed alongside Paediatric Allergy
services– Eczema education programme
• Capital projects: move of clinical services to Guys
Clinical News!
Biological therapies approved for psoriasis
generic name brand name
other name skin joints
T cell targeted
alefacept Amevive LFA3TIP +
efalizumab Raptiva anti CD11a +
TNF blockers
etanercept Enbrel TNF-R + +
infliximab Remicade anti-TNF + +
adalimumab Humira anti-TNF +
Qualifying clinical categories for patients with severe disease*
• At risk of developing (or has developed) clinically important drug-related toxicity
• Intolerant to standard therapy• Unresponsive to standard therapy • Disease only controlled by repeated inpatient Rx• Standard therapy contra-indicated due to co-existent co-
morbidity• Life threatening clinical situation• Associated psoriatic arthritis fulfilling the British Society
of Rheumatology eligibility criteria
*BJD 2005; 153:486-497
Toxicity: Anti TNFs versus EfalizumabAdverse effect Anti TNF therapy
(etanercept/infliximab)Efalizumab
Tuberculosis Yes – RR 4-8 x Not reported
Other infections Yes – listeriosis, hepatitis (B/C), HIV
Yes
Demyelination Yes ? RR ? Polyradiculopathy
Cardiac problems Yes ? RR Not reported
Thrombocytopenia No Yes 1:500 to 1:1000Drug hepatitis Yes NoDisease flare Not reported ‘efalizumab rash’
? PsAAll infections ? Size of riskCANCER ? Size of risk
Fewer patients treated overall with efalizumab compared to anti-TNF agents
NICE guidance on skin cancer• ‘Referral guidelines for suspected cancer’
– issued June 2005– covers all cancers (98 pages)– includes specific recommendations on skin– www.nice.org.uk/CG027
• ‘Improving outcomes for people with skin tumours including melanoma’ (IOG)– issued February 2006– huge document (177 pages)– www.nice.org.uk– 3 years allowed for full implementation from date of
publication
Referral guidelines for suspected cancer: skin cancer• Much of the guideline content is
incorporated into the IOG • Suspected melanomas and SCCs should
be referred urgently (ie 2 week cancer wait proformas)
• BCCs should be referred non urgently• Avoid excision of melanoma in primary
care
Referral guidelines for suspected cancer: pigmented lesions
7 point checklistMajor features (2)
– Change in size– Irregular shape– Irregular colour
Minor features (1)– > 7mm– Inflammation– Oozing– Sensation
Emphasis on observation over 8 weeks prior to referralfor low suspicion lesions
Key Recommendations of Skin Cancer IOG
MDT working
• Cancer Networks should establish two levels of skin cancer MDT – Local hospital based MDT (LSMDT) – Specialist MDTs based in Cancer Centres (SSMDT).
• All clinicians who treat patients with any type of skin cancer should be a member of a skin cancer MDT, whether they work in the community or in a hospital setting
• Expected attendance for GPs – 4x per year
Who can treat what and where?
Precancerous Lesions (AKs, Bowen’s) May be treated and followed up by any GP If there is doubt about the diagnosis the patient
should be referred to the local hospital skin cancer specialist.
Low risk BCC May be diagnosed, treated and followed up by a
doctor working in the community who is a member of the local MDT, or a hospital specialist (‘normally a Dermatologist’).
Who can treat what and where?
High risk BCC, SCC and MM • All patients with skin lesions which are
suspicious of these skin cancers, including all suspicious pigmented lesions and skin lesions where the diagnosis is uncertain , should be referred to a hospital specialist (Dermatologist).
• GPs will no longer ‘be allowed’ to treat these cancers.
High risk BCCs• Histological subtype
– Morphoiec/infiltrating– Micronodular– Basosquamous
• Histological features– Invasion below dermis– Perineural invasion
• Site• Other factors
– Size, immunosuppression– recurrence