“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

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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 Presentation

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Page 1: “Working together better” Dermatology 12 th  April 2007

“Working together better”Dermatology

12th April 2007

Catherine SmithClinical Lead for Dermatology

St Johns Institute of DermatologyGSTT

Page 2: “Working together better” Dermatology 12 th  April 2007

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

Page 3: “Working together better” Dermatology 12 th  April 2007

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

Page 4: “Working together better” Dermatology 12 th  April 2007

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

Page 5: “Working together better” Dermatology 12 th  April 2007

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

Page 6: “Working together better” Dermatology 12 th  April 2007

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

Page 7: “Working together better” Dermatology 12 th  April 2007

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

Page 8: “Working together better” Dermatology 12 th  April 2007

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

Page 9: “Working together better” Dermatology 12 th  April 2007

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

Page 10: “Working together better” Dermatology 12 th  April 2007

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

Page 11: “Working together better” Dermatology 12 th  April 2007

Inflammatory skin disease(ie: excluding benign skin lesions

and skin cancer)

Page 12: “Working together better” Dermatology 12 th  April 2007

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’)

Page 13: “Working together better” Dermatology 12 th  April 2007

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)

Page 14: “Working together better” Dermatology 12 th  April 2007

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

Page 15: “Working together better” Dermatology 12 th  April 2007

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

Page 16: “Working together better” Dermatology 12 th  April 2007

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%)

Page 17: “Working together better” Dermatology 12 th  April 2007

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)

Page 18: “Working together better” Dermatology 12 th  April 2007

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

Page 19: “Working together better” Dermatology 12 th  April 2007

Clinical News!

Page 20: “Working together better” Dermatology 12 th  April 2007

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 +

Page 21: “Working together better” Dermatology 12 th  April 2007

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

Page 22: “Working together better” Dermatology 12 th  April 2007

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

Page 23: “Working together better” Dermatology 12 th  April 2007

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

Page 24: “Working together better” Dermatology 12 th  April 2007

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

Page 25: “Working together better” Dermatology 12 th  April 2007

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

Page 26: “Working together better” Dermatology 12 th  April 2007

Key Recommendations of Skin Cancer IOG

Page 27: “Working together better” Dermatology 12 th  April 2007

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

Page 28: “Working together better” Dermatology 12 th  April 2007

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’).

Page 29: “Working together better” Dermatology 12 th  April 2007

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.

Page 30: “Working together better” Dermatology 12 th  April 2007

High risk BCCs• Histological subtype

– Morphoiec/infiltrating– Micronodular– Basosquamous

• Histological features– Invasion below dermis– Perineural invasion

• Site• Other factors

– Size, immunosuppression– recurrence